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Adult Stem Cell Therapy Tackles Diabetes Complications …

September 5th, 2015 5:47 am

By: Brenda Neugent

By Brenda Neugent

Despite a degree of controversy surrounding stem cell therapy, more scientists are starting to discover that adult stem cells are like tiny superheroes with the potential to ease the symptoms of a multitude of serious health problems.

Among the most effective uses for stem cells include inflammation-based diseases such as type 2 diabetes as well as autoimmune disorders like type 1 diabetes and rheumatoid arthritis.

Traditionally, the disease and its complication are treated with insulin as well as drugs that help reduce pain, protect organs and prevent additional damage by helping regulate blood glucose levels.

Adult stem cell therapy removes a patients stem cells stored in body fat and injects them into the abdomen where the majority of the immune system lives and helps treats most of the complications associated with diabetes.

Stem cells are like a small but powerful medical team, according to Dr. Todd Malan, the chief cell therapy at Okyanos, one of the leaders in stem cell technology. They are blank slates that can serve a wide range of purposes, including:

Repairing the lining of blood vessels so blood flows more smoothly. Because they increase blood flow, stem cells can also reverse damage to the beta cells of the pancreas tasked with making insulin, so there is more of the hormone available naturally; Improving the communication between cells, so cells are better able to take in glucose, reducing the amount of sugar in the blood; Restoring nerve function, so the pain of peripheral neuropathy is reduced; and Alleviating inflammation, lessening stress on the body and reducing the release of abnormal levels of inflammatory messengers.

Once the stem cells enter the body, they immediately realize where the bodys inflammation exists and heads there to fix it. This includes tissue repair, the creation of new blood vessels, building cartilage or muscles to fix the damage.

Adult stem cells can reverse, prevent and slow down much of the damage caused by high blood sugar levels.

Stem cells from your body are much better at the cell to cell communication, said Malan, and immediately realize they have a lot of jobs to do.

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Personalized Medicine Conferences | Europe | Worldwide …

September 5th, 2015 5:47 am

OMICS Internationalinvites all the participants across the globe to attend 3rd International Conference on Predictive, Preventive and Personalized Medicine & Molecular Diagnostics during September 01-03, 2015 Valencia, Spain.

Personalized Medicine 2015scientific program paves a way to gather visionaries through the research talks and presentations and put forward many thought provoking strategies in Personalized Medicine.

OMICS Internationalis devotedly involved in conducting International conferences 2014-2015 Europe, across USA (Baltimore, Chicago, Las Vegas, Philadelphia, and San Antonio) and almost all other parts of the world

Personalized Medicine 2015 will serve as an impulse for the advancement of molecular analysis by connecting scientists all across the world at conferences and exhibitions that would create an environment conducive for information exchange, generation of new ideas and acceleration of applications. Personalized Medicine promises many medical innovations, and has the potential to change the way treatments are discovered and used.

Personalized Medicine is referred as individualized therapy which means the prescription of specific treatments and therapeutics. Biomarker is a biological characteristic which can be molecular, anatomic, physiologic and chemical change drug development research which turns biomarkers into companion diagnostics. Personalized medicine therapeutics and companion diagnostic market have huge opportunities for growth in healthcare and will improve therapeutic effectiveness and reduce the severity of adverse effects approach to drug therapies. Personalized cancer medicine is self-made samples of translating cancer genetics into medical. Genomic medicine can contribute to personalized medicine Genomics by revealing genomic variations; have an effect on health, sickness and drug response.

Please, submit your abstract according to our format as early as possible and take advantage of early bird registration. All abstracts will be reviewed by the OCM/Review Panel.

As the hardest problem with science can only be solved by the Opencollaboration with Scientifc Community, Series of Conferences are Organized by Omics International Confereses, for more details have a glance atConference Series

Track 1:Current Focus on Personalized Medicine

Personalized medicine is an emerging practice of medicine that uses an individual's genetic profile to guide decisions made in regard to the prevention, diagnosis, and treatment of disease. Knowledge of a patient's genetic profile can help doctors select the proper medication or therapy and administer it using the proper dose or regimen. Used for the treatment asPersonalized cancer medicine,Diabetes- related disease: risk assessment & management,Personalized medicine: New strategies and economic implications,Implications of personalized medicine in treatment of HIV,Applications of personalized medicine in rare diseases,Translational Medicine.

Track 2:Clinical aspects of Personalized Medicine in Human, Animal models

Personalized medicine is based on intraspecies differences. It is axiomatic that small differences in genetic make-up can result in dramatic differences in response to drugs or disease andSocietal impact of personalized medicine. To express this in more general terms: in any given complex system, small changes in initial conditions can result in dramatically different outcomes. Despite human variability and intraspecies variation in other species, nonhuman species are still the primary model for ascertaining data forPersonalized medicine health improvement in Human.We call this practice into question and conclude that human-based research should be the primary means for obtaining data about human diseases and responses to drugs.Strategies in the development and application of personalized medicinewas developed for the accurate results inPersonalized medicine health improvement in Human and Animal Models.

Track 3:Genetics of Ebola Outbreak

Sequence analysis of Ebola virus Genomeis the second through the sixth genes of the Ebola virus (EBO) genome indicates that it is organized similarly to rhabdoviruses and paramyxoviruses and is virtually the same as Marburg virus (MBG). Scientists usedgenomic sequencing technologiesto identify the origin and track transmission of the Ebola virus in the current outbreak in Africa.

Track 4:Molecular Diagnostics and Therapeutics

Molecular diagnosticsis a technique used to analyzebiological markersin thegenomeandproteome,realizing the value of personalized medicinethe individual'sgenetic codeand how their cells express their genes asproteins, by applyingmolecular biologytomedical testing. The technique is used to diagnose and monitor disease, detect risk, and decide which therapies will work best for individual patients.Therapeutics and diagnosticsare useful in a range of medical specialisms, includinginfectious disease,oncology,human leukocyte antigentyping (which investigates and predictsimmune function),coagulation, and pharmacogenomicsthe genetic prediction of which drugs will work best and even leads totranslational research.

Track 5:Biomarkers

In medicine, abiomarkerand molecular markersare the measurableindicatorof the severity or presence of some disease state. More generally abiomarkeris anything that can be used as an indicator of a particular disease state or some otherphysiologicalstate of an organismDrug-Diagnostic Co-Development. In the current era of stratified medicine and biomarker-driven therapies, the focus has shifted from predictions based on the traditional anatomic staging systems to guide the choice of treatment for an individual patient to an integrated approach using the genetic makeup of the tumor and the genotype of the patient. Genomics and other "omics technologies have largely contributed to the identification and the development of biomarkers likeStratification biomarkers in personalised medicine. The recent surge in high-throughput sequencing of cancer genomes has supported an expanding molecular classification of cancer. These studies have identified putative predictive biomarkers signifying aberrant oncogene pathway activation and may provide a rationale for matching patients with molecularly targeted therapies in clinical trials. Here, we discuss some of the challenges of adapting these data for rare cancers or molecular subsets of certain cancers, which will require aligning the availability of investigational agents, rapid turnaround of clinical grade sequencing, molecular eligibility and reconsideringPersonalizing clinical trials with biomarkersdesign and end points.

Track 6:Nanotechnology and Biotechnology

Nanotechnology("nanotech") is the manipulation of matter on anatomic,molecular, and supramolecularscale. The earliest, widespread description of nanotechnologyreferred to the particular technological goal of precisely manipulating atoms and molecules for fabrication of macroscale products, also now referred to asmolecular nanotechnology. Applications of pharmaceutical nanotools,Cell based therapy,Molecular mechanismsare the techniques and tool in nano technology and biotechnology.

The human metabolome is best understood by analogy to the human genome, i.e., where the human genome is the set of all genes in a human being, the human metabolome is the set of all metabolites in a human being well understood by Role of Metabolics, Bioinformatics, Biosensorsin Personalized Medicine.

Track 7:Predictive Medicine in Pharmaceutical Analysis

Predictive medicineis a field ofmedicinethat entails predicting the probability ofdiseaseand instituting preventive measures in order to either prevent the disease altogether or significantly decrease its impact upon the patient (such as by preventingmortalityor limitingmorbidity).Techniques and assaysincludeNewborn screening,Diagnostic testing,Medical bioinformatics,Prenatal testing,Carrier testing,Preconception testing. Newborn screeningis apublic healthprogram designed to screen infants shortly after birth for a list of conditions that are treatable, but not clinically evident in the newborn period.Prenatal testing: Prenatal testing is used to look for diseases and conditions in a fetus orembryobefore it is born. This type of testing is offered for couples who have an increased risk of having a baby with a genetic or chromosomal disorder. Screening can determine the sex of the fetus.Prenatal testingcan help a couple decide whether toabortthe pregnancy. Like diagnostic testing,prenatal testingcan be noninvasive or invasive. Non-invasive techniques include examinations of the woman's womb throughor maternal serum screens. These non-invasive techniques can evaluate risk of a condition, but cannot determine with certainty if the fetus has a condition.

Track 8:Preventive Medicine

Preventive Medicine is practiced by all physicians to keep their patients healthy. It is also a unique medical specialty recognized by the American Board of Medical Specialties (ABMS). Preventive Medicinefocuses on the health of individuals, communities, and defined populations. It is also used for the treatment forobesity, blindness. TheEpidemiologyDivisionapplies research methods to understand the patterns and causes of health and disease in the populationandto translate this knowledge into programs designed to prevent disease. The division has a long history of involvement in NIH-sponsored multi-site, longitudinal cohort studies, and its faculty oversees many investigator-initiated, NIH-sponsored research projects and trials. Public trust invaccinesis a key to the success of immunization programs worldwide in the era of preventive medicine.

Track 9:Health Care Medicine and P4 Medicine

P4 Medicineis a plan to radically improve the quality of human life via biotechnology. P4 Medicine is a term coined by biologist Leroy Hood, and is short for "Predictive, Preventive, Personalized, andParticipatory Medicine." The premise of P4 Medicine is that, over the next 20 years, medical practice will be revolutionized by biotechnology, to manage a person's health, instead of manage a patient's disease.Internal medicineorgeneralmedicine(in Commonwealth nations) is themedicalspecialty dealing with the prevention, diagnosis, and treatment of adult diseases.Emergency medicineis amedicalspecialty involving care for adult and pediatric patients with acute illnesses or injuries that require immediatemedicalattention.

Track 10:Lifestyle Medicine

Lifestyle Medicine (LM) is the use of lifestyle interventions in the treatment andmanagement of disease. LM is becoming the preferred modality for not only the prevention but thetreatment of most chronic diseases, including Type-2 Diabetes, Coronary Heart Disease, Hypertension, Obesity, Insulin Resistance Syndrome, Osteoporosis, cancer prevention Alsoinclude Aerobic & Resistance exercises for patients with diabetes,Sleep and disease prevention, Intrinsic motivation and health behavior adherence.

Track 11:Genomics

Genomicsis a discipline ingeneticsthat appliesrecombinant DNA,DNA sequencingmethods, andbioinformaticsto sequence, assemble, and analyze the function and structure ofgenomes. Advances in genomics have triggered a revolution in discovery-based research to understand even the most complex biological systems such as the brain. The field includes efforts to determine the entireDNA sequenceandhuman genome varivationof organisms and fine-scalegenetic mapping. The field also includes studies of intragenomic phenomena such as other interactions betweenlociand within thegenome and metagenomics.Comparative genomicsis an exciting new field of biological research in which thegenomesequences of different species human, mouse and a wide variety of other organisms from yeast to chimpanzees are compared.

Track 12:Cancer Immunology & Oncology

Personalized medicine can be used to learn about a person's genetic makeup and to unravel thebiology of their tumor. Using this information, doctors hope to identify prevention, screening, andtreatment strategiesthat may be more effective and cause fewer side effects than would be expected with standard treatments. By performing more genetic tests and analysis, doctors may customize treatment to each patient's needs. Creating a personalized cancer screening and treatment plan includes: Determining the chances that a person will develop cancer and selectingscreening strategiesto lower the risk, Matching patients with treatments that are more likely to be effective and cause fewer side effects,Predicting the risk of recurrence(return of cancer).

Personalized medicine can be used to learn about a person's genetic makeup and to unravel the biology of their tumor. Using this information, doctors hope to identify prevention, screening, and treatment strategies that may be more effective and cause fewer side effects than would be expected with standard treatments. By performing more genetic tests and analysis, doctors may customize treatment to each patient's needs. Creating aPersonalized Cancer Medicineand treatment plan includes: Determining the chances that a person will develop cancer and selecting screeningstrategies to lower therisk, Matching patients with treatments that are more likely to be effectiveand cause fewer side effects, Predicting the risk of recurrence(return of cancer).

Personalized medicine is an evolving field of medicine in which treatments are tailored to the individual patient.Personalized Diagnosticsare medical devices that help doctors decide which treatments to offer patients and which dosage to give, tailored specifically to the patient, says Elizabeth A. Mansfield, Ph.D., Deputy Office Director for Personalized Medicine in FDAs Office of In Vitro Diagnostics and Radiological Health. The companion diagnostic is essential to the safe and effective use of the drug.

Personalized Medicine Diabetesis the use of information about the genetic makeup of a person with diabetes to tailor strategies for preventing, detecting, treating, or monitoring their diabetes. The practice of PMFD involves four processes. First is the identification of genes and biomarkers for diabetes as well as for obesity. Second, is allocation of resources to prevent or detect the diabetes and/or obesity phenotype in high-risk individuals, whose risk is based on their genotype. Third is selection of individualized therapies for affected individuals. Fourth is measurement of circulating biomarkers of diabetes to monitor the response to prevention or therapy.

Personalized Medicine World Conferencewill serve as an impulse for the advancement of molecular analysis by connecting scientists all across the world at conferences and exhibitions that would create an environment conducive for information exchange, generation of new ideas and acceleration of applications.Personalized Medicine Conferencepromises many medical innovations, and has the potential to change the way treatments are discovered and used.

Cancer chemotherapy is in evolution from non-specific cytotoxic drugs that damage both tumour and normal cells to more specific agents and immunotherapy approaches. Targeted agents are directed at unique molecular features of cancer cells, and immunotherapeutics modulate the tumour immune response; both approaches aim to produce greater effectiveness with less toxicity. The development and use of such agents in biomarker-defined populations enables a morePersonalized Medicine Oncologytreatment than previously possible and has the potential to reduce the cost of cancer care.

The term "personalized medicine" is often described as providing "the right patient with the right drug at the right dose at the right time." More broadly,personalized medicine(also known asprecision medicine)may be thought of as the tailoring of medical treatment to the individual characteristics, needs, and preferences of a patient during all stages of care, including prevention, diagnosis, treatment, and follow-up. International expertise Gathering onPersonalized Medicine World Congress.

Personalized medicine will shift medical practices upstream from the reactive treatment of disease, to proactive healthcare management including screening, early treatment, and prevention, and will alter the roles of both physician and patient. Personalized medicine requires a systems approach to implementation. But in a healthcare economy that is highly decentralized and market driven, it is incumbent upon the stakeholders themselves to advocate for a consistent set of policies and legislation that pave the way for the adoption of personalized medicine. To address this need, thePersonalized Medicine Coalition(PMC) was formed as a nonprofit umbrella organization of pharmaceutical, biotechnology, diagnostic, and information technology companies, healthcare providers and payers, patient advocacy groups, industry policy organizations, major academic institutions, and government agencies.

Pharmacogenomics is part of a field called personalized medicine, also called individualized or precision medicine, that aims to customize health care, with decisions and treatments tailored to each individual patient in every way possible.Although genomic testing is still a relatively new development in drug treatment, this field is expanding. Currently, more than 100 drugs have label information regardingPersonalized Medicine Pharmacogenomicsbiomarkers some measurable or identifiable segment of genetic information that can be used to direct the use of a drug.

Advances in human genome research are opening the door to a new paradigm for practicing medicine that promises to transform healthcare. Personalized medicine, the use of marker-assisted diagnosis and targeted therapies derived from an individual's molecular profile, will impact the way drugs are developed and medicine is practiced. The traditional linear process of drug discovery and development will be replaced by an integrated and heuristic approach. In addition,Personalized Medicine Patient Carewill be revolutionized through the use of novel molecular predisposition, screening, diagnostic, prognostic, pharmacogenomic and monitoring markers. Although numerous challenges will need to be met to make personalized medicine a reality, with time, this approach will replace the traditional trial-and-error practice of medicine.

Personalized lifestyle medicine is a newly developed term that refers to an approach to medicine in which an individual's health metrics from point-of-care diagnostics are used to develop lifestyle medicine-oriented therapeutic strategies for improving individual health outcomes in managing chronic disease.Personalized lifestyle medicinecan provide solutions to chronic health problems by harnessing innovative and evolving technologies based on recent discoveries in genomics, epigenetics, systems biology, life and behavioral sciences, and diagnostics and clinical medicine.

The US market for personalized medicines is predicted to grow at the compounded annual growth rate of 9.5% during 2010 to 2015. This growth in future is expected to be driven by different factors like cost savings on treatments, early diagnosis of disease, drug safety, patient compliance, and optimization of therapies. Currently, America dominates the market for personalized medicine; however, advancement in technology and developments in the field of DNA is expected to establishPersonalized Medicine Marketin UK, France, India, China, and Japan.

Rapid advances in technology have made it feasible to identify a persons unique genome. One person differs from another by millions of variations in the genome, and many of these variations affect susceptibility to disease and response to treatments.Greater understanding of individual genomes is allowing scientists and clinicians to begin to personalize" medicine. ThePersonalized Genomic Medicinerevolution will yield more effective medicines with fewer adverse side effects and lead to longer, healthier lives and lower health care costs. The personalized medicine industry in the United States already generates $286 billion per year in revenues and is growing by 11 percent annually, according to PricewaterhouseCoopers.Research at JAX Genomic Medicine will contribute to personalized medicine by revealing how genomic variations affect health, disease and drug response.

The globalPersonalized Medicine Industrywas valued at USD 1,007.88 billion in 2014 and is expected to reach USD 2,452.50 billion in 2022, growing at a CAGR of 11.8% over the forecast period. Key drivers of the market include growing development of next generation sequencing, whole genome technology, companion diagnostics and growing number of retail clinics.

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The Stem Cell Debate: Is it over? – Learn Genetics

September 4th, 2015 5:48 am

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Stem Cells

The Stem Cell Debate: Is It Over?

Stem cell therapies are not new. Doctors have been performing bone marrow stem cell transplants for decades. But when scientists learned how to remove stem cells from human embryos in 1998, both excitement and controversy ensued.

The excitement was due to the huge potential these cells have in curing human disease. The controversy centered on the moral implications of destroying human embryos. Political leaders began to debate over how to regulate and fund research involving human embryonic stem (hES) cells.

Newer breakthroughs may bring this debate to an end. In 2006 scientists learned how to stimulate a patient's own cells to behave like embryonic stem cells. These cells are reducing the need for human embryos in research and opening up exciting new possibilities for stem cell therapies.

Both human embryonic stem (hES) cells and induced pluripotent stem (iPS) cells are pluripotent: they can become any type of cell in the body. While hES cells are isolated from an embryo, iPS cells can be made from adult cells.

Until recently, the only way to get pluripotent stem cells for research was to remove the inner cell mass of an embryo and put it in a dish. The thought of destroying a human embryo can be unsettling, even if it is only five days old.

Stem cell research thus raised difficult questions:

With alternatives to hES cells now available, the debate over stem cell research is becoming increasingly irrelevant. But ethical questions regarding hES cells may not entirely go away.

For now, some human embryos will still be needed for research. iPS cells are not exactly the same as hES cells, and hES cells still provide important controls: they are a gold standard against which the "stemness" of other cells is measured.

Some experts believe it's wise to continue the study of all stem cell types, since we're not sure yet which one will be the most useful for cell replacement therapies.

An additional ethical consideration is that iPS cells have the potential to develop into a human embryo, in effect producing a clone of the donor. Many nations are already prepared for this, having legislation in place that bans human cloning.

Regulations and policies change frequently to keep up with the pace of research, as well as to reflect the views of different political parties. Here President Obama signs an executive order on stem cells, reversing some limits on federal research funding. (White House photo by Chuck Kennedy)

Governments around the globe have passed legislation to regulate stem cell research. In the United States, laws prohibit the creation of embryos for research purposes. Scientists instead receive "leftover" embryos from fertility clinics with consent from donors. Most people agree that these guidelines are appropriate.

Disagreements surface, however, when political parties debate about how to fund stem cell research. The federal government allocates billions of dollars each year to biomedical research. But should taxpayer dollars be used to fund embryo and stem cell research when some believe it to be unethical? Legislators have had the unique challenge of encouraging advances in science and medicine while preserving a respect for life.

U.S. President Bush, for example, limited federal funding to a study of 70 or so hES cell lines back in 2001. While this did slow the destruction of human embryos, many believe the restrictions set back the progress of stem cell research.

President Obama overturned Bush's stem cell policy in 2009 to expand the number of stem cell lines available to researchers. Policy-makers are now grappling with a new question: Should the laws that govern other types of pluripotent stem cells differ from those for hES cells? If so, what new legislation is needed?

APA format: Genetic Science Learning Center (2014, June 22) The Stem Cell Debate: Is It Over?. Learn.Genetics. Retrieved September 04, 2015, from http://learn.genetics.utah.edu/content/stemcells/scissues/ MLA format: Genetic Science Learning Center. "The Stem Cell Debate: Is It Over?." Learn.Genetics 4 September 2015 <http://learn.genetics.utah.edu/content/stemcells/scissues/> Chicago format: Genetic Science Learning Center, "The Stem Cell Debate: Is It Over?," Learn.Genetics, 22 June 2014, <http://learn.genetics.utah.edu/content/stemcells/scissues/> (4 September 2015)

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What is Biotechnology?

September 4th, 2015 5:44 am

Forty years ago, viable monoclonal antibodies, imperceptibly small magic bullets, became available for the first time. First produced in 1975 by Csar Milstein and Georges Khler at the Laboratory of Molecular Biology in Cambridge, England (where Watson and Crick unraveled the structure of DNA), Mabs have had a phenomenally far-reaching effect on our society and daily life. The Lock and Key of Medicine is the first book to tell the extraordinary yet unheralded history of monoclonal antibodies, or Mabs. Though unfamiliar to most nonscientists, these microscopic protein molecules are everywhere, quietly shaping our lives and healthcare. They have radically changed understandings of the pathways of disease, enabling faster, cheaper, and more accurate clinical diagnostic testing. And they lie at the heart of the development of genetically engineered drugs such as interferon and blockbuster personalized therapies such as Herceptin.

Historian of medicine Lara V. Marks recounts the risks and opposition that a daring handful of individuals faced while discovering and developing Mabs, and she addresses the related scientific, medical, technological, business, and social challenges that arose. She offers a saga of entrepreneurs who ultimately changed the healthcare landscape and brought untold relief to millions of patients. Even so, controversies over Mabs remain, which the author explores through the current debates on their cost-effectiveness.

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arthritis | disease | Britannica.com

September 3rd, 2015 1:44 pm

Arthritis,inflammation of the joints and its effects. Arthritis is a general term, derived from the Greek words arthro-, meaning joint, and -itis, meaning inflammation. Arthritis can be a major cause of disability. In the United States, for example, data collected from 2007 to 2009 indicated that 21 million adults were affected by arthritis and experienced limited activity as a result of their condition. Overall, the incidence of arthritis was on the rise in that country, with 67 million adults expected to be diagnosed by 2030. Likewise, each year in the United Kingdom, arthritis and related conditions caused more than 10 million adults to consult their doctors. Although the most common types of arthritis are osteoarthritis and rheumatoid arthritis, a variety of other forms exist, including those secondary to infection and metabolic disturbances.

Osteoarthritis, also known as degenerative joint disease, is the most common form of arthritis, affecting nearly one-third of people over age 65. It is characterized by joint pain and mild inflammation due to deterioration of the articular cartilage that normally cushions joints. Joint pain is gradual in onset, occurring after prolonged activity, and is typically deep and achy in nature. One or multiple joints may be affected, predominantly involving the knee, hips, spine, and fingers.

Approximately 90 percent of individuals experience crepitus (crackling noises) in the affected joint with motion. Muscle weakness and joint laxity or stiffness can occur as people become reluctant to move painful joints. Patients tend to have decreased joint stability and are predisposed to injuries such as meniscal and anterior cruciate ligament tears. Hip arthritis can affect gait, while arthritis of the hands can lead to decreased dexterity. Enlargement of the bony processes surrounding affected joints, called osteophytes (bone spurs), are common.

Joint trauma, increased age, obesity, certain genetic factors and occupations, and hobbies or sports that result in excessive joint stresses can result in the cartilaginous changes leading to osteoarthritis. Damage begins with the development of small cracks in the cartilage that are perpendicular to the joint. Eventually, cartilage erodes and breaks off, facilitating painful bone-on-bone contact. In due course, pathologic bony changes, such as osteophytes and subchondral bone cysts, develop and further restrict joint movement and integrity.

Osteoarthritis may be divided into two types, primary and secondary osteoarthritis. Primary osteoarthritis is age-related, affecting 85 percent of individuals 7579 years of age. Although the etiology is unknown, primary osteoarthritis is associated with decreased water-retaining capacity in the cartilage, analogous to a dried-up rubber band that can easily fall apart. Secondary osteoarthritis is caused by another condition, such as joint trauma, congenital joint malalignment, obesity, hormonal disorders, and osteonecrosis. Treatment for osteoarthritis is directed toward reducing pain and correcting joint mechanics and may include exercise, weight loss, nonsteroidal anti-inflammatory drugs, steroids, and total joint replacement surgery.

Autoimmune arthritis is characterized by joint inflammation and destruction caused by ones own immune system. Genetic predisposition and inciting factors, such as an infection or trauma, can trigger the inappropriate immune response. Rheumatoid arthritis, which is an autoimmune disease, is often associated with elevations in the serum level of an autoantibody called rheumatoid factor, whereas the seronegative arthropathies are not.

Rheumatoid arthritis is a progressive inflammatory condition that can lead to decreased mobility and joint deformities. The worldwide prevalence is 0.8 percent, with a 2:1 predilection for women over men. Disease onset, mainly occurring in the third and fourth decades of life, may be acute or slowly progressive with initial symptoms of fatigue, weakness, malaise, weight loss, and mild, diffuse joint pain. Rheumatoid arthritis tends to affect the hips, knees, elbows, ankles, spine, hands, and feet symmetrically. The disease course is characterized by periods of remission, followed by progressive exacerbations in which specific joints become warm, swollen, and painful. Morning stiffness, typically lasting about two hours, is a hallmark feature of rheumatoid arthritis. Patients with rheumatoid arthritis tend to complain of joint pain after prolonged periods of inactivity, whereas osteoarthritis is typically exacerbated with extended activity. Rheumatoid arthritis can be severely debilitating, resulting in a variety of deformities. Some patients experience complete remission, which typically occurs within two years of disease onset.

Although the exact cause is unknown, rheumatoid arthritis results from the inflammation of the tissues surrounding the joint space. The thin lining of the joint space becomes thick and inflamed, taking on the form of a mass with fingerlike projections (pannus), which invades the joint space and surrounding bone. Initially, this results in joint laxity. However, with progression, the bones can actually undergo fusion (ankylosis), limiting motion.

The effect rheumatoid arthritis has on the hands is a defining characteristic. Clinically, it can be distinguished from osteoarthritis based on the distribution of joints affected in the hands. Rheumatoid arthritis tends to affect the more proximal joints, whereas osteoarthritis tends to affect the more distal joints of the hands and fingers. In severe cases, joint laxity and tendon rupture result in a characteristic deformity of the fingers and wrist.

Rheumatoid nodules are thick fibrous nodules that form as a result of excessive tissue inflammation in rheumatoid arthritis. These nodules are typically present over pressure points, such as the elbows, Achilles tendon, and flexor surfaces of the fingers. Destruction of peripheral blood vessels (vasculitis) from the inflammatory process can occur in any organ, leading to renal failure, myocardial infarction (heart attack), and intestinal infarction (death of part of the intestine). In addition, rheumatoid arthritis is also associated with an increased risk of infections, osteoporosis (thinning of bones), and atherosclerosis (hardening of arteries).

Diagnosis of rheumatoid arthritis is based on the presence of several clinical features: rheumatoid nodules, elevated levels of rheumatoid factor, and radiographic changes. Although rheumatoid factor is found in 70 to 80 percent of people with rheumatoid arthritis, it cannot be used alone as a diagnostic tool, because multiple conditions can be associated with elevated levels of rheumatoid factor.

Since no therapy cures rheumatoid arthritis, treatment is directed toward decreasing symptoms of pain and inflammation. Surgical treatment may include total joint replacement, carpal tunnel release (cutting of the carpal ligament), and tendon repair. Hand splints are used to slow the progression of finger and wrist deformations.

The overall life span of individuals with rheumatoid arthritis is typically shortened by 510 years and is highly dependent on disease severity. Disease severity and the likelihood of extra-articular manifestations are each directly related to serum rheumatoid factor levels.

Several rheumatoid arthritis variants exist. In Sjgren syndrome the characteristic symptoms include dry eyes, dry mouth, and rheumatoid arthritis. Felty syndrome is associated with splenomegaly (enlarged spleen), neutropenia (depressed white blood cell levels), and rheumatoid arthritis. Juvenile rheumatoid arthritis is the most common form of childhood arthritis. Disease etiology and clinical course typically differ from that of adult-onset rheumatoid arthritis, and sufferers are prone to the development of other rheumatologic diseases, including rheumatoid arthritis.

Ankylosing spondylitis, Reiter syndrome, psoriatic arthritis, and arthritis associated with inflammatory bowel disease are a subset of conditions known as spondyloarthropathies. Typically affected are the sacrum and vertebral column, and back pain is the most common presenting symptom. Enthesitis, inflammation at the insertion of a tendon or ligament into bone, is a characteristic feature of spondyloarthropathy. Unlike rheumatoid arthritis, spondyloarthropathies are not associated with elevated levels of serum rheumatoid factor. Spondyloarthropathies occur most frequently in males and in individuals with a genetic variation known as HLA-B27.

Ankylosing spondylitis is the most common type of spondyloarthropathy, affecting 0.1 to 0.2 percent of the population in the United States. In a region of Turkey, prevalence was found to be 0.25 percent, and in the United Kingdom prevalence is estimated to range from 0.1 to 2 percent. In all regions, the condition occurs more frequently in males than in females and typically strikes between ages 15 and 40. Genetic studies have shown that more than 90 percent of all patients with ankylosing spondylitis who are white and of western European descent are HLA-B27 positive.

Ankylosing spondylitis is characterized by arthritis of the spine and sacroiliac joints. Extensive inflammation of the spinal column is present, causing a characteristic bamboo spine appearance on radiographs. Arthritis first occurs in the sacroiliac joints and gradually progresses up the vertebral column, leading to spinal deformity and immobility. Typical symptoms include back pain, which lessens with activity, and heel pain due to enthesitis of the plantar fascia and Achilles tendon. Hip and shoulder arthritis may occur early in the course of the disease.

Reiter syndrome, a type of reactive arthritis, is characterized by the combination of urethritis, conjunctivitis, and arthritis. Patients typically develop acute oligoarthritis (two to four joints affected) of the lower extremities within weeks of gastrointestinal infection or of acquiring a sexually transmitted disease. Reiter arthritis is not considered an infectious arthritis, because the joint space is actually free of bacteria. Instead, an infection outside the joint triggers this form of arthritis. Other symptoms can include fever, weight loss, back pain, enthesitis of the heel, and dactylitis (sausage-shaped swelling of the fingers and toes). Most cases resolve within one year; however, 1530 percent of patients develop chronic, sometimes progressive arthritis. Occurring almost exclusively in men, Reiter syndrome is strongly linked to the HLA-B27 gene variant, which is present in 65 to 96 percent of symptomatic individuals.

Psoriasis is an immune-mediated inflammatory skin condition characterized by raised red plaques with an accompanying silvery scale, which can be painful and itchy at times. Though typically seen on the elbow, knees, scalp, and ears, plaques can occur on any surface of the body. About 10 percent of people with psoriasis (possibly as many as 30 percent in some regions of the world) develop a specific type of arthritis known as psoriatic arthritis.

Psoriatic arthritis typically occurs after psoriasis has been present for many years. In some cases, however, arthritis may precede psoriasis; less often, the two conditions appear simultaneously. Estimates on the prevalence of psoriatic arthritis vary according to population. However, overall, it is thought to affect nearly 1 percent of the general population, with a peak age of onset between 30 and 55. Usually less destructive than rheumatoid arthritis, psoriatic arthritis tends to be mild and slowly progressive, though certain forms, such as arthritis mutilans, can be quite severe. Occasionally the onset of symptoms associated with psoriatic arthritis is acute, though more often it is insidious, initially presenting as oligoarthritis with enthesitis. Over time, arthritis begins to affect multiple joints (polyarthritis), especially the hands and feet, resulting in dactylitis. Typically, the polyarticular pattern of psoriatic arthritis affects a different subset of finger joints than rheumatoid arthritis. It is not until years after peripheral arthritis has occurred that psoriatic arthritis may affect the axial joints, causing inflammation of the sacroiliac joint (sacroiliitis) and intervertebral joints (spondylitis).

Arthritis mutilans is a more severe and much less common pattern (seen in fewer than 5 percent of psoriatic arthritis cases) resulting in bone destruction with characteristic telescoping of the fingers or toes. In addition, individuals with psoriatic arthritis necessitate more aggressive treatment if the onset of the condition occurs before age 20, if there is a family history of psoriatic arthritis, if there is extensive skin involvement, or if the patient has the HLA-DR4 genotype.

Crohn disease and ulcerative colitis, two types of inflammatory bowel disease, are complicated by a spondyloarthropathy in as many as 20 percent of patients. Although arthritis associated with inflammatory bowel disease typically occurs in the lower extremities, up to 20 percent of cases demonstrate symptoms identical to ankylosing spondylitis. Arthritis is usually exacerbated in conjunction with inflammatory bowel disease exacerbations and lasts several weeks thereafter.

Joint inflammation, destruction, and pain can occur as a result of the precipitation of crystals in the joint space. Gout and pseudogout are the two primary types of crystalloid arthritis caused by different types of crystalloid precipitates.

Gout is an extremely painful form of arthritis that is caused by the deposition of needle-shaped monosodium urate crystals in the joint space (urate is a form of uric acid). Initially, gout tends to occur in one joint only, typically the big toe (podagra), though it can also occur in the knees, fingers, elbows, and wrists. Pain, frequently beginning at night, can be so intense that patients are sensitive to even the lightest touch. Urate crystal deposition is associated with the buildup of excess serum uric acid (hyperuricemia), a by-product of everyday metabolism that is filtered by the kidneys and excreted in the urine. Causes of excess uric acid production include leukemia or lymphoma, alcohol ingestion, and chemotherapy. Kidney disease and certain medications, such as diuretics, can depress uric acid excretion, leading to hyperuricemia. Although acute gouty attacks are self-limited when hyperuricemia is left untreated for years, such attacks can recur intermittently, involving multiple joints. Chronic tophaceous gout occurs when, after about 10 years, chalky, pasty deposits of monosodium urate crystals begin to accumulate in the soft tissue, tendons, and cartilage, causing the appearance of large round nodules called tophi. At this disease stage, joint pain becomes a persistent symptom.

Gout is most frequently seen in men in their 40s, due to the fact that men tend to have higher baseline levels of serum uric acid. In the early 21st century the prevalence of gout appeared to be on the rise globally, presumably because of increasing longevity, changing dietary and lifestyle factors, and the increasing incidence of insulin-resistant syndromes.

Pseudogout is caused by rhomboid-shaped calcium pyrophosphate crystals deposition (CPPD) into the joint space, which leads to symptoms that closely resemble gout. Typically occurring in one or two joints, such as the knee, ankles, wrists, or shoulders, pseudogout can last between one day and four weeks and is self-limiting in nature. A major predisposing factor is the presence of elevated levels of pyrophosphate in the synovial fluid. Because pyrophosphate excess can result from cellular injury, pseudogout is often precipitated by trauma, surgery, or severe illness. A deficiency in alkaline phosphatase, the enzyme responsible for breaking down pyrophosphate, is another potential cause of pyrophosphate excess. Other disorders associated with synovial CPPD include hyperparathyroidism, hypothyroidism, hemochromatosis, and Wilson disease. Unlike gout, pseudogout affects both men and women, with more than half at age 85 and older.

Infectious arthritides are a set of arthritic conditions caused by exposure to certain microorganisms. In some instances the microorganisms infiltrate the joint space and cause destruction, whereas in others an infection stimulates an inappropriate immune response leading to reactive arthritis. Typically caused by bacterial infections, infectious arthritis may also result from fungal and viral infections.

Septic arthritis usually affects a single large joint, such as the knee. Although a multitude of organisms may cause arthritis, Staphylococcus aureus is the most common pathogen. Neisseria gonorrhoeae, the bacteria that causes gonorrhea, is a common pathogen affecting sexually active young adults.

The most common way by which bacteria enter the joint space is through the circulatory system after a bloodstream infection. Microorganisms may also be introduced into the joint by penetrating trauma or surgery. Factors that increase the risk of septic arthritis include very young or old age (e.g., infants and the elderly), recent surgery or skin infection, preexisting arthritic condition, immunosuppression, chronic renal failure, and the presence of a prosthetic joint.

Postinfectious arthritis is seen after a variety of infections. Certain gastrointestinal infections, urinary tract infections, and upper respiratory tract infections can lead to arthritic symptoms after the infections themselves have resolved. Examples include Reiter syndrome and arthritis associated with rheumatic fever.

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Arthritis | ASPCA

September 3rd, 2015 1:44 pm

Canine arthritis, also known as osteoarthritis or degenerative joint disease, is characterized by pain and inflammation in a dogs joints. Arthritis is caused by the breaking down of smooth cartilage that covers and protects the bones that form a joint. Once the bones are exposed, painful wear and tear can occur.

Dogs who have canine arthritis may:

A veterinarian may conduct a physical exam, take radiographs and perform other diagnostic tests to help determine the cause of your dogs pain. He or she will also check your dogs medical history for previous injuries and consider possible inherited conditions.

Canine arthritis can occur as a result of:

Note: If a larger dog suffers any injuries or sprains during his growth period, this can cause him to develop arthritis later in life.

Although certain larger breed dogs such as mastiffs and Great Danes are susceptible to arthritis, the condition can develop in all breeds and mixed breeds as the result of joint infection, dislocation, trauma or family genetics. Elder dogs also often develop arthritis as a result of aging.

Keeping your dog fit with exercise and proper nutrition may, in some cases, help prevent arthritis, or possibly slow its progression once the condition has set in. In fact, if your dog is a larger breed, it's necessary to monitor the type and amount of food given when his bones are still growing. However, arthritic conditions cannot always be predicted or prevented, especially those that are inherited.

Once symptoms of arthritis set in, there is no cure. Its important for you to work with your veterinarian to create a program to minimize your dogs pain while keeping him healthy. Some general treatment options may include:

Note: Please do not give your dog human medication without first checking with your vet.

Generally, dogs with arthritis should engage in daily low-impact exercise such as walking or, if possible, swimming.

If your dog has arthritis, here are a few ways that you can make her more comfortable.

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Rheumatoid Arthritis: Medication, Treatment and Diet Facts

September 3rd, 2015 1:44 pm

Rheumatoid Arthritis Rheumatoid Arthritis Overview

Rheumatoid arthritis is a chronic joint disease that damages the joints of the body. It is also a systemic disease that potentially affects internal organs of the body and leads to disability. The joint damage is caused by inflammation of the joint lining tissue. Inflammation is normally a response by the body's immune system to "assaults" such as infections, wounds, and foreign objects. In rheumatoid arthritis, the inflammation is misdirected to attack the joints. Rheumatoid arthritis is often referred to as RA.

Rheumatoid arthritis can be confused with other forms of arthritis, such as osteoarthritis or arthritis associated with infections. Rheumatoid arthritis is an autoimmune disease. This means that the body's immune system mistakenly attacks the tissues it is supposed to protect.

Rheumatoid arthritis most often affects the smaller joints, such as those of the hands and/or feet, wrists, elbows, knees, and/or ankles, but any joint can be affected. The symptoms often lead to significant discomfort and disability.

Although rheumatoid arthritis most often affects the joints, it is a disease of the entire body. It can affect many organs and body systems besides the joints. Therefore, rheumatoid arthritis is referred to as a systemic disease.

Medically Reviewed by a Doctor on 5/11/2015

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Arthritis – Arthritis Causes – Symptoms, Treatments, and …

September 3rd, 2015 1:44 pm

Arthritis is a general term for more than 100 diseases that cause inflammation, pain, stiffness and swelling of joints. Common types of arthritis include:

Osteoarthritis - an ongoing, progressive disease that affects the joints as cartilage breaks down over time. Osteoarthritis is also called degenerative joint disease.

Rheumatoid arthritis - an autoimmune disease that affects the joints of the body with episodes of painful inflammation. Rheumatoid arthritis also affects other organs of the body and can result in the destruction of joints, disability, and, in severe cases, life-threatening complications.

Septic arthritis - arthritis caused by the infection of a joint by microorganisms, such as bacteria or fungi.

Complications of all forms of arthritis can be serious and include destruction of the joints, leading to disability. Rheumatoid arthritis and septic arthritis can also lead to serious or life-threatening complications that can affect almost any organ in the body.

Seek prompt medical care if you have symptoms of arthritis, such as inflammation, pain, stiffness, and swelling of joints. Early diagnosis and treatment can minimize discomfort and reduce the risk of serious complications.

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Arthritis & Joint Pain – Orthopedics Advice from About.com

September 3rd, 2015 1:44 pm

Image Medical Multimedia Group What is Arthritis?

Arthritis is a condition that causes inflammation of joint. While there are many types of arthritis, all types cause joint inflammation. Common complaints of people with arthritis include joint pain, swelling, and stiffness.

Arthritis come in many different types, and can affect any joint. Determining the best treatment for your arthritis will depend on identifying the type of arthritis and determining which joints are affected.

Common symptoms of arthritis include joint pain, swelling, and limited movement. The severity of symptoms of arthritis tends to correspond to the degree of inflammation of the joint.

Once you have determined the type of arthritis, you can review potential treatments for your condition. Most often, doctors will recommend trying simpler treatments for arthritis first to determine if your condition can be managed with minimal intervention.

Joint replacement surgery is generally considered a last-step treatment for the most severe cases of joint arthritis. Joint replacement surgery uses artificial joints to take the place of your worn out joint.

The best way to avoid problems associated with arthritis is to try to prevent progression of the condition. For people who have had arthritis in one joint, it is important to prevent the progression of arthritis in other joints.

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Foods and Arthritis | The Physicians Committee

September 3rd, 2015 1:44 pm

Millions of people suffer from painful and swollen joints associated with arthritis. In the past, many doctors told arthritis patients that dietary changes would not help them. However, this conclusion was based on older research with diets that included dairy products, oil, poultry, or meat.1,2 New research shows that foods may be a more frequent contributor to arthritis than is commonly recognized. It is clear that, at least for some people, a healthier menu is the answer.

Arthritis is actually a group of different diseases. Osteoarthritis is a gradual loss of cartilage and overgrowth of bone in the joints, especially the knees, hips, spine, and fingertips. Over 20 million Americans, mostly over age 45, suffer from osteoarthritis, which seems to be the result of accumulated wear and tear. Although it can cause painful episodes, it is characterized by only transient stiffness and does not cause major interference with the use of the hands.

Rheumatoid arthritis, which affects over 2 million people, is a more aggressive form of the disease. It causes painful, inflamed joints, which sometimes become damaged.

Rheumatoid arthritis is one of medicine's mysteries. There were no medical reports of the disease until the early 1800s. Some have suspected that a virus or bacterium may play a role, perhaps by setting off an autoimmune reaction. Genetics may also be a factor, in that it may influence susceptibility to the disease.

For years people have suspected that foods are an important factor in the development of rheumatoid arthritis. Many notice an improvement in their condition when they avoid dairy products, citrus fruits, tomatoes, eggplant and certain other foods.

Initially, the evidence was anecdotal. A woman from the Midwest once suffered from painful arthritis. Today she is a picture of health, thin and athletic, and her arthritis is totally gone. It seemed that dairy products were to blame for her arthritis, for when she eliminated them from her diet, the arthritis disappeared completely.

Another woman, from Wisconsin, also found that her arthritis was clearly linked to dairy products. Although she had been raised on a dairy farm, she learned that staying away from dairy products was the key to relieving her symptoms.

A 1989 survey of over one thousand arthritis patients revealed that the foods most commonly believed to worsen the condition were red meat, sugar, fats, salt, caffeine, and nightshade plants (e.g., tomatoes, eggplant).3 Once the offending food is eliminated completely, improvement usually comes within a few weeks. Dairy foods are one of the principle offenders, and the problem is the dairy protein, rather than the fat, so skim products are as much a problem as whole milk.4

An increasing volume of research shows that certain dietary changes do in fact help. For example, polyunsaturated oils and omega-3 supplements have a mild beneficial effect, and researchers have found that vegan diets are beneficial.5 One 2002 study looked at the influence of a very low-fat vegan diet on subjects with moderate-to-severe RA. After only four weeks on the diet, almost all measures of RA symptoms decreased significantly.6 The journal Rheumatology published a study that found a gluten-free vegan diet improved the signs and symptoms of RA.7 An uncooked vegan diet, rich in antioxidants and fiber was shown in another study to decrease joint stiffness and pain in patients with RA.8 Some research studies have looked at fasting followed by a vegetarian or vegan diet. A review of multiple research studies concluded that this dietary treatment might be useful in the treatment of RA.9

Vegan diets dramatically reduce the overall amount of fat in the diet, and alter the composition of fats. This in turn can affect the immune processes that influence arthritis. The omega-3 fatty acids in vegetables may be a key factor, along with the near absence of saturated fat. The fact that patients also lose weight on a vegan diet contributes to the improvement.

In addition, vegetables are rich in antioxidants, which can neutralize free radicals. Oxygen free radicals attack many parts of the body and contribute to heart disease and cancer, and intensify the aging processes generally, including of the joints.

Iron acts as a catalyst, encouraging the production of these dangerous molecules. Vitamins C and E, which are plentiful in a diet made of vegetables and grains, help neutralize free radicals. Meats supply an overload of iron, no vitamin C, and very little vitamin E, whereas vegetables contain more controlled amounts of iron, and generous quantities of antioxidant vitamins.

As well as being helpful in preventing arthritis, antioxidants may also have a role in reducing its symptoms. Some arthritis treatments, including non-steroidal anti-inflammatory drugs, work at least in part by neutralizing free radicals. For the most part, however, vitamins and other antioxidants will be of more use in preventing damage before it occurs, rather than in treating an inflamed joint.10

A diet drawn from fruits, vegetables, grains, and beans therefore appears to be helpful in preventing and, in some cases, ameliorating arthritis.

For four weeks, include generous amounts of foods from the pain-safe list in your routine.

At the same time, scrupulously avoid the major triggers.

It is important to avoid these foods completely, as even a small amount can cause symptoms.

Foods that are not on either list can be consumed, so long as you are emphasizing the arthritis-safe foods and scrupulously avoiding the major triggers.

You may well experience benefits earlier than four weeks, but for some people it can take this long for chronically inflamed joints to cool down.

Pain-safe foods virtually never contribute to arthritis or other painful conditions. These include

After four weeks, if your symptoms have improved or disappeared, the next step is to nail down which one or more of the trigger foods has been causing your problem. Simply reintroduce the foods you have eliminated back into your diet one at a time, every two days.

Have a generous amount of each newly reintroduced food, and see whether your joints flare up again. If so, eliminate the food that seems to have caused the problem, and let your joints cool down again. Then continue to reintroduce the other foods. Wait at least two weeks before trying a problem food a second time. Many people have more than one food trigger.

It is not recommended to bring meats, dairy products, or eggs back into your diet. Not only are they major triggers, but they also encourage hormone imbalances that may contribute to joint pain, and also lead to many other health problems.

1. Dairy products* 2. Corn 3. Meats** 4. Wheat, oats, rye 5. Eggs 6. Citrus fruits 7. Potatoes 8. Tomatoes 9. Nuts 10. Coffee *All dairy products should be avoided: skim or whole cows milk, goats milk, cheese, yogurt, etc. **All meats should be avoided: beef, pork, chicken, turkey, fish, etc.

For some arthritis patients, supplements of certain essential fatty acids have been helpful. They should be thought of as a medicine, rather than a food. A typical regimen would include a tablespoon of flaxseed oil with 500 mg of blackcurrant oil (or three capsules of evening primrose oil) twice each day. If it is helpful, it should be reduced to the lowest effective dose. Some people also benefit from an herb called feverfew, taken two to three times per day. (Caution: Do not take feverfew if you are pregnant.)

These supplements are available in health food stores.

References 1. Panush RS, Carter RL, Katz P, Kowsari B, Longley S, Finnie S. Diet therapy for rheumatoid arthritis. Arthritis and Rheumatism. 1983;26:462-471. 2. Lithell H, Bruce A, Gustafsson IB, et al. A fasting and vegetarian diet treatment trial on chronic inflammatory disorders. Acta Derm Venereol. 1983;63:397-403. 3. Sobel D. Arthritis: What Works. New York, St. Martin's Press, 1989. 4. Skoldstam L, Larsson L, Lindstrom FD. Effects of fasting and lactovegetarian diet on rheumatoid arthritis. Scand J Rheumatol. 1979;8:249-255. 5. Skoldstam L. Fasting and vegan diet in rheumatoid arthritis. Scand J Rheumatol. 1986;15:219-223. 6. McDougall J, Bruce B, Spiller G, Westerdahl J, McDougall M. Effects of a very low-fat, vegan diet in subjects with rheumatoid arthritis. J Altern Complement Med. 2002;8(1):71-75. 7. Hafstrom I, Ringertz B, Spangberg A, von Zweigbergk L, Brannemark S, Nylander I, Ronnelid J, Laasonen L, Klareskog L. A vegan diet free of gluten improves the signs and symptoms of rheumatoid arthritis: the effects on arthritis correlate with a reduction in antibodies to food antigens. Rheumatology (Oxford). 2001;40(10):1175-1179. 8. Hanninen, Kaartinen K, Rauma AL, Nenonen M, Torronen R, Hakkinen AS, Adlercreutz H, Laakso J. Antioxidants in vegan diet and rheumatic disorders. Toxicology. 2000;155(1-3):45-53. 9. Muller H, de Toledo FW, Resch KL. Fasting followed by vegetarian diet in patients with rheumatoid arthritis: a systematic review. Scand J Rheumatol. 2001;30(1):1-10. 10. Merry P, Grootveld M, Lunec J, Blake DR. Oxidative damage to lipids within the inflamed human joint provides evidence of radical-mediated hypoxic-reperfusion injury. Am J Clin Nutr. 1991;53:362S-369S.

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How does gene therapy work? – Genetics Home Reference

September 2nd, 2015 4:45 pm

Gene therapy is designed to introduce genetic material into cells to compensate for abnormal genes or to make a beneficial protein. If a mutated gene causes a necessary protein to be faulty or missing, gene therapy may be able to introduce a normal copy of the gene to restore the function of the protein.

A gene that is inserted directly into a cell usually does not function. Instead, a carrier called a vector is genetically engineered to deliver the gene. Certain viruses are often used as vectors because they can deliver the new gene by infecting the cell. The viruses are modified so they cant cause disease when used in people. Some types of virus, such as retroviruses, integrate their genetic material (including the new gene) into a chromosome in the human cell. Other viruses, such as adenoviruses, introduce their DNA into the nucleus of the cell, but the DNA is not integrated into a chromosome.

The vector can be injected or given intravenously (by IV) directly into a specific tissue in the body, where it is taken up by individual cells. Alternately, a sample of the patients cells can be removed and exposed to the vector in a laboratory setting. The cells containing the vector are then returned to the patient. If the treatment is successful, the new gene delivered by the vector will make a functioning protein.

Researchers must overcome many technical challenges before gene therapy will be a practical approach to treating disease. For example, scientists must find better ways to deliver genes and target them to particular cells. They must also ensure that new genes are precisely controlled by the body.

A new gene is injected into an adenovirus vector, which is used to introduce the modified DNA into a human cell. If the treatment is successful, the new gene will make a functional protein.

The Genetic Science Learning Center at the University of Utah provides information about various technical aspects of gene therapy in Gene Delivery: Tools of the Trade. They also discuss other approaches to gene therapy and offer a related learning activity called Space Doctor.

The Better Health Channel from the State Government of Victoria (Australia) provides a brief introduction to gene therapy, including the gene therapy process and delivery techniques.

Penn Medicines Oncolink describes how gene therapy works and how it is administered to patients.

Next: Is gene therapy safe?

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Arthritis | At A Glance Reports | Publications | Chronic …

September 2nd, 2015 4:43 pm

About 1 out of every 5 US adults has doctor-diagnosed arthritis. The term arthritis includes more than 100 different rheumatic diseases and conditions, the most common of which is osteoarthritis. Other forms of arthritis that occur often are rheumatoid arthritis, lupus, fibromyalgia, and gout.

Symptoms include pain, aching, stiffness, and swelling in or around the joints. Some forms of arthritis, such as rheumatoid arthritis and lupus, can affect multiple organs and cause widespread symptoms.

Many people think of arthritis as a disease that only affects the elderly, but it affects people of all ages, including children. Although the risk of developing arthritis increases with age, nearly two-thirds of people with arthritis are younger than 65. Arthritis is more common among women (26%) than men (19%), and it affects members of all racial and ethnic groups.

As the US population ages, the number of adults with arthritis is expected to increase to 67 million by 2030. The Centers for Disease Control and Prevention (CDC) is leading the nations efforts to help the millions of adults with arthritis to live well and manage their condition.

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About Arthritis

September 2nd, 2015 4:43 pm

You've probably heard the word "arthritis" before. And now, you may be wondering if it could be affecting you. By definition, arthritis means "joint inflammation," and it's used to describe more than 100 different diseases and conditions that affect joints, the tissues that surround joints, and other connective tissue.

Arthritis can affect people differently. It's common in adults 65 and older, but it can affect people of all ages, races, and ethnic groups. In fact, about 1 out of every 5 adults in the United States around 50 million people has reported being diagnosed by their doctor with some form of arthritis.

Osteoarthritis and rheumatoid arthritis have different causes, risk factors, and effects on the body:

Even though they have these differences, osteoarthritis and rheumatoid arthritis often share common symptoms:

Sometimes arthritis symptoms make it harder to do certain activities. By talking to your doctor about your symptoms, he or she may help you find other ways to continue doing some of those activities.

Your doctor can also help evaluate your current treatment and may recommend other, more effective ways to help you manage your arthritis. The sooner you take action and talk to your doctor, the sooner you can start managing your arthritis symptoms more effectively.

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longevity | Chiraan’s Astrology

September 2nd, 2015 1:44 am

AyuhKshinam Ayuhvriddhi

When 8th and ninth lord in 12th then one will lose his longevity by the dishonouring the elders. Aspect of benefics on 8th house and its lord increases the longevity.Having good Ayur yogas also increases the strata of longevity .12th sun for libra ascendant also confers longevity.

One loses his longevity by

Once there was a very learned bramhin by name Srinivasachar in 18th century. He was a great scholar in sanskrit and philososphy . He was very proud of his scholarly aptitude . It was also around same time ,when bhakti movement had gained importance in south India and Das culture was on the rise . Das way of life was initiated by Purandardas [incarnation of Narada] in the south when Vijaynagar empire was at its peak under the able guidance of Vyasateertha [Incarnation of Balhik] a pontiff in the line of Madhvacharya. Das culture mainly emphasised the delivery of Vedic Knowledge in local language [Kannada] through poems and melodious songs for the Lord Vittala .Thus common men and women were suddenly bestowed the nectar of geeta and puranas in the common mans language then prevalent. Vijaydas [ incarnation of sage BHrigu] was also one such illustrious personality of those times. VijayDas was also maternal uncle to Srinivasachar.

Srinivasachar owing to the pride ,he had cultivated, did not recognize the fact that philososphy could be delivered to common man in simple mans language. The philosophy which could not be guaged by immense learning in sanskrit ,how could they be delivered in simple dismal languages.

True ! Sanskrit is a complex language ; its grammar is vast ; its difficult to master it ;perhaps takes many years for the same; Then comes the grasp poetry in sanskrit ! still difficult ; upon that philosophy ; its totally incomprehensible ; Almost all the philosophic literature is available in archaic sanskrit in poetry form ; difficult to decode. it takes many years of study and mastery to exhibit command over such philosophic understandings. All such efforts would seem ridiculous , if somebody claims he understands philosophy although he does not understand sanskrit. Amazing still will be the statement if one says he can express all the intricacies of the Vedas in common mans language! even if we were to accept this ; How come the common man is going to understand them; Can such claim be accepted ?

SrinivasAchar felt these Das culture guys were fooling people in the name of God for common man and dancing around with bells in their anklets;He seriously doubted their credentials and claims of sainthood.

One day VijayDas came visiting to his place and even visited his house. Srinivasachar out of ego and pride did not respect the Learned VijayDas and did not even welcome him in his house. VijayDas went away smiling .But soon after this insult , Srinivasachar started losing out on health.Slowly his health deteriorated. He contracted Kushtha [skin disease ] and slowly his moments became restricted.

SrinivasAchar now contemplated he is heading for Apamrutyu [ his longevity has decreased ]. He however could not comprehend the loss of longevity[ Ayuhkshina] . So to gain longevity he prayed Lord Hanuman in the mountains near Panchamukhi on the banks of TungaBhadra river. After 42 days of Vayustuti Purascharan ,he had a dream , where Lord Hanuman directed him to pray Shri Raghavendra swamy in Mantralaya for further directions. [ Shri Raghavendra has been specially sent from heavens by God to grant the wishes of the humans, hence the direction ].

Srinivas achar spent next few days under austere conditions as penace towards Shri Raghavendra Swamy at Mantralayam. The following night Shri Raghavendra swamy appeared and explained to him the reason for his loss of longevity .[ Disrespect towards very learned VijayDas] ,so he asked him to seek his pardon and blessings.

Srinivas Achar went to VijayDas and sought pardon and accepted the supremacy of poetry and dance in gaining lords Grace . VijayDas directed him to go to his disciple Shri GopalDas [incarnation of Ganapathy] to seek blessings and accept him as Guru .GopalDas was a very learned man , he kept the entire place clean of pebbles lest his disciple would be hurt [ Srinivasachar was troubled by lack of moment and kushtha ] .

When SrinivasAchar came and bowed to GopalDas , he transfered his 40 years of longevity [ through yoga] to a Roti of Jowar[Bhakri] and asked him to eat it to gain a 40 years. When one loses longevity owing to disrespect no austerities can actually increase it . someone has to donate his longevity to make a person live more. [SO never ever lose longevity we would not find anyone to donate life] Without life and longevity all the riches and fame are useless.

Despite donating 40 years GopalDas lived for 80 years of age and gave to this world a wonderful science and technique of Vishwopasana . He rechristened Srinivasachar as JagannathDas [ srinivasachar is incarnation of AHLAD brother of Prahlad , and hence had a very special relationship with Shri Raghavendra swamy ,a incarnation of Prahlad]

JagannathDas gave a magnum opus HARIKATHAMRUTASARA a treatise on the qualities of God Narayana in the comman mans language specially to be read by women and others inelligible for Vedas.

krishnarpanamastu

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Genetics: MedlinePlus Medical Encyclopedia

September 2nd, 2015 1:43 am

Human beings have cells with 46 chromosomes -- 2 chromosomes that determine what sex they are (X and Y chromosomes), and 22 pairs of nonsex (autosomal) chromosomes. Males are "46,XY" and females are "46,XX." The chromosomes are made up of strands of genetic information called DNA. Each chromosome contains sections of DNA called genes, which carry the information needed by your body to make certain proteins.

Each pair of autosomal chromosomes contains one chromosome from the mother and one from the father. Each chromosome in a pair carries basically the same information; that is, each chromosome pair has the same genes. Sometimes there are slight variations of these genes. These variations occur in less than 1% of the DNA sequence. The genes that have these variations are called alleles.

Some of these variations can result in a gene that is abnormal. An abnormal gene may lead to an abnormal protein or an abnormal amount of a normal protein. In a pair of autosomal chromosomes, there are two copies of each gene, one from each parent. If one of these genes is abnormal, the other one may make enough protein so that no disease develops. When this happens, the abnormal gene is called recessive, and the other gene in the pair is called dominant. Recessive genes are said to be inherited in an autosomal recessive pattern.

However, if only one abnormal gene is needed to produce a disease, it leads to a dominant hereditary disorder. In the case of a dominant disorder, if one abnormal gene is inherited from mom or dad, the child will likely show the disease.

A person with one abnormal gene is called heterozygous for that gene. If a child receives an abnormal recessive disease gene from both parents, the child will show the disease and will be homozygous (or compound heterozygous) for that gene.

GENETIC DISORDERS

Almost all diseases have a genetic component. However, the importance of that component varies. Disorders in which genes play an important role (genetic diseases) can be classified as:

A single-gene disorder (also called Mendelian disorder) is caused by a defect in one particular gene. Single gene defects are rare. But since there are about 4,000 known single gene disorders, their combined impact is significant.

Single-gene disorders are characterized by how they are passed down in families. There are six basic patterns of single gene inheritance:

The observed effect of a gene (the appearance of a disorder) is called the phenotype.

In autosomal dominant inheritance, the abnormality or abnormalities usually appear in every generation. Each time an affected woman has a child, that child has a 50% chance of inheriting the disease.

People with one copy of a recessive disease gene are called carriers. Carriers usually don't have symptoms of the disease. But, the gene can often be found by sensitive laboratory tests.

In autosomal recessive inheritance, the parents of an affected individual may not show the disease (they are carriers). On average, the chance that carrier parents could have children who develop the disease is 25% with each pregnancy. Male and female children are equally likely to be affected. For a child to have symptoms of an autosomal recessive disorder, the child must receive the abnormal gene from both parents. Because most recessive disorders are rare, a child is at increased risk of a recessive disease if the parents are related. Related individuals are more likely to have inherited the same rare gene from a common ancestor.

In X-linked recessive inheritance, the chance of getting the disease is much higher in males than females. Since the abnormal gene is carried on the X (female) chromosome, males do not transmit it to their sons (who will receive the Y chromosome from their fathers). However, they do transmit it to their daughters. In females, the presence of one normal X chromosome masks the effects of the X chromosome with the abnormal gene. So, almost all of the daughters of an affected man appear normal, but they are all carriers of the abnormal gene. Each time these daughters bear a son, there is a 50% chance the son will receive the abnormal gene.

In X-linked dominant inheritance, the abnormal gene appears in females even if there is also a normal X chromosome present. Since males pass the Y chromosome to their sons, affected males will not have affected sons. All of their daughters will be affected, however. Sons or daughters of affected females will have a 50% chance of getting the disease.

EXAMPLES OF SINGLE GENE DISORDERS

Autosomal recessive:

X-linked recessive:

Autosomal dominant:

X-linked dominant:

Only a few, rare, disorders are X-linked dominant. One of these is hypophosphatemic rickets, also called vitamin D -resistant rickets.

CHROMOSOMAL DISORDERS

In chromosomal disorders, the defect is due to either an excess or lack of the genes contained in a whole chromosome or chromosome segment.

Chromosomal disorders include:

MULTIFACTORIAL DISORDERS

Many of the most common diseasesare caused byinteractions of several genes and factors in the the environment (for example, illnesses in the mother and medications). These include:

MITOCHONDRIAL DNA-LINKED DISORDERS

Mitochondria are small organisms found in most of the body's cells. They are responsible for energy production inside cells. Mitochondria contain their own private DNA.

In recent years, many disorders have been shown to result from changes (mutations) in mitochondrial DNA. Because mitochondria come only from the female egg, most mitochondrial DNA-related disorders are passed down from the mother.

Mitochondrial DNA-related disorders can appear at any age. They have a wide variety of symptoms and signs. These disorders may cause:

Some other disorders are also known as mitochondrial disorders, but they do not involve mutations in the mitochondrial DNA. These disorders are usually single gene defects and they follow the same pattern of inheritance as other single gene disorders.

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Ology Genetics – AMNH

September 2nd, 2015 1:43 am

Photos: DNA, ladybug, brown eye, blue eye, PCR, Gregor Mendel, peas: AMNH; Starfish: courtesy of AMNH Department of Library Services K4508; Perch fish: courtesy of AMNH Department of Library Services PK241; Illustrations: Louis Pappas, Steve Thurston, Eric Hamilton; DNA, nature/nurture: Kelvin Chan Boy at computer: Jim Steck; Fruit fly: courtesy of Flybase

Did you know that DNA carries all the information a cell needs to make you uniquely you? Take a look at the science of where it ALL begins.

Illustrations Steve Gray

Solve genetic riddles as you wind your way through the star-studded park.

Photos: Dr. Ian Wilmut and Dolly; Dolly and her birth mother, courtesy of the Roslin Institute; Illustrations: Clay Meyer

Investigate the how and why of cloning. This Web page helps kids understand cloning and explains some of the ethical issues involved.

Photos: George Barrowclough: courtesy of R.J. Gutierrez; Humpback whales, Howard Rosenbaum: courtesy of Peter J. Ersts, Center for Biodiversity and Conservation, AMNH; Owl: John and Karen Hollingsworth, U.S. Fish and Wildlife Service; Yael Wyner: courtesy of Yael Wyner; Joel Cracraft: courtesy of Joel Cracraft; Sumatran Tiger: courtesy of Jessie Cohen, Smithsonian's National Zoo; Lemur: courtesy of Duke University Primate Center; Daniela Calcagnotto: Courtesy of Daniela Calcagnotto; Pacu: courtesy of Leonard Lovshin, Department of Fisheries and Allied Aquacultures, Auburn University; St. Vincent parrots, Mike Russello: courtesy of Mike Russello; Illustrations: Louis Pappas, Steve Thurston, Eric Hamilton

Travel around the world with museum scientists: from Madagascar to the Western U.S. to the island of Sumatra in Indonesia.

Photos: George Amato, Lab machines: courtesy of Denis Finnin, AMNH; Caimans: courtesy of Santos Breyer, Crocodilian Photo Gallery; Elephant: courtesy of Jason Lelchuk, AMNH; American Crocodile: courtesy of Julio Caballeros Sigme, Florida Museum of Natural History; Tibetan Antelope: courtesy of George B. Schaller; Products: courtesy of Meg Carlough

Join scientist George Amato on his quest to stop criminals smuggling illegal goods.

All photos: AMNH

Here's a very cool experiment that just might bring a tear to your eye. Use a blender to separate the DNA from an onion.

Illustrations: Daryl Collins

Find out what makes you different from a snail, a tree, or even your best friend!

Photos: Salmon, Florida Panther: courtesy of U.S. Fish and Wildlife Service; Ruffed lemur: courtesy of Duke University Primate Center; Congo Gorilla: courtesy of AMNH Department of Library Services 1636; Spotted owl: courtesy of U.S. Fish and Wildlife Service / photo by J&K Hollingsworth; Sumatran tiger: courtesy of Jessie Cohen, Smithsonian's National Zoo; Grevy's zebra: courtesy of AMNH Department of Library Services K10684; Asian Elephant: courtesy of Jason Lelchuk, AMNH; DNA, tongue curling, earlobe, thumb: courtesy of Denis Finnin, AMNH; Dolly: courtesy of the Roslin Institute; Corn, bananas, dog, bird, eye, flowers, buildings, glacier, human, tomato, cupcake, none: AMNH; Guinea pig: courtesy of AMNH Department of Library Services PK326; Mars: courtesy of David Crisp and the WFPC2 Science Team (Jet Propulsion Laboratory/California Institute of Technology)/NSSDC and NASA; Dusky Seaside Sparrow: courtesy of P.W. Sykes, U.S. Fish and Wildlife Service; Antelope: courtesy of George B. Schaller; Crocodile: courtesy of Santos Breyer, the Crocodilian Photo Gallery; Sea turtle: courtesy of David Vogel, U.S. Fish and Wildlife Service; Illustrations: Cell, Chromosome, DNA: Stephen Blue; Gene: Kelvin Chan; Mononykus dinosaur: Mick Ellison, AMNH; Woolly Mammoth: courtesy of AMNH Department of Library Services 2431, painting by Charles. R. Knight; Dodo Bird: courtesy of AMNH Department of Library Services 6261, Jean Pretre, from Henri-Marie Ducrotay de Blainville, Nouvelles annales du Museum d'Histoire Naturelle, Paris; Sabre tooth tiger: courtesy of AMNH Department of Library Services 1017; painting by Charles R. Knight

Make your opinion count!

Explore the gene scene with these seven books.

Photos: Rob De Salle: courtesy of Denis Finnin, AMNH; Illustrations: Daniel Guidera

Step into the future for a look at what cloning might do for you.

Illustrations: Animals: Steve Thurston; Journal Page: Carl Mehling

Want to figure out the wildlife in your area and the impact of genetics? Start a field journal, and track how your favorite critter looks and behaves.

Illustrations: Eric Hamilton

Send a note to a friend with these colorful letterheads.

Photos: Physics Notebook, Questions, Molecular Lab, Dog: AMNH; Narwhal: courtesy of AMNH Department of Library Services, 26177, Photo by A.S. Rudland and Sons, copied by Thos. Lunt, Feb. 19, 1910 from "The Living Animals of the World," Hutchinson and Co., London; Fruit fly: courtesy of AMNH Department of Library Services 101321; The Genomic Revolution AMNH exhibit pictures: Preparation, DNA Learning Lab, Nature/Nurture wall, Yeast: courtesy of Denis Finnin, AMNH; Chimpanzee: courtesy of AMNH Department of Library Services K12658 Salmon: courtesy of U.S. Fish and Wildlife Service

Find out where Rob has followed his born curiosity.

Photos: Rob DeSalle: Physics Notebook, Questions, Molecular Lab, Dog: AMNH; Narwhal: courtesy of AMNH Department of Library Services, 26177, Photo by A.S. Rudland and Sons, copied by Thos. Lunt, Feb. 19, 1910 from "The Living Animals of the World," Hutchinson and Co., London; Fruit fly: courtesy of AMNH Department of Library Services 101321; The Genomic Revolution AMNH exhibit pictures: Preparation, DNA Learning Lab, Nature/Nurture wall, Yeast: courtesy of Denis Finnin, AMNH; Chimpanzee: courtesy of AMNH Department of Library Services K12658 Salmon: courtesy of U.S. Fish and Wildlife Service; Kids: All people pictures and drawings: courtesy of subjects; Woolly Mammoth: courtesy of AMNH Department of Library Services 2431, painting by Charles. R. Knight Cat: courtesy of subject Farm: AMNH

Find out where Rob, Emily, Logan, and Seth have followed their born curiosity.

Illustrations: Wayne Vincent

What's the human genome project and what does it mean to you? Toby, Annie, and Claudia uncovered the answers.

Illustrations: Daryl Collins

The next time you eat a tomato, ask yourself: What would it taste like if there were a bit of flounder in it? Learn how scientists are using genetics to change the food you eat.

Photos: Monarch Butterfly, courtesy of AMNH Department of Library Services K14898; Grizzly Bear: courtesy of NPS; Sunflower: courtesy of Bruce Fritz, ARS; Chimpanzee: courtesy of AMNH Department of Library Services K12658; African Elephant: courtesy of Miriam Westervelt, U.S. Fish and Wildlife Service; Apple tree: courtesy of Doug Wilson, USDA; Red flour beetle: courtesy of Cereal Research Centre, AAFC; Brown trout: courtesy of Duane River, U.S. Fish and Wildlife Service; Supplies: AMNH; What to Do: (All photos): AMNH; DNA Model, Lady beetle: courtesy of Scott Bauer, ARS Fish, Daisy: AMNH; What You Need illustrations: Stephen Blue

How can you wear a chimp on your wristwithout getting primate elbow? The answer to this riddle is not as tough as it may seem.

Photos: DNA, AMNH; The Genomic Revolution Exhibit: courtesy of Denis Finnin, AMNH; Gene: AMNH; Dolly: courtesy of the Roslin Institute; Chimpanzee: courtesy of AMNH Department of Library Services K12658

How much do you know about what makes you you? Test your genetics knowledge with this interactive quiz.

Photos: People: courtesy of Denis Finnin, AMNH; Illustrations: Louis Pappas, Steve Thurston, Eric Hamilton; People: Jim Steck Genetics illustrations: Stephen Blue

Zoom inside your cells for a fascinating look at chromosomes, DNA, genes, and more!

Photos: Frozen Tissue Collection: All specimens from the Frozen Tissue Collection, frilled leaf-tailed gecko: AMNH / Denis Finnin cryovat, test tubes: AMNH / Craig Chesek humpback whale: John J. Mosesso / NBII coyote: AMNH; Gold: gold sheet mouflon, miniature sacrificial figurine, Spanish coins: AMNH / Craig Chesek Inca necklace: AMNH / Denis Finnin Eureka Bar: AMNH / Roderick Mickens astronaut in space: NASA computer chip: stock.xchng; Leeches: jaw: Eye of Science / Photo Researchers, Inc. bite mark: Geoff Tompkinson / Photo Researchers, Inc. leech feeding on snail: Edward Hendrycks, reproduce courtesy of the Canadian Museum of Nature leeches before and after blood meal, leeches on foot, American Medicinal Leech, Malagobdella vagans, Mark Siddall in swamp: courtesy of Mark Siddall; Dioramas: AMNH / Roderick Mickens; Mythic Creatures: All photos courtesy of American Museum of Natural History; Vietnam: pygmi loris, Tonkin snub-nosed monkey: Tilo Nadler / Frankfurt Zoological Society Oriental pit viper: Robert W. Murphy / Royal Ontario Museum scientists with camera trap: Kevin Frey / AMNH Center for Biodiversity and Conservation saola: European Commission, Social Forestry and Nature Conservation

Put your viewing skills to the test with this mystery photo challenge.

Tracking a gorilla can get hairy. Literally. Just ask George Amato.

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Home > Genetics | Yale School of Medicine

September 2nd, 2015 1:43 am

The information in genomes provides the instruction set for producing each living organism on the planet. While we have a growing understanding of the basic biochemical functions of many of the individual genes in genomes, understanding the complex processes by which this encoded information is read out to orchestrate production of incredibly diverse cell types and organ functions, and how different species use strikingly similar gene sets to nonetheless produce fantastically diverse organismal morphologies with distinct survival and reproductive strategies, comprise many of the deepest questions in all of science. Moreover, we recognize that inherited or acquired variation in DNA sequence and changes in epigenetic states contribute to the causation of virtually every disease that afflicts our species. Spectacular advances in genetic and genomic analysis now provide the tools to answer these fundamental questions.

Members of the Department of Genetics conduct basic research using genetics and genomics of model organisms (yeast, fruit fly, worm, zebrafish, mouse) and humans to understand fundamental mechanisms of biology and disease. Areas of active investigation include genetic and epigenetic regulation of development, molecular genetics, genomics and cell biology of stem cells, the biochemistry of micro RNA production and their regulation of gene expression, and genetic and genomic analysis of diseases in model systems and humans including cancer, cardiovascular and kidney disease, neurodegeneration and regeneration, and neuropsychiatric disease. Members of the Department have also been at the forefront of technology development in the use of new methods for genetic analysis, including new methods for engineering mutations as well as new methods for production and analysis of large genomic data sets.

The Department sponsors a graduate program leading to the PhD in the areas of molecular genetics and genomics, development, and stem cell biology. Admission to the Graduate Program is through the Combined Programs in Biological and Biomedical Sciences (BBS).

In addition to these basic science efforts, the Department is also responsible for providing clinical care in Medical Genetics in the Yale New Haven Health System. Clinical genetics services include inpatient consultation and care, general, subspecialty, cancer and prenatal genetics clinics, and clinical laboratories for cytogenetics, DNA diagnostics, and biochemical diagnostics. The Department sponsors a Medical Genetics Residency program leading to certification by the American Board of Medical Genetics. Admission to the Genetics Residency is directly through the Department.

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Genetics – Biology

September 2nd, 2015 1:43 am

Genetics

Background:

Homunculus in Sperm One question that has always intrigued us humans is Where did we come from? Long ago, Hippocrates and Aristotle proposed the idea of what they called pangenes, which they thought were tiny pieces of body parts. They thought that pangenes came together to make up the homunculus, a tiny pre-formed human that people thought grew into a baby. In the 1600s, the development of the microscope brought the discovery of eggs and sperm. Antonie van Leeuwenhoek, using a primitive microscope, thought he saw the homunculus curled up in a sperm cell. His followers believed that the homunculus was in the sperm, the father planted his seed, and the mother just incubated and nourished the homunculus so it grew into a baby. On the other hand, Regnier de Graaf and his followers thought that they saw the homunculus in the egg, and the presence of semen just somehow stimulated its growth. In the 1800s, a very novel, radical idea arose: both parents contribute to the new baby, but people (even Darwin, as he proposed his theory) still believed that these contributions were in the form of pangenes.

Modern genetics traces its beginnings to Gregor Mendel, an Austrian monk, who grew peas in a monastery garden. Mendel was unique among biologists of his time because he sought quantifiable data, and actually counted the results of his crosses. He published his findings in 1865, but at that time, people didnt know about mitosis and meiosis, so his conclusions seemed unbelievable, and his work was ignored until it was rediscovered in 1900 by a couple of botanists who were doing research on something else. Peas are an ideal organism for this type of research because they are easy to grow and it is easy to control mating.

We will be looking at the sorts of genetic crosses Mendel did, but first, it is necessary to introduce some terminology:

Monohybrid Cross and Probabilities:

A monohybrid cross is a genetic cross where only one gene/trait is being studied. P stands for the parental generation, while F1 and F2 stand for the first filial generation (the children) and second filial generation (the grandchildren). Each parent can give one chromosome of each pair, therefore one allele for each trait, to the offspring. Thus, when figuring out what kind(s) of gametes an individual can produce, it is necessary to choose one of the two alleles for each gene (which presents no problem if they are the same).

Purple Pea Flower White Pea Flower For example, a true-breeding purple-flowered plant (the dominant allele for this gene) would have the genotype PP, and be able to make gametes with either P or P alleles. A true-breeding white-flowered plant (the recessive allele for this gene) would have the genotype pp, and be able to make gametes with either p or p alleles. Note that both of these parent plants would be homozygous. If one gamete from each of these parents got together to form a new plant, that plant would receive a P allele from one parent and a p allele from the other parent, thus all of the F1 generation will be genotype Pp, they will be heterozygous, and since purple is dominant, they will look purple. What if two individuals from the F1 generation are crossed with each other (PpPp)? Since gametes contain one allele for each gene under consideration, each of these individuals could contribute either a P or a p in his/her gametes. Each of these gametes from each parent could pair with each from the other, thus yielding a number of possible combinations for the offspring. We need a way, then, to predict what the possible offspring might be. Actually, there are two ways of doing this. The first is to do a Punnett square (named after Reginald Crandall Punnett). The possible eggs from the female are listed down the left side, and there is one row for each possible egg. The possible sperm from the male are listed across the top, and there is one column for each possible sperm. The boxes at the intersections of these rows and columns show the possible offspring resulting from that sperm fertilizing that egg. The Punnett square from this cross would look like this:

Note that the chance of having a gamete with a P allele is and the chance of a gamete with a p allele is , so the chance of an egg with P and a sperm with P getting together to form an offspring that is PP is =, just like the probabilities involved tossing coins. Thus, the possible offspring include: PP, ( Pp + pP, which are the same (Pp), since P is dominant over p), so = Pp, and pp.

Another way to calculate this is to use a branching, tree diagram:

Note, again, that the chance of Pp is +=. A shorter way of telling how many PP, Pp, and pp could be expected, would be to say that there is a 1:2:1 genotype ratio (that comes from the , , and , above, and by the way, notice that they add up to , so we know we have accounted for everything). The chance of getting at least one dominant allele (either PP or Pp) necessary for purple color (this can be written as P) is +=, so we could say that theres a 3:1 phenotype ratio. These two ratios are classic genotype and phenotype ratios for a monohybrid cross between two heterozygotes.

Mendels Four-Part Theory:

Based on his data, Mendel came up with a four-part theory of how genetics works:

Some special cases:

(Rh factor, by the way, is a totally separate gene with Rh+ [R] and Rh [r] alleles [actually, that gene also has multiple alleles, but the vast majority of people are positive or negative for one particular allele called D]. In the U. S., about 85% of the population is Rh+ [RR and Rr] and 15% Rh [rr], thus the chances of someone being O [having both ii and rr] would be 45% 15% = 6.75%. The rarest blood type in the U. S. would be AB, about 0.45% of the population.]

This is a cross where two traits/genes are under consideration. For example, in peas if R = round, so r = wrinkled, and Y = yellow, so y = green, in a cross between RRYY rryy, the gametes must have ONE ALLELE FOR EACH GENE, so in this case, RRYY could produce gametes with one R AND one Y, or RY, and rryy could produce gametes with one r AND one y, or ry. The F1 would get RY from one parent and ry from the other, thus would all be RrYy. Note that it is necessary to keep the alleles for the same gene together and put the dominant allele (capital letter) first for EACH GENE. In calculating what the F2 generation would be, you must first figure out what gametes (eggs or sperm) each parent can make. It is very important to remember that gametes must have ONE ALLELE FOR EACH GENE, so figure out the possibilities this way:

Thus, each parent could make four kinds of gametes, so the Punnett square would be 44 cells.

This would give the following possible offspring:

Thus the genotype ratio is 1:2:1:2:4:2:1:2:1 and the phenotype ratio is 9:3:3:1. Notice the shorthand used to represent the phenotypes. Since both RR and Rr will look round, rather than writing round pea seeds, we can use R to say its got at least one R, so itll be round.

Try This:

On your own, try IAiRr IBiRr, a cross involving both the ABO blood group and Rh factor. Note, a little later, we will discuss what those blood groups actually are/do.

Genotype and Phenotype Are Not the Same:

It is important to understand the difference between genotype and phenotype. For example, for most of the genes we will be discussing, an organism with the genotype of, say, BB and an organism who is Bb both have at least one dominant allele for that gene, and thus, would both express/show/be the dominant phenotype. If, for example, this was a gene for human eye color, then B would represent the dominant allele which codes for make brown eyes, and b would represent the recessive allele which codes for blue eyes (technically, more like, we dont know how to make brown, so blue is the default). Thus, people whose genotypes are either BB or Bb both have instructions for make brown, so the phenotypes of both are brown eye color.

As another example where many people get confused, an individuals sex is a phenotype, not a genotype! We can talk of a person as having either two X chromosomes (XX) or one X and one Y chromosome (XY). Those are, essentially, genotypes, and there are also a few people who have genotypes such as X (also called XO), XXX, or XXY. Those X and Y chromosomes contain/consist of a number of genes, and factors such as what alleles a person has for each of those genes, how those alleles are expressed, and how that gene expression affects/influences various body processes will all come together to produce that phenotype which we call a persons sex. In humans, if all those alleles are expressed in what we like to think of as being normal, then, usually, X, XX, and XXX are expressed as a female phenotype (with X and XXX producing some other physical characteristics considered to be typical for those genotypes), while the result of how the XY combination is expressed usually results in what we refer to as a male phenotype.

However, while uncommon, it is entirely possible that due to a mutation in some gene, somewhere, that codes for some enzyme or hormone, a person with 2 X chromosomes (XX) can have a male phenotype; can, clearly and unambiguously, be male. Similarly, while also not very common, it is also possible, due to a mutation in some gene, somewhere, that codes for some hormone or enzyme, that a person with an X and a Y chromosome (XY) can have a female phenotype; can, clearly and unambiguously, be female. Interestingly, because of differences in how the genes/alleles are expressed, the XXY combination typically results in a male in humans but results in a female in fruit flies.

Our culture, our way of thinking, is so locked into having/needing to choose between male and female as the only two options, that while in the unambiguous cases just mentioned where a persons expressed phenotype obviously fits our preconception of maleness or femaleness even if their genotype/chromosomes are different from what we might think (and of which we would not even be aware unless we were that persons doctor and maybe not even then), on the other hand, people whose bodies dont exactly and neatly fit into one of those two categories are lumped together in a group and labeled as intersex. Typically, at birth, their parents are advised by medical personnel to choose whether they wish to bring this child up as a boy or a girl, and may even be pressured into having cosmetic surgery performed on the child to make the child look more like the chosen sex assignment, yet it frequently happens as the child grows up, due to the influence of internal factors such as hormones, etc., that he or she does not feel like the sex which the doctors assigned/labeled at birth. On the other hand, if parents try to be more neutral and let the child make that choice when and if the child decides to do so, that tends to expose the child to a lot of ridicule from classmates and even other adults.

Pedigrees:

Sample Pedigree In pedigrees, a circle represents a female and a square represents a male. Filled-in vs. open symbols are used to distinguish between two phenotypes for the gene in question, and a half-filled symbol may be used to designate a carrier (a heterozygous individual who has a recessive allele for some gene, but is not showing that phenotype). Here is a sample pedigree for eye color. If the people with filled-in (dark) symbols have brown eyes and those with open (light) symbols have blue eyes, can you figure out the genotypes of the people marked with *?

Genetic Basis of Behavior, Polyploids:

Some further notes on genetics: We tend to think of genes that control what an organism looks like, etc., but genes can also control behavior of animals. For example, bird songs and other courtship rituals are under genetic control. The most successful competitors live and mate and pass on their genes. On a different subject, many of our horticultural plant varieties are polyploid plants. Typically, like us, plants are diploid. Horticulturists have figured out ways to manipulate plants and make triploid or tetraploid plants. Typically these plants are larger and/or have bigger or more ruffled flowers and/or larger seeds. While triploid plants are usually sterile (with three sets of chromosomes they have trouble doing meiosis), tetraploid plants are usually fertile and can reproduce. I believe I read somewhere that the wheat we eat is actually a hexaploid, resulting in seeds that are quite a bit larger than its grass-like ancestor.

References:

Borror, Donald J. 1960. Dictionary of Root Words and Combining Forms. Mayfield Publ. Co.

Campbell, Neil A., Lawrence G. Mitchell, Jane B. Reece. 1999. Biology, 5th Ed. Benjamin/Cummings Publ. Co., Inc. Menlo Park, CA. (plus earlier editions)

Campbell, Neil A., Lawrence G. Mitchell, Jane B. Reece. 1999. Biology: Concepts and Connections, 3rd Ed. Benjamin/Cummings Publ. Co., Inc. Menlo Park, CA. (plus earlier editions)

Marchuk, William N. 1992. A Life Science Lexicon. Wm. C. Brown Publishers, Dubuque, IA.

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Genetics and Genetic Disorders and Diseases – WebMD

September 2nd, 2015 1:43 am

What are genes?

Genes are the part of a body cell that contain the biological information that parents pass to their children. Genes control the growth and development of cells. Genes are contained in DNA (deoxyribonucleic acid), a substance inside the center (nucleus) of cells that contains instructions for the development of the cell.

You inherit half of your genetic information from your mother and the other half from your father. Genes, alone or in combination, determine what features (genetic traits) a person inherits from his or her parents, such as blood type, hair color, eye color, and other characteristics, including risks of developing certain diseases. Certain changes in genes or chromosomes may cause problems in various body processes or functions.

Many genes together make up larger structures within the cell called chromosomes. Each cell normally contains 23 pairs of chromosomes.

A human has 46 chromosomes (23 pairs). One chromosome from each pair comes from the mother, and one chromosome from each pair comes from the father. One of the 23 pairs determines your sex. These sex chromosomes are called X and Y.

Some genetic disorders are caused when all or part of a chromosome is missing or when an extra chromosome or chromosome fragment is present.

Genetic testing examines a DNA sample for gene changes, or it may analyze the number, arrangement, and characteristics of the chromosomes. Testing may be performed on samples of blood, semen, urine, saliva, stool, body tissues, bone, or hair.

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Genetics – Simple English Wikipedia, the free encyclopedia

September 2nd, 2015 1:43 am

Genetics is a discipline of biology.[1] It is the science of heredity. This includes the study of genes, and the inheritance of variation and traits of living organisms.[2][3][4] In the laboratory, genetics proceeds by mating carefully selected organisms, and analysing their offspring. More informally, genetics is the study of how parents pass some of their characteristics to their children. It is an important part of biology, and gives the basic rules on which evolution acts.

The fact that living things inherit traits from their parents has been known since prehistoric times, and used to improve crop plants and animals through selective breeding. However, the modern science of genetics, which seeks to understand the process of inheritance, only began with the work of Gregor Mendel in the mid-nineteenth century.[5] Although he did not know the physical basis for heredity, Mendel observed that organisms inherit traits via discrete units of inheritance, which are now called genes.

Living things are made of millions of tiny self-contained components called cells. Inside of each cell are long and complex molecules called DNA.[6]DNA stores information that tells the cells how to create that living thing. Parts of this information that tell how to make one small part or characteristic of the living thing red hair, or blue eyes, or a tendency to be tall are known as genes.

Every cell in the same living thing has the same DNA, but only some of it is used in each cell. For instance, some genes that tell how to make parts of the liver are switched off in the brain. What genes are used can also change over time. For instance, a lot of genes are used by a child early in pregnancy that are not used later.

A living thing has two copies of each gene, one from its mother, and one from its father.[7] There can be multiple types of each gene, which give different instructions: one version might cause a person to have blue eyes, another might cause them to have brown. These different versions are known as alleles of the gene.

Since a living thing has two copies of each gene, it can have two different alleles of it at the same time. Often, one allele will be dominant, meaning that the living thing looks and acts as if it had only that one allele. The unexpressed allele is called recessive. In other cases, you end up with something in between the two possibilities. In that case, the two alleles are called co-dominant.

Most of the characteristics that you can see in a living thing have multiple genes that influence them. And many genes have multiple effects on the body, because their function will not have the same effect in each tissue. The multiple effects of a single gene is called pleiotropism. The whole set of genes is called the genotype, and the total effect of genes on the body is called the phenotype. These are key terms in genetics.

We know that man started breeding domestic animals from early times, probably before the invention of agriculture. We do not know when heredity was first appreciated as a scientific problem. The Greeks, and most obviously Aristotle, studied living things, and proposed ideas about reproduction and heredity.[8]

Probably the most important idea before Mendel was that of Charles Darwin, whose idea of pangenesis had two parts. The first, that persistent hereditary units were passed on from one generation to another, was quite right. The second was his idea that they were replenished by 'gemmules' from the somatic (body) tissues. This was entirely wrong, and plays no part in science today.[9] Darwin was right about one thing: whatever happens in evolution must happen by means of heredity, and so an accurate science of genetics is fundamental to the theory of evolution. This 'mating' between genetics and evolution took many years to organise. It resulted in the Modern evolutionary synthesis.

The basic rules of genetics were first discovered by a monk named Gregor Mendel in around 1865. For thousands of years, people had already studied how traits are inherited from parents to their children. However, Mendel's work was different because he designed his experiments very carefully.

In his experiments, Mendel studied how traits were passed on in pea plants. He started his crosses with plants that bred true, and counted characters that were either/or in nature (either tall or short). He bred large numbers of plants, and expressed his results numerically. He used test crosses to reveal the presence and proportion of recessive characters.

Mendel explained the results of his experiment using two scientific laws:

Mendel's laws helped explain the results he observed in his pea plants. Later, geneticists discovered that his laws were also true for other living things, even humans. Mendel's findings from his work on the garden pea plants helped to establish the field of genetics. His contributions were not limited to the basic rules that he discovered. Mendel's care towards controlling experiment conditions along with his attention to his numerical results set a standard for future experiments. Over the years, scientists have changed and improved Mendel's ideas. However, the science of genetics would not be possible today without the early work of Gregor Mendel.

In the years between Mendel's work and 1900 the foundations of cytology, the study of cells, was developed. The facts discovered about the nucleus and cell division were essential for Mendel's work to be properly understood.[10]

At this point, discoveries in cytology merged with the rediscovered ideas of Mendel to make a fusion called cytogenetics, (cyto = cell; genetics = heredity) which has continued to the present day.

During the 1890s several biologists began doing experiments on breeding. and soon Mendel's results were duplicated, even before his papers were read. Carl Correns and Hugo de Vries were the main rediscovers of Mendel's writings and laws. Both acknowledged Mendel's priority, although it is probable that de Vries did not understand his own results until after reading Mendel.[19] Though Erich von Tschermak was originally also credited with rediscovery, this is no longer accepted because he did not understand Mendel's laws.[20] Though de Vries later lost interest in Mendelism, other biologists built genetics into a science.[19]

Mendel's results were replicated, and genetic linkage soon worked out. William Bateson perhaps did the most in the early days to publicise Mendel's theory. The word genetics, and other terminology, originated with Bateson.

Mendel's experimental results have later been the object of some debate. Fisher analyzed the results of the F2 (second filial) ratio and found them to be implausibly close to the exact ratio of 3 to 1.[21] It is sometimes suggested that Mendel may have censored his results, and that his seven traits each occur on a separate chromosome pair, an extremely unlikely occurrence if they were chosen at random. In fact, the genes Mendel studied occurred in only four linkage groups, and only one gene pair (out of 21 possible) is close enough to show deviation from independent assortment; this is not a pair that Mendel studied.[22]

During the process of DNA replication, errors sometimes occur. These errors, called mutations, can have an effect on the phenotype of an organism. In turn, that usually has an effect on the organism's fitness, its ability to live and reproduce successfully.

Error rates are usually very low1 error in every 10100million basesdue to the "proofreading" ability of DNA polymerases.[23][24] Error rates are a thousandfold higher in many viruses. Because they rely on DNA and RNA polymerases which lack proofreading ability, they get higher mutation rates.

Processes that increase the rate of changes in DNA are called mutagenic. Mutagenic chemicals increase errors in DNA replication, often by interfering with the structure of base-pairing, while UV radiation induces mutations by causing damage to the DNA structure.[23] Chemical damage to DNA occurs naturally as well, and cells use DNA repair mechanisms to repair mismatches and breaks in DNAnevertheless, the repair sometimes fails to return the DNA to its original sequence.

In organisms which use chromosomal crossovers to exchange DNA and recombine genes, errors in alignment during meiosis can also cause mutations.[23] Errors in crossover are especially likely when similar sequences cause partner chromosomes to adopt a mistaken alignment; this makes some regions in genomes more prone to mutating in this way. These errors create large structural changes in DNA sequenceduplications, inversions or deletions of entire regions, or the accidental exchanging of whole parts between different chromosomes (called translocation).

Developed by Reginald Punnett, Punnett squares are used by biologists to determine the probability of offspring to having a particular genotype.

If B represents the allele for having black hair and b represents the allele for having white hair, the offspring of two Bb parents would have a 25% probability of having two white hair alleles (bb), 50% of having one of each (Bb), and 25% of having only black hair alleles (BB).

Geneticists (biologists who study genetics) use pedigree charts to record traits of people in a family. Using these charts, geneticists can study how a trait is inherited from person to person.

Geneticists can also use pedigree charts to predict how traits will be passed to future children in a family. For instance, genetic counselors are professionals who work with families who might be affected by genetic diseases. As part of their job, they create pedigree charts for the family, which can be used to study how the disease might be inherited.

Since human beings are not bred experimentally, human genetics must be studied by other means. One recent way is by studying the human genome. Another way, older by many years, is to study twins. Identical twins are natural clones. They carry the same genes, they may be used to investigate how much heredity contributes to individual people. Studies with twins have been quite interesting. If we make a list of characteristic traits, we find that they vary in how much they owe to heredity. For example:

The way the studies are done is like this. Take a group of identical twins and a group of fraternal twins. Measure them for various traits. Do a statistical analysis (such as analysis of variance). This tells you to what extent the trait is inherited. Those traits which are partly inherited will be significantly more similar in identical twins. Studies like this may be carried further, by comparing identical twins brought up together with identical twins brought up in different circumstances. That gives a handle on how much circumstances can alter the outcomes of genetically identical people.

The person who first did twin studies was Francis Galton, Darwin's half-cousin, who was a founder of statistics. His method was to trace twins through their life-history, making many kinds of measurement. Unfortunately, though he knew about mono and dizygotic twins, he did not appreciate the real genetic difference.[25][26] Twin studies of the modern kind did not appear until the 1920s.

The genetics of bacteria, archaea and viruses is a major field or research. Bacterial mostly divide by asexual cell division, but do have a kind of sex by horizontal gene transfer. Bacterial conjugation, transduction and transformation are their methods. In addition, the complete DNA sequence of many bacteria, archaea and viruses is now known.

Although many bacteria were given generic and specific names, like Staphylococcus aureus, the whole idea of a species is rather meaningless for an organism which does not have sexes and crossing-over of chromosomes.[27] Instead, these organisms have strains, and that is how they are identified in the laboratory.

Gene expression is the process by which the heritable information in a gene, the sequence of DNA base pairs, is made into a functional gene product, such as protein or RNA. The basic idea is that DNA is transcribed into RNA, which is then translated into proteins. Proteins make many of the structures and all the enzymes in a cell or organism.

Several steps in the gene expression process may be modulated (tuned). This includes both the transcription and translation stages, and the final folded state of a protein. Gene regulation switches genes on and off, and so controls cell differentiation, and morphogenesis. Gene regulation may also serve as a basis for evolutionary change: control of the timing, location, and amount of gene expression can have a profound effect on the development of the organism. The expression of a gene may vary a lot in different tissues. This is called pleiotropism, a widespread phenomenon in genetics.

Alternative splicing is a modern discovery of great importance. It is a process where from a single gene a large number of variant proteins can be assembled. One particular Drosophila gene (DSCAM) can be alternatively spliced into 38,000 different mRNA.[28]

Epigenetics is the study of changes in gene activity which are not caused by changes in the DNA sequence.[29] It is the study of gene expression, the way genes bring about their phenotypic effects.[30]

These changes in gene activity may stay for the remainder of the cell's life and may also last for many generations of cells, through cell divisions. However, there is no change in the underlying DNA sequence of the organism.[31] Instead, non-hereditary factors cause the organism's genes to behave (express themselves) differently.[32]

Hox genes are a complex of genes whose proteins bind to the regulatory regions of target genes. The target genes then activate or repress cell processes to direct the final development of the organism.[33][34]

There are some kinds of heredity which happen outside the cell nucleus. Normal inheritance is from both parents via the chromosomes in the nucleus of a fertilised egg cell. There are some kinds of inheritance other than this.[35]

Mitochondria and chloroplasts carry some DNA of their own. Their make-up is decided by genes in the chromosomes and genes in the organelle. Carl Correns discovered an example in 1908. The four o'clock plant, Mirabilis jalapa, has leaves which may be white, green or variegated. Correns discovered the pollen had no influence on this inheritance. The colour is decided by genes in the chloroplasts.

This is caused by a symbiotic or parasitic relationship with a microorganism.

In this case nuclear genes in the female gamete are transcribed. The products accumulate in the egg cytoplasm, and have an effect on the early development of the fertilised egg. The coiling of a snail, Limnaea peregra, is determined like this. Right-handed shells are genotypes Dd or dd, while left-handed shells are dd.

The most important example of maternal effect is in Drosophila melanogaster. The protein product maternal-effect genes activate other genes, which in turn activate still more genes. This work won the Nobel Prize in Physiology or Medicine for 1995.[36]

Much modern research uses a mixture of genetics, cell biology and molecular biology. Topics which have been the subject of Nobel Prizes in either chemistry or physiology include:

Many well-known disorders of human behaviour have a genetic component. This means that their inheritance partly causes the behavour, or makes it more likely the problem would occur. Examples include: [37]

Also, normal behaviour is also heavily influenced by heredity:

Originally posted here:
Genetics - Simple English Wikipedia, the free encyclopedia

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