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Genetic Medicine | Department of Pediatrics | University …

July 2nd, 2015 10:42 am

Leadership

Michael Bamshad, MD Professor Division Chief

The Division of Genetic Medicine is committed to providing an outstanding level of patient care, education and research. The faculty have diverse interests and are drawn from several disciplines including clinical genetics, molecular genetics, biochemical genetics, human embryology/teratology and neurology.

A large clinical program of medical genetics operates from Seattle Childrens Hospital staffed by faculty from the Division. These clinical activities concentrate on pediatric genetics but also encompass adult and fetal consultations. At Seattle Children's full IP consultations are available and general genetics clinics occur regularly. Consultative services are also provided to the University of Washington Medical Center and Swedish Hospital. In addition, a variety of interdisciplinary clinical services are provided at Childrens including cardiovascular genetics, skeletal dysplasia, neurofibromatosis, craniofacial genetics, gender disorders, neurogenetics and biochemical genetics as well as others. A very large regional genetics service sponsored by state Departments of Health are provided to multiple outreach clinical sites in both Alaska and Washington.

Our research holds the promise for both continued development of improved molecular diagnostic tools and successful treatment of inherited diseases. Research in the Division is highly patient-driven. It often begins with a physician identifying a particular patients problems and subsequently taking that problem into a laboratory setting for further analysis. The Division has a strong research focus with established research programs in medical genetics information systems, neurogenetic disorders, fetal alcohol syndrome, neuromuscular diseases, human teratology, population genetics/evolution and gene therapy.

The Division offers comprehensive training for medical students, residents, and postdoctoral fellows in any of the areas of our clinical and research programs relevant to medical genetics. Medical Genetics Training Website

Margaret L.P. Adam, MD Associate Professor mpa5@u.washington.edu

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Genetic Medicine – The University of Chicago Department of …

July 2nd, 2015 10:42 am

The Section of Genetic Medicine was created in May 2005 to both build research infrastructure in genetics within the Department of Medicine and to focus translational efforts related to genetics. As a result, the Section of Genetic is shaping the future of precision medicine with very active and successful research programs focused on the quantitative genetics, systems biology and genomics, and bioinformatics and computational biology. The Section provides extremely valuable collaborations with investigators in the Department of Medicine who are seeking to develop new and more powerful ways to identify genetic risk factors for common, complex disorders with almost immediate clinical application.

The Section of Genetic Medicine has a reputation for leading-edge research. In FY 14 the Section was awarded a large grant from the National Cancer Institute to build an Open Genomics Data Commons (OGDC)under the direction of Dr. Robert Grossman and is also home to the NIH funded Silvio O. Conte Center, led by Andrey Rzhetsky, PhD, where computational data-mining has been applied to understand the causes of neuropsychiatric disorders. We invite you to explore our website for more information about the Section.

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Genetic Engineering – humans, body, used, process, plants …

July 2nd, 2015 10:42 am

Photo by: Gernot Krautberger

Genetic engineering is any process by which genetic material (the building blocks of heredity) is changed in such a way as to make possible the production of new substances or new functions. As an example, biologists have now learned how to transplant the gene that produces light in a firefly into tobacco plants. The function of that genethe production of lighthas been added to the normal list of functions of the tobacco plants.

Genetic engineering became possible only when scientists had discovered exactly what is a gene. Prior to the 1950s, the term gene was used to stand for a unit by which some genetic characteristic was transmitted from one generation to the next. Biologists talked about a "gene" for hair color, although they really had no idea as to what that gene was or what it looked like.

That situation changed dramatically in 1953. The English chemist Francis Crick (1916 ) and the American biologist James Watson (1928 ) determined a chemical explanation for a gene. Crick and Watson discovered the chemical structure for large, complex molecules that occur in the nuclei of all living cells, known as deoxyribonucleic acid (DNA).

DNA molecules, Crick and Watson announced, are very long chains or units made of a combination of a simple sugar and a phosphate group.

Amino acid: An organic compound from which proteins are made.

DNA (deoxyribonucleic acid): A large, complex chemical compound that makes up the core of a chromosome and whose segments consist of genes.

Gene: A segment of a DNA molecule that acts as a kind of code for the production of some specific protein. Genes carry instructions for the formation, functioning, and transmission of specific traits from one generation to another.

Gene splicing: The process by which genes are cut apart and put back together to provide them with some new function.

Genetic code: A set of nitrogen base combinations that act as a code for the production of certain amino acids.

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Gene Therapy – Nature

July 2nd, 2015 10:42 am

Included in top indexing databases and has an impact factor of 3.104! The journal website is hosted on http://www.nature.com that gets 8.4 million page views per month Over 69,000 table of contents registrants and 82,706 page views across the Gene Therapy web site on average Easy and quick online submission system Rapid and rigorous peer review Advanced Article Preview (AAP) feature to be available from early March 2015 to all accepted original and review article authors. Accepted articles to be available online within 72 hours of acceptance into production! For further information on AAP please refer to About accepted article preview section Free manuscript deposition service to Pub Med Central on behalf of non-open access authors We regularly promote content alongside that of the Nature branded titles on our subject pages and in collections as well as via social media We also have a number of regional websites reaching a wide and varied audience demographic http://www.nature.com/regions Free online issue

Volume 22, No 7 July 2015 ISSN: 0969-7128 EISSN: 1476-5462

2014 Impact Factor 3.104* 117/289 Biochemistry & Molecular Biology 47/162 Biotechnology & Applied Microbiology 63/167 Genetics & Heredity 43/123 Medicine, Research & Experimental

Editors: J Glorioso, USA N Lemoine, UK

*2014 Journal Citation Reports Science Edition (Thomson Reuters, 2015)

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Gene Therapy now offers authors the option to publish their articles with immediate open access upon publication. Open access articles will also be deposited on PubMed Central at the time of publication and will be freely available immediately. Find out more from our FAQs page.

Reviews by top researchers in the field. See the recent Progress and Prospects articles.

Essential topics explored in depth in Gene Therapy Special Issues.

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eye conditions – All About Vision

July 2nd, 2015 10:42 am

Section Editor: Gary Heiting, OD

Have questions about an eye condition or vision problem? Browse our extensive list of doctor-written and doctor-reviewed articles for reliable, easy-to-understand information.

Please keep in mind that these articles are for general education purposes only. If you suspect you have an eye condition or vision problem or you have injured your eye, see an eye doctor immediately.

Acanthamoeba Keratitis A rare but serious eye infection associated with poor contact lens hygiene and other factors.

Amblyopia (Lazy Eye) Amblyopia is a vision development problem in infants and young children that can lead to permanent vision loss. Learn the symptoms, causes and treatments.

Astigmatism Usually caused by an irregular cornea, astigmatism causes blur at all distances. Also see the Eye Doctor Q&A on astigmatism.

Bell's Palsy This condition causes sudden paralysis of one side of the face. Because it affects blinking, it can cause severe dry eye.

Blepharitis Inflammation of the eyelids associated with chronic eye irritation, watery eyes, foreign body sensation, sensitivity to light and crusty debris at the base of the eyelashes.

Blurry Vision Blurry vision has many causes, from fatigue and eyestrain to serious eye diseases such as glaucoma. A video helps explain blurry vision causes and treatments.

Cataracts The risk of cataracts increases with age. Learn what causes them and how to protect your eyes. See also: Cataract News | FAQ | Eye Doctor Q&A | Congenital Cataracts

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Dental Stem Cell Potential Explored with Dental Pulp Stem …

July 2nd, 2015 10:42 am

Scanning through the headlines, tuning in to morning television shows, stem cells are repeatedly the topic of discussion a discussion that increasingly includes primary teeth.

The discovery of stem cells in dental pulp has led to much research and predictions about their potential uses. Although the full possibilities of tooth-derived stem cells are not yet known, some researchers believe that they could one day be valuable for regenerating dental tissues and possibly other tissues as well.

Pamela Robey, Ph.D., chief, Craniofacial and Skeletal Diseases Branch, National Institute of Dental and Craniofacial Research, says that because no one knows for certain what the full possibilities are for the cells isolated from dental pulp, nor can they accurately predict if or when they'll be used in clinical settings, patients and professionals need to make informed decisions.

"What we do know," she said, "is the cells from dental pulp in baby or wisdom teeth have the ability to make dentin and pulp and they might have the ability to make bone but right now that's all we really know for sure."

Because "the data for other things is not hard yet, we can't say how useful for the future they'll be," she said.

Dr. Jeremy Mao, a professor of dental medicine and director of the Tissue Engineering and Regenerative Medicine Laboratory at Columbia University, believes that dental stem cells and related bioengineering technologies will transform dentistry in a magnitude that is far greater than amalgam and dental implants.

"Some of the technologies may happen 10 years down the road but others may happen within 10 years," he predicted.

Presently, there are no human trials taking place with the dental postnatal cells and there are no clinical applications available. There also is no central place for dentists or patients to read about the latest in dental stem cell research. Dr. Robey advised anyone hearing claims of new evidence and dental stem cells to consult the Web site http://www.clinicaltrials.gov.

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What is Biotechnology? | BIO

July 2nd, 2015 10:41 am

At its simplest, biotechnology is technology based on biology - biotechnology harnesses cellular and biomolecular processes to develop technologies and products that help improve our lives and the health of our planet. We have used the biological processes of microorganisms for more than 6,000 years to make useful food products, such as bread and cheese, and to preserve dairy products.

Modern biotechnology provides breakthrough products and technologies to combat debilitating and rare diseases, reduce our environmental footprint, feed the hungry, use less and cleaner energy, and have safer, cleaner and more efficient industrial manufacturing processes.

Currently, there are more than 250 biotechnology health care products and vaccines available to patients, many for previously untreatable diseases. More than 18 million farmers around the world use agricultural biotechnology to increase yields, prevent damage from insects and pests and reduce farming's impact on the environment. And more than 50 biorefineries are being built across North America to test and refine technologies to produce biofuels and chemicals from renewable biomass, which can help reduce greenhouse gas emissions.

Recent advances in biotechnology are helping us prepare for and meet societys most pressing challenges. Here's how:

Biotech is helping toheal the worldby harnessing nature's own toolbox and using our own genetic makeup to heal and guide lines of research by:

Biotech uses biological processes such as fermentation and harnesses biocatalysts such as enzymes, yeast, and other microbes to become microscopic manufacturing plants. Biotech is helping tofuel the worldby:

Biotech improves crop insect resistance, enhances crop herbicide tolerance and facilitates the use of more environmentally sustainable farming practices. Biotech is helping tofeed the worldby:

Source: Healing, Fueling, Feeding: How Biotechnology is Enriching Your Life

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Arthritis: Facts on Diet, Treatment and Symptoms

July 2nd, 2015 10:41 am

Arthritis facts Arthritis is inflammation of one or more joints. Symptoms of arthritis include pain and limited function of joints. Arthritis sufferers include men and women, children and adults. A rheumatologist is a medical arthritis expert. Earlier and accurate diagnosis can help to prevent irreversible damage and disability. What is arthritis? What causes arthritis?

Arthritis is a joint disorder featuring inflammation. A joint is an area of the body where two different bones meet. A joint functions to move the body parts connected by its bones. Arthritis literally means inflammation of one or more joints.

Arthritis is frequently accompanied by joint pain. Joint pain is referred to as arthralgia.

There are many types of arthritis (over 100 identified, and the number is growing). The types of arthritis range from those related to wear and tear of cartilage (such as osteoarthritis) to those associated with inflammation resulting from an overactive immune system (such as rheumatoid arthritis). Together, the many types of arthritis make up the most common chronic illness in the United States.

The causes of arthritis depend on the form of arthritis. Causes include injury (leading to osteoarthritis), metabolic abnormalities (such as gout and pseudogout), hereditary factors, the direct and indirect effect of infections (bacterial and viral), and a misdirected immune system with autoimmunity (such as in rheumatoid arthritis and systemic lupus erythematosus).

Arthritis is classified as one of the rheumatic diseases. These are conditions that are different individual illnesses, with differing features, treatments, complications, and prognoses. They are similar in that they have a tendency to affect the joints, muscles, ligaments, cartilage, and tendons, and many have the potential to affect other internal body areas.

Medically Reviewed by a Doctor on 5/7/2015

Arthritis - Effective Treatments Question: What kinds of treatments have been effective for your arthritis?

Arthritis - Symptoms Question: What symptoms did you experience with arthritis?

Arthritis - Diet and Fish Oil Question: Do you follow a special diet for arthritis? Does it involve fish oils? Please discuss your diet.

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Swiss Apple Stem Cells for perfect skin. What do plant …

July 1st, 2015 2:50 pm

This active ingredient won the prize in European Innovation Best Active Ingredient in 2008. It is a revolutionary technology designed to protect human skin stem cells with the help of stem cells from a rare Swiss apple. The clinical trials conducted by the company who discovered this ingredient showed that 100% of the participants saw a reduction in fine lines and wrinkles after using a solution containing 2% PhytoCellTech Malus Domestica.

According to the Bible, Adam bit into an apple (coaxed on by us femme fatales) and deprived Earth of Heaven...was he attracted by the delicious taste or did he already know of the amazing youth-boosting properties of this fruit?

PhytoCellTec Malus Domestica is an award-winning patented liposomal preparation, so containing tiny bubbles made out of the same material as cell membranes, based on the stem cells of a rare Swiss apple called Uttwiler Sptlauber that derives from a seedling planted in the middle of the18th century. Uttwiler Sptlauber is an endangered apple variety that is well-known for its ability to be stored for long periods without shrivelling and thus its longevity potential. The apples are rich in phytonutrients, proteins and long-living cells. A novel technology has now been developed enabling the cultivation of rare and endangered species like Uttwiler Sptlauber. Thanks to this technology, plant stem cells can be obtained and incorporated into skin care products to enhance the longevity of skin cells. Not only does it protect the skins own stem cells but has been shown to have excellent age-delaying and anti-wrinkle properties, and is currently one of the most pioneering and exciting ingredients in skin care.

Stem Cells and Longevity

Longevity is related to specific cells called stem cells which have a unique growth characteristic. These cells can make identical copies of themselves as well as differentiate (in other words, split) to become separate, specialised cells. Two basic types of stem cells are present in the human body:

Embryonic stem cells found in blastocysts (structures found in the human pre-embryonic stage) can grow and differentiate into one of the more than 220 different cell types which make up the human body;

Adult stem cells located in some adult tissues can only differentiate into their own or related cell types. These cells act as a repair system for the body but also maintain the normal turnover of regenerative organs such as blood, skin or intestinal tissues.

Research on Stem Cells and Applications

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Stem Cell Assays Reproducible Research on Stem Cells

July 1st, 2015 3:45 am

Cells Weekly is a digest of the most interesting news and events in stem cell research, cell therapy and regenerative medicine. Cells Weekly is posted every Sunday night!

This week was a week of ISSCR 2015, so read all news from the conference here.

1. The price of gene therapy trial failure A year ago, Celladon became the first gene therapy company, which received designation by US FDA Breakthrough Therapy for their MYDICAR platform in heart failure. It means very good data from Phase 1 trial and impressive efficacy in early Phase 2. Despite the recognition and all excitement, a year later, MYDICAR failed to deliver efficacy as result of Phase 2. The fate of the company was unclear. This week, the company warned their investor about potential termination suspension of MYDICAR and other pre-clinical programs, sale/ merger of the company or liquidation:

We are aggressively pursuing that course, said Paul Cleveland, president and chief executive officer of Celladon. If we are unable to identify a merger or sale that provides superior value to our shareholders, we will move forward with a liquidation and distribution of net cash to shareholders. The Company also announced a second reduction in its workforce, with approximately half of the employees not previously notified of termination of employment being expected to depart in the third quarter.

Very bad news for the field! Many lessons to learn

2. Heart peacemaker activity turned on by light The most interesting study from this week came from 2 Israeli scientists. They were able to modulate cardiac pacing in vivo, using optogenetic approach. AVV vector with light-sensitive protein transgene was injected directly into myocardium:

This allowed optogenetic pacing of the hearts at different beating frequencies with blue-light illumination both in vivo and in isolated perfused hearts. Optical mapping confirmed that the source of the new pacemaker activity was the site of ChR2 transgene delivery. Notably, diffuse illumination of hearts where the ChR2 transgene was delivered to several ventricular sites resulted in electrical synchronization

This is fantastic! The author Lior Gepstein says:

Our work is the first to suggest a non-electrical approach to cardiac resynchronization therapy, Gepstein said. Before this, there have been a number of elegant gene therapy and cell therapy approaches for generating biological pacemakers that can pace the heart from a single spot. However it was impossible to use such approaches to activate the heart simultaneously from a number of sites for resynchronization therapy.

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regenerative medicine | Britannica.com

July 1st, 2015 3:45 am

regenerative medicine,cartilage: bronchus repair using bioartificial tissue transplantationHospital Clinic of Barcelona/APthe application of treatments developed to replace tissues damaged by injury or disease. These treatments may involve the use of biochemical techniques to induce tissue regeneration directly at the site of damage or the use of transplantation techniques employing differentiated cells or stem cells, either alone or as part of a bioartificial tissue. Bioartificial tissues are made by seeding cells onto natural or biomimetic scaffolds (see tissue engineering). Natural scaffolds are the total extracellular matrixes (ECMs) of decellularized tissues or organs. In contrast, biomimetic scaffolds may be composed of natural materials, such as collagen or proteoglycans (proteins with long chains of carbohydrate), or built from artificial materials, such as metals, ceramics, or polyester polymers. Cells used for transplants and bioartificial tissues are almost always autogeneic (self) to avoid rejection by the patients immune system. The use of allogeneic (nonself) cells carries a high risk of immune rejection and therefore requires tissue matching between donor and recipient and involves the administration of immunosuppressive drugs.

A variety of autogeneic and allogeneic cell and bioartificial tissue transplantations have been performed. Examples of autogeneic transplants using differentiated cells include blood transfusion with frozen stores of the patients own blood and repair of the articular cartilage of the knee with the patients own articular chondrocytes (cartilage cells) that have been expanded in vitro (amplified in number using cell culture techniques in a laboratory). An example of a tissue that has been generated for autogeneic transplant is the human mandible (lower jaw). Functional bioartificial mandibles are made by seeding autogeneic bone marrow cells onto a titanium mesh scaffold loaded with bovine bone matrix, a type of extracellular matrix that has proved valuable in regenerative medicine for its ability to promote cell adhesion and proliferation in transplantable bone tissues. Functional bioartificial bladders also have been successfully implanted into patients. Bioartificial bladders are made by seeding a biodegradable polyester scaffold with autogeneic urinary epithelial cells and smooth muscle cells.

Another example of a tissue used successfully in an autogeneic transplant is a bioartificial bronchus, which was generated to replace damaged tissue in a patient affected by tuberculosis. The bioartificial bronchus was constructed from an ECM scaffold of a section of bronchial tissue taken from a donor cadaver. Differentiated epithelial cells isolated from the patient and chondrocytes derived from mesenchymal stem cells collected from the patients bone marrow were seeded onto the scaffold.

There are few clinical examples of allogeneic cell and bioartificial tissue transplants. The two most common allogeneic transplants are blood-group-matched blood transfusion and bone marrow transplant. Allogeneic bone marrow transplants are often performed following high-dose chemotherapy, which is used to destroy all the cells in the hematopoietic system in order to ensure that all cancer-causing cells are killed. (The hematopoietic system is contained within the bone marrow and is responsible for generating all the cells of the blood and immune system.) This type of bone marrow transplant is associated with a high risk of graft-versus-host disease, in which the donor marrow cells attack the recipients tissues. Another type of allogeneic transplant involves the islets of Langerhans, which contain the insulin-producing cells of the body. This type of tissue can be transplanted from cadavers to patients with diabetes mellitus, but recipients require immunosuppression therapy to survive.

Cell transplant experiments with paralyzed mice, pigs, and nonhuman primates demonstrated that Schwann cells (the myelin-producing cells that insulate nerve axons) injected into acutely injured spinal cord tissue could restore about 70 percent of the tissues functional capacity, thereby partially reversing paralysis.

embryonic stem cell: scientists conducting research on embryonic stem cellsMauricio LimaAFP/Getty ImagesStudies on experimental animals are aimed at understanding ways in which autogeneic or allogeneic adult stem cells can be used to regenerate damaged cardiovascular, neural, and musculoskeletal tissues in humans. Among adult stem cells that have shown promise in this area are satellite cells, which occur in skeletal muscle fibres in animals and humans. When injected into mice affected by dystrophy, a condition characterized by the progressive degeneration of muscle tissue, satellite cells stimulate the regeneration of normal muscle fibres. Ulcerative colitis in mice was treated successfully with intestinal organoids (organlike tissues) derived from adult stem cells of the large intestine. When introduced into the colon, the organoids attached to damaged tissue and generated a normal-appearing intestinal lining.

In many cases, however, adult stem cells such as satellite cells have not been easily harvested from their native tissues, and they have been difficult to culture in the laboratory. In contrast, embryonic stem cells (ESCs) can be harvested once and cultured indefinitely. Moreover, ESCs are pluripotent, meaning that they can be directed to differentiate into any cell type, which makes them an ideal cell source for regenerative medicine.

Studies of animal ESC derivatives have demonstrated that these cells are capable of regenerating tissues of the central nervous system, heart, skeletal muscle, and pancreas. Derivatives of human ESCs used in animal models have produced similar results. For example, cardiac stem cells from heart-failure patients were engineered to express a protein (Pim-1) that promotes cell survival and proliferation. When these cells were injected into mice that had experienced myocardial infarction (heart attack), the cells were found to enhance the repair of injured heart muscle tissue. Likewise, heart muscle cells (cardiomyocytes) derived from human ESCs improved the function of injured heart muscle tissue in guinea pigs.

Derivatives of human ESCs are likely to produce similar results in humans, although these cells have not been used clinically and could be subject to immune rejection by recipients. The question of immune rejection was bypassed by the discovery in 2007 that adult somatic cells (e.g., skin and liver cells) can be converted to ESCs. This is accomplished by transfecting (infecting) the adult cells with viral vectors carrying genes that encode transcription factor proteins capable of reprogramming the adult cells into pluripotent stem cells. Examples of these factors include Oct-4 (octamer 4), Sox-2 (sex-determining region Y box 2), Klf-4 (Kruppel-like factor 4), and Nanog. Reprogrammed adult cells, known as induced pluripotent stem (iPS) cells, are potential autogeneic sources for cell transplantation and bioartificial tissue construction. Such cells have since been created from the skin cells of patients suffering from amyotrophic lateral sclerosis (ALS) and Alzheimer disease and have been used as human models for the exploration of disease mechanisms and the screening of potential new drugs. In one such model, neurons derived from human iPS cells were shown to promote recovery of stroke-damaged brain tissue in mice and rats, and, in another, cardiomyocytes derived from human iPS cells successfully integrated into damaged heart tissue following their injection into rat hearts. These successes indicated that iPS cells could serve as a cell source for tissue regeneration or bioartificial tissue construction.

Scaffolds and soluble factors, such as proteins and small molecules, have been used to induce tissue repair by undamaged cells at the site of injury. These agents protect resident fibroblasts and adult stem cells and stimulate the migration of these cells into damaged areas, where they proliferate to form new tissue. The ECMs of pig small intestine submucosa, pig and human dermis, and different types of biomimetic scaffolds are used clinically for the repair of hernias, fistulas (abnormal ducts or passageways between organs), and burns.

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Sermorelin – HGH Injections and Testosterone Therapy Programs

June 30th, 2015 11:46 am

HGH (Human Growth Hormone) medications and Sermorelin injectable HGH stimulating medication. Sermorelin is a gH releasing hormone with 29- Amino acids.

ANALYSIS: If you fit the qualifications (including age) then SERMORELIN might be the best choice financially, especially with 1/3 the benefits but at a fraction of the cost of HGH premium brands

*If cost is an issue then SERMORELIN is high recommended instead of doing nothing to address and human growth hormone (HGH) deficiencies due to aging or other factors.

Sermorelin Acetate or Growth Hormone Releasing Hormone (GHRH) is also considered a Sermorelin HGH therapy that produces results by binding to specific receptors thereby increasing the secretion of endogenous growth hormone (HGH) doing do by stimulating the pituitary gland. The body responds to the elevation of HGH which produces an anabolic effect to thetissue, yielding numerous health and wellness benefits. Sermorelin is known to contain 29 amino acids and studies as far back as the 1970s have shownSermorelin results occur by stimulating an increase in Human Growth Hormone (HGH) by the pituitary gland. Some clinics also tout that Sermorelin is better then actual recombinant HGH in many respects. Therapy and Sermorelin price can be substantially lower then the cost of HGH therapies. Many HGH maintenance programs include HGH Sermorelin acetate to be administered at the tail end HGH therapies.

Buy Sermorelin injections and similar Sermorelin products when cost is certainly an issue. BHRT Male patients and BHRT Female patients both benefit with Sermorelin and similar HGH products.

Sermorelin Acetate injection results happen because ofits ability tostimulate the production and release of HGH. Medical studies have found that once sufficient amounts of HGH are produced in the body, Sermorelinthen stimulates the insulin growth factor (IGF-1) in the liver which helps increase new cell growth as well as boost the bodys metabolism

The welcomed side effects with a Sermorelin dosage are: increased energy, better sleep, and weight loss, all which have been linked to the effect of Sermorelin on the pituitary gland and its increase of HGH production. In some people the combination of both of these helps to increase the effectiveness and overall benefits of the treatment. Growth Hormone Releasing Peptide or GHRP-6 has been shown to act similarly as Sermorelin, however binds to different receptors. The rate of HGH secretion is increased when the two are combined and the product is an overall improved outcome in a Sermorelin review. Combinations of GHRP-6 and GHRP-2 HGH products similarly.

Sermorelin reviews show that as we begin to age, our HGH levels decline at a dramatic rate producing side effects that can be unpleasant. In our mid 20s we experience the highest levels of HGH output and by our 40s our HGH levels diminish by as much as 40%. Sermorelinbenefits are well known by todays physicians to be a safe and effective means to stimulate as well as increase HGH production. To begin a protocol of HGH and to ensure its effectiveness will be greatly reliantondiligentblood panel tests which will help dictate proper dosages to avoid any unnecessary side effects. By utilizing the blood panel information and medical documentation, one can implement a long term plan that will help you regain and stabilize healthy hormone levels. The purpose of Sermorelin Therapy is to stimulate the pituitary gland to secrete HGH, and to so naturally. Sermorelin benefits are achieved by following a therapy of nightlydosageswith subcutaneous injections. Unlike HGH Therapy, Sermorelin Therapy tries to address the primary cause of diminishing HGH levels in the body by naturally stimulating the pituitary gland to produce more HGH rather than replenish levels with bio-identical hormones.

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Endocrinology – Wikipedia, the free encyclopedia

June 30th, 2015 11:46 am

Endocrinology (from Greek , endon, "within"; , krn, "to separate"; and -, -logia) is a branch of biology and medicine dealing with the endocrine system, its diseases, and its specific secretions known as hormones. It is also concerned with the integration of developmental events proliferation, growth, and differentiation, and the psychological or behavioral activities of metabolism, growth and development, tissue function, sleep, digestion, respiration, excretion, mood, stress, lactation, movement, reproduction, and sensory perception caused by hormones. Specializations include behavioral endocrinology[1][2][3] and comparative endocrinology.

The endocrine system consists of several glands, all in different parts of the body, that secrete hormones directly into the blood rather than into a duct system. Hormones have many different functions and modes of action; one hormone may have several effects on different target organs, and, conversely, one target organ may be affected by more than one hormone.

In the original 1902 definition by Bayliss and Starling (see below), they specified that, to be classified as a hormone, a chemical must be produced by an organ, be released (in small amounts) into the blood, and be transported by the blood to a distant organ to exert its specific function. This definition holds for most "classical" hormones, but there are also paracrine mechanisms (chemical communication between cells within a tissue or organ), autocrine signals (a chemical that acts on the same cell), and intracrine signals (a chemical that acts within the same cell).[4] A neuroendocrine signal is a "classical" hormone that is released into the blood by a neurosecretory neuron (see article on neuroendocrinology).

Examples of amine hormones

Examples of steroid hormones

Griffin and Ojeda identify three different classes of hormone based on their chemical composition:[5]

Amines, such as norepinephrine, epinephrine, and dopamine (catecholamines), are derived from single amino acids, in this case tyrosine. Thyroid hormones such as 3,5,3-triiodothyronine (T3) and 3,5,3,5-tetraiodothyronine (thyroxine, T4) make up a subset of this class because they derive from the combination of two iodinated tyrosine amino acid residues.

Peptide hormones and protein hormones consist of three (in the case of thyrotropin-releasing hormone) to more than 200 (in the case of follicle-stimulating hormone) amino acid residues and can have a molecular mass as large as 30,000 grams per mole. All hormones secreted by the pituitary gland are peptide hormones, as are leptin from adipocytes, ghrelin from the stomach, and insulin from the pancreas.

Steroid hormones are converted from their parent compound, cholesterol. Mammalian steroid hormones can be grouped into five groups by the receptors to which they bind: glucocorticoids, mineralocorticoids, androgens, estrogens, and progestogens. Some forms of vitamin D, such as calcitriol, are steroid-like and bind to homologous receptors, but lack the characteristic fused ring structure of true steroids.

The earliest study of endocrinology began in China.[6] The Chinese were isolating sex and pituitary hormones from human urine and using them for medicinal purposes by 200 BCE.[6] They used many complex methods, such as sublimation of steroid hormones.[6] Another method specified by Chinese textsthe earliest dating to 1110specified the use of saponin (from the beans of Gleditschia sinensis) to extract hormones, but gypsum (containing calcium sulfate) was also known to have been used.[6]

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Patients at risk for stem cell transplant complications …

June 29th, 2015 3:45 pm

June 26, 2015

Lymphocyte recovery in related and unrelated stem cell transplant recipients generally falls into three patterns that are significantly associated with survival, according to findings from a phase 2 clinical trial published in Biology of Blood & Marrow Transplantation (2015; 21[7]:1237-1245).

This first-of-its-kind research continues the efforts of principal investigator Amir Toor, MD, of the Virginia Commonwealth University Massey Cancer Center in Richmond, to understand the immune system as a dynamical system that can be modeled to improve stem cell transplantation.

"We began considering lymphocyte reconstitution following stem cell transplantation as similar to population growth models. So, we graphed the lymphocyte counts of our patients at various times following their transplant as a logistic function and observed distinct patterns that correlated with clinical outcomes," said Toor.

"Our goal is to use this data to develop models that can predict complications from stem cell transplantation. Then, we may be able to intervene at key points in times with appropriate clinical treatments that will make the most positive impact on patients' outcomes."

The study retrospectively examined lymphocyte recovery and clinical outcome data from a recent phase II clinical trial (Clinical trials.gov identifier NCT00709592) in which 41 patients received a stem cell transplant from related or unrelated donors.

As part of the clinical trial protocol, the patients underwent low-dose radiation therapy and received one of two different doses of antithymocyte globulin (ATG), an immune-modulating drug given before transplantation to guard against graft-versus-host-disease (GVHD). GVHD is a condition that occurs when immune cells from the donor attack the recipient's body.

Following transplantation, the researchers observed that the patients' lymphocytes recovered in one of three general patterns that correlated significantly with survival, relapse, GVHD, and the need for further donor immune cell infusions to treat the cancer.

Group A experienced fast, early lymphoid expansion, culminating in a high absolute lymphoid count (ALC) within 2 months of transplantation. Group B experienced a slower, but steady lymphoid expansion that peaked much later than group A with a lower ALC. Group C experienced very poor lymphocyte recovery that demonstrated an early, but brief lymphoid expansion with a very low ALC.

Group B had the best clinical outcomes with a survival rate of 86%, followed by group A with a survival rate of 67% and group C with 30% survival. Relapse rates between groups A and B were similar at 33% and 29%, respectively, while group C experienced a 90% relapse rate.

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death :: Diagnosis of brain-stem death | Britannica.com

June 29th, 2015 3:43 pm

Diagnosis of brain-stem death

The diagnosis is not technically difficult. In more and more countries, it is made on purely clinical grounds. The aim of the clinical tests is not to probe every neuron within the intracranial cavity to see if it is deadan impossible taskbut to establish irreversible loss of brain-stem function. This is the necessary and sufficient condition for irreversible unconsciousness and irreversible apnea, which together spell a dead patient. Experience has shown that instrumental procedures (such as electroencephalography and studies of cerebral blood flow) that seek to establish widespread loss of cortical function contribute nothing of relevance concerning the cardiac prognosis. Such tests yield answers of dubious reliability to what are widely felt to be the wrong questions. As the concept of brain-stem death is relatively new, most countries rightly insist that the relevant examinations be carried out by physicians of appropriate seniority. These doctors (usually neurologists, anesthetists, or specialists in intensive care) must be entirely separate from any who might be involved in using the patients organs for subsequent transplants.

The diagnosis of brain-stem death involves three stages. First, the cause of the coma must be ascertained, and it must be established that the patient (who will always have been in apneic coma and on a ventilator for several hours) is suffering from irremediable, structural brain damage. Damage is judged irremediable based on its context, the passage of time, and the failure of all attempts to remedy it. Second, all possible causes of reversible brain-stem dysfunction, such as hypothermia, drug intoxication, or severe metabolic upset, must be excluded. Finally, the absence of all brain-stem reflexes must be demonstrated, and the fact that the patient cannot breathe, however strong the stimulus, must be confirmed.

It may take up to 48 hours to establish that the preconditions and exclusions have been met; the testing of brain-stem function takes less than half an hour. When testing the brain-stem reflexes, doctors check for the following normal responses: (1) constriction of the pupils in response to light, (2) blinking in response to stimulation of the cornea, (3) grimacing in response to firm pressure applied just above the eye socket, (4) movements of the eyes in response to the ears being flushed with ice water, and (5) coughing or gagging in response to a suction catheter being passed down the airway. All responses have to be absent on at least two occasions. Apnea, which also must be confirmed twice, is assessed by disconnecting the patient from the ventilator. (Prior to this test, the patient is fully oxygenated by being made to breathe 100 percent oxygen for several minutes, and diffusion oxygenation into the trachea is maintained throughout the procedure. These precautions ensure that the patient will not suffer serious oxygen deprivation while disconnected from the ventilator.) The purpose of this test is to establish the total absence of any inspiratory effort as the carbon dioxide concentration in the blood (the normal stimulus to breathing) reaches levels more than sufficient to drive any respiratory centre cells that may still be alive.

The patient thus passes through a tight double filter of preconditions and exclusions before he is even tested for the presence of a dead brain stem. This emphasis on strict preconditions and exclusions has been a major contribution to the subject of brain-stem death, and it has obviated the need for ancillary investigations. Thousands of patients who have met criteria of this kind have had ventilation maintained: all have developed asystole within a few hours or a few days, and none has ever regained consciousness. There have been no exceptions. The relevant tests for brain-stem death are carried out systematically and without haste. There is no pressure from the transplant team.

The developments in the idea and diagnosis of brain-stem death came as a response to a conceptual challenge. Intensive-care technology had saved many lives, but it had also created many brain-dead patients. To grasp the implications of this situation, society in generaland the medical profession in particularwas forced to rethink accepted notions about death itself. The emphasis had to shift from the most common mechanism of death (i.e., irreversible cessation of the circulation) to the results that ensued when that mechanism came into operation: irreversible loss of the capacity for consciousness, combined with irreversible apnea. These results, which can also be produced by primary intracranial catastrophes, provide philosophically sound, ethically acceptable, and clinically applicable secular equivalents to the concepts of departure of the soul and loss of the breath of life, which were so important to some earlier cultures.

Throughout history, specific cultural contexts have always played a crucial role in how people perceived death. Different societies have held widely diverging views on the breath of life and on how the soul left the body at the time of death. Such ideas are worth reviewing (1) because of the light they throw on important residual elements of popular belief; (2) because they illustrate the distance traveled (or not traveled) between early beliefs and current ones; and (3) because of the relevance of certain old ideas to contemporary debates about brain-stem death and about the philosophical legitimacy of organ transplantation. The following discussion therefore focuses on how certain cultural ideas about death compare or contrast with the modern concept. For an overview of various eschatologies from a cross-cultural perspective, see death rite: Death rites and customs.

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Stem cell clinic opens in Mandaue | Sun.Star

June 28th, 2015 11:45 pm

GOVERNMENT needs to ramp up its efforts to get its share of the global medical tourism market, an industry player said.

Medical tourism in the country is picking up as more foreign patients seek medical services here. As a regional player, we are slowly catching up with our neighbors like Thailand and Korea, said Dr. Roderick Yalung, medical director of Regenestem in the Philippines.

He noted that a lot of hospitals and health and wellness centers in the country are now affiliated with institutions abroad, and that many medical centers and clinics have innovated and now use state-of-the-art facilities.

Yalung believes the Philippines is well positioned for medical tourism because we offer cheaper services yet high-quality medical attention, plus a variety of destinations to offer while patients recuperate.

He pointed out that a breast augmentation package would cost $8,000 to $10,000. This already covers hotel accommodations and round-trip fares plus a visit to a local tourism destination. The same amount would cover only the cost of the procedure, he said, in the United States.

We really have advantages, thats why the industry is calling on the government to fund medical tourism because this could be a revenue driver for the economy, Yalung said. Government support was a key factor in the thriving medical tourism industry in countries like Thailand, Korea and Singapore, he added.

In a 2010 study, the Philippines ranked 11th in the top 15 destinations for medical tourists in the world, with Thailand and Singapore in the top two slots.

According to a 2013 report by the Philippine Institute of Development Studies, one of the problems is the lack of information such as medical tourist arrivals, expenditures, and services.

Yalung was recently in Cebu to open Regenestem, its first clinic in the Visayas and the second clinic in Asia of the Global Stem Cell Group, which offers the most comprehensive and up-to-date stem cell treatments. Regenestem Cebu is located at Block 88 of Oakridge Business Park on A.S. Fortuna in Mandaue City. It also offers services like cosmetic surgery, anti-ageing, dermatology, regenerative medicine, sports and arthritis medicine, and molecular orthopedics.

We decided to open in Cebu because of its robust tourism and we believe there is a ready market for these kinds of medical services, said Yalung.

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Personalized Medicine, Targeted Therapeutics and Companion …

June 28th, 2015 11:44 pm

NEW YORK, June 23, 2015 /PRNewswire/ --

This is a comprehensive account of the market size, segmentation, key players, SWOT analysis, influential technologies, and business and economic environments. The report is supported by over 270 tables & figures over 254 pages. The personalized medicine (global) market is presented as follows:

By Company (e.g., 23andMe, AFFYMETRIX, ATOSSA GENETICS, NODALITY, deCode /Amgen, CELERA, MYRIAD) By Geography (US, UK, EU) By Segment (Targeted therapeutics, Companion Diagnostics, Esoteric tests, Esoteric lab services) By Sub-market (Companion diagnostics & therapeutic, nutrition & wellness, medical technology, pharmacogenomics, consumer genomics)

A wealth of financial data & business strategy information is provided including:

Company financials, sales & revenue figures Business Model Strategies for Diagnostic, Pharmaceutical and Biotechnology Companies Business Model Strategies for Providers. Provider Systems and Academic Medical Centres Business Model Strategies for Payers & Governments Private and Public Funding and Personalized Medicine Reimbursement Revisions to Current Payment Systems and intellectual property How to Gain Market Penetration in the EU Cost-effectiveness and Business Value of Personalized Medicine Consumer genomics and POC market Therapeutics and Companion Diagnostics (e.g., BRAC Analysis, Oncotype Dx , KRAS Mutations) Comprehensive account of company product portfolios & kits

SWOT, Economic & Regulatory Environment specifics include:

Key strengths, weaknesses and threats influencing leading player position within the market Technologies driving the market (e.g., New-Generation Sequencing Technologies, Ultra-High Throughput Sequencing) Top fastest growing market segments and emerging opportunities Top pharmaceutical companies within the IPM by market share and revenue Comprehensive product portfolios, R&D activity and pipeline therapeutics M&A activity and future strategies of top personalized medicine pharmacos Personalized Medicine Regulation (USA, UK, Germany, France, Spain, Italy) CE-marked Personalized Medicine/Diagnostic Tests FDA Advances in Personalized Medicine Regulation

This report highlights a number of significant pharmacos and gives details of their operations, products, financials and business strategy.

23andMe Affymetrix Astex Pharmaceuticals Atossa Genetics CuraGen Celera Corporation (Quest Diagnostics) Celldex Therapeutics deCode Genetics (Amgen) Illumina Genelex Myriad Nodality Qiagen What you will gain:

An in-depth understanding of the global personalized medicine market and it's environment Current market facts, figures and product lines of key players in the industry Emerging trends in key markets such as the US, UK, Germany and France Knowledge of how the personalized medicine market will integrate into the global healthcare market Technical insights into new generation sequencing technologies and ultra-high throughput sequencing Updates on bioinformatics, high throughput systems, genetic analysis kits, companion diagnostics and future technologies FDA approved pharmacogenetic tests and recognized biomarkers Information on key government and regulatory policies Strategies on how to adapt and restructure current business models to this industry

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OPHTHALMOLOGY. What is Ophthalmology? (Opthalmology)

June 28th, 2015 11:44 pm

Ophthalmology is the medicine discipline which deals with the anatomy and diseases of the eye. An ophthalmologist refers to a specialist in both medical and surgical eye problems, as ophthalmologists perform operations on eyes.

The word ophthalmology has Greek , as ophthalmos means eye and logos means a word or a thought. Thereby ophthalmology can literally be translated as the science of eyes. As a discipline, it applies to animal eyes also. However, veterinary medicine is regulated separately in many countries and states. Therefore ophthalmologists treating both humans and animals are rare.

Ophthalmologists are medical doctors (MD/MBBS or D.O.) who have completed a college degree, medical school, and residency in ophthalmology. Ophthalmology was the first medicine discipline to offer board certification which is now a standard practice among all specialties. In many countries, ophthalmologistscan also undergo specialized training in one of the many subspecialities, as the ones listed below.

Ophthalmology sub-specialities:

* Ocular oncology. * Oculoplastics & Orbit surgery. * Ophthalmic pathology.

* Refractive surgery. * Uveitis/Immunology. * Veterinary Formal specialty training programs in veterinary ophthalmology now exist in some countries. * Vitreo-retinal surgery, deals with surgical management of retinal and posterior segment diseases and disorders.

* Anterior segment surgery * Cataracts most general ophthalmologists perform cataract surgery, is not usually considered a subspecialty. * Cornea, ocular surface, and external disease. * Glaucoma. * Medical retina,which deals with treatment of retinal problems through non-surgical means. * Neuro-ophthalmology. * Pediatric ophthalmology/Strabismus (mis-alignment of the eyes)

In america, certification by the American Board of Ophthalmology is a voluntary process. This process involves a written and an oral examination. A candidate who successfully passes becomes a Board Certified Diplomate of the American Board of Ophthalmology. Thus this person is entitled to use the letters D.A.B.O. after his or her name.

The American Academy of Ophthalmology (AAO) is the largest national membership medical association of ophthalmologists in America. +90 percent of practicing U.S. Eye M.D.s are AAO Academy members, and the Academy has more than 7,000 international members. The group has its headquarters in San Francisco, California.

The academy originated as American Academy of Ophthalmology and Otolaryngology (AAOO), founded in 1896 as a medical association of both ophthalmologists and otolaryngologists, but was split in 1979 and divided into separate academies for each specialty. Outside the medical community it promotes public health information.

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Gordie Howe’s Stem Cell Treatment Raises Issues

June 28th, 2015 11:44 pm

Gordie Howes Treatment Raises Source of Stem Cells Issues

The Detroit News is reporting on a controversy surrounding the stem cells used to treat NHL legend Gordie Howe. Howe suffered a stroke on October 26, 2014 and was in declining health. He received stem cell treatment in December, and family members share that his condition has improved a great deal.

The source of the controversy is that the company behind the treatments, Stemedica, didnt initially reveal some of the stem cells came from an aborted fetus.

The paper adds that Dave McGuigan a VP at Stemedica told The Detroit News and other media in February that only adult stem cells were used in the injections Howe received at a clinic in Mexico. However, in a separate investigation, Stemedica told USA Today that some of the stem cells used for Gordie Howe were from a fetus that was aborted at approximately 15 weeks.

When interviewed by USA Today, Stemedicas President, Maynard Howe (not related to Gordie Howe) stated, We just dont want to get people confused about what it is. Theyre really considered legally adult stem cells even if theyre fetal-derived.

While legal definitions may permit Stemedicas position, there are moral and ethical issues as well as matters of law. It is crucial that medical and stem cell providers be clear about the sources and types of stem cells being used. If the information reported by The Detroit News is correct, we view this as a significant breach of trust and ethical conduct. We simply think more is required.

We believe as a matter of faith that life begins at conception. We recognize that many of clients have religious and ethical concerns of their own, and we try to respect them in all we do. Consequently, Soter Healthcare has a specific agreement with our stem cell medical providers at both the lab and the hospitals, to use only Respect for Life Stem Cells. This is our assurance that no stem cells derived from abortion in any form will be used. We believe this is the only contract of its kind in effect today. The fetal cells we obtain and use come following miscarriage, stillbirths or premature infant mortality. To make sure there are no safety issues for a patient, all stem cells are checked and rechecked to make sure they are disease and infection free before treatments.

Being true to our convictions and making sure you always know the type and source of stem cells used in your treatment is how we do business. Anything less is unacceptable.

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NIH Fact Sheet on Human Pluripotent Stem Cell Research …

June 28th, 2015 11:44 pm

The Promise of Stem Cell Research

Human pluripotent stem cells are a unique scientific and medical resource. In 1998, scientists at the University of Wisconsin and at Johns Hopkins University isolated and successfully cultured human pluripotent stem cells. The pluripotent stem cells were derived using non-Federal funds from early-stage embryos donated voluntarily by couples undergoing fertility treatment in an in vitro fertilization (IVF) clinic or from non-living fetuses obtained from terminated first trimester pregnancies. Informed consent was obtained from the donors in both cases. Women voluntarily donating fetal tissue for research did so only after making the decision to terminate the pregnancy.

Because pluripotent stem cells give rise to almost all of the cells types of the body, such as muscle, nerve, heart, and blood, they hold great promise for both research and health care. This advance in human biology continues to generate enthusiasm among scientists, patients suffering from a broad range of diseases, including cancer, heart disease and diabetes, and their families. For example, further research using human pluripotent stem cells may help:

Questions have been raised about the usefulness of adult stem cells in research and treatment, especially as compared to pluripotent stem cells derived from embryos or fetal tissue. Indeed, there is enormous potential for research using such cells. Human adult stem cells have been isolated from tissues such as blood, brain, intestine, skin, and muscle. Furthermore, some adult stem cells have been shown to be more "plastic" than first thoughtthat is, some of these stem cells appear to be capable of developing into different kinds of cells than first predicted.

There is, however, considerable evidence that adult stem cells may have limited potential compared to pluripotent stem cells derived from embryos or fetal tissue. Human adult stem cells have not yet been isolated from all cell and tissue types, and they have not been shown to be capable of developing into all of the different cell and tissue types of the body. Furthermore, adult stem cells are difficult to obtain, since they are often present in only minute quantities. They are difficult to isolate and purify, and their numbers appear to decrease with age. Moreover, adult stem cells may have more DNA damage, and they appear to have a shorter life span than pluripotent stem cells. For all of these reasons, and because of the enormous potential of stem cell approaches to research and treatment, it is vitally important that scientists study and compare both pluripotent and adult stem cells.

The NIH is prohibited from using any appropriated funds for "... (1) the creation of a human embryo or embryos for research purposes; or (2) research in which a human embryo or embryos are destroyed, discarded, or knowingly subjected to risk of injury or death greater than that allowed for research on fetuses in utero under 45 CFR 46.208(a)(2) and section 498(b) of the Public Health Service Act (42 U.S.C. 289g(b))." Because of the enormous potential of human pluripotent stem cells to medical research, the NIH asked the General Counsel of the Department of Health and Human Services (DHHS) to determine whether research utilizing pluripotent stem cells is permissible under existing Federal law governing embryo and fetal tissue research. After careful consideration, the DHHS concluded that because human pluripotent cells are not embryos, current Federal law does not prohibit DHHS funds from being used for research utilizing these cells.

Recognizing the ethical and legal issues surrounding human pluripotent stem cell research and the need for stringent oversight of this class of researchoversight that goes beyond the traditional rigorous NIH scientific peer review processthe NIH issued a moratorium on the funding of this research until Guidelines could be developed and an oversight process could be implemented.

In April 1999, the NIH convened a working group of the Advisory Committee to the Director (ACD), NIH, to provide advice to the ACD relevant to guidelines and oversight for this research. The working group met in public session and included scientists, clinicians, ethicists, lawyers, patients, and patient advocates. During their deliberations, the group considered advice from the National Bioethics Commission, the public, and scientists. Draft guidelines for this research were published for public comment, and, after reviewing and considering all comments received, the NIH Guidelines for Research Using Human Pluripotent Stem Cells (NIH Guidelines) were published in the Federal Register and became effective on August 25, 2000. (Because the NIH Guidelines contained a few incorrect citations and other minor errors, a notice of correction (65 FR 69951) was published on November 21, 2000.) The revised NIH Guidelines and other information about stem cell research can be found at the URL: /news/pages/default.aspx.

The purpose of the NIH Guidelines is to set forth procedures to help ensure that NIH-funded research in this area is conducted in an ethical and legal manner. By issuing these Guidelines, the NIH aims to enhance both the scientific and ethical oversight of this important arena of research and the pace at which scientists can explore its many promises. These Guidelines will encourage openness, provide appropriate Federal oversight, help make certain that all researchers can make use of these critical research tools, and help assure full public access to the practical medical benefits of research using these cells.

The Guidelines prescribe the documentation and assurances that must accompany requests for NIH funding for research using human pluripotent stem cells derived from human embryos or fetal tissue. These include the following:

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