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Stem Cell Therapy: New Hope for Kidney Failure Patients

June 10th, 2015 3:44 pm

Home > Understanding Kidney Disease > Kidney Diseases > Kidney Failure > Kidney Failure Treatment > 2015-06-08 15:16| Font Size A A A

Stem Cell Therapy is also known as stem cell transplant which has tremendous promise to help us understand and treat a range of diseases including chronic kidney disease, especially Kidney Failure. Well then, how does the treatment help renal failure patients? Now, lets see.

Kidney Failure is a medical condition in which the kidneys fail to adequately filter waste products from the body. Along with the progression of illness condition, patients will experience more and more symptoms, and patients will also lose more and more functioning renal cells and tissues. Eventually, Dialysis or Kidney Transplant will be the last choice for patients. But I am sure that the consequence is not what we want. Because patients may suffer from more and more symptoms. As the matter of fact, although kidney failure cannot be cured completely, we still can do useful something so as to stop or at least slow down the progression of illness condition totally.

What is the stem cell therapy?

Fortunately, Stem Cell Therapy can be new hope for kidney failure patients. Briefly, stem cells are characterized by their capacity for self-renewal and ability to differentiate into specialized cell types.

How does it help kidney failure patients?

In recent years, clinical research finds that stem cells can differentiate into inherent kidney cells and renal parenchymal cells, replacing the damaged or necrotic kidney cells and tissues. So stem cell transplant shows an obvious effect on repairing and rebuilding kidney functioning cells. In the condition, the poor renal function can get improvement and kidney will also function normally. Last, patients will also get rid of dialysis and live a improved-quality life.

Is there any risk to take the therapy?

Compared with conventional therapies, stem cells wont cause rejection reaction, have strong differentiated ability, and dont cause any toxicity or side effect. Whats more, after many years research and practices, the success rate of Stem Cell Therapy has been improved largely. Now, it has risen to 90% especially in the specialized kidney disease hospital. I believe most kidney disease patients can get confidence from this success rate.

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Complementary, Alternative, or Integrative Health: Whats …

June 10th, 2015 3:42 pm

Weve all seen the words complementary, alternative, and integrative, but what do they reallymean?

This fact sheet looks into these terms to help you understand them better and gives you a brief picture of NCCIHs mission and role in this areaofresearch.

Many Americansmore than 30 percent of adults and about 12 percent of childrenuse health care approaches developed outside of mainstream Western, or conventional, medicine. When describing these approaches, people often use alternative and complementary interchangeably, but the two terms refer to differentconcepts:

True alternative medicine is uncommon. Most people who use non-mainstream approaches use them along with conventionaltreatments.

There are many definitions of integrative health care, but all involve bringing conventional and complementary approaches together in a coordinated way. The use of integrative approaches to health and wellness has grown within care settings across the United States. Researchers are currently exploring the potential benefits of integrative health in a variety of situations, including pain management for military personnel and veterans, relief of symptoms in cancer patients and survivors, and programs to promote healthybehaviors.

Chronic pain is a common problem among active-duty military personnel and veterans. NCCIH, the U.S. Department of Veterans Affairs, and other agencies are sponsoring research to see whether integrative approaches can help. For example, NCCIH-funded studies are testing the effects of adding mindfulness meditation, self-hypnosis, or other complementary approaches to pain management programs for veterans. The goal is to help patients feel and function better and reduce their need for pain medicines that can have serious sideeffects.

More information on pain management for military personnel andveterans

Cancer treatment centers with integrative health care programs may offer services such as acupuncture and meditation to help manage symptoms and side effects for patients who are receiving conventional cancer treatment. Although research on the potential value of these integrative programs is in its early stages, some studies have had promising results. For example, NCCIH-funded research has suggestedthat:

More information oncancer

Healthy behaviors, such as eating right, getting enough physical activity, and not smoking, can reduce peoples risks of developing serious diseases. Can integrative approaches promote these types of behaviors? Researchers are working to answer this question. Preliminary research suggests that yoga and meditation-based therapies may help smokers quit, and NCCIH-funded studies are testing whether adding mindfulness-based approaches to weight control programs will help people lose weight moresuccessfully.

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Heavier Patients Permanently Damage Fat Stem Cells – Regenexx

June 10th, 2015 3:42 pm

Heavier Patients Permanently Damage Fat Stem Cells

I promised this week that I would delve deeper into the concept of adipose versus bone marrow stem cells.One of the concepts often brought up in support of using fat as a stem cell source is that its a plentiful resource in America. However, does being heavy make for more and better stem cells or does being heavy actually hurt stem cell quality? Regrettably it seems like the research is supporting that the later is more frequently the case heavy people have poor quality fat stem cells.

Stem cells are everywhere in our bodies in our skin, bones, muscles, organs, and fat. There are a good number of stem cells in fat which can be concentrated by breaking down the tissue in a simple procedure that our FDA regrettably categorizes as the creation of a prescriptiondrug. Despite that regulatory classification, there are no shortage of doctors and companies using fat stem cells to treat whatever ails you. Websites advertising the treatment of everything from Arthritis and ALS to MS and impotence using fat stem cells can be found all over the Internet. However, what if obesity itselfactually harmed the quality of the stem cells? The burgeoning fat stem cell industry would have some serious issues to solve.

The concept that the physical attributes of the patient may impact fat stem cells isnt new. For example, prior studies have shown that fat stem cells isolated from olderpatients werent as capable to doing things like creating new blood supply, a critical feat for tissue repair. In addition, other research has revealed that women over 40 have about half the number of fat stem cells as younger patients. Now a new study suggests that not only age, but being heavy negatively impacts fat stem cell health.

The new studylooked at the most common type of fat stem cell treatment being used stromal vascular fraction (SVF). This is digested and centrifuged fat that isolates a mix of cells, the vast minority of which are stem cells. In the research, the investigators looked at SVF from thinnerpatients (thinner than the average person in the U.S.), from very obese patients, and from formerly obese patients who had undergone successful bariatric surgery. Basically, the stem cells from obese women and formerly obese women excreted much more of a bad inflammatory chemical (IL-6) than those from thinner patients. Why is this an issue? Fat stem cells are frequently used to treat diseases where inflammation is out of control, so if they inadvertently secrete inflammatory chemicals, that could make the inflammatory disease worse. This makes sense, as obese men and women often suffer from diseases of chronic inflammation, so its no surprise that their stem cells may play a role in stoking that inflammatory fire.

The upshot? Fat stem cells from older patients tend to perform more poorly than those taken from younger patients. In older women there are also far fewer of them. Now this new research suggests that in obese women, they may function differently by releasing excessive amounts of pro-inflammatory chemicals. Perhaps more concerning is the fact that even after women have lost massive amounts of weight (almost half their body weight in this study), their stem cells still have this problem!

If you liked this post, you may really enjoy this book by the same author - Dr. Chris Centeno

Written by Regenexx Founder, Dr. Chris Centeno, this 150 page book explains the Regenexx approach to patients and orthopedic conditions. Whether youre are an existing patient or simply interested in the human body and how everything in the body ties together, you will enjoy exploring this book in-depth. With hyperlinks to more detailed information, related studies and commentary, this book condenses a huge amount of data and resources into an enjoyable and entertaining read.

Chris Centeno, M.D. is a specialist in regenerative medicine and the new field of Interventional Orthopedics.

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Fat Stem Cell Arthritis Treatments: Are All Fat Stem Cells …

June 10th, 2015 3:42 pm

Fat Stem Cell Arthritis Treatments: Are All Fat Stem Cells Equal?

There are an ever increasing supply of physicians who have taken a weekend course to deliver fat stem cell arthritis treatments. What should patients know? All stem cells are created equal, right? Wrong. Let me explain.

For many patients, the term stem cell means a single type of cell that can help treat disease. However, nothing could be farther from the truth, as there are hundreds of different kinds of stem cells, each with their own properties and uses. As an example of this, a recent paper highlights how fat stem cells taken from two different sources have completely different potentials in helping arthritis.

There are stem cells in your body that keep you alive. Believe it or not, these little repairmen are in every tissue you have. When an injury happens, they spring into action to help repair the local area. We accumulate small injuries everyday, so without these stem cells, we would soon be like an old car where the oil, tires, and windshield wipers were never replaced, a broken downshadow of our former selves.

Fat stem cells make more fat for a living. So if you had trauma to an area where they live, they will help create more fat tissue and the blood supply to support it. This is why theyre so good for cosmetic purposes, as adding fat that will stay in an area can be a big bonus in enhancing appearance. However, what they dont do all day is make cartilage, so fat stem cell use for orthopedics has been shown to be less than optimal in the peer reviewed research. Now a new study shows us just how important the location of stem cell harvest is to their final use.

The new study took fat stem cells from the fat deposits many Americans are trying to decrease and compared them to fat deposits in the knee. The fat stem cells in the knee all came from a very specific spot under the knee cap, the Infra-patellar Fat Pad (IFP). The belly fat stem cells turned out to be better at creating bone, but were quite poor at creating cartilage. The IFP cells were good at making cartilage and less adept at making bone. Why? multiple studies have shown that the daily function of the stem cell impacts its proclivities. So for example, stem cells that are from the heart are better at creating new heart muscle than stem cells taken from fat or bone marrow.

Why is this important? Many fat stem cell clinics often show studies performed by others that use IFP cells to help arthritis, when what theyre actually doing is harvesting the very different belly fat stem cells. Regrettably, the comparison is apples to oranges.

The upshot? A stem cell taken from one part of the body isnt the same as one taken from another. Most of the physicians using stem cells today who learned their craft in a weekend course werent taught this distinction. However, an educated patient, should know the difference!

If you liked this post, you may really enjoy this book by the same author - Dr. Chris Centeno

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biotechnology | Britannica.com

June 10th, 2015 3:41 pm

biotechnology,the use of biology to solve problems and make useful products. The most prominent area of biotechnology is the production of therapeutic proteins and other drugs through genetic engineering.

People have been harnessing biological processes to improve their quality of life for some 10,000 years, beginning with the first agricultural communities. Approximately 6,000 years ago, humans began to tap the biological processes of microorganisms in order to make bread, alcoholic beverages, and cheese and to preserve dairy products. But such processes are not what is meant today by biotechnology, a term first widely applied to the molecular and cellular technologies that began to emerge in the 1960s and 70s. A fledgling biotech industry began to coalesce in the mid- to late 1970s, led by Genentech, a pharmaceutical company established in 1976 by Robert A. Swanson and Herbert W. Boyer to commercialize the recombinant DNA technology pioneered by Boyer and Stanley N. Cohen. Early companies such as Genentech, Amgen, Biogen, Cetus, and Genex began by manufacturing genetically engineered substances primarily for medical and environmental uses.

For more than a decade, the biotechnology industry was dominated by recombinant DNA technology, or genetic engineering. This technique consists of splicing the gene for a useful protein (often a human protein) into production cellssuch as yeast, bacteria, or mammalian cells in culturewhich then begin to produce the protein in volume. In the process of splicing a gene into a production cell, a new organism is created. At first, biotechnology investors and researchers were uncertain about whether the courts would permit them to acquire patents on organisms; after all, patents were not allowed on new organisms that happened to be discovered and identified in nature. But, in 1980, the U.S. Supreme Court, in the case of Diamond v. Chakrabarty, resolved the matter by ruling that a live human-made microorganism is patentable subject matter. This decision spawned a wave of new biotechnology firms and the infant industrys first investment boom. In 1982 recombinant insulin became the first product made through genetic engineering to secure approval from the U.S. Food and Drug Administration (FDA). Since then, dozens of genetically engineered protein medications have been commercialized around the world, including recombinant versions of growth hormone, clotting factors, proteins for stimulating the production of red and white blood cells, interferons, and clot-dissolving agents.

In the early years, the main achievement of biotechnology was the ability to produce naturally occurring therapeutic molecules in larger quantities than could be derived from conventional sources such as plasma, animal organs, and human cadavers. Recombinant proteins are also less likely to be contaminated with pathogens or to provoke allergic reactions. Today, biotechnology researchers seek to discover the root molecular causes of disease and to intervene precisely at that level. Sometimes this means producing therapeutic proteins that augment the bodys own supplies or that make up for genetic deficiencies, as in the first generation of biotech medications. (Gene therapyinsertion of genes encoding a needed protein into a patients body or cellsis a related approach.) But the biotechnology industry has also expanded its research into the development of traditional pharmaceuticals and monoclonal antibodies that stop the progress of a disease. Such steps are uncovered through painstaking study of genes (genomics), the proteins that they encode (proteomics), and the larger biological pathways in which they act.

In addition to the tools mentioned above, biotechnology also involves merging biological information with computer technology (bioinformatics), exploring the use of microscopic equipment that can enter the human body (nanotechnology), and possibly applying techniques of stem cell research and cloning to replace dead or defective cells and tissues (regenerative medicine). Companies and academic laboratories integrate these disparate technologies in an effort to analyze downward into molecules and also to synthesize upward from molecular biology toward chemical pathways, tissues, and organs.

In addition to being used in health care, biotechnology has proved helpful in refining industrial processes through the discovery and production of biological enzymes that spark chemical reactions (catalysts); for environmental cleanup, with enzymes that digest contaminants into harmless chemicals and then die after consuming the available food supply; and in agricultural production through genetic engineering.

Agricultural applications of biotechnology have proved the most controversial. Some activists and consumer groups have called for bans on genetically modified organisms (GMOs) or for labeling laws to inform consumers of the growing presence of GMOs in the food supply. In the United States, the introduction of GMOs into agriculture began in 1993, when the FDA approved bovine somatotropin (BST), a growth hormone that boosts milk production in dairy cows. The next year, the FDA approved the first genetically modified whole food, a tomato engineered for a longer shelf life. Since then, regulatory approval in the United States, Europe, and elsewhere has been won by dozens of agricultural GMOs, including crops that produce their own pesticides and crops that survive the application of specific herbicides used to kill weeds. Studies by the United Nations, the U.S. National Academy of Sciences, the European Union, the American Medical Association, U.S. regulatory agencies, and other organizations have found GMO foods to be safe, but skeptics contend that it is still too early to judge the long-term health and ecological effects of such crops. In the late 20th and early 21st centuries, the land area planted in genetically modified crops increased dramatically, from 1.7 million hectares (4.2 million acres) in 1996 to 160 million hectares (395 million acres) by 2011.

Overall, the revenues of U.S. and European biotechnology industries roughly doubled over the five-year period from 1996 through 2000. Rapid growth continued into the 21st century, fueled by the introduction of new products, particularly in health care.

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Sermorelin Doctors – Growth hormone

June 9th, 2015 9:44 pm

One of the soundest principles throughout life is to focus on perfecting yourself, instead of trying to change the behavior of others. Finding out how to get a Sermorelin Doctors Prescription to eliminate your unhealthy low hgh symptoms is an excellent way to focus your attention on giving your body exactly what it now needs. When you have been struggling with low energy, stubborn belly fat, a lack of sexual desire, and an overall feeling of lethargy, your bodys decreasing human growth hormone levels are usually responsible. However, there is something you can do to eliminate those symptoms and actually significantly improve your overall healthiness and vitality, allowing you to feel and look like the best possible version of yourself! Our safe and highly effective doctor prescribed Sermorelin injections stimulate you pituitary gland to jump-start the restoring of your bodys natural growth hormone supply. As a result, you will experience an amazing increase in energy, stamina and your desire for sexual intimacy. Your stubborn belly fat will rapidly melt away, and your muscle and skin tone will quickly improve. In fact, with our injectable Sermorelin therapy, you will even reduce your risk for heart disease, stroke, osteoporosis and diabetes! That is how important having an adequate supply of hgh actually is to sustaining your overall health and wellness. However, without treatment your low hgh levels will only continue to decline and your symptoms will continue to intensify over time unless you have decided that getting a Sermorelin Doctors Prescription makes more sense than giving up on ever feeling really good again. With the help of our doctors who specialize in Sermorelin therapy for hgh deficiency, you can focus on how great you feel instead of how old and tired youve been feeling. As you experience the astonishing and long-lasting Sermorelin benefits that our treatment provides you with, you will discover that you havent felt this energetic and alive since you were in your twenties! You will notice that as your fresh supply of hgh rejuvenates every cell, system and organ in your body, everything about your lifestyle is greatly enhanced by the benefits of your treatment with our doctor prescribed Sermorelin treatment. From your performance at work to the time that you spend with your family and friends, our proven therapy for increasing your bodys natural growth hormone supply is a life-changing experience! Our doctors know that it is difficult to be happy with your lifestyle when your symptoms associated with low human growth hormone levels take over so we have made it easy and convenient for you to get the help you need. We have also made sure that it is easy and convenient for you to get the facts about treatment with Sermorelin injections just by calling us at our toll-free number. Thats because when it comes to successfully eliminating your unhealthy symptoms, we are dedicated to providing you with a Sermorelin Doctors Prescription that has been created with your own specific needs and goals in mind.

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Global Stem Cells Group, Stem Cell Training and Anti-aging …

June 9th, 2015 9:43 pm

MIAMI (PRWEB) June 08, 2015

Global Stem Cells Group and its subsidiary Stem Cell Training, Inc. have announced plans to conduct a hands-on, two day intensive stem cell training course for physicians and qualified medical professionals Sept. 18 -19, 2015. The training course will be led by anti-aging specialist John P. Salerno, M.D. in Downtown Manhattan.

The founder of The Salerno Center, Salerno practices integrative medicine, combining traditional and alternative healing methods. The course will focus on stem cell therapies for a variety of conditions and treatments including anti-aging therapies. Salerno trained in anti-aging medicine and has opened more than 20 anti-aging medical centers worldwide, including 10 in Japan, three in Brazil and two in Korea.

The Adipose and Bone Marrow Stem Cell Training Course was developed for physicians and high-level practitioners to learn the process through an intensive, hands-on training session that arms participants with clinical protocols and state-of-the-art techniques for isolating and re-integrating adipose- and bone marrow-derived stem cells.

The objective of the training is to teach effective regenerative medicine techniques that can be used to treat patients in-office.

Global Stem Cells Group's Stem Cell Training, Inc. courses have been extended to approximately 35 countries, allowing a global community of physicians to learn how to apply these new stem cell technologies. For more information, visit the Stem Cell Training, Inc. website, email info(at)stemcelltraining(dot)net, or call 305-224-1858.

About Global Stem Cells Group:

Global Stem Cells Group, Inc. is the parent company of six wholly owned operating companies dedicated entirely to stem cell research, training, products and solutions. Founded in 2012, the company combines dedicated researchers, physician and patient educators and solution providers with the shared goal of meeting the growing worldwide need for leading edge stem cell treatments and solutions.

With a singular focus on this exciting new area of medical research, Global Stem Cells Group and its subsidiaries are uniquely positioned to become global leaders in cellular medicine.

Global Stem Cells Group's corporate mission is to make the promise of stem cell medicine a reality for patients around the world. With each of GSCG's six operating companies focused on a separate research-based mission, the result is a global network of state-of-the-art stem cell treatments.

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Researchers identify patients at risk for stem cell …

June 9th, 2015 4:47 am

Amir Toor, M.D., hematologist-oncologist and member of the Developmental Therapeutics research program at VCU Massey Cancer Center is pictured. Credit: VCU Massey Cancer Center

Researchers at VCU Massey Cancer Center's Bone Marrow Transplant Program have recently published findings from a phase 2 clinical trial that demonstrate lymphocyte recovery in related and unrelated stem cell transplant recipients generally falls into three patterns that are significantly associated with survival. This first-of-its-kind research continues the efforts of principal investigator Amir Toor, M.D., 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," says Toor, the lead investigator of the study and hematologist-oncologist and member of the Developmental Therapeutics research program at VCU Massey Cancer Center. "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, recently published in the journal Biology of Blood & Marrow Transplantation, retrospectively examined lymphocyte recovery and clinical outcome data from a recent phase 2 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 anti-thymocyte globulin (ATG), an immune-modulating drug given to guard against graft-versus-host-disease (GVHD) before transplantation. GVHD is a condition where the donor's immune system attacks 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 two 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 percent, followed by group A with a survival rate of 67 percent and group C with 30 percent survival. Relapse rates between groups A and B were similar at 33 and 29 percent, respectively, while group C experienced a 90 percent relapse rate. GVHD was observed in 67 percent of patients in group A, 43 percent of patients in group B and 10 percent of patients in group C. Finally, adoptive immunotherapy with donor cell infusions was required for 13 percent of patients in group A, 21 percent in group B and 70 percent in group C.

The discovery of these patterns in lymphocyte recovery build on prior research by Toor and his team that supports the concept of the immune system working as a dynamical system. In 2013, the Massey Bone Marrow Transplant Program's research team and Massey researcher Masoud Manjili, D.V.M., Ph.D., sequenced DNA from the T cells of 10 stem cell transplant recipients and their donors and found a fractal, self-repeating pattern in the participants' T cell repertoires. This discovery suggested that physicians could potentially sequence the DNA of patients after they undergo stem cell transplantation and predict potential GVHD complications based on the pattern in which their T cell repertoire is developing. Another study of the same participants in 2014 also used whole exome sequencing and found significant variation in minor histocompatability antigens (mHA, which are receptors on the cellular surface of donated organs that are known to give an immunological response in some organ transplants) between the donor-recipient pairs. This variation represents a large and previously unmeasured potential for developing GVHD for which conventional human leucocyte antigen (HLA) testing, the test that matches stem cell transplants with donors, does not measure. This large library of immune targets, in turn, can serve to drive immune complications of transplantation such as GVHD or graft rejection.

Currently, physicians use stochastic models to determine the probability of a patient developing GVHD based on HLA test results. Stochastic models are not precise because they estimate probability by allowing for random variation in one or more variables. Dynamical system modeling, on the other hand, would account for the key variables influencing transplant outcomes and their evolution over time, allowing physicians to personalize therapy based on the extent of a patient's immune recovery following transplantation.

"We've uncovered order in the structure of the immune system, we've found new variables influencing GVHD and we've now shown patterns in lymphocyte reconstitution that identify at-risk patients," says Toor. "Now, we are working to put it all together and develop a model of immune system reconstruction following stem cell transplantation that will allow physicians to make more informed treatment decisions."

Explore further: Predicting the storm: Can computer models improve stem cell transplantation?

More information: Biology of Blood & Marrow Transplantation, http://www.sciencedirect.com/science/ ii/S1083879115001834

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Longevity genes – Supercentenarian

June 8th, 2015 3:51 pm

A handful of genes that control the body's defenses during hard times can also dramatically improve health and prolong life in diverse organisms. Understanding how they work may reveal the keys to extending human life span while banishing diseases of old age

By David A. Sinclair and Lenny Guarente

You can assume quite a bit about the state of a used car just from its mileage and model year. The wear and tear of heavy driving and the passage of time will have taken an inevitable toll. The same appears to be true of aging in people, but the analogy is flawed because of a crucial difference between inanimate machines and living creatures: deterioration is not inexorable in biological systems, which can respond to their environments and use their own energy to defend and repair themselves.

At one time, scientists believed aging to be not just deterioration but an active continuation of an organism's genetically programmed development. Once an individual achieved maturity, "aging genes" began to direct its progress toward the grave. This idea has been discredited, and conventional wisdom now holds that aging really is just wearing out over time because the body's normal maintenance and repair mechanisms simply wane. Evolutionary natural selection, the logic goes, has no reason to keep them working once an organism has passed its reproductive age.

Yet we and other researchers have found that a family of genes involved in an organism's ability to withstand a stressful environment, such as excessive heat or scarcity of food or water, have the power to keep its natural defense and repair activities going strong regardless of age. By optimizing the body's functioning for survival, these genes maximize the individual's chances of getting through the crisis. And if they remain activated long enough, they can also dramatically enhance the organism's health and extend its life span. In essence, they represent the opposite of aging genes--longevity genes.

We began investigating this idea nearly 15 years ago by imagining that evolution would have favored a universal regulatory system to coordinate this well-known response to environmental stress. If we could identify the gene or genes that serve as its master controllers and thereby act as master regulators of an organism's life span, these natural defense mechanisms might be turned into weapons against the diseases and decline that are now apparently synonymous with human aging.

Many recently discovered genes, known by such cryptic names as daf-2, pit-1, amp-1, clk-1 and p66Shc, have been found to affect stress resistance and life span in laboratory organisms, suggesting that they could be part of a fundamental mechanism for surviving adversity. But our own two laboratories have focused on a gene called SIR2, variants of which are present in all organisms studied so far, from yeast to humans. Extra copies of the gene increase longevity in creatures as diverse as yeast, roundworms and fruit flies, and we are working to determine whether it does the same for larger animals, such as mice.

As one of the first longevity genes to have been identified, SIR2 is the best characterized, so we will focus here on its workings. They illustrate how a genetically regulated survival mechanism can extend life and improve health, and growing evidence suggests that SIR2 may be the key regulator of that mechanism.

One of us (Guarente) began by screening yeast colonies for unusually long-lived cells in the hope of finding genes responsible for their longevity. This screen yielded a single mutation in a gene called SIR4, which encodes part of a complex of proteins containing the Sir2 enzyme. The mutation in SIR4 caused the Sir2 protein to gather at the most highly repetitive region of the yeast genome, a stretch containing the genes that encode the protein factories of the cell, known as ribosomal DNA (rDNA). More than 100 of these rDNA repeats exist in the average yeast cell's genome, and they are difficult to maintain in a stable state. Repetitive sequences are prone to "recombining" with one another, a process that in humans can lead to numerous illnesses, such as cancer and Huntington's disease. Our yeast findings suggested that aging in mother cells was caused by some form of rDNA instability that was mitigated by the Sir proteins.

In fact, we found a surprising kind of rDNA instability. After dividing several times, yeast mother cells spin off extra copies of the rDNA as circular rings that pop out of the genome. These extrachromosomal rDNA circles (ERCs) are copied along with the mother cell's chromosomes prior to cell division but remain in the mother cell's nucleus afterward. Thus, a mother cell accumulates an ever increasing number of circles that eventually spell her doom, possibly because copying the ERCs consumes so many resources that she can no longer manage to replicate her own genome.

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Stem cell patents: legal aspects | Europe’s stem cell hub …

June 8th, 2015 3:50 pm

iStockphoto.com/Ssolbergj

*New 18 June 2012*: The EU ban on embryonic stem cell patents is legally flawed, argues a paper and public lecture by Aurora Plomer, Chair of Law and Bioethics at the University of Sheffield, UK. Find out more.

June 2011: Lately there have been several cases on the patentability of inventions related to human embryonic stem cells (hESC) in Europe. Now the first case has reached the European Court of Justice (ECJ), the highest European court, whose decision will be binding for all EU member states.

The judgement of the ECJ is still outstanding. However, the Advocate General Yves Bot offered his opinion on the case, which points towards a complete prohibition of patents for inventions relating to hESC. While the court does not have to follow the opinion, it does so in a majority of the cases.

The case history The current case arose in Germany from a patent of belonging to Prof. Oliver Brstle. The patent covers neural progenitor cells (precursors of nerve cells), neuronal cells derived from these progenitors, and a method for producing them from hESC lines. hESC lines are typically derived from surplus fertilized egg cells, which are produced in large numbers during in vitro fertilization (IVF) and otherwise discarded. Once established, hESC lines can be permanently maintained and proliferated and thus serve as a source of tissue-specific cells, such as neuronal precursors.

Brstles patent was originally filed in 1997 and granted by the German Patent Office in 1999. In 2004 Greenpeace filed a nullity action against the patent based on reasons of ordre public and morality. A decision of the German Federal Patent Court in 2006 rendered the patent partially invalid, eliminating all claims relating to cells derived from hESC lines. Following Brstles appeal against this decision, the German Federal Court of Justice referred the dispute to the ECJ, arguing that its decision in the case depends on the interpretation of Article 6 of the European Biopatent Directive (Art. 6).

The legal situation The EU Biopatent Directive (Directive on the Legal Protection of Biotechnological Inventions 98/44/EC) was meant to assure harmonized patent protection for biotechnological inventions in the EU. The directive also contains exemptions from patentability including Art. 6(1), which states that patents contrary to ordre public and morality are excluded from patentability. To provide national courts and patent offices with guidance on how to interpret this clause, an illustrative list of examples was incorporated in Art. 6(2) of the Biopatent Directive.

One of these examples has now proven to be key for the patentability of stem-cell-based inventions: Art. 6 (2) (c), which states that in particular uses of human embryos for industrial or commercial purposes shall be excluded from patentability. However, there is no definition of any of the terms used in this provision found within the Directive, neither of the term human embryo nor of what is to be understood by uses for industrial or commercial purposes.

Consequently and contrary to the aim of the European legislator to achieve harmonisation, there are significant differences in how the Directive has been implemented in the EU member states, and even more variation in how the corresponding provisions of national patent law have been applied in the member states. As a result, some countries have adopted a rather liberal approach to patenting. For example, in the UK about 100 patents on hESC-based inventions had already been granted by 2009 [1]. Others, such as Germany at least with the first instance ruling of the German Federal Patent Court - have so far opted for a much more restrictive interpretation of the Directive.

The opinion of the Advocate General Yves Bot European Court of Justice: Image by SsolbergjIn his opinion the Advocate General made a suggestion on how Art. 6 (2) (c) of the Biopatent Directive and its terms should be understood. Bot rightly argues that the concept of a human embryo must be subject to a common understanding in all EU member states. Furthermore, he states clearly that hESC are not included in that concept, because they do not in themselves have the capacity to develop into a human being. Nevertheless, he surprisingly took a restrictive approach on patenting of hESC-based inventions: even inventions based on legally established hESC lines are excluded from patentability due to the fact that hESC lines are originally derived from fertilized human eggs.

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stemcellbioethics – home

June 8th, 2015 3:50 pm

While these scenarios may once have seemed like futuristic science fiction, advances in stem cell technology are bringing them closer to possibilities, if not to probabilities. In fact, desperate patients across the globe are traveling to countries such as China, Mexico, and the Dominican Republic to participate in unproven stem cell therapies."

Recently, stem cell science has made rapid progress, revealing entirely new scientific opportunities that will enable the development of future treatments for a wide variety of medical conditions. Many of these experimental or medical breakthroughs will have an unprecedented societal impact. It is imperative to carefully evaluate these developments from diverse viewpoints including ethical, legal, religious, economic, cultural, political, as well as scientific perspectives. Together, these disciplines will shape both public policy and personal health decisions.

We believe that cell biologists, clinicians, and bio- and neuro-ethicists can work together to celebrate advances, while simultaneously helping to inform and protect patients and the broader community concerning what might be considered inappropriate or premature applications of novel stem cell technologies. This will not be an easy process. We must engage in ongoing reasoned and informed discourse to ensure safe and appropriate innovations and applications of this new technology.

These modules were initially designed to accompany the Columbia University classroom course: "Stem Cells: Biology, Ethics, and Applications". We have now adapted the course to supplement any university course that focuses on stem cell research and potential medical and scientific applications. Undergraduate and graduate students as well as all others who have an interest in stem cell science, bioethical and social implications, and regulatory issues should find this course informative.

Within the eight Modules and Supplements of the online course, the reader will find:

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Emerging stem cell science reflects a dynamic and often opposing balance between rapidly progressing and diverse scientific discoveries, and a host of bioethical and societal concerns. Important issues are raised at every level and stage of research, from manipulating a somatic cell into a stem cell, to enrolling a patient in a stem cell clinical trial, to educating legislators and the public. We hope readers of this on-line course will have their curiosity stimulated by the myriad of important and complex ideas raised, and carefully consider the ethical dilemmas generated by stem cell science.

"Stem Cells: Biology, Bioethics, and Applications" is supported by a grant from the New York State STEM Cell Initiative (NYSTEM). It provides information on a range of important and complex topics about stem cell science. We believe students, professors, health care professionals, and the public alike will find the online multidisciplinary course on the current and future research of stem cell technologies and its applications informative and stimulating. The content of this online course was written and prepared by John D. Loike, Ph.D., Director of Special Programs, Center for Bioethics, Columbia University and Ruth L. Fischbach, Ph.D. M.P.E., Director, Center for Bioethics, Columbia University with special assistance from Janet Mindes, Ph.D., Consultant, Center for Bioethics, Columbia University.

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The Immune System | Health | Patient.co.uk

June 8th, 2015 3:49 pm

What is the immune system?

We are surrounded by millions of bacteria, viruses and other microbes (germs) that have the potential to enter our bodies and cause harm. The immune system is the body's defence against pathogens (disease-causing microbes). The immune system is made up of non-specialised defences such as skin and the acidic juice produced by your stomach. But it also has some highly specialised defences which give you immunity against (resistance to) particular pathogens. These defences are special white blood cells called lymphocytes. Other types of white blood cells play an important part in defending your body against infection.

The lymphatic system is also part of the immune system. The lymphatic system is made up of a network of vessels (tubes) which carry fluid called lymph. It contains specialised lymph tissue and all of the structures dedicated to the production of lymphocytes.

The immune system is generally divided into two parts. The first part is the defences you are born with. These form what are known as the innate system.

The second part of your immune system, known as immunity, develops as you grow. Your immunity gives you protection against specific pathogens. Not only can this system recognise particular pathogens, it also has a memory of this. This means that if you encounter a certain pathogen twice, your immune system recognises it the second time around. This usually means your body responds quicker to fight off the infection.

The innate system is found in many different places around the body. First line of defence is your skin. Skin forms a waterproof barrier that prevents pathogens from entering the body. Your body cavities, such as the nose and mouth, are lined with mucous membranes. Mucous membranes produce sticky mucus which can trap bacteria and other pathogens. Other fluids produced by the body help to protect your internal layers from invasion by pathogens. Gastric juice produced by the stomach has high acidity which helps to kill off many of the bacteria in food. Saliva washes pathogens off your teeth and helps to reduce the amount of bacteria and other pathogens in your mouth.

If bacteria or other pathogens manage to get through these initial defences, they encounter a second line of defence. Most of these defences are present in your blood, either as specialised white blood cells or as chemicals released by your cells and tissues.

The second part of your immune system, the part that gives you immunity, involves the activation of lymphocytes. This will be described later on. Lymphocytes are found in your blood and also in specialised lymph tissue such as lymph nodes, the spleen and the thymus.

The first line of defence is your body's skin and mucous membranes, as mentioned above.

If pathogens manage to get through these barriers, they encounter special white blood cells present in your bloodstream. There are different types of white cells, called neutrophils (polymorphs), lymphocytes, eosinophils, monocytes, and basophils.

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Faqs, What Are Stem Cells, What Is Stem Cell Research

June 8th, 2015 3:49 pm

Our Technology

The Cell Surgical Network uses adipose derived stem cells for deployment & clinical research. Early stem cell research has traditionally been associated with the controversial use of embryonic stem cells. The new focus is on non-embryonic adult mesenchymal stem cells which are found in a persons own blood, bone marrow, and fat. Most stem cell treatment centers in the world are currently using stem cells derived from bone marrow.

A recent technological breakthrough enables us to now use adipose (fat) derived stem cells. Autologous stem cells from a persons own fat are easy to harvest safely under local anesthesia and are abundant in quantities up to 2500 times those seen in bone marrow.

Clinical success and favorable outcomes appear to be related directly to the quantity of stem cells deployed. Once these adipose derived stem cells are administered back in to the patient, they have the potential to repair human tissue by forming new cells of mesenchymal origin, such as cartilage, bone, ligaments, tendons, nerve, fat, muscle, blood vessels, and certain internal organs. Stem cells ability to form cartilage and bone makes them potentially highly effective in the treatment of degenerative orthopedic conditions. Their ability to form new blood vessels and smooth muscle makes them potentially very useful in the treatment of peyronies disease and impotence. Stem cells are used extensively in Europe and Asia to treat these conditions.

We have anecdotal and experimental evidence that stem cell therapy is effective in healing and regeneration. Stem cells seek out damaged tissues in order to repair the body naturally. The literature and internet is full of successful testimonials but we are still awaiting definitive studies demonstrating efficacy of stem cell therapy. Such data may take five or ten years to accumulate. In an effort to provide relief for patients suffering from certain degenerative diseases that have been resistant to common modalities of treatment, we are initiating pilot studies as experimental tests of treatment effectiveness with very high numbers of adipose derived stem cells obtained from fat. Adipose fat is an abundant and reliable source of stem cells.

The Cell Surgical Networks cell harvesting and isolation techniques are based on technology from Korea. This new technological breakthrough allows patients to safely receive their own autologous stem cells in extremely large quantities. Our treatments and research are patient funded and we have endeavored successfully to make it affordable. All of our sterile procedures are non-invasive and done under local anesthesia. Patients who are looking for non-surgical alternatives to their degenerative disorders can participate in our trials by filling out our treatment application to determine if they are candidates. The Cell Surgical Network is proud to be state of the art in the new field of Regenerative Medicine. RETURN TO TOP

We are currently in the process of setting up FDA approved protocols for stem cell banking in collaboration with a reputable cryo-technology company. This enables a person to receive autologous stem cells at any time in the future without having to undergo liposuction which may be inconvenient or contraindicated. Having your own stem cells available for medical immediate use is a valuable medical asset.

Provisions are nearly in place for this option and storage of your own stem cells obtained by liposuction at CSN or from fat obtained from cosmetic procedures performed elsewhere should be possible in the near future. RETURN TO TOP

Adult (NonEmbryonic) Mesenchymal Stem Cells are undifferentiated cells that have the ability to replace dying cells and regenerate damaged tissue. These special cells seek out areas of injury, disease and destruction where they are capable of regenerating healthy cells and enabling a persons natural healing processes to be accelerated. As we gain a deeper understanding of their medical function and apply this knowledge, we are realizing their enormous therapeutic potential to help the body heal itself. Adult stem cells have been used for a variety of medical treatments to repair and regenerate acute and chronicially damaged tissues in humans and animals. The use of stem cells is not FDA approved for the treatment of any specific disease in the United States at this time and their use is therefore investigational. Many reputable international centers have been using stem cell therapy to treat various chronic degenerative conditions as diverse as severe neurologic diseases, renal failure, erectile dysfunction, degenerative orthopedic problems, and even cardiac and pulmonary diseases to name a few. Adult stem cells appear to be particularly effective at repairing cartilage in degenerated joints. RETURN TO TOP

Regenerative Medicine is the process of creating living, functional tissues to repair or replace tissue or organ function lost due to damage, or congenital defects. This field holds the promise of regenerating damaged tissues and organs in the body by stimulating previously irreparable organs to heal themselves. (Wikipedia) RETURN TO TOP

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How is your vision after Cataract Surgery? – Eye Care …

June 8th, 2015 3:49 pm

re: "wish there is some way to emulate the vision under different types of settings"

If you do get the Crystalens set for distance and it doesn't provide enough near vision, then you can try some of the options I mentioned above like multifocal contacts, or a corneal inlay (which can be taken out if it doesn't work). Coincidentally,the Kamra inlay was just approved in the US by the FDA yesterday (I see you are in the US, unlike the prior poster). Itsbeen available elsewhere for quite a while. The Raindrop inlayis still in the approval process, but is available elsewhere. I will note that both of those have evolved over time, so if you look for studies the recent ones may be better due to improvements.

How much near vision you get will depend on your eyes, a tiny fraction of people have enough natural depth of focus in their eyes that even with a monofocal they are able to read some without correction, but it is best to plan based on average results.

If you are concerned about getting enough intermediate or near vision if the lens doesn't accommodate much,and don't mind wearing correction for driving, then you could consider getting the Crystalens set for some intermediate distance, e.g.if you set yourself for 0.5D myopia that would be focused at around 2 meters, so that even if it doesn't accommodate, that would give you usable vision for around the household and at computer distance. Setting it a bit closer would ensure even better computer distance and perhaps some reading, e.g. 1D is focused at 1 meter, 1.5D = 66.7 meters = 26.2 inches which is around computer monitor range for many (laptops might be a bit less).This page explains what diopters translate to what focal distance:

https://www.slackbooks.com/excerpts/67956_3.pdf

Studies on lensestry to evaluate the average visual acuity at different distances (with the distances measured in diopters, though sometimes the distance in cm added) which lets you compare lenses. The graphs are called defocus curves, and are explained in this article:

http://crstoday.com/2010/11/feature-story-get-to-know-the-defocus-curve/

For example if you look on this site, and click on the "clinical" tab:

http://www.tecnisiol.com/eu/tecnis-symfony-iol.htm

You will see a defocus curve for the Symfony lens, but the graph also shows the curve for a Tecnis monofocal to see what those are like(though not all monofocals are equal, I don't know how well the Crystalens does as a monofocal if it doesn't accommodate, I hadn't searched for that).

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Color vision – Wikipedia, the free encyclopedia

June 8th, 2015 3:49 pm

Color vision is the ability of an organism or machine to distinguish objects based on the wavelengths (or frequencies) of the light they reflect, emit, or transmit. Colors can be measured and quantified in various ways; indeed, a person's perception of colors is a subjective process whereby the brain responds to the stimuli that are produced when incoming light reacts with the several types of cone cells in the eye. In essence, different people see the same illuminated object or light source in different ways.

Isaac Newton discovered that white light splits into its component colors when passed through a dispersive prism. Newton also found that he could recombine these colors by passing them through a different prism to make white light.

The characteristic colors are, from long to short wavelengths (and, correspondingly, from low to high frequency), red, orange, yellow, green, cyan, blue, and violet. Sufficient differences in wavelength cause a difference in the perceived hue; the just-noticeable difference in wavelength varies from about 1nm in the blue-green and yellow wavelengths, to 10nm and more in the longer red and shorter blue wavelengths. Although the human eye can distinguish up to a few hundred hues, when those pure spectral colors are mixed together or diluted with white light, the number of distinguishable chromaticities can be quite high.[ambiguous]

In very low light levels, vision is scotopic: light is detected by rod cells of the retina. Rods are maximally sensitive to wavelengths near 500nm, and play little, if any, role in color vision. In brighter light, such as daylight, vision is photopic: light is detected by cone cells which are responsible for color vision. Cones are sensitive to a range of wavelengths, but are most sensitive to wavelengths near 555nm. Between these regions, mesopic vision comes into play and both rods and cones provide signals to the retinal ganglion cells. The shift in color perception from dim light to daylight gives rise to differences known as the Purkinje effect.

The perception of "white" is formed by the entire spectrum of visible light, or by mixing colors of just a few wavelengths in animals with few types of color receptors. In humans, white light can be perceived by combining wavelengths such as red, green, and blue, or just a pair of complementary colors such as blue and yellow.[1]

Perception of color begins with specialized retinal cells containing pigments with different spectral sensitivities, known as cone cells. In humans, there are three types of cones sensitive to three different spectra, resulting in trichromatic color vision.

Each individual cone contains pigments composed of opsin apoprotein, which is covalently linked to either 11-cis-hydroretinal or more rarely 11-cis-dehydroretinal.[2]

The cones are conventionally labeled according to the ordering of the wavelengths of the peaks of their spectral sensitivities: short (S), medium (M), and long (L) cone types. These three types do not correspond well to particular colors as we know them. Rather, the perception of color is achieved by a complex process that starts with the differential output of these cells in the retina and it will be finalized in the visual cortex and associative areas of the brain.

For example, while the L cones have been referred to simply as red receptors, microspectrophotometry has shown that their peak sensitivity is in the greenish-yellow region of the spectrum. Similarly, the S- and M-cones do not directly correspond to blue and green, although they are often described as such. The RGB color model, therefore, is a convenient means for representing color, but is not directly based on the types of cones in the human eye.

The peak response of human cone cells varies, even among individuals with so-called normal color vision;[3] in some non-human species this polymorphic variation is even greater, and it may well be adaptive.[4]

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What are the potential uses of human stem cells and the …

June 8th, 2015 3:48 pm

Introduction: What are stem cells, and why are they important? What are the unique properties of all stem cells? What are embryonic stem cells? What are adult stem cells? What are the similarities and differences between embryonic and adult stem cells? What are induced pluripotent stem cells? What are the potential uses of human stem cells and the obstacles that must be overcome before these potential uses will be realized? Where can I get more information? VII. What are the potential uses of human stem cells and the obstacles that must be overcome before these potential uses will be realized?

There are many ways in which human stem cells can be used in research and the clinic. Studies of human embryonic stem cells will yield information about the complex events that occur during human development. A primary goal of this work is to identify how undifferentiated stem cells become the differentiated cells that form the tissues and organs. Scientists know that turning genes on and off is central to this process. Some of the most serious medical conditions, such as cancer and birth defects, are due to abnormal cell division and differentiation. A more complete understanding of the genetic and molecular controls of these processes may yield information about how such diseases arise and suggest new strategies for therapy. Predictably controlling cell proliferation and differentiation requires additional basic research on the molecular and genetic signals that regulate cell division and specialization. While recent developments with iPS cells suggest some of the specific factors that may be involved, techniques must be devised to introduce these factors safely into the cells and control the processes that are induced by these factors.

Human stem cells are currently being used to test new drugs. New medications are tested for safety on differentiated cells generated from human pluripotent cell lines. Other kinds of cell lines have a long history of being used in this way. Cancer cell lines, for example, are used to screen potential anti-tumor drugs. The availability of pluripotent stem cells would allow drug testing in a wider range of cell types. However, to screen drugs effectively, the conditions must be identical when comparing different drugs. Therefore, scientists must be able to precisely control the differentiation of stem cells into the specific cell type on which drugs will be tested. For some cell types and tissues, current knowledge of the signals controlling differentiation falls short of being able to mimic these conditions precisely to generate pure populations of differentiated cells for each drug being tested.

Perhaps the most important potential application of human stem cells is the generation of cells and tissues that could be used for cell-based therapies. Today, donated organs and tissues are often used to replace ailing or destroyed tissue, but the need for transplantable tissues and organs far outweighs the available supply. Stem cells, directed to differentiate into specific cell types, offer the possibility of a renewable source of replacement cells and tissues to treat diseases including maculardegeneration, spinal cord injury, stroke, burns, heart disease, diabetes, osteoarthritis, and rheumatoid arthritis.

Figure 3. Strategies to repair heart muscle with adult stem cells. Click here for larger image.

2008 Terese Winslow

For example, it may become possible to generate healthy heart muscle cells in the laboratory and then transplant those cells into patients with chronic heart disease. Preliminary research in mice and other animals indicates that bone marrow stromal cells, transplanted into a damaged heart, can have beneficial effects. Whether these cells can generate heart muscle cells or stimulate the growth of new blood vessels that repopulate the heart tissue, or help via some other mechanism is actively under investigation. For example, injected cells may accomplish repair by secreting growth factors, rather than actually incorporating into the heart. Promising results from animal studies have served as the basis for a small number of exploratory studies in humans (for discussion, see call-out box, "Can Stem Cells Mend a Broken Heart?"). Other recent studies in cell culture systems indicate that it may be possible to direct the differentiation of embryonic stem cells or adult bone marrow cells into heart muscle cells (Figure 3).

Cardiovascular disease (CVD), which includes hypertension, coronary heart disease, stroke, and congestive heart failure, has ranked as the number one cause of death in the United States every year since 1900 except 1918, when the nation struggled with an influenza epidemic. Nearly 2,600 Americans die of CVD each day, roughly one person every 34 seconds. Given the aging of the population and the relatively dramatic recent increases in the prevalence of cardiovascular risk factors such as obesity and type 2 diabetes, CVD will be a significant health concern well into the 21st century.

Cardiovascular disease can deprive heart tissue of oxygen, thereby killing cardiac muscle cells (cardiomyocytes). This loss triggers a cascade of detrimental events, including formation of scar tissue, an overload of blood flow and pressure capacity, the overstretching of viable cardiac cells attempting to sustain cardiac output, leading to heart failure, and eventual death. Restoring damaged heart muscle tissue, through repair or regeneration, is therefore a potentially new strategy to treat heart failure.

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Biotechnology Industry Organization – Wikipedia, the free …

June 8th, 2015 3:48 pm

The Biotechnology Industry Organization (BIO) is the largest trade organization to serve and represent the biotechnology industry in the United States and around the world.[1][2][3]

Its members include companies that make Pharmaceutical drugs, biofuels, industrial enzymes, and genetically modified crops.[4] It was founded 1993 in Washington, D.C. and Carl B. Feldbaum was the president from BIO's founding until he retired in 2004,[5] and was succeeded by James C. Greenwood. As of 2013, it represents 1,000 biotech companies in all 50 U.S. states, which employ 1.61 million Americans and support an additional 3.4 million jobs.[6]

Rachel King, president and chief executive of GlycoMimetics, is board chairwoman; the first woman to hold this position.[7][8] James Greenwood is President and CEO.[9]

BIO holds a trade meeting each year in the United States, which are essential for the business development and partnering activities that are required in the biotechnology sector, in which it is expensive to develop products, timelines to develop products are long, and regulatory risks are high.[10] In 2013 the conference was held in Chicago and was attended by 13,594 delegates from 47 states, the District of Columbia, Puerto Rico, U.S. Virgin Islands and 62 countries.[11][12]

It also holds regional partnering meetings, for example in China,[13]India,[14] and Europe.[15]

In 2013 it spent $1.98 million on lobbying in the United States.[16] Issues included the amending the Internal Revenue Code to provide an exception from the passive loss rules for investments in high-technology research small business pass-through entities, to include vaccines against seasonal influenza within the definition of taxable vaccines, and to extend, expand, and improve the qualifying therapeutic discovery project program that first became law in 2010.[17][18]

Example of its public lobbying efforts, include support for development of biofuels such as those produced from algae,[19]genetically modified crops,[20] strong intellectual property rights,[21] and for a more efficient and predictable regulatory process for new food and drug products.[22]

In June 2013 it partnered with the Coalition of Small Business Innovators to lobby the U.S. government to modernize the U.S. tax code "to recognize and promote small business innovation as fundamental to the long-term growth of the U.S. economy".[6][23]

It is a member of The Alliance to Feed the Future, an umbrella network, the mission of which is to "raise awareness and improve understanding of the benefits & necessity of modern food production and technology in order to meet global demand".[24][25]

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Stem Cell Therapy in Mexico. You Can Improve Your Life …

June 8th, 2015 3:47 pm

Our Clinic Our clinic has been certified by the COFEPRIS, which is Mexico's regulatory health organization and performs the same functions as the FDA in the United States.

We have received countless testimonials from very satisfied patients, and if you're traveling to Mexico from the U.S. to receive treatments, we will provide you with a personal assistant who will translate from Spanish to English, give you medical passes that you can use to cross the border swiftly, transport you to and from the airport and help you find our office and your hotel in Tijuana.

http://progencell.com. ProgenCell offers an alternative stem cell treatment that is safe and effective. ProgenCell is able to use adult stem cells obtained from your own bone marrow and transfer the stem cells to a different part of your body through an IV (similar to blood transfusion). This stem cell therapy treatment can help relieve pain and even cure diseases. Learn how stem cells can help you today.

Get Started

If you would like to schedule an appointment, you can fill out the form on our website, and our representatives will contact you within 24 hours.

Additionally, if you have any questions or need immediate assistance, call our office at 1-888-443-6235. At ProgenCell we specialize in the treatment of different conditions including the following:

Stem Cell Therapy for Rheumatoid Arthritis This autoimmune disease causes inflammation in the body's tissues and organs. The condition can be present for more than five years before the patient recognizes any symptoms, and usually, rheumatoid arthritis affects the joints first. Stem cell therapy may help this condition. Over time, this type of arthritis can disfigure the joints and prevent them from functioning properly.

By injecting stem cells into areas of the body that have been damaged by the condition, the healthy cells will regenerate the old, weakened tissues, and as the new cells divide, their positive effects will increase.

Stem Cell Therapy for Systemic Lupus The immune system of an individual with systemic lupus will attack the person's own cells, and usually, the disease primarily affects the heart, the lungs and the kidneys.

Physicians treat the condition by prescribing medications that suppress the activity of the immune system, such as corticosteroids and cyclophosphamide. Stem cell therapy may help this condition.

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Stem Cell Kidney Diseases – World Stem Cells, LLC

June 7th, 2015 12:44 pm

Chronic kidney disease(CKD), also known as chronic renal disease, is a progressive loss in renal function over a period of months or years. The symptoms of worsening kidney function are unspecific, and might include feeling generally unwell and experiencing a reduced appetite. Often, chronic kidney disease is diagnosed as a result of screening of people known to be at risk of kidney problems, such as those with high blood pressure or diabetes and those with a blood relative with chronic kidney disease. Chronic kidney disease may also be identified when it leads to one of its recognized complications, such as cardiovascular disease, anemia or pericarditis.

Chronic kidney disease is identified by a blood test for creatinine. Higher levels of creatinine indicate a falling glomerular filtration rate and as a result a decreased capability of the kidneys to excrete waste products. Creatinine levels may be normal in the early stages of CKD, and the condition is discovered if urinalysis (testing of a urine sample) shows that the kidney is allowing the loss of protein or red blood cells into the urine.

To fully investigate the underlying cause of kidney damage, various forms of medical imaging, blood tests and often renal biopsy (removing a small sample of kidney tissue) are employed to find out if there is a reversible cause for the kidney malfunction.

Recent professional guidelines classify the severity of chronic kidney disease in five stages, with stage 1 being the mildest and usually causing few symptoms and stage 5 being a severe illness with poor life expectancy if untreated. Stage 5 CKD is also called established chronic kidney disease and is synonymous with the now outdated terms end-stage renal disease (ESRD), chronic kidney failure (CKF) or chronic renal failure (CRF).

There was no specific treatment unequivocally shown to slow the worsening of chronic kidney disease, until recently. If there is an underlying cause to CKD, such as vasculitis, this may be treated directly with treatments aimed to slow the damage. In more advanced stages, treatments may be required for anemia and bone disease. Severe CKD requires one of the forms of renal replacement therapy; this may be a form of dialysis, but ideally constitutes a kidney transplant or potentially stem cell therapy.

CKD is initially without specific symptoms and can only be detected as an increase in serum creatinine or protein in the urine. As the kidney function decreases:

People with chronic kidney disease suffer from accelerated atherosclerosis and are more likely to develop cardiovascular disease than the general population.

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Stem Cell Therapy – CKD Treatment

June 5th, 2015 5:43 pm

Hi, I am Dr. Shan. I will be looking into your query below and will be guiding you through the process.In this step, you can edit your query and in the next one, if needed, you can talk with our free online service directly.

40% kidney function is so poor that kidneys are unable to do the normal work, and patients are prone to suffer numerous symptoms which can severely affect patients life quality. Well then, what is the prognosis for someone with 40% kidney f...

According to GFR (glomerular filtration rate), 40% kidney function means that you are in the Stage 3 Chronic Kidney Disease which is characterized with decline of renal function. When diagnosed with 40% renal function, many patients are con...

Creatinine 6.8 is extremely high for FSGS patients. Many patients do not know the causes of high creatinine level, and do not know the treatment. Then, is there any treatment to deal with the condition? Causes of high creatinine level in FS...

ESRD (end-stage renal disease) is the last stage of kidney disease and it cant be reversed. When diagnosed with Purpura Nephritis and when it progresses to this stage, what should you do for yourself? Aside from dialysis, is there any avail...

For diabetes, our hospital will use the stem cells treatment to treat. Stem cells transplant is a new treatment in treating diabetes. With the development of medical science and the improvement of medical device, stem cells transplant has b...

Can a patient with 9% kidney function benefit from Stem Cell Therapy? This is a concerned issue by a large amount of kidney disease patients. Well then, what is the answer? Lets have a look at this passage. A person with 9% kidney function...

Prognosis is important to control the illness condition and enhance life quality for kidney failure patients. Stage 3 kidney failure is one of important periods to improve prognosis. Well then, how to make a good prognosis for them? Kidney...

Recently, I browsed the Internet looking for available treatment for Kidney Failure, and I occasionally found that your Stem Cell Therapy. I am interested in this therapy, and could you please tell me that how it treats this kidney disease?...

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