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Global Stem Cells Market – Industry Analysis, Size, Share, Growth, Trends and Forecast, 2012 – 2018

Posted: Published on July 12th, 2013

Albany, New York (PRWEB) July 12, 2013 According to a new market report published by Transparency Market Research "Stem Cells Market (Adult, Human Embryonic , Induced Pluripotent, Rat-Neural, Umbilical Cord, Cell Production, Cell Acquisition, Expansion, Sub-Culture)- Global Industry Analysis, Size, Share, Growth, Trends and Forecast, 2012 - 2018," the market for stem cells was valued at USD 26.23 billion in 2011 and is expected to reach an estimated value of USD 119.51 billion in 2018, growing at a CAGR of 24.2% from 2012 to 2018. Related Report : Coronary Stents Market http://www.transparencymarketresearch.com/coronary-stents-market.html Stem cells are undifferentiated cells which are capable of differentiating into any type of cell that make-up the human body and thus, are capable of producing non-regenerative cells such as neural and myocardial cells. This report estimates the market for global stem cells in terms of revenue (USD billion) for the period 2012 2018, keeping 2011 as the base year. The global stem cells market is mainly segmented into four major sub-types namely market by products, market by technology, market by applications and market by geography. The market by products is segmented into three sub-types, namely adult stem cells, human embryonic stem cells and other type of stem … Continue reading

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Injecting iron supplement lets Stanford scientists track transplanted stem cells

Posted: Published on July 12th, 2013

Public release date: 12-Jul-2013 [ | E-mail | Share ] Contact: Bruce Goldman 650-725-2106 Stanford University Medical Center STANFORD, Calif. A new, noninvasive technique for tracking stem cells after transplantation developed by a cross-disciplinary team of radiologists, chemists, statisticians and materials scientists at the Stanford University School of Medicine could help surgeons determine whether a procedure to repair injured or worn-out knees is successful. The technique, described in a study to be published online July 12 in Radiology, relies on an imaging agent already approved by the U.S. Food and Drug Administration for an entirely different purpose: anemia treatment. Although this study used rodents, the approach is likely to be adapted for use in humans this fall as part of a clinical trial in which mesenchymal stem cells will be delivered to the site of patients' knee injuries. Mesenchymal stem cells are capable of differentiating into bone and cartilage, as well as muscle, fat and tendon, but not into the other cell types that populate the body. Every year, arthritis accounts for 44 million outpatient visits and 700,000 knee-replacement procedures. But the early repair of cartilage defects in young patients may prevent further deterioration of the joint and the need … Continue reading

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Argentine boy heads home after stem cell transplant at Duke

Posted: Published on July 12th, 2013

Durham, N.C. Almost a year ago, when 11-year-old Lautaro Javier left Argentina for medical treatment at Duke University Hospital, his parents didn't know where they would stay or how they would get by in Durham. They felt very much alone. "Like a fish out of water," said Lautaro's father, Eduardo Javier. But they went to the Ronald McDonald House, where they were made to feel comfortable and protected, he said. On Sunday, after 347 days, the Javiers will return home. "This week, it was very hard for us because we had to say goodbye to everybody at the transplant ward, all the nurses, everybody," said Gabriela Veronica de Pablo, Lautaro's mother. "It was very hard to say goodbye." Lautaro has a rare disease called metachromatic leukodystrophy, which causes an enzyme deficiency in his brain. "That leads to damage in the brain and progressive brain disease, which is usually the cause of death," said Dr. Vinod Prasad with Duke's pediatric bone marrow and stem cell transplant program. A stem cell transplant and therapy helped him improve in many areas he can speak more with his family and is able to spend more time on his feet, with assistance. Back home, celebrities … Continue reading

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Aesthetic medicine a safe, painless alternative to surgery

Posted: Published on July 12th, 2013

For years those looking to regain their youthful appearance, and boost their self-confidence in the process, have turned to surgical procedures such as face lifts or plastic surgery. Thankfully, advancements in aesthetic medicine mean patients can now get similar results without having to undergo invasive surgeries. Tsawwassens Dr. Martin Ray of the View Laser Skin Rejuvenation Clinic specializes in non-surgical procedures that offer many advantages to surgery. After a face lift, a patient can spend days or weeks recovering at home with bandages on their face. Thankfully, the modern techniques Ray employs mean a patient can be in and out in under an hour, pain-free. Theres significant things we can do now to improve appearance, without surgery, he says. Ray has been operating a family practice in Tsawwassen since 1986, and in 2006 founded the View Laser Skin Rejuvenation Clinic with his wife, Dr. Judith Fletcher. The clinic offers dermal fillers, laser therapy, microdermabrasion, intense pulse light photofacials, Botox, and much more. The treatments can rejuvenate the skin, reduce acne scarring and the appearance of blood vessels, smooth out wrinkles, and get rid of age spots. Over time we can develop lines on our face that make us look angry … Continue reading

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Stem cell therapy future of medicine? – Video

Posted: Published on July 12th, 2013

Stem cell therapy future of medicine? Everyone is talking about stem cell therapy. But scammers and swindlers are also taking advantage of the fad, prompting the Health Department to step in. Bue... By: Rappler … Continue reading

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Two successful gene therapy trials block inherited diseases in humans

Posted: Published on July 12th, 2013

Gene therapy: not just for mice. Genetic traits, like a bulbous nose or balding, give some people reasons to moan about what they inherited from their parents. But more serious genetic flaws can cause debilitating disease. Now, Italian researchers have come up with a way of treating one such inherited disease and reversing another using a promising new method of gene therapy. The idea behind gene therapy is to replace a faulty gene with a shiny new version that works properly. Modified versions of viruses, which have been sculpted by millions of years of evolution, perfectly penetrate human cells. They act as courriers delivering DNA payloads to defective cells and ensure they are stably inherited. This deceptively simple idea, though, has been challenging to achieve in practice. The first commercial gene therapy product, Glybera, only received regulatory approval in 2012. Part of the reason for this is the difficulty of successfully clearing three hurdles at once: delivering replacement genetic information to the exact cells that need help, getting this information safely translated in high enough volumes to overcome the defects, and stopping the immune system from reacting to normal genes when it has grown used to only seeing mangled ones. … Continue reading

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ViaCyte raises $10.6 million

Posted: Published on July 12th, 2013

SAN DIEGO ViaCyte, a developer of a diabetes treatment from human embryonic stem cells, has raised $10.6 million in a private equity financing. The money will go to ViaCytes therapy for type 1 diabetes, the privately held company said Wednesday. ViaCyte said the financing included its largest existing investors: Johnson & Johnson Development Corp., Sanderling Ventures and Asset Management Co. The cash infusion represents a matching investment to a $10.1 million grant from the California Institute for Regenerative Medicine, the states stem cell agency. ViaCytes product, called VC-01, contains cells derived from human embryonic stem cells. These cells mature into the insulin-producing pancreatic cells destroyed in type 1 diabetes. The cells are enclosed in a semipermeable screen that protects the cells from the immune system, allowing them to receive nutrients and secrete insulin. The device has been tested in animals, and ViaCyte is preparing to begin human clinical trials Assuming all goes well, ViaCyte could start by the first or second quarter of 2014, said Chief Executive Paul Laikind. Only a few companies in the United States have used embryonic stem cells in clinical trials. Most use other kinds derived from nonembryonic sources, such as umbilical cord blood. This is … Continue reading

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Babraham scientists make stem cell discovery

Posted: Published on July 12th, 2013

Epigenetics researchers at the Babraham Institute in Cambridge UK have identified the biological process that leads to global loss of the genomes methylation memory when cells are reprogrammed at fertilisation to the so-called ground-state development. Epigenetics is revolutionising our understanding of genetic inheritance and also helping to explain how our genes can be influenced by the environment. Genomic methylation, which does not alter DNA sequence but essentially marks it in a stable lifelong manner, is accumulated during development and plays a vital role in committing cells to specialised roles in the body. These methylation marks must be erased at the start of each new generation, to restore the ability of a newly fertilised egg to develop into a new organism. Understanding this mechanism of wiping the slate clean is important to appreciate how the developmental capacity of cells is reset and also provides insights that will guide the use of stem cells for therapeutic purposes, which also requires remodelling of genomic methylation. It is known that when adult cells are reprogrammed to stem cell-like cells, they do not completely erase their memory. This unfortunately limits their use in stem cell therapy since these cells will have the tendency to develop … Continue reading

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Billings veterinary clinic conducts city's first dog stem cell therapy treatment

Posted: Published on July 12th, 2013

Thor, an athletic 7-year-old Catahoula leopard hound, lay on a table at the Animal Clinic of Billings, panting lightly while staffers put small bags over his feet and temperature-controlled packs on his chest before the anesthesia kicked in. Not long after he went under, those same staff members carried Thor to an operating table where his owner, Dr. Bobbi Jo Massic, who is also a veterinarian at the clinic, made a small incision in his abdomen, the first step in a cutting-edge process designed to help the alleviate the dogs hip dysplasia and arthritis. By the end of Tuesday, Thor became the very first patient in the clinics brand new animal stem cell therapy program. This is a very exciting day, said Dr. Bryna Felchle, another vet at the clinic who will help spearhead the program. Were launching our very first stem cell therapy right here. The process is widespread across the United States, but Felchle is just the second vet in Montana certified to perform the procedure and the only one in the eastern half of the state. Generally, it involves removing fatty tissue from an animal, separating the stem cells from that tissue, activating the cells and then … Continue reading

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New Method to Produce Blood Cells from Stem Cells Could Yield a Purer, Safer Cell Therapy

Posted: Published on July 12th, 2013

Durham, NC (PRWEB) July 12, 2013 A new protocol for reprogramming induced pluripotent stem cells (iPSCs) into mature blood cells, using just a small amount of the patients own blood and a readily available cell type, is reported on in the current issue of STEM CELLS Translational Medicine. This novel method skips the generally accepted process of mixing iPSCs with either mouse or human stromal cells during the differentiation process and, in essence, ensures no outside and potentially harmful DNA is introduced into the reprogrammed cells. As such, it could lead to a purer, safer therapeutic grade of stem cells for use in regenerative medicine. The discovery of iPSCs holds great promise for regenerative medicine since it is possible to produce patient-specific iPSCs from the individual for potential autologous treatment that is, treatment using the patients own cells. This avoids the possibility of rejection and numerous other harmful side effects. CD34+ cells are a type of blood stem cell that has been linked to proliferation. However, collecting enough CD34+ cells from a patient to produce an adequate amount of blood usually requires a large volume of blood to be taken from the patient. But scientists found a way around this, … Continue reading

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