The Sims 3: Perfect Baby Challenge - Part 4 | Strong Genetics.
Read The Description Please. Challenge Rules: 100 Baby Challenge: http://modthesims.info/t/465479 Perfect Genetics: http://modthesims.info/t/454886 S...

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Lets Play The Sims 3 Perfect Genetics Part 4: Dirty Girl!
Watch as we get a better look into Marina #39;s life before us! My Sims 3 Page: http://mypage.thesims3.com/mypage/becky050890 My Husband #39;s Sims 3 Page: http://mypage.thesims3.com/mypage/gordonwisner2...

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Lets Play The Sims 3 Perfect Genetics Part 4: Dirty Girl! - Video

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Q A Part 5 Muscle Increase In Metabolism Training When Sore Average Genetics Stubborn Fat
0:15 Jason, about how much does a pound of muscle raise your BMR/TDEE? I #39;ve heard its between 7-15 calories per pound of muscle, is that pretty accurate? If ...

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Q&A Part 5 Muscle Increase In Metabolism Training When Sore Average Genetics Stubborn Fat - Video

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EOC Review for Genetics Part I
EOC Review for Genetics Part I.

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PUBLIC RELEASE DATE:

4-Jun-2014

Contact: Karen Kreeger karen.kreeger@uphs.upenn.edu 215-349-5658 University of Pennsylvania School of Medicine

PHILADELPHIA Advances in the understanding of the genetics of coronary artery disease, or CAD, will revitalize the field and lead to more therapeutic targets for new medicines to combat this common disease, suggests a genetics expert from the Perelman School of Medicine at the University of Pennsylvania in a Perspective article in the new issue of Science Translational Medicine.

Daniel J. Rader, MD, chair of the Department of Genetics and associate director of the Institute for Translational Medicine and Therapeutics, asserts that the lagging search for new heart medicines could be jump-started by a wide-angle hunt for relevant genetic variants in humans.

According the America Heart Association, the death rate from heart disease has fallen about 39 percent during the past 10-most-recent years for which statistics are available. Still, heart disease is the number-one cause of death in the United States, killing almost 380,000 people a year.

Although progress has been made in decreasing the risk of heart disease, with the single greatest contribution made by statins to reduce levels of low-density lipoprotein cholesterol (LDL-C) in millions of people, the burden of the disease remains high. "Despite this clear unmet need, however, many biopharmaceutical companies have begun to back away from efforts to discover and develop therapies for this prevalent disease," writes Rader, citing seven drugs that have failed in phase 3 clinical trials in the last three to five years.

The single biggest issue facing the development of new therapeutics for heart disease is confidence before expensive human trials are underway that the target of a new drug has a high probability of success in reducing disease. Animal models of atherosclerosis, however, have not proven reliable at predicting new therapies that are effective in humans. In contrast, Rader says, basing drug targets on human genetics can provide greater confidence that a therapeutic targeted to a particular pathway will show clinical benefit in reducing major cardiovascular events in people. As with recent successes in cancer immunotherapy, a targeted, personalized approach to developing new treatments has proved attractive to big pharma.

Human genetic data strongly support the concept that reducing LDL-C by any means is associated with a lower cardiovascular risk. This association is consistent with LDL-C being a causal factor in the development of cardiovascular disease. Indeed, the discovery that mutations in the gene PCSK9 reduce LDL-C and protect against CAD launched a major effort to develop inhibitors of PCSK9, which markedly reduce LDL-C and are in late-stage clinical development.

Similar genetic data for triglycerides were recently published, suggesting that specific proteins regulating this blood chemical might be viable therapeutic targets. On the other hand, human genetic data provide little support for raising high-density lipoprotein cholesterol (HDL-C) because genetic variants associated with increased HDL-C are not generally associated with decreased cardiovascular risk.

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Genetics provide blueprint for new heart disease therapies

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Newswise PHILADELPHIA Advances in the understanding of the genetics of coronary artery disease, or CAD, will revitalize the field and lead to more therapeutic targets for new medicines to combat this common disease, suggests a genetics expert from the Perelman School of Medicine at the University of Pennsylvania in a Perspective article in the new issue of Science Translational Medicine.

Daniel J. Rader, MD, chair of the Department of Genetics and associate director of the Institute for Translational Medicine and Therapeutics, asserts that the lagging search for new heart medicines could be jump-started by a wide-angle hunt for relevant genetic variants in humans.

According the America Heart Association, the death rate from heart disease has fallen about 39 percent during the past 10-most-recent years for which statistics are available. Still, heart disease is the number-one cause of death in the United States, killing almost 380,000 people a year.

Although progress has been made in decreasing the risk of heart disease, with the single greatest contribution made by statins to reduce levels of low-density lipoprotein cholesterol (LDL-C) in millions of people, the burden of the disease remains high. Despite this clear unmet need, however, many biopharmaceutical companies have begun to back away from efforts to discover and develop therapies for this prevalent disease, writes Rader, citing seven drugs that have failed in phase 3 clinical trials in the last three to five years.

The single biggest issue facing the development of new therapeutics for heart disease is confidence before expensive human trials are underway that the target of a new drug has a high probability of success in reducing disease. Animal models of atherosclerosis, however, have not proven reliable at predicting new therapies that are effective in humans. In contrast, Rader says, basing drug targets on human genetics can provide greater confidence that a therapeutic targeted to a particular pathway will show clinical benefit in reducing major cardiovascular events in people. As with recent successes in cancer immunotherapy, a targeted, personalized approach to developing new treatments has proved attractive to big pharma.

Human genetic data strongly support the concept that reducing LDL-C by any means is associated with a lower cardiovascular risk. This association is consistent with LDL-C being a causal factor in the development of cardiovascular disease. Indeed, the discovery that mutations in the gene PCSK9 reduce LDL-C and protect against CAD launched a major effort to develop inhibitors of PCSK9, which markedly reduce LDL-C and are in late-stage clinical development.

Similar genetic data for triglycerides were recently published, suggesting that specific proteins regulating this blood chemical might be viable therapeutic targets. On the other hand, human genetic data provide little support for raising high-density lipoprotein cholesterol (HDL-C) because genetic variants associated with increased HDL-C are not generally associated with decreased cardiovascular risk.

Although circulating biomarkers such as LDLs and triglycerides, commonly measured in standard blood lipid panels, are useful for guiding drug development programs focused on reducing CAD, Rader contends that many of the genetically validated targets for CAD will not have well-established circuiting biomarkers. Some of the most interesting new targets for atherosclerotic cardiovascular disease are likely to come from genetic studies of common and rare variants, comparing individuals with early disease with those who are free of disease, says Rader.

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Genetics Provide Blueprint for New Heart Disease Therapies, Writes Penn Medicine Researcher

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gene therapy,also called gene transfer therapy, introduction of a normal gene into an individuals genome in order to repair a mutation that causes a genetic disease. When a normal gene is inserted into the nucleus of a mutant cell, the gene most likely will integrate into a chromosomal site different from the defective allele; although this may repair the mutation, a new mutation may result if the normal gene integrates into another functional gene. If the normal gene replaces the mutant allele, there is a chance that the transformed cells will proliferate and produce enough normal gene product for the entire body to be restored to the undiseased phenotype.

Human gene therapy has been attempted on somatic (body) cells for diseases such as cystic fibrosis, adenosine deaminase deficiency, familial hypercholesterolemia, cancer, and severe combined immunodeficiency (SCID) syndrome. Somatic cells cured by gene therapy may reverse the symptoms of disease in the treated individual, but the modification is not passed on to the next generation. Germinal gene therapy aims to place corrected cells inside the germ line (e.g., cells of the ovary or testis). If this is achieved, these cells will undergo meiosis and provide ... (200 of 506 words)

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gene therapy (medicine) -- Encyclopedia Britannica

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MIAMI (PRWEB) June 04, 2014

GlobalStemCellsGroup.com, its subsidiary Stem Cell Training, Inc. and Bioheart, Inc. have announced a new 16 CME online credit course for physicians. Working at their own pace from the privacy of home or office, physicians can learn how to implement regenerative medicine techniques in their own practices.

Taught by stem cell and regenerative medicine expert Kristin Comella, the online course provides didactic lectures on regenerative medicine and scientifically validated protocols. Lecture topics include:

Included in the online coursework are training videos, training booklets, detailed protocols and power point presentations with instructions and images for:

Medical professionals can also choose to combine the online coursework with one-on-one training with a regenerative medicine specialist.

For more information, visit the Global Stem Cells website,, email bnovas(at)regenestem(dot)com, or call 305-224-1858.

About the 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 Groups corporate mission is to make the promise of stem cell medicine a reality for patients around the world. With each of GSCGs 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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Global Stem Cells Group Announces Accredited Online Stem Cell Training Course

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Arthritic hip, knee, and thumbs 9 months after stem cell therapy by Dr Harry Adelson
Raymond and Nina describe their outcomes from stem cell therapy by Dr Harry Adelson for their various arthritic pains http://www.docereclinics.com.

By: Harry Adelson, N.D.

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New York, NY (PRWEB) June 04, 2014

The Animal Medical Center of New York is offering stem cell therapy provided through Vet-Stem and long-term management in a clinical trial for qualifying cats with chronic kidney disease (CKD). The ultimate goal of this study is to investigate the use of stem cells (obtained from the patients own fat) in aiding the enhancement of renal (kidney) function by their regenerative capabilities, with the goal of improving survival in cats with CKD.

Currently there are no therapeutic options for cats with CKD other than renal transplantation, which is not typically an option for most owners. Most efforts aim at improving uremic signs with food, dietary supplements, and antacids, but there are no current methods for improving function of the kidney directly. CKD is the leading cause of death in older cats, and 35% of cats will develop CKD at some point.

Since renal failure is so common in cats and renal cell death is the ultimate result, improving the health and environment of the cells that remain could improve the overall function of the kidneys and ultimately improve the survival times and quality of life in patients. The aim is to use the cats own adipose (fat) derived stem cells to improve renal function directly, as stem cells are thought to improve, repair, and aid in the growth of damaged tissue.

The potential health benefits of using stem cells to combat CKD include renal regeneration, anti-fibrotic effects, a decrease in proteinuria (also called urine albumin or an abnormal amount of protein in the urine), and an improvement in the Glomerular Filtration Rate (GFR used to help measure kidney function). AMC is offering free fat collection, isolation of the stem cells from the fat, and intra-arterial injection for qualifying cats, as well as free follow-up for three years. Qualifying cats must be diagnosed with IRIS Stage 3 CKD that have had no other experimental therapies. Potential candidates must undergo a full workup and have no history of urinary tract stone disease or the presence of other concurrent, unrelated disease.

Allyson Berent, DVM, DACVIM and Catherine E. Langston, DVM, DACVIM will be leading the three year study, and invite owners with a cat that has been diagnosed with CKD to call 212.329.8763 for more information on qualifying for the clinic trial. To learn more about the study go to http://www.amcny.org/clinicaltrials. To watch a short special interest film about one cats success go to http://www.vet-stem.com/pr_detail.php?id=49.

The Animal Medical Center in New York City is a federally recognized 501(c)(3) non-profit veterinary center that has been a national leader in animal care since 1910. As an academic veterinary hospital, The AMC promotes the health and well-being of companion animals through advanced treatment, research and education. Stem Cell Therapy through Vet-Stem has been offered at AMC since 2008 to treat pain associated with chronic osteoarthritis. To find out more about AMC and their stem cell therapy services for osteoarthritis go to http://www.amcny.org/surgery/neurosurgery/stem-cell-therapy.

Vet-Stem, Inc. was formed in 2002 to bring regenerative medicine to the veterinary profession. The privately held company is working to develop therapies in veterinary medicine that apply regenerative technologies while utilizing the natural healing properties inherent in all animals. As the first company in the United States to provide an adipose-derived stem cell service to veterinarians for their patients, Vet-Stem, Inc. pioneered the use of regenerative stem cells in veterinary medicine. The company holds exclusive licenses to over 50 patents including world-wide veterinary rights for use of adipose derived stem cells. In the last decade over 10,000 animals have been treated using Vet-Stem, Inc.s services, and Vet-Stem is actively investigating stem cell therapy for immune-mediated and inflammatory disease, as well as organ disease and failure. For more on Vet-Stem, Inc. and Veterinary Regenerative Medicine visit http://www.vet-stem.com or call 858-748-2004.

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Animal Medical Center of New York Seeks Candidates for Clinical Trial for Cats with Chronic Kidney Disease to Receive ...

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A NEW method of helping bone marrow stem cells "mature" is pushing science closer to being able to treat brain injuries by creating specific cells capable of repairing damaged areas.

By modifying the surface of these cells and ensuring the proper environment, these otherwise easy-to-obtain marrow cells could drive brain regeneration.

Although this is only a small step forward, the hope is that these techniques could one day help treat those who have suffered brain damage, including those resulting from a stroke.

Nationally, there are 420,000 Australians living with the effects of stroke in Australia.

There are about 50,000 new and recurrent strokes each year, about 29,000 of those in Queensland and New South Wales.

National Stroke Foundation spokeswoman Professor Richard Linley said the research had the potential to help stroke patients, but was clearly in the very early stages of development.

Queensland University of Technology researcher Rachel Okolicsanyi said while the capability of these marrow stem cells has been understood for some time, this research into influencing how they mature could create techniques to convert them into brain or neural cells.

Ms Okolicsanyi, with supervisors Dr Larisa Haupt and Professor Lyn Griffiths , will now attempt to nail down a technique that will deliver routine results.

Ms Okolicsanyi's work was published in the journal Developmental Biology.

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New stem cell methods may help brain injuries

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PUBLIC RELEASE DATE:

3-Jun-2014

Contact: Sandra Hutchinson s3.hutchinson@qut.edu.au 61-731-389-449 Queensland University of Technology

A QUT scientist is hoping to unlock the potential of stem cells as a way of repairing neural damage to the brain.

Rachel Okolicsanyi, from the Genomics Research Centre at QUT's Institute of Health and Biomedical Innovation, said unlike other cells in the body which were able to divide and replicate, once most types of brain cells died, the damage was deemed irreversible.

Ms Okolicsanyi is manipulating adult stem cells from bone marrow to produce a population of cells that can be used to treat brain damage.

"My research is a step in proving that stem cells taken from the bone marrow can be manipulated into neural cells, or precursor cells that have the potential to replace, repair or treat brain damage," she said.

Ms Okolicsanyi's research has been published in Developmental Biology journal, and outlines the potential stem cells have for brain damage repair.

"What I am looking at is whether or not stem cells from the bone marrow have the potential to differentiate or mature into neural cells," she said.

"Neural cells are those cells from the brain that make everything from the structure of the brain itself, to all the connections that make movement, voice, hearing and sight possible."

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Unlocking the potential of stem cells to repair brain damage

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GOLTRY, Okla. Armed with stem cells, a Goltry area woman will be heading to Milwaukee next week to join in her brothers cancer fight.

Jeni Sumner was the only match among family members tested to donate stem cells to her younger brother, Ed Dee.

To me, Ive been given a gift. I know everybodys congratulating me and saying its a wonderful thing, and not taking it away from that, but I think Ive been given just a tremendous gift, Sumner said.

Along with helping her brother, Sumner is trying to encourage others to join the bone marrow donor registry.

I think a lot of people are afraid to join because they might get called, because they dont know what its like to be a donor, she said. I want more people to become aware of what its actually like to be a donor.

Sumner set up a Facebook page It Doesnt Hurt - To Save a Life to chronicle everything she will go through, as a donor, during the procedure.

Its an unknown for me, but its nothing compared to what my brothers going through, she said. I know the feeling that I got when I got the call from the doctor saying that I was his donor. The relief and the joy that I felt that our family doesnt have to look anymore. If anything happens, were covered because we have a donor, we have a match. The feeling that I got was incredible, she said.

Dee, of Milwaukee, Wis., was diagnosed with acute myelogenous leukemia last year. Sumner said he went into remission last October.

Unfortunately, the cancer came back. This type of leukemia is a very dangerous and aggressive form. He, every couple of weeks, would go in for a blood test and this March he was informed that his leukemia had come back, she said. His doctors feel that a stem cell transplant would be the best for him, at this time.

Following the return of the cancer, Dee went through five days of rigorous chemotherapy to put him back into remission. He recently finished a lower dose session of chemo, Sumner said.

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Using stem cells, woman joins brothers cancer fight

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Boston, MA (PRWEB) June 03, 2014

Today, Dr. James L. Sherley, the Director of Bostons Adult Stem Cell Technology Center, LLC (ASCTC) described a new technology for identification of new drug candidates that are toxic to adult stem cell cells in the human body. The new AlphaSTEM technology is the first of its kind to address a long-standing unmet need in the pharmaceutical industry.

Dr. Sherley presented the AlphaSTEM technology at the 7th Annual Massachusetts Life Sciences Innovation Day (MALSI Day 2014; http://www.mattcenter.org/malsi-day-2014/home.html) at the Harvard Club of Boston. ASCTC is one of a select number of start-up companies invited to present posters on their newest innovative biotechnologies at the all day event, which features the best and brightest life sciences innovations of the year.

Just as adult stem cells are crucial for life and normal organ function, their safety is crucial for successful treatment with new drugs. Even if a new drug has high activity against a disease or disorder; it will not be an effective treatment, if it is also too toxic to adult stem cells.

Adult stem cells are found in all renewing tissues and organs of the human body, like hair, skin, liver, and even the brain. They are responsible for replacing old mature tissue cells with new young cells. They are also essential cells for repairing injured tissues and wounds.

Some drugs are known to harm adult stem cells. Examples of these are many cancer drugs. Cancer drugs are often administered at the highest doses at which patients can tolerate the adverse effects of the drugs on adult stem cells. ASCTCs AlphaSTEM technology could accelerate discovery of better cancer drugs with less adult stem cell toxicity.

The major application proposed for the new AlphaSTEM technology is use by pharmaceutical companies to identify adult stem cell-toxic drugs before initiating clinical trials with them or entering the marketplace. Drug failure in clinical trials due to safety concerns is a major unrecovered cost of drug development. Chronic adult stem cell toxicity that now may go undetected until after marketing can result in tragic deaths for patients and catastrophic injury liabilities for the responsible drug companies. The Merck drug Vioxx is an example of such an unfortunate mishap.

The problem faced by the Food and Drug Administration (FDA) and the pharmaceutical industry is how to monitor drug effects on adult stem cells, when the cells are difficult to identify, isolate, produce, and count. The solution presented by ASCTC was a computer simulation approach based on the universal tissue cell production properties of adult stem cells.

ASCTC partnered with AlphaSTAR Corporation, a leading global provider of simulation technologies, to develop the AlphaSTEM software program that can simulate the culture multiplication of adult tissue stem cells found in any human tissue. AlphaSTEM technology not only has the power to detect drug toxicity against adult stem cells, but also against other specialized types of tissue cells specifically.

Director Sherley predicted that the introduction of AlphaSTEM technology into the pharmaceutical industry would have many immediate benefits. With relatively inexpensive detection of drugs destined to fail in expensive clinical trials, the new technology could save billions of currently wasted dollars, reducing overall drug development costs in the U.S. by as much as 20%. These savings could accelerate the rate of arrival of new effective drugs to patients by a comparable reduction in time. AlphaSTEM technology may also reduce the occurrence of drugs thought safe, but which actual have a lurking toxicity that emerges as lethal to some patients with wider and longer use.

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The Adult Stem Cell Technology Center, LLC Announces New Technology for Preventing Catastrophic Adult Stem Cell ...

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4 hours ago A-DNA (left) B-DNA (right)

(Phys.org) Scientists have discovered that bacteria can reshape their DNA to survive dehydration.

The research, published today in the journal Journal of the Royal Society Interface, shows that bacterial DNA can change from the regular double helix known as B-DNA, to the more compact A-DNA form, when faced with hostile conditions such as dehydration.

Crucially, scientists have pinpointed a unique process in DNA, called the B-A-B transition, which allows it to change its structure in response to environmental change. Without impacting on the ability of the bacteria to function and reproduce, this unique structural alteration sees the B-DNA change to A-DNA, and then revert back to its original B-DNA form to ensure the bacteria survive.

Associate Professor Bayden Wood, from Monash University said the study gives vital new information on how bacteria can survive periods of time in arid environments.

"Our findings may be important in understanding how dormant bacteria that are transferred from dry surfaces may become active and reproduce in the human body,' Associate Professor Wood said.

PhD student and first author of the paper, Donna Whelan said the most common form of DNA found in most organisms is B-DNA. However, the A-form has been thought to show protective qualities to allow bacterial spores to survive high UV exposure and other extreme environmental conditions.

"Our research, which utilised infrared light to investigate the structure of DNA inside live bacteria, demonstrates that bacteria can survive by adopting the A-DNA form after the majority of water is removed and that really is groundbreaking," Donna Whelan said.

The new findings build on research led by Associate Professor Wood and Donna Whelan in 2011 at the Australian Synchrotron, which indicated the same B-A-B DNA transition occurs in all cell types. Significantly, the team has now discovered this change may have a biological function in bacteria, potentially assisting them to survive dehydration.

Associate Professor Bayden Wood said the ability for DNA to transform and then change back again in human cells had puzzled scientists until now.

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'Clever' DNA may help bacteria survive

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stem cell therapy-treatment for adhd by dr alok sharma, mumbai, india
improvement seen in just 5 days after stem cell therapy treatment for Global Developmental Delay with Attention Deficit Hyperactivity Disorder predominantly Hyperactivity Disorder by dr alok...

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Hawaii: Fear over GM plants and pesticides | Global 3000
The Hawaiian archipelago has become the largest genetic engineering testing ground in the world for the global seed producers. If anything should happen to go wrong, the risk is minimal. California...

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Hawaii: Fear over GM plants and pesticides | Global 3000 - Video

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Genetic Engineering Presentation

By: Dylan Hynds

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Genetic Engineering Presentation - Video

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Genetic engineering and the Vedas
Harvard biophysicist D. P. Dupey writes, "We may lead ourselves down a blind alley by adhering dogmatically to the assumption that life can be explained enti...

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Omicia - Advancing Personalized Medicine and Clinical Genomics
The analysis and clinical interpretation of genomic information is rapidly changing the landscape of disease research, diagnostics, drug development, and disease management. Omicia is developing...

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Omicia - Advancing Personalized Medicine and Clinical Genomics - Video

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BRITNEY HILL MAY 26 2014 LAS VEGAS NV spinal cord injury, paralyzed below her waist, now walking
Britney Hill May 26 2014.... One year later. Britney Hill, paralyzed from the waist down in an ATV accident on May 26 2013. She has been going through rehabilitation now for one year. She...

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BRITNEY HILL MAY 26 2014 LAS VEGAS NV spinal cord injury, paralyzed below her waist, now walking - Video

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NIBSC/SCIENCE PHOTO LIBRARY

Embryonic stem cells may have the ability to repair damaged tissue.

A landmark stem-cell trial is sputtering back to life two-and-a-half years after it was abandoned by the California company that started it. But it now faces a fresh set of challenges, including a field that is packed with competitors.

The trial aims to test whether cells derived from human embryonic stem cells can help nerves to regrow in cases of spinal-cord injury. It was stopped abruptly in 2011 by Geron of Menlo Park, California (see Nature 479, 459; 2011); the firm said at the time that it wanted to focus on several promising cancer treatments instead. Now, a new company Asterias Biotherapeutics, also of Menlo Park plans to resurrect the trial with a US$14.3-million grant that it received on 29May from the California Institute for Regenerative Medicine (CIRM), the states stem-cell-funding agency.

But the field has moved on since Geron treated its first patient in 2010, and the therapy that Asterias inherited is no longer the only possibility for spinal-cord injury. StemCells, a biotechnology company in Newark, California, has treated 12 patients in a safety study of a different type of stem cell, and it plans to start a more advanced trial this year to test effectiveness. And another entrant to the field, Neuralstem of Germantown, Maryland, received regulatory approval in January 2013 to begin human tests of its stem-cell product.

Gerons human trial was the first approved to use cells derived from human embryonic stem cells. But regulators halted it twice, once citing concerns about the purity and predictability of the cells being implanted, and again after the company reported seeing microscopic cysts in the spinal cords of rats that had been treated in preclinical studies. The worry was that the cysts could be teratomas uncontrolled growths that can form from embryonic stem cells, a feared side effect of treatment. Geron later said that the growths were not teratomas, and the US Food and Drug Administration allowed the trial to proceed. But after injecting the cells into five of the ten intended patients, the company said that it had run out of money for the trial.

Geron founder Michael West and former chief executive Thomas Okarma then formed Asterias, which bought Gerons stem-cell therapy last year. The company plans first to treat three patients with spinal-cord damage in the neck, using a low dose of the stem cells; it will then treat different people with higher doses to see if the therapy can restore any sensation or function in the trunk or limbs.

The five patients previously treated by Geron, whom Asterias continues to track, had cord damage at chest level. On 22May, Asterias reported that none of those five had experienced serious side effects from the treatment or developed immune responses to it.

Researchers say that the continuation of the former Geron trial is important because it uses a type of cell different from the fetus-derived ones used by StemCells and Neuralstem. Geron surgically implanted embryonic stem cells that had been coaxed in vitro to grow into immature myelinated glial cells, which insulate nerve fibres when mature. The other companies are using partially differentiated cells derived from fetal brain tissue, which might produce substances that protect surviving tissue and make new connections in the neural circuitry.

Its very good for the field, because we now have multiple cell lines being tested in very similar populations of patients, and this will help us define what is needed to make this approach work, says Martin Marsala, a neuroscientist at the University of California, San Diego, whose work has shown that Neuralstems cells can develop into working neurons and restore movement to rats with cord injuries in the neck.

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Funding windfall rescues abandoned stem-cell trial

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stem cell therapy - treatment for mr with delayed milestones by dr alok sharma, mumbai, india
after stem cell therapy treatment for mental retardation with delayed milestones by dr alok sharma, mumbai, india. Stem Cell Therapy done date 18/02/2013 After Stem Cell Therapy OT assessment:...

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(2009-04a) David Steenblock MS DO - Bone marrow stem cell therapy
David Steenblock MS DO - Bone marrow stem cell therapy 2009-04-16 part 1 April 16, 2009 Visit the Silicon Valley Health Institute (aka Smart Life Forum) at http://www.svhi.com Silicon Valley...

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(2009-04a) David Steenblock MS DO - Bone marrow stem cell therapy - Video

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Hundreds join bone marrow register at ACLT in memory of Kevin Kararwa

12:15pm Tuesday 3rd June 2014 in News By Louisa Clarence-Smith, Reporter

Hundreds of people have come forward to join the bone marrow register following the death of leukaemia patient Kevin Kararwa.

The 24-year-old business student launched the #KillLeukaemia4Kevin campaign to save others from the life-threatening cancer after doctors gave him two weeks to live.

ACLT co-founder Beverley De-Gale OBE explains how to join the bone marrow register

His final wishes were to raise 24,000 for the African Caribbean Leukaemia Trust (ACLT) and inspire 2,400 people to join the bone marrow register - 100 for every year he lived.

Speaking from his hospital bed four days before his death, Mr Kararwa said: "Most people are not aware that ethnic minorities struggle to find bone marrow transplants.

"I would like to be the catalyst in creating awareness like never before."

To show solidarity to the campaign The Wimbledon Guardian's Nick Hitchens and Louisa Clarence-Smith visited the ACLT centre in Garnett Road, Croydon, to join the register.

Signing up simply involves filling out a form with personal details and taking a cheek swab sample.

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VIDEO: Hundreds join bone marrow register in memory of Kevin Kararwa

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