Stem Cells Solutions 2ns Draft
By: Andrew McGill
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Stem Cells Solutions 2ns Draft - Video
Posted: June 4, 2014 at 2:42 pm
Posted: June 4, 2014 at 2:42 pm
Neural Stem Cells
In this video we want to summaryze the progenitor cells of the Central Nervous System: The Neural Stem Cells. NSC are a multipotent cells that generate the main phenotype of the Nervous System....
By: Ernesto Caballero Garrido
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Neural Stem Cells - Video
Posted: June 4, 2014 at 2:42 pm
FDA vs stem cells booster
According to Food and Drugs Administration (FDA) all stem cell products are not effective meanwhile FDA also advise the bad effect of artex water color. Subs...
By: ABS-CBN News
Posted: June 4, 2014 at 2:41 pm
Bharat Book Presents : Stem Cell Research Products Opportunities, Tools, and Technolo
To know more : https://www.bharatbook.com/biotechnology-market-research-reports-90809/stem-cell-research-products-opportunities-tools-and-technologies.html Bharatbook.com announces a new...
By: Deepa Kamath
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Bharat Book Presents : Stem Cell Research Products Opportunities, Tools, and Technolo - Video
Posted: June 4, 2014 at 6:45 am
(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...
By: Silicon Valley Health Institute
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(2009-04a) David Steenblock MS DO - Bone marrow stem cell therapy - Video
Posted: June 4, 2014 at 6:44 am
Dr. Mark Penn, founder and CMO of Juventas Therapeutics
While the optimal treatment for heart failure was provided to a group of patients, they were still having symptoms. However when a new drug therapy based in regenerative medicine was given to these patients they showed clinically meaningful improvements in end systolic volumes, end diastolic volumes, ejection fraction and NTproBNP levels.
The drug, produced by Cleveland, Ohio-based Juventas Therapeutics, called JVS-100, is a non-viral gene therapy that expresses SDF-1 and promotes endogenous stem cell repair of the heart in patients with severe heart failure.
"What was remarkable about the improvement is that this drug was given to patients who had heart failures stemming from heart attacks that occurred - on average- about eleven years ago," said Dr. Mark Penn, founder and CMO of Juventas Therapeutics, and director of Cardiovascular Research at Summa Health System in Akron, Ohio.
Penn presented phase II clinical data last month at the European Society of Cardiology- Heart Failure Congress in Athens, Greece.
The field of regenerative medicine, which is the process of replacing, engineering or regenerating human cells, tissues or organs to restore or establish normal function, has come a long way. Penn explained that 14 years ago that stem cell based repairs lacked molecular signals that orchestrated the repairs. "Doing research we asked what drives stem cell repair? We saw that newly injured tissue was sending some signal to ask for it to be repaired. And in 2000 we discovered SDF-1 could aid that signal. Now our theory is validated that the gene therapy is a key factor for recruiting stem cells to the site for any injured tissue."
The therapy showed an 80% chance of a significant decrease in mortality for high risk heart failure patients.
With this success, Penn hopes to start next summer of 2015 on a larger trial of 300-400 patients. When that trial is initiated the company will have to move from manufacturing the drug for clinic studies to a commercial scale. Once the drug has regulatory approval the company will decide where to manufacture.
When asked about the reason for the success of the company, Penn says that "the company has always been driven by data. We had no preconceived ideas that this should work. We designed good trials, looked at the data and that told us where to go."
With regard to the financial side of the business, the company has worked with venture investors. And they have formed partnerships. The company has on-going collaborative research programs with Cleveland Clinic, Center for Stem Cell & Regenerative Medicine, Global Cardiovascular Innovation Center and Summa Health System.
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New Drug-Based Approach to Regenerative Medicine for Heart Failure
Posted: June 3, 2014 at 5:57 pm
"It's a tiny wee finger prick test," says senior nurse Patsy Scouse to calm the nervous first-time donor having his hemoglobin levels tested at a blood donation centre in Edinburgh.
The Scottish National Blood Transfusion Service receives donations from about four percent of the UK's population. Currently, stocks are stable, although the service is always trying to recruit new donors.
The collection may take place in a clinical environment, the nurse says, but the clinic "wants this experience, especially for first-time donors, to be really positive so they can go out and feel they've done a really good thing."
But the service is also working on potential new technologies to secure blood supplies in the future, including "artificial blood."
Mass-produced and clean
Mark Turner, medical director of the Blood Transfusion Service, is looking into how blood could be synthesized in the future.
"We've known for some time that it's possible to produce red blood cells from so called adult stem cells, but you can't produce large amounts of blood in that way because of the restrictive capacity of those cells to proliferate," he explains. What scientists can do, he adds, is to derive pluripotent stem cells - stem cell lines - either from embryos or from adult tissue.
These cells are processed in the laboratory to produce larger numbers of cells, Turner told DW.
"It may be possible in due course to manufacture blood on a very large scale, but we're a very long way from that at the present time," he says. "At the moment, our focus is on trying to achieve production of red blood cells which are of the right kind of quality and safety, that they would be fit for human trials."
From the lab to clinical trials
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Artificial blood made from human stem cells could plug the donations hole
Posted: June 3, 2014 at 5:57 pm
A Littlestown resident went through a five-day procedure to give bone marrow stem cells to a man living in France
By Adam Michael
@goodoletwonames on Twitter
John Sibirtzeff will never meet the man who used his stem cells to heal. He'll never know exactly what his affliction was, and he's OK with that.
A month ago, Sibirtzeff spent five days in Washington D.C. donating bone marrow stem cells that would be used to heal a 69-year-old man living in France.
"I'll never know who the recipient was," he said. "I'll never know if he was American or French, military or non."
When Sibirtzeff, of Littlestown, was in Navy boot camp in 2007, he opted into the C.W. Bill Young Department of Defense Marrow Donor Program. Naval doctors drew a vial of his blood and stored it after identifying his type. In 2011, Sibirtzeff finished his tour of duty, but his name remained on the donor list.
This past January, the program contacted Sibirtzeff requesting that he return for testing, as he was a potential match for a 69-year-old man living in France.
According to the program's website, salutetolife.org, 70 percent of patients are unable to find a match within their families. Sibirtzeff's receiver was among them.
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Everyday Hero: Littlestown man donates bone marrow stem cells to stranger
Posted: June 3, 2014 at 5:47 pm
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:...
By: Neurogen Brain and Spine Institute
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stem cell therapy - treatment for mr with delayed milestones by dr alok sharma, mumbai, india - Video
Posted: June 3, 2014 at 5:47 pm
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