My Stem Cell Therapy Fundraiser
Explain how I was able to raise funds toward my Stem Cell Therapy to treat Multiple Sclerosis...
By: Tiffany Talks Multiple Sclerosis
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My Stem Cell Therapy Fundraiser - Video
Posted: August 15, 2013 at 5:44 pm
My Stem Cell Therapy Fundraiser
Explain how I was able to raise funds toward my Stem Cell Therapy to treat Multiple Sclerosis...
By: Tiffany Talks Multiple Sclerosis
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My Stem Cell Therapy Fundraiser - Video
Posted: August 15, 2013 at 5:44 pm
Hello Doctor Zee 24 Taas Dr Nandini Gokulchandran talk show on stem cell therapy treatment
Hello Doctor Zee 24 Taas Dr Nandini Gokulchandran talks about Brain Related different types diseases and for them effective Stem Cell Therapy Treatments Stem...
By: Neurogen Brain and Spine Institute
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Hello Doctor Zee 24 Taas Dr Nandini Gokulchandran talk show on stem cell therapy treatment - Video
Posted: August 15, 2013 at 5:44 pm
Poway, California (PRWEB) August 15, 2013
Robert J. Harman, DVM, Chief Executive Officer of Vet-Stem, Inc., a leading Regenerative Veterinary MedicineTM company located in San Diego, California, has been invited back to speak at the Adult Stem Cell Therapy and Regenerative Medicine Conference in Cleveland, Ohio August 19-21, 2013. The conference is presented by The National Center for the Regenerative Medicine (NCRM), Case Western Reserve University (CWRU), Cleveland Clinic (CC), and University Hospitals Case Medical Center (UHCMC) to bring together a global perspective on regenerative medicine and adult stem cell therapy.
Dr. Harman is scheduled as the first speaker of Session II titled Disease Models for Adult Stem Cell Therapy, and his presentation is One Medicine Natural Veterinary Disease Models.
He stands alone in his expertise in the field of Regenerative Veterinary Medicine among the 273 attendees from 100 institutions in 17 countries that make up the conference. Dr. Harman draws his knowledge from more than 10,000 horse, dog and cat patients treated over the last 10 years in both the U.S. and Canada using proprietary Vet-Stem technology.
Dr. Harman is sharing the podium with Case Western Reserve Universitys own Dr. Arnold Caplan, and revolutionary regenerative medicine companies such as BioTime, Terumo BCT, STROMALab, and Pfizer. Dr. Caplan, a technology pioneer in cell-based therapies in Regenerative Medicine, is a scientific advisor to Vet-Stem, Inc.
About Vet-Stem, Inc.
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.
Posted: August 15, 2013 at 5:44 pm
by Buena Bernal Posted on 08/15/2013 7:59 PM |Updated 08/16/2013 12:05 AM
PROBE STEM CELL THERAPY. Rep Paulino 'Doy' Leachon files a resolution to probe the conduct of stem cell therapy in the Philippines. Photo grabbed from islandsentinel.com
MANILA, Philippines - Rep Paulino Salvador "Doy" Leachon of Oriental Mindoro's 1st district filed on Thusday, August 15, a house resolution calling for a congressional inquiry in aid of legislation on the conduct of stem cell therapy in the country.
House Resolution 215 was filed a day after Leachon's scheduled privilege speech, calling for the resignation of Health Secretary Enrique Ona over the cabinet official's stand on stem cell therapy.
READ: Leachon asks Ona to resign over stem cell issue
The 40-year-old lawmaker also urged concerned government agencies to step up their regulatory oversight. These agencies include the Department of Health (DOH), the Food and Drug Administration (FDA), and the Professional Regulation Commission (PRC).
First attempt to regulate
Government regulation of stem cell treatment is still in its infancy stage, with the guidelines for accreditation of facilities released only in March.
It is DOH's first attempt at regulating the practice, despite the therapy having been administered by Filipino physicians for years now.
The types of stem cell treatment that are allowed, prohibited, and restricted (i.e. allowed but with limitations) in the facilities to be accredited by August 31 are listed in the released guidelines.
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Solon calls for probe into stem cell therapy
Posted: August 14, 2013 at 11:48 pm
“Jerry Brown's
veto of AB926
which would allow young women to be paid for multiple egg extractions
for scientific research is one for the gals. In western Ireland
women secreted away their 'butter
and eggs'
money in anticipation of hard times. In my day every smart girl had
her 'mad money' to escape a bad situation. Secret cash for young
women is a great idea, but not when it turns on multiple cycles of
pumping powerful hormones associated (in other contexts) with ovarian
cancer into young women's bodies to produce 30 or 60 eggs a month.
That's not promoting gender equity no matter what some of our best
Democratic women leaders have to say. Selling sperm and selling eggs
are a totally different matter. One is pleasurable and safe,
the other is a complicated and invasive procedure. We need good
science and good research and freedom of choice and action. We
also need protection from false advertising. There are no
evidence based, long term studies of the effects of these hormone
injections on women ten or twenty years after the fact. Let's fund
those needed longitudinal and cohort studies and hope for the best.
In the meantime, women had best stick to 'butter and eggs' money. It
doesn't pay a lot, but it's less painful and a heck of a lot safer.”
Posted: August 14, 2013 at 11:44 pm
A newly beating heart is part-mouse, part-human. For the first time, a mouse heart has been made to pulse again by stripping it of its own cells and rebuilding it with human ones (see video above).
To create the hybrid heart, Lei Yang at the University of Pittsburgh and colleagues took the heart from a mouse and, in a process that lasted 10 hours, removed all its cells. The remaining protein scaffold was then repopulated with human heart precursor cells stem cells that had differentiated into the three types of cell required for a heart. After a few weeks, the organ started to beat again. "Our engineered hearts contain about 70 per cent human heart precursor cells, which provide enough mechanical force for contraction," says Yang.
The precursor cells were derived from induced pluripotent stem cells generated from human skin cells, and were then turned into cardiac precursor cells. A previous study used human embryonic cells to achieve similar results, but the success rate in converting them to beating heart cells was very low.
Although the designer hearts do beat rhythmically, they aren't strong enough to pump blood effectively and the team found that the heart's rhythm differed from a normal mouse's heart. Yang thinks this is because the added cells were not as mature as adult heart cells or properly synchronised. "We did not rebuild the whole cardiac conduction system, which could control the rhythmic beatings of a heart," he says. The team's next step will be to improve the mechanical and electrical synchronisation of the heartbeat.
The study builds on previous work by Yang and colleagues where human heart precursor cells, derived from embryonic stem cells, successfully differentiated into different heart cells when injected into a mouse heart. In another recent study, a rat's heart was bioengineered by seeding a scaffold with another rat's stem cells.
Yang's long-term goal is to create human hearts that can be used for transplants, for drug testing and to better understand how a heart develops. "Using our method, we could generate both muscle and vascular-like structures in the engineered heart constructs," says Yang. "We hope to make a piece of human heart tissue soon but our dream is to regenerate a human heart organ."
The main challenge is to scale up the system to work with human heart scaffolds. There, the biggest problem will be the sheer number of cells needed to reseed a human heart.
Journal reference: Nature Communications, DOI: 10.1038/ncomms3307
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Posted: August 14, 2013 at 11:44 pm
Scientists said Tuesday they had used stem cells to grow human heart tissue that contracted spontaneously in a petri dish -- marking progress in the quest to manufacture transplant organs.
A team from the University of Pittsburgh, Pennsylvania, used induced pluripotent stem (iPS) cells generated from human skin cells to create precursor heart cells called MCPs. iPS cells are mature human cells "reprogrammed" into a versatile, primitive state from which they can be prompted to develop into any kind of cell of the body.
The primitive heart cells created in this way were attached to a mouse heart "scaffold" from which the researchers had removed all mouse heart cells, they wrote in the journal Nature Communications. The scaffold is a network of non-living tissue composed of proteins and carbohydrates to which cells adhere and grow on.
Placed on the 3D scaffold, the precursor cells grew and developed into heart muscle, and after 20 days of blood supply the reconstructed mouse organ "began contracting again at the rate of 40 to 50 beats per minute," said a University of Pittsburgh statement.
"It is still far from making a whole human heart," added senior researcher Lei Yang.
Ways have to be found to make the heart contract strongly enough to pump blood effectively and to rebuild the heart's electrical conduction system.
"However, we provide a novel resource of cells -- iPS cell-derived MCPs -- for future heart tissue engineering," Yang told AFP by email. "We hope our study would be used in the future to replace a piece of tissue damaged by a heart attack, or perhaps an entire organ, in patients with heart disease."
According to the World Health Organisation, an estimated 17 million people die of cardiovascular ailments every year, most of them from heart disease. Due to a shortage of donor organs, "end-stage heart failure is irreversible," said the study. More than half of patients with heart disease do not benefit from drugs.
"Heart tissue engineering holds a great promise... based on the reconstruction of patient-specific cardiac muscle," the researchers wrote.
Last month, scientists in Japan said they had grown functional human liver tissue from stem cells in a similar process. Creating lab-grown tissue to replenish organs damaged by accident or disease is a Holy Grail for the pioneering field of stem cell research.
Posted: August 14, 2013 at 11:44 pm
Washington, August 13 : Researchers have created a novel technique that lays down the groundwork for major advances in regenerative medicine, drug screening and biomedical research.
Using human pluripotent stem cells and DNA-cutting protein from meningitis bacteria, researchers from the Morgridge Institute for Research and Northwestern University were able to create a more efficient way to target and repair defective genes.
The team reported that the new method is much simpler than previous methods.
Zhonggang Hou of the Morgridge Institute's regenerative biology team and Yan Zhang of Northwestern University served as first authors on the study; James Thomson, director of regenerative biology at the Morgridge Institute, and Erik Sontheimer, professor of molecular biosciences at Northwestern University, served as principal investigators.
Hou said that with this system, there is the potential to repair any genetic defect, including those responsible for some forms of breast cancer, Parkinson's and other diseases.
He said that the fact that it can be applied to human pluripotent stem cells opens the door for meaningful therapeutic applications.
Zhang said the Northwestern University team focused on Neisseria meningitidis bacteria as it is a good source of the Cas9 protein needed for precisely cleaving damaged sections of DNA.
She said that they were able to guide this protein with different types of small RNA molecules, allowing them to carefully remove, replace or correct problem genes.
She asserted that this represents a step forward from other recent technologies built upon proteins such as zinc finger nucleases and TALENs.
These previous gene correction methods required engineered proteins to help with the cutting. Hou said scientists can synthesize RNA for the new process in as little as one to three days - compared with the weeks or months needed to engineer suitable proteins.
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New method brings regenerative medicine closer to reality
Posted: August 14, 2013 at 11:42 pm
Stem Cell Therapy Treatment for Congenital Muscular Dystrophy by Dr Alok Sharma, Mumbai, India.
Improvement seen in just 5 day after Stem Cell Therapy Treatment for Congenital Muscular Dystrophy by Dr Alok Sharma, Mumbai, India. After Stem Cell Therapy ...
By: Neurogen Brain and Spine Institute
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Stem Cell Therapy Treatment for Congenital Muscular Dystrophy by Dr Alok Sharma, Mumbai, India. - Video
Posted: August 14, 2013 at 11:42 pm
NewsLife: DOH calls for registration of stem cell therapy operators
NewsLife - DOH calls for registration of stem cell therapy operators (Reported By: Noel Perfecto) - [August 12, 2013] For more news, visit: #9659;http://www.ptvne...
By: PTV PH
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NewsLife: DOH calls for registration of stem cell therapy operators - Video