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Stem Cell Treatment for Charge Syndrome – Video

Posted: March 17, 2012 at 3:02 pm

14-10-2011 21:22 http://www.StemCellTreatment.org Stem cell treatment for Charge Syndrome was performed on Braulio and as you can see in this video he has improved drastically. He is now walking and his eyesight has improved. Charge syndrome is a serious condition and obviously difficult to live with. If you suffer or know someone who suffers from this condition please contact the American Stem Cell & Anti Aging Center at http

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Controversial scientist plans to clone a mammoth

Posted: March 17, 2012 at 5:46 am

South Korean Hwang Woo Suk was long regarded as a cloning pioneer - until he was charged with having faked much of his stem cell research. Now, he is back with a new project: he wants to clone a woolly mammoth.

South Korean researcher and cloning pioneer Hwang Woo Suk hasn't been in the scientific spotlight ever since he claimed to have successfully created human embryonic stem cells by cloning six years ago, and that research turned out to be fake.

Now, the controversial veterinarian and researcher is in the headlines again. He wants to use frozen tissue samples to recreate an animal that last walked the earth some 10,000 years ago: a woolly mammoth.

Hwang Woo Su successfully cloned Snuppy in 2005

The scientist recently signed an accord to that effect with a university in Russia's Sakha Republic.

Vast areas of the republic are covered in permafrost that has begun to thaw over the years due to climate change, uncovering the well-preserved remains of several mammoths that had lain frozen in the ice for more than 10.000 years.

To clone new life from the remains, Hwang needs an intact cell nucleus that he hopes could contain the animal's entire genetic information. The scientist would then have to replace the nuclei of egg cells from a related species - in this case an Indian elephant - with those taken from the mammoth's cells.

It is possible - in principle. Three years ago, as part of a mammoth cloning project in Japan, researchers there managed to clone a mouse from the cells of a rodent that had been frozen for 16 years. Nothing has been heard of this project since then.

Fragmented DNA

Alex Greenwood, a biologist at the Leibniz Institute for Zoo and Wildlife Research (IZW) in Berlin, is skeptical about the mammoth-cloning project. A first look into the microscope may give scientists reason for hope because they can discern contours of cells and even cell nuclei in the mammoth tissue. But the structures are not intact, Greenwood said, "They are frozen imprints of ancient cells."

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Eastday-Big stem cell breakthrough

Posted: March 17, 2012 at 5:46 am

A NEW stem cell therapy treatment to develop new bones for patients with bone loss and new skin for recipients of plastic surgery has been developed, doctors from Shanghai No.9 People's Hospital announced yesterday.

In the procedure, medical staff use a special machine to collect stem cells from a patient's blood. The stem cells adhere to a base made of a special biological material.

The stem cells are then transplanted into the patient's body, where they grow into either new bones or skin tissue, while the base is absorbed by the human body.

"So far the practice has been successful in treating patients with bone and skin loss," said Dr Dai Kerong from Shanghai Jiao Tong University's translational medicine institute at Shanghai No.9 hospital. "The stem cell technology will be used to develop corneas for blind people as well as treating heart attack and stroke patients by developing new heart and cerebral tissue."

The technology is patented in China and abroad and will be licensed within one or two years, according to Dai.

China has established 51 translational medicine centers to boost the introduction of laboratory research into clinical use.

The complicated procedures and documentation required often prevent doctors from introducing lab success into clinical practice.

Dai said one reagent developed by No. 9 hospital's doctors for in vitro fertilization received a license in Europe within six months and has been used in clinical practice "while this would take at least five years in China."

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‘Forged’ brain cells offers hope for Huntington’s disease treatment

Posted: March 16, 2012 at 8:59 pm

Washington, Mar 16 (ANI): A special type of brain cell forged from stem cells could help restore the muscle coordination deficits that cause the uncontrollable spasms characteristic of Huntington's disease, a new study has suggested.

Huntington's disease, the debilitating congenital neurological disorder that progressively robs patients of muscle coordination and cognitive ability, is a condition without effective treatment, a slow death sentence.

"This is really something unexpected," said Su-Chun Zhang, a University of Wisconsin-Madison neuroscientist and the senior author of the new study, which showed that locomotion could be restored in mice with a Huntington's-like condition.

Zhang is an expert at making different types of brain cells from human embryonic or induced pluripotent stem cells.

In the new study, his group focused on what are known as GABA neurons, cells whose degradation is responsible for disruption of a key neural circuit and loss of motor function in Huntington's patients.

GABA neurons, Zhang explained, produce a key neurotransmitter, a chemical that helps underpin the communication network in the brain that coordinates movement.

In the laboratory, Zhang and his colleagues at the UW-Madison Waisman Center have learned how to make large amounts of GABA neurons from human embryonic stem cells, which they sought to test in a mouse model of Huntington's disease.

The goal of the study, Zhang noted, was simply to see if the cells would safely integrate into the mouse brain.

To their astonishment, the cells not only integrated but also project to the right target and effectively re-established the broken communication network, restoring motor function.

The results of the study were surprising, Zhang explained, because GABA neurons reside in one part of the brain, the basal ganglia, which plays a key role in voluntary motor coordination.

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RBCC Closes Deal with Game Changing Biotech Firm

Posted: March 16, 2012 at 8:58 pm

NOKOMIS, Fla.--(BUSINESS WIRE)--

With the global demand for biotechnology solutions to mounting health concerns growing every day, Rainbow Coral Corp. (OTCBB: RBCC.OB - News) has been working hard to deliver the kinds of breakthroughs that doctors, scientists, and researchers the world over are begging for.

Today, Rainbow BioSciences, the biotech division of Rainbow Coral Corp. (OTCBB: RBCC.OB - News) announced that it has signed a deal to acquire an interest in the cutting-edge biotech firm Nano3D Biosciences, Inc. (n3D). One of the hottest emerging biotech developers in the world, n3D is producing new tools that could challenge long-held assumptions about healthcareand change lives in the process.

The agreement is the culmination of months of work and negotiations. N3D is a terrific fit with RBCCs aggressive focus on company growth. The companys new breakthrough cell-culturing technology, the Bio-Assembler, is fully commercialized already. RBCCs participation will provide n3D with the funds for marketing and distributing the Bio-Assembler to new markets as cellular research in the biotech sector explodes around the globe.

The acquisition has RBCC well-positioned to participate in the potentially dramatic upside that many bioscience companies realize at this stage. N3Ds Bio-Assembler could be poised to revolutionize the way stem cell research and the study of other living tissues is conducted worldwide, with the potential to ultimately reduce the development timeline for new life-saving drug therapies.

For more information on Rainbow BioSciences, RBCCs biotechnology division, please visit http://www.rainbowbiosciences.com/investors.

Rainbow BioSciences will develop new medical and research technology innovations to compete alongside companies such as Cell Therapeutics, Inc. (NASDAQ: CTIC - News), Biogen Idec Inc. (NASDAQ: BIIB - News), Abbott Laboratories (NYSE: ABT - News) and Elan Corp. (NYSE: ELN - News).

About Rainbow BioSciences

Rainbow BioSciences, LLC, is a wholly owned subsidiary of Rainbow Coral Corp. (OTCBB: RBCC.OB - News). The company continually seeks out new partnerships with biotechnology developers to deliver profitable new medical technologies and innovations. For more information on our growth-oriented business initiatives, please visit our website at [www.RainbowBioSciences.com]. For investment information and performance data on the company, please visit http://www.RainbowBioSciences.com/investors.

Notice Regarding Forward-Looking Statements

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Gov. Perry’s stem-cell firm draws FDA scrutiny

Posted: March 16, 2012 at 8:57 pm

The U.S. Food and Drug Administration has received a complaint alleging the Houston company involved in Gov. Rick Perry's unregulated adult stem-cell operation is a potential danger to patients and not in compliance with federal law.

In an eight-page letter sent last month, University of Minnesota bioethicist Leigh Turner called on the FDA to investigate Celltex Therapeutics Corp., which banks people's stem cells for future reinjection in the event of disease or injury. Perry was the company's first customer last year.

"It appears their business plan involves injecting or infusing on a for-profit, commercial basis non-FDA-approved adult stem cells into paying customers," Turner wrote in the Feb. 21 letter. "This plan conflicts with FDA regulations governing human stem cells."

An FDA spokeswoman declined comment, but Turner said an agency official told him the matter has been assigned to an investigator and is being taken seriously.

Celltex co-founder David Eller said Tuesday night he is confident the company will "meet all FDA specifications." He emphasized that Celltex doesn't administer stem cells, but stores and processes them at the behest of doctors who later reinject them into patients.

Dr. Stanley Jones, a Houston orthopedic surgeon, injected Perry's stem cells during his back surgery in July.

The plan by Celltex and Perry to make Texas a leader in the therapy have been controversial since details about the governor's procedure became known last summer. The therapy, drawing on the ability of adult stem cells to replenish dying cells, is promising but thought by most medical researchers to need much more clinical study before it is commercialized.

Stem cells are a kind of medicine known as biologics, therapy involving living cells rather than chemicals. Most medical experts say that adult stem-cell therapy involves more than the "minimal manipulation" the agency allows without its oversight because the cells are isolated, cultured in a laboratory and stored for some period of time before being reinjected.

The FDA has recently stepped up enforcement of unregulated adult stem cell activity, though legal experts interviewed last fall by the Chronicle said it was unclear whether the agency would look into Perry's procedure because he seemed fully informed and unharmed by it.

The Texas Medical Board is currently considering a policy that would require providers of stem cells and other experimental drugs to use them only with the permission of independent review committees that assess trials for patient safety. The policy comes up for final approval in April.

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Scientists Make Big Leap in Eye Research by Growing Retina Structures – Video

Posted: March 16, 2012 at 3:36 pm

14-03-2012 13:25 Could synthetic stem cells mean the end of certain forms of blindness? Scientists at the University of Wisconsin have created basic retina structures, giving hope to many with eye damage that their vision could be repaired someday. The retina structures were created by synthesizing stem cells from a patient's blood, and successfully sent important information to the brain that helps humans see. Scientists can create the stem cells from a simple blood test, and the ability to build the retina structures from the cells—and isolate which layers need repair—will allow researchers to further study degenerative diseases like retinitis pigmentosa. The study is still in its primordial phases, but it could lead to some big leaps forward in research and maybe even some day the ability to generate new cells for patients whose eyes are going bad. Just think: Someday grandma may stop asking you where she put her reading glasses!

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Gov. Perry's stem-cell firm draws FDA scrutiny

Posted: March 16, 2012 at 3:36 pm

The U.S. Food and Drug Administration has received a complaint alleging the Houston company involved in Gov. Rick Perry's unregulated adult stem-cell operation is a potential danger to patients and not in compliance with federal law.

In an eight-page letter sent last month, University of Minnesota bioethicist Leigh Turner called on the FDA to investigate Celltex Therapeutics Corp., which banks people's stem cells for future reinjection in the event of disease or injury. Perry was the company's first customer last year.

"It appears their business plan involves injecting or infusing on a for-profit, commercial basis non-FDA-approved adult stem cells into paying customers," Turner wrote in the Feb. 21 letter. "This plan conflicts with FDA regulations governing human stem cells."

An FDA spokeswoman declined comment, but Turner said an agency official told him the matter has been assigned to an investigator and is being taken seriously.

Celltex co-founder David Eller said Tuesday night he is confident the company will "meet all FDA specifications." He emphasized that Celltex doesn't administer stem cells, but stores and processes them at the behest of doctors who later reinject them into patients.

Dr. Stanley Jones, a Houston orthopedic surgeon, injected Perry's stem cells during his back surgery in July.

The plan by Celltex and Perry to make Texas a leader in the therapy have been controversial since details about the governor's procedure became known last summer. The therapy, drawing on the ability of adult stem cells to replenish dying cells, is promising but thought by most medical researchers to need much more clinical study before it is commercialized.

Stem cells are a kind of medicine known as biologics, therapy involving living cells rather than chemicals. Most medical experts say that adult stem-cell therapy involves more than the "minimal manipulation" the agency allows without its oversight because the cells are isolated, cultured in a laboratory and stored for some period of time before being reinjected.

The FDA has recently stepped up enforcement of unregulated adult stem cell activity, though legal experts interviewed last fall by the Chronicle said it was unclear whether the agency would look into Perry's procedure because he seemed fully informed and unharmed by it.

The Texas Medical Board is currently considering a policy that would require providers of stem cells and other experimental drugs to use them only with the permission of independent review committees that assess trials for patient safety. The policy comes up for final approval in April.

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'Forged' brain cells offers hope for Huntington's disease treatment

Posted: March 16, 2012 at 3:36 pm

Washington, Mar 16 (ANI): A special type of brain cell forged from stem cells could help restore the muscle coordination deficits that cause the uncontrollable spasms characteristic of Huntington's disease, a new study has suggested.

Huntington's disease, the debilitating congenital neurological disorder that progressively robs patients of muscle coordination and cognitive ability, is a condition without effective treatment, a slow death sentence.

"This is really something unexpected," said Su-Chun Zhang, a University of Wisconsin-Madison neuroscientist and the senior author of the new study, which showed that locomotion could be restored in mice with a Huntington's-like condition.

Zhang is an expert at making different types of brain cells from human embryonic or induced pluripotent stem cells.

In the new study, his group focused on what are known as GABA neurons, cells whose degradation is responsible for disruption of a key neural circuit and loss of motor function in Huntington's patients.

GABA neurons, Zhang explained, produce a key neurotransmitter, a chemical that helps underpin the communication network in the brain that coordinates movement.

In the laboratory, Zhang and his colleagues at the UW-Madison Waisman Center have learned how to make large amounts of GABA neurons from human embryonic stem cells, which they sought to test in a mouse model of Huntington's disease.

The goal of the study, Zhang noted, was simply to see if the cells would safely integrate into the mouse brain.

To their astonishment, the cells not only integrated but also project to the right target and effectively re-established the broken communication network, restoring motor function.

The results of the study were surprising, Zhang explained, because GABA neurons reside in one part of the brain, the basal ganglia, which plays a key role in voluntary motor coordination.

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Campus Connection: UW research hints at potential for Huntington’s treatment

Posted: March 16, 2012 at 3:36 pm

Todd Finkelmeyer has been covering higher education for the Capital Times since April 2008. He started contributing to the newspaper in 1990, was hired full-time in 1994 and has since covered everything from the Super Bowl to stem cell research. Follow his Campus Connection blog for the latest on higher education news in the Madison area.

Researchers working on the University of Wisconsin-Madison campus have found a way to use neurons derived from human embryonic stem cells to restore muscle coordination in mice inflicted with a Huntingtons disease-like condition.

The findings, which were reported Thursday in the journal Cell Stem Cell by a team of scientists who work at the university's Waisman Center, could one day help lead to new therapies for Huntington's disease, the debilitating disorder that affects both muscle coordination and cognitive ability. There currently are no effective treatments.

This is very exciting, and next well try to move onto different models, particularly in primates, to see whether this actually works in a larger brain, says Su-Chun Zhang, a UW-Madison neuroscientist and the senior author of the study.

Zhang, who specializes in producing different types of brain cells from stem cells, explains that this particular research focused on GABA neurons -- the cells that deteriorate and thus disrupt the brains circuitry that leads to the loss of motor function in patients with Huntington's. He notes the GABA neurons make a chemical that plays an important role in helping to link the communication network in the brain with movement.

Zhang and co-workers in the lab figured out how to produce large amounts of these GABA neurons from human embryonic stem cells, which they tested in mice with a Huntingtons-like ailment. Initially, the researchers were just trying to see whether or not these cells could safely integrate into the mouse brain. They were stunned to see that the cells not only successfully merged into the brain, but that they also eventually sent signals to the proper targets and rewired broken circuitry to restore motor functions.

This was quite surprising, says Zhang. These human neurons actually projected a long distance to another place in the brain and hooked up at the circuit, which is essential for our movement coordination. This is very critical, because in order for cell therapies to work for Huntingtons, the circuit has to be re-formed.

He notes scientists generally didnt believe it was possible for this circuitry to be rewired in older brains. In the mature brain, the nerve cells do not project a long distance, particularly into the correct target, Zhang explains. But that happened with these cells. So the point is, these stem cells somehow know where to go.

Its not clear how relevant this information will be in finding treatments for Huntingtons, but the UW-Madison scientists are hopeful their research can be used as another building block of information that can one day lead to treatments for the debilitating disease.

According to the Huntington's Disease Society of America, more than a quarter of a million Americans have the ailment or are at risk of inheriting the disease from an affected parent.

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