header logo image


Page 10«..9101112

Archive for the ‘Stem Cell kidney Failure’ Category

Celldex Reports First Quarter 2012 Financial Results

Friday, May 4th, 2012

NEEDHAM, Mass.--(BUSINESS WIRE)--

Celldex Therapeutics, Inc. (NASDAQ: CLDX - News) today reported financial results for the first quarter ended March 31, 2012. Celldex reported a net loss of $13.5 million, or $0.27 per share, for the first quarter of 2012 compared to a net loss of $10.1 million, or $0.31 per share, for the first quarter of 2011. At March 31, 2012, Celldex reported cash, cash equivalents and marketable securities of $92.1 million, which the Company believes will be sufficient to meet estimated working capital requirements and fund planned program development into 2014, including enrollment of both the pivotal ACT IV study and the ReACT Phase 2 study for rindopepimut (CDX-110).

In the first quarter of 2012, Celldex continued to advance multiple late- and mid-stage product candidates, said Anthony S. Marucci, President and Chief Executive Officer. First, for rindopepimut, we have made very real progress with our pivotal Phase 3 global registration study in patients with newly diagnosed EGFRvIII-positive glioblastoma (ACT IV) and our randomized Phase 2 study in recurrent EGFRvIII-positive patients (ReACT). Second, in collaboration with Rockefeller University, Celldex initiated a Phase 1 study of CDX-301 (Mobista), a potent stem cell mobilizer and dendritic cell growth factor, to support subsequent trials for patients requiring hematopoietic stem cell transplantation. On the business front, Celldex raised total net proceeds of $51.9 million which will provide continued financial support, particularly for our later-stage product candidates.

First quarter and recent highlights:

The Company has

Upcoming events:

Further Financial Highlights

The net loss of $13.5 million for the first quarter of 2012 represents an increased loss of approximately $3.5 million when compared to the net loss for the same period in 2011, primarily due to an increase in research and development (R&D) expense in 2012.

Revenues for the first quarter of 2012 decreased when compared to revenues in 2011, primarily because of lower product royalty revenues related to Rotarix.

In the first quarter of 2012, R&D expense increased by approximately $3.9 million compared to the first quarter of 2011. Changes in R&D expense between 2012 and 2011 reflect higher clinical trial costs of $3.7 million primarily due to initiation and upfront expenses related to the ACT IV and ReACT rindopepimut studies.

Read the original post:
Celldex Reports First Quarter 2012 Financial Results

Read More...

Transforming scar tissue into beating heart muscle may help repair cardiac damage

Sunday, April 22nd, 2012

London, Apr 19 : Researchers including one of Indian origin have declared a research breakthrough in mice that shows promise to restore hearts damaged by heart attacks-by converting scar-forming cardiac cells into beating heart muscle.

Gladstone Institutes scientists previously transformed such cells into cardiac muscle-like cells in petri dishes.

But Gladstone postdoctoral scholar Li Qian, PhD, along with researchers in the laboratory of Deepak Srivastava, MD, has now accomplished this transformation in living animals-and with even greater success.

The results may have broad human-health implications.

"The damage from a heart attack is typically permanent because heart-muscle cells-deprived of oxygen during the attack-die and scar tissue forms," said Dr. Srivastava, who directs cardiovascular and stem cell research at Gladstone, an independent and nonprofit biomedical-research institution.

"But our experiments in mice are a proof of concept that we can reprogram non-beating cells directly into fully functional, beating heart cells-offering an innovative and less invasive way to restore heart function after a heart attack."

In laboratory experiments with mice that had experienced a heart attack, Drs. Qian and Srivastava delivered three genes that normally guide embryonic heart development-together known as GMT-directly into the damaged region.

Within a month, non-beating cells that normally form scar tissue transformed into beating heart-muscle cells. Within three months, the hearts were beating even stronger and pumping more blood.

"These findings could have a significant impact on heart-failure patients-whose damaged hearts make it difficult for them to engage in normal activities like walking up a flight of stairs," said Dr. Qian, who is also a California Institute for Regenerative Medicine postdoctoral scholar and a Roddenberry Fellow.

"This research may result in a much-needed alternative to heart transplants-for which donors are extremely limited. And because we are reprogramming cells directly in the heart, we eliminate the need to surgically implant cells that were created in a petri dish."

See more here:
Transforming scar tissue into beating heart muscle may help repair cardiac damage

Read More...

National Stem Cell Foundation – Video

Wednesday, March 14th, 2012

17-02-2012 10:42 NSCF funds clinical trials to: • Induce drug-free tolerance for transplanted kidneys • Effectively cure inherited red blood cell disorders like sickle cell disease (SCD) and thalassemia •Permanently correct fatal childhood enzyme deficiencies For more information visit nationalstemcellfoundation.org.

See original here:
National Stem Cell Foundation - Video

Read More...

New Hope For Organ Transplant Recipients

Friday, March 9th, 2012

Organ transplant patients usually spend a lifetime on expensive and often dangerous anti-rejection drugs. But experts have announced that such drugs may not even be needed in the future, thanks to a new study that suggests patients receiving an organ that is less than a perfect match can be protected against rejection by a second transplant of the donors imperfectly matched stem cells. The study is being hailed as a game-changer for transplantation.

Experts announced the success of kidney transplants for a small number of patients, using a relatively new technique known as normothermic perfusion. This involves the warming of the kidney with oxygenated blood after it has been in cold storage. This technique also boosts the function of damaged kidneys from marginal donors, such as the elderly or those with high blood pressure and diabetes, and also reduces the risk of the organ being rejected.

Also, an injection of stem cells given with the kidney transplant could remove the need for patients to take anti-rejection drugs the rest of their lives to suppress the immune system. Preliminary tests of the technique were successful in a small number of patients.

The researchers, publishing their study in the journal Science Translational Medicine, said the research could have a major impact on transplant science.

The key issue with transplantation is the immune systems recognition that the new organ is a foreign invader and bombards it. To prevent this from occurring, patients take powerful drugs to suppress their immune systems, and must do this for life. However, the drugs can have dangerous side effects, and in some instances, are ineffective, causing even more danger to the patient.

The study, carried out at the University of Louisville and the Northwestern Memorial Hospital in Chicago, involved eight patients.

Transplants came from a live donor, who also underwent a procedure to draw stem cells from the blood. The transplant recipients body was prepared using radiotherapy and chemotherapy to suppress their own immune system. The transplant was then performed, with the stem cells injected a few days afterwards. The idea is that the stem cells will help generate a modified immune system that no longer attacks the organ or its new owner.

The patients were still given anti-rejection drugs after the transplant. However, the aim was to reduce doses slowly, hopefully withdrawing them altogether over time. Five of the eight patients were able to do this within a year.

One of those is 47-year-old Lindsay Porter, from Chicago.

I hear about the challenges recipients have to face with their medications and it is significant, she said in a press statement. Its almost surreal when I think about it because I feel so healthy and normal.

Link:
New Hope For Organ Transplant Recipients

Read More...

Scientists offer a glimpse of life without immune-suppressing drugs

Thursday, March 8th, 2012

Lindsay Porter's kidneys weighed 16 pounds before her transplant.

STORY HIGHLIGHTS

(CNN) -- By the time Lindsay Porter had her kidneys removed two years ago, they were bulging -- covered in cysts -- and together weighed 16 pounds.

Her abdominal area was so distended, "I looked nine months pregnant, and people regularly asked when I was due," Porter said.

As she prepared for a transplant to address her polycystic kidney disease, Porter, 47, had mixed feelings -- relief to have found a donor, tinged with resignation. She was looking forward to both a new kidney, and a lifetime on immune system-suppressing drugs.

"You get this brand new shiny kidney, and then they give you drugs that eventually destroy it," said Porter.

But that scenario may eventually change, if results of a new pilot study are replicated in a larger group of patients. The study, published Wednesday in the journal Science Translational Medicine, describes eight kidney transplant patients, including Porter, who received a stem cell therapy that allowed donor and recipient immune cells to coexist in the same body.

The effect, in a handful of those patients, was to trick the recipient's immune system into recognizing the donated kidney as its own.

When it works, patients become a sort of medical rarity called a chimera.

"Chimerism is a condition wherein two different genetic cell populations are present in the body, and both cell types are tolerated," said Dr. Anthony Atala, director of the Institute for Regenerative Medicine at Wake Forest Baptist Medical Center, who was not involved in the study, via e-mail.

Read more from the original source:
Scientists offer a glimpse of life without immune-suppressing drugs

Read More...

Respite home lets families with ailing children get away

Tuesday, February 28th, 2012

The Pincus family, of Manassas, Va. at the respite house in Pinnacle Falls. From left: Lori, Lauren, Brooke, Lacey, Lexus, Blake, Don. The family spent a week at the Believe in Tomorrow Foundation respite house in Pinnacle Falls, Zirconia last year. The foundation provides respite homes for military families with critically-ill children and is celebrating the one-year anniversary of the Pinnacle Falls property. Blake suffered from lymphoma cancer and now is waiting for a kidney transplant.

Buy Photo Photo provided Published: Monday, February 27, 2012 at 11:40 p.m. Last Modified: Monday, February 27, 2012 at 11:40 p.m.

ZIRCONIA - It's been a year since the Pincus family found much-needed relaxation in the Blue Ridge Mountains at a respite house nestled in the Pinnacle Falls development.

Don and Lori Pincus' son, 17-year-old Blake, was diagnosed with a type of lymphoma cancer in 2009, and that eventually led them to the Believe in Tomorrow Foundation.

In 2011, the Pincuses became the first family to vacation at the foundation's respite house at Pinnacle Falls in Zirconia. Now the foundation is celebrating the one-year anniversary of the home that serves military families with children battling life-threatening illnesses.

Blake received a kidney transplant from his mom when he was just 2 years old. In May 2009, he was diagnosed with Post-Transplant Lymphoproliferative Disorder.

Between 2009 and 2010, Blake and his family stayed at the Believe In Tomorrow Children's House at Johns Hopkins and at St. Casimir while he underwent multiple rounds of chemotherapy and radiation treatments, followed by a bone marrow and stem-cell transplant to prevent the disease from returning.

Although the transplant was successful, renal failure caused by the treatments has forced Blake to remain on dialysis until he can get another kidney transplant.

Blake is doing well as he waits, said his father, Don.

"He keeps a great attitude and takes everything in stride," he added.

Don Pincus is a retired U.S. Army Corps of Engineers lieutenant colonel who worked at the Office of the Chief of Engineers at the Pentagon. He said his seven-member family from Manassas, Va., needed a break from the hustle and bustle of the city. He and his wife, Lori, and Blake and his four sisters — Lauren, Lacey, Brooke and Lexus — found that break at Pinnacle Falls.

"It was quite relaxing," Don Pincus said. "It was a relief to get out there and enjoy the mountainside."

The Pincuses spent a lot of time outdoors — hiking, exploring waterfalls and playing sports. While indoors, they shot pool and competed in Xbox Connect and Wii video games.

"The kids had a ball," Don Pincus said.

The family also visited Hendersonville eateries, including Hot Dog World and TCBY Yogurt. The owners of TCBY, Roger and Linda Freed, have worked for several years with families that have children battling cancer.

"I will do anything I can do for the children and to put a smile on their faces," Linda Freed said.

The Pinnacle Falls house is Believe in Tomorrow's fifth respite property and the second to support military families with ill children. To date, the Henderson County home has hosted 26 families.

Several contributors, volunteers and community supporters constructed the 3,300-square-foot home and continue its upkeep. Debbie Walsh of Hendersonville has volunteered with Believe in Tomorrow since 2007 and prepares the home for incoming families.

"What they (the foundation) do is such a great story," she said.

Inside, Walsh ensures everything is in place and ready for the families.

"Every time I come here, I think about the families that come here to relax and enjoy themselves," she said.

And the organization plans to have plenty more families visit the mountain getaway. Believe in Tomorrow will stay committed to serving the needs of military families, said Brian Morrison, founder and CEO.

"We are thrilled to be able to expand our military respite housing initiative to this area of the country and are eager to host many more families as they cross the threshold of the Believe in Tomorrow House at Pinnacle Falls," Morrison said.

Reach Schulman at 828-694-7890 or mark.schulman@blueridgenow.com.

See original here:
Respite home lets families with ailing children get away

Read More...

Fibrosis – Targeting MicroRNA-21 May Have Therapeutic Benefit

Wednesday, February 22nd, 2012

Editor's Choice
Academic Journal
Main Category: Genetics
Article Date: 21 Feb 2012 - 10:00 PST

email to a friend   printer friendly   opinions  

Current Article Ratings:

Patient / Public: Healthcare Prof:
Fibrosis is a harmful build-up of excessive fibrous tissue that results in scarring, and ultimately, the loss of organ function. Although it can affect any tissue and organ system, it is most common in the heart, liver, lung, peritoneum, and kidney. The fibrotic scar tissue consists of extra-cellular matrix proteins, such as type I collagen, proteoglycans and fibronectin.

Regulus, a biopharmaceutical leader in the discovery and development of innovative medications that targets microRNAs, has discovered a number of microRNAs that impair the physiological regulatory mechanism in fibrosis, and has announced their new preclinical study results in the Science Translational Medicine journal, demonstrating that miR-21 contributed to fibrogenesis, and that it can be a suitable candidate as a target for anti-fibrotic therapies.

MicroRNA in humans are small RNA molecules that are typically 20 to 25 nucleotides in length, which do not encode proteins, but regulate gene expression. Discovered in the last decade, they represent one of the most exciting scientific breakthroughs in recent history. Researchers have discovered over 700 microRNAs in the human genome, with more than a third of all human genes thought to be regulated by microRNAs.

Given that a single microRNA is able to regulate entire networks of genes, these molecules are considered master regulators of the human genome. microRNAs have demonstrated their integral role in several biological processes, such as in immune response, cell-cycle control, metabolism, viral replication, stem cell differentiation and human development.

Most microRNAs are conserved across multiple species, which suggests that these molecules have an evolutionary importance as modulators of critical biological pathways. microRNA expression or function, has demonstrated to substantially alter in many states if diseases, such as cancer, heart failure and viral infections.

By targeting microRNAs with anti-miRs, antisense oligonucleotide inhibitors of microRNAs, or miR-mimics, double-stranded oligonucleotides to replace microRNA function, research has discovered a new potential for a novel class of therapeutics that provide a unique approach for the treatment of diseases by modulating entire biological pathways.

Neil W. Gibson, Ph.D., Regulus' Chief Scientific Officer announced:

"We are pleased with the published results demonstrating that targeting miR-21 with proprietary anti-miR oligonucleotides is effective at preventing kidney fibrosis in preclinical models. We plan to select an anti-miR-21 development candidate this year for advancement into the clinic in the near future and are excited about the potential to bring this innovative treatment to patients with fibrotic diseases."

Dr. Duffield, M.D., Ph.D. Associate Professor of Medicine, in the Division of Nephrology, at the University of Washington explained:

"Expression of miR-21 was found to be increased in fibrotic kidney samples from animal models and human patient samples. Genetic deletion of miR-21 in preclinical models protected kidneys from fibrosis and treatment with anti-miRs targeting miR-21 also blocked fibrosis in preclinical models. Taken together, these data suggest that anti-miR-21 could have a therapeutic benefit in patients with chronic kidney disease."

The study focused on fibrosis targets miR-21 that increase cells in fibrotic tissues of humans. According to Regulus' earlier preclinical research, therapeutic oligonucleotides targeting miR-21 (anti-miR-21) has the ability to lower fibrosis in preclinical models through reducing the expression of extracellular matrix proteins. Even though many people are currently affected by fibrosis-related disease, few therapies are available to specifically treat this devastating illness.

Regulus and collaborators from the University of Washington examined the effect of miR-21 in kidney fibrosis, and even though they discovered no overt abnormality when genetically deleting miR-21 in mice, they did observe that these miR-21 knock out mice experienced less fibrosis in response to kidney injury, which was pheno-copied in wild-type mice treated with anti-miR-21 oligonucleotides.

The researchers analyzed gene expression profiles and detected groups of genes, especially those involved in lipid metabolism and enhanced oxygen radical production, that were involved in metabolic pathways that were up-regulated in the absence of miR-21. They observed that by systematically administering anti-miR-21, the harmful effects of miR-21 in kidney injuries were successfully reversed.

The results of the two mouse model studies prove that miR-21 contributes to fibrogenesis and epithelial injury in the kidneys. Furthermore, the findings support that miR-21 is a suitable candidate target for anti-fibrotic therapies.

Written by Petra Rattue
Copyright: Medical News Today
Not to be reproduced without permission of Medical News Today

Visit our genetics section for the latest news on this subject. "MicroRNA 21 Promotes Fibrosis of the Kidney by Silencing Metabolic Pathways"
Science Translational Medicine Please use one of the following formats to cite this article in your essay, paper or report:

MLA

Petra Rattue. "Fibrosis - Targeting MicroRNA-21 May Have Therapeutic Benefit." Medical News Today. MediLexicon, Intl., 21 Feb. 2012. Web.
22 Feb. 2012. <http://www.medicalnewstoday.com/articles/241959.php&gt;

APA

Please note: If no author information is provided, the source is cited instead.


Rate this article:
(Hover over the stars then click to rate) Patient / Public:
or Health Professional:

Please note that we publish your name, but we do not publish your email address. It is only used to let you know when your message is published. We do not use it for any other purpose. Please see our privacy policy for more information.

If you write about specific medications or operations, please do not name health care professionals by name.

All opinions are moderated before being included (to stop spam)

Contact Our News Editors

For any corrections of factual information, or to contact the editors please use our feedback form.

Please send any medical news or health news press releases to:

Note: Any medical information published on this website is not intended as a substitute for informed medical advice and you should not take any action before consulting with a health care professional. For more information, please read our terms and conditions.


More:
Fibrosis - Targeting MicroRNA-21 May Have Therapeutic Benefit

Read More...

Pathfinder Presents Preliminary Data on New Regenerative Approach to Diabetes Treatment

Wednesday, February 22nd, 2012

CAMBRIDGE, Mass., Feb. 21, 2012 (GLOBE NEWSWIRE) -- Pathfinder Cell Therapy, Inc. ("Pathfinder," or "the Company") (OTCQB:PFND.PK - News), a biotechnology company focused on the treatment of diabetes and other diseases characterized by organ-specific cell damage, today presented preliminary data highlighting the potential of the Company's unique cell-based therapy for treating diabetes at the 7th Annual New York Stem Cell Summit. Richard L. Franklin, M.D., Ph.D., Founder, CEO and President of Pathfinder, provided an overview of the Company's Pathfinder Cell ("PC") technology, and presented preclinical evidence demonstrating how treatment with PCs was able to reverse the symptoms of diabetes in two different mouse models.

Pathfinder Cells are a newly identified non-stem cell mammalian cell type that has the ability to stimulate regeneration of damaged tissue without being incorporated into the new tissue. In today's presentation, Dr. Franklin showed how recent experiments performed using a non-obese diabetic (NOD) mouse strain were supportive of earlier data that demonstrated complete reversal of diabetes in mice. The earlier results, which used a drug-induced diabetic mouse model, were published in Rejuvenation Research1. Though preliminary, the recent results are encouraging because the NOD mouse model is widely used and highly regarded as being predictive of human type-1 diabetes.

In three separate experiments using this model, 30-50% of the mice treated with PCs at the onset of diabetes returned to normal blood glucose levels. Of the mice that responded well to treatment, the effects tended to be long lasting, up to two months in some cases after just two doses. These results, which were generated by intravenous injection of PC's derived from rat pancreatic tissue, further demonstrate the remarkable ability of Pathfinder Cells to elicit their positive effect regardless of the organ, or even species, of origin.

"We are very encouraged by these preclinical results using NOD mice. This model is the gold standard for type-1 diabetes and the fact that recent experiments mirror what we've seen in previous models may be highly significant," stated Dr. Franklin. "We have many questions to answer about how PCs act in the body, but we believe, based on previous experiments, that PCs may stimulate regeneration of damaged islet cells that produce insulin. The current NOD mouse data also suggest that PCs may have an effect in modulating the auto-immune process in type 1 diabetes. We continue to conduct experiments aimed at elucidating the optimal dosing and other factors that may be responsible for producing a robust and long-lasting response, as this will be critical as we start to think about how PCs may be used in treating human diabetes."

In his presentation today, Dr. Franklin also provided further insight into the mechanism of action of PCs, based on recent animal experiments. It was observed previously that PCs produce microvesicles, which are known to play a role in intercellular communication, but through mechanisms that are poorly understood. In a recent experiment, Pathfinder was able to isolate these microvesicles from the PCs and treat animals directly with an injection containing microvesicles only. Remarkably, both PC- and microvesicle-treated mice exhibited similar reductions in blood glucose compared to controls using the same drug-induced diabetes mouse model. This suggests, not only that the microvesicles produced by PCs are central to the mechanism of action, but that the microvesicles alone appear to be sufficient to produce the full effect.

Dr. Franklin commented, "If confirmed, this finding could have a significant positive impact on the future of PC-based therapy. Due to the relatively small amount of material contained within the microvesicles, determining the specific factor(s) that are responsible for regenerating damaged tissue could be more straightforward than we first anticipated, bringing us closer to understanding the mechanism of action. There may also be a number of potential manufacturing and storage benefits to using microvesicles versus PCs that will be interesting to explore in parallel as we work to advance this innovative new therapeutic approach closer to human clinical development."

The New York Stem Cell Summit brings together cell therapy company executives, researchers, investors and physicians to explore investment opportunities in cell therapy research and innovation. More information can be found at http://www.stemcellsummit.com.

Presentation details Event: 7th Annual New York Stem Cell Summit Date: Tuesday, February 21, 2012 Place: Bridgewaters New York, 11 Fulton Street, New York, NY Time: 3:35 pm ET

About Pathfinder

Pathfinder is developing a novel cell-based therapy and has generated encouraging preclinical data in models of diabetes, renal disease, myocardial infarction, and critical limb ischemia, a severe form of peripheral vascular disease. Leveraging its internal discovery of Pathfinder Cells ("PCs") Pathfinder is pioneering a new field in regenerative medicine.

PCs are a newly identified mammalian cell type present in very low quantities in a variety of organs, including the kidney, liver, pancreas, lymph nodes, myometrium, bone marrow and blood. Early studies indicate that PCs stimulate regeneration of damaged tissues without the cells themselves being incorporated into the newly generated tissue. Based on testing to date, the cells appear to be "immune privileged," and their effects appear to be independent of the tissue source of PCs. For more information please visit: http://www.pathfindercelltherapy.com.

FORWARD LOOKING STATEMENTS

This press release contains forward-looking statements. You should be aware that our actual results could differ materially from those contained in the forward-looking statements, which are based on management's current expectations and are subject to a number of risks and uncertainties, including, but not limited to, our inability to obtain additional required financing; costs and delays in the development and/or FDA approval, or the failure to obtain such approval, of our product candidates; uncertainties or differences in interpretation in clinical trial results, if any; our inability to maintain or enter into, and the risks resulting from our dependence upon, collaboration or contractual arrangements necessary for the development, manufacture, commercialization, marketing, sales and distribution of any products; competitive factors; our inability to protect our patents or proprietary rights and obtain necessary rights to third party patents and intellectual property to operate our business; our inability to operate our business without infringing the patents and proprietary rights of others; general economic conditions; the failure of any products to gain market acceptance; technological changes; and government regulation. We do not intend to update any of these factors or to publicly announce the results of any revisions to these forward-looking statements.

1Karen Stevenson, Daxin Chen, Alan MacIntyre, Liane M McGlynn, Paul Montague, Rawiya Charif, Murali Subramaniam, W.D. George, Anthony P. Payne, R. Wayne Davies, Anthony Dorling, and Paul G. Shiels. Rejuvenation Research. April 2011, 14(2): 163-171. doi:10.1089/rej.2010.1099

Excerpt from:
Pathfinder Presents Preliminary Data on New Regenerative Approach to Diabetes Treatment

Read More...

Kidney Cure Center – Video

Tuesday, February 21st, 2012

29-01-2012 13:44 Stem Cell to Cure Kidney Problem. More Details Visit : http://www.kidneycurecenter.com

Here is the original post:
Kidney Cure Center - Video

Read More...

Rob Waddell’s Story – Combination Kidney/Adult Stem Cell Transplant – Video

Tuesday, February 21st, 2012

15-02-2012 13:33 Hear from one of NSCF's post-transplant patients, the father of four. Rob requires no anti-rejection medication more than two years after a combination kidney/stem cell transplant in a clinical trial NSCF funds. NSCF currently supports research and clinical trial collaborations between Duke University, Northwestern University and University of Louisville. NSCF funds clinical trials to: • Induce drug-free tolerance for transplanted kidneys • Effectively cure inherited red blood cell disorders like sickle cell disease (SCD) and thalassemia •Permanently correct fatal childhood enzyme deficiencies For more information visit nationalstemcellfoundation.org.

Original post:
Rob Waddell's Story - Combination Kidney/Adult Stem Cell Transplant - Video

Read More...

Regulus Announces New Publication Showing Potential Therapeutic Benefit of Targeting microRNA-21 in Fibrosis

Friday, February 17th, 2012

LA JOLLA, Calif., Feb. 16, 2012  /PRNewswire/ -- Regulus Therapeutics Inc., a biopharmaceutical company leading the discovery and development of innovative medicines targeting microRNAs, today announced that new preclinical data investigating the role of microRNA-21 (miR-21) in the treatment of kidney fibrosis has been published in the journal Science Translational Medicine. Regulus' lead program for fibrosis targets miR-21, which is up-regulated in fibrotic tissues of humans. Previous preclinical studies by Regulus scientists and collaborators have shown that therapeutic oligonucleotides targeting miR-21 (anti-miR-21) can decrease fibrosis in preclinical models by reducing the expression of extracellular matrix proteins.  Despite the current burden of fibrosis-related human disease, there are few therapies that can specifically treat this devastating disease.

"We are pleased with the published results demonstrating that targeting miR-21 with proprietary anti-miR oligonucleotides is effective at preventing kidney fibrosis in preclinical models," said Neil W. Gibson, Ph.D., Regulus' Chief Scientific Officer.  "We plan to select an anti-miR-21 development candidate this year for advancement into the clinic in the near future and are excited about the potential to bring this innovative treatment to patients with fibrotic diseases."

"Expression of miR-21 was found to be increased in fibrotic kidney samples from animal models and human patient samples. Genetic deletion of miR-21 in preclinical models protected kidneys from fibrosis and treatment with anti-miRs targeting miR-21 also blocked fibrosis in preclinical models," said Dr. Duffield, M.D., Ph.D. Associate Professor of Medicine, in the Division of Nephrology, at the University of Washington. "Taken together, these data suggest that anti-miR-21 could have a therapeutic benefit in patients with chronic kidney disease."

In the published study, Regulus and its collaborators from the University of Washington investigated the role of miR-21 in kidney fibrosis. Genetic deletion of miR-21 in mice resulted in no overt abnormality, however, these miR-21 knock out mice suffered less fibrosis in response to kidney injury, which was pheno-copied in wild-type mice treated with anti-miR-21 oligonucleotides. Analysis of gene expression profiles identified groups of genes involved in metabolic pathways that were up-regulated in the absence of miR-21, in particular genes involved in lipid metabolism and enhanced oxygen radical production.  Systemic administration of anti-miR-21 effectively reversed the deleterious effects of miR-21 in kidney injuries.  These animal studies demonstrate that miR-21 contributes to fibrogenesis and epithelial injury in the kidney in two mouse models and is a candidate target for anti-fibrotic therapies. 

The journal article titled, "MicroRNA 21 Promotes Fibrosis of the Kidney by Silencing Metabolic Pathways," is now available in Science Translational Medicine and on the publications page of the Regulus website at http://www.regulusrx.com.   

About Fibrosis

Fibrosis is the harmful build-up of excessive fibrous tissue leading to scarring and ultimately the loss of organ function. Fibrosis can affect any tissue and organ system, and is most common in the heart, liver, lung, peritoneum, and kidney. The fibrotic scar tissue is made up of extracellular matrix proteins such as type I collagen, proteoglycans and fibronectin. Regulus has identified several microRNAs that are dysregulated in fibrosis.  Results from this new preclinical study demonstrate that miR-21 contributed to fibrogenesis and is a candidate target for anti-fibrotic therapies. 

About microRNAs

The discovery of microRNA in humans during the last decade is one of the most exciting scientific breakthroughs in recent history. microRNAs are small RNA molecules, typically 20 to 25 nucleotides in length, that do not encode proteins but instead regulate gene expression. More than 700 microRNAs have been identified in the human genome, and over one-third of all human genes are believed to be regulated by microRNAs. A single microRNA can regulate entire networks of genes. As such, these molecules are considered master regulators of the human genome. microRNAs have been shown to play an integral role in numerous biological processes, including the immune response, cell-cycle control, metabolism, viral replication, stem cell differentiation and human development. Most microRNAs are conserved across multiple species, indicating the evolutionary importance of these molecules as modulators of critical biological pathways. Indeed, microRNA expression, or function, has been shown to be significantly altered in many disease states, including cancer, heart failure and viral infections. Targeting microRNAs with anti-miRs, antisense oligonucleotide inhibitors of microRNAs, or miR-mimics, double-stranded oligonucleotides to replace microRNA function opens potential for a novel class of therapeutics and offers a unique approach to treating disease by modulating entire biological pathways. 

About Regulus Therapeutics, Inc.

Regulus Therapeutics is a biopharmaceutical company leading the discovery and development of innovative medicines targeting microRNAs. Regulus is using a mature therapeutic platform based on technology that has been developed over 20 years and tested in more than 5,000 humans. The company works with a broad network of academic collaborators and leverages the oligonucleotide drug discovery and development expertise of its founding companies, Alnylam Pharmaceuticals (NASDAQ:ALNY) and Isis Pharmaceuticals (NASDAQ:ISIS). Regulus is advancing microRNA therapeutics toward clinical development in several areas, including fibrosis, hepatitis C, immuno-inflammatory diseases, metabolic diseases and oncology. Regulus' intellectual property estate contains both the fundamental and core patents in the field and includes over 600 patents and more than 300 pending patent applications pertaining primarily to chemical modifications of oligonucleotides targeting microRNAs for therapeutic applications. In April 2008, Regulus formed a major alliance with GlaxoSmithKline to discover and develop microRNA therapeutics for immuno-inflammatory diseases. In February 2010, Regulus and GlaxoSmithKline entered into a new collaboration to develop and commercialize microRNA therapeutics targeting microRNA-122 for the treatment of hepatitis C infection. In June 2010, Regulus and sanofi-aventis entered into the largest-to-date strategic alliance for the development of microRNA therapeutics with an initial focus on fibrosis.

For more information, please visit http://www.regulusrx.com. Regulus is also on YouTube at http://www.youtube.com/user/RegulusRx#p/f and on Twitter at http://www.twitter.com/regulusrx.

Forward-Looking Statements

This press release includes forward-looking statements regarding the future therapeutic and commercial potential of Regulus' business plans, technologies and intellectual property related to microRNA therapeutics being discovered and developed by Regulus, including statements regarding the therapeutic potential of targeting microRNA -21 for treating fibrosis and kidney injury. Any statement describing Regulus' goals, expectations, financial or other projections, intentions or beliefs is a forward-looking statement and should be considered an at-risk statement. Such statements are subject to certain risks and uncertainties, particularly those inherent in the process of discovering, developing and commercializing drugs that are safe and effective for use as human therapeutics, and in the endeavor of building a business around such products. Such forward-looking statements also involve assumptions that, if they never materialize or prove correct, could cause the results to differ materially from those expressed or implied by such forward-looking statements. Although these forward-looking statements reflect the good faith judgment of Regulus' management, these statements are based only on facts and factors currently known by Regulus. As a result, you are cautioned not to rely on these forward-looking statements. These and other risks concerning Regulus', Alnylam's, and Isis' programs are described in additional detail in Alnylam's and Isis' annual reports on Form 10-K for the year ended December 31, 2010, and its most recent quarterly report on Form 10-Q.  Copies of these and other documents are available from Alnylam or Isis.

 

Continued here:
Regulus Announces New Publication Showing Potential Therapeutic Benefit of Targeting microRNA-21 in Fibrosis

Read More...

Pathfinder to Present at New York Stem Cell Summit

Friday, February 17th, 2012

CAMBRIDGE, Mass., Feb. 16, 2012 (GLOBE NEWSWIRE) -- Pathfinder Cell Therapy, Inc. ("Pathfinder," or "the Company") (OTCQB:PFND.PK - News), a biotechnology company focused on the treatment of diseases characterized by organ-specific cell damage, today announced that Richard L. Franklin, M.D., Ph.D., Founder, CEO and President of Pathfinder, will present at the 7th Annual New York Stem Cell Summit being held on Tuesday, February 21, 2012.

Event: 7th Annual New York Stem Cell Summit
Date: Tuesday, February 21, 2012
Place: Bridgewaters New York, 11 Fulton Street, New York, NY
Time: 3:35 pm ET

Dr. Franklin will be providing an overview of the Company's novel Pathfinder Cell therapy.

The New York Stem Cell Summit brings together stem cell company executives, researchers, investors and physicians to explore investment opportunities in stem cell research and innovation. More information can be found at http://www.stemcellsummit.com.

About Pathfinder

Pathfinder is developing a novel cell-based therapy and has generated encouraging preclinical data in models of diabetes, renal disease, myocardial infarction, and critical limb ischemia, a severe form of peripheral vascular disease. Leveraging its internal discovery of Pathfinder Cells ("PCs") Pathfinder is pioneering a new field in regenerative medicine.

PCs are a newly identified mammalian cell type present in very low quantities in a variety of organs, including the kidney, liver, pancreas, lymph nodes, myometrium, bone marrow and blood. Early studies indicate that PCs stimulate regeneration of damaged tissues without the cells themselves being incorporated into the newly generated tissue. Based on testing to date, the cells appear to be "immune privileged," and their effects appear to be independent of the tissue source of PCs. For more information please visit: http://www.pathfindercelltherapy.com.

FORWARD LOOKING STATEMENTS

This press release contains forward-looking statements. You should be aware that our actual results could differ materially from those contained in the forward-looking statements, which are based on management's current expectations and are subject to a number of risks and uncertainties, including, but not limited to, our inability to obtain additional required financing; costs and delays in the development and/or FDA approval, or the failure to obtain such approval, of our product candidates; uncertainties or differences in interpretation in clinical trial results, if any; our inability to maintain or enter into, and the risks resulting from our dependence upon, collaboration or contractual arrangements necessary for the development, manufacture, commercialization, marketing, sales and distribution of any products; competitive factors; our inability to protect our patents or proprietary rights and obtain necessary rights to third party patents and intellectual property to operate our business; our inability to operate our business without infringing the patents and proprietary rights of others; general economic conditions; the failure of any products to gain market acceptance; technological changes; and government regulation. We do not intend to update any of these factors or to publicly announce the results of any revisions to these forward-looking statements.

Here is the original post:
Pathfinder to Present at New York Stem Cell Summit

Read More...

Following a trail of blood: A new diagnostic tool comes of age

Wednesday, February 15th, 2012

Public release date: 14-Feb-2012
[ | E-mail | Share ]

Contact: Joseph Caspermeyer
Joseph.Caspermeyer@asu.edu
Arizona State University

Blood tests have been a mainstay of diagnostic medicine since the late 19th century, offering a wealth of information concerning health and disease. Nevertheless, blood derived from the human umbilical cord has yet to be fully mined for its vital health information, according to Rolf Halden, a researcher at Arizona State University's Biodesign Institute.

In a new study appearing in the journal Environmental Health Perspectives, Halden's team performs detailed analyses of umbilical cord blood (UCB), identifying a total of 1,210 proteins using mass spectroscopy. The findings represent a 6-fold increase in the number UCB proteins thus far described?a significant advance: "Mapping of the full spectrum of proteins detectable in cord blood is the first, crititcal step in the discovery of biomarkers to improve human health," Halden says.

The proteins identified are associated with 138 different metabolic and disease pathways and provide invaluable information for the identification of biomarkers?early warning indices of disease, toxic exposure or disruptions in cellular processes. In addition to presenting intriguing candidates for new biomarkers in UCB, the study also identified 38 proteins corresponding to existing FDA-approved biomarkers for adult blood.

The UCB samples were pooled from 12 newborns, whose maternal backgrounds varied in terms of ethnicity, educational background, body weight, exposure to environmental toxins and also, to cigarette smoke. The research improves prospects for early disease diagnosis, by prioritizing biomarkers based on known proteins linked with disease.

According to Halden, the use of UCB as a diagnostic tool offers a number of attractive advantages. It is a readily acquired diagnostic biofluid?no invasive procedures are needed and relatively large volumes of fluid can be easily obtained. With the aid of modern high-throughput mass spectroscopy, UCB can be rapidly screened to reveal hundreds of proteins in parallel from a single sample having a volume of as small as 1/125th of an ounce. Most importantly, such early screening may provide critical information on likely health trajectories for newborns.

For a wide variety of diseases, early detection offers the best prospect for successful intervention and treatment. Further, many adult afflictions including chronic heart and kidney disease, diabetes and obesity may have their roots in fetal and early childhood development. Previous research has already established a well-documented link between fetal exposure to certain environmental contaminants and unfavorable health outcomes, for example in the case of in utero exposure to cigarette smoke constituents.

Halden's team hoped to expand knowledge of the UCB protein content or proteome, using a limited starting volume of fluid. This is important, as cord blood is a precious resource, exploited for other medical uses. Stem cells obtained from UCB for example are used for bone marrow transplantation and other therapeutic purposes. Once UCB proteins were identified in the tested sample pool, they were compared with known and proposed biomarkers in order to produce a concise list of candidate proteins of diagnostic value in medicine.

The team sought to comprehensively evaluate the diagnostic potential of the UCB proteome, with minimal bias relating to individual health histories. To do this, samples from the 12 newborns were combined into a composite. Among the UCB donors, 6 were African American, 5 were Caucasian and one was Asian.

Of the proteins detected in UCB, around 25 percent were previously detected in adults. Halden's group was able to obtain the protein data with as little as 240 microliters of blood. He emphasizes that new methods for evaluating UCB for newborns are highly desireable, given a spectrum of disorders of rising incidence in the general population, including diabetes, chronic heart and kidney disease and obesity.

The highest priority proteins examined in the current study were those already approved for adult diagnoses by the FDA. These biomarkers include those associated with thyroid deficiencies, chronic kidney dysfunction, and cardiovascular diseases. Future research will determine if such biomarkers are diagnostically appropriate for infants as well.

A second priority was to identify proteins of known function associated with disruptions of normal cell processes. While these proteins have not been FDA approved for diagnostic purposes, they are nevertheless linked with particular diseases or with toxic exposure. These include proteins involved with cardiac arrhythmia and sudden heart failure, maturity onset diabetes of the young (MODY), acute kidney injury, lymphoblastic leukemia, pancreatic cancer and other serious diseases.

Mass spectroscopic analysis of UCB offers the prospect of a global approach to assessing health risks in newborns, allowing the simultaneous observation of numerous indicators of health and disease. The technique should be an invaluable aid to early diagnosis for a range of conditions, with the potential to dramatically improve health outcomes.

###

The study is a multi-institutional effort involving researchers from Arizona State University, Johns Hopkins University, and George Washington University. It was conducted with funding from the National Institute of Environmental Health Sciences (NIEHS).

Rolf Halden is the Associate Director of the Swette Center for Environmental Biotechnology at the Biodesign Institute and Co-Director of the Center for Health Information and Research. He holds a professorship in the School of Sustainable Engineering and the Built Environment at ASU.

Written by: Richard Harth
Science Writer: The Biodesign Institute
richard.harth@asu.edu

[ | E-mail | Share ]

 

AAAS and EurekAlert! are not responsible for the accuracy of news releases posted to EurekAlert! by contributing institutions or for the use of any information through the EurekAlert! system.

Here is the original post:
Following a trail of blood: A new diagnostic tool comes of age

Read More...

U.S. begins stem cell trial for hearing loss

Monday, February 13th, 2012

WASHINGTON -- U.S. researchers have begun a groundbreaking trial to test the potential of umbilical cord blood transplants, a kind of stem cell therapy, to treat and possibly reverse hearing loss in infants.

The phase I trial follows promising studies on mice showing that such transplants were able to rebuild the structures of the inner ear, and some anecdotal evidence from humans, sparking hope of a cure for some forms of deafness.

One of those people is two-year-old Finn McGrath, who suffered brain damage after being deprived of oxygen during a prolonged and complicated delivery, according to his mother, Laura.

"His doctors told us he was at high risk for cerebral palsy, vision issues, hearing problems and mental retardation," she said in an interview with AFP.

Finn’s early days were an all-out struggle to survive, so for his parents, learning that he had failed his hearing tests and had damaged hair cells — the sensory receptors in the inner ear that pick up sounds — was almost an afterthought.

He had organ failure, breathing problems, and his cerebral palsy left him unable to roll, crawl or walk, hold his head up, talk or eat.

As his parents searched for ways to help him, they came upon stories online that told of studies using cord blood to help children with cerebral palsy and other disorders.

Prior to his birth, the McGraths had arranged to privately bank his umbilical cord blood, a procedure that costs around $2,000 plus storage fees, and remains controversial among pediatricians.

Private companies such as the Cord Blood Registry, which is funding the Texas study on hearing loss, urge expecting parents to bank their umbilical cord blood and reserve it for personal use as a way to protect their family.

That advice runs counter to the guidelines issues by the American Academy of Pediatrics in 2007, which calls such claims "unsubstantiated" and says banking for personal or family use "should be discouraged" but is "encouraged" if it is to be stored in a bank for public use.

Since Finn’s parents had already banked his, they enrolled him in cord blood trial for cerebral palsy in North Carolina and he received his first transplant in November 2009 when he was about seven weeks old.

A second transfusion followed and by May, his parents began to notice a change.

Nighttime noises, like an alarm on his food pump or the sound of ripping medical tape, would suddenly startle him awake, his mother recalled.

"He started vocalizing sounds and we could tell that he was anticipating things that we would say. Like, if he had heard a story a number of times or a song, he would smile like he recognized the song or the story."

Finn had a third infusion in September 2010, when he was one year old. Four months later, an otoacoustic emissions test (OAE), which plays a sound and picks up vibrations in the cochlea and hair cells, came back normal.

The early hearing tests that showed hearing loss were not exactly the same as the later tests that came back normal, so McGrath is cautious about comparing them directly, but she believes the cord blood transfusions may have helped.

"All I can tell you is anecdotally he was not able to hear for probably the first three or four months of his life, and then when he was about six to eight months old, he started hearing."

The hearing trial in Texas aims to take a first step in testing the safety, and later the efficacy, of transfusing cord blood in children age six weeks to 18 months who have sustained post-birth sensorineural hearing loss.

Some reasons that children lose their hearing at or after birth may include oxygen deprivation, head injury, infection, strong doses of antibiotics or loud noises.

Sensorineural hearing loss affects approximately six per 1,000 children, and there is no available medical treatment. Hearing aids or cochlear implants are typically offered to boost the ability of the damaged tissues.

"Stem cell therapy may potentially repair the damaged structures of the inner ear and restore normal hearing," lead investigator Samer Fakhri told AFP.

"We are at the initial stages of this process and the results are looking promising," Fakhri added.

Research using stem cells in cord blood, known as hematopoietic cells, is already under way on some types of brain injury, cerebral palsy, juvenile diabetes, kidney and lung disease, he said.

The new study at Memorial Hermann-Texas Medical Center is being funded by the Cord Blood Registry, and those eligible must have already banked their own umbilical cord blood with CBR.

But to Stephen Epstein, an otolaryngologist in Maryland, that does not pose a conflict of interest, because separate medical institutions in Texas and Georgia are conducting the Food and Drug Administration-approved research.

"If both of them can reproduce the same results then I would say it has some validity to it," said Epstein, who is not involved in the study.

"This is certainly a welcome, acceptable experiment, but it should be looked at with caution and time will tell."

One patient is already enrolled and the study, which runs for one year, has room for nine more.

While Finn McGrath still faces many challenges due to his cerebral palsy, his mother is grateful for the things he can do.

"I don’t know how much worse off he would have been without the stem cell transfusion," McGrath said, pointing to his normal cognition, lack of seizures, good hearing and vision.

"We remain hopeful that he will continue to improve."

© Copyright (c) AFP

Link:
U.S. begins stem cell trial for hearing loss

Read More...

Adult Stem Cell Scientist Stem Cell Nutrition Pioneer.flv – Video

Tuesday, January 31st, 2012

10-09-2011 19:18 http://www.rhemat.stemtechbiz.com e mail chris@rhemat.co.za The Roll of Stem Cells in your Body Support the Natural Healing System of the Body

Read more from the original source:
Adult Stem Cell Scientist Stem Cell Nutrition Pioneer.flv - Video

Read More...

http://stemcellremedy.com Stem Cell Remedy User Forum

Tuesday, January 31st, 2012

05-10-2011 13:45 stemcellremedy.com Stem Cell Remedy User Forum and Blog is a global collaborative effort of regular individuals and trained researchers from organizations across the world focused on helping patients, friends and families, while avoiding the politics associated with other types of research a The sixteenth installment of my original series, "Discovering Religion". In this episode I discuss the current actions of Christian Americans to suppress modern-day scientific advancements. In particular, I address the movement by Christians to outlaw embryonic stem cell, a stance they have no justification from the Bible in taking -- a situation that very closely parallels the Church's suppression of Roger Bacon and Galileo Galilei's scientific discoveries. Additional information I could not include in the video Diabetes: Giving insulin to children with Type I Diabetes is a viable means of treating this disease, however; after 15-20 years of living with type I diabetes, the danger continues to grow, possibly leading to kidney failure, heart disease, blindness, brain damage, and premature death. This is why stem cell research is so crucial to patients suffering from this serious condition. Bone Marrow Transplants: There are many patients, both child and adult, in need of bone marrow transplants that would greatly benefit from the use of stem cells. For 2/3 of them, there is no donor with an acceptable genetic match. However, even when a match is found, it is never perfect. With stem ...

The rest is here:
http://stemcellremedy.com Stem Cell Remedy User Forum

Read More...

january twenty second two thousand ten | two years later. she was here. – Video

Tuesday, January 31st, 2012

23-01-2012 19:28 "Left this world a little better just because I was here." Yesterday, the 22nd of January, marked a devastating and unforgettable day for all those who knew, loved and followed precious Layla Grace Marsh's story as she battled fiercely against the disease that claimed her life. After a routine check-up following her stem cell transplant Layla's parents were given the news that instead of getting better she had new tumors. Not only were they back in her abdomen but they were now crowding and invading her kidney. Her only good kidney. Precious Layla Grace was sent home with no treatment options aimed toward a cure. She was sent home to pass away. On the 9th of March, 2010 Layla gave up the fight for her "sparky" (sparkly) wings and has been her family's guardian angel ever since. Layla was full of life, happiness, love, fearlessness, determination, spunk, wit, joy and above all, strength. She loved wearing her flower beanies, babylegs and tutus. A smile was always flashed across her cheeky little face and she would often claim that she "had a good day" despite all the shit she was going through at the time. Layla lived, she loved and her legacy on how to do this is still here. I will never forget you. Miss you, boo. This video is dedicated to my wonderful friend through Twitter, Melly. Thank you for motivating me to finish this video even if I had to "cut it off where I finished." Seeing Layla's face and making videos (especially those commemorating certain painful milestones) are ...

Read this article:
january twenty second two thousand ten | two years later. she was here. - Video

Read More...

Please Help Vanessa – Video

Tuesday, January 31st, 2012

13-01-2012 12:10 http://www.justgiving.com/vanessa-appeal In Feb 2009, Vanessa, then aged 8, was diagnosed with Stage 4 (High-Risk) Neuroblastoma, a very rare, aggressive and difficult to treat form of childhood cancer. Fewer than 100 children in the UK are diagnosed with neuroblastoma each year, most of which are below the age of 5 and generally have a better prognosis as the older the child is the worse the prognosis is. Since Feb 09, Vanessa has undergone many different treatments at Yorkhill Hospital in Glasgow, these include; 12 rounds of High Dose Chemotherapy, two 7 hour surgical operations, the removal of one of her kidneys, a stem cell transplant, Radiotherapy, Retinoic Acid treatment and Immunotherapy treatment......all of which was agonising to watch as parents never mind to have to endure as a child! Having undergone all this difficult and often very painful treatment the fact remained that due to a high relapse rate the long term prognosis for Vanessa's survival remained very poor with less than a 40% survival rate. All the same, Vanessa finished her treatment at Yorkhill Hospital in Aug 2010 and was given the all clear. In Dec 2011 after routine scans, we were given the devastating news that Vanessa had relapsed. She has many hotspots on the skull, neck, spine, leg and knees. The UK doctors have told us that this time round there is very little chance of survival; "much less than 10%" they said, as we do not have any relapse protocols in the UK. This is due to the Government not ...

Go here to read the rest:
Please Help Vanessa - Video

Read More...

RNL BIO brings an artist his normal life back from severe rheumatoid. by stem cell therapy – Video

Friday, December 23rd, 2011

John Lawson Cullison, Jr., an artist lost his ability to paint due to the effects of arthritis. This incurable condition is due to the degeneration in cartilage tissue and symptoms include: pain, tenderness in the joints, stiffness, loss of flexibility, bone spurs and severe swelling. Pain management and joint replacement surgery are the typical means to treating this condition

Read more:
RNL BIO brings an artist his normal life back from severe rheumatoid. by stem cell therapy - Video

Read More...

63 year old stroke victim was greatly improved through stem cell therapy – Video

Friday, December 23rd, 2011

Mr. Kim had cerebral hemorrhage seven years ago.

Read more:
63 year old stroke victim was greatly improved through stem cell therapy - Video

Read More...

Page 10«..9101112


2024 © StemCell Therapy is proudly powered by WordPress
Entries (RSS) Comments (RSS) | Violinesth by Patrick