With the $700,000 Institute of Medicine inquiry into the performance of the California stem cell agency half complete – at least publicly – the blue-ribbon panel seems to be coming up short on comments from outside of the agency itself.

The major public effort by the IOM to secure comments is the passive posting of forms to be filled out on the IOM web site.

How many responses has the IOM received on those forms? The IOM has not disclosed that information despite two inquiries earlier this month by the California Stem Cell Report.

The prestigious institute is undertaking the study of $3 billion agency under contract with CIRM, which is paying the IOM $700,000. Some CIRM directors have expressed hope that the IOM findings will help build support for another multi-billion dollar state bond measure to renew financing for CIRM. It is scheduled to run out of money for new grants in five years.

So far, the IOM panel has held two public meetings, one in Washington, D.C., and one in the San Francisco area. The final California hearing is scheduled for April 10 in Irvine with the last public meetings scheduled for later this year in Washington.

So far, the panel has heard only from CIRM employees or directors as well as researchers who have received tens of millions of dollars in CIRM grants. The IOM has not heard publicly from a single independent witness.

The IOM has posted on its web site forms seeking comments from the public, grant recipients, beneficiary institutions and businesses. However, passive postings of forms are unlikely to generate more than a relative handful of responses. To produce significant numbers requires aggressive and targeted follow-up.

It is also unclear exactly what the IOM is doing to seek information from biotech businesses and unsuccessful grant applicants. Some businesses have complained publicly about the tiny share of funding that industry has received. And some CIRM directors have expressed concern for several years about the inadequacies of business funding.

On Feb. 12, the California Stem Cell Report queried the IOM about its efforts at outreach, asking for specifics on what is being done. Christine Stencel, a spokeswoman for the IOM, replied,

"The IOM has been obtaining and compiling lists of organizations and people to circulate the questionnaires as widely as possible among target groups. For example, IOM has sent a notice to some 300 stakeholder groups encouraging participation."

Other specifics were not forthcoming. (The full text of the questions and responses can be found here.)

On Feb. 15, the California Stem Cell Report followed up with these additional questions,

"Regarding the 300 stakeholder groups, how are those defined? Please give me a few examples.

"Based on your response, is it correct to say that the IOM is not sending out questionnaires directly to all CIRM grant applicants, including those who were rejected?

"Is it correct to say that no special effort -- other than that described in your response -- is being made to seek responses from stem cell businesses?

"The failure to provide numbers on the responses so far would indicate that the numbers are so small that the IOM is choosing not to disclose them. If that is not the case, please email me the numbers."

As of this writing, the IOM has not responded to those questions. We will carry its response verbatim when we receive it.

Source:
http://californiastemcellreport.blogspot.com/feeds/posts/default?alt=rss

Here is the text of the questions submitted Feb. 12 by the California Stem Cell Report to the Institute of Medicine concerning its attempts to secure comments on the operation of the $3 billion California stem cell agency along with the IOM response.

The response from Christine Stencel, a spokeswoman for the IOM, follows these questions from the California Stem Cell Report.

"I will be writing a piece on Wednesday dealing with the online surveys that IOM has posted. For that piece, please tell me very, very  specifically what the IOM is doing to generate responses. For example, is the IOM buying ads in newspapers or online, asking the public to fill out the forms? Is it hiring a polling firm to call households for responses?  Also please tell me exactly what is being done to generate responses on all the other surveys that have been posted.

"Additionally, please tell me how many responses that the IOM has received so far in each category on the survey forms for CIRM grantees, industry partners and leadership. Thank you."

The IOM response on Feb. 15:

"The IOM has been obtaining and compiling lists of organizations and people to circulate the questionnaires as widely as possible among target groups. For example, IOM has sent a notice to some 300 stakeholder groups encouraging participation. We do not have the resources to hire a polling firm or place ads.

"The purpose of these questionnaires is to extend the committee's information gathering beyond in-person meetings and the standard listing of an email address or phone number for the study on the project website. Not all people who might have useful experiences or perspectives on CIRM may be able to attend the in-person meetings and not all may visit the project website and find the study contact information. This is a proactive effort to reach more people.

"Anyone who knows of individuals or organizations with information on CIRM that would be useful for the committee's knowledge can share the links to the questionnaires with them. This will help spread the word and get the committee insights they need.

"I don't have information on the number of responses so far. Ultimately, as noted at the top of each survey, the responses will be aggregated and de-identified and placed in the public access file in addition to being shared with the committee.

"I trust this will be useful for your readers."

The California Stem Cell Report then asked the following questions on Feb. 15.

"Thank you for your response. A few follow-up questions:
Regarding the 300 stakeholder groups, how are those defined? Please give me a few examples.

"Based on your response, is it correct to say that the IOM is not sending out questionnaires directly to all CIRM grant applicants, including those who were rejected?

"Is it correct to say that no special effort -- other than that described in your response -- is being made to seek responses from stem cell businesses?

"The failure to provide numbers on the responses so far would indicate that the numbers are so small that the IOM is choosing not to disclose them. If that is not the case, please email me the numbers. Thank you."

The IOM had not responded to the follow-up questions as of this writing on Feb. 21.

Source:
http://californiastemcellreport.blogspot.com/feeds/posts/default?alt=rss

Press TV

Iran's NIGEB holds international stem cell workshop Press TV Iran's National Institute of Genetic Engineering and Biotechnology (NIGEB) has held an international stem cell workshop in the capital city of Tehran, Press TV reported. A number of university professors and researchers from Turkey, Iraq, ...

Source:
http://news.google.com/news?q=genetic-engineering&output=rss

Breakthrough stem cell research at Scripps Research Institute in La Jolla, Calif. has the potential to revive endangered species. Researchers at the Center for Regenerative Medicine are aiming to turn stem cells into gametes. Once new eggs and sperm are created, “test tube babies” can be born, possibly preserving a species.

In 1972, researchers preserved skin cells of certain endangered species at the Frozen Zoo, hoping that future technology would help to revive populations, and today Scripps researchers are combining the frozen skin cells with human stem cells to generate stem cells specific to the animal. Stem cells are turned into gametes through re-programming, a process in which retroviruses are used to bring the cells back to earlier stages of development. Last month, scientists created mouse sperm cells through this process.

Scientists view this method of species preservation as a last resort when cheaper, simpler means have failed. For instance, the white rhino, whose population is numbered at seven in the world, would benefit immensely since other methods of trying to save the species have failed. Scientists also hope to help the drill, a West African primate threatened by hunting and habitat degradation.

—compiled by Michelle Lim

Go here to read the rest:
One Response to “Rescuing the white rhino?”

LOS ANGELES, CA--(Marketwire -02/24/12)- A2Z Health Expo today announced it will hold its 5th annual Health Expo at the Skirball Cultural Center in Los Angeles, CA on Thursday, March 22, 2012 from 4pm to 10pm. According to Dr. Ben Drillings, Director, the keynote speaker for the event will be the co-founder of the Samueli Foundation, Susan Samueli, PhD. Mrs. Samueli serves on the Board and Advisory Board of the Susan Samueli Center for Integrated Medicine (SSCIM) at UC Irvine. SSCIM promotes integrative medicine by providing education, scientific research and a model of clinical care that emphasizes healing of the whole person. Mrs. Samueli was honored with the UCI Medal in March 2000, the 2002 Ellen Cooperman Angel Award Recipient from the John Wayne Cancer Institute and the 2005 General William Lyon Crystal Vision Philanthropy Award from the Orangewood Children's Foundation. In 2006, Susan and Henry Samueli became the owners of the NHL franchise the Anaheim Ducks. The topic of Mrs. Samueli at the expo is: "Integrated Clinic in the 21st Century: Innovations, New Models & Challenges."

The A2Z Health Expo event is focusing on bringing together healthcare professionals, philanthropists, academicians, that are interested in learning more about the integrated clinic model. The expo aims to build a network relationship and sharing of ideas within the health community. Attendees include MDs, Chiropractors, Massage Therapists, Nutritionists, Schools & Spa owners, and general public.

Joining Mrs. Samueli are a bevy of prestigious speakers: Kerry Crofton, PhD., the author of the award-winning book, Wireless Radiation Rescue, and co-founder and executive Director of the International Advisory Board Doctors for Safer Schools; Dr. Nathan Newman, innovator of Stem Cell Lift -- cutting edge cosmetic surgery, without cutting;
And Ms. Alexa Zaledonis, who is the current chair of the National Certification Board for Therapeutic Massage & Bodywork as well as the owner of Even Keel Wellness Spa.

Dr. Drillings is urging the healthcare community to come and learn about the integrated clinic model. This is a must see expo!

The Skirball Cultural Center is located at 2701 N. Sepulveda Blvd., Los Angeles, CA 90049. To register to the event, please visit http://www.a2zhealthexpo.com or email us at expo@a2zhealthexpo.com or call (818) 700-0286.

Link:
Susan Samueli, PhD of the Susan Samueli Center for Integrative Medicine UC Irvine to Headline A2Z Health Expo in Los ...

Bar Harbor – Yijun Ruan, Ph.D., an American geneticist who has pioneered new techniques to sequence and map DNA to better understand cancer growth and stem cell properties, will be the first scientist to join the new Jackson Laboratory for Genomic Medicine (JAX Genomic Medicine) in Farmington, Conn.

Ruan is currently associate director and senior group leader at the Genome Institute of Singapore and professor of biochemistry at the National University of Singapore. He is also an investigator with the Encyclopedia of DNA Elements (ENCODE) project, an international consortium of research groups funded by the National Human Genome Research Institute.
Ruan said he was attracted by The Jackson Laboratory’s famously collaborative research environment, and plans to “take a community approach to tackle genomic questions through intensive collaboration.” Through innovating new technologies and studying how the human and mouse genomes are regulated, he said his goal is to translate research findings into personalized medicine. Ruan has also been appointed director of JAX Genomic Sciences, and will be bringing his current research program and team with him to JAX Genomic Medicine.
JAX Genomic Medicine will unite doctors, patients, scientists and industry to find new ways to tailor disease diagnosis, prevention and treatment to each person’s unique genetic makeup, or genome. Ruan and other recruits will begin initial operations this year in leased space while a 173,000-square-foot permanent facility is designed and built. Construction will begin in 2013, and the new facility will open in 2014.
“Yijun’s broad interests in genome biology, coupled with his innovative approach to developing new research techniques, make him an ideal member of the new JAX Genomic Medicine research team,” said Bob Braun, Ph.D., Jackson’s associate director and chair of research.
After earning BS and MS degrees in microbiology from Huazhong Agricultural University in Wuhan, China, Ruan obtained his Ph.D. in plant molecular biology from the University of Maryland, College Park, where he also conducted postgraduate research. Following scientific appointments at Monsanto Co. in St. Louis and Large Scale Biology Corp. in Vacaville, Calif., Ruan was recruited to the Genome Institute of Singapore (GIS) in 2002. Edison Liu, M.D., former director of GIS and now president and CEO of The Jackson Laboratory, credits Ruan for building the institute’s state-of-the-art genomic technology platforms and its award-winning genome biology programs.
Ruan is an author of 70 research papers and holds patents in Japan, Singapore and the United Kingdom for the DNA analysis techniques he helped to develop. A U.S. citizen, Ruan is married and has two children.
In addition to recruiting research faculty, JAX Genomic Medicine is currently hiring a site director, science coordinator, senior human resources manager, facilities manager and senior financial analyst in Connecticut. Job announcements are on The Jackson Laboratory’s website at http://www.jax.org/careers/connecticut.html.
Braun notes that The Jackson Laboratory is expanding the research faculty at its headquarters campus in Bar Harbor, Maine, as well as recruiting faculty in Connecticut.
The Jackson Laboratory is an independent, nonprofit biomedical research institution and National Cancer Institute-designated Cancer Center based in Bar Harbor, Maine, with a facility in Sacramento, Calif., afuture institute in Farmington, Conn., and a total staff of about 1,400. Its mission is to discover the genetic basis for preventing, treating and curing human disease, and to enable research and education for the global biomedical community.

For more health news, pick up a copy of the Mount Desert Islander.

Read more here:
First researcher joins The Jackson Lab for Genomic Medicine in Conn.

NEW YORK & PETACH TIKVAH, Israel--(BUSINESS WIRE)--

BrainStorm Cell Therapeutics Inc. (OTCBB: BCLI.OB - News), a developer of innovative stem cell technologies for neurodegenerative disorders, announced that NurOwn™, its autologous stem cell therapy for amyotrophic lateral sclerosis (ALS), or Lou Gehrig's Disease, was profiled yesterday on CNBC. In the Feature Story about the impact of Iran's nuclear threat, Israeli business and scientific leaders were interviewed about Israel's thriving economy and cutting edge technologies. Among those leaders that met with CNBC were Brainstorm’s President Mr. Chaim Lebovits and Prof. Dimitrios Karussis, Principal Investigator of Brainstorm's Phase I/II clinical trial currently underway at the Hadassah Medical Center in Jerusalem.

Brainstorm recently announced positive initial results from the clinical trial, resulting in approval from Hadassah's Helsinki committee to proceed with the trial. Accordingly, additional patients have been enrolled in the study, and Brainstorm will announce additional results in the coming months.

To see the video online, follow the link at: http://video.cnbc.com/gallery/?video=3000074883

To read the Feature Story online, follow the link at: http://www.cnbc.com/id/46484576

Safe Harbor Statement
Statements in this announcement other than historical data and information constitute "forward-looking statements" and involve risks and uncertainties that could cause BrainStorm Cell Therapeutics Inc.'s actual results to differ materially from those stated or implied by such forward-looking statements. The potential risks and uncertainties include risks associated with BrainStorm's limited operating history, history of losses; minimal working capital, dependence on its license to Ramot's technology; ability to adequately protect the technology; dependence on key executives and on its scientific consultants; ability to obtain required regulatory approvals; and other factors detailed in BrainStorm's annual report on Form 10-K and quarterly reports on Form 10-Q available at http://www.sec.gov. The Company does not undertake any obligation to update forward-looking statements made by us.

Read more here:
BrainStorm Featured on CNBC

More Topics: Choose a Sector Accounting Firms Advertising/Media/Communications Capital CEO/Board General Business Health/Biotech Internet/Technology Investment Firms Law Firms Mergers & Acquisitions Money Managers People Private Companies Public Companies Venture Capital

Posted February 23, 2012

WASHINGTON -- The Stem Cell Action Coalition opposes Virginia House Bill No.1, the so-called Virginia "personhood bill." The Virginia Senate Committee on Education and Health is scheduled to take the matter up this week.

The language of the personhood bill states, in part, that the laws of Virginia "shall be interpreted and construed to acknowledge on behalf of unborn children at every stage of development all of the rights, privileges and immunities available to other persons, citizens and residents." The bill further states "unborn children shall include the offspring of human beings from the moment of conception until birth at every stage of biological development."

HB 1 arguably would apply to every aspect of Virginia law thus profoundly impacting inheritance, adoption, guardianship, civil and criminal liability by according the same rights as adults and children to a single cell.

The personhood bill would surely interfere with reproductive and related rights of women and couples along several fronts. These interferences include making it exceedingly difficult for couples in Virginia to seek in vitro fertilization as a means of creating families and donating for research IVF-created embryos not needed for implantation or not sufficiently healthy for implantation. Moreover, the law would prevent the pursuit of medical research in Virginia that utilizes human embryonic stem cells.

In this twisted new world, Virginia researchers deriving embryonic stem cells from donated embryos might be charged with capital crimes, even murder. Couples donating embryos to research might be designated as accessories to these crimes. Microscopic embryos, consisting of a few cells in lab dishes or frozen in IVF clinics might be designated as wards of the state and by mandate have legal guardians appointed on their behalf.

Human embryonic stem cell research has been described by scientists as the "gold standard" for those seeking to develop cures based on stem cell technology for many diseases and maladies such as Parkinson's, ALS, diabetes, MS, macular degeneration and other causes of blindness, spinal cord injuries, and other medical conditions for which there is no known cure.

Bernard Siegel, J.D., spokesperson for the Coalition and executive director of the Genetics Policy Institute commented, "It is a sad day indeed when the Commonwealth of Virginia should become an outpost for extremism by impeding potentially lifesaving scientific research. Thomas Jefferson would be appalled. The wise voters of Colorado (twice) and Mississippi overwhelmingly rejected personhood amendments to their state constitutions.

The profound implications of the personhood bill cannot be wished away by its sponsors. Passage of this bill would be an affront to couples trying to avail themselves of modern infertility treatments, stem cell researchers targeting cures and to all Virginians suffering from chronic and life threatening disease. Passage of HB 1 is akin to crushing hope.

Human embryonic stem cell research holds the promise of discovering the root causes of disease, serves as a tool for drug discovery, and will surely lead to regenerative medicines and cell therapies for repairing or replacing damaged tissues and organs.

Microscopic cells in a lab dish, that by a couples' decision, will never be implanted in a womb, should not be defined as 'people'," Siegel continued.

HB 1 represents a concerted move by opponents of all forms of early termination of pregnancy and medical research involving human embryos to attempt to pass laws to define "person" as the being that comes into existence at conception. In addition to Virginia, similar efforts to pass "personhood" legislation are underway in Oklahoma, Mississippi and in other states.

The Stem Cell Action Coalition has 75 nonprofit affiliated organizations including patient groups, medical philanthropies, scientific and medical societies and public interest organizations all dedicated to advancing scientifically meritorious and ethically responsible research.

The Stem Cell Action Coalition serves as an engine to unite the pro-cures community. It recognizes that human embryonic stem cell research must be a national public health priority at all branches and levels of government, not only as a matter of the medical health of the individuals who comprise the United States, but also as a matter of national financial health. The Coalition sponsors a web site http://www.stemcellaction.org and can be found on Twitter @StemCellAction and on Facebook at http://www.facebook.com/stemcellaction.

To find out more about the company in this article and to see if you
have business connections, click below:

The Stem Cell Action Coalition Please enable JavaScript to view the comments powered by Disqus. blog comments powered by

Here is the original post:
Stem Cell Action Coalition Opposes Virginia Personhood Bill

Friday, Feb. 24, 2012

Japan has made great strides in the fight against leukemia in the last two decades that have seen bone marrow transplants increase, while the implementation of a nationwide donor program also has contributed significantly.

But the donor pool still needs to be expanded further to give more patients on the waiting list a chance of finding a marrow match, and a better shot at undergoing the life-saving surgery.

As of the end of 2011, about 400,000 potential donors were registered with the Japan Marrow Donor Program and around 13,700 patients in total had received bone marrow transplants since its inception in 1991. Approximately 34,600 patients have sought transplants since the program started.

But many patients still die before a suitable donor match is found, and the program is looking to expand the donor pool through raising public awareness about bone marrow donations. Undergoing a transplant in time can eradicate the cancer, which attacks the body's blood-forming tissues, including bone marrow and the lymphatic system.

"I wish more people would join the program and that all patients could be given the chance to survive," said former leukemia patient Chikako Kimura, 39, who had one of the early bone marrow transplants during the program's first years.

Kimura was diagnosed with acute myelogenous leukemia in 1991, a year after graduating from high school and starting to work. That spring, she felt constantly tired but shrugged it off as resulting from the rigors of her job.

That December, however, Kimura saw a doctor about swelling in her legs. She was immediately hospitalized and started to receive treatment, but didn't learn she had leukemia until several years later.

Kimura was not informed she had leukemia until spring 1993, when her doctor told her a donor with bone marrow matching her type had been found and encouraged to her to undergo a transplant. A year earlier, the doctor had put her on the waiting list of the fledgling bone marrow donor program.

Initially, she balked at the proposal as her condition had been stabilized through chemotherapy. But she eventually decided to take a chance.

"I was really lucky to find a matching donor so soon, given the small pool of donors at the time," Kimura recalled.

According to the foundation that set up the program, more than 527,000 people have registered as potential bone marrow donors since January 1992.

The donor pool swelled after a TV campaign was launched in July 2005 featuring Masami Ihara, a former captain of Japan's national soccer team, who appealed for more people to register. The high-profile campaign helped raise public awareness over the issue and led to a flood of inquiries to the four toll-free numbers the foundation set up.

"From the first day (of the TV ads), we had our hands full answering phone calls" from the public asking how to become donors, said Hidehiko Okubo of the foundation.

The TV campaign was later amended to use the images of actress Masako Natsume, who died of leukemia in 1985, and singer Minako Honda, who died in 2005.

The easing of criteria that must be met before being allowed to register as a donor and an increase in locations nationwide where people can register also helped to boost donor numbers.

The donor pool has now expanded to a level where more than 90 percent of leukemia patients on the waiting list can expect to find at least one suitable match.

But even if they find a potential donor, logistical or other reasons currently prevent about 40 percent of leukemia patients from actually receiving transplants. And it remains extremely difficult to find donors for some patients with rare white blood cell types.

The foundation's Okubo said trying to cure leukemia only by bone marrow transplants has its limits, and noted another kind of transplant was granted the green light in October 2010.

The procedure, which uses hematopoietic stem cells extracted from the blood of healthy people, had until 2010 only been allowed in Japan for transplants involving family members.

While 33 medical facilities are capable of performing such transplants, only two leukemia patients have been operated on so far.

The new procedure is expected to increase the number of people willing to become donors, as it involves fewer health risks than bone marrow transplants.

More than 18 years on from her transplant, Kimura now works as a nurse. "Many people have supported me. I wanted to be of some help to other people," she explained.

Read more from the original source:
More bone marrow donors sought

The method, developed over several years in the lab of Prof. Ehud Shapiro of the Institute's Biological Chemistry, and Computer Science and Applied Mathematics Departments, uses mutations in specific genetic markers to determine which cells are most closely related and how far back they share a common parent cell, to create a sort of family tree for cells. Shapiro and members of his lab, including Drs. Shalev Itzkovitz and Rivka Adar, together with Prof. Nava Dekel and research student Yitzhak Reizel of the Biological Regulation Department, used their method to see if ova could be descended from bone-marrow stem cells. Their findings indicated that any relationship between the two types was too distant for one to be an ancestor of the other.

These scientists also found, surprisingly, that the ova of older mice had undergone more cell divisions than those of younger mice. This could be the result of replenishment during adulthood, but an alternate theory holds that all eggs are created before birth, and those that undergo fewer divisions are simply selected earlier on for ovulation. Further experimentation, says Shapiro, will resolve the issue.

Cell lineage trees are similar to modern evolutionary and taxonomic trees based on genome comparisons between organisms. Shapiro and his team used mutations in cells that are passed on to daughter cells over an organism's lifetime (though not on to the next generation). By comparing a number of genetic sequences called microsatellites – areas where mutations occur like clockwork – they can place cells on trees to reveal their developmental history.

A number of papers published by Shapiro, his team and collaborators in recent months have demonstrated the power and versatility of this method. One study, for instance, lent support to the notion that the adult stem cells residing in tiny crypts in the lining of the colon do not harbor, as thought, "immortal DNA strands." Immortal strands may be retained by dividing stem cells if they always relegate the newly-synthesized DNA to the differentiating daughter cell and keep the original stand in the one that remains a stem cell.

A second study addressed an open question about developing muscle cells. Here they found that two kinds of progenitor cell - myogenic cells, which eventually give rise to muscle fiber, and non-myogenic cells – found within the same muscle are more closely related than similar cells in different muscles.

One immediate advantage of the cell lineage analysis method developed by Shapiro's team is that it is non-invasive and retrospective, and as such can be applied to the study of human cell lineages. Most other studies of development rely on genetically engineered lab animals in which the stem cells are tagged with fluorescent markers. In addition to providing a powerful new research method that does not rely on such markers, Shapiro believes that it could one day be adapted as a diagnostic tool that might, for instance, reveal the history of an individual's cancer and help doctors determine the best course of treatment.

Provided by Weizmann Institute of Science (news : web)

Visit link:
Lineage trees reveal cells' histories

Newswise — The International Society for Stem Cell Research (ISSCR) is pleased to announce the winner of the 2012 McEwen Award for Innovation, a coveted prize in the field of stem cell research and regenerative medicine. The 2012 recipient is Rudolf Jaenisch, MD, Founding Member of the Whitehead Institute for Biomedical Research and Professor of Biology at the Massachusetts Institute of Technology in recognition of his pioneering discoveries in the areas of genetic and epigenetic control of development in mice that directly impact the future potential of embryonic stem cells and induced pluripotent stem cells for therapeutic utility.

The McEwen Award for Innovation is supported by the McEwen Centre for Regenerative Medicine in Toronto, Ontario, Canada. The $100,000 award honors original thinking and groundbreaking research pertaining to stem cells or regenerative medicine that opens new avenues of exploration towards the understanding or treatment of human disease or affliction.

“Rudolf Jaenisch has consistently contributed new and groundbreaking discoveries to stem cell biology and regenerative medicines that have changed the way stem cell research is conducted, said Fred H. Gage, PhD, ISSCR President. “Importantly, Rudolf not only has an uncanny sense of the next big question, but also conducts his experiments with such thoughtful and critical experimental design that his results have an immediate impact. This critical attention to detail and experimental design has greatly benefited the many gifted students that have passed through his lab and now populate many of the major stem cell centers throughout the world. Rudolf is very deserving of this award.”

Winner of the inaugural McEwen Award for Innovation in 2011, Shinya Yamanaka, MD, PhD, ISSCR President-Elect agrees. “Dr. Rudolf Jaenisch has always been on the cutting-edge of our field and his research has been a source of inspiration not only for myself, but has influenced the careers of some of our most esteemed colleagues.”

Dr. Jaenisch will be presented with the award at the ISSCR 10th Annual Meeting, in Yokohama, Japan, on Wednesday, June 13, 2012.
***
The International Society for Stem Cell Research is an independent, nonprofit membership organization established to promote and foster the exchange and dissemination of information and ideas relating to stem cells, to encourage the general field of research involving stem cells and to promote professional and public education in all areas of stem cell research and application.

Comment/Share

Continued here:
ISSCR Honors Stem Cell Research Pioneer with Prestigious McEwen Award for Innovation

22-02-2012 02:19 Department of Obstetrics and Gynecology, Buddhist Tzu-Chi Medical Center, Hualien, Taiwan, speaking on "Human umbilical cord mesenchymal stem cells support prolonged expansion of human embryonic stem cells without tumorigenesis" at the International Conference of Stem Cells and Regenerative Medicine for Neurodegenerative Diseases to be held at the Tzu-Chi Hospital in Hualien, Taiwan on April 22-24, 2010.

Read more from the original source:
Dah-Ching Ding, "Human umbilical cord mesenchymal stem cells support prolonged expansion of... - Video

22-02-2012 04:19 Osamu Honmou, Sapporo Medical University, Sapporo, "Transplantation of bone marrow stem cells" at the International Conference of Stem Cells and Regenerative Medicine for Neurodegenerative Diseases to be held at the Tzu-Chi Hospital in Hualien, Taiwan on April 22-24, 2010.

See original here:
Osamu Honmou, "Transplantation of bone marrow stem cells" - Video

22-02-2012 05:16 Waisan Poon, Chinese U, Hong Kong, speaking on, "Clinical trial of umbilical cord blood stem cells in spinal cord injury" at the International Conference of Stem Cells and Regenerative Medicine for Neurodegenerative Diseases to be held at the Tzu-Chi Hospital in Hualien, Taiwan on April 22-24, 2010.

Read the original:
Waisan Poon, "Clinical trial of umbilical cord blood stem cells in spinal cord injury" - Video

Bioethicists debate how to remain impartial as a bioethics journal editor joins a company that peddles unproven stem cell therapies.

By Sabrina Richards | February 22, 2012

Bioethicists are debating how, or even whether, one can remain impartial when working for industry as Glenn McGee, founder and editor of the American Journal of Bioethics, joins CellTex, a company that banks patients’ cells for untested stem cell therapies, reported Nature. McGee, who joined CellTex in December of last year and will step down from AJOB on March 1, says he hopes to bring ethical standards to CellTex’s stem cell trials.

CellTex licenses therapies from RNL Bio, a South Korea-based company that converts patients’ fat cells into patient-specific mesenchymal stem cells, which the company claims can be reinjected to treat conditions like spinal cord injury. To date, no clinical trials have been completed that back these claims.

Though criticism has been leveled at McGee for joining CellTex while remaining at AJOB, observers also wonder whether bioethicists can work in industry at all. McGee has argued that bioethicists have a place in industry, thereby helping bioethics to have a practical purpose. Others, such as Insoo Hyun, a stem-cell bioethicist at Case Western Reserve University in Cleveland, Ohio, are doubtful. Hyun developed patient consent procedure for egg donation for Woo Suk Hwang, the infamous Korean stem cell researcher whose claims of human cloning later proved fraudulent.

“I know firsthand how difficult it is to separate conflict of interest—to maintain the role of bioethicist,” Hyun told Nature. “I know you need to not be too chummy with enterprises trying to speed ahead in stem cells.”

Teenage Tourrette’s Outbreak?

By Edyta Zielinska

School-district officials in northwestern New York State are puzzled by a spate of high school students reporting symptoms of the neuropsychiatric disorder.

Wireless Drug Chip

By Jef Akst

The world’s first programmable drug-delivery chip passes the test, accurately and safely delivering an osteoporosis drug.

News from AAAS

By Jef Akst

A roundup of recent research announced last weekend at the annual conference of the American Association for the Advancement of Science (AAAS).

More:
Bioethics Backlash

Published Wednesday, February 22, 2012 12:12 AM By MAGGIE KIELY
maggie.kiely@theeagle.com

Two Texas A&M cancer awareness organizations are encouraging people to participate in an event that could save lives.

From 11 a.m. to 3 p.m. on March 1 and March 2 at the Recreation Center, residents will have an opportunity to register their bone marrow into a global data base used to help patients waiting for a donor match.

Spearheading the drive are Christina Ruiz, president of the Texas A&M Cancer Society, and Courtney Hawes, president of Texas A&M American Childhood Cancer Organization.

The two campus groups have teamed up with DKMS, a global bone marrow donor center, for the event.

Registering bone marrow involves swabbing the inside of the person's cheek to gather tissue used to determine the DNA type.

Amy Roseman, donor recruitment coordinator for DKNS Texas region, said finding a match is a challenge for many patients.

"What we're looking for is a genetic twin, so it's really hard to find a match," she said. "Within a family, a patient only has a 30 percent chance of matching a relative."

Each year, there are about 20,000 patients seeking a match, but only four out of 10 are successful, she said.

That's why it's so important to increase the size of the bone marrow data base: "The more the marrower," said Roseman.

Roseman said that 80 percent of patients in need of bone marrow donations are looking for blood stem cells, while only 20 percent -- mainly children -- require a full transplant.

Giving the stem cells involves a process similar to donating blood, she said.

To donate bone marrow, the donor is put under anesthesia while doctors draw tissue from the pelvic bone.

All of the procedures are paid for by DKNS, she said.

Ruiz, a junior molecular and cell biology major, said her plan is to become an oncologist.

Cancer entered her world in middle school when her best friend's mother was diagnosed with lymphoma.

The friend's mom, who had been her after-school caretaker, died her freshman year, but because of two bone marrow transplants, she was able to live longer than expected.

Hawes said several of her family members have been diagnosed with a rare form of cancer since her middle school years, which is what prompted her to join the campus cancer society as a freshman.

She founded ACCO last summer and has recruited about 30 members since, she said.

The cancer society has about 40 members, Ruiz said, adding that most of their work centers around raising awareness about cancer prevention and ways people can contribute to research or treatments.

Josh Lemon, a freshman visualization major from Waco, said he was diagnosed with Ewing sarcoma -- a rare form of bone cancer -- two years ago as a senior in high school.

Even though he didn't receive a bone marrow transplant, he did require a platelet transfusion, which wouldn't have been possible without a donor.

"For me, it was very beneficial that someone had donated," he said. "You never know, you may know someone who will be affected by cancer."

For more information about what it takes to register or become a bone marrow donor, visit getswabbed.org.

Read more from the original source:
A&M to host bone marrow donor drive

TYLER, TX (KLTV) -

Over the last 3 months, life has changed drastically for Cody Chandler, a Tyler doctor diagnosed with leukemia just after Thanksgiving.

A bone marrow drive will be hosted Wednesday afternoon in his honor, and one of the main things Chandler stresses now is his new-found passion to get people who need bone marrow transplants the help they need.

"To be very honest, I didn't realize the severity of it. I was like, leukemia, what do you mean leukemia? And he said, you have cancer, and we need to start chemo tomorrow," Chandler recalls.

Chandler is a young father, husband, and doctor. He describes himself as being "pretty healthy" before he was diagnosed with acute myeloid leukemia in November.

"The severity of the diagnosis doesn't really hit you until you unfortunately start looking at statistics, and what it's going to take for me to get treated and get healthy and to live past 5 years," he said. "And I don't think I can explain that feeling. I think the real definition of being humbled, I've really learned what humility means."

Chandler's cancer is currently in remission and he continues to have chemo treatments. But if he relapses, he'll have to have a bone marrow transplant. Heart to Heart Hospice in Tyler is hosting a bone marrow drive Wednesday afternoon to get people on the national registry.

"They wanted to reach out and help and let people know how simple the process is to get into the registry and how simple the process is now to donate," said April Brown, the host of Wednesday's blood drive.

To join the registry, it only takes someone 15 seconds to swab their cheek and a few minutes to fill out some paperwork. And Brown says the bone marrow donation process is much easier than people think.

"They put an IV in both arms. They take the blood out and it goes into a machine that separates the stem cells and they'll collect the stem cells and the blood goes back into the arm," she said.

A process Chandler says he now realizes the importance of -- he wishes he could help Leslie Harris, a young Arkansas mother given 6 months to live without a bone marrow transplant.

"I would give her my bone marrow if I could, and I can't, but there's a million people in the upper East Texas region that could. There's 100,000 people in Tyler that could, with a 15-second swab, can maybe save somebody's life, and the reality is it could actually save someone exactly like me," Chandler said.

If you'd like to attend today's bone marrow drive, it's being held at Heart to Heart Hospice here in Tyler from 1 to 6 pm.

If you'd like to help but can't make it, there are a few ways you can do so.

You can donate to the Chandler family at http://www.comfortforcody.com.

And you can find out more about becoming a bone marrow donor at http://www.getswabbed.org.

Copyright 2012 KLTV. All rights reserved.

Read the rest here:
Bone marrow drive held Wednesday for Tyler doctor

An important new study by a team of scientists at RhinoCyte™ Inc., Louisville, Ky., details promising results on the effectiveness of olfactory (nasal) stem cells in repairing spinal cord damage resulting from the most common cause of these injuries — contusions (bruising) due to major trauma such as is seen in auto accidents, falls or combat. This could have major implication for the estimated 5 million people worldwide affected by spinal cord injuries – 1.275 million of them in the United States alone, where the cost of treatment exceeds $40.5 billion each year.

Louisville, Kentucky (PRWEB) February 22, 2012

An important new study released by a team of scientists at RhinoCyte™ Inc., Louisville, Ky., details promising results on the effectiveness of olfactory (nasal) stem cells in repairing spinal cord damage resulting from the most common cause of these injuries — contusions (bruising) due to major trauma. Their study is featured in the current issue of the Journal of Neurodegeneration and Regeneration.

The study, led by Dr. Fred Roisen, has great implication for the estimated 5 million people worldwide affected by spinal cord injuries – 1.275 million of them in the United States alone, where the cost of treatment exceeds $40.5 billion each year. Current treatment options are limited to retaining and retraining mobility; no drug therapies are available, but studies pertaining to stem cell treatments are showing great promise for these as well as other neurodegenerative conditions.

A previous study by the group made national headlines when lab rats whose spinal cords had been partially cut in the region of the animal’s neck in a way that disabled their front right paws were able to regain significant use of their paws after being injected with olfactory stem cells. The investigative team took the cells from the olfactory neurosensory epithelium — the part of the nose that controls the sense of smell — in adult volunteer donors who were already undergoing elective sinus surgery. The removal of the stem cells has no effect on the patients’ ability to smell. Also, the minimally invasive surgery is frequently done on an outpatient basis so the cells are readily available and, as such, are a potentially promising source of therapeutic stem cells.

The researchers isolated the stem cells and increased their numbers in the laboratory by growing them in an enriched solution. The cells were then injected into a group of lab rats. Twelve weeks later, these animals had regained control of their affected paws while a control group that received no cells had not.

This latest study continued that original work, by concentrating on contusions caused by blunt force trauma such as that resulting from an automobile accident or a fall. Spinal cord and head trauma are common among soldiers suffering serious combat injuries, too.

Two independent sets of experiments were conducted, beginning two weeks after the rats had received contusions administered in a computer-controlled surgery. In the first group, 27 out of 41 rats were injected with olfactory stem cells, while the remainder received none. In the second group, 16 rats were treated with olfactory stem cells, 11 received no treatment and 10 received stem cells grown from human skin to see how the olfactory cells compared with another stem cell source.

The results once again showed great promise, with 40 percent of the rats treated with the olfactory-derived stem cells showing significant improvement after just six weeks, compared to 30 percent of those treated with human skin-derived cells and only 9 percent of those receiving no treatment. In addition, the olfactory stem cell-treated rats showing the highest rate of improvement recovered much faster than the other groups.

“This is very exciting on numerous levels,” said Dr. Roisen. “As an autologous cell source — that is, the patient is both the donor and the recipient — olfactory stem cells bypass the time a patient must wait while a suitable donor is found, which can be critical to the outcome of the patient’s treatment. They also eliminate the need for immunosuppressive drugs, which have numerous negative side effects.

“And just as importantly, stem cells taken from the nose of an adult do away with the ethical concerns associated with using embryonic stem cells.”

The researchers are in the final stages of their enabling studies, which are scheduled to be completed by summer; Phase 1 safety studies could begin as soon as early next year.

Dr. Roisen is chief science officer and co-founder of RhinoCtye™, and a professor and chair of the University of Louisville School of Medicine’s Department of Anatomical Sciences and Neurobiology. The original work forming the basis for the contusion study was conducted by Dr. Roisen’s group at UofL and has been licensed to RhinoCtye™ (http://www.rhinocyte.com), a company he co-founded in 2005 with Dr. Chengliang Lu and Dr. Kathleen Klueber to develop and commercialize diagnostic tools and therapies for stem cell treatment of multiple degenerative and traumatic neurological diseases. RhinoCyte™ currently has three patents for olfactory stem cell treatments approved in the United States, Australia and Israel, with others pending worldwide.

###

Laurel Harper
Laurel92@msn.com
502-550-0089
Email Information

Read more:
Nasal Stem Cells Show Promise in Repairing Spinal Cord Damage Caused by Contusion

Monkeys suffering from Parkinson's disease show a marked improvement when human embryonic stem cells are implanted in their brains, in what a Japanese researcher said Wednesday was a world first.

A team of scientists transplanted the stem cells into four primates that were suffering from the debilitating disease.

The monkeys all had violent shaking in their limbs -- a classic symptom of Parkinson's disease -- and were unable to control their bodies, but began to show improvements in their motor control after about three months, Kyoto University associate professor Jun Takahashi told AFP.

About six months after the transplant, the creatures were able to walk around their cages, he said.

"Clear improvements were confirmed in their movement," he said.

Parkinson's disease is a progressive neurological illness linked to a decrease in dopamine production in the brain. There is currently no medical solution to this drop off in a key neurotransmitter.

The condition, which generally affects older people, gained wider public recognition when Hollywood actor Michael J. Fox revealed he was a sufferer.

Takahashi said at the time of the implant about 35 percent of the stem cells had already grown into dopamine neuron cells, with around 10 percent still alive after a year.

He said he wants to improve the effectiveness of the treatment by increasing the survival rate of dopamine neuron cells to 70 percent.

"The challenge before applying it to a clinical study is to raise the number of dopamine neuron cells and to prevent the development of tumours," he said.

"I would like to make this operation more effective and safe" before clinical trials, Takahashi said.

Takahashi said so far he had used embryonic stem cells, which are harvested from foetuses, but would likely switch to so-called Induced Pluripotent Stem (iPS) cells, which are created from human skin, for the clinical trial.

His team, which has also transplanted iPS cells into monkeys, are now looking to see if the primates with Parkinson's disease show similar improvements in their motor control.

Scientists say the use of human embryonic stem cells as a treatment for cancer and other diseases holds great promise, but the process has drawn fire from religious conservatives, among others.

Opponents say harvesting the cells, which have the potential to become any cell in the human body, is unethical because it involves the destruction of an embryo.

The Japanese government currently has no guidelines on the use of human stem cells in clinical research.

In October last year, the Court of Justice of the European Union banned the patenting of stem cells when their extraction causes the destruction of a human embryo, a ruling that could have repercussions on medical research.

Scientists warned that the ruling would damage stem cell research in Europe, while the Catholic church hailed it as a victory for the protection of human life.

See more here:
Stem cell implants boost monkeys with Parkinson's

Global leader in animal stem cell technology is poised for significant expansion through new partnership with top U.S. companion animal health distribution company.

Las Vegas, Nevada (PRWEB) February 22, 2012

MediVet-America, the global leader in veterinary stem cell technology and regenerative medicine, has entered into a distribution partnership with Butler Schein Animal Health, a division of Henry Schein, the leading companion animal health distribution company in the U.S., to sell and distribute stem cell kits and equipment to veterinarians serving the nation’s fast-growing $50 billion pet industry.

The announcement was made today at the Western Veterinary Conference in Las Vegas by Jeremy Delk, CEO of MediVet-America.

The two companies will partner to sell and distribute MediVet-America’s advanced stem cell technology to more than 26,000 veterinary clinics nationwide. Adult animal stem cell technology uses the body’s own regenerative healing power to help treat dogs, cats, horses and other animals suffering from painful arthritis, hip dysplasia and tendon, ligament and cartilage injuries and other ailments.

The Adipose-Derived Stem Cell Procedure Kit and state of the art equipment, co-developed with Medical Australia, enable veterinarians to remove a small sample of fat, separate the stem cells, then activate and inject them into affected areas.

“We are pleased to be teaming up with Butler Schein, the largest companion animal health distribution company in the nation,” said Delk. “Their strong track record in sales and distribution will further fuel our rapid growth and bring this breakthrough technology to more leading veterinary practices across the country.”

To introduce the distribution partnership, Delk said MediVet-America has developed an exclusive program of product and service offers that will be made available only to Butler Schein customers.

Veterinary practitioners in more than 200 markets throughout 42 states now perform the drug-free procedure entirely in their own clinics more quickly, effectively and economically than earlier generation animal stem cell therapy. MediVet-America’s new treatment, developed in Australia, is available in 26 countries worldwide.

“This exciting partnership will allow even more of our colleagues unparalleled access to MediVet-America’s superior technology, providing the most affordable and efficacious stem cell therapy in the industry,” said Mike Hutchinson, D.V.M., the world’s leading animal stem cell practitioner. Dr. Hutchinson, who has spoken around the world about stem cell therapy, most recently in Tokyo, has performed more than 300 procedures over the last 18 months in his practice near Pittsburgh, PA.

Partnering with the leading animal health manufacturers in the world, Butler Schein maintains an order-fill ratio greater than 98 percent, and is positioned to bring the broadest selection of veterinary products and strategic business solutions to veterinarians, including:

    A comprehensive product offering for companion animal, equine and large animal practices including biologicals, diagnostics, nutritionals, parasiticides and pharmaceuticals

    Technology hardware and software solutions     Capital equipment, supply products and repair services     Practice design and remodeling, client marketing and financial solutions

Stem cells are basic biological cells with the ability to differentiate into specialized tissue cells and regenerate new cells to replace or repair damaged tissue. The stem cells used in veterinary medicine are not embryonic, which have attracted controversy over the years, but are taken from adipose (fat) tissue of the adult animal.

Americans spent an estimated $50.8 billion in 2011 on their companion animals, according to the American Pet Products Association, up from $28.5 billion in 2001. MediVet-America’s stem cell treatment costs about $1,800 for small animals, $2,400 for horses. Stem cells also can be frozen and banked for future use through MediVet Lab Services.

MEDIVET-AMERICA

A research and development company and global leader in veterinary stem cell technology, MediVet-America provides innovative cell applications for the therapeutic care of animals. Headquartered in Nicholasville, Kentucky, MediVet-America develops advanced cellular designed kits and services for the treatment of arthritis and degenerative joint disease. The company also offers MediVet Lab Services in multiple locations around the world that provides technical support for in-house stem cell vets, as well as regional and national Adipose stem cell processing and cryo banking services for pets at a young age or for a maintenance program, autologous conditioned serum processing, and cell counting for in-house stem cell procedures. http://www.MediVet-America.com

BUTLER SCHEIN ANIMAL HEALTH

Butler Schein Animal Health is the leading U.S. companion animal health distribution company. Headquartered in Dublin, Ohio, the company operates through 18 distribution centers and 12 telecenters. Approximately 900 Butler Schein Animal Health team members, including 300 field sales representatives and 200 telesales and customer support representatives, serve animal health customers in all 50 states. http://www.ButlerShein.com

###

Dick Roberts
Roberts Communications
(412) 535-5000
Email Information

See original here:
MediVet-America Partners With Butler Schein Animal Health to Distribute World's Leading Animal Stem Cell Technology to ...