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Scientists Report First Success in Cloning Human Stem Cells

Posted: May 17, 2013 at 8:46 am

Its been 17 years since Dolly the sheep was cloned from a mammary cell. And now scientists applied the same technique to make the first embryonic-stem-cell lines from human skin cells.

Ever since Ian Wilmut, an unassuming embryologist working at the Roslin Institute just outside Edinburgh stunned the world by cloning the first mammal, Dolly, scientists have been asking: Could humans be cloned in the same way? Putting aside the ethical challenges the question raised, the query turned out to involve more wishful thinking than scientific success. Despite the fact that dozens of other species have been cloned using the technique, called nuclear transfer, human cells have remained stubbornly resistant to the process.

Until now. Shoukhrat Mitalipov, a professor at Oregon Health & Science University, and his colleagues report in the journal Cell that they have successfully reprogrammed human skin cells back to their embryonic state. The purpose of the study, however, was not to generate human clones but to produce lines of embryonic stem cells. These can develop into muscle, nerve, or other cells that make up the bodys tissues. The process, he says, took only a few months, a surprisingly short period to reach such an important milestone.

(MORE:Stem-Cell Research: The Quest Resumes)

Nuclear transfer involves inserting a fully developed cell in Mitalipovs study, the cells came from the skin of fetuses into the nucleus of an egg, and then manipulating the egg to start dividing, a process that normally only occurs after it has been fertilized by a sperm. After several days, the ball of cells that results contains a blanket of embryonic stem cells endowed with the genetic material of the donor skin cell, which have the ability to generate every cell type from that donor. In Dollys case, those cells were allowed to continue developing into an embryo that was then transferred to a ewe to produce a cloned sheep. But Mitalipov says his process with the human cells isnt designed to generate a human clone, but rather just to create the embryonic stem cells. These could then be manipulated to create heart, nerve or other cells that can repair or treat disease.

I think this is a really important advance, says Dieter Egli, an investigator at the New York Stem Cell Foundation. I have a very high confidence that versions of this technique will work very well; its something that the field has been waiting for. Egli is among the handful of scientists who have been working to perfect the technique with human cells and, in 2011, succeeded in producing human stem cells, but with double the number of chromosomes. In 2004, Hwang Woo-suk, a veterinary scientist at Seoul National University, claimed to have succeeded in achieving the feat, but later admitted to faking the data. Instead of generating embryonic-stem-cell lines via nuclear transfer, Hwangs group produced the stem cells from days-old embryos, a technique that had already been established by James Thomson at University of Wisconsin in 1998.

That scandal, as well as ethical concerns about the dangers of encouraging work that could lead to human cloning, dried up interest in getting the process to work with human cells. Then came a breakthrough in 2007, when Shinya Yamanaka of Kyoto University succeeded in reprogramming adult skin cells back to their embryonic state simply by dousing them in a concoction of four genetic factors and some growth media. That technique for generating embryonic-like stem cells (called induced pluripotent stem cells, or iPS cells) bypassed the need for transferring the cells into eggs, as Wilmut had done, and also averted the ethical issues attached to extracting stem cells from embryos as Thomson had done. Plus, the iPS cells had the advantage that patients could generate their own stem cells and potentially grow new cells they might need to treat or avert diseases like diabetes, Alzheimers or heart problems.

Except that researchers still couldnt prove that the heart, nerve, muscle and other cells they made from the iPS cells were exactly like the ones generated from the embryonic stem cells. The gold standard embryonic stem cells still came from embryos themselves, including ones that were made through nuclear transfer.

(MORE: Stem-Cell Miracle? New Therapies May Cure Chronic Conditions Like Alzheimers)

Now that the technique appears to work with human cells, the process could be another source of generating stem cells that may ultimately treat patients, says Mitalipov. His group is especially interested in promoting the technique for treating mitochondrial diseases these organelles posses a different set of DNA than that contained in the nucleus of cells, and are responsible for generating the energy needed for cells to function. But because they lie outside the nucleus, transferring cells from a patient with mitochondrial diseases into a donor egg that has a healthy set of mitochondrial DNA would generate populations of cells that are free of disease.

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Scientists Report First Success in Cloning Human Stem Cells

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US researchers make embryonic stem cells from skin

Posted: May 17, 2013 at 8:46 am

US researchers have reported a breakthrough in stem cell research, describing how they have turned human skin cells into embyronic stem cells for the first time.

The method described Wednesday by Oregon State University scientists in the journal Cell, would not likely be able to create human clones, said Shoukhrat Mitalipov, senior scientist at the Oregon National Primate Research Center.

But it is an important step in research because it does not require the use of embryos in creating the type of stem cell capable of transforming into any other type of cell in the body.

The technique involves transplanting an individual's DNA into an egg cell that has been stripped of genetic material, a variation of a method called somatic cell nuclear transfer.

"A thorough examination of the stem cells derived through this technique demonstrated their ability to convert just like normal embryonic stem cells, into several different cell types, including nerve cells, liver cells and heart cells," said Mitalipov.

He added that since the reprogrammed cells use genetic material from the patient, there is no concern about transplant rejection.

"While there is much work to be done in developing safe and effective stem cell treatments, we believe this is a significant step forward in developing the cells that could be used in regenerative medicine," Mitalipov said.

Another advantage of this approach is that it does not use fertilized embryos to obtain stem cells, a technique that raises major ethical issues because the embryo is destroyed.

Since the birth of the sheep Dolly in 1996 in the United Kingdom, the first cloned animal, researchers have cloned some 20 species including goats and rabbits, but never monkeys or primates whose biologies and reproduction is more complex.

Years of research on monkey cells using the same technique have not successfully produced any monkey clones.

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US researchers make embryonic stem cells from skin

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Researchers make embryonic stem cells from skin

Posted: May 17, 2013 at 8:46 am

US researchers have reported a breakthrough in stem cell research, describing how they have turned human skin cells into embryonic stem cells for the first time.

The method described Wednesday by Oregon Health and Science University scientists in the journal Cell, would not likely be able to create human clones, said Shoukhrat Mitalipov, senior scientist at the Oregon National Primate Research Center.

But it is an important step in research because it does not require the use of embryos in creating the type of stem cell capable of transforming into any other type of cell in the body.

The technique involves transplanting an individual's DNA into an egg cell that has been stripped of genetic material, a variation of a method called somatic cell nuclear transfer.

"A thorough examination of the stem cells derived through this technique demonstrated their ability to convert just like normal embryonic stem cells, into several different cell types, including nerve cells, liver cells and heart cells," said Mitalipov.

He added that since the reprogrammed cells use genetic material from the patient, there is no concern about transplant rejection.

"While there is much work to be done in developing safe and effective stem cell treatments, we believe this is a significant step forward in developing the cells that could be used in regenerative medicine," Mitalipov said.

Another advantage of this approach is that it does not use fertilized embryos to obtain stem cells, a technique that raises major ethical issues because the embryo is destroyed.

Since the birth of the sheep Dolly in 1996 in the United Kingdom, the first cloned animal, researchers have cloned some 20 species including goats and rabbits, but never monkeys or primates whose biologies and reproduction is more complex.

Years of research on monkey cells using the same technique have not successfully produced any monkey clones.

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Researchers make embryonic stem cells from skin

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Scientists Use Cloning Technique to Produce Human Stem Cells

Posted: May 17, 2013 at 8:46 am

WEDNESDAY, May 15 (HealthDay News) -- Scientists report they've used a cloning technique to reprogram an ordinary human skin cell to become an embryonic stem cell. In turn, the new stem cell has the potential to transform into any type of cell in the body.

Besides marking a breakthrough in stem cell technology, which has the potential to one day cure a myriad of illnesses, the achievement has some concerned that scientists are moving a step closer to human cloning.

That's because the new stem cell is genetically identical to cells from the person from whom it was derived. Stem cells can differentiate into cells for all of the tissue types that the body needs, such as nerves, muscle and bone.

While Dolly the Sheep was cloned in 1996, and other species have been cloned since, researchers have been unable to clone a primate such as a monkey, chimpanzee or human. However, the technological advances described in the new study are such that "it's a matter of time before they produce a cloned monkey," Jose Cibelli, a cloning expert at Michigan State University who wasn't involved in the study, told the Wall Street Journal.

The new research was published online May 15 in the journal Cell, and was led by Shoukhrat Mitalipov, a senior scientist at the Oregon National Primate Research Center, in partnership with researchers at Oregon Health & Science University (OHSU).

The research involved a version of what's known as somatic cell nuclear transfer, where the cell's nucleus -- which contains all a person's genetic information -- is transferred into an egg cell that has had all of its DNA removed. Once the new nucleus is in place, the unfertilized egg cell proceeds to develop and produce stem cells, according to an OHSU news release.

"Stem cells derived through this technique demonstrated their ability to convert just like normal embryonic stem cells, into several different cell types, including nerve cells, liver cells and heart cells," Mitalipov said in the news release. "While there is much work to be done in developing safe and effective stem cell treatments, we believe this is a significant step forward in developing the cells that could be used in regenerative medicine."

Regenerative medicine is the term used to describe therapies where stem cells are used to regenerate tissues lost to illness or injury.

One key point in the new research: Creation of the new, functioning embryonic stem cell did not involve the use of fertilized embryos, the focus of heated debate over the past decade.

Mitalipov's team says the road to success was not easy, because human egg cells seem to be more fragile than those from other species. That meant that methods had to be tested in monkeys first, in a trial-and-error fashion, before moving to human eggs.

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Scientists Use Cloning Technique to Produce Human Stem Cells

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Scientists clone human stem cells for the first time

Posted: May 17, 2013 at 8:46 am

For all its promise, embryonic stem cell research has been slow going in the last few decades. Ethical quandaries and scientific difficulty have conspired to keep the next big advance just out of reach, but a new study published this week in the journal Cell could kick off a new age of interest in stem cell therapies. Researchers from Oregon Health & Science University have managed to clone human embryonic stem cells using unfertilized eggs and human skin cells.

The process is very similar to the method used over a decade ago to clone Dolly the sheep, but the aim here was not to produce a human clone. Rather, scientists wanted to make a line of stem cells that would not be rejected by a recipients own immune system, In fact, according to Professor Shoukhrat Mitalipov from Oregon Health & Science University, it is unlikely the embryos used in the study had any hope of developing into viable human clones.

To create these new stem cell lines, researchers removed the DNA from donated unfertilized human eggs. A skin cell from a different individual was then inserted into the egg cell. The trick that made this advance possible is in finding a way to entice that cell to begin dividing. Mitalipov and his team eventually found that exposure to precisely-timed electric pulses and a chemical bath with a bit of caffeine did the trick.

The result is a small bundle of embryonic stem cells that match the genotype of the skin cell donor, not the egg donor. Stem cells created in this process are known as pluripotent, because they can differentiate to become a wide variety of cell types. They could conceivably be turned into cardiac muscle, nerve cells, pancreatic cells, or any number of other tissues to treat disease.

Additionally, the maturation process is well established for the cells in this study. They actually appear to become functional adult cells when harvested. Researchers even managed to create cardiac cells that contract just like the real thing. Previous stem cell discoveries using only regressed skin cells come with many unanswered questions, thus the continued use of human embryos.

Having a way to manufacture stem cells that match a persons DNA is revolutionary in stem cell therapy. If you implant cells that dont match someones genotype, they are likely to be rejected. This is why transplant patients must take immunosuppressive drugs. This process could lead to treatments where doctors create new tissues to treat patients that are essentially their own cells.

Other researchers are anxious to attempt the process themselves, and hopefully confirm Mitalipovs results. The entire paper is online if you want to check it out.

Now read:Scientists end our dreams of cloning dinosaurs

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Scientists clone human stem cells for the first time

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Stem cells’ breakthrough in cloned human embryos

Posted: May 17, 2013 at 8:46 am

Stem cells breakthrough in cloned human embryos

(WAM) / 17 May 2013

Scientists have finally recovered stem cells from cloned human embryos, a longstanding goal that could lead to new treatments for such illnesses as Parkinsons disease and diabetes.

A prominent expert called the work a landmark, but noted that a different, simpler technique now under development may prove more useful.

Stem cells can turn into any cell of the body, so scientists are interested in using them to create tissue for treating disease. Transplanting brain tissue might treat Parkinsons disorder, for example, and pancreatic tissue might be used for diabetes.

But transplants run the risk of rejection, so more than a decade ago, researchers proposed a way around that: Create tissue from stem cells that bear the patients own DNA, obtained with a process called therapeutic cloning.

If DNA from a patient is put into a human egg, which is then grown into an early embryo, the stem cells from that embryo would provide a virtual genetic match. So in theory, tissues created from them would not be rejected by the patient.

That idea was met with some ethical objections because harvesting the stem cells involved destroying human embryos.

Scientists have tried to get stem cells from cloned human embryos for about a decade, but theyve failed. Generally, thats because the embryos stopped developing before producing the cells. In 2004, a South Korean scientist claimed to have got stem cells from cloned human embryos, but that turned out to be a fraud.

In Wednesdays edition of the journal Cell, however, scientists in Oregon report harvesting stem cells from six embryos created from donated eggs. Two embryos had been given DNA from skin cells of a child with a genetic disorder, and the others had DNA from fetal skin cells.

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Stem cells’ breakthrough in cloned human embryos

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Cytomedix to Present at the World Stem Cells & Regenerative Medicine Congress 2013

Posted: May 17, 2013 at 8:46 am

GAITHERSBURG, MD--(Marketwired - May 17, 2013) - Cytomedix, Inc. (OTCQX: CMXI), a regenerative therapies company commercializing and developing innovative platelet and adult stem cell technologies, announced today that Edward Field, the Company's Chief Operating Officer, has been invited to make a presentation on Partnering & Collaboration at the World Stem Cells & Regenerative Medicine Congress 2013, which will be held May 21-23, 2013 in London, United Kingdom.

Presentation Details

Time: Tuesday, May 21, 2013 @ 11:55am BST (6:55 am EST)

Track Title: Commercialisation through Collaboration: What Does Partnering In This Industry Actually Look Like?

Location: Victoria Park Plaza Hotel, London, UK

During the presentation, Mr. Field will highlight Cytomedix's two collaborations that are advancing clinical stage therapies.The first is a collaboration with the National Institute of Health (NIH) and the Cardiovascular Cell Therapy Research Network (CCTRN) for conduct of the PACE study, an 80 patient, double-blind, placebo-controlled clinical trial designed to look at the safety and efficacy of ALD-301 in peripheral artery disease patients diagnosed with intermittent claudication.This is the first ever randomized clinical trial to look at the benefits of autologous stem cell therapy in this indication.The second collaboration is with Duke University Medical Center, which is conducting a Phase 1 clinical study with ALD-451 in patients that have been treated for glioblastomas, which is the most aggressive form of brain cancer.This open-label study is designed to enroll up to 12 patients and is intended to demonstrate the safety and feasibility of ALD-451 when administered intravenously in patients with grade IV malignant glioma following surgery, radiation therapy and treatment with temozolomide.

About the World Stem Cells Regenerative Medicine Congress 2013The World Stem Cells & Regenerative Medicine Congress 2013 is Europe's largest and most senior conference for the stem cell research and regenerative medicine community.It is now in its 8th year. Topics covered will include streamlining clinical development, commercialising a stem cell-based therapy and exploiting alternative sources of funding. For more information please visit: http://www.terrapinn.com/2013/stemcells/index.stm.

About Cytomedix, Inc. Cytomedix, Inc. is a fully integrated regenerative medicine company commercializing and developing innovative platelet and adult stem cell separation products that enhance the body's natural healing processes. The Company's advanced autologous technologies offer clinicians a new treatment paradigm for wound and tissue repair. The Company's patient-derived PRP systems are marketed by Cytomedix in the U.S. and distributed internationally. Our commercial products include the AutoloGel System, cleared by the FDA for wound care and the Angel Whole Blood Separation System. The Company is developing novel regenerative therapies using our proprietary ALDH Bright Cell ("ALDH") technology to isolate a unique, biologically active population of a patient's own stem cells. A Phase 2 trial evaluating the use of ALDHbr for the treatment of ischemic stroke is underway. For additional information please visit http://www.cytomedix.com.

Safe Harbor Statement - Statements contained in this press release not relating to historical facts are forward-looking statements that are intended to fall within the safe harbor rule for such statements under the Private Securities Litigation Reform Act of 1995. The information contained in the forward-looking statements is inherently uncertain, and Cytomedix' actual results may differ materially due to a number of factors, many of which are beyond Cytomedix' ability to predict or control, including among many others, risks and uncertainties related to the Company's ability to successfully execute its Angel and AutoloGel sales strategies, to achieve AutoloGel expected reimbursement rates in 2013, to meet its stroke trial enrollment rates, the Company's ability to successfully integrate the Aldagen acquisition, the Company's ability to expand patient populations as contemplated, its ability to provide Medicare patients with access as expected, the Company's expectations of favorable future dialogue with potential strategic partners, and its ability to successfully manage contemplated clinical trials, to manage and address the capital needs, human resource, management, compliance and other challenges of a larger, more complex and integrated business enterprise, viability and effectiveness of the Company's sales approach and overall marketing strategies, commercial success or acceptance by the medical community, competitive responses, the Company's ability to raise additional capital and to continue as a going concern, and Cytomedix's ability to execute on its strategy to market the AutoloGel System as contemplated. To the extent that any statements made here are not historical, these statements are essentially forward-looking. The Company uses words and phrases such as "believes," "forecasted," "projects," "is expected," "remain confident," "will" and/or similar expressions to identify forward-looking statements in this press release. Undue reliance should not be placed on forward-looking information. These forward-looking statements are subject to known and unknown risks and uncertainties that could cause actual events to differ from the forward-looking statements. More information about some of these risks and uncertainties may be found in the reports filed with the Securities and Exchange Commission by Cytomedix, Inc. Cytomedix operates in a highly competitive and rapidly changing business and regulatory environment, thus new or unforeseen risks may arise. Accordingly, investors should not place any reliance on forward-looking statements as a prediction of actual results. Except as is expressly required by the federal securities laws, Cytomedix undertakes no obligation to update or revise any forward-looking statements, whether as a result of new information, changed circumstances or future events or for any other reason. Additional risks that could affect our future operating results are more fully described in our U.S. Securities and Exchange Commission filings, including our Annual Report for the year ended December 31, 2012, as amended to date, and other subsequent filings. These filings are available at http://www.sec.gov.

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Cytomedix to Present at the World Stem Cells & Regenerative Medicine Congress 2013

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TaiGen Biotechnology Announces Submission of New Drug Application for Nemonoxacin in Taiwan and Mainland China

Posted: May 17, 2013 at 8:44 am

TAIPEI, Taiwan, May 16, 2013 /PRNewswire/ --TaiGen Biotechnology Company, Limited ("TaiGen") today announced that they have submitted New Drug Application (NDA) for the oral formulation of nemonoxacin with the Taiwan Food and Drug Administration (TFDA) and China Food and Drug Administration (CFDA). Approval is expected in the first half of 2014. Nemonoxacin is the first pharmaceutical product to fall under the Cross-Strait Cooperation Agreement on Medicine and Public Health Affairs of the Economic Cooperation Framework Agreement (ECFA) between Taiwan and mainland China. It is also the first new drug from Taiwan to meet the requirements of CFDA's Category 1.1 New Drug. Drugs under this classification have to be new chemical entities (NCEs) that have not been marketed in any country in the world. Nemonoxacin, thus, represents a landmark in the continued development of cross-strait relationship between the pharmaceutical industry and regulatory agencies.

Nemonoxacin is a NCE, broad spectrum antibiotic with excellent efficacy and safety profile. The NDA submission for nemonoxacin is supported by a pivotal Phase 3 trial with 532 patients in community-acquired pneumonia (CAP). The trial was conducted in both Taiwan and mainland China (441 patients from mainland China and 91 patients from Taiwan) that met all primary and secondary endpoints including non-inferiority to the comparator, levofloxacin. TaiGen is currently conducting Phase 2 trial for the intravenous formulation of nemonoxacin in moderate to severe CAP patients. In addition to CAP, nemonoxacin has also shown efficacy in diabetic foot infections in a Phase 2 trial conducted in the US, Taiwan, and South Africa. In the clinical trials conducted to this point, nemonoxacin have demonstrated excellent activity against drug-resistant bacteria such as methicillin-resistant Staphylococcus aureus (MRSA) and quinolone-resistant MRSA as well as quinolone-resistant Streptococcus pneumoniae. TaiGen owns the worldwide patent portfolio of nemonoxacin that protects composition, use, and processes until 2029.

Dr. Ming-Chu Hsu, President and Chief Executive Officer of TaiGen, said, "Since the founding of TaiGen, we have been focusing on the development of First-in-class and Best-in-class novel drugs. The submission of the NDA for nemonoxacin is the culmination of efforts by our experienced management team and all the staff at TaiGen. I am very pleased with the groundbreaking achievement of using one NDA dossier for submissions to TFDA and CFDA. Not only nemonoxacin is our first product to the market, it is also an indication that a world class medicine can be discovered and developed in Taiwan. TaiGen is well positioned to advance in the world's fastest pharmaceutical market, mainland China."

In June 2012, TaiGen signed an agreement with Zhejiang Medicine Company, Limited ("ZMC") to out-license the exclusive marketing and manufacturing rights of nemonoxacin in China. ZMC is a leading manufacturer and marketer of antibiotics in China and is a publicly listed company in the Shanghai Stock Exchange. This partnership combines TaiGen's R&D expertise and ZMC's antibiotic marketing knowhow to compete in China's US$11 billion antibiotic market.

About TaiGen Biotechnology

TaiGen Biotechnology is a leading research-based and product-driven biotechnology company in Taiwan with a wholly-owned subsidiary in Beijing, mainland China. In addition to nemonoxacin, TaiGen has two other in-house discovered NCEs in clinical development under IND with US FDA: TG-0054, a chemokine receptor antagonist for stem cell transplantation and chemosensitization, in Phase 2 and TG-2349, a HCV protease inhibitor for treatment of chronic hepatitis infection, in Phase 2. Both TG-0054 and TG-2349 are currently in clinical trials in patients in the US.

Disclaimer

Certain statements in this press release are forward-looking. These statements may be identified by the use of forward-looking words such as "anticipate," "believe," "forecast," "estimated" and "intend," among others. These forward-looking statements are based on TaiGen's current expectations and actual results could differ materially. There are a number of factors that could cause actual events to differ materially from those indicated by such forward-looking statements. These factors include, but are not limited to, substantial competition; our need for additional financing; uncertainties of patent protection and litigation; uncertainties of government or third party payer reimbursement; limited sales and marketing efforts and dependence upon third parties; and risks related to failure to obtain regulatory authority clearances or approvals and noncompliance with regulatory regulations. As with any drugs under development, there are significant risks in the development, regulatory approval and commercialization of new products. There are no guarantees that future clinical trials discussed in this press release will be completed or successful or that any product will receive regulatory approval for any indication or prove to be commercially successful. TaiGen does not undertake an obligation to update or revise any forward-looking statement.

TaiGen Contact:

Peter W. Tsao, PhD, Vice President ofBusiness Development Tel: +886-2-8177-7072 ext 1705 ptsao@taigenbiotech.com.tw

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TaiGen Biotechnology Announces Submission of New Drug Application for Nemonoxacin in Taiwan and Mainland China

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Oregon-style Stem Cell Cloning Research Illegal in California: No Pay for Eggs in Golden State

Posted: May 16, 2013 at 11:42 pm

The good news out of Oregon is that
some diligent scientists in the Beaver State have accomplished a
major advance in stem cell research --- the cloning of human stem
cells.

That bad news is that their research
would have been illegal in California, and probably will be banned
for decades, if not longer – thanks to Proposition 71 of 2004.
The proposition was the ballot
initiative that created the $3 billion California stem cell agency,
which is hailed internationally as being one of the world leaders in
financing stem cell science. Unfortunately, the 10,000-word
initiative also contains language that was aimed at winning voter
approval of the measure -- not promoting good science.
The team writing the initiative, led by
Robert Klein, the former and first chairman of the stem cell agency,
put in a provision that made it illegal to pay women for their eggs.
The Oregon researchers paid women $3,000 to $7,000 each for their eggs, reflecting the current market rate based on prices paid in
connection with IVF. In some cases for IVF, the compensation is
dramatically higher. (See here and here.) Stem cell researchers in
recent years in the United States have found that they cannot secure
an adequate number of donors without matching IVF donor compensation.
While compensation for eggs is a matter
of some controversy, strong cases have been made that women
should make their own decisions about selling their eggs – not the what some call the nanny state. Of course, that should occur under well-regulated
situations. But Proposition 71 backers wanted to remove any possible
campaign objections by opponents of stem cell research, and so they
inserted the ban along with management minutia and other dubious
material.
Can't that be changed, one might ask?
Not without a herculean effort. That means another ballot measure or
a super, super majority vote in the California legislature plus the
signature of the governor. Imagine a measure on the ballot to
allow women to sell their eggs. The uproar would be heard
internationally. In 2004, when Proposition 71 was approved, it would
have been better to leave the compensation issue unaddressed. Then it
could have been dealt with through regulation or normal legislation,
both of which are far more flexible than ballot measures that alter
the state Constitution and state law.
Our quick and limited survey of the
news coverage indicated that many of the mainstream media stories
omitted the price of the eggs, which may suggest that the issue of
compensation is becoming moot.
In related news about the Oregon
accomplishment, UC Davis stem cell researcher Paul Knoepfler has
posted a good look at the some of the misinformation that is
surfacing on the Internet about the research, including its
implications.
He said,

“Keep in mind that on day one of the
iPS cell era in the stem cell field we had a huge number of
misconceptions because we simply had so much to learn. Same is true
here.”

Jessica Cussins over at the
Berkeley-based Biopolitical Times also has a solid roundup of the
coverage of the Oregon research and the analysis of its significance.
Here are links to two blog items from
the California stem cell agency on the Oregon research, including one
dealing with “cloning hysteria” and a more general look.

Source:
http://feedproxy.google.com/~r/blogspot/uqpFc/~3/A4AXZfPs3dc/oregon-style-stem-cell-cloning-research.html

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Apple Cell Serum Review – Apple Stem Cells Aging Creams Offer Hope for Aging and Damaged Skin – Video

Posted: May 16, 2013 at 5:45 am


Apple Cell Serum Review - Apple Stem Cells Aging Creams Offer Hope for Aging and Damaged Skin
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Apple Cell Serum Review - Apple Stem Cells Aging Creams Offer Hope for Aging and Damaged Skin - Video

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