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Supreme Essence of Torricelumn 3 – Video

Posted: January 17, 2013 at 1:41 am


Supreme Essence of Torricelumn 3
Watch how Elizabeth Grant Skin Care #39;s new Supreme Essence of Torricelumn trade; works on the epidermal structure to revive the look of aging skin. Elizabeth Grant #39;s original superior moisturizing compound is enhanced with advanced stem cell technology and amino acids to create a supreme skin care treatment. Plant stem cells contain molecules that can help to repair and rejuvenate the skin #39;s systems through superior antioxidant activity and soothing anti-inflammatory properties. Amino acids, known as #39;the building blocks of life #39;, are essential to the #39;Natural Moisturizing Factor #39;, which helps to maintain a healthy skin barrier. A healthy skin barrier is important to help retain moisture and block the entry of foreign particles, which may damage skin. An original ground-breaking formula, advanced by superior innovative ingredients.

By: babywitz

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Supreme Essence of Torricelumn 3 - Video

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MSstationRadio Promo February 5th, 2013 – Video

Posted: January 17, 2013 at 1:41 am


MSstationRadio Promo February 5th, 2013
Dr. Neil Riordan, PhD will educate us about Stem Cells.

By: judilecoq

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Moiz Mohammed – Immunosuppressive Effects of Mesenchymal Stem Cells in Neonates – Video

Posted: January 17, 2013 at 1:41 am


Moiz Mohammed - Immunosuppressive Effects of Mesenchymal Stem Cells in Neonates
Rutgers #39; Molecular Biology undergraduate, Moiz Mohammed discusses his research on Bronchopulmonary Dysplasia, a lung disease found in premature babies.

By: Rutgers

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Moiz Mohammed - Immunosuppressive Effects of Mesenchymal Stem Cells in Neonates - Video

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AFTER SHIPPING IN PETAKA G3 – Video

Posted: January 17, 2013 at 1:41 am


AFTER SHIPPING IN PETAKA G3
Simple method of shipping without dry-ice and expanding mammalian cells including stem cells

By: PetakaTechnology

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Katie M Stem Cell Research Infomercial – Video

Posted: January 17, 2013 at 1:41 am


Katie M Stem Cell Research Infomercial
Infomercial for AP Lang

By: skatepunk23ify

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California Stem Cell Face-Off: CIRM Directors Wrestle with Tough IOM Recommendations

Posted: January 16, 2013 at 11:50 pm

Two days next week at the posh
Claremont Hotel in the Berkeley hills could settle the fate of
California's $3 billion stem cell agency.

At 9 a.m. next Wednesday, the governing
board of the state research effort will begin a critical, two-day
public session. On the table will be the $700,000, blue-ribbon
report from the prestigious Institute of Medicine (IOM). The study
recommends sweeping changes in the structure and operations of the
California Institute of Regenerative Medicine (CIRM), as the stem
cell agency is formally known.
The IOM report alone poses major
challenges for the agency. But the recommendations are freighted with
even more significance. Below the surface lies the hard fact of
CIRM's dwindling resources and possible demise. In less than four
years – without either renewed public support or private
contributions – the research effort will begin a shriveling,
downward spiral.
Claremont Hotel

The IOM report places a special burden
on the agency governing board. The board paid the IOM to evaluate its
performance. In 2010, then CIRM Chairman Robert Klein trumpeted the
value of an IOM study, saying it would serve as a springboard for a
new, multibillion-dollar state bond measure for the agency(see here and here). Given the
state's difficult financial condition – not to mention the position
of potential private sector investors – winning approval of that
kind of investment will be more than difficult. 

California's major newspapers already have editorially backed the IOM proposals. Indeed, if the
directors choose to ignore the major IOM recommendations, they will
hand opponents a devastating weapon, one that could be used to convince voters to reject
any proposal for continued funding. The board
would also give private investors more major reasons to say no to
CIRM pitches for cash.
Under Klein's leadership, the 29-member
board has rejected similar proposals for changes in the past. When
the IOM presented the study to the board just last month, the
reception was not much different. Several board members bristled. One
influential board member, Sherry Lansing, chair of the University of
California
board of regents, said the directors' “hands are tied”
because some of the recommendations might require a vote of the people. Her comments echoed similar statements from Klein in 2009,
when he said board members would violate their oath of office if they
supported recommendations for changes that he opposed.
The IOM discussion in December,
however, was relatively brief and less than definitive. Klein has
been off the board since June 2011, replaced by Los Angeles bond
financier Jonathan Thomas, who is regarded as a welcome change by a
number of board members.
Nonetheless, the recommendations of the IOM could mean that some members of the board would lose their seats; others would lose important roles in the grant-award process or
within the agency itself. Conflict of interest rules would be
tightened. In some ways, the board would lose power, which would be
shifted to the president. The board would no longer vote on
individual applications – only a slate recommended by reviewers.
Applicants for CIRM awards would be directly affected, being barred
from making the sort of direct and public appeals that clogged the
CIRM board meetings last year. And that would be just the beginning.
Thomas, the CIRM chairman, is expected
to make his recommendations for action on the report, although they
have not yet been posted on the CIRM web site. Under what might be considered “normal” leadership, Thomas would be testing sentiment
among board members via personal conversations and phone calls.
However, in California that would be illegal – a violation of open
meeting laws that bar what are called “serial meetings” at nearly
all public agencies.
Thomas' task is not easy. Rounding up a
majority vote for anything significant among 29 strong-minded
individuals is not simple. But it is even more difficult when facing
a board that has a tradition of consensus management and
oversight.
The site of next week's meetings is
interesting. The nearly 100-year-old, iconic Claremont hotel has a
troubled financial history. It was up for sale for $80 million last
spring but there were no takers. In the early 20th century, the
property on which it is located was lost and won in a checkers game
in Oakland, or so the story goes.
The stakes are also high for the
California stem cell agency. Moves next week by directors could
easily determine whether CIRM becomes nothing more than an
interesting scientific footnote or establishes a path that will lead
it to long-lasting leadership in regenerative medicine.

Source:
http://feedproxy.google.com/~r/blogspot/uqpFc/~3/SS09uwQmVDQ/california-stem-cell-face-off-cirm.html

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NeoStem’s Subsidiary, Progenitor Cell Therapy, Enters Into a Cell Therapy Manufacturing Services Agreement With …

Posted: January 16, 2013 at 6:46 pm

ALLENDALE, N.J. and OXFORD, United Kingdom, Jan. 16, 2013 (GLOBE NEWSWIRE) -- NeoStem, Inc. (NYSE MKT:NBS) and its subsidiary, Progenitor Cell Therapy LLC ("PCT"), together with Adaptimmune Limited and Adaptimmune LLC (collectively, "Adaptimmune"), announced today a Services Agreement under which PCT will provide services to support Adaptimmune's NYESO-1c259-T cell therapy product being developed for multiple oncology indications (for more information with respect to Adaptimmune's clinical trials, see clinicaltrials.gov, identifiers NCT01350401, NCT01343043 and NCT01352286).

PCT's services will include the transfer and qualification of Adaptimmune's manufacturing process for its NYESO-1c259-T cell therapy product candidate at PCT's facility in Allendale, New Jersey and subsequent manufacturing of the product for Adaptimmune's clinical trials.

Adaptimmune develops products containing unique engineered T cell receptors for the treatment of cancer and infectious diseases. The company has a research base in Oxford, UK and a clinical base in Philadelphia, Pennsylvania.

In December, at the American Society of Hematology conference, Adaptimmune announced encouraging preliminary results from its expanded multiple myeloma trial. Related trials in melanoma and sarcoma are also recruiting patients.

PCT is an internationally recognized contract development and manufacturing organization with facilities in Allendale, New Jersey and Mountain View, California. The company has expertise in GMP manufacture for cell therapies, including dendritic cells, stem cells and T cells. Notably, PCT provided manufacturing for the pivotal studies for Dendreon's Provenge(R), the first cell therapy approved for cancer treatment.

"With our sights set on future pivotal trials for our T cell therapy products, we have invested significant effort towards establishing capabilities within Adaptimmune that support expansion of our clinical platform in terms of both scale and compliance with FDA requirements beyond phase I/II. Our relationship with PCT is an important component," said James Noble, Chief Executive Officer of Adaptimmune. "PCT's impressive level of experience in the burgeoning field of cell therapy, combined with their flexible capacity and professionalism, are among the reasons we selected them for this critical role for our T cell product."

"We are excited to enter into this agreement with Adaptimmune, an innovator for T cell therapy to treat cancers," said Robert A. Preti, PhD, President and Chief Scientific Officer of PCT. "Given our extensive experience with technology transfer, process qualification and GMP manufacturing, we feel PCT will be an asset to Adaptimmune as it develops its product for the U.S. commercial market."

Dr. Robin L. Smith, NeoStem's Chairman and Chief Executive Officer, stated that, "PCT's expertise is recognized globally as demonstrated by the services agreement executed with Adaptimmune. As PCT continues to expand its GMP manufacturing capabilities and focus to support the development of an increasingly wide range of cell therapies under development, it remains focused on providing outstanding client services."

About Adaptimmune

Adaptimmune focuses on the use of T cell therapy to treat cancer and infectious disease. It aims to use the body's own machinery -- the T cell -- to target and destroy cancerous or infected cells.

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Stem Cells May Hold Promise for Lou Gehrig’s Disease (ALS)

Posted: January 16, 2013 at 12:50 pm

SAN DIEGO, Jan. 14, 2013 /PRNewswire-USNewswire/ -- Apparent stem cell transplant success in mice may hold promise for people with amyotrophic lateral sclerosis (ALS), or Lou Gehrig's disease. The results of the study will be presented at the American Academy of Neurology's 65th Annual Meeting in San Diego, March 16 to 23, 2013.

"There have been remarkable strides in stem cell transplantation when it comes to other diseases, such as cancer and heart failure," said study author Stefania Corti, MD, PhD, with the University of Milan in Italy and a member of the American Academy of Neurology. "ALS is a fatal, progressive, degenerative disease that currently has no cure. Stem cell transplants may represent a promising avenue for effective cell-based treatment for ALS and other neurodegenerative diseases."

For the study, mice with an animal model of ALS were injected with human neural stem cells taken from human induced pluripotent stem cells (iPSCs). iPSC are adult cells such as skin cells that have been genetically reprogrammed to an embryonic stem cell-like state. Neurons are a basic building block of the nervous system, which is affected by ALS. After injection, the stem cells migrated to the spinal cord of the mice, matured and multiplied.

The study found that stem cell transplantation significantly extended the lifespan of the mice by 20 days and improved their neuromuscular function by 15 percent.

"Our study shows promise for testing stem cell transplantation in human clinical trials," said Corti.

The study was supported by AriSLA - The Italian Foundation for Research on Amyotrophic Lateral Sclerosis (ALS).

Learn more about ALS at http://www.aan.com/patients.

The American Academy of Neurology, an association of more than 25,000 neurologists and neuroscience professionals, is dedicated to promoting the highest quality patient-centered neurologic care. A neurologist is a doctor with specialized training in diagnosing, treating and managing disorders of the brain and nervous system such as Alzheimer's disease, stroke, migraine, multiple sclerosis, brain injury, Parkinson's disease and epilepsy.

For more information about the American Academy of Neurology, visit http://www.aan.com or find us on Facebook, Twitter, Google+ and YouTube.

SOURCE American Academy of Neurology

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Stem Cells May Hold Promise for Lou Gehrig's Disease (ALS)

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Court lifts cloud over embryonic stem cells

Posted: January 16, 2013 at 12:50 pm

Researchers are keen to compare induced pluripotent stem cells (pictured) with their embryonic cousins.

SILVIA RICCARDI/SPL

The US Supreme Courts decision last week to throw out a lawsuit that would have blocked federal funding of all research on human embryonic stem cells cleared the gloom that has hung over the field for more than three years. Yet the biggest boost from the decision might go not to work on embryonic stem (ES) cells, but to studies of their upstart cousins, induced pluripotent stem (iPS) cells, which are created by reprogramming adult cells into a stem-cell-like state.

At first glance, iPS-cell research needs no help. Researchers flocked to the field soon after a recipe for deriving the cells from adult mouse cells was announced in 2006, partly because this offered a way to skirt the thorny ethical issues raised by extracting cells from human embryos. But the real allure of iPS cells was the promise of genetically matched tissues. Adult cells taken from a patient could be used to create stem cells that would, in turn, generate perfectly matched specialized tissues replacement neurons, say for cell therapy. Although the number of published papers from iPS-cell research has not yet caught up with that of ES-cell work (see Inducing a juggernaut), US funding for each approach is now roughly matched at about US$120 million a year.

C. T. Scott et al. Cell 145, 820826 (2011)

But, as iPS cells crop up in ever more labs, ES cells generally cheaper, better behaved and backed by an extra decades worth of data promise to have an important supporting role. Ever since iPS cells were described, researchers have been trying to understand just how similar they are to ES cells. iPS cells begin with different patterns of gene expression, and they can also acquire mutations during the reprogramming process, which means that every iPS cell must be thoroughly evaluated before it can be used in any study. Human ES cells will always be the standard to which other cells will be compared, says Roger Pedersen, who studies how stem cells retain embryo-like states at the University of Cambridge, UK.

Federally supported ES-cell research was shut down in the United States on 23August 2010, a year after a lawsuit was filed by two opponents of human ES-cell research, and remained frozen for more than two weeks (see Fifteen years of controversy). Many investigators shied away from the field for fear of having to shut down again. The Supreme Courts move has reassured investigators such as Candace Kerr, who studies early development of the brain at the University of Maryland School of Medicine in Baltimore. As a young scientist working towards tenure, she felt particularly vulnerable to the threat of ES-cell funding being stopped. So she switched to iPS cells in 2010, while the lawsuit was working its way through the US court system. With the litigation over, she says she need not hesitate or fear adding to her work with experiments using ES cells, which she finds much easier to prompt into neurons than iPS cells. I am excited and relieved by this decision, she says.

The tussles over whether or not US federal funds can be used for research involving human embryonic stem cells have a long history.

November 1998 Paper announces the isolation of embryonic stem (ES) cells from human embryos.

August 2001 US President George W. Bush restricts federal funding for work on human ES cells to a few extant lines.

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Genea Stem Cells (GSC): 25 New Disease Specific Pluripotent Stem Cell Lines Placed On The NIH Registry

Posted: January 16, 2013 at 12:50 pm

SYDNEY, AUSTRALIA--(BUSINESS WIRE)--

Genea Stem Cells Pty Ltd (GSC), a supplier and developer of disease-specific human stem cells, today announced that 25 of its disease specific embryonic pluripotent stem cell lines have been placed on the USA National Institutes of Health (NIH) human stem cell registry. These embryonic stem cell lines are now all available commercially for use in medical research.

These cell lines include one disease free pluripotent cell line and 24 others with individual mutations that give rise to several severe diseases such as cancer (breast cancer, Wilms tumor and Von HippelLindau syndrome), Huntingtons disease, muscular dystrophy (including CMT, FSHD and Myotonic) and cystic fibrosis as well as some rarer genetic diseases such as Trisomy 5, macular dystrophy, incontinentia pigmenti, juvenile retinoschisis, alpha thalassemia and autosomal dominant torsion dystonia. All these cell lines are genetically unmodified and have been derived in compliance with international regulatory and ethical guidelines.

GSC has the worlds largest private bank of pluripotent human embryonic stem cells with more than 100 individual lines expressing almost 30 different genetic diseases. The Company is also developing multiple differentiated cell lines from these pluripotent lines and currently offer GABAergic neurons and vascular smooth muscle cells. These are the only commercially available differentiated disease affected cell lines in the world and GSC is willing to work with drug developers globally to custom-make disease-specific differentiated cell lines for use in in vitro research.

Dr Uli Schmidt, General Manager of GSC, commented: It is a tribute to all the hard work and diligence of our scientists in Sydney that so many of our lines have been accepted by the NIH. We believe that this year will see substantial commercial take up of these perfect in vitro research tools.

GSC will be exhibiting (booth 1536) this week at the Society for Lab Automation and Screening (SLAS) 2013 conference and exhibition in Orlando, Florida. [12-16 January 2013].

- ends -

About Genea Stem Cells

Genea Stem Cells (GSC) supplies and develops disease-specific pluripotent and differentiated human embryonic stem cells for use in drug development and research. All of our cellular products are genetically unmodified human cells - the most accurate in vitro reflection of clinical conditions, promising more predictive disease models and thereby reducing the need for animal studies. GSC provides the following products for use in drug development and medical research:

As well as providing the above products, GSC also works collaboratively with industry for custom-developed cell-based assay solutions in drug development.

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