Monthly Archives: September 2014

Wise Young, M.D., Ph.D., Announced as 12th New Jersey Symposium on Biomaterials Science Dinner Speaker

Posted: September 4, 2014 at 8:52 am

Piscataway, NJ (PRWEB) September 04, 2014

Dr. Young has organized a twenty-five center clinical trial network in China, Hong Kong, and Taiwan to test a new therapy for chronic spinal cord injuries using transplantation of umbilical cord blood stem cells, lithium, and intense physical rehabilitation. Phase II clinical trials have been completed and preparations are being made for Phase III trials in China, Norway, India, and the United States. Dr. Young will speak the evening of October 6th on Running Clinical Trials for Spinal Cord Injury Therapies in the US and China: Differences and Lessons Learned.

Dr. Young is the Founding Director of the W. M. Keck Center for Collaborative Neuroscience at Rutgers, the State University of New Jersey. He is a Distinguished Professor in the Department of Cell Biology and Neuroscience and also holds the Richard H. Shindell Chair in Neuroscience. The Keck Center was established in 1997 to develop effective treatments for spinal cord injuries and to move these discoveries from laboratory to human lives as rapidly as possible. The research conducted at the Center also is applicable to many other devastating conditions of the central nervous system.

Registration for the 12th NJ Symposium on Biomaterials Science is available at http://www.njbiomaterials.org/biomaterials-symposia.htm

The New Jersey Center for Biomaterials (NJCBM) was founded in 1997. Based at Rutgers, the State University of New Jersey, the center spans academia, industry, and government. Staffed by biomaterial scientists, the Center works to improve health care and quality of life by developing advanced biomedical products for tissue repair and replacement as well as the delivery of pharmaceutical agents. The Centers technologies have been translated into clinical and pre-clinical products including surgical meshes, cardiovascular stents, bone regeneration scaffolds, and ocular drug delivery systems.

Media Contact:

Louli Kourkounakis (732) 445 0488 ext. 40001 symposium(at)dls(dot)rutgers(dot)edu

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Wise Young, M.D., Ph.D., Announced as 12th New Jersey Symposium on Biomaterials Science Dinner Speaker

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Co-workers honor doctor by registering as bone marrow donors

Posted: September 4, 2014 at 8:51 am

PASCAGOULA, MS (WLOX) -

Nearly 120 doctors, nurses, technicians and other Singing River Health System employees lined up to register as a bone marrow donor in honor of their co-worker, Dr. Jeremy Simpler, who is battling cancer.

"I don't want to get emotional, but very, very devastating when we found this out because he is wonderful. He's a people person. He treated us like family," Singing River Health System Surgical Tech Patricia Taylor said.

A stranger, who gave 40 seconds to get his or her cheeks swabbed, could end up saving Simpler's life. Now, his co-workers want to repay that favor.

"Every day, we have someone looking for a match," Mattie Coburn, with the Mississippi Marrow Donor Program said.

Coburn said 70 percent of patients who need a transplant rely on the registry, because they do not have a match in their family.

There are two different ways donors are asked to donate.

"Bone marrow transplant, it is outpatient. You are put to sleep under anesthesia. We are going to go to the hip and pelvic bone with a sterile needle and syringe," Coburn said. "You are not going to feel it. We keep you overnight for observation, and release you with a Band-Aid over where the needles were. PBSC, peripheral blood stem cell, is similar to giving platelets. We draw blood, separate the cells, you get your blood back."

Three years ago, Singing River Health System Dr. Clinton Hull donated bone marrow.

"It was a really good feeling," Hull said. "The last communication I had through the bone marrow service was the patient had returned to their daily activities and living, so that makes me feel really good."

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Transplanted stem cells help prevent bladder fibrosis after spinal cord injury

Posted: September 4, 2014 at 8:50 am

PUBLIC RELEASE DATE:

3-Sep-2014

Contact: Robert Miranda cogcomm@aol.com Cell Transplantation Center of Excellence for Aging and Brain Repair

Putnam Valley, NY. (Sept. 3, 2014) A team of researchers from Korea and Canada have found that transplantation of B10 cells (a stable immortalized human bone marrow derived mesenchymal stem cell line; B10 hMSC) directly into the bladder wall of mice modeled with spinal cord injury (SCI) helped inhibit the development of bladder fibrosis and improved bladder function by promoting the growth of smooth muscle cells in the bladder.

The study will be published in a future issue of Cell Transplantation and is currently freely available on-line as an unedited early e-pub at: http://www.ingentaconnect.com/content/cog/ct/pre-prints/content-CT-1227_Lee.

Spinal cord injury (SCI) can cause severe lower urinary tract dysfunction and conditions such as overactive bladder, urinary retention and increased bladder thickness and fibrosis. HMSCs, multipotent cells that can differentiate into a variety of cell types, including bone cells, cartilage cells, and fat cells, have been transplanted into injured spinal cords to help patients regain motor function.

In this study, mice receiving the B10 hMSCs injected directly into the bladder wall experienced improved bladder function while an untreated control group did not.

"Human MSCs can secrete growth factors," said study co-author Seung U. Kim of the Division of Neurology at the University of British Columbia Hospital, Vancouver, Canada. "In a previous study, we showed that B 10 cells secrete various growth factors including hepatocyte growth factor (HGF) and that HGF inhibits collagen deposits in bladder outlet obstructions in rats more than hMSCs alone. In this study, the SCI control group that did not receive B10 cells showed degenerated spinal neurons and did not recover. The B10-injected group appeared to have regenerated bladder smooth muscle cells."

Four weeks after the onset of SCI, the treatment group received the B10 cells transplanted directly into the bladder wall. To track the transplanted B10 cells via magnetic resonance imaging (MRI), the researchers labeled them with fluorescent magnetic particles.

"HGF plays an essential role in tissue regeneration and angiogenesis and acts as a potent antifibrotic agent," explained Kim.

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Transplanted stem cells help prevent bladder fibrosis after spinal cord injury

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Stem Cell Beauty: The Online Shop Revolutionizing the Beauty Industry

Posted: September 4, 2014 at 8:49 am

Los Angeles, California (PRWEB) September 03, 2014

Stem Cell technology is the future; looking younger and better without plastic surgery is here now. Stem Cell Beautys debut product line StemLife is spearheading the current beauty renaissance. Among websites that provide stem cell beauty products, Stem Cell Beauty is in a league of its own.

Science is always advancing, why shouldn't your beauty products? questions Albert Faleski, Director of Operations at StemCellBeauty.com.

Most products on the shelves are outdated, whereas we take a different approach to find a formula that works with your body, reinvigorating your own stem cells to provide actual results.

The science behind StemLife is nothing short of groundbreaking. Its trademarked FixT Technology was achieved through reverse engineering to understand how the body maintains and heals itself with our own endogenous combinations of adult stem cells. With this knowledge they developed a means to mimic the natural stem cell processes in our body. Unlike other beauty brands, StemLife uses specific combinations of stem cell types, each cultured under specific state-dependent conditions, using cell types and states that are ideal for the particular tissue. It then creates a set of molecules from multiple stem cell types that is complete and fully formed, rendering maximum benefit and efficiency. This approach of stem cell skin care is extremely unique.

Other leading stem cell-based beauty companies use simpler technology where one stem cell type is chosen to make their molecules. This one-size fits all approach is not efficient and lacks the complexity of StemLifes FixT technology. Some companies mash the cells without allowing their molecules to fully process, which again leads to underachieving results. Many of the largest companies have made no attempt to use new science to formulate better products, providing their customers with over-priced serums proven to be archaic.

StemLifes cutting edge formula is shaping the future of hair regrowth as well, providing an ultramodern solution to those looking to slow the hands of time. Their most popular product, The Advanced Hair Treatment for Women, is essentially the hidden gem the world has been waiting for.

Its popularity stems back to the fact that it actually works. Faleski explained.

Were not big on gimmicks. We prefer showing our customer actual people who have had actual results with our products. After seeing life-changing hair growth with their own eyes, we are confident new customers will try it and have amazing results of their own. The Advanced Hair Treatment for Women is an incredible product that sells itself.

StemLifes most interesting product to date is the Natural Lash & Brow Lash Extend. This product boasts ingredients that are formulated to generate eyelash growth. In a market where eyelash extensions have been the go-to fix for longer lashes, being able to naturally grow them is a revolutionary concept.

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Stem Cell Beauty: The Online Shop Revolutionizing the Beauty Industry

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Dr Adam Miller Talks Modern Medicine – Video

Posted: September 4, 2014 at 8:44 am


Dr Adam Miller Talks Modern Medicine
Dr. Miller has experience as an oral and facial cosmetic surgeon, sleep apnea specialist, skin cancer expert, and is stem cell/ regenerative medicine and Age Management certified. He helped...

By: adam miller

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Latest Study on Stem Cell Therapy Shows Promising Signs of Recovery for Stroke Patients and Support for StemGenex …

Posted: September 4, 2014 at 8:41 am

La Jolla, CA (PRWEB) September 03, 2014

A new study, published on Aug. 8th, 2014 in Stem Cells Translational Medicine, has shown the positive effect stem cell therapy has had on a group of patients only 6 months after their treatment. Researchers observed significant improvements in disease-related complications in each of the 5 patients included in the study. Post-treatment brain scans of each patient revealed that stroke-related damage was reduced over time. Further, at six-month follow-ups patients demonstrated improvements in standard measures of stroke-related disability and impairment.

Researchers are being cautiously optimistic when considering these results. Similar improvements are often seen in stroke patients as part of the normal recovery process and state that more thorough studies will need to be completed. Nonetheless, the findings are absolutely astounding as the five patients included in this study suffered severe strokes. Four out of five of the patients had the most serious type of stroke. Normally only 4% of these patients survive and are able to live independently after six months of a stroke occurrence.

Clinical studies for stem cell treatment are currently being offered by StemGenex to patients diagnosed with Stroke and other degenerative neurological diseases. Innovation is truly a driving force for StemGenex. Stroke Patients who receive stem cell treatment through StemGenex receive multiple therapeutic modalities they simply cannot find elsewhere under one roof, said Jeremiah McDole, Director of Scientific Research and Development at StemGenex. Offering targeted therapies that deliver stem cells past the blood brain barrier is essential to providing effective treatment for patients with neurological disorders.

StemGenex takes a unique approach of compassion and empowerment while providing access to the latest stem cell therapies for degenerative neurological diseases including Multiple Sclerosis, Parkinsons Alzheimers disease, and others. Rita Alexander, founder of StemGenex and the companys first stem cell patient, insists that all patients be treated like they are one of our loved ones. Hope, compassion, and the relentless pursuit for an end to these diseases are the primary focus.

To find out more about stem cell therapy, contact StemGenex either by phone at (800) 609-7795 or email Contact@stemgenex.com

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Latest Study on Stem Cell Therapy Shows Promising Signs of Recovery for Stroke Patients and Support for StemGenex ...

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Cord blood stem cells a life saviour

Posted: September 4, 2014 at 1:51 am

Dubai: Stem cells harvested from the umbilical cord blood can save lives.

Of the 3,377 stem cells collected so far at the Dubai Cord Blood and Research Centre (DCRC), nine have been used for life-saving transplants in children in cases of leukaemia and other blood diseases.

Advocating the importance of public donation of cord blood stem cells to help form a substantial registry of stem cells for the UAE, Kareema Salim Al Arrayed, head of DCRC, said: Since the inception of this centre in 2006, we have seen an increase in the awareness levels about cord blood banking and this has directly attributed to an increase in the number of people who save their cord blood at our cord blood bank. However, we need to raise awareness that cord blood stem cells can be donated. Presently, more than 80 diseases can be cured with the help of stem cells and this includes leukaemia, and treatment of genetic disorders such as thalassaemia.

She added: The DCRC encourages families to donate cord blood stem cells so that we have a strong UAE public registry to help people in need. Stem cells are the future of medicine and public banking is a trend that is catching on globally due to the several diseases stem cells can cure.

Many women today opt for cord blood collection at the time of birth and DCRC provides pregnant women and their families a guided tour of the centre and its facilities to engender their interest in preserving stem cells for their families or for the purpose of donation.

The DCRC was established in 2006 and the prime objective of the centre is to retrieve a newborns umbilical cord blood at birth and extract the haemopoietic stem cells and carry out its cryopreservation. The DCRC spokesperson explained that the umbilical cord blood is what remains in the placenta following birth. The placenta is the temporary organ that transfers oxygen and nutrients to the baby via the umbilical cord while in the mothers uterus. Until recently, in most cases, the umbilical cord and the placenta were discarded after birth. In the last decade, scientists and researchers have discovered that the umbilical cord blood could supply stem cells, the hidden treasure of life. These stem cells can be used to replace blood-forming cells in a person being treated for cancer or other life-threatening diseases such as haemoglobinopathies, leukaemia, immune system deficiencies and numerous genetic diseases and it holds out hope for incurable diseases.

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Can Extended Breastfeeding stem cells Cure Autism 2014 – Video

Posted: September 3, 2014 at 9:41 pm


Can Extended Breastfeeding stem cells Cure Autism 2014

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Central biobank for drug research

Posted: September 3, 2014 at 3:45 am

Sep 01, 2014 The biobank comprises three cryotanks, equipped with cooled protective hoods, and a transfer station from which the sample containers are transported via a rail system. There is enough space for approximately 60,000 samples. Credit: Fraunhofer IBMT

For the development of new drugs it is crucial to work with stem cells, as these allow scientists to study the effects of new active pharmaceutical ingredients. But it has always been difficult to derive enough stem cells of the right quality and in the right timeframe. A central biobank is about to remedy the situation.

Human stem cells allow scientists to assess how patients are likely to respond to new drugs and to examine how illnesses come about. For a few years now, it has been possible to take tissue samples from adults and use reverse programming to artificially produce stem cells, which have the potential to create any kind of cell found in the human body. Before this discovery, pharmaceutical researchers had to use adult stem cells or primary cells, which have a more limited potential. Another option is to use stem cells derived from human embryos, but quite apart from the ethical considerations these cells are available only in limited diversity. The new technique makes it possible for instance to reprogram adult skin or blood cells so that they behave in a similar way to embryonic stem cells and can become any type of cell. "These are known as induced pluripotent stem cells, or iPS cells for short," says Dr. Julia Neubauer from the Fraunhofer Institute for Biomedical Engineering IBMT in St. Ingbert, Germany. Although an increasing number of local biobanks have emerged in recent years, none of them fulfills the requirements of the pharmaceutical industry and research institutions. What is needed is a supply of 'ready-to-use' stem cells, which means large numbers of consistently characterized, systematically catalogued cells of suitable quality.

At the beginning of 2014, the IBMT teamed up with 26 industry and research partners to launch a project aimed at establishing a central biobank the European Bank for induced pluripotent Stem Cells (EBiSC) to generate iPS cells from patients with specific diseases or genetic mutations (http://ebisc.org/). Six months into the project and the first cells are available for use in the development of new drugs. By its three-year mark, it is hoped the project will be in a position to offer over 1000 defined and characterized cell lines comprising a hundred million cells. Such quantities are needed because a single drug screening involves testing several million cells. The main biobank facility is being built in the English city of Cambridge and an identical "mirror site" will be set up at the IBMT's Sulzbach location in Germany.

Gently freezing cells

The IBMT was brought on board for EBiSC by virtue of the comprehensive expertise it gained through participation in the EU's "Hyperlab" and "CRYSTAL" projects. For EBiSC, IBMT scientists are responsible for freezing the cells and for automating cell cultivation and the biobank itself. For an efficient long-term storage of functional stem cells, they have to be cooled down to temperatures of below 130 degrees Celsius in a controlled way. The scientists have to prepare the cells so they can survive the cold shock of nitrogen gas. The IBMT has, for instance, developed technologies that allow cells to be frozen in an extremely gentle way. "Cells don't like being removed from the surface they are grown on, but that's what people used to do in order to freeze them. Our method allows the cells to stay adherent," explains Neubauer.

Just as with foodstuffs, stem cells depend on an unbroken cold chain to preserve their functionality and viability. The scientists store the cells in special containers or cryotanks each measuring one by two meters. To remove a particular sample, the scientists have to open the cryotank. The problem is that this exposes all the other samples to warmer ambient air, causing them to begin to thaw out. "It's just like when you go to your refrigerator at home it's not a good idea to leave the door open too long," says Neubauer. She and her colleagues at the IBMT and industry partner Askion GmbH have together developed a stem cell biobank complete with protective hoods that protect the other samples whenever the cryotank is opened. In addition to maintaining the temperature, the hoods help keep another key shelf-life criterion, humidity, at a constant level.

Flawless freezing is important, but it is just as important to automate the whole process. "That not only guarantees consistency, it's what makes it possible to provide large quantities of cells of the required quality in the first place," says Neubauer. And the scientists' cooling process already boasts a finished technology. In their automated biobank, each cell sample is labelled with barcodes to allow them to be tracked. The samples travel along a conveyor belt to the individual cyrotanks, and a computer monitors the entire freezing and storage process.

Now the scientists are working on automating cell cultivation or the multiplying of the cells. There are essentially two possible approaches. One is to use robots that translate each preparation step into a mechanical one. The other is to use stirred bioreactors that provide free-moving cells with the ideal supply of nutrients and oxygen. Both technologies feature in the IBMT's portfolio. "By the time the project is completed, we'll know which is the better method for what we're trying to do," says Neubauer.

Explore further: Animal-free reprogramming of adult cells improves safety

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Scientists' new approach can provide better treatment for cancer

Posted: September 3, 2014 at 3:45 am

Researchers have recently found a method to expand blood stem cells that could lead to new and better cancer treatment, it has been reported.

Scientists from the University Of Colorado School Of Medicine have reported the breakthrough discovery of a process to expand production of stem cells used to treat cancer patients. These findings could have implications that extend beyond cancer, including treatments for inborn immunodeficiency and metabolic conditions and autoimmune diseases.

Researchers from the Charles C. Gates Center for Regenerative Medicine and Stem Cell Biology and Taiga Biotechnologies, Inc. said they have uncovered the keys to the molecular code that appear to regulate the ability of blood stem cells to reproduce and retain their stem-like characteristics.

The team developed protein products that can be directly administered to blood stem cells to encourage them to multiply without permanent genetic modifications. The technology described in the article has worked with blood stem cells obtained from cord blood, adult bone marrow or peripheral blood from adults.

Taiga Biotechnologies are now in the process of setting up first-in-human clinical trials with the blood stem cell expansion approaches described in the article. The clinical applications for expanded human blood stem cells vary from inborn immunodeficiency conditions, like SCID and sickle cell anemia, to metabolic conditions, like Hurler's disease or Gaucher syndrome.

Autoimmune diseases that could be affected include severe multiple sclerosis and lupus. And the types of cancer that could be treated as a result of this research include leukemia, lymphoma, myeloma and other types of solid tumors.

The article is published in PLOS ONE. (ANI)

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