Upper Dublin girl names semi-finalist for medical school scholarship

Jennifer Deasy has suffered from migraines since she was 11 years old more than half the 18-year-old Upper Dublin girls life. And she has an idea that just may ease the pain a bit for her and other migraine sufferers.

It also could net her a medical school scholarship.

Basically, her idea is to cure migraines with stem cell treatment.

Deasy has been named one of 12 semi-finalists for a National Academy Medical School Scholarship Challenge sponsored by the National Academy of Future Physicians and Medical Scientists.

Three of the 12 will be selected to present their research proposals at the November Congress of Future Medical Leaders in Washington, D.C., according to an academy press release. One will receive a medical school scholarship up to $185,000, with $10,000 scholarships going to the runners-up.

The winners will be determined by scholars attending the November Congress.

Deasy was one of 3,100 honor high school students who attended the February Congress, where students were challenged to identify an unsolved medical/scientific/world health problem and create an original investigation to solve that problem.

My guidance counselor nominated me to attend the February Congress, said Deasy, a 2014 Upper Dublin High School grad and current freshman at Franklin & Marshall. Attending medical school has been a dream for as long as I can remember.

I always found [medicine] cool and interesting, she said, noting her dad is an oral surgeon, three uncles are doctors and one is a nurse. She hopes to become a neurologist, both seeing patients and doing research on the brain and its workings with different hormones and how they can affect brain function, like seizures and migraines.

Pain medication or caffeine pills are currently used to treat migraine symptoms, she said. It is not known what causes the severe headaches often accompanied by nausea, and there is no cure. Continued...

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Upper Dublin girl names semi-finalist for medical school scholarship

Beat tennis elbow with stem cell injections: Patients are …

By Roger Dobson for the Daily Mail

Published: 18:06 EST, 22 September 2014 | Updated: 18:06 EST, 22 September 2014

Scientists believe stem cells will provide a more effective solution fortendon injuries

Patients are receiving jabs of their own cells in an attempt to heal hard-to-treat tendon injuries, such as tennis elbow.

The treatment, which has previously been used on injured racehorses, uses a patient's stem cells to super-charge the body's natural repair mechanisms.

Millions of Britons suffer tendon injuries. Tendons are the tough bands of tissue that connect muscle to bone. They can become damaged through wear and tear or injury, causing inflammation or tears.

Such damage is notoriously difficult to treat because tendons have a very poor blood supply, so healing compounds cannot reach the injury site. As a result, tough scar tissue often forms around the tendon, significantly hampering movement and flexibility.

Treatments include non-steroidal anti-inflammatory drugs (NSAIDs), steroid injections and physiotherapy, but experts say they have limited success. Scientists believe stem cells - which have the ability to turn into different types of cells in the body - will provide a more effective solution.

Early-stage laboratory studies, as well as reports from treating racehorses, have shown that, over several weeks, the stem cells encourage the growth of new tendon tissue and reduce scar tissue.

This may be because stem cells can recruit compounds called growth factors that help regenerate damaged tissue.

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Germantown's Next Healthcare pairs with NFL player

Company plans for the future of stem cell use

by Samantha Schmieder

Staff Writer

Next Healthcare Inc. of Germantown recently launched a partnership with Arizona Cardinals wide reciever Larry Fitzgerald to promote its newest venture, CelBank Pro to other professional athletes.

Next Healthcares CelBank is the collection of cell samples and storage of their blood, skin or stem cells to be used in the future. Stem cells are unspecialized cells that are able to renew themselves through cell division and can be scientifically manipulated to become another type of cell with a more specialized function. They offer hope to provide new ways to fight disease or injuries, according to the National Institutes of Health.

Essentially we are in the business of banking cells for people, Vin Singh, the founder and CEO of Next Healthcare, said.

While CelBank is geared toward anyone interested in using their own cells later in their life, CelBank Pro is geared toward sports players who are very likely to get injured or just worn down during their career.

Skin cells and stem cells are stored at a healthy time at someones life for later use in regenerative medicine, Singh said.

In 2006 and 2007, Singh, who lives in Boyds, heard about a method in Japan that was able to turn adult skin cells into stem cells. Singh decided to build Next Healthcare around these induced pluripotent stem cells, or iPS cells.

For me that was the real spark. I heard about that and thought, Wow, this is an amazing, revolutionary breakthrough, Singh said. Thats where the idea came from, what can we do with that technology. There has to be something that I can do for consumers to give them an advantage.

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Germantown's Next Healthcare pairs with NFL player

Germantown

Company plans for the future of stem cell use

by Samantha Schmieder

Staff Writer

Next Healthcare Inc. of Germantown recently launched a partnership with Arizona Cardinals wide reciever Larry Fitzgerald to promote its newest venture, CelBank Pro to other professional athletes.

Next Healthcares CelBank is the collection of cell samples and storage of their blood, skin or stem cells to be used in the future. Stem cells are unspecialized cells that are able to renew themselves through cell division and can be scientifically manipulated to become another type of cell with a more specialized function. They offer hope to provide new ways to fight disease or injuries, according to the National Institutes of Health.

Essentially we are in the business of banking cells for people, Vin Singh, the founder and CEO of Next Healthcare, said.

While CelBank is geared toward anyone interested in using their own cells later in their life, CelBank Pro is geared toward sports players who are very likely to get injured or just worn down during their career.

Skin cells and stem cells are stored at a healthy time at someones life for later use in regenerative medicine, Singh said.

In 2006 and 2007, Singh, who lives in Boyds, heard about a method in Japan that was able to turn adult skin cells into stem cells. Singh decided to build Next Healthcare around these induced pluripotent stem cells, or iPS cells.

For me that was the real spark. I heard about that and thought, Wow, this is an amazing, revolutionary breakthrough, Singh said. Thats where the idea came from, what can we do with that technology. There has to be something that I can do for consumers to give them an advantage.

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Germantown

BioKidz: the Children of the Stem Cell Revolution to go Global

(PRWEB UK) 22 September 2014

BioKidz is a simple concept which aims to engage children in the importance of stem cell medicine. Aimed at an audience of 4-9 year olds, the company now aims to use it in the 21 countries in which it operates.

BioEden has been invited to speak with parents and teachers later this month, as the BioKidz site aims to be a good source of scientific information for primary school teachers.

The BioEden proposition is very simple one: harvest the stem cells from a naturally shed baby tooth, store the viable cells for future therapeutic use, and guarantee that the cells will be available when needed.

As stem cell medicine is now becoming commonplace, it is important that there is a stem cell match when needed. The easiest way to do this is by harvesting and storing one's own cells, and there is no easier way than from naturally shed teeth.

The company admits that they could be putting the ordinary tooth fairy out of business, but they hasten to add that BioKidz have their own hero in the form of a Super Tooth Fairy who works within their own stem cell laboratories.

Children can meet BioEden the Super Tooth Fairy by visiting http://www.bioeden.com.

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BioKidz: the Children of the Stem Cell Revolution to go Global

Beat tennis elbow with stem cell injections: Patients are receiving jabs to heal hard-to-treat tendon injuries

By Roger Dobson for the Daily Mail

Published: 18:06 EST, 22 September 2014 | Updated: 18:06 EST, 22 September 2014

Scientists believe stem cells will provide a more effective solution fortendon injuries

Patients are receiving jabs of their own cells in an attempt to heal hard-to-treat tendon injuries, such as tennis elbow.

The treatment, which has previously been used on injured racehorses, uses a patient's stem cells to super-charge the body's natural repair mechanisms.

Millions of Britons suffer tendon injuries. Tendons are the tough bands of tissue that connect muscle to bone. They can become damaged through wear and tear or injury, causing inflammation or tears.

Such damage is notoriously difficult to treat because tendons have a very poor blood supply, so healing compounds cannot reach the injury site. As a result, tough scar tissue often forms around the tendon, significantly hampering movement and flexibility.

Treatments include non-steroidal anti-inflammatory drugs (NSAIDs), steroid injections and physiotherapy, but experts say they have limited success. Scientists believe stem cells - which have the ability to turn into different types of cells in the body - will provide a more effective solution.

Early-stage laboratory studies, as well as reports from treating racehorses, have shown that, over several weeks, the stem cells encourage the growth of new tendon tissue and reduce scar tissue.

This may be because stem cells can recruit compounds called growth factors that help regenerate damaged tissue.

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Beat tennis elbow with stem cell injections: Patients are receiving jabs to heal hard-to-treat tendon injuries

Bone paste could provide treatment for ostoeporosis …

About three million Briton currently suffer osteoporosis which is affected by a number factors such as genes, a lack of exercise and poor diet and results in about 60,000 hip, 50,000 wrist and 120,000 spinal fractures every year, according to the National Osteoporosis Society, costing about 1.7 billion in health and social care.

Dr Ifty Ahmed, a researcher at Nottingham University, said his team wanted to provide a preventative treatment, strengthening the bones of those at risk before they suffered a fracture.

Speaking at the Regener8 conference on regenerative medicine, in Leeds last week, he said: Our aim would be to use screening to spot people who are at risk, then strengthen their bones before they get fractures.

It means that rather than waiting until people have a fall and break something, we would try to stop that ever happening, along with the consequences, loss of independence, surgery and secondary illnesses.

Previous attempts have been made to find ways of strengthening thinning bones but the difficulties of protecting the fragile stem cells has meant no such treatments have yet been developed.

Dr Ahmeds team hope to overcome this problem by puncturing the tiny hollow spheres of calcium phosphate allowing the stem cells to migrate inside them where they are protected.

The experimental treatment has not yet been trialled on humans.

It would involve extracting stem cells from a patients bone marrow and mixing them with the microspheres before injecting the paste into the vulnerable bones.

Dr Ahmed said: "If it works, this kind of treatment could be done in a day.

Until now the team have been funded by the Engineering and Physical Sciences Research Council but they are now looking for a commercial partner.

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Scientists Report Highly Efficient Method for Making Stem …

At NYU Langone Medical Center, scientists have found a way to boost dramatically the efficiency of the process for turning adult cells into so-called pluripotent stem cells by combining three well-known compounds, including vitamin C.

"This big boost in efficiency gives us an opportunity now to study stem cell programming mechanisms at high resolution," says Matthias Stadtfeld, PhD, assistant professor of cell biology and a member of the Skirball Institute of Biomolecular Medicine and the Helen L. and Martin S. Kimmel Center for Stem Cell Biology at NYU Langone Medical Center, who led the research."This is a very exciting advance," says Ruth Lehmann, PhD, director of the Kimmel Center for Stem Cell Biology and the Skirball Institute at NYU Langone and chair of the Department of Cell Biology. "The new technology developed by the Stadtfeld lab to reprogram differentiated cells efficiently and effectively brings the prospect of stem cell technology for safe use in regenerative medicine ever so much closer."

The standard method for reprogramming skin, blood, or other tissue-specific cell types into "induced pluripotent stem cells" (iPSCs) was reported in 2006 by the laboratory of Kyoto University's Shinya Yamanaka, who later won a Nobel Prize for the achievement. The method involves the artificial expression of four key genes dubbed OKSM (for Oct4, Klf4, Sox2 and myc) whose collective activity slowly prods cells into an immature state much like that of an early embryonic cell. In principle, one could take a sample of cells from a person, induce the cells to become iPSCs, then multiply the iPSCs in a lab dish and stimulate them to mature towards desired adult cell types such as blood, brain or heartwhich then could be used to replace injured or diseased tissue in that same individual.

But there are many formidable technical obstacles, among which is the low efficiency of currently used protocols. Converting most cell types into stable iPSCs occurs at rates of 1 percent or less, and the process can take weeks.Researchers throughout the world have been searching for ways to boost this efficiency, and in some cases have reported significant gains. These procedures, however, often alter vital cellular genes, which may cause problems for potential therapies. For the new study, reported online today in Stem Cell Reports, Dr. Stadtfeld and his laboratory team decided to take a less invasive approach and investigate chemical compounds that transiently modulate enzymes that are present in most cells.

"We especially wanted to know if these compounds could be combined to obtain stem cells at high efficiency," Dr. Stadtfeld says.Two of these compounds influence well known signaling pathways, called Wnt and TGF-, which regulate multiple growth-related processes in cells. The third is vitamin C (also known as ascorbic acid). Best known as a powerful antioxidant, the vitamin was recently discovered to assist in iPSC induction by activating enzymes that remodel chromatinthe spiral scaffold for DNAto regulate gene expression.Simon Vidal, a graduate student in the Stadtfeld lab, and Bhishma Amlani, a postdoctoral researcher, looked first at mouse skin fibroblasts, the most common cell type used for iPSC research. Adding to fibroblasts engineered to express OKSM either vitamin C, a compound to activate Wnt signaling, or a compound to inhibit TGF- signaling increased iPSC-induction efficiency weakly to about 1% after a week of cell culture.

Combining any two worked a bit better. But combining all three brought the efficiency to about 80 percent in the same period of time.In another series of experiments the team worked with blood progenitor cells, which usually replace blood cells lost after injury or infection. The OKSM method on its own can slowly convert these cells to stem cells with up to 30 percent efficiency. Using OKSM together with the three compounds brought the efficiency to nearly 100 percent in less than a week. The researchers also achieved nearly 100-percent yield in mouse liver progenitor cells.Dr. Stadtfeld expects that these dramatic increases in conversion rates of adult cells into embryonic-like stem cells will facilitate future studies of the iPSC induction process, simply by making that induction a more predictable event.

"It's just a lot easier this way to study the mechanisms that govern reprogramming, as well as detect any undesired features that might develop in iPSCs," he said.Vitamin C and the two compounds used to manipulate the Wnt and TGF- pathways are widely studied and considered to have few unknown or hazardous effects, the researchers said. By contrast, the use of OKSM has in some cases caused undesired features in iPSCs, such as developmental defects. By making iPSC induction more rapid and efficient, though, Dr. Stadtfeld's new technique might also make the resulting stem cells safer. "Conceivably it reduces the risk of abnormalities by smoothening out the reprogramming process," Dr. Stadtfeld says. "That's one of the issues we're following up."

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Molecule boosts stem cells in cord blood: Canadian study

TORONTO Canadian researchers have found a way to boost the number of stem cells in umbilical cord blood so more patients with leukemia and other blood-related cancers could receive potentially life-saving transplants.

The key to the breakthrough technique is a molecule developed at the Universite de Montreal, coupled with a bioreactor designed at the University of Toronto, which allows scientists to significantly expand the number of stem cells from a single unit of cord blood.

Basically its going to give access to about 10 times as many cords in (cord blood) banks, said Dr. Guy Sauvageau, principal investigator of stem cell genetics at the Institute for Research in Immunology and Cancer at the Montreal university. Its as if you were to multiply by 10 today the number of cord blood units in the world.

The molecule, called UM171, was discovered serendipitously. It had been created by a chemist at the institute working on another program but didnt work for its intended purpose, so they just threw it in what we call a library of compounds, Sauvageau said Thursday from Montreal.

When his research team began testing compounds from among thousands in the library, UM171 was the only one that really worked.

Stem cells from donated umbilical cord blood are able to give rise to all the types of cells that make up blood, including the immune cells that protect the body and fight infection. The same is true of bone marrow, but finding a suitable donor is more difficult.

For some people with blood-related cancers like leukemia, myeloma and lymphoma, getting a stem cell transplant to replace their own blood system is often the treatment of last resort.

But the biggest hurdle for doctors is finding enough cord blood stem cells that are a compatible match and wont cause severe rejection symptoms in recipients, he said. Typically, there are not enough stem cells in a single cord blood unit to regenerate an adults blood system; only five per cent of cord blood bank units can be used for large adults.

And theres another reason why this is becoming more of a problem, because we have more and more ethnic groups in our society and these peoples access to a matched unrelated donor is more limited than for most Caucasians.

That was the case for Mai Duong of Montreal, who is fighting her second bout of leukemia. The 34-year-old mother had made a desperate online plea and a global search for a donor of either bone marrow or cord blood stem cells for a transplant. On Tuesday, doctors announced an unidentified woman had donated her infants umbilical cord to the Vietnamese-Canadian to help save her life.

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Molecule boosts stem cells in cord blood: Canadian study