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Study Shows Most Commonly Mutated Gene in Cancer may have a Role in Stroke

Posted: Published on June 23rd, 2012

Reported in CELL, Stony Brook pathologist uncovers new p53 mechanism triggering necrosis Newswise STONY BROOK, N.Y., June 22, 2012 The gene p53 is the most commonly mutated gene in cancer. p53 is dubbed the guardian of the genome because it blocks cells with damaged DNA from propagating and eventually becoming cancerous. However, new research led by Ute M. Moll, M.D., Professor of Pathology at Stony Brook University School of Medicine, and colleagues, uncovers a novel role for p53 beyond cancer in the development of ischemic stroke. The research team identified an unexpected critical function of p53 in activating necrosis, an irreversible form of tissue death, triggered during oxidative stress and ischemia. The findings are detailed online in Cell. Ischemia-associated oxidative damage leads to irreversible necrosis which is a major cause of catastrophic tissue loss. Elucidating its signaling mechanism is of paramount importance. p53 is a central cellular stress sensor that responds to multiple insults including oxidative stress and is known to orchestrate apoptotic and autophagic types of cell death. However, it was previously unknown whether p53 can also activate oxidative stress-induced necrosis, a regulated form of cell death that depends on the mitochondrial permeability transition pore (PTP) pore. We identified … Continue reading

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Notre Dame establishes professorships in adult stem cell research

Posted: Published on June 23rd, 2012

Public release date: 22-Jun-2012 [ | E-mail | Share ] Contact: William Gilroy gilroy.6@nd.edu 574-631-4127 University of Notre Dame Alumnus Michael Gallagher and his wife, Elizabeth, have made a $5 million gift to establish the Elizabeth and Michael Gallagher Family Professorships in Adult Stem Cell Research at the University of Notre Dame. Their gift, which will fund three new endowed professorships in adult and all forms of non-embryonic stem cell research, will strengthen Notre Dame's leadership in the field of stem cell research and enhance the University's effective dialogue between the biomedical research community and the Catholic Church on matters related to the use and application of stem cells and regenerative medicine. "As a Catholic university, Notre Dame carries a mantle of responsibility to use our scholarship and resources to help alleviate human suffering, and, in this area of research in particular, to do so with deep respect for the sanctity of all human life," said Rev. John I. Jenkins, C.S.C., the University's president. "These new professorships will enable us to effectively build upon an already strong foundation in this critically important field. We are tremendously grateful to the Gallaghers for making this possible with their transformative gift." Despite years … Continue reading

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Study Shows Most Commonly Mutated Gene in Cancer may have a Role in Stroke

Posted: Published on June 23rd, 2012

Reported in CELL, Stony Brook pathologist uncovers new p53 mechanism triggering necrosis Newswise STONY BROOK, N.Y., June 22, 2012 The gene p53 is the most commonly mutated gene in cancer. p53 is dubbed the guardian of the genome because it blocks cells with damaged DNA from propagating and eventually becoming cancerous. However, new research led by Ute M. Moll, M.D., Professor of Pathology at Stony Brook University School of Medicine, and colleagues, uncovers a novel role for p53 beyond cancer in the development of ischemic stroke. The research team identified an unexpected critical function of p53 in activating necrosis, an irreversible form of tissue death, triggered during oxidative stress and ischemia. The findings are detailed online in Cell. Ischemia-associated oxidative damage leads to irreversible necrosis which is a major cause of catastrophic tissue loss. Elucidating its signaling mechanism is of paramount importance. p53 is a central cellular stress sensor that responds to multiple insults including oxidative stress and is known to orchestrate apoptotic and autophagic types of cell death. However, it was previously unknown whether p53 can also activate oxidative stress-induced necrosis, a regulated form of cell death that depends on the mitochondrial permeability transition pore (PTP) pore. We identified … Continue reading

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Notre Dame establishes professorships in adult stem cell research

Posted: Published on June 23rd, 2012

Public release date: 22-Jun-2012 [ | E-mail | Share ] Contact: William Gilroy gilroy.6@nd.edu 574-631-4127 University of Notre Dame Alumnus Michael Gallagher and his wife, Elizabeth, have made a $5 million gift to establish the Elizabeth and Michael Gallagher Family Professorships in Adult Stem Cell Research at the University of Notre Dame. Their gift, which will fund three new endowed professorships in adult and all forms of non-embryonic stem cell research, will strengthen Notre Dame's leadership in the field of stem cell research and enhance the University's effective dialogue between the biomedical research community and the Catholic Church on matters related to the use and application of stem cells and regenerative medicine. "As a Catholic university, Notre Dame carries a mantle of responsibility to use our scholarship and resources to help alleviate human suffering, and, in this area of research in particular, to do so with deep respect for the sanctity of all human life," said Rev. John I. Jenkins, C.S.C., the University's president. "These new professorships will enable us to effectively build upon an already strong foundation in this critically important field. We are tremendously grateful to the Gallaghers for making this possible with their transformative gift." Despite years … Continue reading

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University of Nevada School of Medicine researcher reviews muscular dystrophy therapies

Posted: Published on June 23rd, 2012

Public release date: 21-Jun-2012 [ | E-mail | Share ] Contact: Mike Wolterbeek mwolterbeek@unr.edu University of Nevada, Reno RENO, Nev. Leading muscular dystrophy researcher Dean Burkin, of the University of Nevada School of Medicine summarizes the impact of a new protein therapeutic, MG53, for the treatment of Duchenne muscular dystrophy in an article published this week in Science Translational Medicine. "This is a focus article in which we summarize the impact of MG53 protein therapy as a treatment option and discuss the increasing number of new protein therapeutics being developed for the muscular dystrophies, including laminin-111 developed in our laboratory," Burkin, a pharmacological researcher and associate professor, said. The article, "A Molecular Bandage for Diseased Muscle," co-authored by Ryan Wuebbles, a post-doctoral student in Burkin's lab in the University's Center for Molecular Medicine, is a review of the current status of therapeutic developments in the muscular dystrophy research field. These therapies represent significant strides and show great promise in treatment of muscular dystrophy. Approaches to treat Duchenne muscular dystrophy include gene replacement therapy, gene repair and myoblast cell transfer. In a study on MG53 by Noah Weislander and colleagues, presented in the same issue of Science Translational Medicine, it was … Continue reading

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Predicting treatment response in central nervous system diseases

Posted: Published on June 23rd, 2012

Public release date: 22-Jun-2012 [ | E-mail | Share ] Contact: Mary Rice mary.rice@riceconseil.eu European Society of Human Genetics Nuremberg, Germany: The commonly-used epilepsy drug, valproic acid (VPA), can have a highly beneficial effect on some babies born with spinal muscular atrophy (SMA), the number one genetic killer during early infancy. But in about two-thirds of such cases it is either damaging or simply has no effect. Now, for the first time, researchers have found a way to identify which patients are likely to respond well to VPA prior to starting treatment. Their results have major implications, not just for SMA patients, but for other conditions treated with the drug such as migraine and epilepsy, and may even provide the conditions for turning VPA non-responders into responders, the researchers say. Dr. Lutz Garbes, from the Institute of Human Genetics, University of Cologne, Germany, will tell the annual conference of the European Society of Human Genetics tomorrow (Sunday) that he and his colleagues had analysed blood RNA samples from a small group of SMA patients who had been treated with VPA. They found, as expected, that only about one third of patients responded well. In an attempt to discover whether blood … Continue reading

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LAUSD Partners with Center for Autism and Related Disorders to Provide Behavioral Health Training to 6,000+ Staff

Posted: Published on June 23rd, 2012

Los Angeles, CA (PRWEB) June 22, 2012 The Los Angeles Unified School District (LAUSD), the second largest school district in the nation, has selected the Center for Autism and Related Disorders CARD eLearning program to provide the district with intense training in evidence-based principles of behavioral health treatment for individuals with autism spectrum disorders (ASD). Over 6,000 LAUSD teachers and support staff will participate in the training. The Center for Autism and Related Disorders, Inc. (CARD) is the worlds largest provider of state-of-the-art, early intensive behavioral intervention for individuals with autism spectrum disorders. In addition to providing treatment for thousands of children worldwide, CARD develops and utilizes technology to increase access to training for professionals who work with individuals who have been diagnosed with ASD. The CARD eLearning program (http://www.cardelearning.com) trains educators and other professionals in the principles of applied behavior analysis (ABA), which has been empirically proven to be the most effective treatment for individuals with ASD and is recommended by the American Academy of Pediatrics and the U.S. Surgeon General. CARD eLearning is a 20-hour online training course designed to facilitate effective intervention for children with autism spectrum disorders by equipping users with foundational knowledge in ABA. The … Continue reading

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InVivo Therapeutics’ CEO Frank Reynolds To Appear on FOX & Friends National Morning Program on #1 Rated Cable Network

Posted: Published on June 23rd, 2012

CAMBRIDGE, Mass.--(BUSINESS WIRE)-- InVivo Therapeutics Holdings Corp. (NVIV), a developer of groundbreaking technologies for the treatment of spinal cord injuries (SCI), today announced that CEO Frank Reynolds is scheduled to appear on Fox & Friends on Fox News Channel for a live interview in NYC on Sunday June 24, 2012 at 8:45am EDT. Fox & Friends is a national morning program on the #1 rated cable network. InVivo Therapeutics has pioneered a new treatment using a biocompatible polymer-based scaffold to provide structural support to a damaged spinal cord. The device sparesspinal cordtissue from scarring while improving functional recovery after a traumatic SCI. In addition to the scaffold and its application for acute and chronic SCI, Reynolds will discuss new hydrogel technologies under development by InVivo. Our technology is a true platform that can be leveraged to create many neurotrauma products. InVivo is developing technologies to treat both acute and chronic injuries, as well as therapies for other nervous system conditions such as pain due to nerve compression and other peripheral nerve injuries. Were currently under review at FDA for our first SCI treatment, and we look forward to receiving approval to begin those human studies in 2012, said Reynolds. Reynolds … Continue reading

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Matheny recieves two 'Spirit of Somerset' awards

Posted: Published on June 23rd, 2012

Matheny needs to grow in order to take care of those families who need them. With those words, the Rev. John Graf, co-chair of the Spirit of Somerset Awards, introduced Matheny Medical and Educational Center president Steve Proctor and The Friends of Matheny recording secretary Jean Wadsworth to accept their Spirit of Somerset Awards for Education, given June 13 at a special ceremony at the Grounds for Sculpture. Proctor talked about the origins of Matheny and how the original school was founded by Walter and Marguerite Matheny, whose son Chuck had cerebral palsy. He described how Matheny has evolved into a special hospital for children and adults with medically complex developmental disabilities and how difficult it is for parents to decide that their child would be better off living at the hospital, rather than at home. Wadsworth, a past president of The Friends of Matheny and a resident of Basking Ridge, recalled how, nearly 30 years ago, a small group of relative newcomers to the Somerset Hills organized a fundraising group to support what was then the Matheny School. In the intervening years, The Friends has raised over $3 million to support the work of what has become the Matheny … Continue reading

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RPI breaks ground on Rensselaer Center for Stem Cell Research

Posted: Published on June 23rd, 2012

Posted at: 06/22/2012 3:10 PM | Updated at: 06/22/2012 5:29 PM By: WNYT Staff TROY - Stem cells have been heralded as the frontier from which great medical treatments will come. Whether or not that materializes, New York wants to be in on the action. So Friday, ground was broken on the Rensselaer Center for Stem Cell Research. Located on the RPI campus, the state is providing a grant of almost $2.5 million over four years to get it built. And through it's funding, the state is very forward looking and it is foster a strong stem cell research community here in New York State, said Shirley Ann Jackson, president of RPI. RPI has already started working in this area, partnering with Albany Medical College and the University at Albany. This expands the scope of that work, with the hopes of finding new medicines and cures for a variety of illness and traumatic injuries. Go here to see the original: RPI breaks ground on Rensselaer Center for Stem Cell Research … Continue reading

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