Sentences with phrase «medical genetic research»
Medical genetic research in all species is progressing rapidly.
https://cgejournal.biomedcentral.com/ Not exact matches
But rather than buying up a genetic research outfit, it decided to build its own in the form of the Regeneron Genetics Center (RGC), an ambitious four - year old effort to sequence as many exomes (the protein - encoding part of the genome) as possible, pair them with medical records, and accelerate drug development.
A 4 - year - old who asks about his genetic condition won't understand the neuroscience behind his disability and a 10 - year - old doesn't need to know about all the latest medical research behind why he takes a certain medication.
The Genetic Interest Group, Great Ormond Street Hospital for Children NHS Trust and UCL Institute for Child Health have written to health minister Lord Darzi calling for an amendment to the human fertilisation and embryology bill which would allow parents to consent to their child's genetic material being used in medical reGenetic Interest Group, Great Ormond Street Hospital for Children NHS Trust and UCL Institute for Child Health have written to health minister Lord Darzi calling for an amendment to the human fertilisation and embryology bill which would allow parents to consent to their child's genetic material being used in medical regenetic material being used in medical research.
In my case, funding from the Howard Hughes Medical Institute's Precollege Science Education Program Initiative for Biomedical Research Institutions and the Science Education Partnership Award from the National Center for Research Resources at the National Institutes of Health enable the Genetic Science Learning Center to provide postdoctoral training for research scientists transitioning into science education Research Institutions and the Science Education Partnership Award from the National Center for Research Resources at the National Institutes of Health enable the Genetic Science Learning Center to provide postdoctoral training for research scientists transitioning into science education Research Resources at the National Institutes of Health enable the Genetic Science Learning Center to provide postdoctoral training for research scientists transitioning into science education research scientists transitioning into science education careers.
Hendrik recovered several short gene fragments, which represented just one - ten - thousandth of 1 percent of the bee's total genetic information.With George as a co-author, it was Hendrik's first scientific paper, published in Medical Science Research in 1992.
Investigators at the Medical University of South Carolina (MUSC) report pre-clinical research showing that a genetic variant encoded in neutrophil cystolic factor 1 (NCF1) is associated with increased risk for autoimmune diseases, including systemic lupus erythematosus (SLE), rheumatoid arthritis, and Sjögren's syndrome, in the January 2017 issue of Nature Genetics.
«The next step of progress is to use this knowledge to decipher what potential impact the genetic variants can have on the health of individuals, when we conduct health - related research,» added Professor Michael Pepper, Unit Director of the South African Medical Research Council's (SAMRC) Stem Cell Research and Therapy Unit, Faculty of Health Sciences at the University of Presearch,» added Professor Michael Pepper, Unit Director of the South African Medical Research Council's (SAMRC) Stem Cell Research and Therapy Unit, Faculty of Health Sciences at the University of PResearch Council's (SAMRC) Stem Cell Research and Therapy Unit, Faculty of Health Sciences at the University of PResearch and Therapy Unit, Faculty of Health Sciences at the University of Pretoria.
Working with an international group of scientists from Cardiff University, Stanford University and Duke University in addition to screening post-mortem brain samples from the Stanley Medical Research Institute, the scientists are the first to identify a molecular genetic component of the blood brain barrier with the development of schizophrenia.
Over the course of a year, a committee led by Green and Leslie Biesecker, chief of the Genetic Disease Research Branch at the National Human Genome Research Institute in Bethesda, Maryland, has been weighing how to handle «incidental findings» that turn up when a genome or exome is sequenced for some other medical reason.
Researchers from the Stowers Institute for Medical Research in collaboration with Fred Hutchinson Cancer Research Center researchers have identified an unprecedented genetic survival strategy that would be right at home in an Agatha Christie murder mystery novel.
Hungary's Medical Research Council (ETT), which advises the government on health policy, has asked public prosecutors to investigate a genetic - diagnostic company that certified that a member of parliament did not have Roma or Jewish heritage.
One of many researchers lending support to the cause is genome scientist and Nobelist John Sulston of the University of Manchester, U.K., who warns that «gene patents can have a chilling impact on research, obstruct the development of new genetic tests, and interfere with medical care.»
A research team at Cincinnati Children's Hospital Medical Center is leveraging semantic capabilities to find the underlying genetic causes of cardiovascular diseases.
Professor Johann de Bono, Regius Professor of Cancer Research at The Institute of Cancer Research, London, and Consultant Medical Oncologist at The Royal Marsden NHS Foundation Trust, said, «Our study identifies, for the first time, genetic changes that allow prostate cancer cells to become resistant to the precision medicine olaparib.
The St. Laurent Institute, a non-profit medical research institute focused on the systems biology of disease, today announced in a study published in the July edition of Genome Biology, that genetic matter, previously ignored by the scientific community, may play an important role in cancer.
Until now, the largest genetic map for humans was created by the Marshfield Medical Research Foundation in Marshfield, Wisconsin.
The two Univerity of Washington studies, «Great ape genetic diversity and population history,» published in Nature, and «Evolution and diversity of copy number variation in the great ape lineage,» published in Genome Research, are funded by NIH grant HG002385 and support from the Howard Hughes Medical Institute.
«The research provided us the deepest survey to date of great ape genetic diversity with evolutionary insights into the divergence and emergence of great - ape species,» noted Eichler, a UW professor of genome sciences and a Howard Hughes Medical Institute Investigator.
Advocates of the measure consider its protections crucial to the advance of medical research and personalized medicine, both of which rely increasingly on genetic testing.
Genome - wide association studies, which try to find correlations between particular genetic variations and disease diagnoses, are a staple of modern medical research.
Genetic tests could be performed only for research or medical reasons, ruling out their use by employers or insurance companies to screen applicants.
New research shows that the response to medical treatment depends on genetic factors.
«To date, research into resilience has tended to take into account a very extensive range of social, psychological, and even genetic factors that positively influence mental flexibility, such as social support, certain personality traits, and typical behavior patterns,» explained Professor Raffael Kalisch, one of the authors of the current publication and the director of the Neuroimaging Center, a central research platform of the Mainz University Medical Center and the Research Center on Translational Neurosresearch into resilience has tended to take into account a very extensive range of social, psychological, and even genetic factors that positively influence mental flexibility, such as social support, certain personality traits, and typical behavior patterns,» explained Professor Raffael Kalisch, one of the authors of the current publication and the director of the Neuroimaging Center, a central research platform of the Mainz University Medical Center and the Research Center on Translational Neurosresearch platform of the Mainz University Medical Center and the Research Center on Translational NeurosResearch Center on Translational Neurosciences.
The artificial DNA, or XNAs, are «simple chemical alternatives to store and propagate genetic information,» says team leader Philipp Holliger of the Medical Research Council Laboratory of Molecular Biology in Cambridge, England.
A study by scientists at the Children's Medical Center Research Institute at UT Southwestern (CRI) is providing insight into the genetic basis of neuropsychiatric disorders.
Last year, the plans ran into a last - minute hitch when the Medical Research Council withdrew its support after research showed that tamoxifen can alter genetic material in rats» liver cells (This Week, 14 MarcResearch Council withdrew its support after research showed that tamoxifen can alter genetic material in rats» liver cells (This Week, 14 Marcresearch showed that tamoxifen can alter genetic material in rats» liver cells (This Week, 14 March 1992).
Professor Jeremy Pearson, Associate Medical Director at the BHF, which part - funded the study, said: «By using the power of very large scale genetic studies, this research is the first to show that the known association between increased height and a lower risk of coronary heart disease is at least in part due to genetics, rather than purely down to nutrition or lifestyle factors.
A chance meeting with Dr. James R. Lupski, the Cullen Professor and Vice Chair of Molecular and Human Genetics and professor of pediatrics at Baylor, at a medical meeting in Istanbul, Turkey would lead to Karaca's recruitment as a trainee in Lupski's lab where the research took off and eventually the team unveiled new clues about the genetic malfunction that may be causing the disorder in these families.
The first is that it could just be one last random mutation that finally provides the cells with the genetic wherewithal to become malignant, says David Thomas, a cancer researcher at the Garvan Institute of Medical Research in Sydney, Australia.
Released by Health Minister Tanya Plibersek, Strategic Review of Health and Medical Research in Australia — Better Health Through Research, known as the McKeon Review, recommended strengthening the country's IP system and argued against outlawing patents on human genetic material.
The study, published by Nature Genetics, was funded by the Medical Research Council (MRC) using detailed genetic data provided by UK Biobank and data provided by other countries, and supported by the Wellcome Trust.
«This [patent] would not have been an issue if Myriad and Genetic Technologies had remained strategically sensitive,» notes Julian Clark, head of business development at the Walter and Eliza Hall Institute of Medical Research in Melbourne.
Each of the working groups is responsible for developing a proposal for a set of genomes to sequence that would advance knowledge in one of three important scientific areas: identifying areas in genetic research where the application of high - throughput sequencing resources would rapidly lead to significant medical advances; understanding of the human genome; and understanding the evolutionary biology of genomes.
The Woodlands, Texas — May 11, 2006 — Lexicon Genetics Incorporated (Nasdaq: LEXG) announced today that it was awarded a grant from the United States Army Medical Research & Materiel Command (USAMRMC) for the identification of targets that may be important in the development of drugs to prevent or treat spinal muscular atrophy (SMA), a neurodegenerative disorder and the leading genetic cause of death in early childhood.
The Coriell Institute for Medical Research is a not - for - profit research organization «dedicated to understanding human genetic diseases and providing the highest quality genetic resourcesResearch is a not - for - profit research organization «dedicated to understanding human genetic diseases and providing the highest quality genetic resourcesresearch organization «dedicated to understanding human genetic diseases and providing the highest quality genetic resources».
To address the growing need for medical staff in the insurance industry to understand genetic testing, the National Human Genome Research Institute (NHGRI) has collaborated with the Blue Cross Blue Shield Association to produce this educational webinar series.
Other gene banks, such as Iceland's deCODE project, store human genetic material for medical research.
Now researchers led by the Wellcome Trust - Medical Research Council Cambridge Stem Cell Institute have managed to induce a ground state by rewiring the genetic circuitry in human embryonic stem (ES) cells and in adult cells that have been induced into a pluripotent state.
The meeting will give the opportunity to update information on techniques and models in transgenesis and genetic engineering.It is intended for Master, PhD and medical students with a background in molecular biology and genetics as an introduction to future work in these rapidly developing areas of research.
«We're pleased to fund this project that will bring together well - established and highly regarded research groups throughout the world to enable an unprecedented sharing and analysis of Alzheimer genetic data,» said William Thies, Ph.D., Alzheimer's Association Chief Medical and Scientific Officer, and Philippe Lagayette, President of the Fondation Plan Alzheimer in France.
Having determined a strategy and a work plan Genetic Alliance UK then seeks resources to implement it from a wide range of potential funders including National Governments, the EU, the pharmaceutical and medical devices industry, the Medical Research Council, Wellcome Trust, The Big Lottery and medical devices industry, the Medical Research Council, Wellcome Trust, The Big Lottery and Medical Research Council, Wellcome Trust, The Big Lottery and others.
Finally we have the genetic blueprint that will unveil the mysteries of the mouse and will prove invaluable for human medical research.»
Mats Hansson is the director of the Centre for Research Ethics & Bioethics at the University of Uppsala and has conducted extensive research in biomedical ethics as principal investigator in multi-disciplinary research projects dealing with issues ranging from ethical, social and legal aspects of the implementation of genetic diagnosis in clinical practice and the use of human tissue materials in research, to clinical and medicalResearch Ethics & Bioethics at the University of Uppsala and has conducted extensive research in biomedical ethics as principal investigator in multi-disciplinary research projects dealing with issues ranging from ethical, social and legal aspects of the implementation of genetic diagnosis in clinical practice and the use of human tissue materials in research, to clinical and medicalresearch in biomedical ethics as principal investigator in multi-disciplinary research projects dealing with issues ranging from ethical, social and legal aspects of the implementation of genetic diagnosis in clinical practice and the use of human tissue materials in research, to clinical and medicalresearch projects dealing with issues ranging from ethical, social and legal aspects of the implementation of genetic diagnosis in clinical practice and the use of human tissue materials in research, to clinical and medicalresearch, to clinical and medical ethics.
«Genetic counseling and testing are not well - matched to medical need,» said Allison Kurian, associate professor of medicine and of health research and policy at Stanford University School of Medicine.
The study entitled «A multi-national Arab genome - wide association study identifies new genetic associations for Rheumatoid Arthritis», has now been published in the prestigious medical journal Arthritis & Rheumatology; and was supported by grant from the Qatar National Research Fund, a member of Qatar Foundation.
Recently, research led by Charis Eng, M.D., Ph.D., Chair of Cleveland Clinic's Genomic Medicine Institute and published in the March 26 issue of the Journal of the American Medical Association (http://jama.ama-assn.org/cgi/content/abstract/299/12/1437), suggests genetic variety may be associated with decreased cancer risk.
Her work has led to advances in understanding the ethical aspects of physical and mental illness research, societal implications for genetic innovation, the role of stigma in health disparities, the impact of medical student and physician health issues and optimal approaches to fostering professionalism in medicine.
Published in the Journal of Medical Ethics Affleck PG Is it ethical to deny genetic research participants individualised results?
Hieter and Jeannie Lee, a professor at Harvard Medical School and the Massachusetts General Hospital (and 2018 GSA President), were co-chairs of 2016's Allied Genetics Conference, which brought together over 3,000 attendees from seven different genetic research communities to exchange ideas and findings.