Categoría: Noticias
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Genetic study redefines a form of excessive sweating as a treatable neurological condition
An international research team led by Dr. Frank Bosmans (Vrije Universiteit Brussel) has discovered a major genetic cause of hyperhidrosis (chronic and excessive sweating). The study, published in Science Advances, provides strong evidence that a genet…
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Which genes make people more susceptible to depression and other psychiatric disorders?
A study by the University of Barcelona has identified nearly 20 genes that could contribute to some people being more susceptible to depression, anxiety and traits such as irritability and neuroticism. These genes are regulated by the RBFOX1 gene, whic…
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Which genes make people more susceptible to depression and other psychiatric disorders?
A study by the University of Barcelona has identified nearly 20 genes that could contribute to some people being more susceptible to depression, anxiety and traits such as irritability and neuroticism. These genes are regulated by the RBFOX1 gene, whic…
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Q&A: A new model reveals hidden disease signatures and predicts health outcomes
Sarah Urbut, MD, Ph.D., of the Mass General Brigham Heart and Vascular Institute, is the lead author of a paper published in Nature, «A Bayesian framework for longitudinal EHR and genetic discovery.» Pradeep Natarajan, MD, MMSc, also of the Heart and V…
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Q&A: A new model reveals hidden disease signatures and predicts health outcomes
Sarah Urbut, MD, Ph.D., of the Mass General Brigham Heart and Vascular Institute, is the lead author of a paper published in Nature, «A Bayesian framework for longitudinal EHR and genetic discovery.» Pradeep Natarajan, MD, MMSc, also of the Heart and V…
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Missing metabolite may drive rare childhood brain disorder, new biosensor reveals
Scientists at Children’s Medical Center Research Institute at UT Southwestern (CRI) have discovered why babies born with a rare inborn error of metabolism called GPT2 deficiency suffer from severe neurological impairment. Using their newly developed bi…
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Missing metabolite may drive rare childhood brain disorder, new biosensor reveals
Scientists at Children’s Medical Center Research Institute at UT Southwestern (CRI) have discovered why babies born with a rare inborn error of metabolism called GPT2 deficiency suffer from severe neurological impairment. Using their newly developed bi…
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Researchers uncover novel pathway that causes epilepsy
Researchers have uncovered a novel biological pathway that can lead to seizures when disrupted. The findings also provide a new approach to improve the diagnosis of epilepsy, for which a genetic cause cannot be found in about 50% of individuals with th…
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Researchers uncover novel pathway that causes epilepsy
Researchers have uncovered a novel biological pathway that can lead to seizures when disrupted. The findings also provide a new approach to improve the diagnosis of epilepsy, for which a genetic cause cannot be found in about 50% of individuals with th…
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Global Parkinson’s gene map uncovers regional differences across 11 world regions
Parkinson’s disease is the second most common neurodegenerative disease worldwide after Alzheimer’s disease and, according to the World Health Organization, one of the fastest-growing neurological disorders. Yet genetic research into the disease has so…