Potential new drug target in Lou Gehrig's disease
Two proteins conspire to promote a lethal neurological disease, according to a study published online this week in the Journal of Experimental Medicine.
Nov 14, 2011
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Two proteins conspire to promote a lethal neurological disease, according to a study published online this week in the Journal of Experimental Medicine.
Nov 14, 2011
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In a set of identical twins, investigators led by researchers at Massachusetts General Hospital (MGH) and Children's Hospital Philadelphia (CHOP) have identified a mitochondrial disease not previously reported.
Oct 14, 2022
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Researchers at Vanderbilt University Medical Center, in collaboration with Seaside Therapeutics in Cambridge, Mass., have achieved a milestone in the development of a potential new treatment for fragile X syndrome, the most ...
Sep 16, 2011
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The largest study of its kind into childhood developmental disorders has discovered that jumping genes cause genetic changes in some patients with undiagnosed neurodevelopmental diseases. The research from the Wellcome Sanger ...
Oct 11, 2019
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(Medical Xpress)—A multinational research project led by the Universities of Dundee and Glasgow has identified a genetic determinant of hypertension (or high blood pressure), which could inform treatment of the condition ...
Nov 22, 2012
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A study led by researchers at Universitat Jaume I de Castellón has identified one of the genetic causes underlying the higher rate of melanoma in men. The results have been published in Biology of Sex Differences.
Jul 25, 2016
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Scientists have harnessed powerful data analysis tools and three-dimensional studies of genomic geography to implicate new risk genes for osteoporosis, the chronic bone-weakening condition that affects millions of people. ...
Mar 21, 2019
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Intellectual disability due to Fragile X and Down syndromes involves similar molecular pathways report researchers in The EMBO Journal. The two disorders share disturbances in the molecular events that regulate the way nerve ...
Aug 3, 2012
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Per Magnus, director of the Norwegian Mother and Child Cohort Study (MoBa) at the NIPH, together with two researchers from the UK and Denmark, have written a commentary article in the latest issue of the prestigious journal ...
Jan 27, 2017
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New research published Online First in The Lancet suggests that a high proportion of severe intellectual disability results from genetic causes that are not inherited. These findings are good news for parents, indicating ...
Sep 26, 2012
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