News tagged with gene fmr1
Study links Fragile X Syndrome proteins and RNA editing mistakes at nerve-muscle junction
The most common form of heritable cognitive impairment is Fragile X Syndrome, caused by mutation or malfunction of the FMR1 gene. Loss of FMR1 function is also the most common genetic cause of autism. Understanding ...
Neuroscience
Oct 30, 2011 |
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Fragile X makes brain cells talk too much, research shows
The most common inherited form of mental retardation and autism, fragile X syndrome, turns some brain cells into chatterboxes, scientists at Washington University School of Medicine in St. Louis report.
Neuroscience
Feb 20, 2013 |
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Boosting natural marijuana-like brain chemicals treats fragile X syndrome symptoms
American and European scientists have found that increasing natural marijuana-like chemicals in the brain can help correct behavioral issues related to fragile X syndrome, the most common known genetic cause of autism.
Autism spectrum disorders
Sep 25, 2012 |
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A striking link is found between the Fragile-X gene and mutations that cause autism
A team led by scientists at Cold Spring Harbor Laboratory (CSHL) publishes research today indicating a striking association between genes found disrupted in children with autism and genes that are targets of FMRP, the protein ...
Genetics
Apr 25, 2012 |
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Genetic defect causing fragile X-related disorders more common than thought
A single genetic defect on the X chromosome that can result in a wide array of conditions—from learning and emotional difficulties to primary ovarian insufficiency in women and tremors in middle-aged men—occurs at a much ...
Genetics
Dec 20, 2012 |
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Stem cell research paves way for progress on dealing with Fragile X retardation
Researchers at the Hebrew University of Jerusalem have achieved, for the first time, the generation of neuronal cells from stem cells of Fragile X patients. The discovery paves the way for research that will examine restoration ...
Medical research
May 22, 2012 |
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