AFQ056
National Institutes of Health
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Abstract 1. AFQ056 phenotyping results indicate that CYP1A1 is responsible for the formation of the oxidative metabolite, M3. In…
Fragile X syndrome (FXS) is the most common form of inherited intellectual disability and the leading single-gene cause of autism…
BackgroundFragile X syndrome (FXS), the leading cause of inherited mental retardation, is due to expansion and methylation of a…
L-dopa is the most effective, currently available treatment for Parkinson's disease (PD), but it leads to the development of…
A simple, sensitive, and selective liquid chromatography/tandem mass spectrometry method was validated for the identification and…
Fragile X syndrome (FXS) is an X-linked condition associated with intellectual disability and behavioral problems. It is caused…
Reference EPFL-CONF-178514View record in Web of Science Record created on 2012-06-25, modified on 2016-08-09
Epigenetic modification of the FMR1 gene in fragile X syndrome is associated with differential response to the mGluR5 antagonist…
The present invention is the use of a compound which acts as a mGluR5 antagonist in the gastrointestinal tract disorders, urinary…