ReviewJournal of neural transmission (Vienna, Austria : 1996)2026
Unraveling mGluR5 dysfunction in autism spectrum disorder: a multi-level analysis of genetic, molecular, and neurobiological mechanisms.
Review in Journal of neural transmission (Vienna, Austria : 1996), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Abstract
purpose of reviewThis review summarizes the current evidence regarding the role of metabotropic glutamate receptor 5 (mGluR5) in autism spectrum disorder (ASD) integrating genetic, molecular, neuroimaging, and therapeutic evidence to evaluate the mGluR5 related pathways in ASD mechanisms and evaluate its potential as a therapeutic target. RECENT
findingsGenetic studies report 25-fold peripheral GRM5 downregulation in ASD patients, with specific variants (rs905646, rs762724) showing biased paternal transmission and associations with increased symptom severity. Advances in super resolution imaging demonstrate that mGluR5 is confined to perisynaptic nanodomains with restricted lateral mobility, forming localized signaling microdomains critical for synaptic modulation. First in-human positron emission tomography (PET) studies using [
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