Work

Disrupted Homer scaffolds mediate abnormal mGluR5 function in a mouse model of fragile X syndrome

Year: 2012

Type: article

Source: Nature Neuroscience

DOI: 10.1038/nn.3033

Authors: Jennifer A Ronesi, Katie A Collins, Seth A Hays, Nien-Pei Tsai, Weirui Guo, Shari G Birnbaum, Jia-Hua Hu, Paul F Worley, Jay R Gibson, Kimberly M Huber

Institutions: The University of Texas Southwestern Medical Center, Johns Hopkins University, Johns Hopkins Medicine

Language: English

Topic: Genetics and Neurodevelopmental Disorders

Subfield: Genetics

Field: Biochemistry, Genetics and Molecular Biology

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: green

Funders: Autism Speaks, National Institutes of Health, National Institute of General Medical Sciences, National Institute of Neurological Disorders and Stroke, Eunice Kennedy Shriver National Institute of Child Health and Human Development

Awards: G285256626, G3115002321, G3302808937, G363963801, G3848173923, G3958605144, Mechanisms of mGluR5 function and dysfunction in mouse autism models, G5154890648, G5854036800, Cell and Molecular Biology Training Grant, G67592071

OpenAlex ID: W2134906491

FWCI: 15.22

Cites: 50

Cited by: 250

Related to: 10