Loss of Wdfy3 in mice alters cerebral cortical neurogenesis reflecting aspects of the autism pathology
Year: 2014
Type: article
Source: Nature Communications
DOI: 10.1038/ncomms5692
Language: English
Subfield: Cognitive Neuroscience
Field: Neuroscience
Domain: Life Sciences
Open Access status: bronze
Funders: Simons Foundation, Nancy Lurie Marks Family Foundation, Regeneron Pharmaceuticals, Shriners Hospitals for Children, Simons Foundation Autism Research Initiative, National Institutes of Health, U.S. Public Health Service, University of California, Davis, National Institute of Mental Health, National Human Genome Research Institute, National Center for Research Resources, Eunice Kennedy Shriver National Institute of Child Health and Human Development
Awards: G1320710445, G2024429596, Production of Targeted Null Mutations for 10,000 Genes in C57BL/6 ES Cells, Wdfy3, a novel regulator of neuronal migration and connectivity, G5816300381, Defective Forebrain Development in Mutant Mice, UCD KOMP Project Repository, High-throughput targeted mutagenesis of mouse stem cell lines
OpenAlex ID: W2059543801
