Work

A MYT1L syndrome mouse model recapitulates patient phenotypes and reveals altered brain development due to disrupted neuronal maturation

Year: 2021

Type: article

Source: Neuron

DOI: 10.1016/j.neuron.2021.09.009

Authors: Jiayang Chen, Mary E. Lambo, Xia Ge, Joshua T. Dearborn, Yating Liu, Katherine B. McCullough, Raylynn G. Swift, Dora R. Tabachnick, Lucy Tian, Kevin Noguchi, Joel R. Garbow, John N. Constantino, Harrison W. Gabel, Keith B. Hengen, Susan E. Maloney, Joseph D. Dougherty

Institutions: Washington University in St. Louis, Alvin J. Siteman Cancer Center

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: bronze

Funders: Washington University in St. Louis, National Institutes of Health, Intellectual and Developmental Disabilities Research Center, Center for Cellular Imaging, Washington University, National Institute of Mental Health, National Center for Advancing Translational Sciences, Eunice Kennedy Shriver National Institute of Child Health and Human Development

Awards: REGULATION OF MAMMALIAN SOCIAL BEHAVIOR BY THE GTF2I FAMILY OF PROTEINS, G1633233004, G1904872316, G2519494799, G2754895010, G2824222223, G9000052771, G9000066151, G9000248306

OpenAlex ID: W3203099629

FWCI: 5.293

Cites: 93

Cited by: 60

Related to: 10