16p11.2 Deletion Syndrome Mice Display Sensory and Ultrasonic Vocalization Deficits During Social Interactions-Reference-Cited by-同舟云学术

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16p11.2 Deletion Syndrome Mice Display Sensory and Ultrasonic Vocalization Deficits During Social Interactions

Published:2015-02-07 Issue:5 Volume:8 Page:507-521
ISSN:1939-3792
Container-title:Autism Research
language:en
Short-container-title:Autism Research

Author:

Yang Mu¹,Mahrt Elena J.²,Lewis Freeman¹,Foley Gillian¹,Portmann Thomas³⁴,Dolmetsch Ricardo E.³⁵,Portfors Christine V.²,Crawley Jacqueline N.¹

Affiliation:

1. Department of Psychiatry and Behavioral Sciences; University of California Davis School of Medicine; Sacramento CA 95817

2. School of Biological Sciences; College of Arts and Sciences, Washington State University Vancouver; Vancouver WA 98686

3. Department of Neurobiology; Stanford University School of Medicine; Stanford CA 94305

4. Drug Discovery Program; Circuit Therapeutics Inc.; Menlo Park CA 94025

5. Novartis Institutes for Biomedical Research; Cambridge MA 02139

Funder

Simons Foundation

National Institute of Mental Health Intramural Research Program

National Institutes of Health Pioneer Award

National Science Foundation

the Swiss National Science Foundation

Publisher

Wiley

Subject

Genetics (clinical),Neurology (clinical),General Neuroscience

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/aur.1465/fullpdf

Reference77 articles.

1. Deletions of 16p11.2 and 19p13.2 in a family with intellectual disability and generalized epilepsy;Bassuk;American Journal of Medical Genetics. Part A,2013

2. Extending the phenotype of recurrent rearrangements of 16p11.2: deletions in mentally retarded patients without autism and in normal individuals;Bijlsma;European Journal of Medical Genetics,2009

3. Transcriptional consequences of 16p11.2 deletion and duplication in mouse cortex and multiplex autism families;Blumenthal;American Journal of Human Genetics,2014

4. Autism-relevant social abnormalities and cognitive deficits in engrailed-2 knockout mice;Brielmaier;PLos One,2012

5. Hormonal regulation of chemosignals of female mice that elicit ultrasonic vocalizations from males;Byatt;Hormones and Behavior,1986

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1. Chromosome 16p11.2 microdeletion syndrome with microcephaly and Dandy-Walker malformation spectrum: expanding the known phenotype;Human Genomics;2024-09-04

2. Neurocognitive profiles of 22q11.2 and 16p11.2 deletions and duplications;Molecular Psychiatry;2024-07-24

3. Understanding copy number variations through their genes: a molecular view on 16p11.2 deletion and duplication syndromes;Frontiers in Pharmacology;2024-06-14

4. Adenosine mediates the amelioration of social novelty deficits during rhythmic light treatment of 16p11.2 deletion female mice;Molecular Psychiatry;2024-05-13

5. The gut metabolite indole-3-propionic acid activates ERK1 to restore social function and hippocampal inhibitory synaptic transmission in a 16p11.2 microdeletion mouse model;Microbiome;2024-03-28

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