Heterozygosity of murine Crkl does not recapitulate behavioral dimensions of human 22q11.2 hemizygosity-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

Heterozygosity of murine Crkl does not recapitulate behavioral dimensions of human 22q11.2 hemizygosity

Published:2020-12-10 Issue:5 Volume:20 Page:
ISSN:1601-1848
Container-title:Genes, Brain and Behavior
language:en
Short-container-title:Genes, Brain and Behavior

Author:

Yamauchi Takahira¹,Kang Gina¹,Hiroi Noboru¹²³^ORCID

Affiliation:

1. Department of Pharmacology University of Texas Health Science Center at San Antonio San Antonio Texas

2. Department of Cellular and Integrative Physiology University of Texas Health Science Center at San Antonio San Antonio Texas

3. Department of Cell Systems and Anatomy University of Texas Health Science Center at San Antonio San Antonio Texas

Funder

Eunice Kennedy Shriver National Institute of Child Health and Human Development

National Institute of Mental Health

National Institute on Deafness and Other Communication Disorders

Publisher

Wiley

Subject

Behavioral Neuroscience,Neurology,Genetics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/gbb.12719

Reference53 articles.

1. Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci

2. Refinement and Discovery of New Hotspots of Copy-Number Variation Associated with Autism Spectrum Disorder

3. Genomic Rearrangements and Gene Copy-Number Alterations as a Cause of Nervous System Disorders

4. Maternal approach behaviors toward neonatal calls are impaired by mother's experiences of raising pups with a risk gene variant for autism

5. Tbx1: identification of a 22q11.2 gene as a risk factor for autism spectrum disorder in a mouse model

Cited by 3 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Inborn errors of immunity associated with defects of thymic development;Pediatric Allergy and Immunology;2022-08

2. ATAD3B and SKIL polymorphisms associated with antipsychotic-induced QTc interval change in patients with schizophrenia: a genome-wide association study;Translational Psychiatry;2022-02-08

3. Two novel mouse models mimicking minor deletions in 22q11.2 deletion syndrome revealed the contribution of each deleted region to psychiatric disorders;Molecular Brain;2021-04-12

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线，采集、加工和组织学术论文而形成的新型学术文献查询和分析系统，可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容，当前同舟云学术共收录了国内外主流学术期刊6万余种，收集的期刊论文及会议论文总量共计约1.5亿篇，并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询！咨询电话：010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号京ICP备18003416号-3