Brain-specific Foxp1 deletion impairs neuronal development and causes autistic-like behaviour-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

Brain-specific Foxp1 deletion impairs neuronal development and causes autistic-like behaviour

Published:2014-09-30 Issue:5 Volume:20 Page:632-639
ISSN:1359-4184
Container-title:Molecular Psychiatry
language:en
Short-container-title:Mol Psychiatry

Author:

Bacon C,Schneider M,Le Magueresse C,Froehlich H,Sticht C,Gluch C,Monyer H,Rappold G A

Publisher

Springer Science and Business Media LLC

Subject

Cellular and Molecular Neuroscience,Psychiatry and Mental health,Molecular Biology

Link

http://www.nature.com/articles/mp2014116.pdf

Reference39 articles.

1. Talkowski ME, Rosenfeld JA, Blumenthal I, Pillalamarri V, Chiang C, Heilbut A et al. Sequencing chromosomal abnormalities reveals neurodevelopmental loci that confer risk across diagnostic Boundaries. Cell 2012; 149: 525–537.

2. Hamdan FF, Daoud H, Rochefort D, Piton A, Gauthier J, Langlois M et al. De novo mutations in FOXP1 in cases with intellectual disability, autism, and language impairment. Am J Hum Genet 2010; 87: 671–678.

3. Horn D, Kapeller J, Rivera-Brugues N, Moog U, Lorenz-Depiereux B, Eck S et al. Identification of FOXP1 deletions in three unrelated patients with mental retardation and significant speech and language deficits. Hum Mutat 2010; 31: E1851–E1860.

4. O'Roak BJ, Deriziotis P, Lee C, Vives L, Schwartz JJ, Girirajan S et al. Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations. Nat Genet 2011; 43: 585–589.

5. Le Fevre AK, Taylor S, Malek NH, Horn D, Carr CW, Abdul-Rahman OA et al. FOXP1 mutations cause intellectual disability and a recognizable phenotype. Am J Med Genet A 2013; 161: 3166–3175.

Cited by 108 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. Human-unique brain cell clusters are associated with learning disorders and human episodic memory activity;Molecular Psychiatry;2024-09-03

2. Knockout of the longevity gene Klotho perturbs aging and Alzheimer’s disease-linked brain microRNAs and tRNA fragments;Communications Biology;2024-06-11

3. Cell type specific roles of FOXP1 during early neocortical murine development;2024-06-08

4. Tactile sensory processing deficits in genetic mouse models of autism spectrum disorder;Journal of Neurochemistry;2024-06-04

5. Deciphering autism heterogeneity: a molecular stratification approach in four mouse models;2024-05-29

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