Brain-specific Foxp1 deletion impairs neuronal development and causes autistic-like behaviour
出版年份 2014 全文链接
标题
Brain-specific Foxp1 deletion impairs neuronal development and causes autistic-like behaviour
作者
关键词
-
出版物
MOLECULAR PSYCHIATRY
Volume 20, Issue 5, Pages 632-639
出版商
Springer Nature
发表日期
2014-09-30
DOI
10.1038/mp.2014.116
参考文献
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注意:仅列出部分参考文献,下载原文获取全部文献信息。- FOXP1mutations cause intellectual disability and a recognizable phenotype
- (2013) Anna K. Le Fevre et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- Sequencing Chromosomal Abnormalities Reveals Neurodevelopmental Loci that Confer Risk across Diagnostic Boundaries
- (2012) Michael E. Talkowski et al. CELL
- The distinct and overlapping phenotypic spectra of FOXP1 and FOXP2 in cognitive disorders
- (2012) Claire Bacon et al. HUMAN GENETICS
- Autistic-like social behaviour in Shank2-mutant mice improved by restoring NMDA receptor function
- (2012) Hyejung Won et al. NATURE
- Absence of CNTNAP2 Leads to Epilepsy, Neuronal Migration Abnormalities, and Core Autism-Related Deficits
- (2011) Olga Peñagarikano et al. CELL
- Basal Ganglia Shapes Predict Social, Communication, and Motor Dysfunctions in Boys With Autism Spectrum Disorder
- (2011) Anqi Qiu et al. JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY
- An aetiological Foxp2 mutation causes aberrant striatal activity and alters plasticity during skill learning
- (2011) C A French et al. MOLECULAR PSYCHIATRY
- Shank3 mutant mice display autistic-like behaviours and striatal dysfunction
- (2011) João Peça et al. NATURE
- Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations
- (2011) Brian J O'Roak et al. NATURE GENETICS
- Foxp2 Regulates Gene Networks Implicated in Neurite Outgrowth in the Developing Brain
- (2011) Sonja C. Vernes et al. PLoS Genetics
- De Novo Mutations in FOXP1 in Cases with Intellectual Disability, Autism, and Language Impairment
- (2010) Fadi F. Hamdan et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Three hypotheses for developmental defects that may underlie some forms of autism spectrum disorder
- (2010) John LR Rubenstein CURRENT OPINION IN NEUROLOGY
- Identification of FOXP1 deletions in three unrelated patients with mental retardation and significant speech and language deficits
- (2010) Denise Horn et al. HUMAN MUTATION
- The neurobiology of repetitive behavior: Of mice…
- (2010) Marieke Langen et al. NEUROSCIENCE AND BIOBEHAVIORAL REVIEWS
- Foxp1 is an essential transcriptional regulator for the generation of quiescent naive T cells during thymocyte development
- (2009) X. Feng et al. BLOOD
- FOXP2 as a molecular window into speech and language
- (2009) Simon E. Fisher et al. TRENDS IN GENETICS
- Hox Repertoires for Motor Neuron Diversity and Connectivity Gated by a Single Accessory Factor, FoxP1
- (2008) Jeremy S. Dasen et al. CELL
- Impaired Synaptic Plasticity and Motor Learning in Mice with a Point Mutation Implicated in Human Speech Deficits
- (2008) Matthias Groszer et al. CURRENT BIOLOGY
- Ultrasonic vocalization impairment of Foxp2 (R552H) knockin mice related to speech-language disorder and abnormality of Purkinje cells
- (2008) E. Fujita et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
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