标题
Transcriptional Regulation by FOXP1, FOXP2, and FOXP4 Dimerization
作者
关键词
FOXP proteins, <em class=EmphasisTypeItalic >FOXP2</em>-regulated genes, Neurodevelopment, Autism
出版物
JOURNAL OF MOLECULAR NEUROSCIENCE
Volume 55, Issue 2, Pages 437-448
出版商
Springer Nature
发表日期
2014-07-15
DOI
10.1007/s12031-014-0359-7
参考文献
相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。- The Role of the FOXP Family of Transcription Factors in ASD
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- Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations
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- The E646D-ATP13A4 Mutation Associated with Autism Reveals a Defect in Calcium Regulation
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- FOXP2 as a molecular window into speech and language
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- Clinical and cytogenetic characterization of 13 Dutch patients with deletion 9p syndrome: Delineation of the critical region for a consensus phenotype
- (2008) Mariëlle E.M. Swinkels et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- Cooperative regulation in development by SMRT and FOXP1
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- Expression ofFOXP2in the developing monkey forebrain: Comparison with the expression of the genesFOXP1,PBX3, andMEIS2
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- Expression ofFoxp4in the developing and adult rat forebrain
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- A Functional Genetic Link between Distinct Developmental Language Disorders
- (2008) Sonja C. Vernes et al. NEW ENGLAND JOURNAL OF MEDICINE
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