polyglutamine

forkhead box P2 ; Homo sapiens







7 Article(s)
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PMID
Title
Pub. Year
#Total Relationships
1 29212017 Control of Huntington's Disease-Associated Phenotypes by the Striatum-Enriched Transcription Factor Foxp2. 2017 Dec 5 1
2 27933109 Functional characterization of rare FOXP2 variants in neurodevelopmental disorder. 2016 2
3 26497390 Contactin‑associated protein‑like 2 expression in SH‑SY5Y cells is upregulated by a FOXP2 mutant with a shortened poly‑glutamine tract. 2015 Dec 3
4 15737702 Absence of causative mutations and presence of autism-related allele in FOXP2 in Japanese autistic patients. 2005 Apr 1
5 15108192 Association between the FOXP2 gene and autistic disorder in Chinese population. 2004 May 15 1
6 11894222 FOXP2 is not a major susceptibility gene for autism or specific language impairment. 2002 May 2
7 10880297 The SPCH1 region on human 7q31: genomic characterization of the critical interval and localization of translocations associated with speech and language disorder. 2000 Aug 1