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GoPubMed Proteins lists recent and important papers and reviews for proteins. Page last changed on 19 Dec 2016.

FCH and double SH3 domains 1

FCHSD1, A030002D08Rik
Top mentioned proteins: ACID, FBP17, SRGAP1, beta 2-adrenoceptor, N-WASP
Papers on FCHSD1
Transcription factor Sp4 regulates expression of nervous wreck 2 to control NMDAR1 levels and dendrite patterning.
Gill et al., Boston, United States. In Dev Neurobiol, 2015
Here we report that Sp4 activates transcription of Nervous Wreck 2 (Nwk2; also known as Fchsd1) and, further, that Nwk2, an F-BAR domain-containing protein, mediates Sp4-dependent regulation of dendrite patterning and cell surface expression of NR1.
Pharmacogenetic predictor of extrapyramidal symptoms induced by antipsychotics: multilocus interaction in the mTOR pathway.
Lafuente et al., Barcelona, Spain. In Eur Neuropsychopharmacol, 2015
In Cohort 1, we identified a four-way interaction, including the rs1130214 (AKT1), rs456998 (FCHSD1), rs7211818 (Raptor) and rs1053639 (DDIT4), that correctly predicted 97 of the 114 patients (85% accuracy).
FCHSD1 and FCHSD2 are expressed in hair cell stereocilia and cuticular plate and regulate actin polymerization in vitro.
Xu et al., Jinan, China. In Plos One, 2012
Mammalian FCHSD1 and FCHSD2 are homologous proteins containing an amino-terminal F-BAR domain and two SH3 domains near their carboxyl-termini.
Characterization of RUSC1 and RUSC2 genes in silico.
Katoh et al., Narashino, Japan. In Oncol Rep, 2004
We have previously cloned (or identified) and characterized novel genes encoding SH3 domain proteins, such as MAP3K10, FNBP1L, FNBP2, FCHSD1, FCHSD2, LASP2 and MPP7.
Identification and characterization of human FCHO2 and mouse Fcho2 genes in silico.
Katoh et al., Narashino, Japan. In Int J Mol Med, 2004
FNBP1, FNBP1L, CIP4/TRIP10, FNBP2, SRGAP1/ARHGAP13, SRGAP2/ARHGAP14, ARHGAP4, FCHSD1, and FCHSD2 constitute the FCFBS superfamily characterized by FES-CIP4 homology (FCH) domain, Formin-binding FNBP1-FNBP2 homology (FBH) domain, and SRC homology 3 (SH3) domain.
Identification and characterization of human FCHSD1 and FCHSD2 genes in silico.
Katoh et al., Tokyo, Japan. In Int J Mol Med, 2004
Complete coding sequence of human FCHSD1 was derived from FLJ00007 (NM_033449.1)
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