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DIAPH1 gene

Known as: hDIA1, LFHL1, DIAPH1 
National Institutes of Health

Related topics

Related topics

2 relations
DEAFNESS, AUTOSOMAL DOMINANT 1 (disorder)DIAPH1 protein, human

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2018
2018
Phosphoproteomic insights into processes influenced by the kinase-like protein DIA1/C3orf58
Many kinases are still ‘orphans,’ which means knowledge about their substrates, and often also about the processes they regulate… 
2015
2015
The effects of prior high intensity double poling on subsequent diagonal stride skiing characteristics
PurposeTo investigate the influence of prior high intensity double poling (DP) on physiological and biomechanical responses… 
2013
2013
The Rho Guanine Nucleotide Exchange Factor Syx Regulates the Balance of Dia and ROCK Activities To Promote Polarized-Cancer-Cell Migration
ABSTRACT The role of RhoA in promoting directed cell migration has been complicated by studies showing that it is activated both… 
2013
2013
Immediate Translation of Formin DIAPH1 mRNA after Its Exiting the Nucleus Is Required for Its Perinuclear Localization in Fibroblasts
DIAPH1 is a formin protein which promotes actin polymerization, stabilizes microtubules and consequently is involved in… 
2010
2010
Nano-mechanical properties of living cells expressing constitutively active RhoA effectors.
2008
2008
Functional interactions between phosphatase POPX2 and mDia modulate RhoA pathways
Rho GTPases and their downstream effectors regulate changes in the actin cytoskeleton that underlie cell motility and adhesion… 
2004
2004
Identification and characterization of human DIAPH3 gene in silico.
Formin homology proteins with FH1 and FH2 domains are signaling effectors for assembly and polarization of actin filaments. FH1… 
2004
2004
Identification and characterization of human FHDC1, mouse Fhdc1 and zebrafish fhdc1 genes in silico.
Formin homology proteins, implicated in organogenesis and carcinogenesis, are actin regulators with scaffold function. FMNL1… 
2004
2004
Characterization of FMN2 gene at human chromosome 1q43.
Mouse Formin (Fmn1) is an actin regulator interacting with Profilin, SRC, EMS1, FNBP1, FNBP2, FNBP3, FNBP4, WBP4 and alpha… 
Review
1999
Review
1999
Genomics and hearing impairment.
Hearing impairment is clinically and genetically heterogeneous. There are >400 disorders in which hearing impairment is a… 
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