Two Deafness-causing (DFNA20/26) Actin Mutations Affect Arp2/3-dependent Actin Regulation
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Biochemistry
Reference34 articles.
1. Mutations in the γ-actin gene (ACTG1) are associated with dominant progressive deafness (DFNA20/26);Zhu;Am. J. Hum. Genet.,2003
2. A novel missense mutation in ACTG1 causes dominant deafness in a Norwegian DFNA20/26 family, but ACTG1 mutations are not frequent among families with hereditary hearing impairment;Rendtorff;Eur. J. Hum. Genet.,2006
3. In vivo and in vitro effects of two novel γ-actin (ACTG1) mutations that cause DFNA20/26 hearing impairment;Morín;Hum. Mol. Genet.,2009
4. Effects of human deafness γ-actin mutations (DFNA20/26) on actin function;Bryan;J. Biol. Chem.,2006
5. An actin-filament-binding interface on the Arp2/3 complex is critical for nucleation and branch stability;Goley;Proc. Natl. Acad. Sci. U.S.A.,2010
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1. The non–muscle actinopathy–associated mutation E334Q in cytoskeletal γ– actin perturbs interaction of actin filaments with myosin and ADF/cofilin family proteins;2023-09-10
2. The actin cytoskeleton in hair bundle development and hearing loss;Hearing Research;2023-09
3. β-actin plasticity is modulated by coordinated actions of histidine 73 methylation, nucleotide type, and ions;2022-12-17
4. Bound nucleotide can control the dynamic architecture of monomeric actin;Nature Structural & Molecular Biology;2022-03-24
5. DFNA20/26 and Other ACTG1-Associated Phenotypes: A Case Report and Review of the Literature;Audiology Research;2021-10-18
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