Effects of human deafness gamma-actin mutations (DFNA20/26) on actin function.

No abstract is available for this paper.

• Publication year

  2006

• Venue

  Journal of Biological Chemistry

• Publication date

  Unknown publication date

• Fields of study

  Biology, Medicine

• Identifiers
  PMID 16690605
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

• Differential interaction of cardiac, skeletal muscle, and yeast tropomyosins with fluorescent (pyrene235) yeast actin.

  2006cited by this paper
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• Differential distribution of beta- and gamma-actin in guinea-pig cochlear sensory and supporting cells.

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• Mitochondrial movement and inheritance in budding yeast.

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• Structural basis of actin filament nucleation and processive capping by a formin homology 2 domain

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• Role of the N‐terminal negative charges of actin in force generation and cross‐bridge kinetics in reconstituted bovine cardiac muscle fibres

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• A Mammalian Actin Substitution in Yeast Actin (H372R) Causes a Suppressible Mitochondria/Vacuole Phenotype*

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• A type V myosin (Myo2p) and a Rab-like G-protein (Ypt11p) are required for retention of newly inherited mitochondria in yeast cells during cell division.

  2004cited by this paper
• Actin mutations are one cause of congenital fibre type disproportion

  2004cited by this paper
• Live cell imaging of mitochondrial movement along actin cables in budding yeast.

  2004cited by this paper
• Nonmuscle myosin heavy-chain gene MYH14 is expressed in cochlea and mutated in patients affected by autosomal dominant hearing impairment (DFNA4).

  2004cited by this paper
• A mutation in the gamma actin 1 (ACTG1) gene causes autosomal dominant hearing loss (DFNA20/26)

  2003cited by this paper
• The mouse Formin mDia1 is a potent actin nucleation factor regulated by autoinhibition.

  2003cited by this paper
• Actin assembly and endocytosis: from yeast to mammals.

  2003cited by this paper
• Biochemical Consequences of the Cardiofunk (R177H) Mutation in Yeast Actin*

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  2003cited by this paper
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  2003cited by this paper
• Mutations in the gamma-actin gene (ACTG1) are associated with dominant progressive deafness (DFNA20/26).

  2003cited by this paper
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• From flies' eyes to our ears: Mutations in a human class III myosin cause progressive nonsyndromic hearing loss DFNB30

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• Regulation of Yeast Actin Behavior by Interaction of Charged Residues across the Interdomain Cleft*

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• An actin nucleation mechanism mediated by Bni1 and Profilin

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• Erratum: Formins direct Arp2/3-independent actin filament assembly to polarize cell growth in yeast

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• Yeast formins regulate cell polarity by controlling the assembly of actin cables

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• Locking the hydrophobic loop 262-274 to G-actin surface by a disulfide bridge prevents filament formation.

  2002cited by this paper
• Effect of Polymerization on the Subdomain 3/4 Loop of Yeast Actin*

  2002cited by this paper
• Formins direct Arp2/3-independent actin filament assembly to polarize cell growth in yeast

  2002cited by this paper
• Arp2/3 complex and actin dynamics are required for actin-based mitochondrial motility in yeast

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• Direct real-time observation of actin filament branching mediated by Arp2/3 complex using total internal reflection fluorescence microscopy

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• The second ADF/cofilin actin-binding site exists in F-actin, the cofilin-G-actin complex, but not in G-actin.

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• Visualization of mitochondrial movement in yeast.

  2001cited by this paper
• MYO6, the human homologue of the gene responsible for deafness in Snell's waltzer mice, is mutated in autosomal dominant nonsyndromic hearing loss.

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• Mechanisms that regulate mechanosensory hair cell differentiation.

  2001cited by this paper
• Tropomyosin-dependent Filament Formation by a Polymerization-defective Mutant Yeast Actin (V266G,L267G)*

  2000cited by this paper
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  2000cited by this paper
• Mutations in the skeletal muscle α-actin gene in patients with actin myopathy and nemaline myopathy

  1999cited by this paper
• Interaction in Vivo and in Vitro between the Yeast Fimbrin, SAC6P, and a Polymerization-defective Yeast Actin (V266G and L267G)*

  1999cited by this paper
• Three-dimensional imaging of the yeast actin cytoskeleton through the budding cell cycle.

  1998cited by this paper
• Domain motions in actin.

  1998cited by this paper
• Association of unconventional myosin MYO15 mutations with human nonsyndromic deafness DFNB3.

  1998cited by this paper
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  1998cited by this paper
• Beryllium Fluoride and Phalloidin Restore Polymerizability of a Mutant Yeast Actin (V266G,L267G) with Severely Decreased Hydrophobicity in a Subdomain 3/4 Loop*

  1997cited by this paper
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  1997cited by this paper
• Characterization of unconventional MYO6, the human homologue of the gene responsible for deafness in Snell's waltzer mice.

  1997cited by this paper
• The Effects of Severely Decreased Hydrophobicity in a Subdomain 3/4 Loop on the Dynamics and Stability of Yeast G-actin*

  1997cited by this paper
• Nonsyndromic deafness DFNA1 associated with mutation of a human homolog of the Drosophila gene diaphanous.

  1997cited by this paper
• Sorting of actin isoforms in chicken auditory hair cells.

  1997cited by this paper
• Mutations in the myosin VIIA gene cause non-syndromic recessive deafness

  1997cited by this paper
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  1996cited by this paper
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  1996cited by this paper
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• Removal of the amino-terminal acidic residues of yeast actin. Studies in vitro and in vivo.

  1992cited by this paper
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  1991cited by this paper
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  1990cited by this paper
• Atomic model of the actin filament

  1990cited by this paper
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• A system of shuttle vectors and yeast host strains designed for efficient manipulation of DNA in Saccharomyces cerevisiae.

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  1980cited by this paper
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