Pages that link to "Q42827680"
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The following pages link to Myopathy mutations in alpha-skeletal-muscle actin cause a range of molecular defects. (Q42827680):
Displaying 37 items.
- Phenotypes of myopathy-related actin mutants in differentiated C2C12 myotubes (Q21284158) (← links)
- A mutation of beta -actin that alters depolymerization dynamics is associated with autosomal dominant developmental malformations, deafness, and dystonia (Q24546532) (← links)
- Allele-specific effects of human deafness gamma-actin mutations (DFNA20/26) on the actin/cofilin interaction (Q24650132) (← links)
- A method for rapidly screening functionality of actin mutants and tagged actins (Q24804053) (← links)
- Association of a Novel ACTA1 Mutation With a Dominant Progressive Scapuloperoneal Myopathy in an Extended Family (Q27345132) (← links)
- Structure of the F-actin-tropomyosin complex (Q28253185) (← links)
- Near-atomic resolution for one state of F-actin (Q30301084) (← links)
- Congenital myopathies: diseases of the actin cytoskeleton. (Q30343979) (← links)
- Conditional dominant mutations in the Caenorhabditis elegans gene act-2 identify cytoplasmic and muscle roles for a redundant actin isoform (Q30476857) (← links)
- In vivo and in vitro effects of two novel gamma-actin (ACTG1) mutations that cause DFNA20/26 hearing impairment (Q30489007) (← links)
- Zebrafish models for nemaline myopathy reveal a spectrum of nemaline bodies contributing to reduced muscle function (Q30661724) (← links)
- The Effects of Disease Models of Nuclear Actin Polymerization on the Nucleus. (Q30819346) (← links)
- The pathogenesis of ACTA1-related congenital fiber type disproportion (Q33280093) (← links)
- Phenotypes induced by NM causing alpha-skeletal muscle actin mutants in fibroblasts, Sol 8 myoblasts and myotubes (Q33417852) (← links)
- Dynamic regulation of sarcomeric actin filaments in striated muscle (Q34235998) (← links)
- Cell and molecular biology of nuclear actin. (Q34944464) (← links)
- Phenotypes of myopathy-related beta-tropomyosin mutants in human and mouse tissue cultures (Q34988373) (← links)
- Mutations and polymorphisms of the skeletal muscle alpha-actin gene (ACTA1). (Q34989619) (← links)
- Thoracic aortic aneurysm (TAAD)-causing mutation in actin affects formin regulation of polymerization (Q36217357) (← links)
- Protein misfolding disorders: pathogenesis and intervention (Q36501365) (← links)
- Functional effects of nemaline myopathy mutations on human skeletal alpha-actin (Q36744184) (← links)
- Actin-ADF/cofilin rod formation in Caenorhabditis elegans muscle requires a putative F-actin binding site of ADF/cofilin at the C-terminus (Q37322303) (← links)
- Actin isoform expression patterns during mammalian development and in pathology: insights from mouse models (Q37417675) (← links)
- Skeletal muscle α-actin diseases (actinopathies): pathology and mechanisms. (Q38028847) (← links)
- Myopathy-causing actin mutations promote defects in serum-response factor signalling (Q39750008) (← links)
- alpha-Skeletal muscle actin mutants causing different congenital myopathies induce similar cytoskeletal defects in cell line cultures (Q39885443) (← links)
- A Mutation in the ACTA1 gene Manifesting Nemaline Myopathy with Central Nervous System Lesions (Q42338874) (← links)
- Nemaline myopathy and non-fatal hypertrophic cardiomyopathy caused by a novel ACTA1 E239K mutation (Q45956684) (← links)
- Functional characterization of the human α-cardiac actin mutations Y166C and M305L involved in hypertrophic cardiomyopathy (Q47696386) (← links)
- Switch from actin alpha1 to alpha2 expression and upregulation of biomarkers for pressure overload and cardiac hypertrophy in taurine-deficient mouse heart (Q48380316) (← links)
- Mammalian Actins: Isoform-Specific Functions and Diseases (Q49145326) (← links)
- Electron cryomicroscopy as a powerful tool in biomedical research. (Q55267707) (← links)
- Nuclear actin: from discovery to function (Q57470054) (← links)
- Congenital myopathies (Q57588284) (← links)
- Mutations in actin, which are equivalent to human cardiomyopathy mutations, cause abnormal actin aggregation in nematode striated muscle (Q64102070) (← links)
- Congenital myopathies (Q82029849) (← links)
- G65V Substitution in Actin Disturbs Polymerization Leading to Inhibited Cell Elongation in Cotton (Q91708211) (← links)