Alteration of tropomyosin function and folding by a nemaline myopathy-causing mutation.
about
Mutations in genes encoding fast-twitch contractile proteins cause distal arthrogryposis syndromesTropomyosin requires an intact N-terminal coiled coil to interact with tropomodulin.Abnormal actin binding of aberrant β-tropomyosins is a molecular cause of muscle weakness in TPM2-related nemaline and cap myopathyChanges in cross-bridge cycling underlie muscle weakness in patients with tropomyosin 3-based myopathy.Tropomyosin-based regulation of the actin cytoskeleton in time and space.Dual roles of tropomyosin as an F-actin stabilizer and a regulator of muscle contraction in Caenorhabditis elegans body wall muscleMuscle weakness in TPM3-myopathy is due to reduced Ca2+-sensitivity and impaired acto-myosin cross-bridge cycling in slow fibres.Novel deletion of lysine 7 expands the clinical, histopathological and genetic spectrum of TPM2-related myopathies.Tropomodulins and tropomyosins: working as a teamDisease severity and thin filament regulation in M9R TPM3 nemaline myopathy.Localization of the binding interface between leiomodin-2 and α-tropomyosin.The cardiomyopathy-associated K15N mutation in tropomyosin alters actin filament pointed end dynamics.Actin regulation by tropomodulin and tropomyosin in neuronal morphogenesis and function.Tropomyosin interacts with phosphorylated HSP27 in agonist-induced contraction of smooth muscle.
P2860
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P2860
Alteration of tropomyosin function and folding by a nemaline myopathy-causing mutation.
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2000 nî lūn-bûn
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2000 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
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2000 թվականի դեկտեմբերին հրատարակված գիտական հոդված
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2000年の論文
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2000年論文
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2000年論文
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2000年論文
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name
Alteration of tropomyosin function and folding by a nemaline myopathy-causing mutation.
@ast
Alteration of tropomyosin function and folding by a nemaline myopathy-causing mutation.
@en
Alteration of tropomyosin function and folding by a nemaline myopathy-causing mutation.
@nl
type
label
Alteration of tropomyosin function and folding by a nemaline myopathy-causing mutation.
@ast
Alteration of tropomyosin function and folding by a nemaline myopathy-causing mutation.
@en
Alteration of tropomyosin function and folding by a nemaline myopathy-causing mutation.
@nl
prefLabel
Alteration of tropomyosin function and folding by a nemaline myopathy-causing mutation.
@ast
Alteration of tropomyosin function and folding by a nemaline myopathy-causing mutation.
@en
Alteration of tropomyosin function and folding by a nemaline myopathy-causing mutation.
@nl
P2093
P2860
P1433
P1476
Alteration of tropomyosin function and folding by a nemaline myopathy-causing mutation
@en
P2093
N J Greenfield
S E Hitchcock-DeGregori
P2860
P304
P356
10.1016/S0006-3495(00)76554-4
P407
P577
2000-12-01T00:00:00Z