A myopathy-related actin mutation increases contractile function.
about
Novel myosin-based therapies for congenital cardiac and skeletal myopathiesPathophysiological concepts in the congenital myopathies: blurring the boundaries, sharpening the focusAlterations at the cross-bridge level are associated with a paradoxical gain of muscle function in vivo in a mouse model of nemaline myopathyX-ray diffraction from flight muscle with a headless myosin mutation: implications for interpreting reflection patternsNemaline myopathy-related skeletal muscle α-actin (ACTA1) mutation, Asp286Gly, prevents proper strong myosin binding and triggers muscle weakness.Multimodal MRI and (31)P-MRS investigations of the ACTA1(Asp286Gly) mouse model of nemaline myopathy provide evidence of impaired in vivo muscle function, altered muscle structure and disturbed energy metabolismSkeletal muscle α-actin diseases (actinopathies): pathology and mechanisms.Sarcomere Dysfunction in Nemaline Myopathy.Distinct underlying mechanisms of limb and respiratory muscle fiber weaknesses in nemaline myopathy.Dysfunctional sarcomere contractility contributes to muscle weakness in ACTA1-related nemaline myopathy (NEM3).
P2860
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P2860
A myopathy-related actin mutation increases contractile function.
description
2012 nî lūn-bûn
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2012年の論文
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2012年論文
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2012年論文
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2012年論文
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2012年論文
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2012年論文
@zh-tw
2012年论文
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2012年论文
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2012年论文
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name
A myopathy-related actin mutation increases contractile function.
@en
A myopathy-related actin mutation increases contractile function.
@nl
type
label
A myopathy-related actin mutation increases contractile function.
@en
A myopathy-related actin mutation increases contractile function.
@nl
prefLabel
A myopathy-related actin mutation increases contractile function.
@en
A myopathy-related actin mutation increases contractile function.
@nl
P2093
P2860
P1476
A myopathy-related actin mutation increases contractile function.
@en
P2093
Hiroyuki Iwamoto
Isabelle Pénisson-Besnier
Johan Lindqvist
Julien Ochala
Meishan Li
Naoto Yagi
P2860
P2888
P304
P356
10.1007/S00401-012-0962-Z
P577
2012-02-23T00:00:00Z