The E22K mutation of myosin RLC that causes familial hypertrophic cardiomyopathy increases calcium sensitivity of force and ATPase in transgenic mice
about
Understanding cardiomyopathy phenotypes based on the functional impact of mutations in the myosin motorMyofilament Calcium Sensitivity: Role in Regulation of In vivo Cardiac Contraction and RelaxationThe effect of myosin RLC phosphorylation in normal and cardiomyopathic mouse heartsCardiac myosin light chain kinase is necessary for myosin regulatory light chain phosphorylation and cardiac performance in vivoIn the thick of it: HCM-causing mutations in myosin binding proteins of the thick filamentAcceleration of stretch activation in murine myocardium due to phosphorylation of myosin regulatory light chainHypertrophic cardiomyopathy associated Lys104Glu mutation in the myosin regulatory light chain causes diastolic disturbance in miceTAZ expression as a prognostic indicator in colorectal cancer.Signaling to myosin regulatory light chain in sarcomeresEffect of alanine replacement of l17 and f19 on the aggregation and neurotoxicity of arctic-type aβ40A chemical genomics approach to identification of interactions between bioactive molecules and alternative reading frame proteins.Single myosin cross-bridge orientation in cardiac papillary muscle detects lever-arm shear strain in transduction.The R21C Mutation in Cardiac Troponin I Imposes Differences in Contractile Force Generation between the Left and Right Ventricles of Knock-In MiceStructural and functional aspects of the myosin essential light chain in cardiac muscle contraction.Mice deleted for heart-type cytochrome c oxidase subunit 7a1 develop dilated cardiomyopathy.Malignant familial hypertrophic cardiomyopathy D166V mutation in the ventricular myosin regulatory light chain causes profound effects in skinned and intact papillary muscle fibers from transgenic mice.Discrete effects of A57G-myosin essential light chain mutation associated with familial hypertrophic cardiomyopathyIncreased myofilament Ca2+-sensitivity and arrhythmia susceptibility.Molecular mechanisms of sarcomere dysfunction in dilated and hypertrophic cardiomyopathy.Kinetics of a single cross-bridge in familial hypertrophic cardiomyopathy heart muscle measured by reverse Kretschmann fluorescence.Single molecule kinetics in the familial hypertrophic cardiomyopathy D166V mutant mouse heart.Molecular and Functional Effects of a Splice Site Mutation in the MYL2 Gene Associated with Cardioskeletal Myopathy and Early Cardiac Death in Infants.Fluorescence lifetime of actin in the familial hypertrophic cardiomyopathy transgenic heart.
P2860
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P2860
The E22K mutation of myosin RLC that causes familial hypertrophic cardiomyopathy increases calcium sensitivity of force and ATPase in transgenic mice
description
2005 nî lūn-bûn
@nan
2005 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
2005 թվականի օգոստոսին հրատարակված գիտական հոդված
@hy
2005年の論文
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2005年論文
@yue
2005年論文
@zh-hant
2005年論文
@zh-hk
2005年論文
@zh-mo
2005年論文
@zh-tw
2005年论文
@wuu
name
The E22K mutation of myosin RL ...... and ATPase in transgenic mice
@ast
The E22K mutation of myosin RL ...... and ATPase in transgenic mice
@en
The E22K mutation of myosin RL ...... and ATPase in transgenic mice
@nl
type
label
The E22K mutation of myosin RL ...... and ATPase in transgenic mice
@ast
The E22K mutation of myosin RL ...... and ATPase in transgenic mice
@en
The E22K mutation of myosin RL ...... and ATPase in transgenic mice
@nl
prefLabel
The E22K mutation of myosin RL ...... and ATPase in transgenic mice
@ast
The E22K mutation of myosin RL ...... and ATPase in transgenic mice
@en
The E22K mutation of myosin RL ...... and ATPase in transgenic mice
@nl
P2093
P3181
P356
P1476
The E22K mutation of myosin RL ...... and ATPase in transgenic mice
@en
P2093
Danuta Szczesna-Cordary
Georgianna Guzman
Jiaju Zhao
Jianqin Wei
Olga Hernandez
Zoraida Diaz-Perez
P304
P3181
P356
10.1242/JCS.02492
P407
P577
2005-08-15T00:00:00Z