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T Kobayashi et al.
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OM Hernandez et al.
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A Sanbe et al.
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Effects of the mutation R145G in human cardiac troponin I on the kinetics of the contraction-relaxation cycle in isolated cardiac myofibrils
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K Harada et al.
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Impact of beta-myosin heavy chain expression on cardiac function during stress
M Krenz et al.
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WGL Kerrick et al.
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Prevalence and spectrum of thin filament mutations in an outpatient referral population with hypertrophic cardiomyopathy
SL Van Driest et al.
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J Köhler et al.
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Hypertrophic cardiomyopathy - Distribution of disease genes, spectrum of mutations, and implications for a molecular diagnosis strategy
P Richard et al.
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Activation of striated muscle: Nearest-neighbor regulatory-unit and cross-bridge influence on myofilament kinetics
JM Robinson et al.
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Myofilament calcium sensitivity and cardiac disease - Insights from troponin I isoforms and mutants
MV Westfall et al.
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The off rate of Ca2+ from troponin C is regulated by force-generating cross bridges in skeletal muscle
Y Wang et al.
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Functional analysis of a troponin I (R145G) mutation associated with familial hypertrophic cardiomyopathy
R Lang et al.
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Two mutations in troponin I that cause hypertrophic cardiomyopathy have contrasting effects on cardiac muscle contractility
D Burton et al.
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Functional consequences of the mutations in human cardiac troponin I gene found in familial hypertrophic cardiomyopathy
F Takahashi-Yanaga et al.
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The genetic basis for cardiomyopathy: from mutation identification to mechanistic paradigms
JG Seidman et al.
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An abnormal Ca2+ response in mutant sarcomere protein-mediated familial hypertrophic cardiomyopathy
D Fatkin et al.
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Transgenic modeling of a cardiac troponin I mutation linked to familial hypertrophic cardiomyopathy
J James et al.
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Clinical features of hypertrophic cardiomyopathy caused by a Lys183 deletion mutation in the cardiac troponin I gene
H Kokado et al.
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Altered regulatory properties of human cardiac troponin I mutants that cause hypertrophic cardiomyopathy
K Elliott et al.
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Altered regulation of cardiac muscle contraction by troponin T mutations that cause familial hypertrophic cardiomyopathy
D Szczesna et al.
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Deletion in the cardiac troponin I gene in a family from northern Sweden with hypertrophic cardiomyopathy
S Morner et al.
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Effect of Arg145Gly mutation in human cardiac troponin I on the ATPase activity of cardiac myofibrils
F Takahashi-Yanaga et al.
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