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Steven Marston

Showing results (11-20 of 32) with videos related to

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Journal of Muscle Research and Cell Motility|April 29, 2019
Troponin structure and function: a view of recent progressSteven Marston, Juan Eiros Zamora
Neuromuscular Disorders : NMD|November 4, 2008
Genotype-phenotype correlations in ACTA1 mutations that cause congenital myopathiesJuan-Juan Feng, Steven Marston
Journal of Molecular and Cellular Cardiology|May 7, 2002
In vitro motility analysis of thin filaments from failing and non-failing human heart: troponin from failing human hearts induces slower filament sliding and higher Ca(2+) sensitivityAdam Knott, Ian Purcell, Steven Marston
Journal of Muscle Research and Cell Motility|February 12, 2004
Cooperative inhibition of actin filaments in the absence of tropomyosinSaira Ansari, Mohammed El-Mezgueldi, Steven Marston
Neuromuscular Disorders : NMD|January 22, 2004
Functional characterisation of a mutant actin (Met132Val) from a patient with nemaline myopathySteven Marston, Mahmooda Mirza, Hassan Abdulrazzak, et al.
American Journal of Physiology. Heart and Circulatory Physiology|October 4, 2015
A dilated cardiomyopathy mutation blunts adrenergic response and induces contractile dysfunction under chronic angiotensin II stressRoss Wilkinson, Weihua Song, Natalia Smoktunowicz, et al.
Frontiers in Physiology|April 9, 2020
Pressure Overload Is Associated With Low Levels of Troponin I and Myosin Binding Protein C Phosphorylation in the Hearts of Patients With Aortic StenosisO'neal Copeland, Andrew Messer, Andrew Jabbour, et al.
Journal of Muscle Research and Cell Motility|November 8, 2011
How do MYBPC3 mutations cause hypertrophic cardiomyopathy?Steven Marston, O'Neal Copeland, Katja Gehmlich, et al.
Biophysical Reviews|July 22, 2020
Donor hearts in the Sydney Heart Bank: reliable control but is it 'normal' heart?Steven Marston, Adam Jacques, Christopher Bayliss, et al.
The Biochemical Journal|February 21, 2002
Two mutations in troponin I that cause hypertrophic cardiomyopathy have contrasting effects on cardiac muscle contractilityDavid Burton, Hassan Abdulrazzak, Adam Knott, et al.
Pageof 4

Showing results (11-20 of 32) with videos related to

Sort By:
Pageof 4
Journal of Muscle Research and Cell Motility|April 29, 2019
Troponin structure and function: a view of recent progressSteven Marston, Juan Eiros Zamora
Neuromuscular Disorders : NMD|November 4, 2008
Genotype-phenotype correlations in ACTA1 mutations that cause congenital myopathiesJuan-Juan Feng, Steven Marston
Journal of Molecular and Cellular Cardiology|May 7, 2002
In vitro motility analysis of thin filaments from failing and non-failing human heart: troponin from failing human hearts induces slower filament sliding and higher Ca(2+) sensitivityAdam Knott, Ian Purcell, Steven Marston
Journal of Muscle Research and Cell Motility|February 12, 2004
Cooperative inhibition of actin filaments in the absence of tropomyosinSaira Ansari, Mohammed El-Mezgueldi, Steven Marston
Neuromuscular Disorders : NMD|January 22, 2004
Functional characterisation of a mutant actin (Met132Val) from a patient with nemaline myopathySteven Marston, Mahmooda Mirza, Hassan Abdulrazzak, et al.
American Journal of Physiology. Heart and Circulatory Physiology|October 4, 2015
A dilated cardiomyopathy mutation blunts adrenergic response and induces contractile dysfunction under chronic angiotensin II stressRoss Wilkinson, Weihua Song, Natalia Smoktunowicz, et al.
Frontiers in Physiology|April 9, 2020
Pressure Overload Is Associated With Low Levels of Troponin I and Myosin Binding Protein C Phosphorylation in the Hearts of Patients With Aortic StenosisO'neal Copeland, Andrew Messer, Andrew Jabbour, et al.
Journal of Muscle Research and Cell Motility|November 8, 2011
How do MYBPC3 mutations cause hypertrophic cardiomyopathy?Steven Marston, O'Neal Copeland, Katja Gehmlich, et al.
Biophysical Reviews|July 22, 2020
Donor hearts in the Sydney Heart Bank: reliable control but is it 'normal' heart?Steven Marston, Adam Jacques, Christopher Bayliss, et al.
The Biochemical Journal|February 21, 2002
Two mutations in troponin I that cause hypertrophic cardiomyopathy have contrasting effects on cardiac muscle contractilityDavid Burton, Hassan Abdulrazzak, Adam Knott, et al.
Pageof 4