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Interaction analyses elucidate the pathophysiology of HCM-causing missense mutations in cardiac myosin binding protein-C.
Published 2001Journal article -
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Mutation analysis of genes encoding Subunits of AMP-activated protein kinase (AMPK) in inherited cardiomyopathies
Published 2002Conference item -
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Gly126Arg substitution causes anomalous behaviour of α-skeletal and β-smooth tropomyosins during the ATPase cycle.
Published 2014Journal article -
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Synchronous in situ ATPase activity, mechanics, and Ca2+ sensitivity of human and porcine myocardium.
Published 2009Journal article -
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Mutation analysis of genes encoding subunits of AMP-activated protein kinase (AMPK) in inherited cardiomyopathies
Published 2002Conference item -
128
Molecular mechanisms of dysfunction of muscle fibres associated with Glu139 deletion in TPM2 gene
Published 2017Journal article -
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A novel interaction between the C5 and C8 domains of myosin binding protein-C and its modulation by HCM mutations
Published 2002Journal article -
130
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Comparison of the functional effects of mutations in troponin T which cause dilated and hypertrophic cardiomyopathies
Published 2002Journal article -
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Mechanical effects of human cardiac troponin C mutation Gly159Asp in exchanged rabbit psoas fibres
Published 2004Conference item -
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Patient-specific fluid simulation of transcatheter mitral valve replacement in mitral annulus calcification
Published 2022-12-01Get full text
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135
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Mutations in tropomyosin that cause DCM, affect cooperativity of cardiac muscle thin filaments
Published 2007Conference item -
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Flexing the principal gradient of the cerebral cortex to suit changing semantic task demands
Published 2022-09-01Get full text
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