HCM and DCM mutations in thin filament proteins have opposite effects on regulation of contractility in vitro

ग्रंथसूची विवरण
मुख्य लेखकों:	Redwood, C, Robinson, P, Mirza, M, Knott, A, Marston, S, Watkins, H
स्वरूप:	Conference item
प्रकाशित:	2003

HCM and DCM mutations in cardiac thin filament proteins have opposite effects on the regulation of contractility in vitro
द्वारा: Redwood, C, और अन्य
प्रकाशित: (2003)

HCM and DCM mutations in thin filament proteins have opposite effects on in vitro motility
द्वारा: Marston, S, और अन्य
प्रकाशित: (2002)

Effects of DCM mutations in thin filament regulatory proteins on contractile function
द्वारा: Robinson, P, और अन्य
प्रकाशित: (2005)

In vitro motility studies of HCM and DCM mutations in cardiac muscle actin
द्वारा: Dyer, E, और अन्य
प्रकाशित: (2007)

Mutations in tropomyosin that cause DCM, affect cooperativity of cardiac muscle thin filaments
द्वारा: Marston, S, और अन्य
प्रकाशित: (2007)

Two DCM mutations in cardiac tropomyosin alter thin filament function by different mechanisms
द्वारा: Marston, S, और अन्य
प्रकाशित: (2007)

Hypertrophic and dilated cardiomyopathycausing mutations of troponin and alpha-tropomyosin have opposite effects on thin filament calcium binding
द्वारा: Robinson, P, और अन्य
प्रकाशित: (2007)

Autosomal dominant HCM and DCM phenotype caused by a novel mutation in phospholamban
द्वारा: Carballo, S, और अन्य
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Two mutations in troponin I that cause hypertrophic cardiomyopathy have contrasting effects on cardiac muscle contractility.
द्वारा: Burton, D, और अन्य
प्रकाशित: (2002)

Evidence for haploinsufficiency as the mechanism of action of MyBP-C mutations that cause HCM
द्वारा: Carballo, S, और अन्य
प्रकाशित: (2008)

Dilated and hypertrophic cardiomyopathy mutations in troponin and alpha-tropomyosin have opposing effects on the calcium affinity of cardiac thin filaments.
द्वारा: Robinson, P, और अन्य
प्रकाशित: (2007)

Dilated cardiomyopathy mutations in thin-filament regulatory proteins reduce contractility, suppress systolic Ca²⁺, and activate NFAT and Akt signaling
द्वारा: Robinson, P, और अन्य
प्रकाशित: (2020)

Modulation of thin filament activation by breakdown or isoform switching of thin filament proteins: physiological and pathological implications.
द्वारा: Marston, S, और अन्य
प्रकाशित: (2003)

Dilated cardiomyopathy mutations in three thin filament regulatory proteins result in a common functional phenotype.
द्वारा: Mirza, M, और अन्य
प्रकाशित: (2005)

Alterations in thin filament regulation induced by a human cardiac troponin T mutant that causes dilated cardiomyopathy are distinct from those induced by troponin T mutants that cause hypertrophic cardiomyopathy.
द्वारा: Robinson, P, और अन्य
प्रकाशित: (2002)

The effect of HCM mutations in troponin T and troponin I on the calcium binding of human cardiac troponin
द्वारा: Redwood, C, और अन्य
प्रकाशित: (2001)

Functional effects of mutations in troponin T and tropomyosin which cause dilated cardiomyopathy
द्वारा: Robinson, P, और अन्य
प्रकाशित: (2003)

MiR-1-3p that correlates with left ventricular function of HCM can serve as a potential target and differentiate HCM from DCM
द्वारा: Mengmeng Li, और अन्य
प्रकाशित: (2018-06-01)

Mouse HCM Model Expression E99K ACTC Mutation Reproduces the Clinical HCM Phenotype
द्वारा: Song, W, और अन्य
प्रकाशित: (2009)

The effect of mutations in alpha-tropomyosin (E40K and E54K) that cause familial dilated cardiomyopathy on the regulatory mechanism of cardiac muscle thin filaments.
द्वारा: Mirza, M, और अन्य
प्रकाशित: (2007)

Using fluorescence emission spectroscopy to asses the Ca2+ affinity of reconstituted troponin and thin filaments containing cardiomyopathy causing mutations of troponin and alpha-tropomyosin
द्वारा: Robinson, P, और अन्य
प्रकाशित: (2007)

Mavacamten rescues increased myofilament calcium sensitivity and dysregulation of Ca2+ flux caused by thin filament hypertrophic cardiomyopathy mutations
द्वारा: Sparrow, AJ, और अन्य
प्रकाशित: (2020)

A revised method of troponin exchange in permeabilised cardiac trabeculae using vanadate: functional consequences of a HCM-causing mutation in troponin I.
द्वारा: Preston, L, और अन्य
प्रकाशित: (2006)

Interaction analyses elucidate the pathophysiology of HCM-causing missense mutations in cardiac myosin binding protein-C.
द्वारा: Moolman-Smook, J, और अन्य
प्रकाशित: (2001)

Value of MRI derived parameters in the discrimination of familial left ventricular noncompaction (LVNC), DCM and HCM in comparison to healthy volunteers
द्वारा: Hassfeld Sabine, और अन्य
प्रकाशित: (2011-02-01)

Functional investigation of troponin with the homozygous HCM mutation, TNNT2 K280N, obtained from an explanted heart
द्वारा: Bayliss, C, और अन्य
प्रकाशित: (2012)

Familial Dilated Cardiomyopathy Caused by an Alpha-Tropomyosin Mutation: The Distinctive Natural History of Sarcomeric DCM
द्वारा: Lakdawala, N, और अन्य
प्रकाशित: (2009)

Cardiomyopathy-Causing Mutations in Thin Filament Regulatory Proteins Acutely Affeect Ca2+-Buffering and Ca2+-Dependent Signalling In Situ
द्वारा: Robinson, P, और अन्य
प्रकाशित: (2013)

P123The rescue of Ca2+ cycling abnormalities conferred by HCM-causing mutations with analogues of the green tea polyphenol epigallocatechin-3-gallate.
द्वारा: Robinson, P, और अन्य
प्रकाशित: (2014)

The HCM-associated cardiac Troponin T mutation K280N causes reduced responsiveness to protein kinase A
द्वारा: Van Der Velden, J, और अन्य
प्रकाशित: (2012)

Cardiomyopathy-causing mutations in cardiac thin filament regulatory proteins acutely affect Ca2+ buffering and Ca2+ dependant signalling in situ
द्वारा: Robinson, P, और अन्य
प्रकाशित: (2012)

Comparison of the functional effects of mutations in troponin T which cause dilated and hypertrophic cardiomyopathies
द्वारा: Robinson, P, और अन्य
प्रकाशित: (2002)

The nemaline myopathy-causing E117K mutation in β-tropomyosin reduces thin filament activation.
द्वारा: Karpicheva, O, और अन्य
प्रकाशित: (2013)

Mutations in fast skeletal troponin I, troponin T and beta-tropomyosin that cause distal arthrogryposis all enhance thin filament activation
द्वारा: Robinson, P, और अन्य
प्रकाशित: (2005)

A novel interaction between the C5 and C8 domains of myosin binding protein-C and its modulation by HCM mutations
द्वारा: Flashman, E, और अन्य
प्रकाशित: (2002)

Investigation of a truncated cardiac troponin T that causes familial hypertrophic cardiomyopathy: Ca(2+) regulatory properties of reconstituted thin filaments depend on the ratio of mutant to wild-type protein.
द्वारा: Redwood, C, और अन्य
प्रकाशित: (2000)

Patients with hypertrophic cardiomyopathy (HCM) and HCM gene carriers have attenuated myocardial oxygenation response to vasodilator stress - a potential mechanism for sudden cardiac death.
द्वारा: Dass, S, और अन्य
प्रकाशित: (2012)

Investigation of troponin I mutations causing familial hypertrophic cardiomyopathy
द्वारा: Abdulrazzak, H, और अन्य
प्रकाशित: (2001)

Effects of hypertrophic cardiomyopathy mutations in troponin I on contractility of skinned cardiac muscle fibres
द्वारा: Burton, D, और अन्य
प्रकाशित: (2002)

Functional effects of the DCM mutant Gly159Asp troponin C in skinned muscle fibres.
द्वारा: Preston, L, और अन्य
प्रकाशित: (2007)

HCM and DCM mutations in thin filament proteins have opposite effects on regulation of contractility in vitro

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