(Q36369921)

13 August 2017

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title

Sarcomeric protein mutations in dilated cardiomyopathy (English)

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13 August 2017

Audrey N Chang

1

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PubMed ID

16416045

13 August 2017

James D Potter

series ordinal

2

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13 August 2017

1 September 2005

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13 August 2017

Heart Failure Reviews

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13 August 2017

10

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13 August 2017

3

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13 August 2017

225-235

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https://scigraph.springernature.com/pub.10.1007/s10741-005-5252-6

13 August 2017

0 references

cites work

Two novel mutations in the beta-myosin heavy chain gene associated with dilated cardiomyopathy

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS10741-005-5252-6

Novel mutation in the alpha-tropomyosin gene and transition from hypertrophic to hypocontractile dilated cardiomyopathy.

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS10741-005-5252-6

alpha-Tropomyosin mutations Asp(175)Asn and Glu(180)Gly affect cardiac function in transgenic rats in different ways

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS10741-005-5252-6

A novel missense mutation in the myosin binding protein-C gene is responsible for hypertrophic cardiomyopathy with left ventricular dysfunction and dilation in elderly patients

21 January 2018

1 reference

12 December 2020

Cardiac troponin T Arg92Trp mutation and progression from hypertrophic to dilated cardiomyopathy

1 reference

12 December 2020

Hypertrophic cardiomyopathy in cardiac myosin binding protein-C knockout mice

1 reference

12 December 2020

Phosphorylation of both serine residues in cardiac troponin I is required to decrease the Ca2+ affinity of cardiac troponin C.

1 reference

12 December 2020

Thin-filament-based modulation of contractile performance in human heart failure

1 reference

12 December 2020

Structural interpretation of the mutations in the beta-cardiac myosin that have been implicated in familial hypertrophic cardiomyopathy

1 reference

12 December 2020

Severe disease expression of cardiac troponin C and T mutations in patients with idiopathic dilated cardiomyopathy

1 reference

12 December 2020

Actin mutations in dilated cardiomyopathy, a heritable form of heart failure

1 reference

12 December 2020

Metavinculin mutations alter actin interaction in dilated cardiomyopathy.

1 reference

12 December 2020

Cardiac titin: an adjustable multi-functional spring

1 reference

12 December 2020

A direct regulatory role for troponin T and a dual role for troponin C in the Ca2+ regulation of muscle contraction

1 reference

12 December 2020

Tcap gene mutations in hypertrophic cardiomyopathy and dilated cardiomyopathy

1 reference

12 December 2020

The unique amino-terminal peptide of cardiac troponin I regulates myofibrillar activity only when it is phosphorylated

1 reference

12 December 2020

Effects of two familial hypertrophic cardiomyopathy-causing mutations on alpha-tropomyosin structure and function

1 reference

12 December 2020

A familial hypertrophic cardiomyopathy alpha-tropomyosin mutation causes severe cardiac hypertrophy and death in mice

1 reference

12 December 2020

Effects of two familial hypertrophic cardiomyopathy-causing mutations on alpha-tropomyosin structure and function.

1 reference

12 December 2020

Mutations that alter the surface charge of alpha-tropomyosin are associated with dilated cardiomyopathy

1 reference

12 December 2020

Identification of sites phosphorylated in bovine cardiac troponin I and troponin T by protein kinase C and comparative substrate activity of synthetic peptides containing the phosphorylation sites

1 reference

12 December 2020

Disruption of muscle architecture and myocardial degeneration in mice lacking desmin

1 reference

12 December 2020

Familial hypertrophic cardiomyopathy mutations from different functional regions of troponin T result in different effects on the pH and Ca2+ sensitivity of cardiac muscle contraction

1 reference

12 December 2020

Sensing stretch is fundamental

1 reference

12 December 2020

Mutations of TTN, encoding the giant muscle filament titin, cause familial dilated cardiomyopathy.

1 reference

12 December 2020

Altered regulation of cardiac muscle contraction by troponin T mutations that cause familial hypertrophic cardiomyopathy

1 reference

12 December 2020

MLP-deficient mice exhibit a disruption of cardiac cytoarchitectural organization, dilated cardiomyopathy, and heart failure

1 reference

12 December 2020

Different functional properties of troponin T mutants that cause dilated cardiomyopathy

1 reference

12 December 2020

Cardiac troponin I phosphorylation increases the rate of cardiac muscle relaxation

1 reference

12 December 2020

Structure of C protein purified from cardiac muscle

1 reference

12 December 2020

Novel troponin T mutation in familial dilated cardiomyopathy with gender-dependant severity

1 reference

12 December 2020

Hypertrophic cardiomyopathy: two homozygous cases with "typical" hypertrophic cardiomyopathy and three new mutations in cases with progression to dilated cardiomyopathy

1 reference

12 December 2020

Differential regulation of cardiac actomyosin S-1 MgATPase by protein kinase C isozyme-specific phosphorylation of specific sites in cardiac troponin I and its phosphorylation site mutants

1 reference

12 December 2020

Characterization of troponin T dilated cardiomyopathy mutations in the fetal troponin isoform

1 reference

12 December 2020

Mutations in the muscle LIM protein and α-actinin-2 genes in dilated cardiomyopathy and endocardial fibroelastosis

1 reference

12 December 2020

The cardiac mechanical stretch sensor machinery involves a Z disc complex that is defective in a subset of human dilated cardiomyopathy

1 reference

12 December 2020

Effect of Hypertrophic Cardiomyopathy Mutations in Human Cardiac Muscle α -tropomyosin (Asp175Asn and Glu180Gly) on the Regulatory Properties of Human Cardiac Troponin Determined by in vitro Motility Assay

1 reference

12 December 2020

Electron microscopy of C-protein molecules from chicken skeletal muscle

1 reference

12 December 2020

Report of the 1995 World Health Organization/International Society and Federation of Cardiology Task Force on the Definition and Classification of cardiomyopathies.

1 reference

12 December 2020

Intracellular Action of Matrix Metalloproteinase-2 Accounts for Acute Myocardial Ischemia and Reperfusion Injury

1 reference

12 December 2020

The NH2 terminus of titin spans the Z-disc: its interaction with a novel 19-kD ligand (T-cap) is required for sarcomeric integrity

1 reference

12 December 2020

Novel mutations in sarcomeric protein genes in dilated cardiomyopathy.

1 reference

12 December 2020

Mutation screening in dilated cardiomyopathy: prominent role of the beta myosin heavy chain gene

1 reference

12 December 2020

Gene mutations in adult Japanese patients with dilated cardiomyopathy

1 reference

12 December 2020

A Matrix Metalloproteinase Induction/Activation System Exists in the Human Left Ventricular Myocardium and Is Upregulated in Heart Failure

1 reference

12 December 2020

Increased protein kinase C activity and expression of Ca2+-sensitive isoforms in the failing human heart

1 reference

12 December 2020

Inotropic stimulation induces cardiac dysfunction in transgenic mice expressing a troponin T (I79N) mutation linked to familial hypertrophic cardiomyopathy

1 reference

12 December 2020

A novel mutation Lys273Glu in the cardiac troponin T gene shows high degree of penetrance and transition from hypertrophic to dilated cardiomyopathy

1 reference

12 December 2020

Phosphorylation switches specific for the cardiac isoform of myosin binding protein-C: a modulator of cardiac contraction?

1 reference

12 December 2020

A mutation in the N-terminus of troponin I that is associated with hypertrophic cardiomyopathy affects the Ca(2+)-sensitivity, phosphorylation kinetics and proteolytic susceptibility of troponin

1 reference

12 December 2020

Cardiac troponin I mutants. Phosphorylation by protein kinases C and A and regulation of Ca(2+)-stimulated MgATPase of reconstituted actomyosin S-1

1 reference

12 December 2020

Molecular and integrated biology of thin filament protein phosphorylation in heart muscle

1 reference

12 December 2020

Molecular and cellular aspects of troponin cardiomyopathies

1 reference

12 December 2020

Troponin I phosphorylation in the normal and failing adult human heart

1 reference

12 December 2020

Alteration of myosin cross bridges by phosphorylation of myosin-binding protein C in cardiac muscle

1 reference

12 December 2020

Tissue-specific expression and alpha-actinin binding properties of the Z-disc titin: implications for the nature of vertebrate Z-discs

1 reference

12 December 2020

Passive stiffness changes caused by upregulation of compliant titin isoforms in human dilated cardiomyopathy hearts

1 reference

12 December 2020

Calsarcins, a novel family of sarcomeric calcineurin-binding proteins

1 reference

12 December 2020

Structural mechanism of muscle contraction.

1 reference

12 December 2020

Novel mutation in cardiac troponin I in recessive idiopathic dilated cardiomyopathy

1 reference

12 December 2020

Mutations in sarcomere protein genes as a cause of dilated cardiomyopathy

1 reference

12 December 2020

Titin mutations as the molecular basis for dilated cardiomyopathy

1 reference

12 December 2020

Ca(2+)-desensitizing effect of a deletion mutation Delta K210 in cardiac troponin T that causes familial dilated cardiomyopathy.

1 reference

12 December 2020

Solution scattering suggests cross-linking function of telethonin in the complex with titin

1 reference

12 December 2020

Downregulation of matrix metalloproteinases and reduction in collagen damage in the failing human heart after support with left ventricular assist devices

1 reference

12 December 2020

Familial dilated cardiomyopathy

1 reference

12 December 2020

Novel cardiac troponin T mutation as a cause of familial dilated cardiomyopathy

1 reference

12 December 2020

10.1007/S10741-005-5252-6

Identifiers

DOI

1 reference

13 August 2017

1 reference

PubMed ID

16416045