(Q42473760)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20600154%20AND%20SRC:MED&resulttype=core&format=json

7 February 2020

title

Investigation of a transgenic mouse model of familial dilated cardiomyopathy (English)

1 reference

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7 February 2020

13

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7 February 2020

Daniel J Stuckey

3

1 reference

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7 February 2020

Catherine Mansfield

6

1 reference

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7 February 2020

Michael Ferenczi

7

1 reference

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7 February 2020

Sian E. Harding

11

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7 February 2020

author name string

Weihua Song

1

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7 February 2020

Emma Dyer

2

1 reference

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7 February 2020

Man-Ching Leung

4

1 reference

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7 February 2020

Massimiliano Memo

5

1 reference

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7 February 2020

Ke Liu

8

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7 February 2020

Charles Redwood

9

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7 February 2020

Kristen Nowak

10

1 reference

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7 February 2020

Kieran Clarke

12

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7 February 2020

Steven Marston

14

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7 February 2020

publication date

17 June 2010

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Journal of Molecular and Cellular Cardiology

7 February 2020

published in

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7 February 2020

volume

49

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7 February 2020

page(s)

380-389

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7 February 2020

issue

3

1 reference

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

7 February 2020

cites work

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.05.009

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

7 January 2021

1 reference

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Mutations in sarcomere protein genes as a cause of dilated cardiomyopathy

7 January 2021

1 reference

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Sarcomeric protein mutations in dilated cardiomyopathy

7 January 2021

1 reference

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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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.05.009

Dilated cardiomyopathy mutations in three thin filament regulatory proteins result in a common functional phenotype

7 January 2021

1 reference

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The effect of mutations in alpha-tropomyosin (E40K and E54K) that cause familial dilated cardiomyopathy on the regulatory mechanism of cardiac muscle thin filaments.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.05.009

Dilated and hypertrophic cardiomyopathy mutations in troponin and alpha-tropomyosin have opposing effects on the calcium affinity of cardiac thin filaments.

7 January 2021

1 reference

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Identification and functional characterization of cardiac troponin I as a novel disease gene in autosomal dominant dilated cardiomyopathy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.05.009

Different functional properties of troponin T mutants that cause dilated cardiomyopathy

7 January 2021

1 reference

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Functional consequences of hypertrophic and dilated cardiomyopathy-causing mutations in alpha-tropomyosin.

7 January 2021

1 reference

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.05.009

Cardiac troponin T mutation R141W found in dilated cardiomyopathy stabilizes the troponin T-tropomyosin interaction and causes a Ca2+ desensitization

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.05.009

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.05.009

α-Actin isoform distribution in normal and failing human heart: a morphological, morphometric, and biochemical study

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.05.009

Transgenic overexpression of cardiac actin in the mouse heart suggests coregulation of cardiac, skeletal and vascular actin expression.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.05.009

Are transgenic mice the 'alkahest' to understanding myocardial hypertrophy and failure?

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.05.009

With great power comes great responsibility: using mouse genetics to study cardiac hypertrophy and failure

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.05.009

Knock-in mouse model of dilated cardiomyopathy caused by troponin mutation

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.05.009

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.05.009

Dilated cardiomyopathy mutant tropomyosin mice develop cardiac dysfunction with significantly decreased fractional shortening and myofilament calcium sensitivity

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.05.009

Characterization of the role of gamma2 R531G mutation in AMP-activated protein kinase in cardiac hypertrophy and Wolff-Parkinson-White syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.05.009

Novel MRI method to detect altered left ventricular ejection and filling patterns in rodent models of disease

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.05.009

Left ventricular pressure-volume relationship in a murine model of congestive heart failure due to acute viral myocarditis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.05.009

Reduced contraction and altered frequency response of isolated ventricular myocytes from patients with heart failure

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.05.009

Differential cross-bridge kinetics of FHC myosin mutations R403Q and R453C in heterozygous mouse myocardium

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.05.009

Troponin phosphorylation and regulatory function in human heart muscle: dephosphorylation of Ser23/24 on troponin I could account for the contractile defect in end-stage heart failure

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.05.009

Functional analysis of a unique troponin c mutation, GLY159ASP, that causes familial dilated cardiomyopathy, studied in explanted heart muscle.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.05.009

Direct comparison of magnetic resonance imaging and conductance microcatheter in the evaluation of left ventricular function in mice

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.05.009

Genetic analysis of the interaction between cardiac and skeletal actin gene expression in striated muscle of the mouse

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.05.009

Variability in the ratio of mutant to wildtype myosin heavy chain present in the soleus muscle of patients with familial hypertrophic cardiomyopathy. A new approach for the quantification of mutant to wildtype protein

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.05.009

A Mutant Tropomyosin That Causes Hypertrophic Cardiomyopathy Is Expressed In Vivo and Associated With an Increased Calcium Sensitivity

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.05.009

The pathogenesis of ACTA1-related congenital fiber type disproportion

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.05.009

Fatal hypertrophic cardiomyopathy and nemaline myopathy associated with ACTA1 K336E mutation

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.05.009

Altered regulatory properties of human cardiac troponin I mutants that cause hypertrophic cardiomyopathy

7 January 2021

1 reference

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Functional studies of yeast actin mutants corresponding to human cardiomyopathy mutations

7 January 2021

1 reference

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Increased Ca2+-sensitivity of the contractile apparatus in end-stage human heart failure results from altered phosphorylation of contractile proteins

7 January 2021

1 reference

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Myofilament dysfunction in cardiac disease from mice to men.

7 January 2021

1 reference

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Is depressed myocyte contractility centrally involved in heart failure?

7 January 2021

1 reference

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Myosin binding protein C phosphorylation in normal, hypertrophic and failing human heart muscle

7 January 2021

1 reference

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Sarcomeric dysfunction in heart failure.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.05.009

A mouse model of familial hypertrophic cardiomyopathy

7 January 2021

1 reference

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