(Q24314590)

Troponin I3, cardiac type

1 reference

Troponin T2, cardiac type

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cardiac muscle contraction

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dilated cardiomyopathy

1 reference

Idiopathic dilated cardiomyopathy

inferred from title

1 reference

inferred from title

author

Hugh Christian Watkins

6

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Jens Mogensen

object named as

Jens Mogensen

1

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author name string

Ross T Murphy

2

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Tony Shaw

3

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Ajay Bahl

4

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Charles Redwood

5

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Margaret Burke

7

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Perry M Elliott

8

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William J McKenna

Journal of the American College of Cardiology

9

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language of work or name

English

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publication date

16 November 2004

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published in

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volume

44

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issue

10

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page(s)

2033-40

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cites work

Titin mutations as the molecular basis for dilated cardiomyopathy

1 reference

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Interactions at the NH2-terminal interface of cardiac troponin I modulate myofilament activation

1 reference

https://api.crossref.org/works/10.1016%2FJ.JACC.2004.08.027

7 January 2021

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

1 reference

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Beneficial effects of metoprolol in idiopathic dilated cardiomyopathy. Metoprolol in Dilated Cardiomyopathy (MDC) Trial Study Group

1 reference

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7 January 2021

The Genetic Basis for Cardiomyopathy

1 reference

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The genetic basis for cardiomyopathy: from mutation identification to mechanistic paradigms

1 reference

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7 January 2021

Comparison of carvedilol and metoprolol on clinical outcomes in patients with chronic heart failure in the Carvedilol Or Metoprolol European Trial (COMET): randomised controlled trial

1 reference

https://api.crossref.org/works/10.1016%2FJ.JACC.2004.08.027

7 January 2021

Novel mutation in cardiac troponin I in recessive idiopathic dilated cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016%2FJ.JACC.2004.08.027

7 January 2021

Familial dilated cardiomyopathy

1 reference

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7 January 2021

Troponin T: genetics, properties and function

1 reference

https://api.crossref.org/works/10.1016%2FJ.JACC.2004.08.027

7 January 2021

Troponin I: inhibitor or facilitator

1 reference

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7 January 2021

Vertebrate tropomyosin: distribution, properties and function

1 reference

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7 January 2021

https://api.crossref.org/works/10.1016%2FJ.JACC.2004.08.027

1 reference

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FJ.JACC.2004.08.027

7 January 2021

Cardiac troponin T is essential in sarcomere assembly and cardiac contractility

1 reference

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7 January 2021

Guidelines for the study of familial dilated cardiomyopathies. Collaborative Research Group of the European Human and Capital Mobility Project on Familial Dilated Cardiomyopathy.

1 reference

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7 January 2021

Cardiac troponin T lysine 210 deletion in a family with dilated cardiomyopathy

1 reference

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7 January 2021

Effect of enalapril on mortality and the development of heart failure in asymptomatic patients with reduced left ventricular ejection fractions

1 reference

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7 January 2021

Mutations in sarcomere protein genes as a cause of dilated cardiomyopathy

1 reference

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7 January 2021

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

1 reference

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Roles for the troponin tail domain in thin filament assembly and regulation. A deletional study of cardiac troponin T.

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

1 reference

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7 January 2021

Folding and function of the troponin tail domain. Effects of cardiomyopathic troponin T mutations

1 reference

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

1 reference

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Hypertrophic cardiomyopathy: the interrelation of disarray, fibrosis, and small vessel disease

1 reference

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Critical analysis of endomyocardial biopsies from patients suspected of having cardiomyopathy. I: Morphological and morphometric aspects

1 reference

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Comparison of fluorescent SSCP and denaturing HPLC analysis with direct sequencing for mutation screening in hypertrophic cardiomyopathy

1 reference

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7 January 2021

Echocardiographic measurements in normal subjects from infancy to old age.

1 reference

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

1 reference

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7 January 2021

Troponin and tropomyosin: proteins that switch on and tune in the activity of cardiac myofilaments

1 reference

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7 January 2021

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

1 reference

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7 January 2021