(Q45089593)

9 December 2017

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

1 reference

familial dilated cardiomyopathy

9 December 2017

dilated cardiomyopathy

1 reference

based on heuristic

inferred from title

1 reference

based on heuristic

inferred from title

author name string

Christopher B Stefanelli

1

1 reference

9 December 2017

Amnon Rosenthal

2

1 reference

9 December 2017

Andrei B Borisov

3

1 reference

9 December 2017

Gregory J Ensing

4

1 reference

9 December 2017

Mark W Russell

5

1 reference

9 December 2017

1 September 2004

1 reference

Molecular Genetics and Metabolism

9 December 2017

1 reference

9 December 2017

83

1 reference

9 December 2017

1-2

1 reference

9 December 2017

188-196

1 reference

Frequency and phenotypes of familial dilated cardiomyopathy.

9 December 2017

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2004.04.013

Many roads lead to a broken heart: the genetics of dilated cardiomyopathy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2004.04.013

Dilated cardiomyopathy and heart failure caused by a mutation in phospholamban

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2004.04.013

AT1 receptor A/C1166 polymorphism contributes to cardiac hypertrophy in subjects with hypertrophic cardiomyopathy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2004.04.013

Mechanisms of the pathogenesis of troponin T-based familial hypertrophic cardiomyopathy.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2004.04.013

Mutations in the genes for cardiac troponin T and alpha-tropomyosin in hypertrophic cardiomyopathy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2004.04.013

Patients with familial hypertrophic cardiomyopathy caused by a Phe110Ile missense mutation in the cardiac troponin T gene have variable cardiac morphologies and a favorable prognosis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2004.04.013

Mutations in sarcomere protein genes as a cause of dilated cardiomyopathy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2004.04.013

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2004.04.013

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2004.04.013

Disease-causing mutations in cardiac troponin T: identification of a critical tropomyosin-binding region

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2004.04.013

Functional consequences of troponin T mutations found in hypertrophic cardiomyopathy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2004.04.013

Cardiac troponin T and familial hypertrophic cardiomyopathy: an energetic affair

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2004.04.013

Decreased energetics in murine hearts bearing the R92Q mutation in cardiac troponin T

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2004.04.013

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.YMGME.2004.04.013

Different functional properties of troponin T mutants that cause dilated cardiomyopathy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2004.04.013

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2004.04.013

Regulatory properties of the NH2- and COOH-terminal domains of troponin T. ATPase activation and binding to troponin I and troponin C

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2004.04.013

Gender differences in the presentation of adult obstructive hypertrophic cardiomyopathy with resting gradient: a study of 122 patients

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2004.04.013

Survival after the onset of congestive heart failure in Framingham Heart Study subjects

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2004.04.013

Sex Hormones and Cardiomyopathic Phenotype Induced by Cardiac β2-Adrenergic Receptor Overexpression

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2004.04.013

Myocyte death in the failing human heart is gender dependent

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2004.04.013

Ca(2+) loading and adrenergic stimulation reveal male/female differences in susceptibility to ischemia-reperfusion injury

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2004.04.013

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2004.04.013

The molecular genetic basis for hypertrophic cardiomyopathy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2004.04.013

10.1016/J.YMGME.2004.04.013

7 January 2021

Identifiers

DOI

1 reference

9 December 2017

1 reference