Functional analysis of a troponin I (R145G) mutation associated with familial hypertrophic cardiomyopathy (Q43860686)

27 November 2017

title

Functional analysis of a troponin I (R145G) mutation associated with familial hypertrophic cardiomyopathy (English)

1 reference

27 November 2017

Rosalyn Lang

1

1 reference

27 November 2017

Aldrin V Gomes

2

1 reference

27 November 2017

Jiaju Zhao

3

1 reference

27 November 2017

Philippe R Housmans

4

1 reference

27 November 2017

Todd Miller

5

1 reference

27 November 2017

James D Potter

6

1 reference

27 November 2017

language of work or name

English

0 references

publication date

18 January 2002

1 reference

Journal of Biological Chemistry

27 November 2017

number of pages

9

1 reference

based on heuristic

inferred from page(s)

published in

1 reference

27 November 2017

volume

277

1 reference

27 November 2017

issue

14

1 reference

27 November 2017

page(s)

11670-11678

1 reference

A molecular basis for familial hypertrophic cardiomyopathy: a beta cardiac myosin heavy chain gene missense mutation

27 November 2017

cites work

1 reference

https://api.crossref.org/works/10.1074/JBC.M108912200

Mutations in either the essential or regulatory light chains of myosin are associated with a rare myopathy in human heart and skeletal muscle

21 January 2018

1 reference

https://api.crossref.org/works/10.1074/JBC.M108912200

Alpha-tropomyosin and cardiac troponin T mutations cause familial hypertrophic cardiomyopathy: a disease of the sarcomere

21 January 2018

1 reference

https://api.crossref.org/works/10.1074/JBC.M108912200

Cardiac myosin binding protein-C gene splice acceptor site mutation is associated with familial hypertrophic cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1074/JBC.M108912200

Mutations in the cardiac myosin binding protein-C gene on chromosome 11 cause familial hypertrophic cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1074/JBC.M108912200

Mutations in the cardiac troponin I gene associated with hypertrophic cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1074/JBC.M108912200

Alpha-cardiac actin is a novel disease gene in familial hypertrophic cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1074/JBC.M108912200

Structural analysis of the titin gene in hypertrophic cardiomyopathy: identification of a novel disease gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1074/JBC.M108912200

First mutation in cardiac troponin C, L29Q, in a patient with hypertrophic cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1074/JBC.M108912200

Molecular genetic basis of hypertrophic cardiomyopathy: genetic markers for sudden cardiac death

21 January 2018

1 reference

https://api.crossref.org/works/10.1074/JBC.M108912200

Structural aspects of troponin-tropomyosin regulation of skeletal muscle contraction

21 January 2018

1 reference

https://api.crossref.org/works/10.1074/JBC.M108912200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074/JBC.M108912200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074/JBC.M108912200

Preparation of troponin and its subunits

21 January 2018

1 reference

https://api.crossref.org/works/10.1074/JBC.M108912200

The time-course of Ca2 exchange with calmodulin, troponin, parvalbumin, and myosin in response to transient increases in Ca2

21 January 2018

1 reference

https://api.crossref.org/works/10.1074/JBC.M108912200

Effects of halothane and isoflurane on the intracellular Ca2 transient in ferret cardiac muscle

21 January 2018

1 reference

https://api.crossref.org/works/10.1074/JBC.M108912200

Molecular cloning of human cardiac troponin I using polymerase chain reaction

21 January 2018

1 reference

https://api.crossref.org/works/10.1074/JBC.M108912200

Cloning and expression in Escherichia coli of the cDNA encoding human cardiac troponin I

21 January 2018

1 reference

https://api.crossref.org/works/10.1074/JBC.M108912200

Isolation and characterization of the human cardiac troponin I gene (TNNI3)

21 January 2018

1 reference

https://api.crossref.org/works/10.1074/JBC.M108912200

Relationship between force and intracellular [Ca2 ] in tetanized mammalian heart muscle

21 January 2018

1 reference

https://api.crossref.org/works/10.1074/JBC.M108912200

Effects of phosphorylation and mutation R145G on human cardiac troponin I function.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074/JBC.M108912200

21 January 2018

Identifiers

DOI

10.1074/JBC.M108912200

1 reference

27 November 2017

1 reference