Mutations in the cardiac troponin I gene associated with hypertrophic cardiomyopathy (Q28244969)

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R. Nagai

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O. Okazaki

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H. Nakamura

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M. Matsuzaki

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T. Sakamoto

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Y. Koga

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T. Imaizumi

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full work available at URL

9 November 2024

language of work or name

English

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publication date

August 1997

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http://www.nature.com/articles/ng0897-379

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http://www.nature.com/articles/ng0897-379.pdf

9 November 2024

file format

Portable Document Format

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

9 November 2024

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16

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issue

4

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page(s)

379-82

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cites work

1 reference

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

21 April 2017

1 reference

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

21 April 2017

1 reference

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

21 April 2017

1 reference

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

21 April 2017

1 reference

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

21 April 2017

1 reference

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

21 April 2017

1 reference

Hypertrophic cardiomyopathy. Interrelations of clinical manifestations, pathophysiology, and therapy (1).

21 April 2017

1 reference

Molecular basis of familial cardiomyopathies

21 January 2018

1 reference

Muscle abnormalities in Drosophila melanogaster heldup mutants are caused by missing or aberrant troponin-I isoforms

21 January 2018

1 reference

Mapping a gene for familial hypertrophic cardiomyopathy to chromosome 14q1

21 January 2018

1 reference

7 January 2021

A disease locus for familial hypertrophic cardiomyopathy maps to chromosome 1q3.

1 reference

7 January 2021

A familial hypertrophic cardiomyopathy locus maps to chromosome 15q2.

1 reference

7 January 2021

Mapping of a novel gene for familial hypertrophic cardiomyopathy to chromosome 11

1 reference

7 January 2021

Molecular structure and evolutionary origin of human cardiac muscle actin gene

1 reference

7 January 2021

Complete sequence and organization of the human cardiac beta-myosin heavy chain gene

1 reference

7 January 2021

Mapping TNNC1, the gene that encodes cardiac troponin I in the human and the mouse

1 reference

7 January 2021

Mapping the locus for familial hypertrophic cardiomyopathy to chromosome 11 in a family with a case of apical hypertrophic cardiomyopathy of the Japanese type

1 reference

7 January 2021

Familial Hypertrophic cardiomyopathy with Wolff-Parkinson-White syndrome maps to a locus on chromosome 7q3

1 reference

7 January 2021

The troponin complex and regulation of muscle contraction

1 reference

7 January 2021

The relationship between biological activity and primary structure of troponin I from white skeletal muscle of the rabbit

1 reference

7 January 2021

Calcium dependence of the distance between Cys-98 of troponin C and Cys-133 of troponin I in the ternary troponin complex. Resonance energy transfer measurements

1 reference

7 January 2021

Altered cardiac troponin T in vitro function in the presence of a mutation implicated in familial hypertrophic cardiomyopathy

1 reference

7 January 2021

A myosin missense mutation, not a null allele, causes familial hypertrophic cardiomyopathy

1 reference

7 January 2021