(Q28244969)

1

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H Harada

2

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J E Park

3

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H Nishi

4

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M Satoh

5

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M Takahashi

6

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S Hiroi

7

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T Sasaoka

8

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N Ohbuchi

9

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T Nakamura

10

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T Koyanagi

11

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T H Hwang

12

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J A Choo

13

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K S Chung

14

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A Hasegawa

15

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R Nagai

16

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O Okazaki

17

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H Nakamura

18

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M Matsuzaki

19

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T Sakamoto

20

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Y Koga

22

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T Imaizumi

23

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T Sasazuki

https://scigraph.springernature.com/pub.10.1038/ng0897-379

24

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language of work or name

English

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publication date

August 1997

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published in

Nature Genetics

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volume

16

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page(s)

379-82

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issue

4

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exact match

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cites work

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

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

https://api.crossref.org/works/10.1038%2FNG0897-379

Molecular basis of familial cardiomyopathies

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0897-379

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0897-379

Mapping a gene for familial hypertrophic cardiomyopathy to chromosome 14q1

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0897-379

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0897-379

7 January 2021

A familial hypertrophic cardiomyopathy locus maps to chromosome 15q2.

1 reference

https://api.crossref.org/works/10.1038%2FNG0897-379

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0897-379

7 January 2021

Molecular structure and evolutionary origin of human cardiac muscle actin gene

1 reference

https://api.crossref.org/works/10.1038%2FNG0897-379

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0897-379

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0897-379

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

https://api.crossref.org/works/10.1038%2FNG0897-379

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0897-379

7 January 2021

The troponin complex and regulation of muscle contraction.

1 reference

https://api.crossref.org/works/10.1038%2FNG0897-379

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0897-379

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

https://api.crossref.org/works/10.1038%2FNG0897-379

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0897-379

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0897-379

7 January 2021