A cardiac myosin binding protein C mutation in the Maine Coon cat with familial hypertrophic cardiomyopathy. (Q30351668)

20 June 2017

A cardiac myosin binding protein C mutation in the Maine Coon cat with familial hypertrophic cardiomyopathy. (English)

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20 June 2017

5

Jeffrey A Towbin

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20 June 2017

Kathryn M Meurs

1

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20 June 2017

Ximena Sanchez

2

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20 June 2017

Ryan M David

3

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20 June 2017

Neil E Bowles

4

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20 June 2017

Peter J Reiser

6

1 reference

20 June 2017

Judith A Kittleson

7

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20 June 2017

Marcia J Munro

8

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20 June 2017

Keith Dryburgh

9

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20 June 2017

Kristin A Macdonald

10

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20 June 2017

Mark D Kittleson

11

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20 June 2017

19 October 2005

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20 June 2017

Human Molecular Genetics

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20 June 2017

14

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20 June 2017

23

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20 June 2017

3587-3593

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Hypertrophic cardiomyopathy: distribution of disease genes, spectrum of mutations, and implications for a molecular diagnosis strategy

20 June 2017

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI386

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/10.1093%2FHMG%2FDDI386

A newly created splice donor site in exon 25 of the MyBP-C gene is responsible for inherited hypertrophic cardiomyopathy with incomplete disease penetrance

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI386

Expression and functional assessment of a truncated cardiac troponin T that causes hypertrophic cardiomyopathy. Evidence for a dominant negative action

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI386

Familial hypertrophic cardiomyopathy in maine coon cats: an animal model of human disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI386

Myosin binding protein C: structural abnormalities in familial hypertrophic cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI386

Structural evidence for the interaction of C-protein (MyBP-C) with actin and sequence identification of a possible actin-binding domain.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI386

COOH-terminal truncated cardiac myosin-binding protein C mutants resulting from familial hypertrophic cardiomyopathy mutations exhibit altered expression and/or incorporation in fetal rat cardiomyocytes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI386

Assignment of the human gene for the sarcomeric M-band protein myomesin (MYOM1) to 18p11.31-p11.32

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI386

The conserved, hydrophilic and arginine-rich N-terminal domain of cucumovirus coat proteins contributes to their anomalous electrophoretic mobilities in sodium dodecylsulfate-polyacrylamide gels.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI386

Anomalous electrophoretic mobility of Drosophila phosphorylated H1 histone: is it related to the compaction of satellite DNA into heterochromatin?

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI386

21 January 2018

Identifiers

DOI

10.1093/HMG/DDI386

1 reference

20 June 2017

1 reference