(Q47772454)

5 February 2018

title

Cardiac Myosin-binding protein C and hypertrophic cardiomyopathy (English)

1 reference

5 February 2018

author

Gisèle Bonne

series ordinal

2

1 reference

5 February 2018

author name string

L Carrier

series ordinal

1

1 reference

5 February 2018

K Schwartz

series ordinal

3

1 reference

5 February 2018

publication date

1 May 1998

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5 February 2018

Trends in Cardiovascular Medicine

published in

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5 February 2018

volume

8

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5 February 2018

issue

4

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5 February 2018

page(s)

151-157

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5 February 2018

Genetic dissection of Drosophila myofibril formation: effects of actin and myosin heavy chain null alleles.

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

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A molecular map of the interactions between titin and myosin-binding protein C. Implications for sarcomeric assembly in familial hypertrophic cardiomyopathy

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Drosophila melanogaster troponin-T mutations engender three distinct syndromes of myofibrillar abnormalities

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A mouse model of familial hypertrophic cardiomyopathy

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Effects of phosphorylated and unphosphorylated C-protein on cardiac actomyosin ATPase

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Alterations in Ca2+ sensitive tension due to partial extraction of C-protein from rat skinned cardiac myocytes and rabbit skeletal muscle fibers

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Phosphorylation of a myofibrillar protein of Mr 150 000 in perfused rat heart, and the tentative indentification of this as C-protein

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Mutations in the cardiac troponin I gene associated with hypertrophic cardiomyopathy

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Expression of a mutation causing hypertrophic cardiomyopathy disrupts sarcomere assembly in adult feline cardiac myocytes

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Expression of a mutant (Arg92Gln) human cardiac troponin T, known to cause hypertrophic cardiomyopathy, impairs adult cardiac myocyte contractility

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7 January 2021

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High-resolution crystal structures of tyrosine kinase SH3 domains complexed with proline-rich peptides

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A new protein of the thick filaments of vertebrate skeletal myofibrils. Extractions, purification and characterization

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7 January 2021

The major myosin-binding domain of skeletal muscle MyBP-C (C protein) resides in the COOH-terminal, immunoglobulin C2 motif.

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Novel splice donor site mutation in the cardiac myosin-binding protein-C gene in familial hypertrophic cardiomyopathy. Characterization Of cardiac transcript and protein

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

Contractile protein mutations and heart disease

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7 January 2021

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

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7 January 2021

Familial hypertrophic cardiomyopathy: a genetic model of cardiac hypertrophy

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7 January 2021

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

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7 January 2021

Alteration of myosin cross bridges by phosphorylation of myosin-binding protein C in cardiac muscle

1 reference

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7 January 2021

Molecular pathology of familial hypertrophic cardiomyopathy caused by mutations in the cardiac myosin binding protein C gene.

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7 January 2021

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Identifiers

DOI

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30 July 2022

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Fatcat

https://api.fatcat.wiki/v0/release/opjufzfqdjg7lpfufcjshwomfy

30 July 2022

mapped directly with Wikidata item

https://api.fatcat.wiki/v0/release/opjufzfqdjg7lpfufcjshwomfy

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30 July 2022