(Q34018918)

30 July 2017

title

Association of 25 bp deletion in MYBPC3 gene with left ventricle dysfunction in coronary artery disease patients (English)

1 reference

30 July 2017

main subject

coronary artery disease

1 reference

7

Balraj Mittal

1 reference

30 July 2017

Anshika Srivastava

1

1 reference

30 July 2017

Naveen Garg

2

1 reference

30 July 2017

Tulika Mittal

3

1 reference

30 July 2017

Roopali Khanna

4

1 reference

30 July 2017

Shipra Gupta

5

1 reference

30 July 2017

Prahlad Kishore Seth

6

1 reference

30 July 2017

language of work or name

English

0 references

publication date

7 September 2011

1 reference

30 July 2017

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30 July 2017

volume

6

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30 July 2017

issue

9

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30 July 2017

page(s)

e24123

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Creative Commons Attribution 4.0 International

30 July 2017

copyright license

start time

7 September 2011

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

cites work

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Limited distribution of a cardiomyopathy-associated variant in India

5 July 2018

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Molecular basis of hereditary cardiomyopathy: abnormalities in calcium sensitivity, stretch response, stress response and beyond

5 July 2018

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Sarcomere mutations in cardiomyopathy with left ventricular hypertrabeculation

5 July 2018

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5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3168477

A common MYBPC3 (cardiac myosin binding protein C) variant associated with cardiomyopathies in South Asia

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3168477

MYBPC3 gene variations in hypertrophic cardiomyopathy patients in India

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3168477

Cardiac myosin binding protein C phosphorylation is cardioprotective

5 July 2018

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Ethnic differences in the prevalence and aetiology of left ventricular systolic dysfunction in the community: the Harrow heart failure watch

5 July 2018

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Impairment of the ubiquitin-proteasome system by truncated cardiac myosin binding protein C mutants

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3168477

SCN5A mutation associated with dilated cardiomyopathy, conduction disorder, and arrhythmia

5 July 2018

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ABCC9 mutations identified in human dilated cardiomyopathy disrupt catalytic KATP channel gating

5 July 2018

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

5 July 2018

1 reference

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Association between aldosterone synthase (CYP11B2) gene polymorphism and left ventricular volume in patients with dilated cardiomyopathy

5 July 2018

1 reference

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5 July 2018

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Changes in cardiac contractility related to calcium-mediated changes in phosphorylation of myosin-binding protein C.

5 July 2018

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Mutations in beta-myosin S2 that cause familial hypertrophic cardiomyopathy (FHC) abolish the interaction with the regulatory domain of myosin-binding protein-C

5 July 2018

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Use of the Friedewald formula to estimate LDL-cholesterol in patients with chronic renal failure on dialysis.

5 July 2018

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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

5 July 2018

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The pathogenesis of atherosclerosis: a perspective for the 1990s

5 July 2018

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5 July 2018

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5 July 2018

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Novel mutation in cardiac troponin I in recessive idiopathic dilated cardiomyopathy

5 July 2018

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Biomolecular interactions between human recombinant β-MyHC and cMyBP-Cs implicated in familial hypertrophic cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0024123

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/10.1371%2FJOURNAL.PONE.0024123

Novel deletions in MYH7 and MYBPC3 identified in Indian families with familial hypertrophic cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0024123

Phenotypic deficits in mice expressing a myosin binding protein C lacking the titin and myosin binding domains

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0024123

Age-dependent declines in proteasome activity in the heart

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0024123

Sarcomeric genotyping in hypertrophic cardiomyopathy

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3168477

Pharmacy's glaucoma alert

29 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21915287

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

4-Hydroxy-2-nonenal-mediated impairment of intracellular proteolysis during oxidative stress. Identification of proteasomes as target molecules

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21915287

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1371/JOURNAL.PONE.0024123

1 reference

30 July 2017

0 references

1 reference

30 July 2017

1 reference