Sarcomere gene mutations in hypertrophy and heart failure (Q34626686)

3 August 2017

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title

Sarcomere gene mutations in hypertrophy and heart failure (English)

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3 August 2017

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3

J G Seidman

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3 August 2017

4

Christine E Seidman

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3 August 2017

1

Hiroyuki Morita

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3 August 2017

Ryozo Nagai

2

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3 August 2017

language of work or name

English

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publication date

25 May 2010

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Journal of Cardiovascular Translational Research

3 August 2017

published in

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3 August 2017

volume

3

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3 August 2017

issue

4

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3 August 2017

page(s)

297-303

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Human genome sequencing using unchained base reads on self-assembling DNA nanoarrays

3 August 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3049265

Cardiac ankyrin repeat protein gene (ANKRD1) mutations in hypertrophic cardiomyopathy

7 July 2018

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Diagnostic, prognostic, and therapeutic implications of genetic testing for hypertrophic cardiomyopathy

7 July 2018

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Cardiac myosin-binding protein C mutations and hypertrophic cardiomyopathy: haploinsufficiency, deranged phosphorylation, and cardiomyocyte dysfunction

7 July 2018

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Genetic evaluation of cardiomyopathy--a Heart Failure Society of America practice guideline

7 July 2018

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

7 July 2018

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Heart disease and stroke statistics--2009 update: a report from the American Heart Association Statistics Committee and Stroke Statistics Subcommittee

7 July 2018

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Adverse events in families with hypertrophic or dilated cardiomyopathy and mutations in the MYBPC3 gene

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3049265

Mutations in sarcomere protein genes in left ventricular noncompaction

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3049265

Shared genetic causes of cardiac hypertrophy in children and adults

7 July 2018

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Genome-wide mapping of modifier chromosomal loci for human hypertrophic cardiomyopathy

7 July 2018

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Mutations in JPH2-encoded junctophilin-2 associated with hypertrophic cardiomyopathy in humans

7 July 2018

1 reference

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Myozenin 2 is a novel gene for human hypertrophic cardiomyopathy

7 July 2018

1 reference

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Structural abnormalities of the inferoseptal left ventricular wall detected by cardiac magnetic resonance imaging in carriers of hypertrophic cardiomyopathy mutations

7 July 2018

1 reference

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Single-gene mutations and increased left ventricular wall thickness in the community: the Framingham Heart Study

7 July 2018

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7 July 2018

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Sequence variations in PCSK9, low LDL, and protection against coronary heart disease

7 July 2018

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Gene-specific modifying effects of pro-LVH polymorphisms involving the renin-angiotensin-aldosterone system among 389 unrelated patients with hypertrophic cardiomyopathy

7 July 2018

1 reference

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Alpha-myosin heavy chain: a sarcomeric gene associated with dilated and hypertrophic phenotypes of cardiomyopathy

7 July 2018

1 reference

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Genetic causes of human heart failure

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3049265

Tcap gene mutations in hypertrophic cardiomyopathy and dilated cardiomyopathy

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3049265

Proposal for contemporary screening strategies in families with hypertrophic cardiomyopathy

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3049265

Multiple Rare Alleles Contribute to Low Plasma Levels of HDL Cholesterol

7 July 2018

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Sudden death in young athletes

7 July 2018

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

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3049265

Mutations in the human muscle LIM protein gene in families with hypertrophic cardiomyopathy

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3049265

Hypertrophic cardiomyopathy: a systematic review

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3049265

Sarcomere protein gene mutations in hypertrophic cardiomyopathy of the elderly

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3049265

The Genetic Basis for Cardiomyopathy

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3049265

Mutations in the gene for cardiac myosin-binding protein C and late-onset familial hypertrophic cardiomyopathy

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3049265

Prevalence of hypertrophic cardiomyopathy in a general population of young adults. Echocardiographic analysis of 4111 subjects in the CARDIA Study. Coronary Artery Risk Development in (Young) Adults

7 July 2018

1 reference

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Prognostic implications of echocardiographically determined left ventricular mass in the Framingham Heart Study

7 July 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS12265-010-9188-4

Genetic counseling and cardiac care in predictively tested hypertrophic cardiomyopathy mutation carriers: the patients' perspective.

21 January 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3049265

Identification of a metavinculin missense mutation, R975W, associated with both hypertrophic and dilated cardiomyopathy

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3049265

Glycogen storage diseases presenting as hypertrophic cardiomyopathy.

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3049265

Myosin binding protein C mutations and compound heterozygosity in hypertrophic cardiomyopathy

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3049265

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

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3049265

The genetic basis for cardiomyopathy: from mutation identification to mechanistic paradigms

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3049265

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

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3049265

Sex hormone receptor gene variation associated with phenotype in male hypertrophic cardiomyopathy patients

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3049265

Mutations in the genes for sarcomeric proteins in Japanese patients with onset sporadic hypertrophic cardiomyopathy after age 40 years

26 October 2018

1 reference

12 December 2020

M-mode echocardiographic predictors of six- to seven-year incidence of coronary heart disease, stroke, congestive heart failure, and mortality in an elderly cohort (the Cardiovascular Health Study)

1 reference

12 December 2020

Assessment of Diastolic Function With Doppler Tissue Imaging to Predict Genotype in Preclinical Hypertrophic Cardiomyopathy

1 reference

12 December 2020

Mutations in the cardiac myosin-binding protein C gene are the predominant cause of familial hypertrophic cardiomyopathy in eastern Finland

1 reference

12 December 2020

Molecular epidemiology of hypertrophic cardiomyopathy

1 reference

12 December 2020

An Atypical Variant of Fabry's Disease in Men with Left Ventricular Hypertrophy

1 reference

12 December 2020

10.1007/S12265-010-9188-4

Identifiers

DOI

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Dimensions Publication ID

3 August 2017

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3 August 2017

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