(Q34027457)

30 July 2017

1 reference

title

Molecular genetics of hypertrophic cardiomyopathy. (English)

1 reference

hypertrophic cardiomyopathy

30 July 2017

1 reference

1 reference

Towbin JA

1

1 reference

30 July 2017

1 March 2000

1 reference

30 July 2017

7

1 reference

Current cardiology reports

inferred from page(s)

published in

1 reference

30 July 2017

2

1 reference

30 July 2017

2

1 reference

30 July 2017

134-140

1 reference

https://scigraph.springernature.com/pub.10.1007/s11886-000-0010-9

30 July 2017

0 references

cites work

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

1 reference

https://api.crossref.org/works/10.1007%2FS11886-000-0010-9

Familial hypertrophic cardiomyopathy: from mutations to functional defects

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11886-000-0010-9

Cardiac myosin binding protein C gene is specifically expressed in heart during murine and human development

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11886-000-0010-9

Human cardiac troponin T: cloning and expression of new isoforms in the normal and failing heart

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11886-000-0010-9

Codon 102 of the cardiac troponin T gene is a putative hot spot for mutations in familial hypertrophic cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11886-000-0010-9

Troponin I isoform expression in human heart

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11886-000-0010-9

Characteristics and prognostic implications of myosin missense mutations in familial hypertrophic cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11886-000-0010-9

Clinical features and prognostic implications of familial hypertrophic cardiomyopathy related to the cardiac myosin-binding protein C gene.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11886-000-0010-9

Isoform Transitions of the Myosin Binding Protein C Family in Developing Human and Mouse Muscles

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11886-000-0010-9

The molecular basis for tropomyosin isoform diversity

21 January 2018

1 reference

12 December 2020

Dilated cardiomyopathy in homozygous myosin-binding protein-C mutant mice

1 reference

12 December 2020

Mapping a gene for familial hypertrophic cardiomyopathy to chromosome 14q1

1 reference

12 December 2020

Altered interactions among thin filament proteins modulate cardiac function

1 reference

12 December 2020

Mutations in either the essential or regulatory light chains of myosin are associated with a rare myopathy in human heart and skeletal muscle

1 reference

12 December 2020

Structural analysis of the titin gene in hypertrophic cardiomyopathy: identification of a novel disease gene

1 reference

12 December 2020

Angiotensin-converting enzyme polymorphism in hypertrophic cardiomyopathy and sudden cardiac death

1 reference

12 December 2020

Actin mutations in dilated cardiomyopathy, a heritable form of heart failure

1 reference

12 December 2020

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

1 reference

12 December 2020

The role of cytoskeletal proteins in cardiomyopathies

1 reference

12 December 2020

Genetics of neonatal cardiomyopathy

1 reference

12 December 2020

Familial hypertrophic cardiomyopathy is a genetically heterogeneous disease

1 reference

12 December 2020

Mice expressing mutant myosin heavy chains are a model for familial hypertrophic cardiomyopathy

1 reference

12 December 2020

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

1 reference

12 December 2020

Right bundle branch block, persistent ST segment elevation and sudden cardiac death: A distinct clinical and electrocardiographic syndrome

1 reference

12 December 2020

Molecular cloning of human cardiac troponin T isoforms: expression in developing and failing heart.

1 reference

12 December 2020

Sudden death in young competitive athletes. Clinical, demographic, and pathological profiles.

1 reference

12 December 2020

Genomic organisation, alternative splicing and polymorphisms of the human cardiac troponin T gene

1 reference

12 December 2020

Etiologies of cardiomyopathy and heart failure

1 reference

12 December 2020

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

1 reference

12 December 2020

Organization and sequence of human cardiac myosin binding protein C gene (MYBPC3) and identification of mutations predicted to produce truncated proteins in familial hypertrophic cardiomyopathy

1 reference

12 December 2020

Alpha-tropomyosin and cardiac troponin T mutations cause familial hypertrophic cardiomyopathy: a disease of the sarcomere

1 reference

12 December 2020

Neonatal cardiomyopathy in mice homozygous for the Arg403Gln mutation in the alpha cardiac myosin heavy chain gene

1 reference

12 December 2020

A familial hypertrophic cardiomyopathy locus maps to chromosome 15q2.

1 reference

12 December 2020

The influence of the angiotensin I converting enzyme genotype in familial hypertrophic cardiomyopathy varies with the disease gene mutation

1 reference

12 December 2020

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

1 reference

12 December 2020

Sudden death due to troponin T mutations

1 reference

12 December 2020

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

1 reference

12 December 2020

Mutations in the genes for cardiac troponin T and alpha-tropomyosin in hypertrophic cardiomyopathy

1 reference

12 December 2020

A mouse model of familial hypertrophic cardiomyopathy

1 reference

12 December 2020

The management of hypertrophic cardiomyopathy

1 reference

12 December 2020

Hypertrophic cardiomyopathy

1 reference

12 December 2020

Development and progression of left ventricular hypertrophy in children with hypertrophic cardiomyopathy

1 reference

12 December 2020

Phosphorylation switches specific for the cardiac isoform of myosin binding protein-C: a modulator of cardiac contraction?

1 reference

12 December 2020

Angiotensin-converting enzyme gene polymorphism in Japanese patients with hypertrophic cardiomyopathy

1 reference

12 December 2020

Molecular diversity of myofibrillar proteins: gene regulation and functional significance

1 reference

12 December 2020

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

1 reference

12 December 2020

Mutations in the cardiac troponin I gene associated with hypertrophic cardiomyopathy

1 reference

12 December 2020

Exclusion of cardiac myosin heavy chain and actin gene involvement in hypertrophic cardiomyopathy of several French families

1 reference

12 December 2020

Alpha-cardiac actin is a novel disease gene in familial hypertrophic cardiomyopathy

1 reference

12 December 2020

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

1 reference

12 December 2020

A mouse model of myosin binding protein C human familial hypertrophic cardiomyopathy

1 reference

12 December 2020

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

1 reference

12 December 2020

10.1007/S11886-000-0010-9

Identifiers

DOI

1 reference

PubMed ID

10980884

Dimensions Publication ID

30 July 2017

0 references

1 reference

PubMed ID

10980884