(Q44454565)

English

Hypertrophic cardiomyopathy due to sarcomeric gene mutations is characterized by impaired energy metabolism irrespective of the degree of hypertrophy

scientific article published in May 2003

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

3 December 2017

Hypertrophic cardiomyopathy due to sarcomeric gene mutations is characterized by impaired energy metabolism irrespective of the degree of hypertrophy (English)

1 reference

Europe PubMed Central

PubMed publication ID

3 December 2017

hypertrophic cardiomyopathy

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inferred from title

Hugh Christian Watkins

10

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Europe PubMed Central

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3 December 2017

Andrew M. Blamire

object named as

Andrew M Blamire

5

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author name string

Jenifer G Crilley

1

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Europe PubMed Central

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3 December 2017

Ernest A Boehm

2

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3 December 2017

Edward Blair

3

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3 December 2017

Bheeshma Rajagopalan

4

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3 December 2017

Peter Styles

6

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3 December 2017

William J McKenna

7

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3 December 2017

Ingegerd Ostman-Smith

8

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3 December 2017

Kieran Clarke

9

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3 December 2017

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publication date

1 May 2003

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Europe PubMed Central

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3 December 2017

Journal of the American College of Cardiology

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Europe PubMed Central

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3 December 2017

41

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3 December 2017

10

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3 December 2017

1776-1782

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3 December 2017

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

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

1 reference

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

1 reference

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7 January 2021

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

1 reference

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7 January 2021

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Familial hypertrophic cardiomyopathy: from mutations to functional defects

1 reference

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The molecular genetic basis for hypertrophic cardiomyopathy

1 reference

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Sudden death due to troponin T mutations

1 reference

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Properties of mutant contractile proteins that cause hypertrophic cardiomyopathy

1 reference

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Functional analyses of troponin T mutations that cause hypertrophic cardiomyopathy: insights into disease pathogenesis and troponin function

1 reference

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Diastolic dysfunction and altered energetics in the alphaMHC403/+ mouse model of familial hypertrophic cardiomyopathy

1 reference

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Deficit of in vivo mitochondrial ATP production in patients with Friedreich ataxia

1 reference

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Maternally inherited cardiomyopathy: a new phenotype associated with the A to G AT nt.3243 of mitochondrial DNA (MELAS mutation)

1 reference

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The use of NMR spectroscopy for the understanding of disease.

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

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

1 reference

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Magnetic resonance spectroscopy evidence of abnormal cardiac energetics in Xp21 muscular dystrophy

1 reference

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Measurement of myocardial pH by saturation transfer in man

1 reference

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Myocardial phosphocreatine-to-ATP ratio is a predictor of mortality in patients with dilated cardiomyopathy

1 reference

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7 January 2021

based on heuristic

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Mutations in cis can confound genotype-phenotype correlations in hypertrophic cardiomyopathy

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

Experience from clinical genetics in hypertrophic cardiomyopathy: proposal for new diagnostic criteria in adult members of affected families

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

31P NMR spectroscopy detects metabolic abnormalities in asymptomatic patients with hypertrophic cardiomyopathy

1 reference

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7 January 2021

based on heuristic

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Diastolic dysfunction in hypertensive heart disease is associated with altered myocardial metabolism

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

Cardiac energetics are abnormal in Friedreich ataxia patients in the absence of cardiac dysfunction and hypertrophy: an in vivo 31P magnetic resonance spectroscopy study.

1 reference

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7 January 2021

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Intracellular compartmentation, structure and function of creatine kinase isoenzymes in tissues with high and fluctuating energy demands: the 'phosphocreatine circuit' for cellular energy homeostasis

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2802%2903009-7

7 January 2021

based on heuristic

inferred from DOI database lookup

Energetics and function of the failing human heart with dilated or hypertrophic cardiomyopathy

1 reference

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7 January 2021

based on heuristic

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Increased adenosine monophosphate-activated protein kinase activity in rat hearts with pressure-overload hypertrophy

1 reference

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7 January 2021

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inferred from DOI database lookup

Progressive loss of myocardial ATP due to a loss of total purines during the development of heart failure in dogs: a compensatory role for the parallel loss of creatine

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

Skeletal muscle expression and abnormal function of beta-myosin in hypertrophic cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2802%2903009-7

7 January 2021

based on heuristic

inferred from DOI database lookup

Single-molecule mechanics of R403Q cardiac myosin isolated from the mouse model of familial hypertrophic cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2802%2903009-7

7 January 2021

based on heuristic

inferred from DOI database lookup

Cardiac troponin T mutations: correlation between the type of mutation and the nature of myofilament dysfunction in transgenic mice

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

Mutations in the gamma(2) subunit of AMP-activated protein kinase cause familial hypertrophic cardiomyopathy: evidence for the central role of energy compromise in disease pathogenesis

1 reference

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Identification of a gene responsible for familial Wolff-Parkinson-White syndrome

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The AMP-activated protein kinase--fuel gauge of the mammalian cell?

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Identifiers

10.1016/S0735-1097(02)03009-7

1 reference

Europe PubMed Central

PubMed publication ID

3 December 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

3 December 2017

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