Hypertrophic cardiomyopathy: histopathological features of sudden death in cardiac troponin T disease

scientific article published on 01 September 2001

Hypertrophic cardiomyopathy: histopathological features of sudden death in cardiac troponin T disease is …
instance of (P31):
scholarly articleQ13442814

External links are
P356DOI10.1161/HC3701.095952
P698PubMed publication ID11560853

P2093author name stringElliott PM
McKenna WJ
Davies MJ
Baboonian C
Davison F
Varnava AM
P433issue12
P407language of work or nameEnglishQ1860
P921main subjecthypertrophic cardiomyopathyQ1364270
P304page(s)1380-1384
P577publication date2001-09-01
P1433published inCirculationQ578091
P1476titleHypertrophic cardiomyopathy: histopathological features of sudden death in cardiac troponin T disease
P478volume104

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cites work (P2860)
Q41687674A One Health Approach to Hypertrophic Cardiomyopathy
Q54345908A low prevalence of MYH7/MYBPC3 mutations among familial hypertrophic cardiomyopathy patients in India.
Q38028220A potential role for integrin signaling in mechanoelectrical feedback
Q33161569A primer on arrhythmias in patients with hypertrophic cardiomyopathy
Q46413646A window to the heart: can zebrafish mutants help us understand heart disease in humans?
Q37413343Abnormal blood pressure response to exercise occurs more frequently in hypertrophic cardiomyopathy patients with the R92W troponin T mutation than in those with myosin mutations
Q28570951Aldosterone, through novel signaling proteins, is a fundamental molecular bridge between the genetic defect and the cardiac phenotype of hypertrophic cardiomyopathy
Q52725150Allele-specific differences in transcriptome, miRNome, and mitochondrial function in two hypertrophic cardiomyopathy mouse models.
Q34275552American College of Cardiology/European Society of Cardiology clinical expert consensus document on hypertrophic cardiomyopathy. A report of the American College of Cardiology Foundation Task Force on Clinical Expert Consensus Documents and the Euro
Q36824519Analysis of the molecular pathogenesis of cardiomyopathy-causing cTnT mutants I79N, ΔE96, and ΔK210.
Q37410985Antifibrotic effects of antioxidant N-acetylcysteine in a mouse model of human hypertrophic cardiomyopathy mutation
Q35115012Association of noninvasively measured left ventricular mechanics with in vitro muscle contractile performance: a prospective study in hypertrophic cardiomyopathy patients.
Q36826251Athletic Cardiac Adaptation in Males Is a Consequence of Elevated Myocyte Mass
Q28187589Autopsy findings in siblings with hypertrophic cardiomyopathy caused by Arg92Trp mutation in the cardiac troponin T gene showing dilated cardiomyopathy-like features
Q46049216Cardiac troponin T is essential in sarcomere assembly and cardiac contractility
Q21328674Cardiac troponin mutations and restrictive cardiomyopathy
Q38724869Cardiac troponin structure-function and the influence of hypertrophic cardiomyopathy associated mutations on modulation of contractility
Q34388932Cardiac-specific over-expression of epidermal growth factor receptor 2 (ErbB2) induces pro-survival pathways and hypertrophic cardiomyopathy in mice
Q90533953Catecholamine response to exercise in patients with non-obstructive hypertrophic cardiomyopathy
Q48177445Clinical outcomes associated with sarcomere mutations in hypertrophic cardiomyopathy: a meta-analysis on 7675 individuals
Q46135637Decreased contractility due to energy deprivation in a transgenic rat model of hypertrophic cardiomyopathy
Q35771997Delayed hyperenhancement in magnetic resonance imaging of left ventricular hypertrophy caused by aortic stenosis and hypertrophic cardiomyopathy: visualisation of focal fibrosis
Q37372239Delineation of Molecular Pathways Involved in Cardiomyopathies Caused by Troponin T Mutations
Q92543202Differences in microRNA-29 and Pro-fibrotic Gene Expression in Mouse and Human Hypertrophic Cardiomyopathy
Q79299051Different Coronary Blood Flow Increase in Left Ventricular Hypertrophy Due to Hypertension Compared to Hypertrophic Cardiomyopathy at Elevated Heart Rate
Q33764571Diffuse interstitial fibrosis assessed by cardiac magnetic resonance is associated with dispersion of ventricular repolarization in patients with hypertrophic cardiomyopathy
Q51730904Distinct ECG Phenotypes Identified in Hypertrophic Cardiomyopathy Using Machine Learning Associate With Arrhythmic Risk Markers.
Q37652430Effect of cellular and extracellular pathology assessed by T1 mapping on regional contractile function in hypertrophic cardiomyopathy
Q84448571Effect of heterogeneities in the cellular microstructure on propagation of the cardiac action potential
Q34188103Effects of two familial hypertrophic cardiomyopathy mutations in alpha-tropomyosin, Asp175Asn and Glu180Gly, on the thermal unfolding of actin-bound tropomyosin
Q37255253Evolving molecular diagnostics for familial cardiomyopathies: at the heart of it all
Q35063399Fetal cardiac troponin isoforms rescue the increased Ca2+ sensitivity produced by a novel double deletion in cardiac troponin T linked to restrictive cardiomyopathy: a clinical, genetic, and functional approach
Q21129229Gene regulation, alternative splicing, and posttranslational modification of troponin subunits in cardiac development and adaptation: a focused review
Q63440935Genetic and clinical profile of Indian patients of idiopathic restrictive cardiomyopathy with and without hypertrophy
Q37125766Genetic determinants of cardiac hypertrophy
Q38125385Genetic testing for inherited cardiac disease
Q38169914Genetics of sudden cardiac death caused by ventricular arrhythmias
Q40526444Higher copeptin levels are associated with worse outcome in patients with hypertrophic cardiomyopathy
Q35762855Histologic characterization of hypertrophic cardiomyopathy with and without myofilament mutations
Q42515078Hypertrophic Cardiomyopathy: Genetics, Pathogenesis, Clinical Manifestations, Diagnosis, and Therapy
Q42339402Hypertrophic cardiomyopathy in daily practice: an introduction on diagnosis, prognosis and treatment
Q50022359Hypertrophic cardiomyopathy-linked mutation in troponin T causes myofibrillar disarray and pro-arrhythmic action potential changes in human iPSC cardiomyocytes.
Q35087752Hypertrophic cardiomyopathy: from gene defect to clinical disease
Q37070209Hypertrophic cardiomyopathy: the genetic determinants of clinical disease expression
Q92225133Identification of Myocardial Disarray in Patients With Hypertrophic Cardiomyopathy and Ventricular Arrhythmias
Q24292763Idiopathic restrictive cardiomyopathy is part of the clinical expression of cardiac troponin I mutations
Q36371337Impact of Mendelian inheritance in cardiovascular disease
Q37054964Impaired contractile function due to decreased cardiac myosin binding protein C content in the sarcomere
Q37680390Increased myofilament Ca2+-sensitivity and arrhythmia susceptibility.
Q37415192Induction and reversal of cardiac phenotype of human hypertrophic cardiomyopathy mutation cardiac troponin T-Q92 in switch on-switch off bigenic mice
Q38046158Insights and challenges in hypertrophic cardiomyopathy, 2012.
Q79372098Is sudden cardiac death predictable in LEOPARD syndrome?
Q39099962L71F mutation in rat cardiac troponin T augments crossbridge recruitment and detachment dynamics against α-myosin heavy chain, but not against β-myosin heavy chain
Q28235380Long-term follow-up of R403WMYH7 and R92WTNNT2 HCM families: mutations determine left ventricular dimensions but not wall thickness during disease progression
Q37949516Mechanisms of disease: hypertrophic cardiomyopathy
Q34641881Modifier genes for hypertrophic cardiomyopathy
Q37675919Molecular basis of hereditary cardiomyopathy: abnormalities in calcium sensitivity, stretch response, stress response and beyond
Q34021080Molecular genetics and pathogenesis of hypertrophic cardiomyopathy
Q39038606Murine Electrophysiological Models of Cardiac Arrhythmogenesis
Q37816783Mutation type is not clinically useful in predicting prognosis in hypertrophic cardiomyopathy.
Q28264798Mutations in Troponin that cause HCM, DCM AND RCM: what can we learn about thin filament function?
Q36593277Myofibrillar remodeling in cardiac hypertrophy, heart failure and cardiomyopathies
Q41896456Myofilament Ca sensitization increases cytosolic Ca binding affinity, alters intracellular Ca homeostasis, and causes pause-dependent Ca-triggered arrhythmia.
Q30484558Myofilament Ca2+ sensitization causes susceptibility to cardiac arrhythmia in mice.
Q49957679Myofilament Calcium-Buffering Dependent Action Potential Triangulation in Human-Induced Pluripotent Stem Cell Model of Hypertrophic Cardiomyopathy
Q34474908Narrative review: harnessing molecular genetics for the diagnosis and management of hypertrophic cardiomyopathy
Q35880670Novel insights on the relationship between T-tubular defects and contractile dysfunction in a mouse model of hypertrophic cardiomyopathy.
Q93174381Pathogenic troponin T mutants with opposing effects on myofilament Ca2+ sensitivity attenuate cardiomyopathy phenotypes in mice
Q88564292Postmortem cardiac magnetic resonance in sudden cardiac death
Q47886356Prevalence and age-dependence of malignant mutations in the beta-myosin heavy chain and troponin T genes in hypertrophic cardiomyopathy: a comprehensive outpatient perspective
Q37445574Prognostic factors in chronic heart failure. A review of serum biomarkers, metabolic changes, symptoms, and scoring systems
Q41698138Right ventricle myectomy
Q34195775Somatic events modify hypertrophic cardiomyopathy pathology and link hypertrophy to arrhythmia
Q80482543Sudden Cardiac Death
Q36242912Surgical correction of hypertrophic obstructive cardiomyopathy in a patient with severe hypertrophy and septal myocardial fibrosis
Q73429825Surgical pathology of subaortic septal myectomy associated with hypertrophic cardiomyopathy. A study of 204 cases (1996-2000)
Q37738593Taxonomy of segmental myocardial systolic dysfunction
Q41997993The effect of cardiomyopathy mutation (R97L) in mouse cardiac troponin T on the muscle length-mediated recruitment of crossbridges is modified divergently by α- and β-myosin heavy chain
Q37636605The genetics of cardiomyopathy: genotyping and genetic counseling
Q37034674The mystery of sudden death: mechanisms for risks
Q37239549The role of Akt/GSK-3beta signaling in familial hypertrophic cardiomyopathy
Q28307606Thin filament mutations: developing an integrative approach to a complex disorder
Q38520406Toward clinical risk assessment in hypertrophic cardiomyopathy with gadolinium cardiovascular magnetic resonance.
Q30245043Update on hypertrophic cardiomyopathy and a guide to the guidelines.
Q83568905[Clinical and genetic aspects of hypertrophic and dilated cardiomyopathy]
Q79748186[What is late gadolinium enhancement in hypertrophic cardiomyopathy?]

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