Pages that link to "Q24292234"
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The following pages link to Sarcomere protein gene mutations in hypertrophic cardiomyopathy of the elderly (Q24292234):
Displaying 50 items.
- Troponin I3, cardiac type (Q21108986) (← links)
- Myosin heavy chain 6 (Q21119515) (← links)
- Myosin binding protein C3 (Q21120896) (← links)
- Cardiac alpha-myosin (MYH6) is the predominant sarcomeric disease gene for familial atrial septal defects (Q21134934) (← links)
- Cardiomyopathy classification: ongoing debate in the genomics era (Q21284968) (← links)
- Mutation in myosin heavy chain 6 causes atrial septal defect (Q24296801) (← links)
- Genome-wide association analysis identifies multiple loci related to resting heart rate (Q24624928) (← links)
- A common MYBPC3 (cardiac myosin binding protein C) variant associated with cardiomyopathies in South Asia (Q24645034) (← links)
- Genetic Misdiagnoses and the Potential for Health Disparities (Q26316693) (← links)
- Chamber Specific Gene Expression Landscape of the Zebrafish Heart (Q27324640) (← links)
- Functional modulation of cardiac form through regionally confined cell shape changes (Q27334821) (← links)
- Genetics of hypertrophic cardiomyopathy in eastern Finland: few founder mutations with benign or intermediary phenotypes (Q28248327) (← links)
- Mutations in Troponin that cause HCM, DCM AND RCM: what can we learn about thin filament function? (Q28264798) (← links)
- Shared genetic causes of cardiac hypertrophy in children and adults (Q28276100) (← links)
- α-cardiac myosin heavy chain (MYH6) mutations affecting myofibril formation are associated with congenital heart defects (Q28288720) (← links)
- Familial hypertrophic cardiomyopathy associated with cardiac beta-myosin heavy chain and troponin I mutations. (Q30366945) (← links)
- Prediction of protein-destabilizing polymorphisms by manual curation with protein structure (Q30424149) (← links)
- Adverse events in families with hypertrophic or dilated cardiomyopathy and mutations in the MYBPC3 gene (Q33379935) (← links)
- Myosin-binding Protein C Compound Heterozygous Variant Effect on the Phenotypic Expression of Hypertrophic Cardiomyopathy (Q33647442) (← links)
- The Genetic Challenges and Opportunities in Advanced Heart Failure (Q33653498) (← links)
- Toward transcriptional therapies for the failing heart: chemical screens to modulate genes (Q33683749) (← links)
- Echocardiography in patients with hypertrophic cardiomyopathy: usefulness of old and new techniques in the diagnosis and pathophysiological assessment (Q33763883) (← links)
- Hypertrophic cardiomyopathy: from genetics to treatment (Q33992358) (← links)
- Experimental therapies in hypertrophic cardiomyopathy (Q33997765) (← links)
- Association of 25 bp deletion in MYBPC3 gene with left ventricle dysfunction in coronary artery disease patients (Q34018918) (← links)
- Genetics of sudden cardiac death (Q34203505) (← links)
- Late onset sporadic dilated cardiomyopathy caused by a cardiac troponin T mutation (Q34248530) (← links)
- Comparative echocardiographic and clinical features of hypertrophic cardiomyopathy in 5 breeds of cats: a retrospective analysis of 344 cases (2001-2011). (Q34263302) (← links)
- American 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 (Q34275552) (← links)
- The role of sarcomere gene mutations in patients with idiopathic dilated cardiomyopathy (Q34327150) (← links)
- High prevalence of Arginine to Glutamine substitution at 98, 141 and 162 positions in Troponin I (TNNI3) associated with hypertrophic cardiomyopathy among Indians (Q34372769) (← links)
- Two novel mutations of the MYBPC3 gene identified in Chinese families with hypertrophic cardiomyopathy (Q34425285) (← links)
- Narrative review: harnessing molecular genetics for the diagnosis and management of hypertrophic cardiomyopathy (Q34474908) (← links)
- Sarcomere gene mutations in hypertrophy and heart failure (Q34626686) (← links)
- Myocardial fibrosis as an early manifestation of hypertrophic cardiomyopathy (Q34629550) (← links)
- Identifying sarcomere gene mutations in hypertrophic cardiomyopathy: a personal history (Q34772983) (← links)
- Cardiac troponin I Pro82Ser variant induces diastolic dysfunction, blunts β-adrenergic response, and impairs myofilament cooperativity (Q34980505) (← links)
- Genetics and clinical destiny: improving care in hypertrophic cardiomyopathy (Q34999606) (← links)
- Diltiazem treatment for pre-clinical hypertrophic cardiomyopathy sarcomere mutation carriers: a pilot randomized trial to modify disease expression (Q35070184) (← links)
- Hypertrophic cardiomyopathy: from gene defect to clinical disease (Q35087752) (← links)
- Knockdown of embryonic myosin heavy chain reveals an essential role in the morphology and function of the developing heart (Q35176657) (← links)
- Mutations of the beta myosin heavy chain gene in hypertrophic cardiomyopathy: critical functional sites determine prognosis (Q35581582) (← links)
- Unexpectedly low mutation rates in beta-myosin heavy chain and cardiac myosin binding protein genes in Italian patients with hypertrophic cardiomyopathy. (Q35590181) (← links)
- Familial hypertrophic cardiomyopathy: clinical features, molecular genetics and molecular genetic testing (Q35623368) (← links)
- Myosin binding protein C: structural abnormalities in familial hypertrophic cardiomyopathy (Q35759293) (← links)
- The pathology of hypertrophic cardiomyopathy (Q35771667) (← links)
- Familial screening and genetic counselling in hypertrophic cardiomyopathy: the Rotterdam experience (Q35812684) (← links)
- Targeted Next-Generation Sequencing Reveals Hot Spots and Doubly Heterozygous Mutations in Chinese Patients with Familial Cardiomyopathy (Q35829323) (← links)
- Dissociation of structural and functional phenotypes in cardiac myosin-binding protein C conditional knockout mice (Q36303049) (← links)
- Molecular genetics in hypertrophic cardiomyopathy: towards individualized management of the disease (Q36344118) (← links)