Hypertrophic Cardiomyopathy
|
0.800 |
Biomarker
|
disease |
GENOMICS_ENGLAND |
|
|
|
Hypertrophic Cardiomyopathy
|
0.800 |
Biomarker
|
disease |
HPO |
|
|
|
Hypertrophic Cardiomyopathy
|
0.800 |
Biomarker
|
disease |
CLINGEN |
Troponin T isoform expression in humans. A comparison among normal and failing adult heart, fetal heart, and adult and fetal skeletal muscle.
|
1934353 |
1991 |
Hypertrophic Cardiomyopathy
|
0.800 |
CausalMutation
|
disease |
CLINVAR |
Alpha-tropomyosin and cardiac troponin T mutations cause familial hypertrophic cardiomyopathy: a disease of the sarcomere.
|
8205619 |
1994 |
Hypertrophic Cardiomyopathy
|
0.800 |
Biomarker
|
disease |
CLINGEN |
Alpha-tropomyosin and cardiac troponin T mutations cause familial hypertrophic cardiomyopathy: a disease of the sarcomere.
|
8205619 |
1994 |
Hypertrophic Cardiomyopathy
|
0.800 |
CausalMutation
|
disease |
CLINVAR |
Mutations in the genes for cardiac troponin T and alpha-tropomyosin in hypertrophic cardiomyopathy.
|
7898523 |
1995 |
Hypertrophic Cardiomyopathy
|
0.800 |
Biomarker
|
disease |
BEFREE |
Expression and functional assessment of a truncated cardiac troponin T that causes hypertrophic cardiomyopathy. Evidence for a dominant negative action.
|
8958207 |
1996 |
Hypertrophic Cardiomyopathy
|
0.800 |
CausalMutation
|
disease |
CLINVAR |
Clinical manifestations of hypertrophic cardiomyopathy with mutations in the cardiac beta-myosin heavy chain gene or cardiac troponin T gene.
|
8951566 |
1996 |
Hypertrophic Cardiomyopathy
|
0.800 |
CausalMutation
|
disease |
CLINVAR |
Expression and functional assessment of a truncated cardiac troponin T that causes hypertrophic cardiomyopathy. Evidence for a dominant negative action.
|
8958207 |
1996 |
Hypertrophic Cardiomyopathy
|
0.800 |
CausalMutation
|
disease |
CLINVAR |
Expression of a mutant (Arg92Gln) human cardiac troponin T, known to cause hypertrophic cardiomyopathy, impairs adult cardiac myocyte contractility.
|
9201030 |
1997 |
Hypertrophic Cardiomyopathy
|
0.800 |
CausalMutation
|
disease |
CLINVAR |
Sudden death due to troponin T mutations.
|
9060892 |
1997 |
Hypertrophic Cardiomyopathy
|
0.800 |
Biomarker
|
disease |
CLINGEN |
A truncated cardiac troponin T molecule in transgenic mice suggests multiple cellular mechanisms for familial hypertrophic cardiomyopathy.
|
9637714 |
1998 |
Hypertrophic Cardiomyopathy
|
0.800 |
CausalMutation
|
disease |
CLINVAR |
A truncated cardiac troponin T molecule in transgenic mice suggests multiple cellular mechanisms for familial hypertrophic cardiomyopathy.
|
9637714 |
1998 |
Hypertrophic Cardiomyopathy
|
0.800 |
Biomarker
|
disease |
CLINGEN |
Cardiac troponin T mutations result in allele-specific phenotypes in a mouse model for hypertrophic cardiomyopathy.
|
10449439 |
1999 |
Hypertrophic Cardiomyopathy
|
0.800 |
CausalMutation
|
disease |
CLINVAR |
Altered regulatory function of two familial hypertrophic cardiomyopathy troponin T mutants.
|
10529204 |
1999 |
Hypertrophic Cardiomyopathy
|
0.800 |
CausalMutation
|
disease |
CLINVAR |
The origins of hypertrophic cardiomyopathy-causing mutations in two South African subpopulations: a unique profile of both independent and founder events.
|
10521296 |
1999 |
Hypertrophic Cardiomyopathy
|
0.800 |
CausalMutation
|
disease |
CLINVAR |
A new mutation of the cardiac troponin T gene causing familial hypertrophic cardiomyopathy without left ventricular hypertrophy.
|
10525521 |
1999 |
Hypertrophic Cardiomyopathy
|
0.800 |
GeneticVariation
|
disease |
CLINVAR |
A new mutation of the cardiac troponin T gene causing familial hypertrophic cardiomyopathy without left ventricular hypertrophy.
|
10525521 |
1999 |
Hypertrophic Cardiomyopathy
|
0.800 |
CausalMutation
|
disease |
CLINVAR |
Ca2+ sensitization and potentiation of the maximum level of myofibrillar ATPase activity caused by mutations of troponin T found in familial hypertrophic cardiomyopathy.
|
10085122 |
1999 |
Hypertrophic Cardiomyopathy
|
0.800 |
Biomarker
|
disease |
CLINGEN |
Identification of a contractile deficit in adult cardiac myocytes expressing hypertrophic cardiomyopathy-associated mutant troponin T proteins.
|
10330428 |
1999 |
Hypertrophic Cardiomyopathy
|
0.800 |
Biomarker
|
disease |
CLINGEN |
Functional consequences of a carboxyl terminal missense mutation Arg278Cys in human cardiac troponin T.
|
10405326 |
1999 |
Hypertrophic Cardiomyopathy
|
0.800 |
CausalMutation
|
disease |
CLINVAR |
Functional consequences of the deletion mutation deltaGlu160 in human cardiac troponin T.
|
10731693 |
2000 |
Hypertrophic Cardiomyopathy
|
0.800 |
CausalMutation
|
disease |
CLINVAR |
Altered regulation of cardiac muscle contraction by troponin T mutations that cause familial hypertrophic cardiomyopathy.
|
10617660 |
2000 |
Hypertrophic Cardiomyopathy
|
0.800 |
GeneticVariation
|
disease |
CLINVAR |
Homozygous mutation in cardiac troponin T: implications for hypertrophic cardiomyopathy.
|
11034944 |
2000 |
Hypertrophic Cardiomyopathy
|
0.800 |
GeneticVariation
|
disease |
CLINVAR |
Disease-causing mutations in cardiac troponin T: identification of a critical tropomyosin-binding region.
|
11606294 |
2001 |