Cardiomyopathy, Dilated
|
0.630 |
Biomarker
|
group |
HPO |
|
|
|
Cardiomyopathy, Dilated
|
0.630 |
CausalMutation
|
group |
CLINVAR |
Mutations in sarcomere protein genes as a cause of dilated cardiomyopathy.
|
11106718 |
2000 |
Cardiomyopathy, Dilated
|
0.630 |
CausalMutation
|
group |
CLINVAR |
Novel cardiac troponin T mutation as a cause of familial dilated cardiomyopathy.
|
11684629 |
2001 |
Cardiomyopathy, Dilated
|
0.630 |
CausalMutation
|
group |
CLINVAR |
Cardiac troponin T lysine 210 deletion in a family with dilated cardiomyopathy.
|
11862580 |
2002 |
Cardiomyopathy, Dilated
|
0.630 |
GeneticVariation
|
group |
BEFREE |
TNNT2 mutations can also lead to dilated cardiomyopathy, a leading cause of heart failure.
|
11967535 |
2002 |
Cardiomyopathy, Dilated
|
0.630 |
CausalMutation
|
group |
CLINVAR |
Ca(2+)-desensitizing effect of a deletion mutation Delta K210 in cardiac troponin T that causes familial dilated cardiomyopathy.
|
11773635 |
2002 |
Cardiomyopathy, Dilated
|
0.630 |
CausalMutation
|
group |
CLINVAR |
Cardiac troponin T mutation R141W found in dilated cardiomyopathy stabilizes the troponin T-tropomyosin interaction and causes a Ca2+ desensitization.
|
14654368 |
2003 |
Cardiomyopathy, Dilated
|
0.630 |
CausalMutation
|
group |
CLINVAR |
Different functional properties of troponin T mutants that cause dilated cardiomyopathy.
|
12923187 |
2003 |
Cardiomyopathy, Dilated
|
0.630 |
CausalMutation
|
group |
CLINVAR |
Severe disease expression of cardiac troponin C and T mutations in patients with idiopathic dilated cardiomyopathy.
|
15542288 |
2004 |
Cardiomyopathy, Dilated
|
0.630 |
GeneticVariation
|
group |
CLINVAR |
Severe disease expression of cardiac troponin C and T mutations in patients with idiopathic dilated cardiomyopathy.
|
15542288 |
2004 |
Cardiomyopathy, Dilated
|
0.630 |
CausalMutation
|
group |
CLINVAR |
Dilated cardiomyopathy mutations in three thin filament regulatory proteins result in a common functional phenotype.
|
15923195 |
2005 |
Cardiomyopathy, Dilated
|
0.630 |
GeneticVariation
|
group |
CLINVAR |
Dilated cardiomyopathy mutations in three thin filament regulatory proteins result in a common functional phenotype.
|
15923195 |
2005 |
Cardiomyopathy, Dilated
|
0.630 |
CausalMutation
|
group |
CLINVAR |
Characterization of troponin T dilated cardiomyopathy mutations in the fetal troponin isoform.
|
15623536 |
2005 |
Cardiomyopathy, Dilated
|
0.630 |
CausalMutation
|
group |
CLINVAR |
Mutation screening in dilated cardiomyopathy: prominent role of the beta myosin heavy chain gene.
|
15769782 |
2005 |
Cardiomyopathy, Dilated
|
0.630 |
GeneticVariation
|
group |
CLINVAR |
Novel troponin T mutation in familial dilated cardiomyopathy with gender-dependant severity.
|
15464434 |
2005 |
Cardiomyopathy, Dilated
|
0.630 |
Biomarker
|
group |
CTD_human |
Knock-in mouse model of dilated cardiomyopathy caused by troponin mutation.
|
17556660 |
2007 |
Cardiomyopathy, Dilated
|
0.630 |
GeneticVariation
|
group |
CLINVAR |
Dilated and hypertrophic cardiomyopathy mutations in troponin and alpha-tropomyosin have opposing effects on the calcium affinity of cardiac thin filaments.
|
17932326 |
2007 |
Cardiomyopathy, Dilated
|
0.630 |
Biomarker
|
group |
MGD |
Knock-in mouse model of dilated cardiomyopathy caused by troponin mutation.
|
17556660 |
2007 |
Cardiomyopathy, Dilated
|
0.630 |
CausalMutation
|
group |
CLINVAR |
Dilated and hypertrophic cardiomyopathy mutations in troponin and alpha-tropomyosin have opposing effects on the calcium affinity of cardiac thin filaments.
|
17932326 |
2007 |
Cardiomyopathy, Dilated
|
0.630 |
CausalMutation
|
group |
CLINVAR |
The role of cardiac troponin T quantity and function in cardiac development and dilated cardiomyopathy.
|
18612386 |
2008 |
Cardiomyopathy, Dilated
|
0.630 |
CausalMutation
|
group |
CLINVAR |
[Association of TNNT2 gene mutations with idiopathic dilated cardiomyopathy in a Chengdu population].
|
19253838 |
2008 |
Cardiomyopathy, Dilated
|
0.630 |
GeneticVariation
|
group |
CLINVAR |
Mutations in sarcomere protein genes in left ventricular noncompaction.
|
18506004 |
2008 |
Cardiomyopathy, Dilated
|
0.630 |
GeneticVariation
|
group |
CLINVAR |
Coding sequence mutations identified in MYH7, TNNT2, SCN5A, CSRP3, LBD3, and TCAP from 313 patients with familial or idiopathic dilated cardiomyopathy.
|
19412328 |
2008 |
Cardiomyopathy, Dilated
|
0.630 |
CausalMutation
|
group |
CLINVAR |
Mutations in sarcomere protein genes in left ventricular noncompaction.
|
18506004 |
2008 |
Cardiomyopathy, Dilated
|
0.630 |
CausalMutation
|
group |
CLINVAR |
Clinical and functional characterization of TNNT2 mutations identified in patients with dilated cardiomyopathy.
|
20031601 |
2009 |