Cardiomyopathy, Dilated
|
0.630 |
CausalMutation
|
group |
CLINVAR |
Disease-related cardiac troponins alter thin filament Ca2+ association and dissociation rates.
|
22675533 |
2012 |
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 |
Cardiac troponin T lysine 210 deletion in a family with dilated cardiomyopathy.
|
11862580 |
2002 |
Cardiomyopathy, Dilated
|
0.630 |
CausalMutation
|
group |
CLINVAR |
Clinical and functional characterization of TNNT2 mutations identified in patients with dilated cardiomyopathy.
|
20031601 |
2009 |
Cardiomyopathy, Dilated
|
0.630 |
Biomarker
|
group |
MGD |
Gene-Targeted Mice with the Human Troponin T R141W Mutation Develop Dilated Cardiomyopathy with Calcium Desensitization.
|
27936050 |
2016 |
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 |
CausalMutation
|
group |
CLINVAR |
The role of cardiac troponin T quantity and function in cardiac development and dilated cardiomyopathy.
|
18612386 |
2008 |
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 |
GeneticVariation
|
group |
CLINVAR |
Dilated cardiomyopathy mutations in three thin filament regulatory proteins result in a common functional phenotype.
|
15923195 |
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 |
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 |
Novel Genetic Variants in BAG3 and TNNT2 in a Swedish Family with a History of Dilated Cardiomyopathy and Sudden Cardiac Death.
|
28669108 |
2017 |
Cardiomyopathy, Dilated
|
0.630 |
CausalMutation
|
group |
CLINVAR |
Familial dilated cardiomyopathy mutations uncouple troponin I phosphorylation from changes in myofibrillar Ca²⁺ sensitivity.
|
23539503 |
2013 |
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 |
Patient-specific induced pluripotent stem cells as a model for familial dilated cardiomyopathy.
|
22517884 |
2012 |
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 |
Biomarker
|
group |
CTD_human |
Therapeutic effect of {beta}-adrenoceptor blockers using a mouse model of dilated cardiomyopathy with a troponin mutation.
|
19477965 |
2009 |
Cardiomyopathy, Dilated
|
0.630 |
GeneticVariation
|
group |
CLINVAR |
Evaluation of ACMG-Guideline-Based Variant Classification of Cancer Susceptibility and Non-Cancer-Associated Genes in Families Affected by Breast Cancer.
|
27153395 |
2016 |
Cardiomyopathy, Dilated
|
0.630 |
CausalMutation
|
group |
CLINVAR |
The landscape of genetic variation in dilated cardiomyopathy as surveyed by clinical DNA sequencing.
|
24503780 |
2014 |
Cardiomyopathy, Dilated
|
0.630 |
GeneticVariation
|
group |
CLINVAR |
Sarcomere gene mutations in isolated left ventricular noncompaction cardiomyopathy do not predict clinical phenotype.
|
21551322 |
2011 |
Cardiomyopathy, Dilated
|
0.630 |
Biomarker
|
group |
BEFREE |
Novel Genetic Variants in BAG3 and TNNT2 in a Swedish Family with a History of Dilated Cardiomyopathy and Sudden Cardiac Death.
|
28669108 |
2017 |
Cardiomyopathy, Dilated
|
0.630 |
GeneticVariation
|
group |
CLINVAR |
Multiple Species Comparison of Cardiac Troponin T and Dystrophin: Unravelling the DNA behind Dilated Cardiomyopathy.
|
29367539 |
2017 |
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 |
GeneticVariation
|
group |
CLINVAR |
Dilated cardiomyopathy caused by a novel TNNT2 mutation-added value of genetic testing in the correct identification of affected subjects.
|
19324435 |
2010 |
Cardiomyopathy, Dilated
|
0.630 |
GeneticVariation
|
group |
CLINVAR |
A novel arginine to tryptophan (R144W) mutation in troponin T (cTnT) gene in an indian multigenerational family with dilated cardiomyopathy (FDCM).
|
24992688 |
2014 |