Cardiomyopathy, Dilated
|
0.210 |
Biomarker
|
group |
MGD |
|
|
|
Patent ductus arteriosus
|
0.200 |
Biomarker
|
disease |
MGD |
|
|
|
Seizures
|
0.100 |
GeneticVariation
|
phenotype |
CLINVAR |
|
|
|
Poor school performance
|
0.100 |
GeneticVariation
|
phenotype |
CLINVAR |
|
|
|
Coronary Artery Disease
|
0.020 |
Biomarker
|
disease |
BEFREE |
<b>Conclusions:</b> These data indicate that TCF21 antagonizes the MYOCD-SRF pathway through multiple mechanisms, further establishing a role for this CAD associated gene in fundamental SMC processes and indicating the importance of smooth muscle response to vascular stress and phenotypic modulation of this cell type in CAD risk.
|
31815603 |
2020 |
Disseminated Malignant Neoplasm
|
0.010 |
AlteredExpression
|
phenotype |
BEFREE |
Disseminated cancer cells employ L1CAM (cell adhesion molecule L1) to spread on capillaries and activate the mechanotransduction effectors YAP (Yes-associated protein) and MRTF (myocardin-related transcription factor).
|
30038252 |
2018 |
Cardiomyopathy, Dilated
|
0.210 |
AlteredExpression
|
group |
BEFREE |
Myocardin and HOP mRNA levels were estimated by both northern blot hybridization and semiquantitative RT-PCR in human ventricular preparations in end-stage failure due to dilated cardiomyopathy (DCM), as well as in nonfailing donor hearts.
|
12920479 |
2003 |
Cardiomyopathy, Familial Idiopathic
|
0.020 |
AlteredExpression
|
disease |
BEFREE |
Myocardin and HOP mRNA levels were estimated by both northern blot hybridization and semiquantitative RT-PCR in human ventricular preparations in end-stage failure due to dilated cardiomyopathy (DCM), as well as in nonfailing donor hearts.
|
12920479 |
2003 |
Dementia due to Alzheimer's disease (disorder)
|
0.010 |
Biomarker
|
disease |
BEFREE |
MYOCD in vivo gene transfer to mouse pial arteries increased contractile protein content and diminished CBF responses produced by brain activation in wild-type mice and in two AD models, the Dutch/Iowa/Swedish triple mutant human amyloid beta-peptide (Abeta)-precursor protein (APP)- expressing mice and APPsw(+/-) mice.Silencing Srf had the opposite effect.
|
17215356 |
2007 |
Neoplasms
|
0.050 |
AlteredExpression
|
group |
BEFREE |
Myocardin expression is reduced in multiple types of human tumors.
|
17292825 |
2007 |
Neoplasm Metastasis
|
0.020 |
AlteredExpression
|
phenotype |
BEFREE |
Myocardin-related transcription factors and SRF are required for cytoskeletal dynamics and experimental metastasis.
|
19198601 |
2009 |
Tumor Cell Invasion
|
0.020 |
Biomarker
|
phenotype |
BEFREE |
Myocardin had the opposite effects of miR‑135b, which suppressed proliferation, migration and invasion in MG63 cells.
|
25190111 |
2014 |
Arteriosclerosis
|
0.040 |
AlteredExpression
|
disease |
BEFREE |
Myocardin levels are reduced during atherosclerosis, in association with phenotypic switching of smooth muscle cells.
|
25614278 |
2015 |
Atherosclerosis
|
0.040 |
AlteredExpression
|
disease |
BEFREE |
Myocardin levels are reduced during atherosclerosis, in association with phenotypic switching of smooth muscle cells.
|
25614278 |
2015 |
LATERAL MENINGOCELE SYNDROME
|
0.030 |
Biomarker
|
disease |
BEFREE |
MYOCD, a key gene associated with smooth muscle differentiation, is amplified in a subset of both retroperitoneal and extremity LMS.
|
26541895 |
2016 |
LIMB-MAMMARY SYNDROME
|
0.030 |
Biomarker
|
disease |
BEFREE |
MYOCD, a key gene associated with smooth muscle differentiation, is amplified in a subset of both retroperitoneal and extremity LMS.
|
26541895 |
2016 |
Malignant transformation
|
0.020 |
Biomarker
|
phenotype |
BEFREE |
Myocardin is frequently repressed during human malignant transformation, and restoration of myocardin expression in sarcoma cells contributes to the inhibition of malignant growth.
|
27156566 |
2016 |
Malignant Neoplasms
|
0.030 |
AlteredExpression
|
group |
BEFREE |
Myocardin is frequently repressed during human malignant transformation, and restoration of myocardin expression in sarcoma cells contributes to the inhibition of malignant growth.
|
27156566 |
2016 |
SMITH-MCCORT DYSPLASIA 1
|
0.020 |
AlteredExpression
|
disease |
BEFREE |
Myocardin expression represents a contractile and differentiated SMC phenotype.
|
28012646 |
2017 |
Myocardial Infarction
|
0.010 |
Biomarker
|
disease |
BEFREE |
Myocardin expression is upregulated upon H<sub>2</sub>O<sub>2</sub> and ischemia/reperfusion, and knockdown of myocardin inhibits autophagy and attenuates myocardial infarction. p53 regulates cardiomyocytes autophagy and myocardial ischemia/reperfusion injury by regulating myocardin expression.
|
29295976 |
2018 |
Heart failure
|
0.010 |
AlteredExpression
|
disease |
BEFREE |
A possible dual consequence of increased myocardin and decreased HOP expression levels on serum response factor-dependent cardiac-specific expression in the normal heart and at heart failure is discussed.
|
12920479 |
2003 |
Congestive heart failure
|
0.010 |
AlteredExpression
|
disease |
BEFREE |
A possible dual consequence of increased myocardin and decreased HOP expression levels on serum response factor-dependent cardiac-specific expression in the normal heart and at heart failure is discussed.
|
12920479 |
2003 |
Neoplasms
|
0.050 |
Biomarker
|
group |
BEFREE |
At stage I, among the tumors reclassified as molecular leiomyosarcomas (ie, genomic index ≥10), the poor prognostic markers were: 5p gain (overall survival P=0.0008), genomic index at cut-off=35 (overall survival P=0.0193), 13p loss including RB1 (overall survival P=0.0096) and 17p gain including MYOCD gain (overall survival P=0.0425).
|
29327710 |
2018 |
leiomyosarcoma
|
0.030 |
Biomarker
|
disease |
BEFREE |
At stage I, among the tumors reclassified as molecular leiomyosarcomas (ie, genomic index ≥10), the poor prognostic markers were: 5p gain (overall survival P=0.0008), genomic index at cut-off=35 (overall survival P=0.0193), 13p loss including RB1 (overall survival P=0.0096) and 17p gain including MYOCD gain (overall survival P=0.0425).
|
29327710 |
2018 |
Atrial Fibrillation
|
0.400 |
GeneticVariation
|
disease |
GWASCAT |
Biobank-driven genomic discovery yields new insight into atrial fibrillation biology.
|
30061737 |
2018 |