Colorectal Neoplasms
|
0.300 |
Biomarker
|
group |
CTD_human |
Expression of protein kinase C isoenzymes in colorectal cancer tissue and their differential activation by different bile acids.
|
7705931 |
1995 |
Drug abuse
|
0.300 |
Biomarker
|
group |
CTD_human |
Genome wide association for addiction: replicated results and comparisons of two analytic approaches.
|
20098672 |
2010 |
Drug Use Disorders
|
0.300 |
Biomarker
|
group |
CTD_human |
Genome wide association for addiction: replicated results and comparisons of two analytic approaches.
|
20098672 |
2010 |
Liver neoplasms
|
0.300 |
Biomarker
|
group |
CTD_human |
Multiple genes exhibit phenobarbital-induced constitutive active/androstane receptor-mediated DNA methylation changes during liver tumorigenesis and in liver tumors.
|
19233941 |
2009 |
Cardiomyopathies, Primary
|
0.300 |
Biomarker
|
group |
CTD_human |
Protein kinase Cepsilon overexpression alters myofilament properties and composition during the progression of heart failure.
|
15242976 |
2004 |
Myocardial Diseases, Secondary
|
0.300 |
Biomarker
|
group |
CTD_human |
Protein kinase Cepsilon overexpression alters myofilament properties and composition during the progression of heart failure.
|
15242976 |
2004 |
Substance Use Disorders
|
0.300 |
Biomarker
|
group |
CTD_human |
Genome wide association for addiction: replicated results and comparisons of two analytic approaches.
|
20098672 |
2010 |
Substance-Related Disorders
|
0.300 |
Biomarker
|
group |
CTD_human |
Genome wide association for addiction: replicated results and comparisons of two analytic approaches.
|
20098672 |
2010 |
Cardiomyopathies
|
0.300 |
Biomarker
|
group |
CTD_human |
Protein kinase Cepsilon overexpression alters myofilament properties and composition during the progression of heart failure.
|
15242976 |
2004 |
Drug Dependence
|
0.300 |
Biomarker
|
group |
CTD_human |
Genome wide association for addiction: replicated results and comparisons of two analytic approaches.
|
20098672 |
2010 |
Peripheral Nervous System Diseases
|
0.300 |
Biomarker
|
group |
CTD_human |
Alcohol consumption enhances antiretroviral painful peripheral neuropathy by mitochondrial mechanisms.
|
20726883 |
2010 |
Hypertensive disease
|
0.200 |
Biomarker
|
group |
RGD |
Protein kinase C isozymes in hypertension and hypertrophy: insight from SHHF rat hearts.
|
15792354 |
2005 |
Cardiovascular Diseases
|
0.100 |
GeneticVariation
|
group |
GWASCAT |
Leveraging Polygenic Functional Enrichment to Improve GWAS Power.
|
30595370 |
2019 |
Malignant Neoplasms
|
0.040 |
Biomarker
|
group |
BEFREE |
Thus, PKCε appears to become specifically engaged in a programme of controls that are required to support cell-cycle progression in transformed cells, advocating for PKCε as a potential cancer therapeutic target.<b>Implications:</b> The close relationship between PKCε dependency for mitotic spindle organization and the nonfunctionality of the TOPO2A-dependent G<sub>2</sub> checkpoint, a hallmark of transformed cells, strongly suggests PKCε as a therapeutic target in cancer.<i>Mol Cancer Res; 16(1); 3-15.©2017 AACR</i>.
|
29021232 |
2018 |
Malignant Neoplasms
|
0.040 |
Biomarker
|
group |
BEFREE |
This surprising capacity indicates PKCε as a novel predictive marker protein in molecular cancer therapy with EGFR tyrosine kinase inhibitors.
|
21964064 |
2012 |
Malignant Neoplasms
|
0.040 |
Biomarker
|
group |
BEFREE |
Suppression of the PKCε-encoding gene achieved through the antisense cDNA, suppression of PKCε with RNAi and inhibition achieved with translocation-inhibitory peptides may provide novel treatment strategies for cancer.
|
21441608 |
2011 |
Malignant Neoplasms
|
0.040 |
Biomarker
|
group |
BEFREE |
Protein kinase C ε (PKCε) has emerged as an oncogenic protein kinase and plays important roles in cancer cell survival, proliferation, and invasion.
|
30209539 |
2018 |
Primary malignant neoplasm
|
0.040 |
Biomarker
|
group |
BEFREE |
Suppression of the PKCε-encoding gene achieved through the antisense cDNA, suppression of PKCε with RNAi and inhibition achieved with translocation-inhibitory peptides may provide novel treatment strategies for cancer.
|
21441608 |
2011 |
Primary malignant neoplasm
|
0.040 |
Biomarker
|
group |
BEFREE |
Thus, PKCε appears to become specifically engaged in a programme of controls that are required to support cell-cycle progression in transformed cells, advocating for PKCε as a potential cancer therapeutic target.<b>Implications:</b> The close relationship between PKCε dependency for mitotic spindle organization and the nonfunctionality of the TOPO2A-dependent G<sub>2</sub> checkpoint, a hallmark of transformed cells, strongly suggests PKCε as a therapeutic target in cancer.<i>Mol Cancer Res; 16(1); 3-15.©2017 AACR</i>.
|
29021232 |
2018 |
Primary malignant neoplasm
|
0.040 |
Biomarker
|
group |
BEFREE |
This surprising capacity indicates PKCε as a novel predictive marker protein in molecular cancer therapy with EGFR tyrosine kinase inhibitors.
|
21964064 |
2012 |
Primary malignant neoplasm
|
0.040 |
Biomarker
|
group |
BEFREE |
Protein kinase C ε (PKCε) has emerged as an oncogenic protein kinase and plays important roles in cancer cell survival, proliferation, and invasion.
|
30209539 |
2018 |
Neoplasms
|
0.020 |
AlteredExpression
|
group |
BEFREE |
By immunohistochemistry, we found that the expression of PKCε was up-regulated in RCCs and was associated with tumor Fuhrman grade and T stage in clear cell RCCs.
|
21955404 |
2011 |
Neoplasms
|
0.020 |
AlteredExpression
|
group |
BEFREE |
Our data showed that knockdown of PKCε expression inhibited proliferation, induced apoptosis and decreased invasiveness of human glioma cell lines U251 and U87, as well as suppressed the growth of U87 cell-derived tumors in nude mice.
|
24888992 |
2015 |
Cardiomyopathy, Dilated
|
0.010 |
Biomarker
|
group |
BEFREE |
Employing LC-MS/MS, we determined the presence of phosphorylation sites at S5/S6 in cTnI from wild type mouse hearts as well as in hearts of mice chronically expressing active protein kinase C-ε (PKCε) and exhibiting severe dilated cardiomyopathy (DCM).
|
22940544 |
2013 |
Herpes Simplex Infections
|
0.010 |
Biomarker
|
group |
BEFREE |
Here, we employ a highly defective herpes simplex virus vector (vHDNP) that expresses dominant negative PKCepsilon (DNPKCepsilon) as a strategy to demonstrate that PKCepsilon is essential for: (i) maintenance of basal phosphorylation and normal TRPV1 responses to capsaicin (CAPS), a TRPV1 agonist and (ii) enhancement of TRPV1 responses by phorbol esters.
|
18973552 |
2008 |