Cholestasis
|
0.300 |
Biomarker
|
disease |
CTD_human |
Role of fibrinogen and protease-activated receptors in acute xenobiotic-induced cholestatic liver injury.
|
20974703 |
2011 |
Hepatitis, Toxic
|
0.300 |
Biomarker
|
disease |
CTD_human |
Role of fibrinogen and protease-activated receptors in acute xenobiotic-induced cholestatic liver injury.
|
20974703 |
2011 |
Peliosis Hepatis
|
0.300 |
Biomarker
|
disease |
CTD_human |
Role of fibrinogen and protease-activated receptors in acute xenobiotic-induced cholestatic liver injury.
|
20974703 |
2011 |
Hepatitis, Drug-Induced
|
0.300 |
Biomarker
|
disease |
CTD_human |
Role of fibrinogen and protease-activated receptors in acute xenobiotic-induced cholestatic liver injury.
|
20974703 |
2011 |
Drug-Induced Acute Liver Injury
|
0.300 |
Biomarker
|
disease |
CTD_human |
Role of fibrinogen and protease-activated receptors in acute xenobiotic-induced cholestatic liver injury.
|
20974703 |
2011 |
Chemical and Drug Induced Liver Injury
|
0.300 |
Biomarker
|
disease |
CTD_human |
Role of fibrinogen and protease-activated receptors in acute xenobiotic-induced cholestatic liver injury.
|
20974703 |
2011 |
Chemically-Induced Liver Toxicity
|
0.300 |
Biomarker
|
disease |
CTD_human |
Role of fibrinogen and protease-activated receptors in acute xenobiotic-induced cholestatic liver injury.
|
20974703 |
2011 |
Malignant neoplasm of prostate
|
0.100 |
AlteredExpression
|
disease |
BEFREE |
Par-4 drives trafficking and activation of Fas and Fasl to induce prostate cancer cell apoptosis and tumor regression.
|
11585763 |
2001 |
Malignant neoplasm of prostate
|
0.100 |
Biomarker
|
disease |
BEFREE |
Par-4 but not Bcl-2 was detected in the secretory epithelium of benign prostatic tumors and in primary and metastatic prostate cancers that are apt to undergo apoptosis.
|
9989812 |
1999 |
Malignant neoplasm of prostate
|
0.100 |
Biomarker
|
disease |
BEFREE |
This review discusses salient features of molecules such as, Bcl-2, Bcl-(XL), NF-kappaB, Akt, PTEN and Par-4 that play a significant role in the regulation of prostate cancer and focuses on the prospects of effectively utilizing their potential for the therapy of hormone-sensitive and hormone-resistant prostate cancer.
|
14965337 |
2004 |
Malignant neoplasm of prostate
|
0.100 |
Biomarker
|
disease |
BEFREE |
These results establish the cooperation between Par-4 and PTEN as relevant for the development of prostate cancer and implicate the NF-kappaB pathway as a critical event in prostate tumorigenesis.
|
19470463 |
2009 |
Malignant neoplasm of prostate
|
0.100 |
AlteredExpression
|
disease |
BEFREE |
The primary form of therapy for prostate cancer is androgen ablation resulting in apoptosis and expression of apoptotic genes (i.e. par-4).
|
14767530 |
2004 |
Malignant neoplasm of prostate
|
0.100 |
Biomarker
|
disease |
BEFREE |
AKT inhibition and Par-4 induction suppressed prostate cancer progression in preclinical models.
|
28494348 |
2017 |
Malignant neoplasm of prostate
|
0.100 |
Biomarker
|
disease |
BEFREE |
Par-4 for molecular therapy of prostate cancer.
|
12643472 |
2003 |
Malignant neoplasm of prostate
|
0.100 |
Biomarker
|
disease |
BEFREE |
Par-4 deficiency cooperates with PTEN haploinsufficiency in prostate cancer initiation and progression and their simultaneous inactivation, in addition to enhancing Akt activation, sets in motion a unique mechanism involving the synergistic activation of NFkappaB.
|
19625770 |
2009 |
Malignant neoplasm of prostate
|
0.100 |
Biomarker
|
disease |
BEFREE |
PAR4, the most recently identified PAR member, was reported to be overexpressed during the progression of colon and prostate cancers.
|
21635966 |
2011 |
Malignant neoplasm of prostate
|
0.100 |
Biomarker
|
disease |
BEFREE |
Par-4 inducible apoptosis in prostate cancer cells.
|
14755681 |
2004 |
Prostate carcinoma
|
0.080 |
Biomarker
|
disease |
BEFREE |
This review discusses salient features of molecules such as, Bcl-2, Bcl-(XL), NF-kappaB, Akt, PTEN and Par-4 that play a significant role in the regulation of prostate cancer and focuses on the prospects of effectively utilizing their potential for the therapy of hormone-sensitive and hormone-resistant prostate cancer.
|
14965337 |
2004 |
Prostate carcinoma
|
0.080 |
Biomarker
|
disease |
BEFREE |
Par-4 deficiency cooperates with PTEN haploinsufficiency in prostate cancer initiation and progression and their simultaneous inactivation, in addition to enhancing Akt activation, sets in motion a unique mechanism involving the synergistic activation of NFkappaB.
|
19625770 |
2009 |
Prostate carcinoma
|
0.080 |
AlteredExpression
|
disease |
BEFREE |
Par-4 drives trafficking and activation of Fas and Fasl to induce prostate cancer cell apoptosis and tumor regression.
|
11585763 |
2001 |
Prostate carcinoma
|
0.080 |
Biomarker
|
disease |
BEFREE |
Par-4 for molecular therapy of prostate cancer.
|
12643472 |
2003 |
Prostate carcinoma
|
0.080 |
Biomarker
|
disease |
BEFREE |
AKT inhibition and Par-4 induction suppressed prostate cancer progression in preclinical models.
|
28494348 |
2017 |
Prostate carcinoma
|
0.080 |
Biomarker
|
disease |
BEFREE |
These results establish the cooperation between Par-4 and PTEN as relevant for the development of prostate cancer and implicate the NF-kappaB pathway as a critical event in prostate tumorigenesis.
|
19470463 |
2009 |
Prostate carcinoma
|
0.080 |
AlteredExpression
|
disease |
BEFREE |
The primary form of therapy for prostate cancer is androgen ablation resulting in apoptosis and expression of apoptotic genes (i.e. par-4).
|
14767530 |
2004 |
Prostate carcinoma
|
0.080 |
Biomarker
|
disease |
BEFREE |
Par-4 inducible apoptosis in prostate cancer cells.
|
14755681 |
2004 |