Retinal Diseases
|
0.010 |
PosttranslationalModification
|
group |
BEFREE |
PF4 antagonizes retinal neovascularization via inhibiting PRAS40 phosphorylation in a mouse model of oxygen-induced retinopathy.
|
31740404 |
2020 |
Arteriosclerosis
|
0.010 |
Biomarker
|
disease |
BEFREE |
Indeed, we previously found PRAS40 gene therapy to improve metabolic profile; however, its function in endothelial cells and its role in atherosclerosis remain unknown.
|
31728028 |
2019 |
Atherosclerosis
|
0.010 |
Biomarker
|
disease |
BEFREE |
Indeed, we previously found PRAS40 gene therapy to improve metabolic profile; however, its function in endothelial cells and its role in atherosclerosis remain unknown.
|
31728028 |
2019 |
Malignant neoplasm of gallbladder
|
0.010 |
Biomarker
|
disease |
BEFREE |
This study also elucidates phospho-PRAS40 as a clinical marker in GBC and the role of PIM1 as a therapeutic target in GBC.
|
30666556 |
2019 |
Gallbladder Carcinoma
|
0.010 |
Biomarker
|
disease |
BEFREE |
This study also elucidates phospho-PRAS40 as a clinical marker in GBC and the role of PIM1 as a therapeutic target in GBC.
|
30666556 |
2019 |
Gallbladder adenocarcinoma
|
0.010 |
Biomarker
|
disease |
BEFREE |
Tissue microarray-based immunohistochemical labeling of phospho-PRAS40 (T246) revealed moderate to strong staining in 77% of the primary gallbladder adenocarcinoma cases.
|
30666556 |
2019 |
Malignant neoplasm of prostate
|
0.010 |
Biomarker
|
disease |
BEFREE |
Importantly, inhibiting the BLM-AKT-PRAS40 axis induced PC cell apoptosis.
|
31210839 |
2019 |
Prostate carcinoma
|
0.010 |
Biomarker
|
disease |
BEFREE |
Importantly, inhibiting the BLM-AKT-PRAS40 axis induced PC cell apoptosis.
|
31210839 |
2019 |
Hurthle Cell Tumor
|
0.010 |
Biomarker
|
disease |
BEFREE |
These results suggest that 14-3-3η may be involved in promoting tumorigenesis in pituitary oncocytoma by interacting with PRAS40 (T246) via the mTOR signaling pathway.
|
31849836 |
2019 |
Oncocytic Neoplasm
|
0.010 |
Biomarker
|
disease |
BEFREE |
These results suggest that 14-3-3η may be involved in promoting tumorigenesis in pituitary oncocytoma by interacting with PRAS40 (T246) via the mTOR signaling pathway.
|
31849836 |
2019 |
Oxyphilic Adenoma
|
0.010 |
Biomarker
|
disease |
BEFREE |
These results suggest that 14-3-3η may be involved in promoting tumorigenesis in pituitary oncocytoma by interacting with PRAS40 (T246) via the mTOR signaling pathway.
|
31849836 |
2019 |
Idiopathic pulmonary arterial hypertension
|
0.010 |
Biomarker
|
disease |
BEFREE |
The phosphorylation of Akt<sup>T308</sup>, proline-rich Akt1 substrate 1 (PRAS40) and S6KT<sup>229</sup> was also notably increased in the PAH model compared with the control.
|
31281449 |
2019 |
Neointimal hyperplasia
|
0.010 |
Biomarker
|
disease |
BEFREE |
In an in vivo model of atherogenic remodeling, mice with induced endothelium-specific PRAS40 deficiency showed enhanced endothelial pro-inflammatory activation as well as increased neointimal hyperplasia and atherosclerotic lesion formation.
|
31728028 |
2019 |
Squamous non-small cell lung cancer
|
0.010 |
Biomarker
|
disease |
BEFREE |
Decrease in phospho-PRAS40 plays a role in the synergy between erlotinib and crizotinib in an EGFR and cMET wild-type squamous non-small cell lung cancer cell line.
|
31078602 |
2019 |
Stage 0 Gallbladder Cancer AJCC v8
|
0.010 |
Biomarker
|
disease |
BEFREE |
This study also elucidates phospho-PRAS40 as a clinical marker in GBC and the role of PIM1 as a therapeutic target in GBC.
|
30666556 |
2019 |
Stage IIA Gallbladder Cancer AJCC v8
|
0.010 |
Biomarker
|
disease |
BEFREE |
This study also elucidates phospho-PRAS40 as a clinical marker in GBC and the role of PIM1 as a therapeutic target in GBC.
|
30666556 |
2019 |
Stage IIB Gallbladder Cancer AJCC v8
|
0.010 |
Biomarker
|
disease |
BEFREE |
This study also elucidates phospho-PRAS40 as a clinical marker in GBC and the role of PIM1 as a therapeutic target in GBC.
|
30666556 |
2019 |
Stage III Gallbladder Cancer AJCC v8
|
0.010 |
Biomarker
|
disease |
BEFREE |
This study also elucidates phospho-PRAS40 as a clinical marker in GBC and the role of PIM1 as a therapeutic target in GBC.
|
30666556 |
2019 |
Stage IV Gallbladder Cancer AJCC v8
|
0.010 |
Biomarker
|
disease |
BEFREE |
This study also elucidates phospho-PRAS40 as a clinical marker in GBC and the role of PIM1 as a therapeutic target in GBC.
|
30666556 |
2019 |
Atherosclerotic lesion
|
0.010 |
Biomarker
|
disease |
BEFREE |
In an in vivo model of atherogenic remodeling, mice with induced endothelium-specific PRAS40 deficiency showed enhanced endothelial pro-inflammatory activation as well as increased neointimal hyperplasia and atherosclerotic lesion formation.
|
31728028 |
2019 |
Glioblastoma
|
0.010 |
PosttranslationalModification
|
disease |
BEFREE |
In this retrospective analysis of treatment-naïve samples of the OSAG 101-BSA-05 trial cohort, we identify the EGFR signaling activity markers phosphorylated PRAS40 and phosphorylated ribosomal protein S6 as predictive markers for treatment efficacy of the EGFR-blocking antibody nimotuzumab in MGMT promoter unmethylated GBs.
|
30129426 |
2018 |
Adult Glioblastoma
|
0.010 |
PosttranslationalModification
|
disease |
BEFREE |
In this retrospective analysis of treatment-naïve samples of the OSAG 101-BSA-05 trial cohort, we identify the EGFR signaling activity markers phosphorylated PRAS40 and phosphorylated ribosomal protein S6 as predictive markers for treatment efficacy of the EGFR-blocking antibody nimotuzumab in MGMT promoter unmethylated GBs.
|
30129426 |
2018 |
Squamous cell carcinoma of esophagus
|
0.010 |
Biomarker
|
disease |
BEFREE |
Down-regulation of Rictor enhances cell sensitivity to PI3K inhibitor LY294002 by blocking mTORC2-medicated phosphorylation of Akt/PRAS40 in esophageal squamous cell carcinoma.
|
30119206 |
2018 |
Childhood Glioblastoma
|
0.010 |
PosttranslationalModification
|
disease |
BEFREE |
In this retrospective analysis of treatment-naïve samples of the OSAG 101-BSA-05 trial cohort, we identify the EGFR signaling activity markers phosphorylated PRAS40 and phosphorylated ribosomal protein S6 as predictive markers for treatment efficacy of the EGFR-blocking antibody nimotuzumab in MGMT promoter unmethylated GBs.
|
30129426 |
2018 |
Glioblastoma Multiforme
|
0.010 |
PosttranslationalModification
|
disease |
BEFREE |
In this retrospective analysis of treatment-naïve samples of the OSAG 101-BSA-05 trial cohort, we identify the EGFR signaling activity markers phosphorylated PRAS40 and phosphorylated ribosomal protein S6 as predictive markers for treatment efficacy of the EGFR-blocking antibody nimotuzumab in MGMT promoter unmethylated GBs.
|
30129426 |
2018 |