Von Hippel-Lindau Syndrome
|
0.010 |
Biomarker
|
disease |
BEFREE |
We determined the role of the VHL tumor suppressor gene in the regulation of the uPA system in RCC.
|
10485495 |
1999 |
Ventricular Fibrillation
|
0.300 |
Biomarker
|
disease |
CTD_human |
Ventricular fibrillation after intrapleural urokinase.
|
9083243 |
1997 |
Venous Thrombosis
|
0.300 |
Therapeutic
|
phenotype |
CTD_human |
Thrombolytic therapy in heparin-associated thrombocytopenia with thrombosis.
|
3488869 |
1986 |
Venous Thrombosis
|
0.300 |
Therapeutic
|
phenotype |
CTD_human |
Clinical and economic outcomes in thrombolytic treatment of peripheral arterial occlusive disease and deep venous thrombosis.
|
15557913 |
2004 |
Venous Thrombosis
|
0.300 |
Therapeutic
|
phenotype |
CTD_human |
Fibrinogenolysis and fibrinolysis in normal volunteers and patients with thrombosis after infusion of urokinase.
|
3161212 |
1985 |
Venous Thrombosis
|
0.300 |
Therapeutic
|
phenotype |
CTD_human |
Controlled multicenter pilot study of urokinase- heparin and streptokinase in deep vein thrombosis.
|
6359570 |
1983 |
Vasogenic Cerebral Edema
|
0.300 |
Biomarker
|
phenotype |
CTD_human |
Massive cerebral edema after recanalization post-thrombolysis.
|
11677890 |
2001 |
Vasogenic Brain Edema
|
0.300 |
Biomarker
|
phenotype |
CTD_human |
Massive cerebral edema after recanalization post-thrombolysis.
|
11677890 |
2001 |
Vasculitis, Hemorrhagic
|
0.300 |
Therapeutic
|
phenotype |
CTD_human |
Pathological improvement of IgA nephropathy and Henoch-Schönlein purpura nephritis with urokinase therapy.
|
9002298 |
1996 |
Vasculitis, Hemorrhagic
|
0.300 |
Therapeutic
|
phenotype |
CTD_human |
Efficacy of methylprednisolone and urokinase pulse therapy for severe Henoch-Schönlein nephritis.
|
12671112 |
2003 |
Vascular occlusion
|
0.010 |
Biomarker
|
disease |
BEFREE |
Whether high concentrations of t-PA, u-PA and PAI 1 antigen can predict future vascular occlusion in children with APCR requires a more extensive multicentre study.
|
9083758 |
1997 |
Vascular Diseases
|
0.010 |
AlteredExpression
|
group |
BEFREE |
In SSc, the downregulation of miR-193b induces the expression of uPA, which increases the number of vascular smooth muscle cells in an uPAR-independent manner and thereby contributes to the proliferative vasculopathy with intimal hyperplasia characteristic for SSc.
|
25384965 |
2016 |
Usual Interstitial Pneumonia
|
0.300 |
Therapeutic
|
disease |
CTD_human |
The role of urokinase in idiopathic pulmonary fibrosis and implication for therapy.
|
18491991 |
2008 |
Urinary tract infection
|
0.010 |
AlteredExpression
|
group |
BEFREE |
These data suggest that UTI significantly down-regulates tumor cell uPA mRNA expression and protein secretion, and that UTI binding to the cells is necessary to exert the UTI's action.
|
11018722 |
2000 |
Unipolar Depression
|
0.010 |
GeneticVariation
|
disease |
BEFREE |
Depression and fatigue during chronic IFN-α administration were associated with alterations in the expression (OAS2) and transcriptional control (CREB/ATF) of genes linked to behavioral disorders including CFS and major depression, further supporting an immune contribution to these diseases.
|
22152193 |
2012 |
Ulcerative Colitis
|
0.100 |
GeneticVariation
|
disease |
GWASCAT |
Analysis of five chronic inflammatory diseases identifies 27 new associations and highlights disease-specific patterns at shared loci.
|
26974007 |
2016 |
Tumor-Associated Vasculature
|
0.010 |
Biomarker
|
disease |
BEFREE |
A bispecific immunotoxin (IT) called DTAT13 was synthesized in order to target simultaneously the urokinase-type plasminogen activator receptor (uPAR)-expressing tumor neovasculature and IL-13 receptor expressing glioblastoma cells with the goal of intratumoral administration for brain tumors.
|
15047912 |
2004 |
tumor vasculature
|
0.010 |
Biomarker
|
phenotype |
BEFREE |
MV-m-uPA targeted murine tumor vasculature after systemic administration, as shown by dual (CD31 and MV-N) staining of tumor capillaries in the MDA-MB-231 model.
|
19208845 |
2009 |
Tumor Progression
|
0.100 |
Biomarker
|
phenotype |
BEFREE |
Urokinase-type plasminogen activator (uPA) is a serine protease that is involved in cancer progression, especially invasion and metastasis including prostate cancer. uPA activation is mediated by transactivation of uPAR and epidermal growth factor receptor (EGF-R) in prostate cancer progression.
|
21308698 |
2011 |
Tumor Progression
|
0.100 |
Biomarker
|
phenotype |
BEFREE |
A large body of evidence support that among the various components of the PA system, urokinase-type plasminogen activator (uPA), its receptor (uPAR), and plasminogen activator inhibitor-1 and -2 (PAI-1 and PAI-2) play a major role in tumor progression and metastasis.
|
29484286 |
2018 |
Tumor Progression
|
0.100 |
Biomarker
|
phenotype |
BEFREE |
Urokinase-type plasminogen activator (u-PA) contributes to tumor progression in prostate cancer (CaP).
|
11676474 |
2001 |
Tumor Progression
|
0.100 |
Biomarker
|
phenotype |
BEFREE |
Only full length uPAR mediates tumor progression.
|
25003596 |
2014 |
Tumor Progression
|
0.100 |
AlteredExpression
|
phenotype |
BEFREE |
Although, uPA is dysregulate in tumor progression, its expression is finely regulated at both enzymatic activity and at protein expression as well, which allow cancer cells efficiently survive, proliferate, and spread into neighbouring tissues and distant organs.
|
28820062 |
2017 |
Tumor Progression
|
0.100 |
Biomarker
|
phenotype |
BEFREE |
Urokinase-type plasminogen activator (uPA) is a serine protease that is causally involved in cancer progression, especially invasion and metastasis.
|
12023852 |
2002 |
Tumor Progression
|
0.100 |
Biomarker
|
phenotype |
BEFREE |
Cancer invasion and metastasis are highly complex processes and a serine protease urokinase-type plasminogen activator/urokinase-type plasminogen activator receptor system has been postulated to play a central role in the mediation of cancer progression.
|
17075310 |
2006 |