Von Hippel-Lindau Syndrome
|
0.020 |
Biomarker
|
disease |
BEFREE |
We obtained several possible cellular partners including VBP1, a binding factor for VHL tumor suppressor protein.
|
18315953 |
2008 |
Von Hippel-Lindau Syndrome
|
0.020 |
AlteredExpression
|
disease |
BEFREE |
Identification of a novel protein (VBP-1) binding to the von Hippel-Lindau (VHL) tumor suppressor gene product.
|
8674032 |
1996 |
Malignant Neoplasms
|
0.010 |
Biomarker
|
group |
BEFREE |
VBP1 represses cancer metastasis by enhancing HIF-1α degradation induced by pVHL.
|
29121446 |
2018 |
Neoplasm Metastasis
|
0.010 |
Biomarker
|
phenotype |
BEFREE |
Furthermore, VBP1 suppresses HIF-1α-induced epithelial-mesenchymal transition in vitro and tumor metastasis in vivo.
|
29121446 |
2018 |
Primary malignant neoplasm
|
0.010 |
Biomarker
|
group |
BEFREE |
VBP1 represses cancer metastasis by enhancing HIF-1α degradation induced by pVHL.
|
29121446 |
2018 |
Secondary Neoplasm
|
0.010 |
Biomarker
|
group |
BEFREE |
Furthermore, VBP1 suppresses HIF-1α-induced epithelial-mesenchymal transition in vitro and tumor metastasis in vivo.
|
29121446 |
2018 |
Hepatitis B
|
0.010 |
AlteredExpression
|
disease |
BEFREE |
Hepatitis B virus X protein enhances NFkappaB activity through cooperating with VBP1.
|
18315953 |
2008 |
Liver carcinoma
|
0.010 |
Biomarker
|
disease |
BEFREE |
These results implicate the important role of HBx in the development of hepatocellular carcinoma through its interaction with VBP1.
|
18315953 |
2008 |
Myeloproliferative disease
|
0.010 |
Biomarker
|
group |
LHGDN |
Molecular pathogenesis of Philadelphia chromosome negative myeloproliferative disorders.
|
15572213 |
2005 |
Renal Cell Carcinoma
|
0.010 |
Biomarker
|
disease |
LHGDN |
Parathyroid hormone-related protein is an essential growth factor for human clear cell renal carcinoma and a target for the von Hippel-Lindau tumor suppressor gene.
|
14729622 |
2004 |
Pheochromocytoma
|
0.010 |
AlteredExpression
|
disease |
BEFREE |
Moreover, expression of the human VBP1 gene was investigated in cerebellum and in various tumours of VHL patients encompassinghaemangioblastomas, renal cell carcinomas and pheochromocytomas.
|
9931330 |
1999 |
Conventional (Clear Cell) Renal Cell Carcinoma
|
0.010 |
GeneticVariation
|
disease |
BEFREE |
We have investigated the possible roles of CUL2 and VBP1 in renal tumorigenesis by analyzing sporadic RCC of known VHL mutation or hypermethylation status, including CC-RCC without VHL inactivation (n = 40); CC-RCC with VHL inactivation (n = 35); and non-CC-RCC (n = 14).
|
10441001 |
1999 |
Carcinogenesis
|
0.010 |
Biomarker
|
phenotype |
BEFREE |
We have investigated the possible roles of CUL2 and VBP1 in renal tumorigenesis by analyzing sporadic RCC of known VHL mutation or hypermethylation status, including CC-RCC without VHL inactivation (n = 40); CC-RCC with VHL inactivation (n = 35); and non-CC-RCC (n = 14).
|
10441001 |
1999 |
Adrenal Gland Pheochromocytoma
|
0.010 |
AlteredExpression
|
disease |
BEFREE |
Moreover, expression of the human VBP1 gene was investigated in cerebellum and in various tumours of VHL patients encompassinghaemangioblastomas, renal cell carcinomas and pheochromocytomas.
|
9931330 |
1999 |
Neoplasms
|
0.010 |
AlteredExpression
|
group |
BEFREE |
Identification of a novel protein (VBP-1) binding to the von Hippel-Lindau (VHL) tumor suppressor gene product.
|
8674032 |
1996 |