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Published in 2025 at "Molecular Biology Reports"
DOI: 10.1007/s11033-025-10272-1
Abstract: von Hippel-Lindau (VHL) hereditary cancer syndrome is caused by mutations in the VHL tumor suppressor gene and is characterized by a predisposition to form various types of tumors, including renal cell carcinomas, hemangioblastomas, and pheochromocytomas.…
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Keywords:
protein kinase;
degradation;
renal carcinoma;
pkc ... See more keywords
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Published in 2020 at "Open Biology"
DOI: 10.1098/rsob.200109
Abstract: The von Hippel–Lindau protein (pVHL) is a tumour suppressor mainly known for its role as master regulator of hypoxia-inducible factor (HIF) activity. Functional inactivation of pVHL is causative of the von Hippel–Lindau disease, an inherited…
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Keywords:
pvhl;
dependent independent;
neglected functions;
pvhl neglected ... See more keywords
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Published in 2025 at "Science Advances"
DOI: 10.1126/sciadv.adt8800
Abstract: BRCA1-associated protein 1 (BAP1) can function as a tumor suppressor or oncogene depending on context, but its role in colorectal cancer (CRC) is not well understood. Here, we demonstrate that BAP1 suppresses CRC progression primarily…
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Keywords:
bap1;
ufmylation;
tumor suppressor;
tumor ... See more keywords
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Published in 2020 at "PLoS Genetics"
DOI: 10.1371/journal.pgen.1009183
Abstract: Loss of von Hippel-Lindau protein pVHL function promotes VHL diseases, including sporadic and inherited clear cell Renal Cell Carcinoma (ccRCC). Mechanisms controlling pVHL function and regulation, including folding and stability, remain elusive. Here, we have…
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Keywords:
protein;
pvhl;
prefoldin complex;
hippel lindau ... See more keywords