VHLdb
A database of interactors and mutations of the human von Hippel-Lindau tumor suppressor protein (pVHL).
Description
More detailed information about this field from each metasource.
A database of interactors and mutations of the human von Hippel-Lindau tumor suppressor protein (pVHL).
metasource: bio.toolsversion: extracted_at: 2022-11-04T11:30:57.096017
Webpage:
http://vhldb.bio.unipd.it/Webpage
More detailed information about this field from each metasource.
Publications:
Publications
More detailed information about this field from each metasource.
VHLdb: A database of von Hippel-Lindau protein interactors and mutations
PMID: 27511743
metasource: bio.tools
version: extracted_at: 2022-11-04T11:30:57.096017
Publications
More detailed information about this field from each metasource.
VHLdb: A database of von Hippel-Lindau protein interactors and mutations
PMID: 27511743
metasource: bio.tools
version: extracted_at: 2022-11-04T11:30:57.096017
-
VHLdb: A database of von Hippel-Lindau protein interactors and mutations
PubMed citations: 16.
16 articles citing: VHLdb: A database of von Hippel-Lindau protein interactors and mutations
Characterization of the pVHL Interactome in Human Testis Using High-Throughput Library Screening. PMID:35205757
The Role of VHL in the Development of von Hippel-Lindau Disease and Erythrocytosis. PMID:35205407
Evaluation of tumour surveillance protocols and outcomes in von Hippel-Lindau disease in a national health service. PMID:35184155
Identification of a VHL gene mutation in atypical Von Hippel-Lindau syndrome: genotype-phenotype correlation and gene therapy perspective. PMID:34923986
Central Nervous System Hemangioblastoma in a Pediatric Patient Associated With Von Hippel-Lindau Disease: A Case Report and Literature Review. PMID:34109129
Algorithmic assessment of missense mutation severity in the Von-Hippel Lindau protein. PMID:33151962
The E3 ubiquitin-protein ligase MDM2 is a novel interactor of the von Hippel-Lindau tumor suppressor. PMID:32985545
The pVHL neglected functions, a tale of hypoxia-dependent and -independent regulations in cancer. PMID:32603638
Assessing predictors for new post translational modification sites: A case study on hydroxylation. PMID:32569263
Von Hippel-Lindau: implications in development and disease-response. PMID:32175434
von Hippel-Lindau Syndrome: Genetic Study of Case With a Rare Pathogenic Variant With Optic Nerve Hemangioblastoma, a Rare Phenotypic Expression. PMID:32117777
Genotype-phenotype relations of the von Hippel-Lindau tumor suppressor inferred from a large-scale analysis of disease mutations and interactors. PMID:30943211
von Hippel-Lindau mutants in renal cell carcinoma are regulated by increased expression of RSUME. PMID:30890701
Arginine refolds, stabilizes, and restores function of mutant pVHL proteins in animal model of the VHL cancer syndrome. PMID:30194449
Performance of in silico tools for the evaluation of p16INK4a (CDKN2A) variants in CAGI. PMID:28440912
Novel interactions of the von Hippel-Lindau (pVHL) tumor suppressor with the CDKN1 family of cell cycle inhibitors. PMID:28425505
Tags:
Tags
More detailed information about this field from each metasource.
protein structure analysis
metasource: bio.tools
version: extracted_at: 2022-11-04T11:30:57.096017
protein interactions
metasource: bio.tools
version: extracted_at: 2022-11-04T11:30:57.096017
rare diseases
metasource: bio.tools
version: extracted_at: 2022-11-04T11:30:57.096017
Tags
More detailed information about this field from each metasource.
protein structure analysis
metasource: bio.toolsversion: extracted_at: 2022-11-04T11:30:57.096017
protein interactions
metasource: bio.toolsversion: extracted_at: 2022-11-04T11:30:57.096017
rare diseases
metasource: bio.toolsversion: extracted_at: 2022-11-04T11:30:57.096017
protein structure analysis protein interaction rare diseases
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