The von Hippel-Lindau tumor-suppressor gene product forms a stable complex with human CUL-2, a member of the Cdc53 family of proteins (Q24564802)

2

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R A Worrell

3

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D Y Chen

4

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W H Burgess

5

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W M Linehan

6

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R D Klausner

Proceedings of the National Academy of Sciences of the United States of America

7

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language of work or name

English

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publication date

18 March 1997

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published in

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volume

94

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issue

6

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page(s)

2156-61

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cites work

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Binding of the von Hippel-Lindau Tumor Suppressor Protein to Elongin B and C

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Inhibition of Transcription Elongation by the VHL Tumor Suppressor Protein

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Characterization of the VHL tumor suppressor gene product: localization, complex formation, and the effect of natural inactivating mutations

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Cdc53p acts in concert with Cdc4p and Cdc34p to control the G1-to-S-phase transition and identifies a conserved family of proteins

24 March 2017

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The B-type cyclin kinase inhibitor p40SIC1 controls the G1 to S transition in S. cerevisiae

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Cdc53 targets phosphorylated G1 cyclins for degradation by the ubiquitin proteolytic pathway

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Allelic deletions of the VHL gene detected in multiple microscopic clear cell renal lesions in von Hippel-Lindau disease patients

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Negative regulation of hypoxia-inducible genes by the von Hippel-Lindau protein

27 September 2017

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Post-transcriptional regulation of vascular endothelial growth factor mRNA by the product of the VHL tumor suppressor gene

27 September 2017

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Golgi dispersal during microtubule disruption: regeneration of Golgi stacks at peripheral endoplasmic reticulum exit sites

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Von Hippel-Lindau disease and sporadic renal cell carcinoma

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Size control: the regulation of cell numbers in animal development

27 September 2017

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Nuclear/cytoplasmic localization of the von Hippel-Lindau tumor suppressor gene product is determined by cell density

27 September 2017

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Molecular cloning of the von Hippel-Lindau tumor suppressor gene and its role in renal carcinoma

27 September 2017

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Frequent somatic mutations and loss of heterozygosity of the von Hippel-Lindau tumor suppressor gene in primary human renal cell carcinomas.

27 September 2017

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Identification of the von Hippel-Lindau (VHL) gene. Its role in renal cancer

27 September 2017

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Stabilization of vascular endothelial growth factor mRNA by hypoxia and hypoglycemia and coregulation with other ischemia-induced genes

27 September 2017

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Cell cycle: cull and destroy

27 September 2017

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Germline mutations in the Von Hippel-Lindau disease (VHL) gene in families from North America, Europe, and Japan

27 September 2017

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Prevalence of microscopic lesions in grossly normal renal parenchyma from patients with von Hippel-Lindau disease, sporadic renal cell carcinoma and no renal disease: clinical implications

30 May 2018

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Interaction of von Hippel-Lindau tumor suppressor gene product with elongin.

30 May 2018

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Post-transcriptional regulation of vascular endothelial growth factor by hypoxia

30 May 2018

1 reference

Crossref

https://api.crossref.org/works/10.1073%2FPNAS.94.6.2156

VHL gene mutation and clear-cell renal carcinomas

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/9122164

12 December 2020

inferred from PubMed ID database lookup

Cellular proteins that bind the von Hippel-Lindau disease gene product: mapping of binding domains and the effect of missense mutations

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/9122164

12 December 2020

inferred from PubMed ID database lookup

Reversion of deregulated expression of vascular endothelial growth factor in human renal carcinoma cells by von Hippel-Lindau tumor suppressor protein

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/9122164

12 December 2020

inferred from PubMed ID database lookup

Identifiers

DOI

10.1073/PNAS.94.6.2156

1 reference

release_usxyxzouujdq7f5vyh63qsjtzi

0 references

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/usxyxzouujdq7f5vyh63qsjtzi

24 November 2022

mapped directly with Wikidata item

1424979

1 reference

1 reference

1424979

PubMed publication ID

9122164

1 reference