An Important von Hippel-Lindau Tumor Suppressor Domain Mediates Sp1-Binding and Self-Association
Open Access
- 1 December 1999
- journal article
- Published by Elsevier in Biochemical and Biophysical Research Communications
- Vol. 266 (1) , 43-50
- https://doi.org/10.1006/bbrc.1999.1767
Abstract
No abstract availableKeywords
This publication has 25 references indexed in Scilit:
- Structure of the VHL-ElonginC-ElonginB Complex: Implications for VHL Tumor Suppressor FunctionScience, 1999
- Sp1 Is a Critical Regulator of the Wilms' tumor-1 GenePublished by Elsevier ,1997
- Cdc53 Targets Phosphorylated G1 Cyclins for Degradation by the Ubiquitin Proteolytic PathwayCell, 1996
- Cloning of the Rat Homologue of the von Hippel-Lindau Tumor Suppressor Gene and Its Non-somatic Mutation in Rat Renal Cell CarcinomasJapanese Journal of Cancer Research, 1995
- Tumour suppression by the human von Hippel-Lindau gene productNature Medicine, 1995
- Germline mutations in the von Hippel-Lindau disease tumor suppressor gene: Correlations with phenotypeHuman Mutation, 1995
- Somatic mutations of the von Hippel — Lindau disease tumour suppressor gene in non-familial clear cell renal carcinomaHuman Molecular Genetics, 1994
- Identification of intragenic mutations in the Von Hippel — Lindau disease tumour suppressor gene andcorrelation with disease phenotypeHuman Molecular Genetics, 1994
- Mutations of the VHL tumour suppressor gene in renal carcinomaNature Genetics, 1994
- Identification of the von Hippel-Lindau Disease Tumor Suppressor GeneScience, 1993