Endemic Polycythemia in Russia: Mutation in the VHL Gene
- 1 January 2002
- journal article
- Published by Elsevier in Blood Cells, Molecules, and Diseases
- Vol. 28 (1), 57-62
- https://doi.org/10.1006/bcmd.2002.0488
Abstract
No abstract availableKeywords
This publication has 8 references indexed in Scilit:
- C. elegans EGL-9 and Mammalian Homologs Define a Family of Dioxygenases that Regulate HIF by Prolyl HydroxylationCell, 2001
- HIFα Targeted for VHL-Mediated Destruction by Proline Hydroxylation: Implications for O 2 SensingScience, 2001
- Targeting of HIF-α to the von Hippel-Lindau Ubiquitylation Complex by O 2 -Regulated Prolyl HydroxylationScience, 2001
- Pathogenetic mechanisms of polycythemia vera and congenital polycythemic disordersSeminars in Hematology, 2001
- Expression of hypoxia-inducible factor 1: mechanisms and consequencesBiochemical Pharmacology, 1999
- Localization of the Gene Responsible for Familial Benign Polycythemia to Chromosome 11q23Human Heredity, 1999
- The tumour suppressor protein VHL targets hypoxia-inducible factors for oxygen-dependent proteolysisNature, 1999
- Avoiding Recomputation in Linkage AnalysisHuman Heredity, 1994