The HIF2A gene in familial erythrocytosis

New England Journal of Medicine

Volumn 358, Issue 18, 2008, Pages 1966-1967

  Percy, Melanie J ^a   Lucas, Guy S ^b   Lee, Frank S ^c  

^a BELFAST CITY HOSPITAL   (United Kingdom)

^b MANCHESTER ROYAL INFIRMARY   (United Kingdom)

^c UNIVERSITY OF PENNSYLVANIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ERYTHROPOIETIN; HYPOXIA INDUCIBLE FACTOR 1BETA; HYPOXIA INDUCIBLE FACTOR 2ALPHA; HYPOXIA INDUCIBLE FACTOR 1ALPHA;

ANEMIA; DEEP VEIN THROMBOSIS; DNA MODIFICATION; ERYTHROCYTOSIS; ERYTHROPOIESIS; FAMILIAL DISEASE; FAMILY ASSESSMENT; GENE CONTROL; GENE DELETION; GENE FUNCTION; LETTER; NONHUMAN; PRIORITY JOURNAL; PROTEIN VARIANT; GENE EXPRESSION REGULATION; GENE MUTATION; KIDNEY; LIVER; MUTATIONAL ANALYSIS; PROTEIN DEGRADATION;

EID: 42949154362     PISSN: 00284793     EISSN: 15334406     Source Type: Journal    
DOI: None     Document Type: Letter

References (3)

1. Rankin EB, Biju MP, Liu Q, et al. Hypoxia-inducible factor-2 (HIF-2) regulates hepatic erythropoietin in vivo. J Clin Invest 2007;117:1068-77.
2. Gruber M, Hu CJ, Johnson RS, Brown EJ, Keith B, Simon MC. Acute postnatal ablation of Hif-2α results in anemia. Proc Natl Acad Sci U S A 2007;104:2301-6.
3. Percy MJ, Mooney SM, McMullin MF, Flores A, Lappin TR, Lee FS. A common polymorphism in the oxygen-dependent degradation (ODD) domain of hypoxia inducible factor-1alpha (HIF-1α) does not impair Pro-564 hydroxylation. Mol Cancer 2003;2:31.