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Journal Abstract Search
210 related items for PubMed ID: 8598197
1. Role of the duplicated CCAAT box region in gamma-globin gene regulation and hereditary persistence of fetal haemoglobin. Ronchi A, Berry M, Raguz S, Imam A, Yannoutsos N, Ottolenghi S, Grosveld F, Dillon N. EMBO J; 1996 Jan 02; 15(1):143-9. PubMed ID: 8598197 [Abstract] [Full Text] [Related]
2. A single point mutation is the cause of the Greek form of hereditary persistence of fetal haemoglobin. Berry M, Grosveld F, Dillon N. Nature; 1992 Aug 06; 358(6386):499-502. PubMed ID: 1379347 [Abstract] [Full Text] [Related]
3. Regulation of embryonic/fetal globin genes by nuclear hormone receptors: a novel perspective on hemoglobin switching. Filipe A, Li Q, Deveaux S, Godin I, Roméo PH, Stamatoyannopoulos G, Mignotte V. EMBO J; 1999 Feb 01; 18(3):687-97. PubMed ID: 9927428 [Abstract] [Full Text] [Related]
4. Increased gamma-globin expression in a nondeletion HPFH mediated by an erythroid-specific DNA-binding factor. Martin DI, Tsai SF, Orkin SH. Nature; 1989 Mar 30; 338(6214):435-8. PubMed ID: 2467208 [Abstract] [Full Text] [Related]
6. DNA-protein interactions in the proximal zeta-globin promoter: identification of novel CCACCC- and CCAAT-binding proteins. Sabath DE, Koehler KM, Yang WQ, Phan V, Wilson J. Blood Cells Mol Dis; 1998 Jun 30; 24(2):183-98. PubMed ID: 9642099 [Abstract] [Full Text] [Related]
8. HMG-I binds to GATA motifs: implications for an HPFH syndrome. Magis W, Martin DI. Biochem Biophys Res Commun; 1995 Sep 25; 214(3):927-33. PubMed ID: 7575565 [Abstract] [Full Text] [Related]
9. An erythroid-specific DNA binding factor mediates increased gamma-globin expression in hereditary persistence of fetal hemoglobin (HPFH). Martin DI, Orkin SH. Prog Clin Biol Res; 1989 Sep 25; 316A():217-28. PubMed ID: 2480608 [No Abstract] [Full Text] [Related]
13. Human fetal-to-adult globin gene switching in transgenic mice: persistent expression of the G gamma-globin gene in the Japanese HPFH. Katsube T, Tojo H, Sakaguchi T, Fukumaki Y. Biochem Biophys Res Commun; 1993 Jul 15; 194(1):246-52. PubMed ID: 7687430 [Abstract] [Full Text] [Related]