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PUBMED FOR HANDHELDS

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
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  • 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
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  • 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
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  • 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
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  • 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
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  • 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
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  • 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
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  • 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
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