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Journal Abstract Search

249 related items for PubMed ID: 1699206

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  • 27. Sequences located 3' to the breakpoint of the hereditary persistence of fetal hemoglobin-3 deletion exhibit enhancer activity and can modify the developmental expression of the human fetal A gamma-globin gene in transgenic mice.
    Anagnou NP, Perez-Stable C, Gelinas R, Costantini F, Liapaki K, Constantopoulou M, Kosteas T, Moschonas NK, Stamatoyannopoulos G.
    J Biol Chem; 1995 Apr 28; 270(17):10256-63. PubMed ID: 7537267
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  • 30. The Australian type of nondeletional G gamma-HPFH has a C-->G substitution at nucleotide -114 of the G gamma gene.
    Motum PI, Deng ZM, Huong L, Trent RJ.
    Br J Haematol; 1994 Jan 28; 86(1):219-21. PubMed ID: 7516698
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  • 31. A fetal globin gene mutation in A gamma nondeletion hereditary persistence of fetal hemoglobin increases promoter strength in a nonerythroid cell.
    Rixon MW, Gelinas RE.
    Mol Cell Biol; 1988 Feb 28; 8(2):713-21. PubMed ID: 2451123
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  • 32. An embryonic/fetal beta-type globin gene repressor contains a nuclear receptor TR2/TR4 heterodimer.
    Tanabe O, Katsuoka F, Campbell AD, Song W, Yamamoto M, Tanimoto K, Engel JD.
    EMBO J; 2002 Jul 01; 21(13):3434-42. PubMed ID: 12093744
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  • 33. Sardinian G gamma-HPFH: a T----C substitution in a conserved "octamer" sequence in the G gamma-globin promoter.
    Ottolenghi S, Nicolis S, Taramelli R, Malgaretti N, Mantovani R, Comi P, Giglioni B, Longinotti M, Dore F, Oggiano L.
    Blood; 1988 Mar 01; 71(3):815-7. PubMed ID: 2449927
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  • 34. A role for the distal CCAAT box of the gamma-globin gene in Hb switching.
    Katsube T, Fukumaki Y.
    J Biochem; 1995 Jan 01; 117(1):68-76. PubMed ID: 7539789
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  • 35. Developmental regulation of human gamma- and beta-globin genes in the absence of the locus control region.
    Starck J, Sarkar R, Romana M, Bhargava A, Scarpa AL, Tanaka M, Chamberlain JW, Weissman SM, Forget BG.
    Blood; 1994 Sep 01; 84(5):1656-65. PubMed ID: 7520781
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  • 36. Sequence analysis of the gamma-globin gene locus from a patient with the deletion form of hereditary persistence of fetal hemoglobin.
    Stolle CA, Penny LA, Ivory S, Forget BG, Benz EJ.
    Blood; 1990 Jan 15; 75(2):499-504. PubMed ID: 1688505
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  • 37. Factor binding to the human gamma-globin gene distal CCAAT site: candidates for repression of the normal gene or activation of HPFH mutants.
    Partington GA, Patient RK.
    Br J Haematol; 1998 Sep 15; 102(4):940-51. PubMed ID: 9734644
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  • 38. The upstream region of the human gamma-globin gene promoter. Identification and functional analysis of nuclear protein binding sites.
    McDonagh KT, Lin HJ, Lowrey CH, Bodine DM, Nienhuis AW.
    J Biol Chem; 1991 Jun 25; 266(18):11965-74. PubMed ID: 2050690
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  • 39. High levels of human gamma-globin gene expression in adult mice carrying a transgene of deletion-type hereditary persistence of fetal hemoglobin.
    Arcasoy MO, Romana M, Fabry ME, Skarpidi E, Nagel RL, Forget BG.
    Mol Cell Biol; 1997 Apr 25; 17(4):2076-89. PubMed ID: 9121456
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  • 40. The molecular basis of HPFH in a British family identified by heteroduplex formation.
    Craig JE, Sheerin SM, Barnetson R, Thein SL.
    Br J Haematol; 1993 May 25; 84(1):106-10. PubMed ID: 7687855
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