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Journal Abstract Search

469 related items for PubMed ID: 9668525

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  • 3. G gamma A gamma (beta+) hereditary persistence of fetal hemoglobin: the G gamma -158 C-->T mutation in cis to the -175 T-->C mutation of the A gamma-globin gene results in increased G gamma-globin synthesis.
    Coleman MB, Adams JG, Steinberg MH, Plonczynski MW, Harrell AH, Castro O, Winter WP.
    Am J Hematol; 1993 Feb; 42(2):186-90. PubMed ID: 7679879
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  • 4. Greek (A gamma) variant of hereditary persistence of fetal haemoglobin: globin gene organization and studies of expression of fetal haemoglobins in clonal erythroid cultures.
    Papayannopoulou T, Lawn RM, Stamatoyannopoulos G, Maniatis T.
    Br J Haematol; 1982 Mar; 50(3):387-99. PubMed ID: 6175332
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  • 5. A point mutation in the A gamma-globin gene promoter in Greek hereditary persistence of fetal haemoglobin.
    Collins FS, Metherall JE, Yamakawa M, Pan J, Weissman SM, Forget BG.
    Nature; 1982 Mar; 313(6000):325-6. PubMed ID: 2578620
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  • 12. The breakpoint of a large deletion causing hereditary persistence of fetal hemoglobin occurs within an erythroid DNA domain remote from the beta-globin gene cluster.
    Feingold EA, Forget BG.
    Blood; 1989 Nov 01; 74(6):2178-86. PubMed ID: 2478223
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  • 13. 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 01; 17(4):2076-89. PubMed ID: 9121456
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  • 14. Molecular mechanism of high hemoglobin F production in Southeast Asian-type hereditary persistence of fetal hemoglobin.
    Changsri K, Akkarapathumwong V, Jamsai D, Winichagoon P, Fucharoen S.
    Int J Hematol; 2006 Apr 01; 83(3):229-37. PubMed ID: 16720553
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  • 15. The deletion of the distal CCAAT box region of the A gamma-globin gene in black HPFH abolishes the binding of the erythroid specific protein NFE3 and of the CCAAT displacement protein.
    Mantovani R, Superti-Furga G, Gilman J, Ottolenghi S.
    Nucleic Acids Res; 1989 Aug 25; 17(16):6681-91. PubMed ID: 2476717
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  • 18. The T----C substitution at -198 of the A gamma-globin gene associated with the British form of HPFH generates overlapping recognition sites for two DNA-binding proteins.
    Fischer KD, Nowock J.
    Nucleic Acids Res; 1990 Oct 11; 18(19):5685-93. PubMed ID: 1699206
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  • 20. 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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