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Journal Abstract Search

206 related items for PubMed ID: 2987809

  • 1. Beta-thalassemia resulting from a single nucleotide substitution in an acceptor splice site.
    Atweh GF, Anagnou NP, Shearin J, Forget BG, Kaufman RE.
    Nucleic Acids Res; 1985 Feb 11; 13(3):777-90. PubMed ID: 2987809
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  • 2. Abnormal splice in a mutant human beta-globin gene not at the site of a mutation.
    Dobkin C, Pergolizzi RG, Bahre P, Bank A.
    Proc Natl Acad Sci U S A; 1983 Mar 11; 80(5):1184-8. PubMed ID: 6298782
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  • 5. A single-base change at a splice site in a beta 0-thalassemic gene causes abnormal RNA splicing.
    Treisman R, Proudfoot NJ, Shander M, Maniatis T.
    Cell; 1982 Jul 11; 29(3):903-11. PubMed ID: 7151176
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  • 6. Reversibility of IVS 2 missplicing in a mutant human beta-globin gene.
    Dobkin C, Bank A.
    J Biol Chem; 1985 Dec 25; 260(30):16332-7. PubMed ID: 3840804
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  • 7. Beta zero thalassemia caused by a base substitution that creates an alternative splice acceptor site in an intron.
    Metherall JE, Collins FS, Pan J, Weissman SM, Forget BG.
    EMBO J; 1986 Oct 25; 5(10):2551-7. PubMed ID: 3780671
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  • 8. Inactivation of an acceptor RNA splice site by a short deletion in beta-thalassemia.
    Orkin SH, Sexton JP, Goff SC, Kazazian HH.
    J Biol Chem; 1983 Jun 25; 258(12):7249-51. PubMed ID: 6190800
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  • 9. Beta + thalassemia: aberrant splicing results from a single point mutation in an intron.
    Busslinger M, Moschonas N, Flavell RA.
    Cell; 1981 Dec 25; 27(2 Pt 1):289-98. PubMed ID: 6895866
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  • 10. Beta-thalassemia due to two novel nucleotide substitutions in consensus acceptor splice sequences of the beta-globin gene.
    Wong C, Antonarakis SE, Goff SC, Orkin SH, Forget BG, Nathan DG, Giardina PJ, Kazazian HH.
    Blood; 1989 Mar 25; 73(4):914-8. PubMed ID: 2920213
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  • 11. Base substitution at position -88 in a beta-thalassemic globin gene. Further evidence for the role of distal promoter element ACACCC.
    Orkin SH, Antonarakis SE, Kazazian HH.
    J Biol Chem; 1984 Jul 25; 259(14):8679-81. PubMed ID: 6086605
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  • 16. A new mutation in the beta-globin gene (IVS II-850 G-C) found in a Yugoslavian beta-thalassemia heterozygote.
    Jankovic L, Dimovski AJ, Sukarova E, Juricic D, Efremov GD.
    Haematologica; 1992 Jul 25; 77(2):119-21. PubMed ID: 1398296
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  • 17. Functional analysis of a beta-globin gene containing a TATA box mutation from a Kurdish Jew with beta thalassemia.
    Surrey S, Delgrosso K, Malladi P, Schwartz E.
    J Biol Chem; 1985 Jun 10; 260(11):6507-10. PubMed ID: 2987224
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  • 18. The beta zero-thalassemia in an American black family is due to a single nucleotide substitution in the acceptor splice junction of the second intervening sequence.
    Padanilam BJ, Huisman TH.
    Am J Hematol; 1986 Jul 10; 22(3):259-63. PubMed ID: 2424301
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  • 19. A nucleotide change at a splice junction in the human beta-globin gene is associated with beta 0-thalassemia.
    Baird M, Driscoll C, Schreiner H, Sciarratta GV, Sansone G, Niazi G, Ramirez F, Bank A.
    Proc Natl Acad Sci U S A; 1981 Jul 10; 78(7):4218-21. PubMed ID: 6270663
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  • 20. RNA processing errors in patients with beta-thalassemia.
    Ley TJ, Anagnou NP, Pepe G, Nienhuis AW.
    Proc Natl Acad Sci U S A; 1982 Aug 10; 79(15):4775-9. PubMed ID: 6956887
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