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Journal Abstract Search

147 related items for PubMed ID: 6280877

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  • 24. Equal stabilities of normal beta globin and nontranslatable beta0 -39 thalassemic transcripts in cell-free extracts.
    Stolle CA, Payne MS, Benz EJ.
    Blood; 1987 Jul; 70(1):293-300. PubMed ID: 3593968
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  • 25. Processing of human beta-globin mRNA precursor to mRNA is defective in three patients with beta+-thalassemia.
    Maquat LE, Kinniburgh AJ, Beach LR, Honig GR, Lazerson J, Ershler WB, Ross J.
    Proc Natl Acad Sci U S A; 1980 Jul; 77(7):4287-91. PubMed ID: 6933479
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  • 26. Relative stability of alpha- and beta-globin messenger RNAs in homozygous beta+ thalassemia.
    Nienhuis AW, Turner P, Benz EJ.
    Proc Natl Acad Sci U S A; 1977 Sep; 74(9):3960-4. PubMed ID: 71735
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  • 27. Mutation in an intervening sequence splice junction in man.
    Orkin SH, Goff SC, Hechtman RL.
    Proc Natl Acad Sci U S A; 1981 Aug; 78(8):5041-5. PubMed ID: 6946451
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  • 28. Beta Thalassemia: mutations which affect processing of the beta-Globin mRNA precursor.
    Kantor JA, Turner PH, Nienhuis AW.
    Cell; 1980 Aug; 21(1):149-57. PubMed ID: 7407909
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  • 29. Reversal of aberrant splicing of beta-thalassemia allele by antisense RNA in vitro and in vivo.
    Zeng Y, Gu X, Chen Y, Gong L, Ren Z, Huang S.
    Chin Med J (Engl); 1999 Feb; 112(2):107-11. PubMed ID: 11593572
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  • 30. A new method for detection of small modifications in genomic DNA, applied to the human delta-beta globin gene cluster.
    Chebloune Y, Trabuchet G, Poncet D, Cohen-Solal M, Faure C, Verdier G, Nigon VM.
    Eur J Biochem; 1984 Aug 01; 142(3):473-80. PubMed ID: 6088226
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  • 31. Abnormal RNA processing due to the exon mutation of beta E-globin gene.
    Orkin SH, Kazazian HH, Antonarakis SE, Ostrer H, Goff SC, Sexton JP.
    Nature; 1982 Dec 23; 300(5894):768-9. PubMed ID: 7177196
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  • 32. Specific transcription and RNA splicing defects in five cloned beta-thalassaemia genes.
    Treisman R, Orkin SH, Maniatis T.
    Nature; 1983 Apr 14; 302(5909):591-6. PubMed ID: 6188062
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  • 33. The mRNA transcripts from a mutant beta-globin gene derived from splicing at preferential cryptic sites.
    Lossi AM, Bergé-Lefranc JL.
    FEBS Lett; 1989 Oct 09; 256(1-2):163-6. PubMed ID: 2680598
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  • 34. Nonsense codons in human beta-globin mRNA result in the production of mRNA degradation products.
    Lim SK, Sigmund CD, Gross KW, Maquat LE.
    Mol Cell Biol; 1992 Mar 09; 12(3):1149-61. PubMed ID: 1545796
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  • 35. High-level expression of hemoglobin A in human thalassemic erythroid progenitor cells following lentiviral vector delivery of an antisense snRNA.
    Vacek MM, Ma H, Gemignani F, Lacerra G, Kafri T, Kole R.
    Blood; 2003 Jan 01; 101(1):104-11. PubMed ID: 12393543
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