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369 related items for PubMed ID: 8608447

  • 1. Evidence that the decay of nucleus-associated nonsense mRNA for human triosephosphate isomerase involves nonsense codon recognition after splicing.
    Zhang J, Maquat LE.
    RNA; 1996 Mar; 2(3):235-43. PubMed ID: 8608447
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  • 2. At least one intron is required for the nonsense-mediated decay of triosephosphate isomerase mRNA: a possible link between nuclear splicing and cytoplasmic translation.
    Zhang J, Sun X, Qian Y, LaDuca JP, Maquat LE.
    Mol Cell Biol; 1998 Sep; 18(9):5272-83. PubMed ID: 9710612
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  • 3. Intron function in the nonsense-mediated decay of beta-globin mRNA: indications that pre-mRNA splicing in the nucleus can influence mRNA translation in the cytoplasm.
    Zhang J, Sun X, Qian Y, Maquat LE.
    RNA; 1998 Jul; 4(7):801-15. PubMed ID: 9671053
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  • 4. Introns are cis effectors of the nonsense-codon-mediated reduction in nuclear mRNA abundance.
    Cheng J, Belgrader P, Zhou X, Maquat LE.
    Mol Cell Biol; 1994 Sep; 14(9):6317-25. PubMed ID: 8065363
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  • 5. Mammalian nonsense codons can be cis effectors of nuclear mRNA half-life.
    Belgrader P, Cheng J, Zhou X, Stephenson LS, Maquat LE.
    Mol Cell Biol; 1994 Dec; 14(12):8219-28. PubMed ID: 7969159
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  • 9. Evidence to implicate translation by ribosomes in the mechanism by which nonsense codons reduce the nuclear level of human triosephosphate isomerase mRNA.
    Belgrader P, Cheng J, Maquat LE.
    Proc Natl Acad Sci U S A; 1993 Jan 15; 90(2):482-6. PubMed ID: 8421679
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  • 10. Nonsense but not missense mutations can decrease the abundance of nuclear mRNA for the mouse major urinary protein, while both types of mutations can facilitate exon skipping.
    Belgrader P, Maquat LE.
    Mol Cell Biol; 1994 Sep 15; 14(9):6326-36. PubMed ID: 8065364
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  • 13. Cytoplasmic mRNA for human triosephosphate isomerase is immune to nonsense-mediated decay despite forming polysomes.
    Stephenson LS, Maquat LE.
    Biochimie; 1996 Sep 15; 78(11-12):1043-7. PubMed ID: 9150883
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  • 19. A mutated human homologue to yeast Upf1 protein has a dominant-negative effect on the decay of nonsense-containing mRNAs in mammalian cells.
    Sun X, Perlick HA, Dietz HC, Maquat LE.
    Proc Natl Acad Sci U S A; 1998 Aug 18; 95(17):10009-14. PubMed ID: 9707591
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  • 20. A mechanism for exon skipping caused by nonsense or missense mutations in BRCA1 and other genes.
    Liu HX, Cartegni L, Zhang MQ, Krainer AR.
    Nat Genet; 2001 Jan 18; 27(1):55-8. PubMed ID: 11137998
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