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Journal Abstract Search

369 related items for PubMed ID: 1986242

  • 1. Suppression of ribosomal reinitiation at upstream open reading frames in amino acid-starved cells forms the basis for GCN4 translational control.
    Abastado JP, Miller PF, Jackson BM, Hinnebusch AG.
    Mol Cell Biol; 1991 Jan; 11(1):486-96. PubMed ID: 1986242
    [Abstract] [Full Text] [Related]

  • 2. A quantitative model for translational control of the GCN4 gene of Saccharomyces cerevisiae.
    Abastado JP, Miller PF, Hinnebusch AG.
    New Biol; 1991 May; 3(5):511-24. PubMed ID: 1883814
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  • 3. Requirements for intercistronic distance and level of eukaryotic initiation factor 2 activity in reinitiation on GCN4 mRNA vary with the downstream cistron.
    Grant CM, Miller PF, Hinnebusch AG.
    Mol Cell Biol; 1994 Apr; 14(4):2616-28. PubMed ID: 8139562
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  • 6. Gene-specific translational control of the yeast GCN4 gene by phosphorylation of eukaryotic initiation factor 2.
    Hinnebusch AG.
    Mol Microbiol; 1993 Oct; 10(2):215-23. PubMed ID: 7934812
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  • 7. Effect of sequence context at stop codons on efficiency of reinitiation in GCN4 translational control.
    Grant CM, Hinnebusch AG.
    Mol Cell Biol; 1994 Jan; 14(1):606-18. PubMed ID: 8264629
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  • 9. Physical evidence for distinct mechanisms of translational control by upstream open reading frames.
    Gaba A, Wang Z, Krishnamoorthy T, Hinnebusch AG, Sachs MS.
    EMBO J; 2001 Nov 15; 20(22):6453-63. PubMed ID: 11707416
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  • 11. Translation Initiation from Conserved Non-AUG Codons Provides Additional Layers of Regulation and Coding Capacity.
    Ivanov IP, Wei J, Caster SZ, Smith KM, Michel AM, Zhang Y, Firth AE, Freitag M, Dunlap JC, Bell-Pedersen D, Atkins JF, Sachs MS.
    mBio; 2017 Jun 27; 8(3):. PubMed ID: 28655822
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  • 12. Multiple upstream AUG codons mediate translational control of GCN4.
    Mueller PP, Hinnebusch AG.
    Cell; 1986 Apr 25; 45(2):201-7. PubMed ID: 3516411
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  • 13. Ribosome association of GCN2 protein kinase, a translational activator of the GCN4 gene of Saccharomyces cerevisiae.
    Ramirez M, Wek RC, Hinnebusch AG.
    Mol Cell Biol; 1991 Jun 25; 11(6):3027-36. PubMed ID: 2038314
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  • 14. Ribosomal protein L33 is required for ribosome biogenesis, subunit joining, and repression of GCN4 translation.
    Martín-Marcos P, Hinnebusch AG, Tamame M.
    Mol Cell Biol; 2007 Sep 25; 27(17):5968-85. PubMed ID: 17548477
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  • 15. GCD2, a translational repressor of the GCN4 gene, has a general function in the initiation of protein synthesis in Saccharomyces cerevisiae.
    Foiani M, Cigan AM, Paddon CJ, Harashima S, Hinnebusch AG.
    Mol Cell Biol; 1991 Jun 25; 11(6):3203-16. PubMed ID: 2038326
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  • 16. cis-acting sequences involved in the translational control of GCN4 expression.
    Miller PF, Hinnebusch AG.
    Biochim Biophys Acta; 1990 Aug 27; 1050(1-3):151-4. PubMed ID: 2207139
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  • 17. Translation of the yeast transcriptional activator GCN4 is stimulated by purine limitation: implications for activation of the protein kinase GCN2.
    Rolfes RJ, Hinnebusch AG.
    Mol Cell Biol; 1993 Aug 27; 13(8):5099-111. PubMed ID: 8336737
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  • 18. Identification of GCD14 and GCD15, novel genes required for translational repression of GCN4 mRNA in Saccharomyces cerevisiae.
    Cuesta R, Hinnebusch AG, Tamame M.
    Genetics; 1998 Mar 27; 148(3):1007-20. PubMed ID: 9539420
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  • 19. Identification of positive-acting domains in GCN2 protein kinase required for translational activation of GCN4 expression.
    Wek RC, Ramirez M, Jackson BM, Hinnebusch AG.
    Mol Cell Biol; 1990 Jun 27; 10(6):2820-31. PubMed ID: 2188100
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  • 20. Transcriptional-translational regulatory circuit in Saccharomyces cerevisiae which involves the GCN4 transcriptional activator and the GCN2 protein kinase.
    Roussou I, Thireos G, Hauge BM.
    Mol Cell Biol; 1988 May 27; 8(5):2132-9. PubMed ID: 3290651
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