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Journal Abstract Search

436 related items for PubMed ID: 9152512

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  • 3. A basis for new approaches to the chemotherapy of AIDS: novel genes in HIV-1 potentially encode selenoproteins expressed by ribosomal frameshifting and termination suppression.
    Taylor EW, Ramanathan CS, Jalluri RK, Nadimpalli RG.
    J Med Chem; 1994 Aug 19; 37(17):2637-54. PubMed ID: 8064794
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  • 4. Selenium-dependent glutathione peroxidase modules encoded by RNA viruses.
    Zhang W, Ramanathan CS, Nadimpalli RG, Bhat AA, Cox AG, Taylor EW.
    Biol Trace Elem Res; 1999 Nov 19; 70(2):97-116. PubMed ID: 10535520
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  • 5. Selenoprotein synthesis in archaea: identification of an mRNA element of Methanococcus jannaschii probably directing selenocysteine insertion.
    Wilting R, Schorling S, Persson BC, Böck A.
    J Mol Biol; 1997 Mar 07; 266(4):637-41. PubMed ID: 9102456
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  • 6. High-level expression in Escherichia coli of selenocysteine-containing rat thioredoxin reductase utilizing gene fusions with engineered bacterial-type SECIS elements and co-expression with the selA, selB and selC genes.
    Arnér ES, Sarioglu H, Lottspeich F, Holmgren A, Böck A.
    J Mol Biol; 1999 Oct 08; 292(5):1003-16. PubMed ID: 10512699
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  • 8. [Analysis, identification and correction of some errors of model refseqs appeared in NCBI Human Gene Database by in silico cloning and experimental verification of novel human genes].
    Zhang DL, Ji L, Li YD.
    Yi Chuan Xue Bao; 2004 May 08; 31(5):431-43. PubMed ID: 15478601
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  • 11. A -1 frameshift in the HIV-1 env gene is enhanced by arginine deficiency via a hungry codon mechanism.
    Olubajo B, Taylor EW.
    Mutat Res; 2005 Nov 11; 579(1-2):125-32. PubMed ID: 16055159
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  • 12. A model for Sec incorporation with the regions upstream of the UGA Sec codon to play a key role.
    Goto C, Osaka T, Mizutani T.
    Biofactors; 2001 Nov 11; 14(1-4):25-35. PubMed ID: 11568437
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  • 13. The major HIV-1 packaging signal is an extended bulged stem loop whose structure is altered on interaction with the Gag polyprotein.
    Zeffman A, Hassard S, Varani G, Lever A.
    J Mol Biol; 2000 Apr 07; 297(4):877-93. PubMed ID: 10736224
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  • 14. A sequence required for -1 ribosomal frameshifting located four kilobases downstream of the frameshift site.
    Paul CP, Barry JK, Dinesh-Kumar SP, Brault V, Miller WA.
    J Mol Biol; 2001 Jul 27; 310(5):987-99. PubMed ID: 11502008
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  • 15. Sequence and genomic organization of Norwalk virus.
    Jiang X, Wang M, Wang K, Estes MK.
    Virology; 1993 Jul 27; 195(1):51-61. PubMed ID: 8391187
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  • 16. E. coli ribosomes re-phase on retroviral frameshift signals at rates ranging from 2 to 50 percent.
    Weiss RB, Dunn DM, Shuh M, Atkins JF, Gesteland RF.
    New Biol; 1989 Nov 27; 1(2):159-69. PubMed ID: 2562219
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  • 17. SECIS elements in the coding regions of selenoprotein transcripts are functional in higher eukaryotes.
    Mix H, Lobanov AV, Gladyshev VN.
    Nucleic Acids Res; 2007 Nov 27; 35(2):414-23. PubMed ID: 17169995
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  • 18. Stem-loop SL4 of the HIV-1 psi RNA packaging signal exhibits weak affinity for the nucleocapsid protein. structural studies and implications for genome recognition.
    Amarasinghe GK, Zhou J, Miskimon M, Chancellor KJ, McDonald JA, Matthews AG, Miller RR, Rouse MD, Summers MF.
    J Mol Biol; 2001 Dec 14; 314(5):961-70. PubMed ID: 11743714
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  • 19. NMR structures of loop B RNAs from the stem-loop IV domain of the enterovirus internal ribosome entry site: a single C to U substitution drastically changes the shape and flexibility of RNA.
    Du Z, Ulyanov NB, Yu J, Andino R, James TL.
    Biochemistry; 2004 May 18; 43(19):5757-71. PubMed ID: 15134450
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  • 20. Selenium and cellular immunity. Evidence that selenoproteins may be encoded in the +1 reading frame overlapping the human CD4, CD8, and HLA-DR genes.
    Taylor EW.
    Biol Trace Elem Res; 1995 May 18; 49(2-3):85-95. PubMed ID: 8562289
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