BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

440 related articles for article (PubMed ID: 9152512)

  • 1. Genomic structures of viral agents in relation to the biosynthesis of selenoproteins.
    Taylor EW; Nadimpalli RG; Ramanathan CS
    Biol Trace Elem Res; 1997 Jan; 56(1):63-91. PubMed ID: 9152512
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Computational genomic analysis of hemorrhagic fever viruses. Viral selenoproteins as a potential factor in pathogenesis.
    Ramanathan CS; Taylor EW
    Biol Trace Elem Res; 1997 Jan; 56(1):93-106. PubMed ID: 9152513
    [TBL] [Abstract][Full Text] [Related]  

  • 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; 37(17):2637-54. PubMed ID: 8064794
    [TBL] [Abstract][Full Text] [Related]  

  • 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; 70(2):97-116. PubMed ID: 10535520
    [TBL] [Abstract][Full Text] [Related]  

  • 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; 266(4):637-41. PubMed ID: 9102456
    [TBL] [Abstract][Full Text] [Related]  

  • 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; 292(5):1003-16. PubMed ID: 10512699
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Mammalian selenoproteins.
    Zachara BA
    J Trace Elem Electrolytes Health Dis; 1992 Sep; 6(3):137-51. PubMed ID: 1483033
    [TBL] [Abstract][Full Text] [Related]  

  • 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; 31(5):431-43. PubMed ID: 15478601
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Recognition of UGA as a selenocysteine codon in type I deiodinase requires sequences in the 3' untranslated region.
    Berry MJ; Banu L; Chen YY; Mandel SJ; Kieffer JD; Harney JW; Larsen PR
    Nature; 1991 Sep; 353(6341):273-6. PubMed ID: 1832744
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Structure and dynamics of a predicted ferredoxin-like selenoprotein in Japanese encephalitis virus.
    Zhong H; Taylor EW
    J Mol Graph Model; 2004 Dec; 23(3):223-31. PubMed ID: 15530818
    [TBL] [Abstract][Full Text] [Related]  

  • 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; 579(1-2):125-32. PubMed ID: 16055159
    [TBL] [Abstract][Full Text] [Related]  

  • 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; 14(1-4):25-35. PubMed ID: 11568437
    [TBL] [Abstract][Full Text] [Related]  

  • 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; 297(4):877-93. PubMed ID: 10736224
    [TBL] [Abstract][Full Text] [Related]  

  • 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; 310(5):987-99. PubMed ID: 11502008
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Sequence and genomic organization of Norwalk virus.
    Jiang X; Wang M; Wang K; Estes MK
    Virology; 1993 Jul; 195(1):51-61. PubMed ID: 8391187
    [TBL] [Abstract][Full Text] [Related]  

  • 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; 1(2):159-69. PubMed ID: 2562219
    [TBL] [Abstract][Full Text] [Related]  

  • 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; 35(2):414-23. PubMed ID: 17169995
    [TBL] [Abstract][Full Text] [Related]  

  • 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; 314(5):961-70. PubMed ID: 11743714
    [TBL] [Abstract][Full Text] [Related]  

  • 19. An RNA pseudoknot in the 3' end of the arterivirus genome has a critical role in regulating viral RNA synthesis.
    Beerens N; Snijder EJ
    J Virol; 2007 Sep; 81(17):9426-36. PubMed ID: 17581985
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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; 43(19):5757-71. PubMed ID: 15134450
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 22.