BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

194 related articles for article (PubMed ID: 8259677)

  • 1. Analysis of figwort mosaic virus (plant pararetrovirus) polyadenylation signal.
    Sanfaçon H
    Virology; 1994 Jan; 198(1):39-49. PubMed ID: 8259677
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A dissection of the cauliflower mosaic virus polyadenylation signal.
    Sanfaçon H; Brodmann P; Hohn T
    Genes Dev; 1991 Jan; 5(1):141-9. PubMed ID: 1703507
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Proximity to the promoter inhibits recognition of cauliflower mosaic virus polyadenylation signal.
    Sanfaçon H; Hohn T
    Nature; 1990 Jul; 346(6279):81-4. PubMed ID: 2366867
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Upstream sequences other than AAUAAA are required for efficient messenger RNA 3'-end formation in plants.
    Mogen BD; MacDonald MH; Graybosch R; Hunt AG
    Plant Cell; 1990 Dec; 2(12):1261-72. PubMed ID: 1983794
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Two G-rich regulatory elements located adjacent to and 440 nucleotides downstream of the core poly(A) site of the intronless melanocortin receptor 1 gene are critical for efficient 3' end processing.
    Dalziel M; Nunes NM; Furger A
    Mol Cell Biol; 2007 Mar; 27(5):1568-80. PubMed ID: 17189425
    [TBL] [Abstract][Full Text] [Related]  

  • 6. The end of the message: 3'-end processing leading to polyadenylated messenger RNA.
    Wahle E
    Bioessays; 1992 Feb; 14(2):113-8. PubMed ID: 1575710
    [TBL] [Abstract][Full Text] [Related]  

  • 7. The contribution of AAUAAA and the upstream element UUUGUA to the efficiency of mRNA 3'-end formation in plants.
    Rothnie HM; Reid J; Hohn T
    EMBO J; 1994 May; 13(9):2200-10. PubMed ID: 8187773
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Different sequence elements are required for function of the cauliflower mosaic virus polyadenylation site in Saccharomyces cerevisiae compared with in plants.
    Irniger S; Sanfaçon H; Egli CM; Braus GH
    Mol Cell Biol; 1992 May; 12(5):2322-30. PubMed ID: 1373813
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Poly(A) site choice in retroelements: deja vu all over again?
    Imperiale MJ; DeZazzo JD
    New Biol; 1991 Jun; 3(6):531-7. PubMed ID: 1680384
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Elements upstream of the AAUAAA within the human immunodeficiency virus polyadenylation signal are required for efficient polyadenylation in vitro.
    Valsamakis A; Schek N; Alwine JC
    Mol Cell Biol; 1992 Sep; 12(9):3699-705. PubMed ID: 1508176
    [TBL] [Abstract][Full Text] [Related]  

  • 11. In silico analysis of EST and genomic sequences allowed the prediction of cis-regulatory elements for Entamoeba histolytica mRNA polyadenylation.
    Zamorano A; López-Camarillo C; Orozco E; Weber C; Guillen N; Marchat LA
    Comput Biol Chem; 2008 Aug; 32(4):256-63. PubMed ID: 18514032
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Efficient translation of distal cistrons of a polycistronic mRNA of a plant pararetrovirus requires a compatible interaction between the mRNA 3' end and the proteinaceous trans-activator.
    Edskes HK; Kiernan JM; Shepherd RJ
    Virology; 1996 Oct; 224(2):564-7. PubMed ID: 8874519
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Gene VI of figwort mosaic virus (caulimovirus group) functions in posttranscriptional expression of genes on the full-length RNA transcript.
    Gowda S; Wu FC; Scholthof HB; Shepherd RJ
    Proc Natl Acad Sci U S A; 1989 Dec; 86(23):9203-7. PubMed ID: 2594762
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Characterization of the polyomavirus late polyadenylation signal.
    Batt DB; Carmichael GG
    Mol Cell Biol; 1995 Sep; 15(9):4783-90. PubMed ID: 7651395
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Mason-Pfizer monkey virus (MPMV) constitutive transport element (CTE) functions in a position-dependent manner.
    Rizvi TA; Schmidt RD; Lew KA
    Virology; 1997 Sep; 236(1):118-29. PubMed ID: 9299624
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Trypanosoma brucei 5'ETS A'-cleavage is directed by 3'-adjacent sequences, but not two U3 snoRNA-binding elements, which are all required for subsequent pre-small subunit rRNA processing events.
    Hartshorne T; Toyofuku W; Hollenbaugh J
    J Mol Biol; 2001 Nov; 313(4):733-49. PubMed ID: 11697900
    [TBL] [Abstract][Full Text] [Related]  

  • 17. The secondary structure of the adenovirus-2 L4 polyadenylation domain: evidence for a hairpin structure exposing the AAUAAA signal in its loop.
    Sittler A; Gallinaro H; Jacob M
    J Mol Biol; 1995 May; 248(3):525-40. PubMed ID: 7752222
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Analyses of alternative poly(A) signals for use in baculovirus expression vectors.
    Westwood JA; Jones IM; Bishop DH
    Virology; 1993 Jul; 195(1):90-9. PubMed ID: 8100374
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Analysis of cis-sequence of subgenomic transcript promoter from the Figwort mosaic virus and comparison of promoter activity with the cauliflower mosaic virus promoters in monocot and dicot cells.
    Bhattacharyya S; Dey N; Maiti IB
    Virus Res; 2002 Dec; 90(1-2):47-62. PubMed ID: 12457962
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Polyadenylation in rice tungro bacilliform virus: cis-acting signals and regulation.
    Rothnie HM; Chen G; Fütterer J; Hohn T
    J Virol; 2001 May; 75(9):4184-94. PubMed ID: 11287568
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.