BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

189 related articles for article (PubMed ID: 11287614)

  • 1. High-mobility-group proteins NHP6A and NHP6B participate in activation of the RNA polymerase III SNR6 gene.
    Lopez S; Livingstone-Zatchej M; Jourdain S; Thoma F; Sentenac A; Marsolier MC
    Mol Cell Biol; 2001 May; 21(9):3096-104. PubMed ID: 11287614
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Nhp6, an HMG1 protein, functions in SNR6 transcription by RNA polymerase III in S. cerevisiae.
    Kruppa M; Moir RD; Kolodrubetz D; Willis IM
    Mol Cell; 2001 Feb; 7(2):309-18. PubMed ID: 11239460
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A novel upstream RNA polymerase III promoter element becomes essential when the chromatin structure of the yeast U6 RNA gene is altered.
    Martin MP; Gerlach VL; Brow DA
    Mol Cell Biol; 2001 Oct; 21(19):6429-39. PubMed ID: 11533232
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Identical components of yeast transcription factor IIIB are required and sufficient for transcription of TATA box-containing and TATA-less genes.
    Joazeiro CA; Kassavetis GA; Geiduschek EP
    Mol Cell Biol; 1994 Apr; 14(4):2798-808. PubMed ID: 8139577
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Nhp6 is a transcriptional initiation fidelity factor for RNA polymerase III transcription in vitro and in vivo.
    Kassavetis GA; Steiner DF
    J Biol Chem; 2006 Mar; 281(11):7445-51. PubMed ID: 16407207
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Chromatin-mediated transcriptional regulation by the yeast architectural factors NHP6A and NHP6B.
    Moreira JM; Holmberg S
    EMBO J; 2000 Dec; 19(24):6804-13. PubMed ID: 11118215
    [TBL] [Abstract][Full Text] [Related]  

  • 7. TATA-binding protein mutants that are lethal in the absence of the Nhp6 high-mobility-group protein.
    Eriksson P; Biswas D; Yu Y; Stewart JM; Stillman DJ
    Mol Cell Biol; 2004 Jul; 24(14):6419-29. PubMed ID: 15226442
    [TBL] [Abstract][Full Text] [Related]  

  • 8. The Brf and TATA-binding protein subunits of the RNA polymerase III transcription factor IIIB mediate position-specific integration of the gypsy-like element, Ty3.
    Yieh L; Kassavetis G; Geiduschek EP; Sandmeyer SB
    J Biol Chem; 2000 Sep; 275(38):29800-7. PubMed ID: 10882723
    [TBL] [Abstract][Full Text] [Related]  

  • 9. TFIIIC-independent in vitro transcription of yeast tRNA genes.
    Dieci G; Percudani R; Giuliodori S; Bottarelli L; Ottonello S
    J Mol Biol; 2000 Jun; 299(3):601-13. PubMed ID: 10835271
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Mutations in the yeast Nhp6 protein can differentially affect its in vivo functions.
    Kruppa M; Kolodrubetz D
    Biochem Biophys Res Commun; 2001 Feb; 280(5):1292-9. PubMed ID: 11162669
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Distinct roles of transcription factors TFIIIB and TFIIIC in RNA polymerase III transcription reinitiation.
    Ferrari R; Rivetti C; Acker J; Dieci G
    Proc Natl Acad Sci U S A; 2004 Sep; 101(37):13442-7. PubMed ID: 15347814
    [TBL] [Abstract][Full Text] [Related]  

  • 12. TFIIIB placement on a yeast U6 RNA gene in vivo is directed primarily by TFIIIC rather than by sequence-specific DNA contacts.
    Gerlach VL; Whitehall SK; Geiduschek EP; Brow DA
    Mol Cell Biol; 1995 Mar; 15(3):1455-66. PubMed ID: 7862139
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Gene dosage affects the expression of the duplicated NHP6 genes of Saccharomyces cerevisiae.
    Kolodrubetz D; Kruppa M; Burgum A
    Gene; 2001 Jul; 272(1-2):93-101. PubMed ID: 11470514
    [TBL] [Abstract][Full Text] [Related]  

  • 14. High-level activation of transcription of the yeast U6 snRNA gene in chromatin by the basal RNA polymerase III transcription factor TFIIIC.
    Shivaswamy S; Kassavetis GA; Bhargava P
    Mol Cell Biol; 2004 May; 24(9):3596-606. PubMed ID: 15082757
    [TBL] [Abstract][Full Text] [Related]  

  • 15. NHP6A and NHP6B, which encode HMG1-like proteins, are candidates for downstream components of the yeast SLT2 mitogen-activated protein kinase pathway.
    Costigan C; Kolodrubetz D; Snyder M
    Mol Cell Biol; 1994 Apr; 14(4):2391-403. PubMed ID: 8139543
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Architectural transcription factors and the SAGA complex function in parallel pathways to activate transcription.
    Yu Y; Eriksson P; Stillman DJ
    Mol Cell Biol; 2000 Apr; 20(7):2350-7. PubMed ID: 10713159
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A RNA polymerase III-based two-hybrid system to study RNA polymerase II transcriptional regulators.
    Marsolier MC; Prioleau MN; Sentenac A
    J Mol Biol; 1997 May; 268(2):243-9. PubMed ID: 9159467
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Yeast HMG proteins NHP6A/B potentiate promoter-specific transcriptional activation in vivo and assembly of preinitiation complexes in vitro.
    Paull TT; Carey M; Johnson RC
    Genes Dev; 1996 Nov; 10(21):2769-81. PubMed ID: 8946917
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Architecture of a yeast U6 RNA gene promoter.
    Eschenlauer JB; Kaiser MW; Gerlach VL; Brow DA
    Mol Cell Biol; 1993 May; 13(5):3015-26. PubMed ID: 8474459
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Requirement of Nhp6 proteins for transcription of a subset of tRNA genes and heterochromatin barrier function in Saccharomyces cerevisiae.
    Braglia P; Dugas SL; Donze D; Dieci G
    Mol Cell Biol; 2007 Mar; 27(5):1545-57. PubMed ID: 17178828
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.