BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

250 related articles for article (PubMed ID: 25058334)

  • 1. UVB induces a genome-wide acting negative regulatory mechanism that operates at the level of transcription initiation in human cells.
    Gyenis A; Umlauf D; Ujfaludi Z; Boros I; Ye T; Tora L
    PLoS Genet; 2014 Jul; 10(7):e1004483. PubMed ID: 25058334
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Transcription-coupled DNA repair in yeast transcription factor IIE (TFIIE) mutants.
    Lommel L; Gregory SM; Becker KI; Sweder KS
    Nucleic Acids Res; 2000 Feb; 28(3):835-42. PubMed ID: 10637337
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Binding of TBP to promoters in vivo is stimulated by activators and requires Pol II holoenzyme.
    Kuras L; Struhl K
    Nature; 1999 Jun; 399(6736):609-13. PubMed ID: 10376605
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Blockage of RNA polymerase II at a cyclobutane pyrimidine dimer and 6-4 photoproduct.
    Mei Kwei JS; Kuraoka I; Horibata K; Ubukata M; Kobatake E; Iwai S; Handa H; Tanaka K
    Biochem Biophys Res Commun; 2004 Aug; 320(4):1133-8. PubMed ID: 15249207
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Widespread use of TATA elements in the core promoters for RNA polymerases III, II, and I in fission yeast.
    Hamada M; Huang Y; Lowe TM; Maraia RJ
    Mol Cell Biol; 2001 Oct; 21(20):6870-81. PubMed ID: 11564871
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Regulation of RNA polymerase I-dependent promoters by the hepatitis B virus X protein via activated Ras and TATA-binding protein.
    Wang HD; Trivedi A; Johnson DL
    Mol Cell Biol; 1998 Dec; 18(12):7086-94. PubMed ID: 9819395
    [TBL] [Abstract][Full Text] [Related]  

  • 7. TATA-binding protein is limiting for both TATA-containing and TATA-lacking RNA polymerase III promoters in Drosophila cells.
    Trivedi A; Vilalta A; Gopalan S; Johnson DL
    Mol Cell Biol; 1996 Dec; 16(12):6909-16. PubMed ID: 8943346
    [TBL] [Abstract][Full Text] [Related]  

  • 8. UV-induced ubiquitination of RNA polymerase II: a novel modification deficient in Cockayne syndrome cells.
    Bregman DB; Halaban R; van Gool AJ; Henning KA; Friedberg EC; Warren SL
    Proc Natl Acad Sci U S A; 1996 Oct; 93(21):11586-90. PubMed ID: 8876179
    [TBL] [Abstract][Full Text] [Related]  

  • 9. TATA-binding protein-associated factors enhance the recruitment of RNA polymerase II by transcriptional activators.
    Wu SY; Chiang CM
    J Biol Chem; 2001 Sep; 276(36):34235-43. PubMed ID: 11457828
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Recruitment of human TBP selectively activates RNA polymerase II TATA-dependent promoters.
    Majello B; Napolitano G; De Luca P; Lania L
    J Biol Chem; 1998 Jun; 273(26):16509-16. PubMed ID: 9632719
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Genomic study of RNA polymerase II and III SNAPc-bound promoters reveals a gene transcribed by both enzymes and a broad use of common activators.
    James Faresse N; Canella D; Praz V; Michaud J; Romascano D; Hernandez N
    PLoS Genet; 2012; 8(11):e1003028. PubMed ID: 23166507
    [TBL] [Abstract][Full Text] [Related]  

  • 12. RNA polymerase II is released from the DNA template during transcription-coupled repair in mammalian cells.
    Chiou YY; Hu J; Sancar A; Selby CP
    J Biol Chem; 2018 Feb; 293(7):2476-2486. PubMed ID: 29282293
    [TBL] [Abstract][Full Text] [Related]  

  • 13. hTFIIIB-beta stably binds to pol II promoters and recruits RNA polymerase III in a hTFIIIC1 dependent way.
    Kober I; Teichmann M; Seifart KH
    J Mol Biol; 1998 Nov; 284(1):7-20. PubMed ID: 9811538
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Accurate positioning of RNA polymerase II on a natural TATA-less promoter is independent of TATA-binding-protein-associated factors and initiator-binding proteins.
    Weis L; Reinberg D
    Mol Cell Biol; 1997 Jun; 17(6):2973-84. PubMed ID: 9154795
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A transcription factor IIA-binding site differentially regulates RNA polymerase II-mediated transcription in a promoter context-dependent manner.
    Wang J; Zhao S; He W; Wei Y; Zhang Y; Pegg H; Shore P; Roberts SGE; Deng W
    J Biol Chem; 2017 Jul; 292(28):11873-11885. PubMed ID: 28539359
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Promoter-specific dynamics of TATA-binding protein association with the human genome.
    Hasegawa Y; Struhl K
    Genome Res; 2019 Dec; 29(12):1939-1950. PubMed ID: 31732535
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Stably paused genes revealed through inhibition of transcription initiation by the TFIIH inhibitor triptolide.
    Chen F; Gao X; Shilatifard A
    Genes Dev; 2015 Jan; 29(1):39-47. PubMed ID: 25561494
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Immunoaffinity purification and functional characterization of human transcription factor IIH and RNA polymerase II from clonal cell lines that conditionally express epitope-tagged subunits of the multiprotein complexes.
    Kershnar E; Wu SY; Chiang CM
    J Biol Chem; 1998 Dec; 273(51):34444-53. PubMed ID: 9852112
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Genomic Organization of Human Transcription Initiation Complexes.
    Pugh BF; Venters BJ
    PLoS One; 2016; 11(2):e0149339. PubMed ID: 26866362
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Transcription factor IIE binds preferentially to RNA polymerase IIa and recruits TFIIH: a model for promoter clearance.
    Maxon ME; Goodrich JA; Tjian R
    Genes Dev; 1994 Mar; 8(5):515-24. PubMed ID: 7926747
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 13.