BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

874 related articles for article (PubMed ID: 29176831)

  • 21. 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]  

  • 22. Transcription of Nearly All Yeast RNA Polymerase II-Transcribed Genes Is Dependent on Transcription Factor TFIID.
    Warfield L; Ramachandran S; Baptista T; Devys D; Tora L; Hahn S
    Mol Cell; 2017 Oct; 68(1):118-129.e5. PubMed ID: 28918900
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Genome-wide localization analysis of a complete set of Tafs reveals a specific effect of the taf1 mutation on Taf2 occupancy and provides indirect evidence for different TFIID conformations at different promoters.
    Ohtsuki K; Kasahara K; Shirahige K; Kokubo T
    Nucleic Acids Res; 2010 Apr; 38(6):1805-20. PubMed ID: 20026583
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Saccharomyces cerevisiae HMO1 interacts with TFIID and participates in start site selection by RNA polymerase II.
    Kasahara K; Ki S; Aoyama K; Takahashi H; Kokubo T
    Nucleic Acids Res; 2008 Mar; 36(4):1343-57. PubMed ID: 18187511
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Distinct role of Mediator tail module in regulation of SAGA-dependent, TATA-containing genes in yeast.
    Ansari SA; Ganapathi M; Benschop JJ; Holstege FC; Wade JT; Morse RH
    EMBO J; 2012 Jan; 31(1):44-57. PubMed ID: 21971086
    [TBL] [Abstract][Full Text] [Related]  

  • 26. An extensive requirement for transcription factor IID-specific TAF-1 in Caenorhabditis elegans embryonic transcription.
    Walker AK; Shi Y; Blackwell TK
    J Biol Chem; 2004 Apr; 279(15):15339-47. PubMed ID: 14726532
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Kin28 depletion increases association of TFIID subunits Taf1 and Taf4 with promoters in Saccharomyces cerevisiae.
    Knoll ER; Zhu ZI; Sarkar D; Landsman D; Morse RH
    Nucleic Acids Res; 2020 May; 48(8):4244-4255. PubMed ID: 32182349
    [TBL] [Abstract][Full Text] [Related]  

  • 28. The TATA box regulates TATA-binding protein (TBP) dynamics in vivo.
    Tora L; Timmers HT
    Trends Biochem Sci; 2010 Jun; 35(6):309-14. PubMed ID: 20176488
    [TBL] [Abstract][Full Text] [Related]  

  • 29. The new core promoter element XCPE1 (X Core Promoter Element 1) directs activator-, mediator-, and TATA-binding protein-dependent but TFIID-independent RNA polymerase II transcription from TATA-less promoters.
    Tokusumi Y; Ma Y; Song X; Jacobson RH; Takada S
    Mol Cell Biol; 2007 Mar; 27(5):1844-58. PubMed ID: 17210644
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Distinct mutations in yeast TAF(II)25 differentially affect the composition of TFIID and SAGA complexes as well as global gene expression patterns.
    Kirschner DB; vom Baur E; Thibault C; Sanders SL; Gangloff YG; Davidson I; Weil PA; Tora L
    Mol Cell Biol; 2002 May; 22(9):3178-93. PubMed ID: 11940675
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Simultaneous recruitment of coactivators by Gcn4p stimulates multiple steps of transcription in vivo.
    Govind CK; Yoon S; Qiu H; Govind S; Hinnebusch AG
    Mol Cell Biol; 2005 Jul; 25(13):5626-38. PubMed ID: 15964818
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Differential requirement of SAGA components for recruitment of TATA-box-binding protein to promoters in vivo.
    Bhaumik SR; Green MR
    Mol Cell Biol; 2002 Nov; 22(21):7365-71. PubMed ID: 12370284
    [TBL] [Abstract][Full Text] [Related]  

  • 33. A genome-wide housekeeping role for TFIID and a highly regulated stress-related role for SAGA in Saccharomyces cerevisiae.
    Huisinga KL; Pugh BF
    Mol Cell; 2004 Feb; 13(4):573-85. PubMed ID: 14992726
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Architecture of the multi-functional SAGA complex and the molecular mechanism of holding TBP.
    Ben-Shem A; Papai G; Schultz P
    FEBS J; 2021 May; 288(10):3135-3147. PubMed ID: 32946670
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Mot1 associates with transcriptionally active promoters and inhibits association of NC2 in Saccharomyces cerevisiae.
    Geisberg JV; Moqtaderi Z; Kuras L; Struhl K
    Mol Cell Biol; 2002 Dec; 22(23):8122-34. PubMed ID: 12417716
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Two roles for the yeast transcription coactivator SAGA and a set of genes redundantly regulated by TFIID and SAGA.
    Donczew R; Warfield L; Pacheco D; Erijman A; Hahn S
    Elife; 2020 Jan; 9():. PubMed ID: 31913117
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Taspase1 processing alters TFIIA cofactor properties in the regulation of TFIID.
    Malecová B; Caputo VS; Lee DF; Hsieh JJ; Oelgeschläger T
    Transcription; 2015; 6(2):21-32. PubMed ID: 25996597
    [TBL] [Abstract][Full Text] [Related]  

  • 38. TATA-binding protein-associated factor(s) in TFIID function through the initiator to direct basal transcription from a TATA-less class II promoter.
    Martinez E; Chiang CM; Ge H; Roeder RG
    EMBO J; 1994 Jul; 13(13):3115-26. PubMed ID: 7518774
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Structure of SAGA and mechanism of TBP deposition on gene promoters.
    Papai G; Frechard A; Kolesnikova O; Crucifix C; Schultz P; Ben-Shem A
    Nature; 2020 Jan; 577(7792):711-716. PubMed ID: 31969704
    [TBL] [Abstract][Full Text] [Related]  

  • 40. A downstream initiation element required for efficient TATA box binding and in vitro function of TFIID.
    Nakatani Y; Horikoshi M; Brenner M; Yamamoto T; Besnard F; Roeder RG; Freese E
    Nature; 1990 Nov; 348(6296):86-8. PubMed ID: 2234067
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 44.