BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

207 related articles for article (PubMed ID: 9288742)

  • 1. Yeast TAF(II)145 functions as a core promoter selectivity factor, not a general coactivator.
    Shen WC; Green MR
    Cell; 1997 Aug; 90(4):615-24. PubMed ID: 9288742
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Yeast TAF(II)145 required for transcription of G1/S cyclin genes and regulated by the cellular growth state.
    Walker SS; Shen WC; Reese JC; Apone LM; Green MR
    Cell; 1997 Aug; 90(4):607-14. PubMed ID: 9288741
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Structure-function analysis of TAF130: identification and characterization of a high-affinity TATA-binding protein interaction domain in the N terminus of yeast TAF(II)130.
    Bai Y; Perez GM; Beechem JM; Weil PA
    Mol Cell Biol; 1997 Jun; 17(6):3081-93. PubMed ID: 9154807
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. Analysis of selective gene activation in yeast by differential display.
    Shen WC; Green MR
    Methods; 1998 Dec; 16(4):415-22. PubMed ID: 10049649
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Distinct requirements for C.elegans TAF(II)s in early embryonic transcription.
    Walker AK; Rothman JH; Shi Y; Blackwell TK
    EMBO J; 2001 Sep; 20(18):5269-79. PubMed ID: 11566890
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. Impaired core promoter recognition caused by novel yeast TAF145 mutations can be restored by creating a canonical TATA element within the promoter region of the TUB2 gene.
    Tsukihashi Y; Miyake T; Kawaichi M; Kokubo T
    Mol Cell Biol; 2000 Apr; 20(7):2385-99. PubMed ID: 10713163
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Drosophila TAFII150: similarity to yeast gene TSM-1 and specific binding to core promoter DNA.
    Verrijzer CP; Yokomori K; Chen JL; Tjian R
    Science; 1994 May; 264(5161):933-41. PubMed ID: 8178153
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Derepression of DNA damage-regulated genes requires yeast TAF(II)s.
    Li B; Reese JC
    EMBO J; 2000 Aug; 19(15):4091-100. PubMed ID: 10921889
    [TBL] [Abstract][Full Text] [Related]  

  • 11. The histone H3-like TAF is broadly required for transcription in yeast.
    Moqtaderi Z; Keaveney M; Struhl K
    Mol Cell; 1998 Nov; 2(5):675-82. PubMed ID: 9844639
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Enhancement of TBP binding by activators and general transcription factors.
    Li XY; Virbasius A; Zhu X; Green MR
    Nature; 1999 Jun; 399(6736):605-9. PubMed ID: 10376604
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Binding of TFIID to the CYC1 TATA boxes in yeast occurs independently of upstream activating sequences.
    Chen J; Ding M; Pederson DS
    Proc Natl Acad Sci U S A; 1994 Dec; 91(25):11909-13. PubMed ID: 7991556
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Broad, but not universal, transcriptional requirement for yTAFII17, a histone H3-like TAFII present in TFIID and SAGA.
    Apone LM; Virbasius CA; Holstege FC; Wang J; Young RA; Green MR
    Mol Cell; 1998 Nov; 2(5):653-61. PubMed ID: 9844637
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Isolation and characterization of TAF25, an essential yeast gene that encodes an RNA polymerase II-specific TATA-binding protein-associated factor.
    Klebanow ER; Poon D; Zhou S; Weil PA
    J Biol Chem; 1996 Jun; 271(23):13706-15. PubMed ID: 8662725
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Core promoter-specific gene regulation: TATA box selectivity and Initiator-dependent bi-directionality of serum response factor-activated transcription.
    Xu M; Gonzalez-Hurtado E; Martinez E
    Biochim Biophys Acta; 2016 Apr; 1859(4):553-63. PubMed ID: 26824723
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Core promoter-specific function of a mutant transcription factor TFIID defective in TATA-box binding.
    Martinez E; Zhou Q; L'Etoile ND; Oelgeschläger T; Berk AJ; Roeder RG
    Proc Natl Acad Sci U S A; 1995 Dec; 92(25):11864-8. PubMed ID: 8524864
    [TBL] [Abstract][Full Text] [Related]  

  • 18. DNA binding site selection by RNA polymerase II TAFs: a TAF(II)250-TAF(II)150 complex recognizes the initiator.
    Chalkley GE; Verrijzer CP
    EMBO J; 1999 Sep; 18(17):4835-45. PubMed ID: 10469661
    [TBL] [Abstract][Full Text] [Related]  

  • 19. TAF-Containing and TAF-independent forms of transcriptionally active TBP in vivo.
    Kuras L; Kosa P; Mencia M; Struhl K
    Science; 2000 May; 288(5469):1244-8. PubMed ID: 10818000
    [TBL] [Abstract][Full Text] [Related]  

  • 20. CIF, an essential cofactor for TFIID-dependent initiator function.
    Kaufmann J; Verrijzer CP; Shao J; Smale ST
    Genes Dev; 1996 Apr; 10(7):873-86. PubMed ID: 8846923
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.