BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

294 related articles for article (PubMed ID: 14612422)

  • 41. Histone acetyltransferase complexes stabilize swi/snf binding to promoter nucleosomes.
    Hassan AH; Neely KE; Workman JL
    Cell; 2001 Mar; 104(6):817-27. PubMed ID: 11290320
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Histone H2A.Z regulats transcription and is partially redundant with nucleosome remodeling complexes.
    Santisteban MS; Kalashnikova T; Smith MM
    Cell; 2000 Oct; 103(3):411-22. PubMed ID: 11081628
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Targeting activity is required for SWI/SNF function in vivo and is accomplished through two partially redundant activator-interaction domains.
    Prochasson P; Neely KE; Hassan AH; Li B; Workman JL
    Mol Cell; 2003 Oct; 12(4):983-90. PubMed ID: 14580348
    [TBL] [Abstract][Full Text] [Related]  

  • 44. The nucleosome remodeling complex, Snf/Swi, is required for the maintenance of transcription in vivo and is partially redundant with the histone acetyltransferase, Gcn5.
    Sudarsanam P; Cao Y; Wu L; Laurent BC; Winston F
    EMBO J; 1999 Jun; 18(11):3101-6. PubMed ID: 10357821
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Subunits of the yeast SWI/SNF complex are members of the actin-related protein (ARP) family.
    Peterson CL; Zhao Y; Chait BT
    J Biol Chem; 1998 Sep; 273(37):23641-4. PubMed ID: 9726966
    [TBL] [Abstract][Full Text] [Related]  

  • 46. 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]  

  • 47. SWI/SNF and RSC cooperate to reposition and evict promoter nucleosomes at highly expressed genes in yeast.
    Rawal Y; Chereji RV; Qiu H; Ananthakrishnan S; Govind CK; Clark DJ; Hinnebusch AG
    Genes Dev; 2018 May; 32(9-10):695-710. PubMed ID: 29785963
    [TBL] [Abstract][Full Text] [Related]  

  • 48. Catalytic activity of the yeast SWI/SNF complex on reconstituted nucleosome arrays.
    Logie C; Peterson CL
    EMBO J; 1997 Nov; 16(22):6772-82. PubMed ID: 9362491
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Mutations in both the structured domain and N-terminus of histone H2B bypass the requirement for Swi-Snf in yeast.
    Recht J; Osley MA
    EMBO J; 1999 Jan; 18(1):229-40. PubMed ID: 9878065
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Global role for chromatin remodeling enzymes in mitotic gene expression.
    Krebs JE; Fry CJ; Samuels ML; Peterson CL
    Cell; 2000 Sep; 102(5):587-98. PubMed ID: 11007477
    [TBL] [Abstract][Full Text] [Related]  

  • 51. The S. cerevisiae SAGA complex functions in vivo as a coactivator for transcriptional activation by Gal4.
    Larschan E; Winston F
    Genes Dev; 2001 Aug; 15(15):1946-56. PubMed ID: 11485989
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Sth1p, a Saccharomyces cerevisiae Snf2p/Swi2p homolog, is an essential ATPase in RSC and differs from Snf/Swi in its interactions with histones and chromatin-associated proteins.
    Du J; Nasir I; Benton BK; Kladde MP; Laurent BC
    Genetics; 1998 Nov; 150(3):987-1005. PubMed ID: 9799253
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Swi/Snf dynamics on stress-responsive genes is governed by competitive bromodomain interactions.
    Dutta A; Gogol M; Kim JH; Smolle M; Venkatesh S; Gilmore J; Florens L; Washburn MP; Workman JL
    Genes Dev; 2014 Oct; 28(20):2314-30. PubMed ID: 25319830
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Proteomic analysis demonstrates activator- and chromatin-specific recruitment to promoters.
    Sikorski TW; Joo YJ; Ficarro SB; Askenazi M; Buratowski S; Marto JA
    J Biol Chem; 2012 Oct; 287(42):35397-35408. PubMed ID: 22902623
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Activation domain-mediated targeting of the SWI/SNF complex to promoters stimulates transcription from nucleosome arrays.
    Neely KE; Hassan AH; Wallberg AE; Steger DJ; Cairns BR; Wright AP; Workman JL
    Mol Cell; 1999 Oct; 4(4):649-55. PubMed ID: 10549297
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Artificial recruitment of mediator by the DNA-binding domain of Adr1 overcomes glucose repression of ADH2 expression.
    Young ET; Tachibana C; Chang HW; Dombek KM; Arms EM; Biddick R
    Mol Cell Biol; 2008 Apr; 28(8):2509-16. PubMed ID: 18250152
    [TBL] [Abstract][Full Text] [Related]  

  • 57. The interactions of yeast SWI/SNF and RSC with the nucleosome before and after chromatin remodeling.
    Sengupta SM; VanKanegan M; Persinger J; Logie C; Cairns BR; Peterson CL; Bartholomew B
    J Biol Chem; 2001 Apr; 276(16):12636-44. PubMed ID: 11304548
    [TBL] [Abstract][Full Text] [Related]  

  • 58. Histone H3 tail acetylation modulates ATP-dependent remodeling through multiple mechanisms.
    Chatterjee N; Sinha D; Lemma-Dechassa M; Tan S; Shogren-Knaak MA; Bartholomew B
    Nucleic Acids Res; 2011 Oct; 39(19):8378-91. PubMed ID: 21749977
    [TBL] [Abstract][Full Text] [Related]  

  • 59. The Swi/Snf complex is important for histone eviction during transcriptional activation and RNA polymerase II elongation in vivo.
    Schwabish MA; Struhl K
    Mol Cell Biol; 2007 Oct; 27(20):6987-95. PubMed ID: 17709398
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Analysis of a mutant histone H3 that perturbs the association of Swi/Snf with chromatin.
    Duina AA; Winston F
    Mol Cell Biol; 2004 Jan; 24(2):561-72. PubMed ID: 14701730
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 15.