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Journal Abstract Search
544 related items for PubMed ID: 10864329
1. Redundant roles for the TFIID and SAGA complexes in global transcription. Lee TI, Causton HC, Holstege FC, Shen WC, Hannett N, Jennings EG, Winston F, Green MR, Young RA. Nature; 2000 Jun 08; 405(6787):701-4. PubMed ID: 10864329 [Abstract] [Full Text] [Related]
2. A histone fold TAF octamer within the yeast TFIID transcriptional coactivator. Selleck W, Howley R, Fang Q, Podolny V, Fried MG, Buratowski S, Tan S. Nat Struct Biol; 2001 Aug 08; 8(8):695-700. PubMed ID: 11473260 [Abstract] [Full Text] [Related]
8. Adenovirus E1A requires the yeast SAGA histone acetyltransferase complex and associates with SAGA components Gcn5 and Tra1. Kulesza CA, Van Buskirk HA, Cole MD, Reese JC, Smith MM, Engel DA. Oncogene; 2002 Feb 21; 21(9):1411-22. PubMed ID: 11857084 [Abstract] [Full Text] [Related]
9. 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 21; 25(13):5626-38. PubMed ID: 15964818 [Abstract] [Full Text] [Related]
10. SAGA is an essential in vivo target of the yeast acidic activator Gal4p. Bhaumik SR, Green MR. Genes Dev; 2001 Aug 01; 15(15):1935-45. PubMed ID: 11485988 [Abstract] [Full Text] [Related]
11. Analysis of TAF90 mutants displaying allele-specific and broad defects in transcription. Durso RJ, Fisher AK, Albright-Frey TJ, Reese JC. Mol Cell Biol; 2001 Nov 01; 21(21):7331-44. PubMed ID: 11585915 [Abstract] [Full Text] [Related]
12. In-depth profiling of post-translational modifications on the related transcription factor complexes TFIID and SAGA. Mischerikow N, Spedale G, Altelaar AF, Timmers HT, Pijnappel WW, Heck AJ. J Proteome Res; 2009 Nov 01; 8(11):5020-30. PubMed ID: 19731963 [Abstract] [Full Text] [Related]
13. TFIID and Spt-Ada-Gcn5-acetyltransferase functions probed by genome-wide synthetic genetic array analysis using a Saccharomyces cerevisiae taf9-ts allele. Milgrom E, West RW, Gao C, Shen WC. Genetics; 2005 Nov 01; 171(3):959-73. PubMed ID: 16118188 [Abstract] [Full Text] [Related]
14. Distinct requirements for C.elegans TAF(II)s in early embryonic transcription. Walker AK, Rothman JH, Shi Y, Blackwell TK. EMBO J; 2001 Sep 17; 20(18):5269-79. PubMed ID: 11566890 [Abstract] [Full Text] [Related]
15. Differential requirement of SAGA subunits for Mot1p and Taf1p recruitment in gene activation. van Oevelen CJ, van Teeffelen HA, Timmers HT. Mol Cell Biol; 2005 Jun 17; 25(12):4863-72. PubMed ID: 15923605 [Abstract] [Full Text] [Related]
16. A subset of TAF(II)s are integral components of the SAGA complex required for nucleosome acetylation and transcriptional stimulation. Grant PA, Schieltz D, Pray-Grant MG, Steger DJ, Reese JC, Yates JR, Workman JL. Cell; 1998 Jul 10; 94(1):45-53. PubMed ID: 9674426 [Abstract] [Full Text] [Related]
17. TAF9b (formerly TAF9L) is a bona fide TAF that has unique and overlapping roles with TAF9. Frontini M, Soutoglou E, Argentini M, Bole-Feysot C, Jost B, Scheer E, Tora L. Mol Cell Biol; 2005 Jun 10; 25(11):4638-49. PubMed ID: 15899866 [Abstract] [Full Text] [Related]
18. 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 10; 2(5):653-61. PubMed ID: 9844637 [Abstract] [Full Text] [Related]
19. Analysis of selective gene activation in yeast by differential display. Shen WC, Green MR. Methods; 1998 Dec 10; 16(4):415-22. PubMed ID: 10049649 [Abstract] [Full Text] [Related]
20. Molecular architecture of the S. cerevisiae SAGA complex. Wu PY, Ruhlmann C, Winston F, Schultz P. Mol Cell; 2004 Jul 23; 15(2):199-208. PubMed ID: 15260971 [Abstract] [Full Text] [Related] Page: [Next] [New Search]