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96 related items for PubMed ID: 15937931

  • 1. GCN5 and p300 share essential functions during early embryogenesis.
    Phan HM, Xu AW, Coco C, Srajer G, Wyszomierski S, Evrard YA, Eckner R, Dent SY.
    Dev Dyn; 2005 Aug; 233(4):1337-47. PubMed ID: 15937931
    [Abstract] [Full Text] [Related]

  • 2. Developmental potential of Gcn5(-/-) embryonic stem cells in vivo and in vitro.
    Lin W, Srajer G, Evrard YA, Phan HM, Furuta Y, Dent SY.
    Dev Dyn; 2007 Jun; 236(6):1547-57. PubMed ID: 17440986
    [Abstract] [Full Text] [Related]

  • 3. Distinct but overlapping roles of histone acetylase PCAF and of the closely related PCAF-B/GCN5 in mouse embryogenesis.
    Yamauchi T, Yamauchi J, Kuwata T, Tamura T, Yamashita T, Bae N, Westphal H, Ozato K, Nakatani Y.
    Proc Natl Acad Sci U S A; 2000 Oct 10; 97(21):11303-6. PubMed ID: 11027331
    [Abstract] [Full Text] [Related]

  • 4. Loss of Gcn5l2 leads to increased apoptosis and mesodermal defects during mouse development.
    Xu W, Edmondson DG, Evrard YA, Wakamiya M, Behringer RR, Roth SY.
    Nat Genet; 2000 Oct 10; 26(2):229-32. PubMed ID: 11017084
    [Abstract] [Full Text] [Related]

  • 5. GCN5: a supervisor in all-inclusive control of vertebrate cell cycle progression through transcription regulation of various cell cycle-related genes.
    Kikuchi H, Takami Y, Nakayama T.
    Gene; 2005 Feb 28; 347(1):83-97. PubMed ID: 15715965
    [Abstract] [Full Text] [Related]

  • 6. Expression of PCAF, p300 and Gcn5 and more highly acetylated histone H4 in pediatric tumors.
    Armas-Pineda C, Arenas-Huertero F, Pérezpeñia-Diazconti M, Chico-Ponce de León F, Sosa-Sáinz G, Lezama P, Recillas-Targa F.
    J Exp Clin Cancer Res; 2007 Jun 28; 26(2):269-76. PubMed ID: 17725108
    [Abstract] [Full Text] [Related]

  • 7. Roles of HIPK1 and HIPK2 in AML1- and p300-dependent transcription, hematopoiesis and blood vessel formation.
    Aikawa Y, Nguyen LA, Isono K, Takakura N, Tagata Y, Schmitz ML, Koseki H, Kitabayashi I.
    EMBO J; 2006 Sep 06; 25(17):3955-65. PubMed ID: 16917507
    [Abstract] [Full Text] [Related]

  • 8. Loss of Gcn5 acetyltransferase activity leads to neural tube closure defects and exencephaly in mouse embryos.
    Bu P, Evrard YA, Lozano G, Dent SY.
    Mol Cell Biol; 2007 May 06; 27(9):3405-16. PubMed ID: 17325035
    [Abstract] [Full Text] [Related]

  • 9. Critical loss of CBP/p300 histone acetylase activity by caspase-6 during neurodegeneration.
    Rouaux C, Jokic N, Mbebi C, Boutillier S, Loeffler JP, Boutillier AL.
    EMBO J; 2003 Dec 15; 22(24):6537-49. PubMed ID: 14657026
    [Abstract] [Full Text] [Related]

  • 10. Distinct GCN5/PCAF-containing complexes function as co-activators and are involved in transcription factor and global histone acetylation.
    Nagy Z, Tora L.
    Oncogene; 2007 Aug 13; 26(37):5341-57. PubMed ID: 17694077
    [Abstract] [Full Text] [Related]

  • 11. Histone acetyltransferase activity of p300 is required for the promotion of left ventricular remodeling after myocardial infarction in adult mice in vivo.
    Miyamoto S, Kawamura T, Morimoto T, Ono K, Wada H, Kawase Y, Matsumori A, Nishio R, Kita T, Hasegawa K.
    Circulation; 2006 Feb 07; 113(5):679-90. PubMed ID: 16461841
    [Abstract] [Full Text] [Related]

  • 12. Bromodomain and histone acetyltransferase domain specificities control mixed lineage leukemia phenotype.
    Santillan DA, Theisler CM, Ryan AS, Popovic R, Stuart T, Zhou MM, Alkan S, Zeleznik-Le NJ.
    Cancer Res; 2006 Oct 15; 66(20):10032-9. PubMed ID: 17047066
    [Abstract] [Full Text] [Related]

  • 13. [Constructions of Gcn5 shRNAs interfere the histone acetylation modification with stem cell differentiation].
    Zhu J, Wang YX, Zhang XP, Wang JJ, Zhang XF, Tian J.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2006 Feb 15; 23(1):43-6. PubMed ID: 16456784
    [Abstract] [Full Text] [Related]

  • 14. Alteration of working memory but not in anxiety or stress response in p300/CBP associated factor (PCAF) histone acetylase knockout mice bred on a C57BL/6 background.
    Duclot F, Jacquet C, Gongora C, Maurice T.
    Neurosci Lett; 2010 May 21; 475(3):179-83. PubMed ID: 20371377
    [Abstract] [Full Text] [Related]

  • 15. Histone acetyltransferase p300 regulates the transcription of human erythroid-specific 5-aminolevulinate synthase gene.
    Han L, Lu J, Pan L, Wang X, Shao Y, Han S, Huang B.
    Biochem Biophys Res Commun; 2006 Sep 29; 348(3):799-806. PubMed ID: 16904069
    [Abstract] [Full Text] [Related]

  • 16. Distinct roles of GCN5/PCAF-mediated H3K9ac and CBP/p300-mediated H3K18/27ac in nuclear receptor transactivation.
    Jin Q, Yu LR, Wang L, Zhang Z, Kasper LH, Lee JE, Wang C, Brindle PK, Dent SY, Ge K.
    EMBO J; 2011 Jan 19; 30(2):249-62. PubMed ID: 21131905
    [Abstract] [Full Text] [Related]

  • 17. Regulation of histone acetyltransferase activity of p300 and PCAF by proto-oncogene protein DEK.
    Ko SI, Lee IS, Kim JY, Kim SM, Kim DW, Lee KS, Woo KM, Baek JH, Choo JK, Seo SB.
    FEBS Lett; 2006 May 29; 580(13):3217-22. PubMed ID: 16696975
    [Abstract] [Full Text] [Related]

  • 18. Fluorescence analysis of a dynamic loop in the PCAF/GCN5 histone acetyltransferase.
    Zheng Y, Mamdani F, Toptygin D, Brand L, Stivers JT, Cole PA.
    Biochemistry; 2005 Aug 09; 44(31):10501-9. PubMed ID: 16060659
    [Abstract] [Full Text] [Related]

  • 19. Proper Gcn5 histone acetyltransferase expression is required for normal anteroposterior patterning of the mouse skeleton.
    Lin W, Zhang Z, Chen CH, Behringer RR, Dent SY.
    Dev Growth Differ; 2008 Jun 09; 50(5):321-30. PubMed ID: 18430026
    [Abstract] [Full Text] [Related]

  • 20. Transcriptional coactivator p300/CBP-associated factor and p300/CBP-associated factor type B are required for normal estrogen response of the mouse uterus.
    Inoue E, Hanai M, Yamada K, Esashi T, Yamauchi J.
    Biosci Biotechnol Biochem; 2004 Oct 09; 68(10):2209-11. PubMed ID: 15502373
    [Abstract] [Full Text] [Related]


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