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Journal Abstract Search

562 related items for PubMed ID: 7523245

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  • 5. Roles of p300, pocket proteins, and hTBP in E1A-mediated transcriptional regulation and inhibition of p53 transactivation activity.
    Sang N, Avantaggiati ML, Giordano A.
    J Cell Biochem; 1997 Sep 01; 66(3):277-85. PubMed ID: 9257185
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  • 7. Cell cycle-mediated regulation of smooth muscle alpha-actin gene transcription in fibroblasts and vascular smooth muscle cells involves multiple adenovirus E1A-interacting cofactors.
    Wang SX, Elder PK, Zheng Y, Strauch AR, Kelm RJ.
    J Biol Chem; 2005 Feb 18; 280(7):6204-14. PubMed ID: 15576380
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  • 8. Differential interactions of the CREB/ATF family of transcription factors with p300 and adenovirus E1A.
    Lee JS, Zhang X, Shi Y.
    J Biol Chem; 1996 Jul 26; 271(30):17666-74. PubMed ID: 8663457
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  • 14. Insulin gene transcription is mediated by interactions between the p300 coactivator and PDX-1, BETA2, and E47.
    Qiu Y, Guo M, Huang S, Stein R.
    Mol Cell Biol; 2002 Jan 26; 22(2):412-20. PubMed ID: 11756538
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  • 16. Adenoviral E1A-associated protein p300 as a functional homologue of the transcriptional co-activator CBP.
    Lundblad JR, Kwok RP, Laurance ME, Harter ML, Goodman RH.
    Nature; 1995 Mar 02; 374(6517):85-8. PubMed ID: 7870179
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  • 17. Adenovirus E1A N-terminal amino acid sequence requirements for repression of transcription in vitro and in vivo correlate with those required for E1A interference with TBP-TATA complex formation.
    Boyd JM, Loewenstein PM, Tang Qq QQ, Yu L, Green M.
    J Virol; 2002 Feb 02; 76(3):1461-74. PubMed ID: 11773419
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  • 20. Binding of p300/CBP co-activators by polyoma large T antigen.
    Cho S, Tian Y, Benjamin TL.
    J Biol Chem; 2001 Sep 07; 276(36):33533-9. PubMed ID: 11438528
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