87 related articles for article (PubMed ID: 10708567)
1. p300/CBP acts as a coactivator of the cone-rod homeobox transcription factor.
Yanagi Y; Masuhiro Y; Mori M; Yanagisawa J; Kato S
Biochem Biophys Res Commun; 2000 Mar; 269(2):410-4. PubMed ID: 10708567
[TBL] [Abstract][Full Text] [Related]
2. P300/CBP acts as a coactivator to cartilage homeoprotein-1 (Cart1), paired-like homeoprotein, through acetylation of the conserved lysine residue adjacent to the homeodomain.
Iioka T; Furukawa K; Yamaguchi A; Shindo H; Yamashita S; Tsukazaki T
J Bone Miner Res; 2003 Aug; 18(8):1419-29. PubMed ID: 12929931
[TBL] [Abstract][Full Text] [Related]
3. Transcription coactivators p300 and CBP are necessary for photoreceptor-specific chromatin organization and gene expression.
Hennig AK; Peng GH; Chen S
PLoS One; 2013; 8(7):e69721. PubMed ID: 23922782
[TBL] [Abstract][Full Text] [Related]
4. Crx activates opsin transcription by recruiting HAT-containing co-activators and promoting histone acetylation.
Peng GH; Chen S
Hum Mol Genet; 2007 Oct; 16(20):2433-52. PubMed ID: 17656371
[TBL] [Abstract][Full Text] [Related]
5. Barrier to autointegration factor interacts with the cone-rod homeobox and represses its transactivation function.
Wang X; Xu S; Rivolta C; Li LY; Peng GH; Swain PK; Sung CH; Swaroop A; Berson EL; Dryja TP; Chen S
J Biol Chem; 2002 Nov; 277(45):43288-300. PubMed ID: 12215455
[TBL] [Abstract][Full Text] [Related]
6. The photoreceptor-specific nuclear receptor Nr2e3 interacts with Crx and exerts opposing effects on the transcription of rod versus cone genes.
Peng GH; Ahmad O; Ahmad F; Liu J; Chen S
Hum Mol Genet; 2005 Mar; 14(6):747-64. PubMed ID: 15689355
[TBL] [Abstract][Full Text] [Related]
7. FIZ1 is part of the regulatory protein complex on active photoreceptor-specific gene promoters in vivo.
Mali RS; Peng GH; Zhang X; Dang L; Chen S; Mitton KP
BMC Mol Biol; 2008 Oct; 9():87. PubMed ID: 18854042
[TBL] [Abstract][Full Text] [Related]
8. The nuclear receptor coactivators p300/CBP/cointegrator-associated protein (p/CIP) and transcription intermediary factor 2 (TIF2) differentially regulate PKA-stimulated transcriptional activity of steroidogenic factor 1.
Børud B; Hoang T; Bakke M; Jacob AL; Lund J; Mellgren G
Mol Endocrinol; 2002 Apr; 16(4):757-73. PubMed ID: 11923473
[TBL] [Abstract][Full Text] [Related]
9. p300/CBP is required for transcriptional induction by interleukin-4 and interacts with Stat6.
Gingras S; Simard J; Groner B; Pfitzner E
Nucleic Acids Res; 1999 Jul; 27(13):2722-9. PubMed ID: 10373589
[TBL] [Abstract][Full Text] [Related]
10. p300/CREB-binding protein enhances the prolactin-mediated transcriptional induction through direct interaction with the transactivation domain of Stat5, but does not participate in the Stat5-mediated suppression of the glucocorticoid response.
Pfitzner E; Jähne R; Wissler M; Stoecklin E; Groner B
Mol Endocrinol; 1998 Oct; 12(10):1582-93. PubMed ID: 9773981
[TBL] [Abstract][Full Text] [Related]
11. Interference of Crx-dependent transcription by ataxin-7 involves interaction between the glutamine regions and requires the ataxin-7 carboxy-terminal region for nuclear localization.
Chen S; Peng GH; Wang X; Smith AC; Grote SK; Sopher BL; La Spada AR
Hum Mol Genet; 2004 Jan; 13(1):53-67. PubMed ID: 14613968
[TBL] [Abstract][Full Text] [Related]
12. CRX controls retinal expression of the X-linked juvenile retinoschisis (RS1) gene.
Langmann T; Lai CC; Weigelt K; Tam BM; Warneke-Wittstock R; Moritz OL; Weber BH
Nucleic Acids Res; 2008 Nov; 36(20):6523-34. PubMed ID: 18927113
[TBL] [Abstract][Full Text] [Related]
13. The steroid receptor co-activator-1 (SRC-1) potentiates TGF-beta/Smad signaling: role of p300/CBP.
Dennler S; Pendaries V; Tacheau C; Costas MA; Mauviel A; Verrecchia F
Oncogene; 2005 Mar; 24(11):1936-45. PubMed ID: 15688032
[TBL] [Abstract][Full Text] [Related]
14. Modulation of CRX transactivation activity by phosducin isoforms.
Zhu X; Craft CM
Mol Cell Biol; 2000 Jul; 20(14):5216-26. PubMed ID: 10866677
[TBL] [Abstract][Full Text] [Related]
15. Synergism between p68 RNA helicase and the transcriptional coactivators CBP and p300.
Rossow KL; Janknecht R
Oncogene; 2003 Jan; 22(1):151-6. PubMed ID: 12527917
[TBL] [Abstract][Full Text] [Related]
16. Smad-dependent stimulation of type I collagen gene expression in human skin fibroblasts by TGF-beta involves functional cooperation with p300/CBP transcriptional coactivators.
Ghosh AK; Yuan W; Mori Y; Varga J
Oncogene; 2000 Jul; 19(31):3546-55. PubMed ID: 10918613
[TBL] [Abstract][Full Text] [Related]
17. Interaction and functional cooperation between the LIM protein FHL2, CBP/p300, and beta-catenin.
Labalette C; Renard CA; Neuveut C; Buendia MA; Wei Y
Mol Cell Biol; 2004 Dec; 24(24):10689-702. PubMed ID: 15572674
[TBL] [Abstract][Full Text] [Related]
18. Human homologue of yeast Rad23 protein A interacts with p300/cyclic AMP-responsive element binding (CREB)-binding protein to down-regulate transcriptional activity of p53.
Zhu Q; Wani G; Wani MA; Wani AA
Cancer Res; 2001 Jan; 61(1):64-70. PubMed ID: 11196199
[TBL] [Abstract][Full Text] [Related]
19. Murine double minute (MDM2) blocks p53-coactivator interaction, a new mechanism for inhibition of p53-dependent gene expression.
Wadgaonkar R; Collins T
J Biol Chem; 1999 May; 274(20):13760-7. PubMed ID: 10318779
[TBL] [Abstract][Full Text] [Related]
20. The oncoprotein Tax binds the SRC-1-interacting domain of CBP/p300 to mediate transcriptional activation.
Scoggin KE; Ulloa A; Nyborg JK
Mol Cell Biol; 2001 Aug; 21(16):5520-30. PubMed ID: 11463834
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]