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98 related items for PubMed ID: 15963504

  • 1. MafA transcription factor is phosphorylated by p38 MAP kinase.
    Sii-Felice K, Pouponnot C, Gillet S, Lecoin L, Girault JA, Eychène A, Felder-Schmittbuhl MP.
    FEBS Lett; 2005 Jul 04; 579(17):3547-54. PubMed ID: 15963504
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  • 3. Neither MafA/L-Maf nor MafB is essential for lens development in mice.
    Takeuchi T, Kudo T, Ogata K, Hamada M, Nakamura M, Kito K, Abe Y, Ueda N, Yamamoto M, Engel JD, Takahashi S.
    Genes Cells; 2009 Aug 04; 14(8):941-7. PubMed ID: 19624757
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  • 4. Differential targeting of the stress mitogen-activated protein kinases to the c-Jun dimerization protein 2.
    Katz S, Aronheim A.
    Biochem J; 2002 Dec 15; 368(Pt 3):939-45. PubMed ID: 12225289
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  • 6. Roles of Maf family proteins in lens development.
    Reza HM, Yasuda K.
    Dev Dyn; 2004 Mar 15; 229(3):440-8. PubMed ID: 14991699
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  • 8. MafA stability in pancreatic beta cells is regulated by glucose and is dependent on its constitutive phosphorylation at multiple sites by glycogen synthase kinase 3.
    Han SI, Aramata S, Yasuda K, Kataoka K.
    Mol Cell Biol; 2007 Oct 15; 27(19):6593-605. PubMed ID: 17682063
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  • 9. MafA has strong cell transforming ability but is a weak transactivator.
    Nishizawa M, Kataoka K, Vogt PK.
    Oncogene; 2003 Sep 11; 22(39):7882-90. PubMed ID: 12970735
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  • 13. Proteasome activator PA28γ stimulates degradation of GSK3-phosphorylated insulin transcription activator MAFA.
    Kanai K, Aramata S, Katakami S, Yasuda K, Kataoka K.
    J Mol Endocrinol; 2011 Aug 11; 47(1):119-127. PubMed ID: 21830322
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  • 14. The inhaled anesthetic, isoflurane, enhances Ca2+-dependent survival signaling in cortical neurons and modulates MAP kinases, apoptosis proteins and transcription factors during hypoxia.
    Bickler PE, Fahlman CS.
    Anesth Analg; 2006 Aug 11; 103(2):419-29, table of contents. PubMed ID: 16861427
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  • 15. Diosgenin induces hypoxia-inducible factor-1 activation and angiogenesis through estrogen receptor-related phosphatidylinositol 3-kinase/Akt and p38 mitogen-activated protein kinase pathways in osteoblasts.
    Yen ML, Su JL, Chien CL, Tseng KW, Yang CY, Chen WF, Chang CC, Kuo ML.
    Mol Pharmacol; 2005 Oct 11; 68(4):1061-73. PubMed ID: 15998873
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  • 16. Extracellular signal-regulated kinase 1 interacts with and phosphorylates CdGAP at an important regulatory site.
    Tcherkezian J, Danek EI, Jenna S, Triki I, Lamarche-Vane N.
    Mol Cell Biol; 2005 Aug 11; 25(15):6314-29. PubMed ID: 16024771
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  • 17. Self-activation of serine/threonine kinase AfsK on autophosphorylation at threonine-168.
    Tomono A, Mashiko M, Shimazu T, Inoue H, Nagasawa H, Yoshida M, Ohnishi Y, Horinouchi S.
    J Antibiot (Tokyo); 2006 Feb 11; 59(2):117-23. PubMed ID: 16629414
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  • 18. The 5'-AT-rich half-site of Maf recognition element: a functional target for bZIP transcription factor Maf.
    Yoshida T, Ohkumo T, Ishibashi S, Yasuda K.
    Nucleic Acids Res; 2005 Feb 11; 33(11):3465-78. PubMed ID: 15972792
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  • 19. Novel MAF mutation in a family with congenital cataract-microcornea syndrome.
    Hansen L, Eiberg H, Rosenberg T.
    Mol Vis; 2007 Oct 18; 13():2019-22. PubMed ID: 17982426
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  • 20. GSK-3-mediated phosphorylation enhances Maf-transforming activity.
    Rocques N, Abou Zeid N, Sii-Felice K, Lecoin L, Felder-Schmittbuhl MP, Eychène A, Pouponnot C.
    Mol Cell; 2007 Nov 30; 28(4):584-97. PubMed ID: 18042454
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