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Journal Abstract Search

239 related items for PubMed ID: 11315998

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  • 3. Role of N-cadherin and protein kinase C in osteoblast gene activation induced by the S252W fibroblast growth factor receptor 2 mutation in Apert craniosynostosis.
    Lemonnier J, Haÿ E, Delannoy P, Lomri A, Modrowski D, Caverzasio J, Marie PJ.
    J Bone Miner Res; 2001 May; 16(5):832-45. PubMed ID: 11341328
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  • 4. Increased osteoblast apoptosis in apert craniosynostosis: role of protein kinase C and interleukin-1.
    Lemonnier J, Haÿ E, Delannoy P, Fromigué O, Lomri A, Modrowski D, Marie PJ.
    Am J Pathol; 2001 May; 158(5):1833-42. PubMed ID: 11337381
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  • 6. Mitogen-activated protein (MAP) kinases are involved in interleukin-1 (IL-1)-induced IL-6 synthesis in osteoblasts: modulation not of p38 MAP kinase, but of p42/p44 MAP kinase by IL-1-activated protein kinase C.
    Miwa M, Kozawa O, Tokuda H, Uematsu T.
    Endocrinology; 1999 Nov; 140(11):5120-5. PubMed ID: 10537140
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  • 7. Protein kinase calpha but not p44/42 mitogen-activated protein kinase, p38, or c-Jun NH(2)-terminal kinase is required for intercellular adhesion molecule-1 expression mediated by interleukin-1beta: involvement of sequential activation of tyrosine kinase, nuclear factor-kappaB-inducing kinase, and IkappaB kinase 2.
    Chen CC, Chen JJ, Chou CY.
    Mol Pharmacol; 2000 Dec; 58(6):1479-89. PubMed ID: 11093788
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  • 8. Apert syndrome mutant FGFR2 and its soluble form reciprocally alter osteogenesis of primary calvarial osteoblasts.
    Suzuki H, Suda N, Shiga M, Kobayashi Y, Nakamura M, Iseki S, Moriyama K.
    J Cell Physiol; 2012 Sep; 227(9):3267-77. PubMed ID: 22105374
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  • 9. Increased EFG- and PDGFalpha-receptor signaling by mutant FGF-receptor 2 contributes to osteoblast dysfunction in Apert craniosynostosis.
    Miraoui H, Ringe J, Häupl T, Marie PJ.
    Hum Mol Genet; 2010 May 01; 19(9):1678-89. PubMed ID: 20124286
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  • 11. Induction of VEGF gene transcription by IL-1 beta is mediated through stress-activated MAP kinases and Sp1 sites in cardiac myocytes.
    Tanaka T, Kanai H, Sekiguchi K, Aihara Y, Yokoyama T, Arai M, Kanda T, Nagai R, Kurabayashi M.
    J Mol Cell Cardiol; 2000 Nov 01; 32(11):1955-67. PubMed ID: 11040101
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  • 12. Signaling by fibroblast growth factors (FGF) and fibroblast growth factor receptor 2 (FGFR2)-activating mutations blocks mineralization and induces apoptosis in osteoblasts.
    Mansukhani A, Bellosta P, Sahni M, Basilico C.
    J Cell Biol; 2000 Jun 12; 149(6):1297-308. PubMed ID: 10851026
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  • 17. A Pro253Arg mutation in fibroblast growth factor receptor 2 (Fgfr2) causes skeleton malformation mimicking human Apert syndrome by affecting both chondrogenesis and osteogenesis.
    Yin L, Du X, Li C, Xu X, Chen Z, Su N, Zhao L, Qi H, Li F, Xue J, Yang J, Jin M, Deng C, Chen L.
    Bone; 2008 Apr 12; 42(4):631-43. PubMed ID: 18242159
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  • 18. Signal transduction system for interleukin-6 synthesis stimulated by lipopolysaccharide in human osteoblasts.
    Kondo A, Koshihara Y, Togari A.
    J Interferon Cytokine Res; 2001 Nov 12; 21(11):943-50. PubMed ID: 11747626
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  • 20. Involvement of AP-1 in interleukin-1alpha-stimulated MMP-3 expression in human trabecular meshwork cells.
    Fleenor DL, Pang IH, Clark AF.
    Invest Ophthalmol Vis Sci; 2003 Aug 12; 44(8):3494-501. PubMed ID: 12882799
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