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202 related items for PubMed ID: 10942429

  • 1. A Pro250Arg substitution in mouse Fgfr1 causes increased expression of Cbfa1 and premature fusion of calvarial sutures.
    Zhou YX, Xu X, Chen L, Li C, Brodie SG, Deng CX.
    Hum Mol Genet; 2000 Aug 12; 9(13):2001-8. PubMed ID: 10942429
    [Abstract] [Full Text] [Related]

  • 2. P253R fibroblast growth factor receptor-2 mutation induces RUNX2 transcript variants and calvarial osteoblast differentiation.
    Baroni T, Carinci P, Lilli C, Bellucci C, Aisa MC, Scapoli L, Volinia S, Carinci F, Pezzetti F, Calvitti M, Farina A, Conte C, Bodo M.
    J Cell Physiol; 2005 Feb 12; 202(2):524-35. PubMed ID: 15389579
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  • 3. 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
    [Abstract] [Full Text] [Related]

  • 4. Molecular mechanisms in calvarial bone and suture development, and their relation to craniosynostosis.
    Rice DP, Rice R, Thesleff I.
    Eur J Orthod; 2003 Apr 12; 25(2):139-48. PubMed ID: 12737212
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  • 5. Increased expression of protein kinase Calpha, interleukin-1alpha, and RhoA guanosine 5'-triphosphatase in osteoblasts expressing the Ser252Trp fibroblast growth factor 2 receptor Apert mutation: identification by analysis of complementary DNA microarray.
    Lomri A, Lemonnier J, Delannoy P, Marie PJ.
    J Bone Miner Res; 2001 Apr 12; 16(4):705-12. PubMed ID: 11315998
    [Abstract] [Full Text] [Related]

  • 6. TWIST inactivation reduces CBFA1/RUNX2 expression and DNA binding to the osteocalcin promoter in osteoblasts.
    Yousfi M, Lasmoles F, Marie PJ.
    Biochem Biophys Res Commun; 2002 Sep 27; 297(3):641-4. PubMed ID: 12270142
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  • 7. Proline to arginine mutations in FGF receptors 1 and 3 result in Pfeiffer and Muenke craniosynostosis syndromes through enhancement of FGF binding affinity.
    Ibrahimi OA, Zhang F, Eliseenkova AV, Linhardt RJ, Mohammadi M.
    Hum Mol Genet; 2004 Jan 01; 13(1):69-78. PubMed ID: 14613973
    [Abstract] [Full Text] [Related]

  • 8. Integration of FGF and TWIST in calvarial bone and suture development.
    Rice DP, Aberg T, Chan Y, Tang Z, Kettunen PJ, Pakarinen L, Maxson RE, Thesleff I.
    Development; 2000 May 01; 127(9):1845-55. PubMed ID: 10751173
    [Abstract] [Full Text] [Related]

  • 9. A Ser252Trp [corrected] substitution in mouse fibroblast growth factor receptor 2 (Fgfr2) results in craniosynostosis.
    Chen L, Li D, Li C, Engel A, Deng CX.
    Bone; 2003 Aug 01; 33(2):169-78. PubMed ID: 14499350
    [Abstract] [Full Text] [Related]

  • 10. Negative autoregulation of fibroblast growth factor receptor 2 expression characterizing cranial development in cases of Apert (P253R mutation) and Pfeiffer (C278F mutation) syndromes and suggesting a basis for differences in their cranial phenotypes.
    Britto JA, Moore RL, Evans RD, Hayward RD, Jones BM.
    J Neurosurg; 2001 Oct 01; 95(4):660-73. PubMed ID: 11596961
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  • 14. Identical mutations in the FGFR2 gene cause both Pfeiffer and Crouzon syndrome phenotypes.
    Rutland P, Pulleyn LJ, Reardon W, Baraitser M, Hayward R, Jones B, Malcolm S, Winter RM, Oldridge M, Slaney SF.
    Nat Genet; 1995 Feb 01; 9(2):173-6. PubMed ID: 7719345
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  • 15. Apert syndrome mutations in fibroblast growth factor receptor 2 exhibit increased affinity for FGF ligand.
    Anderson J, Burns HD, Enriquez-Harris P, Wilkie AO, Heath JK.
    Hum Mol Genet; 1998 Sep 01; 7(9):1475-83. PubMed ID: 9700203
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  • 16. Identical mutations in three different fibroblast growth factor receptor genes in autosomal dominant craniosynostosis syndromes.
    Bellus GA, Gaudenz K, Zackai EH, Clarke LA, Szabo J, Francomano CA, Muenke M.
    Nat Genet; 1996 Oct 01; 14(2):174-6. PubMed ID: 8841188
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  • 17. The appearance of the feet in Pfeiffer syndrome caused by FGFR1 P252R mutation.
    Rossi M, Jones RL, Norbury G, Bloch-Zupan A, Winter RM.
    Clin Dysmorphol; 2003 Oct 01; 12(4):269-74. PubMed ID: 14564217
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  • 18. Analysis of the mutational spectrum of the FGFR2 gene in Pfeiffer syndrome.
    Cornejo-Roldan LR, Roessler E, Muenke M.
    Hum Genet; 1999 May 01; 104(5):425-31. PubMed ID: 10394936
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  • 20. Thyroid hormone activates fibroblast growth factor receptor-1 in bone.
    Stevens DA, Harvey CB, Scott AJ, O'Shea PJ, Barnard JC, Williams AJ, Brady G, Samarut J, Chassande O, Williams GR.
    Mol Endocrinol; 2003 Sep 01; 17(9):1751-66. PubMed ID: 12805413
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