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Journal Abstract Search

285 related items for PubMed ID: 18391499

  • 1. Roles of FGFR2 and twist in human craniosynostosis: insights from genetic mutations in cranial osteoblasts.
    Marie PJ, Kaabeche K, Guenou H.
    Front Oral Biol; 2008; 12():144-159. PubMed ID: 18391499
    [Abstract] [Full Text] [Related]

  • 2. A role for fibroblast growth factor receptor-2 in the altered osteoblast phenotype induced by Twist haploinsufficiency in the Saethre-Chotzen syndrome.
    Guenou H, Kaabeche K, Mée SL, Marie PJ.
    Hum Mol Genet; 2005 Jun 01; 14(11):1429-39. PubMed ID: 15829502
    [Abstract] [Full Text] [Related]

  • 3. [Clinical and genetic characteristics of craniosynostosis].
    Bessenyei B, Oláh E.
    Orv Hetil; 2014 Mar 02; 155(9):341-7. PubMed ID: 24566698
    [Abstract] [Full Text] [Related]

  • 4. Somatic FGFR and TWIST mutations are not a common cause of isolated nonsyndromic single suture craniosynostosis.
    Anderson PJ, Cox TC, Roscioli T, Elakis G, Smithers L, David DJ, Powell B.
    J Craniofac Surg; 2007 Mar 02; 18(2):312-4. PubMed ID: 17414280
    [Abstract] [Full Text] [Related]

  • 5. Clinical and genetic characteristics of craniosynostosis in Hungary.
    Bessenyei B, Nagy A, Szakszon K, Mokánszki A, Balogh E, Ujfalusi A, Tihanyi M, Novák L, Bognár L, Oláh É.
    Am J Med Genet A; 2015 Dec 02; 167A(12):2985-91. PubMed ID: 26289989
    [Abstract] [Full Text] [Related]

  • 6. Dura in the pathogenesis of syndromic craniosynostosis: fibroblast growth factor receptor 2 mutations in dural cells promote osteogenic proliferation and differentiation of osteoblasts.
    Ang BU, Spivak RM, Nah HD, Kirschner RE.
    J Craniofac Surg; 2010 Mar 02; 21(2):462-7. PubMed ID: 20489451
    [Abstract] [Full Text] [Related]

  • 7. Molecular mechanisms in calvarial bone and suture development, and their relation to craniosynostosis.
    Rice DP, Rice R, Thesleff I.
    Eur J Orthod; 2003 Apr 02; 25(2):139-48. PubMed ID: 12737212
    [Abstract] [Full Text] [Related]

  • 8. A comprehensive screen of genes implicated in craniosynostosis.
    Johnson D.
    Ann R Coll Surg Engl; 2003 Nov 02; 85(6):371-7. PubMed ID: 14629875
    [Abstract] [Full Text] [Related]

  • 9. Craniosynostosis.
    Johnson D, Wilkie AO.
    Eur J Hum Genet; 2011 Apr 02; 19(4):369-76. PubMed ID: 21248745
    [Abstract] [Full Text] [Related]

  • 10. Twist1 dimer selection regulates cranial suture patterning and fusion.
    Connerney J, Andreeva V, Leshem Y, Muentener C, Mercado MA, Spicer DB.
    Dev Dyn; 2006 May 02; 235(5):1345-57. PubMed ID: 16502419
    [Abstract] [Full Text] [Related]

  • 11. Craniosynostosis: genes and mechanisms.
    Wilkie AO.
    Hum Mol Genet; 1997 May 02; 6(10):1647-56. PubMed ID: 9300656
    [Abstract] [Full Text] [Related]

  • 12. NGS targeted screening of 100 Scandinavian patients with coronal synostosis.
    Topa A, Rohlin A, Andersson MK, Fehr A, Lovmar L, Stenman G, Kölby L.
    Am J Med Genet A; 2020 Feb 02; 182(2):348-356. PubMed ID: 31837199
    [Abstract] [Full Text] [Related]

  • 13. Genetic background dependent modifiers of craniosynostosis severity.
    Dudakovic A, Nam HK, Wijnen AJV, Hatch NE.
    J Struct Biol; 2020 Dec 01; 212(3):107629. PubMed ID: 32976998
    [Abstract] [Full Text] [Related]

  • 14. Genetics of craniosynostosis: review of the literature.
    Ciurea AV, Toader C.
    J Med Life; 2009 Dec 01; 2(1):5-17. PubMed ID: 20108486
    [Abstract] [Full Text] [Related]

  • 15. Medical treatment of craniosynostosis: recombinant Noggin inhibits coronal suture closure in the rat craniosynostosis model.
    Shen K, Krakora SM, Cunningham M, Singh M, Wang X, Hu FZ, Post JC, Ehrlich GD.
    Orthod Craniofac Res; 2009 Aug 01; 12(3):254-62. PubMed ID: 19627528
    [Abstract] [Full Text] [Related]

  • 16. Further analysis of the Crouzon mouse: effects of the FGFR2(C342Y) mutation are cranial bone-dependent.
    Liu J, Nam HK, Wang E, Hatch NE.
    Calcif Tissue Int; 2013 May 01; 92(5):451-66. PubMed ID: 23358860
    [Abstract] [Full Text] [Related]

  • 17. Isolated sagittal and coronal craniosynostosis associated with TWIST box mutations.
    Seto ML, Hing AV, Chang J, Hu M, Kapp-Simon KA, Patel PK, Burton BK, Kane AA, Smyth MD, Hopper R, Ellenbogen RG, Stevenson K, Speltz ML, Cunningham ML.
    Am J Med Genet A; 2007 Apr 01; 143A(7):678-86. PubMed ID: 17343269
    [Abstract] [Full Text] [Related]

  • 18. Do Craniosynostosis syndrome phenotypes with both FGFR2 and TWIST mutations have a worse clinical outcome?
    Anderson PJ, Netherway DJ, Cox TC, Roscioli T, David DJ.
    J Craniofac Surg; 2006 Jan 01; 17(1):166-72. PubMed ID: 16432427
    [Abstract] [Full Text] [Related]

  • 19. Genotype and clinical care correlations in craniosynostosis: findings from a cohort of 630 Australian and New Zealand patients.
    Roscioli T, Elakis G, Cox TC, Moon DJ, Venselaar H, Turner AM, Le T, Hackett E, Haan E, Colley A, Mowat D, Worgan L, Kirk EP, Sachdev R, Thompson E, Gabbett M, McGaughran J, Gibson K, Gattas M, Freckmann ML, Dixon J, Hoefsloot L, Field M, Hackett A, Kamien B, Edwards M, Adès LC, Collins FA, Wilson MJ, Savarirayan R, Tan TY, Amor DJ, McGillivray G, White SM, Glass IA, David DJ, Anderson PJ, Gianoutsos M, Buckley MF.
    Am J Med Genet C Semin Med Genet; 2013 Nov 01; 163C(4):259-70. PubMed ID: 24127277
    [Abstract] [Full Text] [Related]

  • 20. Facial skeleton dysmorphology in syndromic craniosynostosis: differences between FGFR2 and no-FGFR2-related syndromes and relationship with skull base and facial sutural patterns.
    Calandrelli R, Pilato F, Massimi L, D'Apolito G, Colosimo C.
    Childs Nerv Syst; 2023 Nov 01; 39(11):3235-3247. PubMed ID: 37195419
    [Abstract] [Full Text] [Related]

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