217 related articles for article (PubMed ID: 18391500)
1. Fibroblast growth factor signaling in cranial suture development and pathogenesis.
Hajihosseini MK
Front Oral Biol; 2008; 12():160-177. PubMed ID: 18391500
[TBL] [Abstract][Full Text] [Related]
2. FGF signaling in craniofacial biological control and pathological craniofacial development.
Hatch NE
Crit Rev Eukaryot Gene Expr; 2010; 20(4):295-311. PubMed ID: 21395503
[TBL] [Abstract][Full Text] [Related]
3. [Genetics of craniofacial development].
van Adrichem LN; Hoogeboom AJ; Wolvius EB
Ned Tijdschr Tandheelkd; 2008 Feb; 115(2):61-8. PubMed ID: 18326400
[TBL] [Abstract][Full Text] [Related]
4. FGFR-associated craniosynostosis syndromes and gastrointestinal defects.
Hibberd CE; Bowdin S; Arudchelvan Y; Forrest CR; Brakora KA; Marcucio RS; Gong SG
Am J Med Genet A; 2016 Dec; 170(12):3215-3221. PubMed ID: 27481450
[TBL] [Abstract][Full Text] [Related]
5. Aberrant bony vasculature associated with activating fibroblast growth factor receptor mutations accompanying Crouzon syndrome.
Tholpady SS; Abdelaal MM; Dufresne CR; Gampper TJ; Lin KY; Jane JA; Morgan RF; Ogle RC
J Craniofac Surg; 2004 May; 15(3):431-5; discussion 436-8. PubMed ID: 15111803
[TBL] [Abstract][Full Text] [Related]
6. Fibroblast growth factors lead to increased Msx2 expression and fusion in calvarial sutures.
Ignelzi MA; Wang W; Young AT
J Bone Miner Res; 2003 Apr; 18(4):751-9. PubMed ID: 12674336
[TBL] [Abstract][Full Text] [Related]
7. Development of the lip and palate: FGF signalling.
Stanier P; Pauws E
Front Oral Biol; 2012; 16():71-80. PubMed ID: 22759671
[TBL] [Abstract][Full Text] [Related]
8. Molecular signaling in pathogenesis of craniosynostosis: the role of fibroblast growth factor and transforming growth factor-β.
Chim H; Manjila S; Cohen AR; Gosain AK
Neurosurg Focus; 2011 Aug; 31(2):E7. PubMed ID: 21806346
[TBL] [Abstract][Full Text] [Related]
9. Phenotypic diversity in patients with craniosynostoses unrelated to Apert syndrome: the role of fibroblast growth factor receptor gene mutations.
Ito S; Sekido K; Kanno H; Sato H; Tanaka M; Yamaguchi K; Yamamoto I
J Neurosurg; 2005 Jan; 102(1 Suppl):23-30. PubMed ID: 16206730
[TBL] [Abstract][Full Text] [Related]
10. Molecular and cellular bases of syndromic craniosynostoses.
Bonaventure J; El Ghouzzi V
Expert Rev Mol Med; 2003 Jan; 5(4):1-17. PubMed ID: 14987407
[TBL] [Abstract][Full Text] [Related]
11. Regulation of cranial suture morphogenesis.
Ogle RC; Tholpady SS; McGlynn KA; Ogle RA
Cells Tissues Organs; 2004; 176(1-3):54-66. PubMed ID: 14745235
[TBL] [Abstract][Full Text] [Related]
12. 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; 18(2):312-4. PubMed ID: 17414280
[TBL] [Abstract][Full Text] [Related]
13. FGF signalling in craniofacial development and developmental disorders.
Nie X; Luukko K; Kettunen P
Oral Dis; 2006 Mar; 12(2):102-11. PubMed ID: 16476029
[TBL] [Abstract][Full Text] [Related]
14. [From gene to disease; craniosynostosis syndromes due to FGFR2-mutation].
van Ravenswaaij-Arts CM; van den Ouweland AM; Hoogeboom AJ; Herbergs J; Pals G
Ned Tijdschr Geneeskd; 2002 Jan; 146(2):63-6. PubMed ID: 11820058
[TBL] [Abstract][Full Text] [Related]
15. Structural basis for fibroblast growth factor receptor activation.
Mohammadi M; Olsen SK; Ibrahimi OA
Cytokine Growth Factor Rev; 2005 Apr; 16(2):107-37. PubMed ID: 15863029
[TBL] [Abstract][Full Text] [Related]
16. Description of a new mutation and characterization of FGFR1, FGFR2, and FGFR3 mutations among Brazilian patients with syndromic craniosynostoses.
Passos-Bueno MR; Sertié AL; Richieri-Costa A; Alonso LG; Zatz M; Alonso N; Brunoni D; Ribeiro SF
Am J Med Genet; 1998 Jul; 78(3):237-41. PubMed ID: 9677057
[TBL] [Abstract][Full Text] [Related]
17. Molecular mechanisms in calvarial bone and suture development, and their relation to craniosynostosis.
Rice DP; Rice R; Thesleff I
Eur J Orthod; 2003 Apr; 25(2):139-48. PubMed ID: 12737212
[TBL] [Abstract][Full Text] [Related]
18. Hearing loss in syndromic craniosynostoses: introduction and consideration of mechanisms.
Agochukwu NB; Solomon BD; Muenke M
Am J Audiol; 2014 Jun; 23(2):135-41. PubMed ID: 24686979
[TBL] [Abstract][Full Text] [Related]
19. The pleiotropic effects of fibroblast growth factor receptors in mammalian development.
McIntosh I; Bellus GA; Jab EW
Cell Struct Funct; 2000 Apr; 25(2):85-96. PubMed ID: 10885578
[TBL] [Abstract][Full Text] [Related]
20. 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; 95(4):660-73. PubMed ID: 11596961
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]