Wilkie AO - Search Results

1

Growth of the normal skull vault and its alteration in craniosynostosis: insights from human genetics and experimental studies.

Morriss-Kay GM, Wilkie AO. Morriss-Kay GM, et al. Among authors: wilkie ao. J Anat. 2005 Nov;207(5):637-53. doi: 10.1111/j.1469-7580.2005.00475.x. J Anat. 2005. PMID: 16313397 Free PMC article. Review.

2

Functions of fibroblast growth factors and their receptors.

Wilkie AO, Morriss-Kay GM, Jones EY, Heath JK. Wilkie AO, et al. Curr Biol. 1995 May 1;5(5):500-7. doi: 10.1016/s0960-9822(95)00102-3. Curr Biol. 1995. PMID: 7583099 Free article. Review.

3

Craniosynostosis: novel insights into pathogenesis and treatment.

Wilkie AO, Wall SA. Wilkie AO, et al. Curr Opin Neurol. 1996 Apr;9(2):146-52. Curr Opin Neurol. 1996. PMID: 8782984 Review.

4

Craniosynostosis: genes and mechanisms.

Wilkie AO. Wilkie AO. Hum Mol Genet. 1997;6(10):1647-56. doi: 10.1093/hmg/6.10.1647. Hum Mol Genet. 1997. PMID: 9300656 Review.

5

Fgfr2 and osteopontin domains in the developing skull vault are mutually exclusive and can be altered by locally applied FGF2.

Iseki S, Wilkie AO, Heath JK, Ishimaru T, Eto K, Morriss-Kay GM. Iseki S, et al. Among authors: wilkie ao. Development. 1997 Sep;124(17):3375-84. doi: 10.1242/dev.124.17.3375. Development. 1997. PMID: 9310332

6

De novo alu-element insertions in FGFR2 identify a distinct pathological basis for Apert syndrome.

Oldridge M, Zackai EH, McDonald-McGinn DM, Iseki S, Morriss-Kay GM, Twigg SR, Johnson D, Wall SA, Jiang W, Theda C, Jabs EW, Wilkie AO. Oldridge M, et al. Among authors: wilkie ao. Am J Hum Genet. 1999 Feb;64(2):446-61. doi: 10.1086/302245. Am J Hum Genet. 1999. PMID: 9973282 Free PMC article.

7

Fgfr1 and Fgfr2 have distinct differentiation- and proliferation-related roles in the developing mouse skull vault.

Iseki S, Wilkie AO, Morriss-Kay GM. Iseki S, et al. Among authors: wilkie ao. Development. 1999 Dec;126(24):5611-20. doi: 10.1242/dev.126.24.5611. Development. 1999. PMID: 10572038

8

Expression patterns of Twist and Fgfr1, -2 and -3 in the developing mouse coronal suture suggest a key role for twist in suture initiation and biogenesis.

Johnson D, Iseki S, Wilkie AO, Morriss-Kay GM. Johnson D, et al. Among authors: wilkie ao. Mech Dev. 2000 Mar 1;91(1-2):341-5. doi: 10.1016/s0925-4773(99)00278-6. Mech Dev. 2000. PMID: 10704861 Free article.

9

Haploinsufficiency of the human homeobox gene ALX4 causes skull ossification defects.

Mavrogiannis LA, Antonopoulou I, Baxová A, Kutílek S, Kim CA, Sugayama SM, Salamanca A, Wall SA, Morriss-Kay GM, Wilkie AO. Mavrogiannis LA, et al. Among authors: wilkie ao. Nat Genet. 2001 Jan;27(1):17-8. doi: 10.1038/83703. Nat Genet. 2001. PMID: 11137991

10

Genetics of craniofacial development and malformation.

Wilkie AO, Morriss-Kay GM. Wilkie AO, et al. Nat Rev Genet. 2001 Jun;2(6):458-68. doi: 10.1038/35076601. Nat Rev Genet. 2001. PMID: 11389462 Review.

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