Morriss-Kay GM - Search Results

1

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. Nat Genet. 2001 Jan;27(1):17-8. doi: 10.1038/83703. Nat Genet. 2001. PMID: 11137991

2

Alx4 and Msx2 play phenotypically similar and additive roles in skull vault differentiation.

Antonopoulou I, Mavrogiannis LA, Wilkie AO, Morriss-Kay GM. Antonopoulou I, et al. J Anat. 2004 Jun;204(6):487-99. doi: 10.1111/j.0021-8782.2004.00304.x. J Anat. 2004. PMID: 15198690 Free PMC article.

3

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.

4

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. 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.

5

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. Am J Hum Genet. 1999 Feb;64(2):446-61. doi: 10.1086/302245. Am J Hum Genet. 1999. PMID: 9973282 Free PMC article.

6

Mutations of ephrin-B1 (EFNB1), a marker of tissue boundary formation, cause craniofrontonasal syndrome.

Twigg SR, Kan R, Babbs C, Bochukova EG, Robertson SP, Wall SA, Morriss-Kay GM, Wilkie AO. Twigg SR, et al. Proc Natl Acad Sci U S A. 2004 Jun 8;101(23):8652-7. doi: 10.1073/pnas.0402819101. Epub 2004 May 27. Proc Natl Acad Sci U S A. 2004. PMID: 15166289 Free PMC article.

7

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. Development. 1997 Sep;124(17):3375-84. doi: 10.1242/dev.124.17.3375. Development. 1997. PMID: 9310332

8

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. Development. 1999 Dec;126(24):5611-20. doi: 10.1242/dev.126.24.5611. Development. 1999. PMID: 10572038

9

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. 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.

10

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.

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