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Items: 1 to 50 of 63

1.

Nprl3 is required for normal development of the cardiovascular system.

Kowalczyk MS, Hughes JR, Babbs C, Sanchez-Pulido L, Szumska D, Sharpe JA, Sloane-Stanley JA, Morriss-Kay GM, Smoot LB, Roberts AE, Watkins H, Bhattacharya S, Gibbons RJ, Ponting CP, Wood WG, Higgs DR.

Mamm Genome. 2012 Aug;23(7-8):404-15. doi: 10.1007/s00335-012-9398-y. Epub 2012 Apr 27.

PMID:
22538705
2.

The evolution of human artistic creativity.

Morriss-Kay GM.

J Anat. 2010 Feb;216(2):158-76. doi: 10.1111/j.1469-7580.2009.01160.x. Epub 2009 Nov 9. Review.

3.

Mechanism of skull suture maintenance and interdigitation.

Miura T, Perlyn CA, Kinboshi M, Ogihara N, Kobayashi-Miura M, Morriss-Kay GM, Shiota K.

J Anat. 2009 Dec;215(6):642-55. doi: 10.1111/j.1469-7580.2009.01148.x. Epub 2009 Oct 6.

4.

Skeletal analysis of the Fgfr3(P244R) mouse, a genetic model for the Muenke craniosynostosis syndrome.

Twigg SR, Healy C, Babbs C, Sharpe JA, Wood WG, Sharpe PT, Morriss-Kay GM, Wilkie AO.

Dev Dyn. 2009 Feb;238(2):331-42. doi: 10.1002/dvdy.21790.

5.

Treatment of mice with retinoids in vivo and in vitro.

Morriss-Kay GM.

Methods Mol Biol. 2008;461:31-6. doi: 10.1007/978-1-60327-483-8_4. Review. No abstract available.

PMID:
19030789
6.

Development and tissue origins of the mammalian cranial base.

McBratney-Owen B, Iseki S, Bamforth SD, Olsen BR, Morriss-Kay GM.

Dev Biol. 2008 Oct 1;322(1):121-32. doi: 10.1016/j.ydbio.2008.07.016. Epub 2008 Jul 22.

7.

Polydactyly in the mouse mutant Doublefoot involves altered Gli3 processing and is caused by a large deletion in cis to Indian hedgehog.

Babbs C, Furniss D, Morriss-Kay GM, Wilkie AO.

Mech Dev. 2008 May-Jun;125(5-6):517-26. doi: 10.1016/j.mod.2008.01.001. Epub 2008 Jan 11.

8.

A point-wise quantification of asymmetry using deformation fields: application to the study of the Crouzon mouse model.

Olafsdóttir H, Lanche S, Darvann TA, Hermann NV, Larsen R, Ersbøll BK, Oubel E, Frangi AF, Larsen P, Perlyn CA, Morriss-Kay GM, Kreiborg S.

Med Image Comput Comput Assist Interv. 2007;10(Pt 2):452-9.

PMID:
18044600
9.

Computational mouse atlases and their application to automatic assessment of craniofacial dysmorphology caused by the Crouzon mutation Fgfr2(C342Y).

Olafsdóttir H, Darvann TA, Hermann NV, Oubel E, Ersbøll BK, Frangi AF, Larsen P, Perlyn CA, Morriss-Kay GM, Kreiborg S.

J Anat. 2007 Jul;211(1):37-52. Epub 2007 Jun 6.

10.

P9 Functions of ALX4 and MSX2 in ossification of the skull vault.

Antonopoulou I, Mavrogiannis L, Wilkie A, Morriss-Kay G.

J Anat. 2002 Nov;201(5):428-9. No abstract available.

11.

P2 Developmental mechanisms underlying polydactyly in the mouse mutant, Doublefoot.

Crick A, Brown J, Morriss-Kay G.

J Anat. 2002 Nov;201(5):426. No abstract available.

12.

8 Doublefoot is epistatic to Sonic hedgehog in the developing mouse limb.

Babbs C, Morriss-Kay G.

J Anat. 2002 Nov;201(5):419. No abstract available.

14.

A gain-of-function mutation of Fgfr2c demonstrates the roles of this receptor variant in osteogenesis.

Eswarakumar VP, Horowitz MC, Locklin R, Morriss-Kay GM, Lonai P.

Proc Natl Acad Sci U S A. 2004 Aug 24;101(34):12555-60. Epub 2004 Aug 17.

15.

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

Antonopoulou I, Mavrogiannis LA, Wilkie AO, Morriss-Kay GM.

J Anat. 2004 Jun;204(6):487-99.

16.

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.

Proc Natl Acad Sci U S A. 2004 Jun 8;101(23):8652-7. Epub 2004 May 27.

17.

Developmental mechanisms underlying polydactyly in the mouse mutant Doublefoot.

Crick AP, Babbs C, Brown JM, Morriss-Kay GM.

J Anat. 2003 Jan;202(1):21-6. Review.

18.

The IIIc alternative of Fgfr2 is a positive regulator of bone formation.

Eswarakumar VP, Monsonego-Ornan E, Pines M, Antonopoulou I, Morriss-Kay GM, Lonai P.

Development. 2002 Aug;129(16):3783-93.

19.
20.
21.

Tissue origins and interactions in the mammalian skull vault.

Jiang X, Iseki S, Maxson RE, Sucov HM, Morriss-Kay GM.

Dev Biol. 2002 Jan 1;241(1):106-16.

22.

A high-resolution genetic, physical, and comparative gene map of the doublefoot (Dbf) region of mouse chromosome 1 and the region of conserved synteny on human chromosome 2q35.

Hayes C, Rump A, Cadman MR, Harrison M, Evans EP, Lyon MF, Morriss-Kay GM, Rosenthal A, Brown SD.

Genomics. 2001 Dec;78(3):197-205.

PMID:
11735226
23.

Derivation of the mammalian skull vault.

Morriss-Kay GM.

J Anat. 2001 Jul-Aug;199(Pt 1-2):143-51. Review.

25.

Genetics of craniofacial development and malformation.

Wilkie AO, Morriss-Kay GM.

Nat Rev Genet. 2001 Jun;2(6):458-68. Review.

PMID:
11389462
26.
27.

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.

Nat Genet. 2001 Jan;27(1):17-8.

PMID:
11137991
29.
30.

Treatment of mice with retinoids in vivo and in vitro. Skeletal staining.

Morriss-Kay GM.

Methods Mol Biol. 1999;97:33-9. Review. No abstract available.

PMID:
10443358
31.

Retinoids and mammalian development.

Morriss-Kay GM, Ward SJ.

Int Rev Cytol. 1999;188:73-131. Review.

PMID:
10208011
32.

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.

Am J Hum Genet. 1999 Feb;64(2):446-61.

33.

Morphogenesis of Doublefoot (Dbf), a mouse mutant with polydactyly and craniofacial defects.

Hayes C, Lyon MF, Morriss-Kay GM.

J Anat. 1998 Jul;193 ( Pt 1):81-91.

34.
35.

Genetic patterning of the developing mouse tail at the time of posterior neuropore closure.

Gofflot F, Hall M, Morriss-Kay GM.

Dev Dyn. 1997 Dec;210(4):431-45.

36.

Sonic hedgehog is not required for polarising activity in the Doublefoot mutant mouse limb bud.

Hayes C, Brown JM, Lyon MF, Morriss-Kay GM.

Development. 1998 Feb;125(3):351-7.

37.
38.

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.

Development. 1997 Sep;124(17):3375-84.

39.

The functional basis of tissue-specific retinoic acid signalling in embryos.

Ward SJ, Morriss-Kay GM.

Semin Cell Dev Biol. 1997 Aug;8(4):429-35.

PMID:
15001081
40.

Apoptotic cell death in neuronal differentiation of P19 EC cells: cell death follows reentry into S phase.

Ninomiya Y, Adams R, Morriss-Kay GM, Eto K.

J Cell Physiol. 1997 Jul;172(1):25-35.

PMID:
9207922
41.

Prorhombomeric subdivision of the mammalian embryonic hindbrain: is it functionally meaningful?

Ruberte E, Wood HB, Morriss-Kay GM.

Int J Dev Biol. 1997 Apr;41(2):213-22. Review.

42.

Craniofacial defects in AP-2 null mutant mice.

Morriss-Kay GM.

Bioessays. 1996 Oct;18(10):785-8. Review.

PMID:
8885715
43.

Embryonic development and pattern formation.

Morriss-Kay GM, Sokolova N.

FASEB J. 1996 Jul;10(9):961-8. Review.

PMID:
8801178
44.
46.

The effects of retinoid status on TGF beta expression during mouse embryogenesis.

Mahmood R, Flanders KC, Morriss-Kay GM.

Anat Embryol (Berl). 1995 Jul;192(1):21-33.

PMID:
7485998
47.

Functions of fibroblast growth factors and their receptors.

Wilkie AO, Morriss-Kay GM, Jones EY, Heath JK.

Curr Biol. 1995 May 1;5(5):500-7. Review.

50.

Analysis of limb reduction defects in babies exposed to chorionic villus sampling.

Firth HV, Boyd PA, Chamberlain PF, MacKenzie IZ, Morriss-Kay GM, Huson SM.

Lancet. 1994 Apr 30;343(8905):1069-71.

PMID:
7909100

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