Dunwoodie SL - Search Results

1

Cited2 is required in trophoblasts for correct placental capillary patterning.

Moreau JL, Artap ST, Shi H, Chapman G, Leone G, Sparrow DB, Dunwoodie SL. Moreau JL, et al. Among authors: dunwoodie sl. Dev Biol. 2014 Aug 1;392(1):62-79. doi: 10.1016/j.ydbio.2014.04.023. Epub 2014 May 5. Dev Biol. 2014. PMID: 24803182 Free article.

2

Axial skeletal defects caused by mutation in the spondylocostal dysplasia/pudgy gene Dll3 are associated with disruption of the segmentation clock within the presomitic mesoderm.

Dunwoodie SL, Clements M, Sparrow DB, Sa X, Conlon RA, Beddington RS. Dunwoodie SL, et al. Development. 2002 Apr;129(7):1795-806. doi: 10.1242/dev.129.7.1795. Development. 2002. PMID: 11923214

3

Diverse requirements for Notch signalling in mammals.

Sparrow DB, Clements M, Withington SL, Scott AN, Novotny J, Sillence D, Kusumi K, Beddington RS, Dunwoodie SL. Sparrow DB, et al. Among authors: dunwoodie sl. Int J Dev Biol. 2002;46(4):365-74. Int J Dev Biol. 2002. PMID: 12141422

4

The expression of the imprinted gene Ipl is restricted to extra-embryonic tissues and embryonic lateral mesoderm during early mouse development.

Dunwoodie SL, Beddington RS. Dunwoodie SL, et al. Int J Dev Biol. 2002;46(4):459-66. Int J Dev Biol. 2002. PMID: 12141432

5

Cited1 is required in trophoblasts for placental development and for embryo growth and survival.

Rodriguez TA, Sparrow DB, Scott AN, Withington SL, Preis JI, Michalicek J, Clements M, Tsang TE, Shioda T, Beddington RS, Dunwoodie SL. Rodriguez TA, et al. Among authors: dunwoodie sl. Mol Cell Biol. 2004 Jan;24(1):228-44. doi: 10.1128/MCB.24.1.228-244.2004. Mol Cell Biol. 2004. PMID: 14673158 Free PMC article.

6

Kousseff syndrome: a causally heterogeneous disorder.

Maclean K, Field MJ, Colley AS, Mowat DR, Sparrow DB, Dunwoodie SL, Kirk EP. Maclean K, et al. Among authors: dunwoodie sl. Am J Med Genet A. 2004 Jan 30;124A(3):307-12. doi: 10.1002/ajmg.a.20418. Am J Med Genet A. 2004. PMID: 14708106

7

Mutated MESP2 causes spondylocostal dysostosis in humans.

Whittock NV, Sparrow DB, Wouters MA, Sillence D, Ellard S, Dunwoodie SL, Turnpenny PD. Whittock NV, et al. Among authors: dunwoodie sl. Am J Hum Genet. 2004 Jun;74(6):1249-54. doi: 10.1086/421053. Epub 2004 Apr 30. Am J Hum Genet. 2004. PMID: 15122512 Free PMC article.

8

Evolution of distinct EGF domains with specific functions.

Wouters MA, Rigoutsos I, Chu CK, Feng LL, Sparrow DB, Dunwoodie SL. Wouters MA, et al. Among authors: dunwoodie sl. Protein Sci. 2005 Apr;14(4):1091-103. doi: 10.1110/ps.041207005. Protein Sci. 2005. PMID: 15772310 Free PMC article.

9

Mutation of the LUNATIC FRINGE gene in humans causes spondylocostal dysostosis with a severe vertebral phenotype.

Sparrow DB, Chapman G, Wouters MA, Whittock NV, Ellard S, Fatkin D, Turnpenny PD, Kusumi K, Sillence D, Dunwoodie SL. Sparrow DB, et al. Among authors: dunwoodie sl. Am J Hum Genet. 2006 Jan;78(1):28-37. doi: 10.1086/498879. Epub 2005 Nov 16. Am J Hum Genet. 2006. PMID: 16385447 Free PMC article.

10

Loss of Cited2 affects trophoblast formation and vascularization of the mouse placenta.

Withington SL, Scott AN, Saunders DN, Lopes Floro K, Preis JI, Michalicek J, Maclean K, Sparrow DB, Barbera JP, Dunwoodie SL. Withington SL, et al. Among authors: dunwoodie sl. Dev Biol. 2006 Jun 1;294(1):67-82. doi: 10.1016/j.ydbio.2006.02.025. Epub 2006 Mar 31. Dev Biol. 2006. PMID: 16579983 Free article.

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