Dunwoodie SL - Search Results

1

Compound heterozygous mutations in RIPPLY2 associated with vertebral segmentation defects.

McInerney-Leo AM, Sparrow DB, Harris JE, Gardiner BB, Marshall MS, O'Reilly VC, Shi H, Brown MA, Leo PJ, Zankl A, Dunwoodie SL, Duncan EL. McInerney-Leo AM, et al. Among authors: dunwoodie sl. Hum Mol Genet. 2015 Mar 1;24(5):1234-42. doi: 10.1093/hmg/ddu534. Epub 2014 Oct 24. Hum Mol Genet. 2015. PMID: 25343988

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

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

5

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.

6

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.

7

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.

8

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.

9

Generation of conditional Cited2 null alleles.

Preis JI, Wise N, Solloway MJ, Harvey RP, Sparrow DB, Dunwoodie SL. Preis JI, et al. Among authors: dunwoodie sl. Genesis. 2006 Dec;44(12):579-83. doi: 10.1002/dvg.20251. Genesis. 2006. PMID: 17133411

10

Disruption of the somitic molecular clock causes abnormal vertebral segmentation.

Sparrow DB, Chapman G, Turnpenny PD, Dunwoodie SL. Sparrow DB, et al. Among authors: dunwoodie sl. Birth Defects Res C Embryo Today. 2007 Jun;81(2):93-110. doi: 10.1002/bdrc.20093. Birth Defects Res C Embryo Today. 2007. PMID: 17600782 Review.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

144 results

Search Page