Dunwoodie SL - Search Results

1

Dll3 and Notch1 genetic interactions model axial segmental and craniofacial malformations of human birth defects.

Loomes KM, Stevens SA, O'Brien ML, Gonzalez DM, Ryan MJ, Segalov M, Dormans NJ, Mimoto MS, Gibson JD, Sewell W, Schaffer AA, Nah HD, Rappaport EF, Pratt SC, Dunwoodie SL, Kusumi K. Loomes KM, et al. Among authors: dunwoodie sl. Dev Dyn. 2007 Oct;236(10):2943-51. doi: 10.1002/dvdy.21296. Dev Dyn. 2007. PMID: 17849441 Free article.

2

Dynamic expression patterns of the pudgy/spondylocostal dysostosis gene Dll3 in the developing nervous system.

Kusumi K, Dunwoodie SL, Krumlauf R. Kusumi K, et al. Among authors: dunwoodie sl. Mech Dev. 2001 Jan;100(1):141-4. doi: 10.1016/s0925-4773(00)00514-1. Mech Dev. 2001. PMID: 11118901 Free article.

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

Novel mutations in DLL3, a somitogenesis gene encoding a ligand for the Notch signalling pathway, cause a consistent pattern of abnormal vertebral segmentation in spondylocostal dysostosis.

Turnpenny PD, Whittock N, Duncan J, Dunwoodie S, Kusumi K, Ellard S. Turnpenny PD, et al. J Med Genet. 2003 May;40(5):333-9. doi: 10.1136/jmg.40.5.333. J Med Genet. 2003. PMID: 12746394 Free PMC article.

5

Dll3 pudgy mutation differentially disrupts dynamic expression of somite genes.

Kusumi K, Mimoto MS, Covello KL, Beddington RS, Krumlauf R, Dunwoodie SL. Kusumi K, et al. Among authors: dunwoodie sl. Genesis. 2004 Jun;39(2):115-21. doi: 10.1002/gene.20034. Genesis. 2004. PMID: 15170697

6

Abnormal vertebral segmentation and the notch signaling pathway in man.

Turnpenny PD, Alman B, Cornier AS, Giampietro PF, Offiah A, Tassy O, Pourquié O, Kusumi K, Dunwoodie S. Turnpenny PD, et al. Dev Dyn. 2007 Jun;236(6):1456-74. doi: 10.1002/dvdy.21182. Dev Dyn. 2007. PMID: 17497699 Free article. Review.

7

Progress in the understanding of the genetic etiology of vertebral segmentation disorders in humans.

Giampietro PF, Dunwoodie SL, Kusumi K, Pourquié O, Tassy O, Offiah AC, Cornier AS, Alman BA, Blank RD, Raggio CL, Glurich I, Turnpenny PD. Giampietro PF, et al. Among authors: dunwoodie sl. Ann N Y Acad Sci. 2009 Jan;1151:38-67. doi: 10.1111/j.1749-6632.2008.03452.x. Ann N Y Acad Sci. 2009. PMID: 19154516 Review.

8

Cyclical expression of the Notch/Wnt regulator Nrarp requires modulation by Dll3 in somitogenesis.

Sewell W, Sparrow DB, Smith AJ, Gonzalez DM, Rappaport EF, Dunwoodie SL, Kusumi K. Sewell W, et al. Among authors: dunwoodie sl. Dev Biol. 2009 May 15;329(2):400-9. doi: 10.1016/j.ydbio.2009.02.023. Epub 2009 Mar 3. Dev Biol. 2009. PMID: 19268448 Free PMC article.

9

Summary of the first inaugural joint meeting of the International Consortium for scoliosis genetics and the International Consortium for vertebral anomalies and scoliosis, March 16-18, 2017, Dallas, Texas.

Giampietro PF, Pourquie O, Raggio C, Ikegawa S, Turnpenny PD, Gray R, Dunwoodie SL, Gurnett CA, Alman B, Cheung K, Kusumi K, Hadley-Miller N, Wise CA. Giampietro PF, et al. Among authors: dunwoodie sl. Am J Med Genet A. 2018 Jan;176(1):253-256. doi: 10.1002/ajmg.a.38550. Epub 2017 Nov 21. Am J Med Genet A. 2018. PMID: 29159998 Free PMC article.

10

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.

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