|The role of hypoxia in development of the Mammalian embryo|
Developmental cell 17 (6), 755-773, 2009
|Mouse Dll3: a novel divergent Delta gene which may complement the function of other Delta homologues during early pattern formation in the mouse embryo|
SL Dunwoodie, D Henrique, SM Harrison, RS Beddington
Development 124 (16), 3065-3076, 1997
|SmcHD1, containing a structural-maintenance-of-chromosomes hinge domain, has a critical role in X inactivation|
ME Blewitt, AV Gendrel, Z Pang, DB Sparrow, N Whitelaw, JM Craig, ...
Nature genetics 40 (5), 663-669, 2008
|Murine T-box transcription factor Tbx20 acts as a repressor during heart development, and is essential for adult heart integrity, function and adaptation|
FA Stennard, MW Costa, D Lai, C Biben, MB Furtado, MJ Solloway, ...
Development 132 (10), 2451-2462, 2005
|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|
SL Dunwoodie, M Clements, DB Sparrow, X Sa, RA Conlon, ...
Development 129 (7), 1795-1806, 2002
|Mutation of the LUNATIC FRINGE gene in humans causes spondylocostal dysostosis with a severe vertebral phenotype|
DB Sparrow, G Chapman, MA Wouters, NV Whittock, S Ellard, D Fatkin, ...
The American Journal of Human Genetics 78 (1), 28-37, 2006
|Divergent functions and distinct localization of the Notch ligands DLL1 and DLL3 in vivo|
I Geffers, K Serth, G Chapman, R Jaekel, K Schuster-Gossler, R Cordes, ...
Journal of Cell Biology 178 (3), 465-476, 2007
|A mechanism for gene-environment interaction in the etiology of congenital scoliosis|
DB Sparrow, G Chapman, AJ Smith, MZ Mattar, JA Major, VC O'Reilly, ...
Cell 149 (2), 295-306, 2012
|Msg1 and Mrg1, founding members of a gene family, show distinct patterns of gene expression during mouse embryogenesis|
SL Dunwoodie, TA Rodriguez, RSP Beddington
Mechanisms of development 72 (1-2), 27-40, 1998
|Mutated MESP2 causes spondylocostal dysostosis in humans|
NV Whittock, DB Sparrow, MA Wouters, D Sillence, S Ellard, ...
The American Journal of Human Genetics 74 (6), 1249-1254, 2004
|Folic acid prevents exencephaly in Cited2 deficient mice|
JPM Barbera, TA Rodriguez, NDE Greene, WJ Weninger, A Simeone, ...
Human molecular genetics 11 (3), 283-293, 2002
|TBX6 null variants and a common hypomorphic allele in congenital scoliosis|
N Wu, X Ming, J Xiao, Z Wu, X Chen, M Shinawi, Y Shen, G Yu, J Liu, ...
New England Journal of Medicine 372 (4), 341-350, 2015
|Notch inhibition by the ligand DELTA-LIKE 3 defines the mechanism of abnormal vertebral segmentation in spondylocostal dysostosis|
G Chapman, DB Sparrow, E Kremmer, SL Dunwoodie
Human molecular genetics 20 (5), 905-916, 2011
|Transcriptional activating activity of Smad4: roles of SMAD hetero-oligomerization and enhancement by an associating transactivator|
T Shioda, RJ Lechleider, SL Dunwoodie, H Li, T Yahata, ...
Proceedings of the National Academy of Sciences 95 (17), 9785-9790, 1998
|Developmental regulation of Notch signaling genes in the embryonic pituitary: Prop1 deficiency affects Notch2 expression|
LT Raetzman, SA Ross, S Cook, SL Dunwoodie, SA Camper, PQ Thomas
Developmental biology 265 (2), 329-340, 2004
|Abnormal vertebral segmentation and the notch signaling pathway in man|
PD Turnpenny, B Alman, AS Cornier, PF Giampietro, A Offiah, O Tassy, ...
Developmental dynamics: an official publication of the American Association …, 2007
|Sp5, a new member of the Sp1 family, is dynamically expressed during development and genetically interacts with Brachyury|
SM Harrison, D Houzelstein, SL Dunwoodie, RSP Beddington
Developmental biology 227 (2), 358-372, 2000
|Novel mutations in DLL3, a somitogenesis gene encoding a ligand for the Notch signalling pathway, cause a consistent pattern of abnormal vertebral segmentation in …|
PD Turnpenny, N Whittock, J Duncan, S Dunwoodie, K Kusumi, S Ellard
Journal of medical genetics 40 (5), 333-339, 2003
|Evolution of distinct EGF domains with specific functions|
MA Wouters, I Rigoutsos, CK Chu, LL Feng, DB Sparrow, SL Dunwoodie
Protein Science 14 (4), 1091-1103, 2005
|Mutation of HAIRY-AND-ENHANCER-OF-SPLIT-7 in humans causes spondylocostal dysostosis|
DB Sparrow, E Guillén-Navarro, D Fatkin, SL Dunwoodie
Human molecular genetics 17 (23), 3761-3766, 2008