Sally L. Dunwoodie
Title
Cited by
Cited by
Year
The role of hypoxia in development of the Mammalian embryo
SL Dunwoodie
Developmental cell 17 (6), 755-773, 2009
4672009
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
4181997
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
2902008
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
2252005
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
2182002
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
2172006
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
1712007
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
1692012
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
1681998
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
1622004
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
1602002
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
1542015
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
1522011
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
1501998
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
1462004
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
1452007
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
1432000
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
1282003
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
1212005
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
1172008
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