Browsing by Author Sparrow, D. B.

Jump to: 0-9 A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
or enter first few letters:  
Showing results 1 to 8 of 8
Issue DateTitleAuthor(s)Citation
2008BMP/SMAD1 signaling sets a threshold for the left/right pathway in lateral plate mesoderm and limits availability of SMAD4Jones, Vanessa; Biben, Christine; Costa, Mauro; Dunwoodie, S. L.; Furtado, Milena B; Harvey, Richard P; Preis, Jost I; Robertson, Elizabeth J.; Saga, Yumiko; Solloway, Mark J; Sparrow, D. B.; Tam, Patrick; Wolstein, Olrit; MedicineBMP/SMAD1 signaling sets a threshold for the left/right pathway in lateral plate mesoderm and limits availability of SMAD4, Genes and Development, vol.22, N/A, 2008,pp 3037-3049
2015Compound heterozygous mutations in RIPPLY2 associated with vertebral segmentation defectsZankl, Andreas; Brown, Matthew; Duncan, Emma; Dunwoodie, Sally; Gardiner, Brooke; Harris, Jessica; Leo, Paul; Marshall, Mhairi; McInerney-Leo, Aideen; O'Reilly, Victoria; Shi, Hongjun; Sparrow, D. B.; Childrens Hospital Westmead: Paediatrics & Child HealthCompound heterozygous mutations in RIPPLY2 associated with vertebral segmentation defects, Human Molecular Genetics, vol.24, 5, 2015,pp 1234-1242
2014Gene-environment interaction demonstrates the vulnerability of the embryonic heartChapman, Bogdan; Chapman, Gavin; Grieve, Stuart; Dunwoodie, S. L.; Harvey, Richard P; James, Alexander C; Johnson, Randall S; Lopes Floro, Kylie; OReilly, Victoria C; Preis, Jost I; Shi, Hongjun; Sparrow, D. B.; Molecular Bioscience; Molecular Bioscience; Northern Clinical School: MedicineGene-environment interaction demonstrates the vulnerability of the embryonic heart, Developmental Biology, vol.391, 1, 2014,pp 99-110
2016Gestational stress induces the unfolded protein response, resulting in heart defectsChapman, Bogdan; Grieve, Stuart; Bewes, Therese; Chapman, G.; Dunwoodie, Sally; Graham, Robert M; Moreau, Julie; O'Reilly, Victoria; Shi, Hongjun; Sparrow, D. B.; Stocker, Roland; Yam, Michelle; Molecular Bioscience; Central Clinical School: MedicineGestational stress induces the unfolded protein response, resulting in heart defects, Development, vol.143, 14, 2016,pp 2561-2572
2006Mutation of the LUNATIC FRINGE gene in humans causes spondylocostal dysostosis with a severe vertebral phenotype.Sillence, David; Chapman, Gavin; Dunwoodie, Sally; Ellard, S.; Fatkin, Diane; Kusumi, K.; Sparrow, D. B.; Turnpenny, P. D.; Whittock, N. V.; Wouters, Merridee A.; Childrens Hospital Westmead: Paediatrics & Child HealthMutation of the LUNATIC FRINGE gene in humans causes spondylocostal dysostosis with a severe vertebral phenotype., The American Journal of Human Genetics, vol.78, 1, 2006,pp N/A-N/A
2006Mutation of the LUNATIC FRINGE gene in humans causes spondylocostal dysostosis with a severe vertebral phenotype.Sillence, David; Chapman, Gavin; Dunwoodie, Sally; Ellard, S.; Fatkin, Diane; Kusumi, K.; Sparrow, D. B.; Turnpenny, P. D.; Whittock, N. V.; Wouters, Merridee A.; Childrens Hospital Westmead: Paediatrics & Child HealthMutation of the LUNATIC FRINGE gene in humans causes spondylocostal dysostosis with a severe vertebral phenotype., The American Journal of Human Genetics, vol.78, 1, 2006,pp N/A-N/A
2015Renal developmental defects resulting from in utero hypoxia are associated with suppression of ureteric β-catenin signalingGrieve, Stuart; Dunwoodie, Sally; Ju, Adler; Kurniawan, Nyoman; Little, Melisssa H.; Moritz, Karen M; Neal, Cailda S; Singh, Reetu R; Sparrow, D. B.; Wilkinson, Lorine; Central Clinical School: MedicineRenal developmental defects resulting from in utero hypoxia are associated with suppression of ureteric β-catenin signaling, Kidney International, vol.87, 5, 2015,pp 975-83
2010Two novel missense mutations in HAIRY-AND-ENHANCER-OF-SPLIT-7 in a family with spondylocostal dysostosis.Sillence, David; Dunwoodie, S. L.; Sparrow, D. B.; Turnpenny, P. D.; Wouters, Merridee A.; Children's Hospital Westmead: Paediatrics & Child HealthTwo novel missense mutations in HAIRY-AND-ENHANCER-OF-SPLIT-7 in a family with spondylocostal dysostosis., European Journal of Human Genetics, vol.18, 6,pp 674-679