Browsing by Author Wouters, Merridee A.

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Showing results 1 to 5 of 5
Issue DateTitleAuthor(s)Citation
2006Mechanism of allosteric regulation of transglutaminase 2 by GTPMatthews, Jacqueline; Stokes, Philippa; Begg, Gillian E; Carrington, Lyle; Graham, Robert M; Husain, Ahsan; Iismaa, Siiri E; Lorand, Laszlo; Wouters, Merridee A.; Molecular & Microbial Bioscien; Molecular & Microbial BioscienMechanism of allosteric regulation of transglutaminase 2 by GTP, National Academy of Sciences 2005, vol.103,(52),2006,pp 19683-19688
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
2015NKX2-5 mutations causative for congenital heart disease retain functionality and are directed to hundreds of targetsWaardenberg, Ashley; Bhattacharya, Shoumo; Blanpain, Cedric; Bondue, Antoine; Bouveret, Romaric; Chapman, G.; Chen, Chiann-mun; de Jong, Danielle; Doan, Tram; Dunwoodie, Sally; Fonoudi, Hananeh; Harvey, R; Kaur, Gurpreet; Mohamed, Stephanie; Plachta, Nicolas; Ramialison, Mirana; Schonrock, Nicole; Wouters, Merridee A.; Childrens Medical Research Institute (CMRI)NKX2-5 mutations causative for congenital heart disease retain functionality and are directed to hundreds of targets, eLife, vol.4, N/A, 2015,pp 1-30
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