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Preview	Issue Date	Title	Author(s)
	2004	In vitro characterization of genetically modified embryonic stem cells as a therapy for murine mucopolysaccharidosis type IIIA	Lau, A.; Hemsley, K.; Meedeniya, A.; Hopwood, J.
	2004	HLS5, a novel RBCC (ring finger, B box, coiled-coil) family member isolated from a hemopoietic lineage switch, is a candidate tumor suppressor	Lalonde, J.; Lim, R.; Ingley, E.; Tilbrook, P.; Thompson, M.; McCulloch, R.; Beaumont, J.; Wicking, C.; Eyre, H.; Sutherland, G.; Howe, K.; Solomon, E.; Williams, J.; Klinken, S.
	2008	The mir-200 family and mir-205 regulate epithelial to mesenchymal transition by targeting ZEB1 and SIP1	Gregory, P.; Bert, A.; Paterson, E.; Barry, S.; Tsykin, A.; Farshid, G.; Vadas, M.; Khew-Goodall, Y.; Goodall, G.
	2008	Maroteaux-Lamy syndrome: Functional characterization of pathogenic mutations and polymorphisms in the arylsulfatase B gene	Garrido, E.; Cormand, B.; Hopwood, J.; Chabas, A.; Grinberg, D.; Vilageliu, L.
	2008	Flightless I: An actin-remodelling protein and an important negative regulator of wound repair	Kopecki, Z.; Cowin, A.
	2002	Mucopolysaccharidosis type VI (Maroteaux-Lamy syndrome): A Y210C mutation causes either altered protein handling or altered protein function of N-acetylgalactosamine 4-sulfatase at multiple points in the vacuolar network	Bradford, T.; Litjens, T.; Parkinson, E.; Hopwood, J.; Brooks, D.
	2008	Mucosal immunology down under: Special interest group in mucosal immunology workshop, Australasian Society for Immunology, Sydney, Australia, 2 December 2007	Cripps, A.; Sutton, P.; Beagley, K.; Robertson, S.; Dunkely, M.
	2009	A UPF3-mediated regulatory switch that maintains RNA surveillance	Chan, W.; Bhalla, A.; Le Hir, H.; Nguyen, L.; Huang, L.; Gecz, J.; Wilkinson, M.
	2004	Mutations of CDKL5 cause a severe neurodevelopmental disorder with infantile spasms and mental retardation	Weaving, L.; Christodoulou, J.; Williamson, S.; Friend, K.; McKenzie, O.; Archer, H.; Evans, J.; Clarke, A.; Pelka, G.; Tam, P.; Watson, C.; Lahooti, H.; Ellaway, C.; Bennetts, B.; Leonard, H.; Gecz, J.
	2001	A recurrent RNA-splicing mutation in the SEDL gene causes X-linked spondyloepiphyseal dysplasia tarda	Tiller, G.; Hannig, V.; Dozier, D.; Carrel, L.; Trevarthen, K.; Wilcox, W.; Mundlos, S.; Haines, J.; Gedeon, A.; Gecz, J.