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Preview	Issue Date	Title	Author(s)
	2005	An index case for the attenuated end of the mucopolysaccharidosis type VI clinical spectrum	Brooks, D.; Gibson, G.; Karageorgos, L.; Hein, L.; Robertson, E.; Hopwood, J.
	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.
	2001	Gentamicin-mediated suppression of Hurler syndrome stop mutations restores a low level of a-L-iduronidase activity and reduces lysosomal glycosaminoglycan accumulation	Keeling, K.; Brooks, D.; Hopwood, J.; Li, P.; Thompson, J.; Bedwell, D.
	2000	Syntaxin 7 is localized to late endosome compartments, associates with Vamp 8, and is required for late endosome-lysosome fusion	Mullock, B.; Smith, C.; Ihrke, G.; Bright, N.; Lindsay, M.; Parkinson, E.; Brooks, D.; Parton, R.; James, D.; Luzio, J.; Piper, R.; Pelham, H.R.B.
	2003	Replacement therapy in Mucopolysaccharidosis type VI: advantages of early onset of therapy	Auclair, D.; Hopwood, J.; Brooks, D.; Lemontt, J.; Crawley, A.
	2002	Immune response to enzyme replacement therapy: single epitope control of antigen distribution from circulation	Glaros, E.; Turner, C.; Parkinson, E.; Hopwood, J.; Brooks, D.
	2000	Regulation of the lysosome-associated membrane protein in a sucrose model of lysosomal storage	Isaac, E.; Karageorgos, L.; Brooks, D.; Hopwood, J.; Meikle, P.