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Preview	Issue Date	Title	Author(s)
	2001	Glycosidase active site mutations in human a-L-iduronidase	Brooks, D.; Fabrega, S.; Hein, L.; Parkinson, E.; Durand, P.; Yogalingam, G.; Matte, U.; Giugliani, R.; Dasvarma, A.; Eslahpazire, J.; Henrissat, B.; Mornon, J.; Hopwood, J.; Lehn, P.
	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.
	1995	In vivo delivery of human α-L-iduronidase in mice implanted with neo-organs	Salvetti, A.; Moullier, P.; Cornet, V.; Brooks, D.; Hopwood, J.; Danos, O.; Heard, J.M.
	2003	Significance of immune response to enzyme-replacement therapy for patients with a lysosomal storage disorder	Brooks, D.; Kakavanos, R.; Hopwood, J.
	2005	Prediction of neuropathology in mucopolysaccharidosis I patients	Fuller, M.; Brooks, D.; Evangelista, M.; Hein, L.; Hopwood, J.; Meikle, P.
	2003	Replacement therapy in Mucopolysaccharidosis type VI: advantages of early onset of therapy	Auclair, D.; Hopwood, J.; Brooks, D.; Lemontt, J.; Crawley, A.
	2003	Identification and characterization of 13 new mutations in mucopolysaccharidosis type I patients	Matte, U.; Yogalingam, G.; Brooks, D.; Leistner, S.; Schwartz, I.; Lima, L.; Norato, D.; Brum, J.; Beesley, C.; Winchester, B.; Giugliani, R.; Hopwood, J.
	2007	Molecular pathology of expanded polyalanine tract mutations in the Aristaless-related homeobox gene	Shoubridge, C.; Cloosterman, D.; Parkinson-Lawrence, E.; Brooks, D.; Gecz, J.
	1997	A membrane protein primarily associated with the lysosomal compartment	Brooks, D.; Bradford, T.; Carlsson, S.; Hopwood, J.
	2005	Analysis of normal and mutant iduronate-2-sulphatase conformation	Parkinson-Lawrence, E.; Turner, C.; Hopwood, J.; Brooks, D.