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Results 1-10 of 72 (Search time: 0.003 seconds).
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PreviewIssue DateTitleAuthor(s)
1998Molecular heterogeneity in mucopolysaccharidosis IVA in Australia and Northern Ireland: nine novel mutations including T312S, a common allele that confers a mild phenotypeYamada, N.; Fukuda, S.; Tomatsu, S.; Muller, V.; Hopwood, J.; Nelson, J.; Kato, Z.; Yamagishi, A.; Sukegawa, K.; Kondo, M.; Orii, T.
1998Evaluation of the lysosome-associated membrane protein LAMP-2 as a marker for lysosomal storage disordersHua, C.; Hopwood, J.; Carlsson, S.; Harris, R.; Meikle, P.
1995Crystallization and preliminary characterisation of human recombinant N-acetylpgalactosamine-4-sulfataseAshby, S.; Clements, P.; Guss, J.; Harvey, J.; Hopwood, J.
1995Quantitative morphometric analysis of trabecular bone architecture in feline mucopolysaccharidosis VIClarke, J.; Byers, S.; Moore, A.; Fazzalari, N.; Hopwood, J.
1995Glucoronate-2-sulphataseBielicki, J.; Freeman, C.; Hopwood, J.
1995N-Acetylgalactosamine-4-sulphataseBielicki, J.; Hopwood, J.
1995N-Acetylgalactosamine-6-sulphataseBielicki, J.; Hopwood, J.
1996Long-term in vitro correction of alpha-L-iduronidase deficiency (Hurler syndrome) in human bone marrowFairbairn, L.; Lashford, L.; Spooncer, E.; McDermott, R.; Lebens, G.; Arrand, J.; Arrand, J.; Bellantuono, I.; Holt, R.; Hatton, C.; Cooper, A.; Besley, G.; Wraith, J.; Anson, D.; Hopwood, J.; Dexter, T.
1997Structure of a human lysosomal sulfataseBond, C.; Clements, P.; Ashby, S.; Collyer, C.; Harrop, S.; Hopwood, J.; Guss, J.
1999Processing of normal lysosomal and mutant N-acetylgalactosamine 4-sulphatase: BiP (immunoglobulin heavy-chain binding protein) may interact with critical protein contact sitesBradford, T.; Gething, M.; Davey, R.; Hopwood, J.; Brooks, D.