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PreviewIssue DateTitleAuthor(s)
2004Transport, enzymatic activity, and stability of mutant sulfamidise (SGSH) identified in patients with mucopolysaccharidosis type III AMuschol, N.; Storch, S.; Balhausen, D.; Beesley, C.; Westermann, J.; Gal, A.; Ullrich, K.; Hopwood, J.; Winchester, B.; Braulke, T.
1996Feline mucopolysaccharidosis type VI - characterization of recombinant N-acetylgalactosamine 4-sulfatase and identification of a mutation causing the diseaseYogalingam, G.; Litjens, T.; Bielicki, J.; Crawley, A.; Muller, V.; Anson, D.; Hopwood, J.
2002Mucopolysaccharidosis 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 networkBradford, T.; Litjens, T.; Parkinson, E.; Hopwood, J.; Brooks, D.
2005Replacing acid ∝-glucosidase in Pompe disease: recombinant and transgenic enzymes are equipotent, but neither completely clears glycogen from type II muscle fibersRaben, N.; Fukuda, T.; Gilbert, A.; de Jong, D.; Thurberg, B.; Mattaliano, R.; Meikle, P.; Hopwood, J.; Nagashima, K.; Nagaraju, K.; Plotz, P.
1995Isolation and characterisation of a recombinant precursor form of lysosomal acid α-glucosidaseFuller, M.; Van der Ploeg, A.; Reuser, A.; Anson, D.; Hopwood, J.
1996Enzyme replacement therapy in a feline model of Maroteaux-Lamy syndromeCrawley, A.; Brooks, D.; Muller, V.; Petersen, B.; Isaac, E.; Bielicki, J.; King, B.; Boulter, C.; Moore, A.; Fazzalari, N.; Anson, D.; Byers, S.; Hopwood, J.
2000Regulation of the lysosome-associated membrane protein in a sucrose model of lysosomal storageIsaac, E.; Karageorgos, L.; Brooks, D.; Hopwood, J.; Meikle, P.

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