1. Adelaide Research & Scholarship

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Results 21-30 of 72 (Search time: 0.004 seconds).
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PreviewIssue DateTitleAuthor(s)
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.
1997Identification of 16 Sulfamidase Gene Mutations Including the Common R74C in Patients With Mucopolysaccharidosis Type IIIa (Sanfilippo A)Bunge, S.; Ince, H.; Steglich, C.; Kleijer, W.; Beck, M.; Zaremba, J.; van Diggelen, O.; Weber, B.; Hopwood, J.; Gal, A.
1995The molecular genetics of mucopolysaccharidosis type I : Diagnostic, clinical and biological implicationsScott, H.; Bunge, S.; Gal, A.; Clarke, L.; Morris, C.; Hopwood, J.
1998Development of a two-dimensional gel electrophoresis database of human lysosomal proteinsChataway, T.; Whittle, A.; Lewis, M.; Bindloss, C.; Moritz, R.; Simpson, R.; Hopwood, J.; Meikle, P.
1997Organ-specific over-sulfation of glycosaminoglycans and altered extracellular matrix in a mouse model of cystic fibrosisHill, W.; Harper, G.; Rozaklis, T.; Boucher, R.; Hopwood, J.
1997Sulfation of chondroitin/dermatan sulfate by cystic fibrosis pancreatic duct cells is not different from control cellsHill, W.; Harper, G.; Rozaklis, T.; Hopwood, J.
1999Prevalence of lysosomal storage disordersMeikle, P.; Hopwood, J.; Clague, A.; Carey, W.
1995A clinically mild case of mucopolysaccharidosis type I - Scheie syndrome (case report)Kozlowski, K.; Nicol, R.; Hopwood, J.
1995Crystallization and preliminary characterisation of human recombinant N-acetylpgalactosamine-4-sulfataseAshby, S.; Clements, P.; Guss, J.; Harvey, J.; Hopwood, J.
1999Autologous transplantation of retrovirally transduced bone marrow or neonatal blood cells into cats can lead to long-term engraftment in the absence of myeloablationSimonaro, C.; Haskins, M.; Abkowitz, J.; Brooks, D.; Hopwood, J.; Zhang, J.B.; Schuchman, E.

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