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PreviewIssue DateTitleAuthor(s)
2003Induction of tolerance to a recombinant human enzyme, acid alpha-glucosidase, in enzyme deficient knockout miceRaben, N.; Nagaraju, K.; Lee, A.; Lu, N.; Rivera, Y.; Jatkar, T.; Hopwood, J.; Plotz, P.
2001Mucopolysaccharidosis type VI: Structural and clinical implications of mutations in N-acetylgalactosamine-4-sulfataseLitjens, T.; Hopwood, J.
2007Long-term intra-articular administration of recombinant human N-acetylgalactosamine-4-sulfatase in feline mucopolysaccharidosis VIAuclair, D.; Hopwood, J.; Lemontt, J.; Chen, L.; Byers, S.
2007Functional correction of CNS lesions in an MPS-IIIA mouse model by intracerebral AAV-mediated delivery of sulfamidase and SUMF1 genesFraldi, A.; Hemsley, K.; Crawley, A.; Lombardi, A.; Lau, A.; Sutherland, L.; Auricchio, A.; Ballabio, A.; Hopwood, J.
2002In utero injection of a-L-iduronidase-carrying retrovirus in canine mucopolysaccharidosis type I: Infection of multiple tissues and neonatal gene expressionMeertens, L.; Zhao, Y.; Rosic-Kablar, S.; Li, L.; Chan, K.; Dobson, H.; Gartley, C.; Lutzko, C.; Hopwood, J.; Kohn, D.; Kruth, S.; Hough, M.; Dube, I.
2003Replacement therapy in Mucopolysaccharidosis type VI: advantages of early onset of therapyAuclair, D.; Hopwood, J.; Brooks, D.; Lemontt, J.; Crawley, A.
2002Immune response to enzyme replacement therapy: single epitope control of antigen distribution from circulationGlaros, E.; Turner, C.; Parkinson, E.; Hopwood, J.; Brooks, D.
2000Enzyme replacement therapy in a feline model of MPS VI: Modification of enzyme structure and dose frequencyByers, S.; Crawley, A.; Brumfield, L.; Nuttall, J.; Hopwood, J.
2009Delivery of recombinant proteins via the cerebrospinal fluid as a therapy option for neurodegenerative lysosomal storage diseasesHemsley, K.; Hopwood, J.
2000Recombinant canine a-L-fucosidase: expression, purification, and characterizationBielicki, J.; Muller, V.; Fuller, M.; Hopwood, J.; Anson, D.

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