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Results 11-20 of 26 (Search time: 0.003 seconds).
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PreviewIssue DateTitleAuthor(s)
1995In vivo delivery of human α-L-iduronidase in mice implanted with neo-organsSalvetti, A.; Moullier, P.; Cornet, V.; Brooks, D.; Hopwood, J.; Danos, O.; Heard, J.M.
2001A novel missense mutation in lysosomal sulfamidase is the basis of MPS III A in a spontaneous mouse mutantBhattacharyya, R.; Gliddon, B.; Beccari, T.; Hopwood, J.; Stanley, P.
1996Correction of Sanfilippo a Skin Fibroblasts By Retroviral Vector-Mediated Gene TransferBielicki, J.; Hopwood, J.; Anson, D.
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.
2005Development of motor deficits in a murine model of mucopolysaccharidosis type IIIA (MPS-IIIA)Hemsley, K.; Hopwood, J.
2003Mouse sulphamidase gene: characterization of the promoter region of the gene and expression in mouse tissuesCostanzi, E.; Beccari, T.; Aisa, M.; Tiribuzi, R.; Hopwood, J.; Orlacchio, A.
2005Over-expression of human lysosomal -mannosidae in mouse embryonic stem cellsRobinson, A.; Crawley, A.; Hopwood, J.
2005Analysis of normal and mutant iduronate-2-sulphatase conformationParkinson-Lawrence, E.; Turner, C.; 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.
2002Immune response to enzyme replacement therapy: single epitope control of antigen distribution from circulationGlaros, E.; Turner, C.; Parkinson, E.; Hopwood, J.; Brooks, D.