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Results 1-10 of 11 (Search time: 0.003 seconds).
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PreviewIssue DateTitleAuthor(s)
1997Mapping of the gene for vascular endothelial growth factor-D in mouse and man to the X chromosomeJenkins, N.; Woollatt, E.; Crawford, J.; Gilbert, D.; Baldwin, M.; Sutherland, G.; Copeland, N.; Achen, M.
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.
2004In vitro characterization of genetically modified embryonic stem cells as a therapy for murine mucopolysaccharidosis type IIIALau, A.; Hemsley, K.; Meedeniya, A.; Hopwood, J.
2004Purification and characterization of recombinant murine sulfamidaseGliddon, B.; Yogalingam, G.; Hopwood, J.
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.
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.
2004Enzyme-replacement therapy from birth delays the development of behavior and learning problems in mucopolysaccharidosis type IIIA miceGliddon, B.; Hopwood, J.
1996Characterization and chromosomal localization of the human A2a adenosine receptor gene - ADORA2ALe, F.; Townsend-Nicholson, A.; Baker, E.; Sutherland, G.; Schofield, P.
2001Purification and characterization of recombinant human lysosomal a-mannosidaseBerg, T.; King, B.; Meikle, P.; Nilssen, O.; Tollersrud, O.; Hopwood, J.