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Results 11-20 of 24 (Search time: 0.002 seconds).
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PreviewIssue DateTitleAuthor(s)
2005Over-expression of human lysosomal -mannosidae in mouse embryonic stem cellsRobinson, A.; Crawley, A.; Hopwood, J.
2005Survival and engraftment of mouse embryonic stem cell-derived implants in the guinea pig brainRobinson, A.; Meedeniya, A.; Hemsley, K.; Auclair, D.; Crawley, A.; Hopwood, J.
2011Enzyme replacement reduces neuropathology in MPS IIIA dogsCrawley, A.; Marshall, N.; Beard, H.; Hassiotis, S.; Walsh, V.; King, B.; Hucker, N.; Fuller, M.; Jolly, R.; Hopwood, J.; Hemsley, K.
2009Examination of intravenous and intra-CSF protein delivery for treatment of neurological diseaseHemsley, K.; Luck, A.; Crawley, A.; Hassiotis, S.; Beard, H.; King, B.; Rozek, T.; Rozaklis, T.; Fuller, M.; Hopwood, J.
2003Prevalence of mucopolysaccharidosis type VI mutations in Siamese catsCrawley, A.; Muntz, F.; Haskins, M.; Jones, B.; Hopwood, J.
1998Mild feline mucopolysaccharidosis type VI. Identification of an N-acetylgalactosamine-4-sulfatase mutation causing instability and increased specific activityYogalingam, G.; Hopwood, J.; Crawley, A.; Anson, D.
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.
1997Enzyme replacement therapy from birth in a feline model of mucopolysaccharidosis type VICrawley, A.; Niedzielski, K.; Isaac, E.; Davey, R.; Byers, S.; Hopwood, J.
1998Two mutations within a feline mucopolysaccharidosis type VI colony cause three different clinical phenotypesCrawley, A.; Yogalingam, G.; Muller, V.; Hopwood, J.
2004Monitoring dose response of enzyme replacement therapy in feline mucopolysaccharidosis type VI by tandem mass spectrometryCrawley, A.; Ramsay, S.; Byers, S.; Hopwood, J.; Meikle, P.