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Results 1-10 of 36 (Search time: 0.004 seconds).
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PreviewIssue DateTitleAuthor(s)
1995Expression, purification and characterization of recombinant human N-acetylgalactosamine-6-sulphataseBielicki, J.; Fuller, M.; Guo, X.H.; Morris, C.; Hopwood, J.; Anson, D.
2013Heparan sulfate proteoglycans containing a glypican 5 core and 2-O-sulfo-induronic acid function as Sonic Hedgehog co-receptors to promote proliferationWitt, R.; Hecht, M.; Pazyra-Murphy, M.; Cohen, S.; Noti, C.; van Kuppevelt, T.; Fuller, M.; Chan, J.; Hopwood, J.; Seeberger, P.; Segal, R.
2012Mass spectrometric quantification of glycogen to assess primary substrate accumulation in the Pompe mouseFuller, M.; Duplock, S.; Turner, C.; Davey, P.; Brooks, D.; Hopwood, J.; Meikle, P.
2012Abnormal gangliosides are localized in lipid rafts in Sanfilippo (MPS3a) mouse brainDawson, G.; Fuller, M.; Hemsley, K.; Hopwood, J.
2008Plasma lipids are altered in Gaucher disease: Biochemical markers to evaluate therapeutic interventionMeikle, P.; Whitfield, P.; Rozaklis, T.; Blacklock, D.; Duplock, S.; Elstein, D.; Zimran, A.; Mengel, E.; Cannell, P.; Hopwood, J.; Fuller, M.
2010Determination of urinary oligosaccharides by high-performance liquid chromatography/electrospray ionization-tandem mass spectrometry: Application to Hunter syndromeNielsen, T.; Rozek, T.; Hopwood, J.; Fuller, M.
2006Characterization of a C57BL/6 congenic mouse strain of mucopolysaccharidosis type IIIACrawley, A.; Gliddon, B.; Auclair, D.; Brodie, S.; Hirte, C.; King, B.; Fuller, M.; Hemsley, K.; Hopwood, J.
2008Glucosylceramide accumulation is not confined to the lysosome in fibroblasts from patients with Gaucher diseaseFuller, M.; Rozaklis, T.; Lovejoy, M.; Zarrinkalam, K.; Hopwood, J.; Meikle, P.
2006Characterization of sulfated oligosaccharides in mucopolysaccharidosis type IIIA by electrospray ionization mass spectrometryMason, K.; Meikle, P.; Hopwood, J.; Fuller, M.
2004Glycosaminoglycan degradation fragments in mucopolysaccharidosis IFuller, M.; Meikle, P.; Hopwood, J.

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