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PreviewIssue DateTitleAuthor(s)
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.
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.
2010Biochemical profiling to predict disease severity in metachromatic leukodystrophyTan, M.; Fuller, M.; Zabidi-Hussin, Z.; Hopwood, J.; Meikle, P.
2012Intrathecal recombinant human 4-sulfatase reduces accumulation of glycosaminoglycans in dura of mucopolysaccharidosis VI catsAuclair, D.; Finnie, J.; Walkley, S.; White, J.; Nielsen, T.; Fuller, M.; Cheng, A.; O'Neill, C.; 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.
2011Screening patients referred to a metabolic clinic for lysosomal storage disordersFuller, M.; Tucker, J.; Lang, D.; Dean, C.; Fietz, M.; Meikle, P.; Hopwood, J.
2014Aminoglycoside-induced premature stop codon read-through of mucopolysaccharidosis type I patient Q70X and W402X mutations in cultured cellsKamei, M.; Kasperski, K.; Fuller, M.; Parkinson-Lawrence, E.; Karageorgos, L.; Belakhov, V.; Baasov, T.; Hopwood, J.; Brooks, D.; Zschocke, J.; Gibson, K.; BRown, G.; Morava, E.; Peters, V.

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