Iminosugars: from botanical curiosities to licensed drugs von Winchester, Bryan G.

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Discovery of a new biomarker for the mucopolysaccharidoses (MPS), dipeptidyl peptidase IV (DPP-IV; CD26), by SELDI-TOF mass spectrometry von Beesley, Clare E., Young, Elisabeth P., Finnegan, Niamh, Jackson, Marie, Mills, Kevin, Vellodi, Ashok, Cleary, Maureen, Winchester, Bryan G.

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Identification and characterisation of an 8.7kb deletion and a novel nonsense mutation in two Italian families with Sanfilippo syndrome type D (mucopolysaccharidosis IIID) von Beesley, Clare E., Concolino, Daniela, Filocamo, Mirella, Winchester, Bryan G., Strisciuglio, Pietro

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A combined defect in the biosynthesis of N- and O-glycans in patients with cutis laxa and neurological involvement: the biochemical characteristics von Wopereis, Suzan, Morava, Éva, Grünewald, Stephanie, Mills, Philippa B., Winchester, Bryan G., Clayton, Peter, Coucke, Paul, Huijben, Karin M.L.C., Wevers, Ron A.

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Identification and characterisation of an 8.7 kb deletion and a novel nonsense mutation in two Italian families with Sanfilippo syndrome type D (mucopolysaccharidosis IIID) von Beesley, Clare E., Concolino, Daniela, Filocamo, Mirella, Winchester, Bryan G., Strisciuglio, Pietro

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Application of magnetic chromatography to the isolation of lysosomes from fibroblasts of patients with lysosomal storage disorders von Diettrich, Ole, Mills, Kevin, Johnson, Andrew W, Hasilik, Andrej, Winchester, Bryan G

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Case of X-linked myopathy with excessive autophagy von Chow, Gabriel, Beesley, Clare E, Robson, Keith, Winchester, Bryan G, Holton, Janice L

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Prenatal Diagnosis of Lysosomal Storage Diseases von Lake, Brian D, Young, Elisabeth P, Winchester, Bryan G

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The chemistry of castanospermine, part V: synthetic modifications at C-1 and C-7 von H Furneaux, Richard, J Gainsford, Graeme, M Mason, Jennifer, C Tyler, Peter, Hartley, Oliver, G Winchester, Bryan

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Non-viral, integrin-mediated gene transfer into fibroblasts from patients with lysosomal storage diseases von Joanna Estruch, Elaine, Lewis Hart, Stephen, Kinnon, Christine, Winchester, Bryan G.

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Mutational analysis of 85 mucopolysaccharidosis type I families : frequency of known mutations, identification of 17 novel mutations and in vitro expression of missense mutations von BEESLEY, Clare E, MEANEY, Cathy A, GREENLAND, Gavin, ADAMS, Vanessa, VELLODI, Ashok, YOUNG, Elisabeth P, WINCHESTER, Bryan G

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Inhibition of Fucosyl Transferase and Fucosidase by a Rigid Bicyclic Mimic of α-L-Fucose von Beacham, Annabel R, Smelt, Kathryn H, Biggadike, Keith, Britten, Christopher J, Hackett, Lucy, Winchester, Bryan G, Nash, Robert J, Griffiths, Rhodri C, Fleet, George W.J

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6R-, and 6S, -6C-methylglucose from D-glucuronolactone: Efficient synthesis of a seven carbon fucose analogue: Inhibition of some enzymes of primary metabolism von Blériot, Yves, Masaguer, Christian F., Charlwood, Joanne, Winchester, Bryan G, Lane, Alexandra L., Crook, Sarah, Watkin, David J., Fleet, George W.J.

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Lysosomal membrane proteins von Winchester, Bryan G.

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6R- and 6S-6C-Methylmannose from d-mannuronolactone. Inhibition of phosphoglucomutase and phosphomannomutase: agents for the study of the primary metabolism of mannose von Martin, Angeles, Watterson, Mark P, Brown, Andrew R, Imtiaz, Faiqa, Winchester, Bryan G, Watkin, David J, Fleet, George W.J

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The underglycosylation of plasma α1-antitrypsin in congenital disorders of glycosylation type I is not random von Mills, Kevin, Mills, Philippa B., Clayton, Peter T., Mian, Nasi, Johnson, Andrew W., Winchester, Bryan G.

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Identification of α1-antitrypsin variants in plasma with the use of proteomic technology von MILLS, Kevin, MILLS, Philippa B, CLAYTON, Peter T, JOHNSON, Andrew W, WHITEHOUSE, David B, WINCHESTER, Bryan G

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Analysis by matrix assisted laser desorption/ ionisation-time of flight mass spectrometry of the post-translational modifications of α1-antitrypsin isoforms separated by two- dimen... von Mills, Philippa B., Mills, Kevin, Johnson, Andrew W., Clayton, Peter T., Winchester, Bryan G.

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A case of X Linked myopathy with autophagy von Chow, G, Beesley, Clare E, Winchester, Bryan G, Holton, Janice

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Mutational analysis of Sanfilippo syndrome type A (MPS IIIA): identification of 13 novel mutations von BEESLEY, CLARE E, YOUNG, ELISABETH P, VELLODI, ASHOK, WINCHESTER, BRYAN G

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