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PreviewIssue DateTitleAuthor(s)
2007N-acetylgalactosamine-6-sulfatase protein detection in MPS IVA patient and unaffected control samplesParkinson-Lawrence, E.; Muller, V.; Hopwood, J.; Brooks, D.
2007Mutational analysis of mucopolysaccharidosis type VI patients undergoing a phase II trial of enzyme replacement therapyKarageorgos, L.; Brooks, D.; Harmatz, P.; Ketteridge, D.; Pollard, A.; Melville, E.; Parkinson-Lawrence, E.; Clements, P.; Hopwood, J.
2012Neonatal gene therapy with a gamma retroviral vector in mucopolysaccharidosis VI catsPonder, K.; O'Malley, T.; Wang, P.; O'Donnell, P.; Traas, A.; Knox, V.; Aguirre, G.; Ellinwood, N.; Metcalf, J.; Wang, B.; Parkinson-Lawrence, E.; Sleeper, M.; Brooks, D.; Hopwood, J.; Haskins, M.
2005Analysis of normal and mutant iduronate-2-sulphatase conformationParkinson-Lawrence, E.; Turner, C.; Hopwood, J.; Brooks, D.
2006Common antigenicity for two glycosidasesKakavanos, R.; Lehn, P.; Callebaut, I.; Meikle, P.; Parkinson-Lawrence, E.; Hopwood, J.; Brooks, D.
2005Immunochemical analysis of CD107a (LAMP-1)Parkinson-Lawrence, E.; Dean, C.; Chang, M.; Hopwood, J.; Meikle, P.; Brooks, D.
2006Immunochemistry of lysosomal storage disordersParkinson-Lawrence, E.; Fuller, M.; Hopwood, J.; Meikle, P.; Brooks, D.
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.