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Results 21-28 of 28 (Search time: 0.002 seconds).
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PreviewIssue DateTitleAuthor(s)
2010Allogeneic stem cell transplantation does not improve neurological deficits in mucopolysaccharidosis type IIIA miceLau, A.; Hannouche, H.; Rozaklis, T.; Hassiotis, S.; 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.
2012Mucopolysaccharidosis type VI in a Miniature Poodle-type dog caused by a deletion in the arylsulphatase B geneJolly, R.; Hopwood, J.; Marshall, N.; Jenkins, K.; Thompson, D.; Dittmer, K.; Thompson, J.; Fedele, A.; Raj, K.; Giger, U.
2010Genetic manipulation of murine embryonic stem cells with enhanced green fluorescence protein and sulfatase-modifying factor I genesZhao, G.; Karageorgos, L.; Hutchinson, R.; Hopwood, J.; Hemsley, K.
2010Embryonic stem cell-derived glial precursors as a vehicle for sulfamidase production in the MPS-IIIA mouse brainRobinson, A.; Zhao, G.; Rathjen, J.; Rathjen, P.; Hutchinson, R.; Eyre, H.; Hemsley, K.; Hopwood, J.
2014Disease stage determines the efficacy of treatment of a paediatric neurodegenerative diseaseHassiotis, S.; Beard, H.; Luck, A.; Trim, P.; King, B.; Snel, M.; Hopwood, J.; Hemsley, K.
2013Neonatal bone marrow transplantation in MPS IIIA miceLau, A.; Shamsani, N.; Winner, L.; Hassiotis, S.; King, B.; Hopwood, J.; Hemsley, K.
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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