Transthyretin interacts with the lysosome-associated membrane protein (LAMP-1) in circulation by Chang, Melissa H Y, Hua, Chi T, Isaac, Elizabeth L, Litjens, Tom, Hodge, Greg, Karageorgos, Litsa E, Meikle, Peter J

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Serotype Conversion in Vibrio cholerae O1 by Stroeher, Uwe H., Karageorgos, Litsa E., Morona, Renato, Manning, Paul A.

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Diagnosis of lysosomal storage disorders: evaluation of lysosome-associated membrane protein LAMP-1 as a diagnostic marker by Meikle, Peter J, Brooks, Doug A, Ravenscroft, Elaine M, Yan, Miao, Williams, Ruth E, Jaunzems, Alvis E, Chataway, Timothy K, Karageorgos, Litsa E, Davey, Richard C, Boulter, Christine D, Carlsson, Sven R, Hopwood, John J

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Genetic Rearrangements in the rfb Regions of Vibrio cholerae O1 and O139 by Stroeher, Uwe H., Jedani, Kathy E., Dredge, B. Kate, Morona, Renato, Brown, Melissa H., Karageorgos, Litsa E., Albert, M. John, Manning, Paul A.

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Regulation of the Lysosome-Associated Membrane Protein in a Sucrose Model of Lysosomal Storage by Isaac, Elizabeth L., Karageorgos, Litsa E., Brooks, Doug A., Hopwood, John J., Meikle, Peter J.

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Structure and sequence of the human sulphamidase gene by Karageorgos, L E, Guo, X H, Blanch, L, Weber, B, Anson, D S, Scott, H S, Hopwood, J J

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A putative pathway for perosamine biosynthesis is the first function encoded within the rfb region of Vibrio cholerae O1 by Stroeher, Uwe H., Karageorgos, Litsa E., Brown, Melissa H., Morona, Renato, Manning, Paul A.

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Lysosomal Biogenesis in Lysosomal Storage Disorders by Karageorgos, Litsa E., Isaac, Elizabeth L., Brooks, Doug A., Ravenscroft, Elaine M., Davey, Richard, Hopwood, John J., Meikle, Peter J.

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Mutational analysis of 105 mucopolysaccharidosis type VI patients by Karageorgos, Litsa, Brooks, Doug A., Pollard, Anthony, Melville, Elizabeth L., Hein, Leanne K., Clements, Peter R., Ketteridge, David, Swiedler, Stuart J., Beck, Michael, Giugliani, Roberto, Harmatz, Paul, Wraith, James E., Guffon, Nathalie, Leão Teles, Elisa, Sá Miranda, M. Clara, Hopwood, John J.

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An index case for the attenuated end of the mucopolysaccharidosis type VI clinical spectrum by Brooks, Doug A., Gibson, Gary J., Karageorgos, Litsa, Hein, Leanne K., Robertson, Evelyn F., Hopwood, John J.

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Aminoglycoside-Induced Premature Stop Codon Read-Through of Mucopolysaccharidosis Type I Patient Q70X and W402X Mutations in Cultured Cells by Kamei, Makoto, Kasperski, Karissa, Fuller, Maria, Parkinson-Lawrence, Emma J., Karageorgos, Litsa, Belakhov, Valery, Baasov, Timor, Hopwood, John J., Brooks, Doug A.

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