CDKN2B expression in adipose tissue of familial combined hyperlipidemia patients[S] von Horswell, Stuart D., Fryer, Lee G.D., Hutchison, Claire E., Zindrou, Dlear, Speedy, Helen E., Town, Margaret-M., Duncan, Emma J., Sivapackianathan, Rasheeta, Patel, Hetal N., Jones, Emma L., Braithwaite, Adam, Salm, Max P.A., Neuwirth, Claire K.Y., Potter, Elizabeth, Anderson, Jonathan R., Taylor, Kenneth M., Seed, Mary, Betteridge, D. John, Crook, Martin A., Wierzbicki, Anthony S., Scott, James, Naoumova, Rossi P., Shoulders, Carol C.

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Genetic and other sources of variation in the activity of serum paraoxonase/diazoxonase in humans: consequences for risk from exposure to diazinon von OʼLeary, Karen A, Edwards, Robert J, Town, Margaret M, Boobis, Alan R

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Immunolocalization of cystinosin, the protein defective in cystinosis von HAQ, Mushfequr R, KALATZIS, Vasiliki, GUBLER, Marie-Claire, TOWN, Margaret M, ANTIGNAC, Corinne, VAN'T HOFF, William G, WOOLF, Adrian S

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Linkage of the gene for cystinosis to markers on the short arm of chromosome 17 von Stephenson, Leah A, Schneider, Jerry A, Mathew, Christopher G, van't Hoff, William, Gahl, William A, Weissenbach, Jean, Town, Margaret M, McDowell, Geraldine A, Polymeropoulos, Mihael H, Farrall, Martin

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A novel gene encoding an integral membrane protein is mutated in nephropathic cystinosis von Hoff, William van't, Bates, Gillian P, Antignac, Corinne, Jean, Geneviève, Forestier, Lionel, Gribouval, Olivier, Whitmore, Scott A, Town, Margaret, Broyer, Michel, Cherqui, Stèphanie, Attard, Marlene, Callen, David F

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Genetic Association of the Serotonin Transporter in Pulmonary Arterial Hypertension von Machado, Rajiv D, Koehler, Rolf, Glissmeyer, Eric, Veal, Colin, Suntharalingam, Jay, Kim, Miryoung, Carlquist, John, Town, Margaret, Elliott, C. Gregory, Hoeper, Marius, Fijalkowska, Anna, Kurzyna, Marcin, Thomson, Jennifer R, Gibbs, Simon R, Wilkins, Martin R, Seeger, Werner, Morrell, Nicholas W, Gruenig, Ekkehard, Trembath, Richard C, Janssen, Bart

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Genome-Wide Scan for Premature Hypertension Supports Linkage to Chromosome 2 in a Large Kyrgyz Family von Kalmyrzaev, Bolot, Aldashev, Almaz, Khalmatov, Mitalib, Polupanov, Andrey, Jumagulova, Ainagul, Mamanova, Lira, Wilkins, Martin R, Town, Margaret

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Severity of phenotype in cystinosis varies with mutations in the CTNS gene : predicted effect on the model of cystinosin von ATTARD, M, JEAN, G, FORESTIER, L, CHERQUI, S, VAN'T HOFF, W, BROYER, M, ANTIGNAC, C, TOWN, M

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Molecular Characterization of CTNS Deletions in Nephropathic Cystinosis: Development of a PCR-Based Detection Assay von Forestier, Lionel, Jean, Geneviève, Attard, Marlene, Cherqui, Stéphanie, Lewis, Cathryn, van't Hoff, William, Broyer, Michel, Town, Margaret, Antignac, Corinne

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Structure of the Human Sarco/Endoplasmic Reticulum Ca2+-ATPase 3 Gene von Dode, Leonard, De Greef, Christine, Mountian, Irina, Attard, Marlene, Town, Margaret M., Casteels, Rik, Wuytack, Frank

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Molecular analysis of cystinosis: probable Irish origin of the most common French Canadian mutation von McGowan-Jordan, J, Stoddard, K, Podolsky, L, Orrbine, E, McLaine, P, Town, M, Goodyer, P, MacKenzie, A, Heick, H

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Clinical and molecular aspects of nephropathic cystinosis von MCDOWELL, G. A, TOWN, M. M, VAN'T HOFF, W, GAHL, W. A

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High-resolution mapping of the gene for cystinosis, using combined biochemical and linkage analysis von JEAN, G, FUCHSHUBER, A, TOWN, M. M, GRIBOUVAL, O, SCHNEIDER, J. A, BROYER, M, VAN'T HOFF, W, NIAUDET, P, ANTIGNAC, C

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Both mutations in G6PD A — are necessary to produce the G6PD deficient phenotype von Town, Margaret, Bautista, Jose M., Mason, Philip J., Luzzatto, Lucio

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Deficiency in red blood cells von M, D, T, M, M, P, V, T, L, L, G, D. K

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Favism in the African type of glucose-6-phosphate dehydrogenase deficiency (A-) von Galiano, S, Gaetani, G F, Barabino, A, Cottafava, F, Zeitlin, H, Town, M, Luzzatto, L

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The production of normal and variant human glucose‐6‐phosphate dehydrogenase in cos cells von MASON, Philip J., VULLIAMY, Tom J., FOULKES, Nicholas S., TOWN, Margaret, HAIDAR, Buran, LUZZATTO, Lucio

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Fine Mapping of the Cystinosis Gene Using an Integrated Genetic and Physical Map of a Region within Human Chromosome Band 17p13 von McDowell, Geraldine, Isogai, Takao, Tanigami, Akira, Hazelwood, Senator, Ledbetter, David, Polymeropoulos, Mihael H., Lichter-Konecki, Uta, Konecki, David, Town, Margaret M., Hoff, William Van’t, Weissenbach, Jean, Gahl, William A.

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A standardized monitor for the control of ethylene oxide sterilization cycles von Dadd, A. H., Stewart, Celia M., Town, Margaret M.

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Quality of Care of People With Type 2 Diabetes in Eight European Countries: Findings from the Guideline Adherence to Enhance Care (GUIDANCE) study von STONE, Margaret A, CHARPENTIER, Guillaume, KHUNTI, Kamlesh, DOGGEN, Kris, KUSS, Oliver, LINDBLAD, Ulf, KELLNER, Christiane, NOLAN, John, PAZDERSKA, Agnieszka, RUTTEN, Guy, TRENTO, Marina

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