Resistance to hepcidin is conferred by hemochromatosis-associated mutations of ferroportin von Drakesmith, Hal, Schimanski, Lisa M., Ormerod, Emma, Merryweather-Clarke, Alison T., Viprakasit, Vip, Edwards, Jon P., Sweetland, Emma, Bastin, Judy M., Cowley, Diana, Chinthammitr, Yingyong, Robson, Kathryn J.H., Townsend, Alain R.M.

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In vitro functional analysis of human ferroportin (FPN) and hemochromatosis-associated FPN mutations von Schimanski, Lisa M., Drakesmith, Hal, Merryweather-Clarke, Alison T., Viprakasit, Vip, Edwards, Jon P., Sweetland, Emma, Bastin, Judy M., Cowley, Diana, Chinthammitr, Yingyong, Robson, Kathryn J.H., Townsend, Alain R.M.

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Factors influencing disease phenotype and penetrance in HFE haemochromatosis von Rochette, J, Le Gac, G, Lassoued, K, Férec, C, Robson, K. J. H

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Global gene expression analysis of human erythroid progenitors von Merryweather-Clarke, Alison T., Atzberger, Ann, Soneji, Shamit, Gray, Nicki, Clark, Kevin, Waugh, Craig, McGowan, Simon J., Taylor, Stephen, Nandi, Asoke K., Wood, William G., Roberts, David J., Higgs, Douglas R., Buckle, Veronica J., Robson, Kathryn J.H.

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Mutations in the β-Tubulin Gene TUBB5 Cause Microcephaly with Structural Brain Abnormalities von Breuss, Martin, Heng, Julian Ik-Tsen, Poirier, Karine, Tian, Guoling, Jaglin, Xavier Hubert, Qu, Zhengdong, Braun, Andreas, Gstrein, Thomas, Ngo, Linh, Haas, Matilda, Bahi-Buisson, Nadia, Moutard, Marie-Laure, Passemard, Sandrine, Verloes, Alain, Gressens, Pierre, Xie, Yunli, Robson, Kathryn J.H., Rani, Deepa Selvi, Thangaraj, Kumarasamy, Clausen, Tim, Chelly, Jamel, Cowan, Nicholas Justin, Keays, David Anthony

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Distinct gene expression program dynamics during erythropoiesis from human induced pluripotent stem cells compared with adult and cord blood progenitors von Merryweather-Clarke, Alison T, Tipping, Alex J, Lamikanra, Abigail A, Fa, Rui, Abu-Jamous, Basel, Tsang, Hoi Pat, Carpenter, Lee, Robson, Kathryn J H, Nandi, Asoke K, Roberts, David J

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Iron overload in the Asian community von Lok, Chun Yu, Merryweather-Clarke, Alison T., Viprakasit, Vip, Chinthammitr, Yingyong, Srichairatanakool, Somdet, Limwongse, Chanin, Oleesky, David, Robins, Anthony J., Hudson, John, Wai, Phyu, Premawardhena, Anuja, de Silva, H. Janaka, Dassanayake, Anuradha, McKeown, Carole, Jackson, Maurice, Gama, Rousseau, Khan, Nasaim, Newman, William, Banait, Gurvinder, Chilton, Andrew, Wilson-Morkeh, Isaac, Weatherall, David J., Robson, Kathryn J.H.

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The effect of altering the 20:5n-3 and 22:6n-3 content of a meal on the postprandial incorporation of n-3 polyunsaturated fatty acids into plasma triacylglycerol and non-esterified... von Burdge, G.C, Sala-Vila, A, West, A.L, Robson, H.J.L, Le Fevre, L. Wilkinson, Powell, J, Calder, P.C

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Inverse Associations of Human Leukocyte Antigen and Malaria Parasite Types in Two West African Populations von KAREN YOUNG, FRODSHAM, Angela, DOUMBO, Ogobara K, GUPTA, Sunetra, DOLO, Amagana, JIANG TING HU, ROBSON, Kathryn J. H, CRISANTI, Andrea, HILL, Adrian V. S, GILBERT, Sarah C

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A Plasmodium falciparum Candidate Vaccine Based on a Six-Antigen Polyprotein Encoded by Recombinant Poxviruses von Prieur, Eric, Gilbert, Sarah C., Schneider, Joerg, Moore, Anne C., Sheu, Eric G., Goonetilleke, Nilu, Kathryn J. H. Robson, Adrian V. S. Hill

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An investigation into the release of cefuroxime axetil from taste-masked stearic acid microspheres: Part 1: The influence of the dissolution medium on the drug release profile and... von Robson, H.J, Craig, D.Q.M, Deutsch, D

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Digenic inheritance of mutations in HAMP and HFE results in different types of haemochromatosis von Merryweather-Clarke, Alison T., Cadet, Estelle, Bomford, Adrian, Capron, Dominique, Viprakasit, Vip, Miller, Anne, McHugh, Paddy J., Chapman, Roger W., Pointon, Jennifer J., Wimhurst, Victoria L.C., Livesey, Karen J., Tanphaichitr, Voravarn, Rochette, Jacques, Robson, Kathryn J.H.

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A highly conserved amino-acid sequence in thrombospondin, properdin and in proteins from sporozoites and blood stages of a human malaria parasite von Robson, Kathryn J. H, Hall, Jennifer R. S, Jennings, M. W, Harris, T. J. R, Marsh, K, Newbold, C. I, Tate, Valerie E, Weatherall, D. J

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Analysis of genes implicated in iron regulation in individuals presenting with primary iron overload von ZAAHL, Monique G, MERRYWEATHER-CLARKE, Alison T, KOTZE, Maritha J, VAN DER MERWE, Schalk, WARNICH, Louise, ROBSON, Kathryn J. H

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Ascorbic acid deficiency, iron overload and alcohol abuse underlie the severe osteoporosis in black African patients with hip fractures--a bone histomorphometric study von Schnitzler, C M, Schnaid, E, MacPhail, A P, Mesquita, J M, Robson, H J

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The origin and spread of the HFE-C282Y haemochromatosis mutation von DISTANTE, S, ROBSON, K. J. H, GRAHAM-CAMPBELL, J, ARNAIZ-VILLENA, A, BRISSOT, P, WORWOOD, Mark

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Synergy between the C2 allele of transferrin and the C282Y allele of the haemochromatosis gene (HFE) as risk factors for developing Alzheimer’s disease von Robson, K J H, Lehmann, D J, Wimhurst, V L C, Livesey, K J, Combrinck, M, Merryweather-Clarke, A T, Warden, D R, Smith, A D

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Iron genes, iron load and risk of Alzheimer’s disease von Lehmann, D J, Worwood, M, Ellis, R, Wimhurst, V L J, Merryweather-Clarke, A T, Warden, D R, Smith, A D, Robson, K J H

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A targeted approach significantly increases the identification rate of patients with undiagnosed haemochromatosis von Cadet, E., Capron, D., Perez, A. S., Crépin, S. N., Arlot, S., Ducroix, J.‐P., Dautréaux, M., Fardellone, P., Leflon, P., Merryweather‐Clarke, A. T., Livesey, K. J., Pointon, J. J., Rose, P., Harcourt, J., Emery, J., Sueur, J. M., Feyt, R., Robson, K. J. H., Rochette, J.

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Recent advances in understanding haemochromatosis: a transition state von Robson, K J H, Merryweather-Clarke, A T, Cadet, E, Viprakasit, V, Zaahl, M G, Pointon, J J, Weatherall, D J, Rochette, J

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