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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TRAP is necessary for gliding motility and infectivity of plasmodium sporozoites von Sultan, A A, Thathy, V, Frevert, U, Robson, K J, Crisanti, A, Nussenzweig, V, Nussenzweig, R S, Ménard, R

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The A-domain and the thrombospondin-related motif of Plasmodium falciparum TRAP are implicated in the invasion process of mosquito salivary glands von Wengelnik, Kai, Spaccapelo, Roberta, Naitza, Silvia, Robson, Kathryn J.H., Janse, Chris J., Bistoni, Francesco, Waters, Andrew P., Crisanti, Andrea

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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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Malarial anemia and STAT6 von Robson, Kathryn J H, Weatherall, David J

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Expression of the SLC11A1 ( NRAMP1) 5′-(GT) n repeat: Opposite effect in the presence of −237C→T von Zaahl, Monique G, Robson, Kathryn J.H, Warnich, Louise, Kotze, Maritha J

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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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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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Multifactorial Iron Man von Robson, Kathryn J.H., Drakesmith, Hal

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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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A retrospective anonymous pilot study in screening newborns for HFE mutations in Scandinavian populations von Merryweather-Clarke, Alison T., Siimonsen, Henrik, Shearman, Jeremy D., Pointon, Jennifer J., Nørgaard-Pedersen, Bent, Robson, Kathryn J.H.

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Hemochromatosis gene ( HFE) mutations in South East Asia: a potential for iron overload von Pointon, Jennifer J, Viprakasit, Vip, Miles, Katie L, Livesey, Karen J, Steiner, Michael, O’Riordan, Sean, Hien, Tran T, Merryweather-Clarke, Alison T, Robson, Kathryn J.H

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Polymorphism in intron 4 of HFE does not compromise haemochromatosis mutation results von Coppin, Hélène, Totaro, Angela, Gasparini, Paolo, Worwood, Mark, Darke, Chris, Rochette, Jacques, Shearman, Jeremy D, Mosser, Annick, Elsey, Terence S, Dooley, James S, David, Véronique, Vandwalle, Jean Luc, Ryan, Eleanor, Borot, Nicolas, Roetto, Antonella, Robson, Kathryn J.H, Crowe, John, Walker, Ann P, Cox, Timothy M, Clare, Michael, Kelly, Alison, Roth, Marie-Paule, Jouanolle, Anne Marie, Bomford, Adrian, Camaschella, Clara, Wallace, Daniel F, Le Gall, Jean-Yves, Pointon, Jennifer J, Halsall, David J, Merryweather-Clarke, Alison T, Saeb-Parsy, Kasra

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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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Global prevalence of putative haemochromatosis mutations von Merryweather-Clarke, A T, Pointon, J J, Shearman, J D, Robson, K J

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A valine deletion of ferroportin 1: a common mutation in hemochromatosis type 4? von Roetto, Antonella, Merryweather-Clarke, Alison T., Daraio, Filomena, Livesey, Karen, Pointon, Jennifer J., Barbabietola, Giuliana, Piga, Antonio, Mackie, Peter H., Robson, Kathryn J.H., Camaschella, Clara

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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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Recombinant vaccinia viruses for the characterization of Plasmodium falciparum-specific cytotoxic T lymphocytes: recognition of processed antigen despite limited re-stimulation eff... von Aidoo, M, Lalvani, A, Whittle, H C, Hill, A V, Robson, K 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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