Frequency of the S65C mutation of HFE and iron overload in 309 subjects heterozygous for C282Y von Wallace, Daniel F., Walker, Ann P., Pietrangelo, Antonello, Clare, Michael, Bomford, Adrian B., Dixon, Jeannette L., Powell, Lawrie W., Subramaniam, V.Nathan, Dooley, James S.

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First phenotypic description of transferrin receptor 2 knockout mouse, and the role of hepcidin von Wallace, D F, Summerville, L, Lusby, P E, Subramaniam, V N

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A novel mutation of HFE explains the classical phenotype of genetic hemochromatosis in a C282Y heterozygote von Wallace, Daniel F., Dooley, James S., Walker, Ann P.

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Autosomal dominant iron overload due to a novel mutation of ferroportin1 associated with parenchymal iron loading and cirrhosis von Wallace, Daniel F., Clark, Roslyn M., Harley, Hugh A.J., Subramaniam, V.Nathan

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A novel mutation in ferroportin 1 is associated with haemochromatosis in a Solomon Islands patient von ARDEN, K. E, WALLACE, D. F, DIXON, J. L, SUMMERVILLE, L, SEARLE, J. W, ANDERSON, G. J, RAMM, G. A, POWELL, L. W, SUBRAMANIAM, V. N

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A simple genetic test identifies 90% of UK patients with haemochromatosis von The, U

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A novel mutation in ferroportin1 is associated with haemochromatosis in a Solomon Islands patient von Arden, K E, Wallace, D F, Dixon, J L, Summerville, L, Searle, J W, Anderson, G J, Ramm, G A, Powell, L W, Subramaniam, V N

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Prohepcidin localises to the Golgi compartment and secretory pathway in hepatocytes von Wallace, Daniel F., Summerville, Lesa, Lusby, Patricia E., Subramaniam, V. Nathan

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Identification of ferroportin disease in the Indian subcontinent von Wallace, D F, Browett, P, Wong, P, Kua, H, Ameratunga, R, Subramaniam, V N

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Ferroportin disease due to the A77D mutation in Australia von Subramaniam, V N, Wallace, D F, Dixon, J L, Fletcher, L M, Crawford, D H

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Purification and partial characterisation of recombinant human hepcidin von Wallace, Daniel F., Jones, Marc D., Pedersen, Palle, Rivas, Lucy, Sly, Lindsay I., Subramaniam, V. Nathan

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Hemojuvelin (HJV)-associated hemochromatosis: analysis of HJV and HFE mutations and iron overload in three families von Wallace, DF, Dixon, JL, Ramm, GA, Anderson, GJ, Powell, LW, Subramaniam, N

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Molecular and cellular characterization of transferrin receptor 2 von Subramaniam, V Nathan, Summerville, Lesa, Wallace, Daniel F

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Non HFE-related haemochromatosis: exclusion of the 1q21 zinc-iron regulated transporter-like ( ZIRTL) gene in juvenile haemochromatosis von Sebastiani, Giada, Wallace, Daniel F., Lioumi, Maria, Goutos, Ioannis, Mitchell, Wayne A., Bomford, Adrian B., Dhillon, A.Paul, Dooley, James S., Ragoussis, Jiannis, Walker, Ann P.

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DIAGNOSIS AND MANAGEMENT OF HAEMOCHROMATOSIS SINCE THE DISCOVERY OF THE HFE GENE: A EUROPEAN EXPERIENCE von Robson, K J H, Merryweather, A T, Pointon, J J, Shearman, J D

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Monocyte-macrophage ferric reductase activity is inhibited by iron and stimulated by cellular differentiation von Partridge, J, Wallace, D F, Raja, K B, Dooley, J S, Walker, A P

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Cloning and Molecular Characterization of a Cross-Homologous Zinc Finger Locus ZNF204 von Partridge, Jason, Wallace, Daniel F., Robertson, Alexis, Fox, Margaret F., Simons, J.Paul, Dooley, James S., Walker, Ann P.

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A 6p22 reference map of leukocyte DNA: exclusion of rearrangement in four cases of atypical haemochromatosis von Wallace, Daniel F, Partridge, Jason, Robertson, Alexis, Simpson, Victoria MA, Worwood, Mark, Bomford, Adrian B, Volz, Armin, Ziegler, Andreas, Dooley, James S, Walker, Ann P

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A Radically Condensed History of Postindustrial Life von Wallace, David Foster

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Peoria von Wallace, David Foster

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