Glucose 6-phosphate dehydrogenase mutations causing enzyme deficiency in a model of the tertiary structure of the human enzyme
NAYLOR, C. E, ROWLAND, P, BASAK, A. K, GOVER, S, MASON, P. J, BAUTISTA, J. M, VULLIAMY, T. J, LUZZATTO, L, ADAMS, M. J
Published in Blood (01.04.1996)
Published in Blood (01.04.1996)
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Multiple glucose 6-phosphate dehydrogenase-deficient variants correlate with malaria endemicity in the Vanuatu Archipelago (southwestern Pacific)
GANCZAKOWSKI, M, TOWN, M, BOWDEN, D. K, VULLIAMY, T. J, KANEKO, A, CLEGG, J. B, WEATHERALL, D. J, LUZZATTO, L
Published in American journal of human genetics (1995)
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Published in American journal of human genetics (1995)
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Diverse Point Mutations in the Human Glucose-6-phosphate Dehydrogenase Gene Cause Enzyme Deficiency and Mild or Severe Hemolytic Anemia
Vulliamy, T. J., D'Urso, M., Battistuzzi, G., Estrada, M., Foulkes, N. S., Martini, G., Calabro, V., Poggi, V., Giordano, R., Town, M., Luzzatto, L., Persico, M. G.
Published in Proceedings of the National Academy of Sciences - PNAS (01.07.1988)
Published in Proceedings of the National Academy of Sciences - PNAS (01.07.1988)
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1.4 Mb candidate gene region for X linked dyskeratosis congenita defined by combined haplotype and X chromosome inactivation analysis
Knight, S W, Vulliamy, T J, Heiss, N S, Matthijs, G, Devriendt, K, Connor, J M, D'Urso, M, Poustka, A, Mason, P J, Dokal, I
Published in Journal of medical genetics (01.12.1998)
Published in Journal of medical genetics (01.12.1998)
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A new glucose-6-phosphate dehydrogenase variant, G6PD Orissa (44 Ala→Gly), is the major polymorphic variant in tribal populations in India
KAEDA, J. S, CHHOTRAY, G. P, MASON, P. J, RANJIT, M. R, BAUTISTA, J. M, REDDY, P. H, STEVENS, D, NAIDU, J. M, BRITT, R. P, VULLIAMY, T. J, LUZZATTO, L
Published in American journal of human genetics (01.12.1995)
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Published in American journal of human genetics (01.12.1995)
Journal Article
Polymorphic Sites in the African Population Detected by Sequence Analysis of the Glucose-6-Phosphate Dehydrogenase Gene Outline the Evolution of the Variants A and A
Vulliamy, T. J., Othman, A., Town, M., Nathwani, A., Falusi, A. G., Mason, P. J., Luzzatto, L.
Published in Proceedings of the National Academy of Sciences - PNAS (01.10.1991)
Published in Proceedings of the National Academy of Sciences - PNAS (01.10.1991)
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Analysis of chimaerism in thalassaemic children undergoing stem cell transplantation
Amrolia, P. J., Vulliamy, T., Vassiliou, G ., Lawson, S., Bryon, J., Kaeda, J., Dokal, I., Johnston, R., Veys, P., Darbyshire, P., Roberts, I. A. G.
Published in British journal of haematology (01.07.2001)
Published in British journal of haematology (01.07.2001)
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Lymphoid transformation in a CML patient in complete cytogenetic remission following treatment with imatinib
Avery, S, Nadal, E, Marin, D, Olavarria, E, Kaeda, J, Vulliamy, T, Brito Babapulle, F, Goldman, J.M, Apperley, J.F
Published in Leukemia research (01.05.2004)
Published in Leukemia research (01.05.2004)
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Clinical and haematological consequences of recurrent G6PD mutations and a single new mutation causing chronic nonspherocytic haemolytic anaemia
Vulliamy, Tom J., Kaeda, Jaspal S., Ait‐Chafa, Dahlila, Mangerini, Rosa, Roper, David, Barbot, Jose, Mehta, Athul B., Athanassiou‐Metaxa, Luzzatto, Lucio, Mason, Philip J.
Published in British journal of haematology (01.06.1998)
Published in British journal of haematology (01.06.1998)
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New haplotype for the Glu104Asp mutation in triose‐phosphate isomerase deficiency and prenatal diagnosis in a Spanish family
Repiso, A., Corrons, J. L. Vives, Vulliamy, T., Killeen, N., Layton, M., Carreras, J., Climent, F.
Published in Journal of inherited metabolic disease (01.01.2005)
Published in Journal of inherited metabolic disease (01.01.2005)
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Exon skipping and translation in patients with frameshift deletions in the dystrophin gene
SHERRATT, T. G, VULLIAMY, T, DUBOWITZ, V, SEWRY, C. A, STRONG, P. N
Published in American journal of human genetics (01.11.1993)
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Published in American journal of human genetics (01.11.1993)
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G6PD Mediterranean accounts for the high prevalence of G6PD deficiency in Kurdish Jews
Oppenheim, A, Jury, C L, Rund, D, Vulliamy, T J, Luzzatto, L
Published in Human genetics (01.04.1993)
Published in Human genetics (01.04.1993)
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G6PD Haplotypes Spanning Xq28 from F8C to Red/Green Color Vision
Filosa, S., Calabrò, V., Lania, G., Vulliamy, T.J., Brancati, C., Tagarelli, A., Luzzatto, L., Martini, G.
Published in Genomics (San Diego, Calif.) (01.07.1993)
Published in Genomics (San Diego, Calif.) (01.07.1993)
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