Hybrid Finite-Discrete Element Simulation of the EDZ Formation and Mechanical Sealing Process Around a Microtunnel in Opalinus Clay von Lisjak, Andrea, Tatone, Bryan S. A., Mahabadi, Omid K., Grasselli, Giovanni, Marschall, Paul, Lanyon, George W., Vaissière, Rémi de la, Shao, Hua, Leung, Helen, Nussbaum, Christophe

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Characterizing the permeability of drillhole core samples of Toki granite, Central Japan to identify factors influencing rock-matrix permeability von Kubo, Taiki, Matsuda, Norihiro, Kashiwaya, Koki, Koike, Katsuaki, Ishibashi, Masayuki, Tsuruta, Tadahiko, Matsuoka, Toshiyuki, Sasao, Eiji, Lanyon, George W.

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Identification of Two Novel Mutations in the Hydroxymethylbilane Synthase Gene in Three Patients from Two Unrelated Families with Acute Intermittent Porphyria von Ong, Patricia M. L., Lanyon, W. George, Hift, Richard J., Halkett, Janet, Cramp, Celia E., Michael R., Moore, Connor, J. Michael

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Detection of four mutations in six unrelated South African patients with acute intermittent porphyria von Ong, Patricia M.L, Lanyon, George W, Hift, Richard J, Halkett, Janet, Moore, Michael R, Mgone, Charles S, Connor, Michael J

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Identification of a new missense point mutation in exon 4 of the Cu/Zn superoxide dismutase (SOD-1) gene in a family with amyotrophic lateral sclerosis von Elshafey, Alaa, Lanyon, W.George, Connor, J.Mlchael

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Characterisation of inherited and sporadic mutations in neurofibromatosis type-1 von Purandare, Smita M., Lanyon, W. George, Connor, J. Michael

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Aberrant RNA splicing in the hMSH2 gene: Molecular identification of three aberrant RNA in Scottish patients with colorectal cancer in the West of Scotland von Davoodi-Semiromi, Abdoreza, Lanyon, George W., Davidson, Rosemary, Connor, Michael J.

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Erythropoietic Protoporphyria: A New Mutation Responsible for Exon Skipping in the Human Ferrochelatase Gene von Remenyik, Éva, Horkay, Irén, Wikonkál, Norbert, Kósa, Ágnes, Lanyon, George W., Paragh, György, Moore, Michael R.

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Identification of five novel mutations in the porphobilinogen deaminase gene von S.Mgone, Charles, Lanyon, W.George, R.Moore, Michael, Louie, Gordon V., Connor, James M.

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Characterisation of a novel splice donor mutation affecting position +1 in intron 18 of the NF-1 gene von Purandare, Smita M., Lanyon, W.George, Arngrimsson, Reynir, Connor, J. Michael

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Detection of mutations in ectopic factor VIII transcripts from nine haemophilia A patients and the correlation with phenotype von BIDICHANDANI, S. I, LANYON, W. G, SHIACH, C. R, LOWE, G. D. O, CONNOR, J. M

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Screening for molecular pathologies in Lesch-Nyhan syndrome von Boyd, Marie, Lanyon, W. George, Connor, J. Michael

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Acute intermittent porphyria: alternative splicing of hydroxymethylbilane synthase mRNA excludes exons 3 and 12 von Ong, Patricia M.L., Lanyon, W.George, Moore, Michael R., Connor, J.Michael

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A novel splice donor mutation affecting position + 3 in intron 6 of the factor VIII gene von Bidichandan, Sanjay I., Shiach, Caroline R., Lanyon, W.George, Connor, J.Michael

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Characterisation of a 5-bp deletion in exon 4 of the factor VIII gene : concordance with slipped-mispairing at DNA replication von BIDICHANDANI, S. I, LANYON, W. G, CONNOR, J. M

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Acute intermittent porphyria: the in vitro expression of mutant hydroxymethylbilane synthase von Ong, P M, Lanyon, W G, Graham, G, Hift, R J, Halkett, J, Moore, M R, Connor, J M

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A novel insertional mutation of a single base in exon 34 of the neurofibromatosis-1 gene von Purandare, Smita M., Davidson, H. Rosemary, Lanyon, W. George, Connor, J. Michael

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Alternative sites of transcription initiation upstream of the canonical cap site in human -γ-globin and β-globin genes von Grindlay, G. Joan, Lanyon, W. George, Allan, Maggi, Paul, John

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AB1 repetitive sequence near the mouse β-major globin gene von Coggins, Lesley W., Vass, J.Keith, Stinson, M.Anne, Lanyon, W.George, Paul, John

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Human Globin Gene Expression and Linkage in Bone Marrow and Fetal Liver von Lanyon, W. George, Ottolenghi, Sergio, Williamson, Robert

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