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Number of items: 6.

Franco-Jarava, C., Comas, D., Orren, A., Hernández-González, M. and Colobran, R. 2017. Complement factor 5 (C5) p.A252T mutation is prevalent in, but not restricted to, sub-Saharan Africa: implications for the susceptibility to meningococcal disease. Clinical and Experimental Immunology 189 (2) , pp. 226-231. 10.1111/cei.12967

Owen, E. Patricia, Würzner, Reinhard, Leisegang, Felicity, Rizkallah, Pierre, Whitelaw, Andrew, Simpson, John, Thomas, Andrew David, Harris, Claire Louise, Giles, Joanna L., Hellerud, Bernt C., Mollnes, Tom E., Morgan, Bryan Paul, Potter, Paul C. and Orren, Ann 2015. A complement C5 gene mutation, c.754G>A:p.A252T, is common in the Western Cape, South Africa and found to be homozygous in seven percent of Black African meningococcal disease cases. Molecular Immunology 64 (1) , pp. 170-176. 10.1016/j.molimm.2014.11.010

Owen, E. P., Leisegang, F., Whitelaw, A., Simpson, J., Baker, S., Würzner, R., Potter, P. and Orren, Ann 2012. Complement component C5 and C6 mutation screening indicated in meningococcal disease in South Africa. South African Medical Journal 102 (6) , pp. 525-527.

Orren, Ann, Owen, E. P., Henderson, H. E., van der Merwe, L., Leisegang, F., Stassen, C. and Potter, P. C. 2012. Complete deficiency of the sixth complement component (C6Q0), susceptibility to Neisseria meningitidis infections and analysis of the frequencies of C6Q0 gene defects in South Africans. Clinical and Experimental Immunology 167 (3) , pp. 459-471. 10.1111/j.1365-2249.2011.04525.x

Thomas, Andrew David, Orren, Ann, Connaughton, J., Feighery, C., Morgan, Bryan Paul and Roberts, Andrew Glyn 2012. Characterization of a large genomic deletion in four Irish families with C7 deficiency. Molecular Immunology 50 (1-2) , pp. 57-59. 10.1016/j.molimm.2011.12.002

Orren, Ann 2000. Screening for complement deficiency. In: Morgan, B. Paul ed. Complement Methods and Protocols, Vol. 150. Methods in Molecular Biology, Springer, pp. 139-158. (10.1385/1-59259-056-X:139)

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