Gene expression profiling of normal and ruptured canine anterior cruciate ligaments

Autor: Clements, D.N. ^{†, ‡}, Carter, S.D. ^†, Innes, J.F. ^†, Ollier, W.E.R. ^‡, Day, P.J.R. ^{‡, §}

Publikováno v: In Osteoarthritis and Cartilage 2008 16(2):195-203

Mannose binding lectin (MBL) genotype distributions with relation to serum levels in UK Caucasoids.

Autor: Crosdale, D.J., Ollier, W.E.R., Thomson, W., Dyert, P.A., Jensenious, J., Johnson, R.W.G., Poulton, K.V.

Publikováno v: European Journal of Immunogenetics. Jun2000, Vol. 27 Issue 3, p111. 7p. 4 Charts, 1 Graph.

Properdin Factor B (Bf) Polymorphism in Saudi Arabs: High Frequency of a 'Rare' Alele Bf S0.7

Autor: Klouda, P.T., Ollier, W.E.R., Hilalic, A. Al, Bacchus, R.A.

Publikováno v: Human Heredity, 1984 Jan 01. 34(4), 269-272.

Externí odkaz: https://www.jstor.org/stable/45101842

Identification of new susceptibility loci for osteoarthritis (arcOGEN): a genome-wide association study

Autor: Zeggini, E., Panoutsopoulou, K., Southam, L., Rayner, N.W., Day-Williams, A.G., Lopes, M.C., Boraska, V., Esko, T., Evangelou, E., Hofman, A., Houwing-Duistermaat, J.J., Ingvarsson, T., Jonsdottir, I., Jonsson, H., Kerkhof, H.J.M., Kloppenburg, M., Bos, S.D., Mangino, M., Metrustry, S., Slagboom, P.E., Thorleifsson, G., Raine, E.V.A., Ratnayake, M., Ricketts, M., Beazley, C., Blackburn, H., Bumpstead, S., Elliott, K.S., Hunt, S.E., Potter, S.C., Shin, S.Y., Yadav, V.K., Zhai, G.J., Sherburn, K., Dixon, K., Arden, E., Aslam, N., Battley, P.K., Carluke, I., Doherty, S., Gordon, A., Joseph, J., Keen, R., Koller, N.C., Mitchell, S., O'Neill, F., Paling, E., Reed, M.R., Rivadeneira, F., Swift, D., Walker, K., Watkins, B., Wheeler, M., Birrell, F., Ioannidis, J.P.A., Meulenbelt, I., Metspalu, A., Rai, A., Salter, D., Stefansson, K., Styrkarsdottir, U., Uitterlinden, A.G., Meurs, J.B.J. van, Chapman, K., Deloukas, P., Ollier, W.E.R., Wallis, G.A., Arden, N., Carr, A., Doherty, M., McCaskie, A., Wilkinson, J.M., Ralston, S.H., Valdes, A.M., Spector, T.D., Loughlin, J., arcOGEN Consortium & arcOGEN Colla

Publikováno v: Lancet, 380(9844), 815-823

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::5dce68dc7cbfc888297764fdc675dea6
https://hdl.handle.net/1887/106407

The PTPN22 gene is associated with juvenile and adult UK Caucasian idiopathic inflammatory myopathy independent of the HLA 8.1 haplotype

Autor: Chinoy, H., Platt, H., Lamb, J.A., Betteridge, Z., Gunawardena, H., Fertig, N., Varsani, H., Davidson, J., Oddis, C.V., McHugh, N.J., Wedderburn, L.R., Ollier, W.E.R., Cooper, R.G.

To examine single-nucleotide polymorphisms (SNPs) of the protein tyrosine phosphatase N22 gene (PTPN22) and to study the relationship between PTPN22 and the HLA region in patients with idiopathic inflammatory myopathies (IIMs).PTPN22 SNPs were assess

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::a79b8080dfa940b6d24f01f2b2674654
https://europepmc.org/articles/PMC4568569/