Found 22 results
Filters: Keyword is Polymorphism, Single Nucleotide  [Clear All Filters]
P. Cho, Gelinas, L., Corbett, N. P., Tebbutt, S. J., Turvey, S. E., Fortuno, E. S., and Kollmann, T. R., Association of common single-nucleotide polymorphisms in innate immune genes with differences in TLR-induced cytokine production in neonates., Genes Immun, vol. 14, no. 4, pp. 199-211, 2013.
E. Fuertes, Brauer, M., MacIntyre, E., Bauer, M., Bellander, T., von Berg, A., Berdel, D., Brunekreef, B., Chan-Yeung, M., Gehring, U., Herbarth, O., Hoffmann, B., Kerkhof, M., Klümper, C., Koletzko, S., Kozyrskyj, A., Kull, I., Heinrich, J., Melén, E., Pershagen, G., Postma, D., Tiesler, C. M. T., and Carlsten, C., Childhood allergic rhinitis, traffic-related air pollution, and variability in the GSTP1, TNF, TLR2, and TLR4 genes: results from the TAG Study., J Allergy Clin Immunol, vol. 132, no. 2, pp. 342-52.e2, 2013.
N. N. Hansel, Ruczinski, I., Rafaels, N., Sin, D. D., Daley, D., Malinina, A., Huang, L., Sandford, A., Murray, T., Kim, Y., Vergara, C., Heckbert, S. R., Psaty, B. M., Li, G., W Elliott, M., Aminuddin, F., Dupuis, J., O'Connor, G. T., Doheny, K., Scott, A. F., H Boezen, M., Postma, D. S., Smolonska, J., Zanen, P., Hoesein, F. A. Mohamed, de Koning, H. J., Crystal, R. G., Tanaka, T., Ferrucci, L., Silverman, E., Wan, E., Vestbo, J., Lomas, D. A., Connett, J., Wise, R. A., Neptune, E. R., Mathias, R. A., Paré, P. D., Beaty, T. H., and Barnes, K. C., Genome-wide study identifies two loci associated with lung function decline in mild to moderate COPD., Hum Genet, vol. 132, no. 1, pp. 79-90, 2013.
F. Aminuddin, Hackett, T. - L., Stefanowicz, D., Saferali, A., Paré, P. D., Gulsvik, A., Bakke, P., Cho, M. H., Litonjua, A., Lomas, D. A., Anderson, W. H., Beaty, T. H., Silverman, E. K., and Sandford, A. J., Nitric oxide synthase polymorphisms, gene expression and lung function in chronic obstructive pulmonary disease., BMC Pulm Med, vol. 13, p. 64, 2013.
J. M. Schuetz, Daley, D., Leach, S., Conde, L., Berry, B. R., Gallagher, R. P., Connors, J. M., Gascoyne, R. D., Bracci, P. M., Skibola, C. F., Spinelli, J. J., and Brooks-Wilson, A. R., Non-Hodgkin lymphoma risk and variants in genes controlling lymphocyte development., PLoS One, vol. 8, no. 9, p. e75170, 2013.
K. R. Thain, Nakada, T. -aki, Boyd, J. H., Russell, J. A., and Walley, K. R., A common polymorphism in the 5' region of the human protein c gene binds USF1., Thromb Res, vol. 130, no. 3, pp. 451-7, 2012.
L. R. Brunham, Lansberg, P. J., Zhang, L., Miao, F., Carter, C., Hovingh, G. K., Visscher, H., Jukema, J. W., Stalenhoef, A. F., Ross, C. J. D., Carleton, B. C., Kastelein, J. J. P., and Hayden, M. R., Differential effect of the rs4149056 variant in SLCO1B1 on myopathy associated with simvastatin and atorvastatin., Pharmacogenomics J, vol. 12, no. 3, pp. 233-7, 2012.
F. Aminuddin, Akhabir, L., Stefanowicz, D., Paré, P. D., Connett, J. E., Anthonisen, N. R., Fahy, J. V., Seibold, M. A., Burchard, E. G., Eng, C., Gulsvik, A., Bakke, P., Cho, M. H., Litonjua, A., Lomas, D. A., Anderson, W. H., Beaty, T. H., Crapo, J. D., Silverman, E. K., and Sandford, A. J., Genetic association between human chitinases and lung function in COPD., Hum Genet, vol. 131, no. 7, pp. 1105-14, 2012.
J. M. Schuetz, Daley, D., Graham, J., Berry, B. R., Gallagher, R. P., Connors, J. M., Gascoyne, R. D., Spinelli, J. J., and Brooks-Wilson, A. R., Genetic variation in cell death genes and risk of non-Hodgkin lymphoma., PLoS One, vol. 7, no. 2, p. e31560, 2012.
K. Hao, Bossé, Y., Nickle, D. C., Paré, P. D., Postma, D. S., Laviolette, M., Sandford, A., Hackett, T. L., Daley, D., Hogg, J. C., W Elliott, M., Couture, C., Lamontagne, M., Brandsma, C. - A., van den Berge, M., Koppelman, G., Reicin, A. S., Nicholson, D. W., Malkov, V., Derry, J. M., Suver, C., Tsou, J. A., Kulkarni, A., Zhang, C., Vessey, R., Opiteck, G. J., Curtis, S. P., Timens, W., and Sin, D. D., Lung eQTLs to help reveal the molecular underpinnings of asthma., PLoS Genet, vol. 8, no. 11, p. e1003029, 2012.
A. J. Sandford, Malhotra, D., H Boezen, M., Siedlinski, M., Postma, D. S., Wong, V., Akhabir, L., He, J. - Q., Connett, J. E., Anthonisen, N. R., Paré, P. D., and Biswal, S., NFE2L2 pathway polymorphisms and lung function decline in chronic obstructive pulmonary disease., Physiol Genomics, vol. 44, no. 15, pp. 754-63, 2012.
D. Daley, Lemire, M., Akhabir, L., Chan-Yeung, M., He, J. Qing, McDonald, T., Sandford, A., Stefanowicz, D., Tripp, B., Zamar, D., Bossé, Y., Ferretti, V., Montpetit, A., Tessier, M. - C., Becker, A., Kozyrskyj, A. L., Beilby, J., McCaskie, P. A., Musk, B., Warrington, N., James, A., Laprise, C., Palmer, L. J., Paré, P. D., and Hudson, T. J., Analyses of associations with asthma in four asthma population samples from Canada and Australia., Hum Genet, vol. 125, no. 4, pp. 445-59, 2009.
J. - Q. He, Foreman, M. G., Shumansky, K., Zhang, X., Akhabir, L., Sin, D. D., Man, S. F. P., DeMeo, D. L., Litonjua, A. A., Silverman, E. K., Connett, J. E., Anthonisen, N. R., Wise, R. A., Paré, P. D., and Sandford, A. J., Associations of IL6 polymorphisms with lung function decline and COPD., Thorax, vol. 64, no. 8, pp. 698-704, 2009.
Y. Bossé, Lemire, M., Poon, A. H., Daley, D., He, J. - Q., Sandford, A., White, J. H., James, A. L., Musk, A. William, Palmer, L. J., Raby, B. A., Weiss, S. T., Kozyrskyj, A. L., Becker, A., Hudson, T. J., and Laprise, C., Asthma and genes encoding components of the vitamin D pathway., Respir Res, vol. 10, p. 98, 2009.
D. Zamar, Tripp, B., Ellis, G., and Daley, D., Path: a tool to facilitate pathway-based genetic association analysis., Bioinformatics, vol. 25, no. 18, pp. 2444-6, 2009.
J. - Q. He, Hallstrand, T. S., Knight, D., Chan-Yeung, M., Sandford, A., Tripp, B., Zamar, D., Bossé, Y., Kozyrskyj, A. L., James, A., Laprise, C., and Daley, D., A thymic stromal lymphopoietin gene variant is associated with asthma and airway hyperresponsiveness., J Allergy Clin Immunol, vol. 124, no. 2, pp. 222-9, 2009.