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Title Author/Creator Date Full Text Reviewed
Add IL12A, MPHOSPH9/CDK2AP1 and RGS1 are novel multiple sclerosis susceptibility loci The International Multiple Sclerosis Genetics Consortium; Esposito, F.; Patsopoulos, N. A.; Lechner-Scott, J.; Goris, A.... More 2010 Reviewed
Add Differential gene expression and cytokine production from neutrophils in asthma phenotypes Baines, K. J.; Simpson, J. L.; Bowden, N. A.; Scott, R. J.; Gibson, P. G. 2010 Reviewed
Add Estrogen receptor polymorphisms and the risk of endometrial cancer Ashton, K. A.; Proietto, A.; Otton, G.; Symonds, I.; McEvoy, M.... More 2009 Reviewed
Add The -149C>T SNP within the ΔDNMT3B gene, is not associated with early disease onset in hereditary non-polyposis colorectal cancer Reeves, S. G.; Mossman, David; Meldrum, C. J.; Kurzawski, G.; Suchy, J.... More 2008 Reviewed
Add Volcanology, geochemistry and structure of the Ordovician Cargo Volcanics in the Cargo-Walli region, central New South Wales Simpson, C. J.; Scott, R. J.; Crawford, A. J.; Meffre, S. 2007 Reviewed
Add Common variants of DNA repair genes and malignant melanoma Debniak, T.; Scott, R. J.; Kowalska, E.; Jakubowska, A.; Gronwald, J.... More 2008 Reviewed
Add Factor V Leiden is associated with pre-eclampsia but not with fetal growth restriction: a genetic association study and meta-analysis Dudding, T.; Heron, J.; Thakkinstian, A.; Nurk, E.; Golding, J.... More 2008 Reviewed
Add Integrin expression in colon cancer cells is regulated by the cytoplasmic domain of the β6 integrin subunit Niu, Jun; Dorahy, Douglas J.; Gu, Xinhua; Scott, R. J.; Draganic, Brian... More 2002 Reviewed
Add Gene profiling in the amygdala in schizophrenia Weidenhofer, J.; Bowden, N. A.; Scott, R. J.; Tooney, P. A. 2004
Add Altered expression of brain related genes in lymphocytes in schizophrenia Bowden, N. A.; Weidenhofer, J. C.; Scott, R. J.; Todd, J.; Case, V.... More 2004
Add Vitamin D receptor variants and breast cancer risk in the Polish population Gapska, P.; Scott, R. J.; Dębniak, T.; Serrano-Fernandez, P.; Huzarski, T.... More 2009 Reviewed
Add A 1q44 deletion, paternal UPD of chromosome 2 and a deletion due to a complex translocation detected in children with abnormal phenotypes using new SNP array technology Talseth-Palmer, B. A.; Bowden, N. A.; Scott, R. J.; Meldrum, C.; Nicholl, J.... More 2009 Reviewed
Add Vitamin D receptor variants and the malignant melanoma risk: a population-based study Gapska, P.; Scott, R. J.; Maleszka, R.; Sulikowski, M.; Lubinski, J.... More 2009 Reviewed
Add Fetal growth and risk of childhood acute lymphoblastic leukemia: results from an Australian case-control study Milne, E.; Royle, J. A.; de Klerk , N. H.; Blair, E.; Bailey, H.... More 2009 Reviewed
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