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Lancet (London, England)|October 23, 2015
Inherited determinants of Crohn's disease and ulcerative colitis phenotypes: a genetic association studyIsabelle Cleynen, Gabrielle Boucher, Luke Jostins, et al.Nature|June 29, 2017
Fine-mapping inflammatory bowel disease loci to single-variant resolutionHailiang Huang, Ming Fang, Luke Jostins, et al.Human Pathology|June 18, 2023
Metastatic solid tumors to the testis: a clinicopathologic evaluation of 157 cases from an international collaborationLuiz M Nova-Camacho, Andres M Acosta, Kiril Trpkov, et al.European Urology|April 11, 2009
Positive surgical margin appears to have negligible impact on survival of renal cell carcinomas treated by nephron-sparing surgeryKarim Bensalah, Allan J Pantuck, Nathalie Rioux-Leclercq, et al.Nature Genetics|January 22, 2008
Genome-wide association scan in women with systemic lupus erythematosus identifies susceptibility variants in ITGAM, PXK, KIAA1542 and other loci, John B Harley, Marta E Alarcón-Riquelme, et al.Nature|February 7, 2014
Fifty thousand years of Arctic vegetation and megafaunal dietEske Willerslev, John Davison, Mari Moora, et al.Cancer Cell|July 2, 2019
Anti-tumor Activity of the Type I PRMT Inhibitor, GSK3368715, Synergizes with PRMT5 Inhibition through MTAP LossAndrew Fedoriw, Satyajit R Rajapurkar, Shane O'Brien, et al.Cancer Discovery|July 12, 2018
Discovery of Selective Estrogen Receptor Covalent Antagonists for the Treatment of ERαWT and ERαMUT Breast CancerXiaoling Puyang, Craig Furman, Guo Zhu Zheng, et al.Gut|April 20, 2023
Genetic coding variant in complement factor B (CFB) is associated with increased risk for perianal Crohn's disease and leads to impaired CFB cleavage and phagocytosisMarzieh Akhlaghpour, Talin Haritunians, Shyam K More, et al.Science Translational Medicine|January 12, 2018
Functional variants in the LRRK2 gene confer shared effects on risk for Crohn's disease and Parkinson's diseaseKen Y Hui, Heriberto Fernandez-Hernandez, Jianzhong Hu, et al.Pageof 191