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Medrxiv : the Preprint Server for Health Sciences|June 12, 2026
Disruption of CTCF binding by germline non-coding variants in CDKN2B suppress CDKN2A expression and predispose to melanomaJessica L Scales, Jayne A Barbour, Alisa M Goldstein, et al.
Journal of Medical Genetics|September 14, 2012
Prediction of breast cancer risk by genetic risk factors, overall and by hormone receptor statusAnika Hüsing, Federico Canzian, Lars Beckmann, et al.
Medrxiv : the Preprint Server for Health Sciences|February 12, 2026
The Metabolome as a Readout for Adverse Social Exposome Influences on Human Health - A Roadmap for Modifiable Factors and Proactive HealthNuanyi Liang, Siamak Mahmoudiandehkordi, Margo B Heston, et al.
Journal for Immunotherapy of Cancer|February 11, 2026
DART/SWOG/NCI phase II anti-CTLA-4/PD-1 trial: clear cell carcinomas of ovary, endometrium, cervixYoung Kwang Chae, Megan Othus, Sandip P Patel, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 23, 2009
Fine mapping and functional analysis of a common variant in MSMB on chromosome 10q11.2 associated with prostate cancer susceptibilityHong Lou, Meredith Yeager, Hongchuan Li, et al.
Journal of the National Cancer Institute|July 28, 2011
Interactions between genetic variants and breast cancer risk factors in the breast and prostate cancer cohort consortiumDaniele Campa, Rudolf Kaaks, Loïc Le Marchand, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 15, 2012
Common genetic variants in the PSCA gene influence gene expression and bladder cancer riskYi-Ping Fu, Indu Kohaar, Nathaniel Rothman, et al.
International Journal of Cancer|January 23, 2015
Association of breast cancer risk loci with breast cancer survivalMyrto Barrdahl, Federico Canzian, Sara Lindström, et al.
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