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The Lancet. Gastroenterology & Hepatology|November 1, 2019
Modifiable pathways for colorectal cancer: a mendelian randomisation analysisAlex J Cornish, Philip J Law, Maria Timofeeva, et al.
Plos Genetics|September 24, 2010
Allelic variation at the 8q23.3 colorectal cancer risk locus functions as a cis-acting regulator of EIF3HAlan M Pittman, Silvia Naranjo, Sanni E Jalava, et al.
Molecular Carcinogenesis|November 3, 2016
Susceptibility loci of CNOT6 in the general mRNA degradation pathway and lung cancer risk-A re-analysis of eight GWASsFei Zhou, Yanru Wang, Hongliang Liu, et al.
International Journal of Cancer|September 9, 2014
Germline polymorphisms and survival of lung adenocarcinoma patients: a genome-wide study in two European patient seriesAntonella Galvan, Francesca Colombo, Elisa Frullanti, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|October 3, 2013
Germline variants and advanced colorectal adenomas: adenoma prevention with celecoxib trial genome-wide association studyJiping Wang, Luis G Carvajal-Carmona, Jen-Hwa Chu, et al.
NPJ Precision Oncology|June 30, 2022
Deciphering associations between three RNA splicing-related genetic variants and lung cancer riskWenjun Yang, Hongliang Liu, Ruoxin Zhang, et al.
Frontiers in Genetics|October 24, 2012
Leveraging ethnic group incidence variation to investigate genetic susceptibility to glioma: a novel candidate SNP approachDaniel I Jacobs, Kyle M Walsh, Margaret Wrensch, et al.
Nature Genetics|June 30, 2009
The common colorectal cancer predisposition SNP rs6983267 at chromosome 8q24 confers potential to enhanced Wnt signalingSari Tuupanen, Mikko Turunen, Rainer Lehtonen, et al.
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