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Nature Genetics|March 19, 2013
The CCND1 c.870G>A polymorphism is a risk factor for t(11;14)(q13;q32) multiple myelomaNiels Weinhold, David C Johnson, Daniel Chubb, et al.
Human Molecular Genetics|April 17, 2014
Identification of susceptibility loci for colorectal cancer in a genome-wide meta-analysisNicola Whiffin, Fay J Hosking, Susan M Farrington, et al.
Gastroenterology|November 18, 2008
Chromosome 8q23.3 and 11q23.1 variants modify colorectal cancer risk in Lynch syndromeJuul T Wijnen, Richard M Brohet, Ronald van Eijk, et al.
Cancer Research|November 1, 2011
Genome-wide high-density SNP linkage search for glioma susceptibility loci: results from the Gliogene ConsortiumSanjay Shete, Ching C Lau, Richard S Houlston, et al.
Blood Advances|August 23, 2019
Clinical significance of DNA methylation in chronic lymphocytic leukemia patients: results from 3 UK clinical trialsTomasz K Wojdacz, Harindra E Amarasinghe, Latha Kadalayil, et al.
Carcinogenesis|July 30, 2010
Inherited variation in immune genes and pathways and glioblastoma riskJudith A Schwartzbaum, Yuanyuan Xiao, Yanhong Liu, et al.
Nature|November 7, 2024
Origins and impact of extrachromosomal DNAChris Bailey, Oriol Pich, Kerstin Thol, et al.
Scientific Reports|May 24, 2019
Publisher Correction: Mendelian randomisation study of the relationship between vitamin D and risk of gliomaHannah Takahashi, Alex J Cornish, Amit Sud, et al.
Familial Cancer|May 11, 2010
Survey of familial glioma and role of germline p16INK4A/p14ARF and p53 mutationLindsay B Robertson, Georgina N Armstrong, Bianca D Olver, et al.
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