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Blood|August 20, 2025
Challenging the Concept of Functional High-Risk Myeloma through Transcriptional and Genetic ProfilingSina Alexandra Beer, David A Cairns, Charlotte Pawlyn, et al.Carcinogenesis|April 7, 2017
Functional variants in DCAF4 associated with lung cancer risk in European populationsHongliang Liu, Zhensheng Liu, Yanru Wang, et al.Scientific Reports|April 13, 2017
Genetic variants of PTPN2 are associated with lung cancer risk: a re-analysis of eight GWASs in the TRICL-ILCCO consortiumYun Feng, Yanru Wang, Hongliang Liu, et al.Blood|October 17, 2013
CYP2B6*6 is an independent determinant of inferior response to fludarabine plus cyclophosphamide in chronic lymphocytic leukemiaGillian G Johnson, Ke Lin, Trevor F Cox, et al.Blood|March 16, 2018
iwCLL guidelines for diagnosis, indications for treatment, response assessment, and supportive management of CLLMichael Hallek, Bruce D Cheson, Daniel Catovsky, et al.Human Molecular Genetics|August 2, 2013
Deciphering the genetic architecture of low-penetrance susceptibility to colorectal cancerNicola Whiffin, Sara E Dobbins, Fay J Hosking, et al.Scientific Reports|October 8, 2016
A Novel Genetic Variant in Long Non-coding RNA Gene NEXN-AS1 is Associated with Risk of Lung CancerHua Yuan, Hongliang Liu, Zhensheng Liu, et al.Plos One|April 1, 2015
Common variation at 1q24.1 (ALDH9A1) is a potential risk factor for renal cancerMarc Y R Henrion, Mark P Purdue, Ghislaine Scelo, et al.Nature Communications|October 2, 2015
Genome-wide association study identifies multiple susceptibility loci for gliomaBen Kinnersley, Marianne Labussière, Amy Holroyd, et al.Cancer Discovery|May 16, 2012
Inherited variation at chromosome 12p13.33, including RAD52, influences the risk of squamous cell lung carcinomaJianxin Shi, Nilanjan Chatterjee, Melissa Rotunno, et al.Pageof 49