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Cancer Research|December 26, 2003
Evaluation of Fanconi Anemia genes in familial breast cancer predispositionSheila Seal, Rita Barfoot, Hiran Jayatilake, et al.
Biostatistics (Oxford, England)|October 20, 2009
PICNIC: an algorithm to predict absolute allelic copy number variation with microarray cancer dataChris D Greenman, Graham Bignell, Adam Butler, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 30, 2008
Subclonal phylogenetic structures in cancer revealed by ultra-deep sequencingPeter J Campbell, Erin D Pleasance, Philip J Stephens, et al.
Blood Advances|May 12, 2019
Efficacy and predictors of response of lenalidomide and rituximab in patients with treatment-naive and relapsed CLLPaolo Strati, Koichi Takahashi, Christine B Peterson, et al.
Discover Oncology|June 17, 2024
Targeting IL-11R/EZH2 signaling axis as a therapeutic strategy for osteosarcoma lung metastasesEswaran Devarajan, R Eric Davis, Hannah C Beird, et al.
Plos One|May 10, 2014
A pathogenic mosaic TP53 mutation in two germ layers detected by next generation sequencingSam Behjati, Mariana Maschietto, Richard D Williams, et al.
Cancer Prevention Research (Philadelphia, Pa.)|September 12, 2020
Effect of Antibiotics on Gut and Vaginal Microbiomes Associated with Cervical Cancer Development in MiceTatiana V Karpinets, Travis N Solley, Megan D Mikkelson, et al.
Blood Advances|January 4, 2018
Copy number alterations detected as clonal hematopoiesis of indeterminate potentialKoichi Takahashi, Feng Wang, Hagop Kantarjian, et al.
Genome Research|August 9, 2018
High-throughput single-cell DNA sequencing of acute myeloid leukemia tumors with droplet microfluidicsMaurizio Pellegrino, Adam Sciambi, Sebastian Treusch, et al.
Nature|May 23, 2007
Chromosomally unstable mouse tumours have genomic alterations similar to diverse human cancersRichard S Maser, Bhudipa Choudhury, Peter J Campbell, et al.
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