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Genes, Chromosomes & Cancer|June 3, 2015
Whole-exome sequencing defines the mutational landscape of pheochromocytoma and identifies KMT2D as a recurrently mutated geneC Christofer Juhlin, Adam Stenman, Felix Haglund, et al.Genome Medicine|February 4, 2017
Longitudinal analysis of treatment-induced genomic alterations in gliomasE Zeynep Erson-Omay, Octavian Henegariu, S Bülent Omay, et al.Nature Communications|February 15, 2017
Integrated genomic analyses of de novo pathways underlying atypical meningiomasAkdes Serin Harmancı, Mark W Youngblood, Victoria E Clark, et al.Nature Communications|April 21, 2018
Integrated genomic analyses of de novo pathways underlying atypical meningiomasAkdes Serin Harmancı, Mark W Youngblood, Victoria E Clark, et al.Nature Genetics|August 23, 2016
Recurrent somatic mutations in POLR2A define a distinct subset of meningiomasVictoria E Clark, Akdes Serin Harmancı, Hanwen Bai, et al.Nature Communications|October 7, 2023
Super-enhancer hijacking drives ectopic expression of hedgehog pathway ligands in meningiomasMark W Youngblood, Zeynep Erson-Omay, Chang Li, et al.Science (New York, N.Y.)|June 20, 2020
Partitioning of cancer therapeutics in nuclear condensatesIsaac A Klein, Ann Boija, Lena K Afeyan, et al.Nature Genetics|December 1, 2015
Integrated genomic characterization of IDH1-mutant glioma malignant progressionHanwen Bai, Akdes Serin Harmancı, E Zeynep Erson-Omay, et al.Journal of Neurosurgery|October 27, 2019
Correlations between genomic subgroup and clinical features in a cohort of more than 3000 meningiomasMark W Youngblood, Daniel Duran, Julio D Montejo, et al.Science (New York, N.Y.)|January 26, 2013
Genomic analysis of non-NF2 meningiomas reveals mutations in TRAF7, KLF4, AKT1, and SMOVictoria E Clark, E Zeynep Erson-Omay, Akdes Serin, et al.Pageof 2