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Proceedings of the National Academy of Sciences of the United States of America|May 2, 2013
Genomic analysis of diffuse pediatric low-grade gliomas identifies recurrent oncogenic truncating rearrangements in the transcription factor MYBL1Lori A Ramkissoon, Peleg M Horowitz, Justin M Craig, et al.
Nature Genetics|April 8, 2014
Recurrent somatic mutations in ACVR1 in pediatric midline high-grade astrocytomaAdam M Fontebasso, Simon Papillon-Cavanagh, Jeremy Schwartzentruber, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|January 5, 2019
Functional Repair Assay for the Diagnosis of Constitutional Mismatch Repair Deficiency From Non-Neoplastic TissueAndrew Y Shuen, Stella Lanni, Gagan B Panigrahi, et al.
Cancer Discovery|December 23, 2020
DNA Polymerase and Mismatch Repair Exert Distinct Microsatellite Instability Signatures in Normal and Malignant Human CellsJiil Chung, Yosef E Maruvka, Sumedha Sudhaman, et al.
Cell|October 24, 2017
Comprehensive Analysis of Hypermutation in Human CancerBrittany B Campbell, Nicholas Light, David Fabrizio, et al.
Nature|April 17, 2020
Germline Elongator mutations in Sonic Hedgehog medulloblastomaSebastian M Waszak, Giles W Robinson, Brian L Gudenas, et al.
Nature Genetics|February 2, 2016
MYB-QKI rearrangements in angiocentric glioma drive tumorigenicity through a tripartite mechanismPratiti Bandopadhayay, Lori A Ramkissoon, Payal Jain, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|January 27, 2021
Clinical Outcomes and Patient-Matched Molecular Composition of Relapsed MedulloblastomaRahul Kumar, Kyle S Smith, Maximilian Deng, et al.
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