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The American Journal of Pathology|September 24, 2016
Braf Mutations Initiate the Development of Rat Gliomas Induced by Postnatal Exposure to N-Ethyl-N-NitrosoureaQi Wang, Kaishi Satomi, Ji Eun Oh, et al.Nature|August 17, 2017
Polylox barcoding reveals haematopoietic stem cell fates realized in vivoWeike Pei, Thorsten B Feyerabend, Jens Rössler, et al.Molecular Oncology|January 29, 2025
Molecular and functional profiling unravels targetable vulnerabilities in colorectal cancerEfstathios-Iason Vlachavas, Konstantinos Voutetakis, Vivian Kosmidou, et al.Human Molecular Genetics|January 14, 2014
Mutation of SALL2 causes recessive ocular coloboma in humans and miceDaniel Kelberman, Lily Islam, Jörn Lakowski, et al.Cold Spring Harbor Molecular Case Studies|December 1, 2016
Integration of genomics and histology revises diagnosis and enables effective therapy of refractory cancer of unknown primary with PDL1 amplificationStefan Gröschel, Martin Bommer, Barbara Hutter, et al.Blood|September 15, 2012
Commonly altered genomic regions in acute myeloid leukemia are enriched for somatic mutations involved in chromatin remodeling and splicingAnna Dolnik, Julia C Engelmann, Maren Scharfenberger-Schmeer, et al.Acta Neuropathologica|April 30, 2021
Rare germline variants in the E-cadherin gene CDH1 are associated with the risk of brain tumors of neuroepithelial and epithelial originAlisa Förster, Frank Brand, Rouzbeh Banan, et al.Nature Cancer|September 7, 2023
Persister cell phenotypes contribute to poor patient outcomes after neoadjuvant chemotherapy in PDACXu Zhou, Jingyu An, Roma Kurilov, et al.Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|August 19, 2016
Targeting Fibroblast Growth Factor Receptor 1 for Treatment of Soft-Tissue SarcomaPriya Chudasama, Marcus Renner, Melanie Straub, et al.JCO Precision Oncology|May 26, 2021
CATCH: A Prospective Precision Oncology Trial in Metastatic Breast CancerMario Hlevnjak, Markus Schulze, Shaymaa Elgaafary, et al.Pageof 7