Ontology highlight
ABSTRACT:
INSTRUMENT(S): Orbitrap Fusion Lumos, LTQ Orbitrap XL, LTQ Orbitrap Elite
ORGANISM(S): Homo Sapiens (human)
TISSUE(S): Liver, Epithelial Cell
DISEASE(S): Hepatocellular Carcinoma
SUBMITTER: Leon Bichmann
LAB HEAD: Hans-Georg Rammensee
PROVIDER: PXD013057 | Pride | 2019-05-06
REPOSITORIES: Pride
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Löffler Markus W MW Mohr Christopher C Bichmann Leon L Freudenmann Lena Katharina LK Walzer Mathias M Schroeder Christopher M CM Trautwein Nico N Hilke Franz J FJ Zinser Raphael S RS Mühlenbruch Lena L Kowalewski Daniel J DJ Schuster Heiko H Sturm Marc M Matthes Jakob J Riess Olaf O Czemmel Stefan S Nahnsen Sven S Königsrainer Ingmar I Thiel Karolin K Nadalin Silvio S Beckert Stefan S Bösmüller Hans H Fend Falko F Velic Ana A Maček Boris B Haen Sebastian P SP Buonaguro Luigi L Buonaguro Luigi L Kohlbacher Oliver O Stevanović Stefan S Königsrainer Alfred A Rammensee Hans-Georg HG
Genome medicine 20190430 1
<h4>Background</h4>Although mutated HLA ligands are considered ideal cancer-specific immunotherapy targets, evidence for their presentation is lacking in hepatocellular carcinomas (HCCs). Employing a unique multi-omics approach comprising a neoepitope identification pipeline, we assessed exome-derived mutations naturally presented as HLA class I ligands in HCCs.<h4>Methods</h4>In-depth multi-omics analyses included whole exome and transcriptome sequencing to define individual patient-specific se ...[more]