类有机物
体外
医学
内科学
人肝
计算生物学
生物
遗传学
神经科学
作者
Charles J. Zhang,Sophia R. Meyer,Matthew J. O’Meara,Sha Huang,Meghan M. Capeling,Daysha Ferrer-Torres,Charlie J. Childs,Jason R. Spence,Robert J. Fontana,Jonathan Z. Sexton
标识
DOI:10.1016/j.jhep.2023.01.019
摘要
Drug-induced liver injury (DILI), both intrinsic and idiosyncratic, causes frequent morbidity, mortality, clinical trial failures and post-approval withdrawal. This suggests an unmet need for improved in vitro models for DILI risk prediction that can account for diverse host genetics and other clinical factors. In this study, we evaluated the utility of human liver organoids (HLOs) for high-throughput DILI risk prediction and in an organ-on-chip system.
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