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dc.contributor.authorBeckwitt, Colin H.
dc.contributor.authorClark, Amanda M.
dc.contributor.authorWheeler, Sarah
dc.contributor.authorTaylor, D. Lansing
dc.contributor.authorStolz, Donna B.
dc.contributor.authorWells, Alan
dc.contributor.authorGriffith, Linda G
dc.date.accessioned2019-03-08T15:24:14Z
dc.date.available2019-03-08T15:24:14Z
dc.date.issued2017-12
dc.date.submitted2017-12
dc.identifier.issn0014-4827
dc.identifier.issn1090-2422
dc.identifier.urihttp://hdl.handle.net/1721.1/120832
dc.description.abstract© 2017 The liver plays critical roles in both homeostasis and pathology. It is the major site of drug metabolism in the body and, as such, a common target for drug-induced toxicity and is susceptible to a wide range of diseases. In contrast to other solid organs, the liver possesses the unique ability to regenerate. The physiological importance and plasticity of this organ make it a crucial system of study to better understand human physiology, disease, and response to exogenous compounds. These aspects have impelled many to develop liver tissue systems for study in isolation outside the body. Herein, we discuss these biologically engineered organoids and microphysiological systems. Keywords: Microphysiologic systems; Organoids; 3D culture systemsen_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (Grant UH3TR000496)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (Grant UH3TR000503)en_US
dc.publisherElsevier BVen_US
dc.relation.isversionofhttp://dx.doi.org/10.1016/J.YEXCR.2017.12.023en_US
dc.rightsCreative Commons Attribution-NonCommercial-NoDerivs Licenseen_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/en_US
dc.sourcePMCen_US
dc.titleLiver ‘organ on a chip’en_US
dc.typeArticleen_US
dc.identifier.citationBeckwitt, Colin H. et al. “Liver ‘organ on a Chip.’” Experimental Cell Research 363, 1 (February 2018): 15–25 © 2017 Elsevieren_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biological Engineeringen_US
dc.contributor.mitauthorGriffith, Linda G
dc.relation.journalExperimental Cell Researchen_US
dc.eprint.versionAuthor's final manuscripten_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dc.date.updated2019-02-11T17:16:02Z
dspace.orderedauthorsBeckwitt, Colin H.; Clark, Amanda M.; Wheeler, Sarah; Taylor, D. Lansing; Stolz, Donna B.; Griffith, Linda; Wells, Alanen_US
dspace.embargo.termsNen_US
dc.identifier.orcidhttps://orcid.org/0000-0002-1801-5548
mit.licensePUBLISHER_CCen_US


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