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To mitigate limitations with de-differentiated cultures, bioengineers have developed advanced techniques\/platforms, including micropatterned cocultures, spheroids\/organoids, bioprinting, and microfluidic devices, for perfusing cell cultures and liver slices. Such techniques improve mature functions and culture lifetime of primary and stem-cell human liver cells. Furthermore, bioengineered liver models display several features of liver diseases including infections with pathogens (e.g., malaria, hepatitis C\/B viruses, Zika, dengue, yellow fever), alcoholic\/nonalcoholic fatty liver disease, and cancer. Here, we discuss features of bioengineered human liver models, their uses for modeling aforementioned diseases, and how such models are being augmented\/adapted for fabricating implantable human liver tissues for clinical therapy. Ultimately, continued advances in bioengineered human liver models have the potential to aid the development of novel, safe, and efficacious therapies for liver disease.<\/jats:p>","DOI":"10.1055\/s-0041-1731016","type":"journal-article","created":{"date-parts":[[2021,6,17]],"date-time":"2021-06-17T23:28:04Z","timestamp":1623972484000},"page":"368-392","source":"Crossref","is-referenced-by-count":10,"title":["Bioengineered Liver Models for Investigating Disease Pathogenesis and Regenerative Medicine"],"prefix":"10.1055","volume":"41","author":[{"given":"David A.","family":"Kukla","sequence":"additional","affiliation":[{"name":"Deparment of Bioengineering, University of Illinois at Chicago, Chicago, Illinois"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Salman R.","family":"Khetani","sequence":"additional","affiliation":[{"name":"Deparment of Bioengineering, University of Illinois at Chicago, Chicago, 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