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Evolution of Novel 3D Culture Systems for Studies of Human Liver Function and Assessments of the Hepatotoxicity of Drugs and Drug Candidates

Andersson, Tommy B.

Basic & clinical pharmacology & toxicology. Volume 121:Issue 4 (2017); pp 234-238 -- John Wiley & Sons, Ltd

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Human hepatocytes and cytochrome P450‐selective inhibitors predict variability in human drug exposure more accurately than human recombinant P450s

Lindmark, Bo et al.

British journal of pharmacology. Volume 175:Number 11 (2018); pp 2116-2129 -- Wiley Blackwell

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Cytochrome P450 Induction and Xeno‐Sensing Receptors Pregnane X Receptor, Constitutive Androstane Receptor, Aryl Hydrocarbon Receptor and Peroxisome Proliferator‐Activated Receptor α at the Crossroads of Toxicokinetics and Toxicodynamics

Hakkola, Jukka et al.

Basic & clinical pharmacology & toxicology. Volume 123 (2018) Supplement 5; pp 42-50 -- John Wiley & Sons, Ltd

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Critical differences in drug metabolic properties of human hepatic cellular models, including primary human hepatocytes, stem cell derived hepatocytes, and hepatoma cell lines

Kvist, Alexander J. et al.

Biochemical pharmacology. Volume 155: (2018, September); pp 124-140 -- Elsevier Science

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