Results 241 to 250 of about 506,903 (380)

In Vitro Assessment of Drug‐Induced Liver Injury Using Three‐Dimensional Cultured HepaSH Cells Derived From Chimeric Mouse Model With Humanized Liver

open access: yesJournal of Applied Toxicology, EarlyView.
ABSTRACT Drug‐induced liver injury (DILI) is a serious adverse event and a common cause of postmarketing drug withdrawal. Despite nonclinical assessments of DILI risk, which are predominantly conducted in experimental animals, DILI remains a frequent adverse event, highlighting the need to improve nonclinical assessments.
Xingming Liu   +7 more
wiley   +1 more source

Roles of Renal Cytochrome P450-Dependent Arachidonic Acid Metabolites in Hypertension.

open access: bronze, 1992
Ken Omata   +7 more
openalex   +2 more sources

Interindividual Variability in Cytochrome P450–Mediated Drug Metabolism

open access: yesDrug Metabolism And Disposition, 2016
T. Tracy   +11 more
semanticscholar   +1 more source

Perinatal Exposure to the Neonicotinoid Thiacloprid Impacts Transcription of Neuroplasticity and Neuroendocrine Markers in Mice but Not in the Zebrafish Model

open access: yesJournal of Applied Toxicology, EarlyView.
ABSTRACT Neonicotinoids are widely used insecticides in agriculture, aquaculture, pet care, and urban pest control. Initially developed to selectively target the insect cholinergic system, their extensive use has raised concerns about adverse effects on nontarget vertebrates.
Kirthana Kunikullaya U   +6 more
wiley   +1 more source

Molecular Genetics of the Human Cytochrome P450-Dependent Monooxygenases.

open access: bronze, 1992
C. Roland Wolf   +6 more
openalex   +2 more sources

Ultra‐Sensitive Quantification of Indoxyl Sulfate and 3‐Carboxy‐4‐Methyl‐5‐Propyl‐2‐Furanpropanoic Acid in Plasma Using Ultra‐Performance Liquid Chromatography Coupled to Quadrupole Time‐of‐Flight Mass Spectrometry

open access: yesJournal of Clinical Laboratory Analysis, EarlyView.
We established and validated a novel ultra‐sensitive method for simultaneous quantification of uremic toxins using ultra‐performance liquid chromatography coupled to quadrupole time‐of‐flight mass spectrometry. This assay met the acceptance criteria of the U.S. Food and Drug Administration bioanalytical method validation guidance.
Jun Negami   +10 more
wiley   +1 more source

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