Results 241 to 250 of about 312,948 (355)
Abstract Aim Tacrolimus dosing in the early post‐kidney transplant period is challenging due to a narrow therapeutic index and substantial interindividual pharmacokinetic (PK) variability. This study aimed to develop and validate mechanism‐informed machine learning (ML) models to support individualized tacrolimus dosing during this critical period ...
Hui Yu +4 more
wiley +1 more source
Identification of factors limiting the efficiency of transplanting extracellular electron transfer chains in <i>Escherichia coli</i>. [PDF]
Philipp L-A +5 more
europepmc +1 more source
Cytochromes P450 and experimental models of drug metabolism
R. Zuber +2 more
semanticscholar +1 more source
Abstract Aim Tacrolimus monitoring is generally performed in whole blood (WB). Most (>85%) of circulating tacrolimus is bound to red blood cells. During pregnancy, WB monitoring might be suboptimal because of physiological changes including increased plasma volume and decreased haematocrit.
Jildau R. Meinderts +7 more
wiley +1 more source
Engineering electron conduits in bacteria for selective biointerfacing and enhanced energy transfer. [PDF]
Kelly AR, Travaglini L, Glover DJ.
europepmc +1 more source
Pharmacogenetic CYP2B6 variants affect steroid hormone metabolism in human breast cancer cells
Common genetic CYP2B6 variants correlate with adverse breast cancer outcome. The oestrogen metabolites estriol and 16‐epiestriol, which are formed downstream of CYP2B6‐catalysed 16α/β‐hydroxytestosterone, may be linked to elevated breast cancer risk and might increase due to the demonstrated CYP2B6 variants‐related metabolic shifts.
Marco Hoffmann +5 more
wiley +1 more source
From coordination to function: Inorganic insights into metalloproteins and metallopeptides in biosystems. [PDF]
Han J.
europepmc +1 more source
The Reaction of Cytochrome Oxidase with Cytochrome c
Quentin H. Gibson +3 more
openaire +1 more source
Aim To evaluate the effects of carbamazepine, a strong cytochrome P450 (CYP)3A4 inducer, on the pharmacokinetics and safety of vepdegestrant, a PROteolysis TArgeting Chimera estrogen receptor degrader. Methods This was a phase 1, open‐label, fixed‐sequence, two‐period study in healthy adult participants.
Hechuan Wang +7 more
wiley +1 more source

