Примери за използване на In vitro studies indicate на Английски и техните преводи на Български
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In vitro studies indicate that varenicline is unlikely to alter the pharmacokinetics of compounds that are primarily metabolised by cytochrome P450 enzymes.
Based on the published literature, in vitro studies indicate that the presence of cimetidine,
In vitro studies indicate that lacosamide may be a weak inhibitor
In vitro studies indicate that pitolisant is neither a substrate
In vitro studies indicate that lumacaftor is a substrate of Breast Cancer Resistance Protein(BCRP).
In vitro studies indicate that irbesartan is primarily oxidised by the cytochrome P450 enzyme CYP2C9; isoenzyme CYP3A4 has negligible effect.
Metabolism and excretion In vitro studies indicate that lenalidomide has no inhibitory effect on CYP1A2,
In vitro studies indicate that irbesartan is primarily oxidised by the cytochrome P450 enzyme CYP2C9;
In vitro studies indicate that lapatinib is a substrate for the transporters BCRP(ABCG1) and p-glycoprotein(ABCB1).
In vitro studies indicate that lenalidomide has no inhibitory effect on human bile salt export pump(BSEP),
Effect of larotrectinib on other transporter substrates In vitro studies indicate that larotrectinib is an inhibitor of OATP1B1.
Active substances that may increase dasatinib plasma concentrations In vitro studies indicate that dasatinib is a CYP3A4 substrate.
Effect of larotrectinib on substrates of PXR regulated enzymes In vitro studies indicate that larotrectinib may induce PXR regulated enzymes(e.g. CYP2C family and UGT).
In vitro studies indicate that vismodegib has the potential to act as an inhibitor of breast cancer resistance protein(BCRP).
In vitro studies indicate that lenalidomide has no inhibitory effect on CYP1A2,
In vitro studies indicate that MMAE is a substrate for CYP3A4/5
In vitro studies indicate that irinotecan, SN-38
In vitro studies indicate that TOOKAD is unlikely to be an inhibitor of CYP450 enzymes.
In vitro studies indicate that larotrectinib does not inhibit CYP1A2,
In vitro studies indicate that the activity of sildenafil against PDE5 in 10-10000 times higher activity against other isoforms of the phosphodiesterase(PDE 1,