Voorbeelden van het gebruik van Vitro study in het Engels en hun vertalingen in het Nederlands
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Medicine
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Programming
An in vitro study shows that zonisamide is a weak inhibitor of P-gp(MDR1)
In an in vitro study, zoledronic acid showed low affinity for the cellular components of human blood,
An in vitro study of azacitidine with cultured human hepatocytes indicates that at concentrations of 1.0 µM to 100 µM(i.e. up to approximately 30-fold higher than clinically achievable concentrations),
In a chromosomal aberration in vitro study with cultured human peripheral lymphocyte cells, florbetapir did not increase the percent
In an in vitro study, temsirolimus inhibited the transport of P-glycoprotein(P-gp) substrates with an IC50 value of 2 µM. In vivo, the effect of P-gp inhibition has not been
In vitro studies.
Effects of other medicinal products on sildenafil In vitro studies.
In vitro studies have shown no inhibition of any subtype of cytochrome P450.
Effects of sildenafil on other medicinal products In vitro studies.
Nateglinide has shown a low potential for protein displacement in in vitro studies.
In in vitro studies, daptomycin was not metabolised by human liver microsomes.
In in vitro studies, the protein binding of amprenavir is approximately 90.
In vitro studies have also indicated that eribulin is not a substrate for OCT1.
In vitro studies have demonstrated that afatinib is a substrate of P-gp and BCRP.
In vitro studies have shown no inhibition of any subtype of cytochrome P450.
In vitro studies indicate that asenapine weakly inhibits CYP2D6.
In vitro studies indicate that dasatinib is a CYP3A4 substrate.
In vitro studies indicate that paliperidone is not an inducer of CYP1A2 activity.
In vitro studies of antiviral activity.
Desloratadine has demonstrated antiallergic properties from in vitro studies.