Examples of using In vitro data in English and their translations into Swedish
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In vitro data show that netupitant is a P-gp inhibitor.
The clinical relevance of these in vitro data is unknown.
In vitro data demonstrate that cabozantinib is a substrate of MRP2.
Grazoprevir is not a P-gp inhibitor based on in vitro data.
Based on in vitro data, afatinib is a moderate inhibitor of P-gp.
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The clinical significance of these in vitro data has not been demonstrated.
In vitro data indicate that ruxolitinib may inhibit P-gp and BCRP.
to human plasma proteins based on in vitro data.
In vitro data show that etravirine has inhibitory properties on CYP2C19.
Aureus exhibited natural in vitro resistance to cefovecin 4 The clinical significance of these in vitro data has not been demonstrated.
In vitro data suggest that fulvestrant does not inhibit CYP450 isoenzymes.
The Applicant concluded that the in vitro data and the negligible clinical relevance of the differences detected were supported by the provided in vivo study.
In vitro data suggest that brivaracetam has a low interaction potential.
The in vitro data show that gamithromycin acts in a bactericidal manner.
The Applicant stated that the presented in vitro data can be predictive of pharmacokinetic bioequivalence for Cmax
In vitro data indicate that cinacalcet is in part metabolised by CYP1A2.
Based upon in vitro data, migalastat is not an inducer of CYP1A2,
In vitro data suggests that netupitant inhibits the efflux of transporter BCRP.
In vitro data indicate that the following species are not susceptible to ceftaroline.
In vitro data indicate that sacubitril inhibits OATP1B1 and OATP1B3 transporters.
In vitro data showed a slight increase of resistance of C. glabrata to voriconazole.
In vitro data suggest that sitagliptin does not inhibit nor induce CYP450 isoenzymes.
In vitro data indicate that enzalutamide may be an inhibitor of the efflux transporter P-gp.
In vitro data indicate that the following species are not susceptible to ceftolozane/tazobactam.
In vitro data indicate that repaglinide is metabolised predominantly by CYP2C8,
In vitro data indicate that this is predominantly mediated by the cytochrome P450 3A4 isoform CYP3A4.
In vitro data indicate that ulipristal acetate
Based on in vitro data, ceritinib also inhibits CYP2A6
Based on in vitro data pasireotide appears to be a substrate of efflux transporter P-gp P-glycoprotein.