Examples of using Data indicate in English and their translations into Croatian
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Colloquial
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Ecclesiastic
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Computer
This data indicate that telavancin is not extensively distributed.
I believe that these data indicate that she is not standing beside the survivors, but in fact against the survivors.
These data indicate manufacturers in the technical description of the material.
The data indicate that boceprevir is eliminated primarily by the liver.
Available data indicate that there may be an increased risk of spontaneous abortion.
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The data indicate presence ofdemixing in the experiments with the real components.
These data indicate that elimination of micafungin is primarily non-renal.
In vitro data indicate that sacubitril inhibits OATP1B1 and OATP1B3 transporters.
In vitro data indicate cobimetinib is not an inhibitor of OAT1, OAT3 or OCT2.
In vitro data indicate that the following species are not susceptible to ceftolozane/tazobactam.
In vitro data indicate that CYP2D6 and CYP3A4 contribute to the limited metabolism of alogliptin.
In vitro data indicate that selexipag could be an inducer of both CYP3A4 and CYP2C9 in the intestine.
Limited data indicate that oseltamivir and the active metabolite are excreted in human milk.
Limited data indicate that the dose should be reduced in patients with moderate renal impairment.
However, these data indicate that clofarabine may accumulate in such patients see figure below.
Initial data indicate, that the satellite was lost not because of someone's sabotage or malicious intent.
In vitro data indicate that IL-5 and reslizumab are unlikely to affect CYP1A2, 3A4 or 2B6 activity.
Our data indicate that employment in theglassblowing industry contributes to the development of chronicrespiratory findings.
Pharmacokinetic data indicate increased systemic exposure to miglustat in patients with renal impairment.
In vitro data indicate that paritaprevir is a substrate for the human hepatic uptake transporters, OATP1B1 and OATP1B3.
In vitro data indicate that silodosin does not have the potential to inhibit or induce cytochrome P450 enzyme systems.
Experimental data indicate that amlodipine binds to both dihydropyridine and non- dihydropyridine binding sites.
Limited published data indicate that growth hormone treatment increases cytochrome P450 mediated antipyrine clearance in man.
Pharmacokinetic data indicate that clofarabine may accumulate in patients with decreased creatinine clearance see section 5.2.
Initial data indicate that the adverse cardiovascular outcomes may be mostly associated with the target heart rate being below 60 bpm;
Pharmacokinetic data indicate that no dose adjustment is necessary in patients with mild to moderate hepatic impairment see section 5.2.
In vitro data indicate that ulipristal acetate may be an inhibitor of BCRP(Breast Cancer Resistance Protein) transporters at the intestinal level.
Data indicate that the binding site involves ribosomal protein L3 and is in the region of the ribosomal P site and peptidyl transferase centre.
Non-clinical data indicate that osimertinib and its metabolite(AZ5104) inhibit the h-ERG channel, and QTc prolonging effect cannot be excluded.
In vitro data indicate that enzalutamide is not a substrate for OATP1B1, OATP1B3, or OCT1; and N-desmethyl enzalutamide is not a substrate for P-gp or BCRP.