Examples of using In in vitro in English and their translations into Croatian
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In in vitro studies, ospemifene and 4-hydroxyospemifene did not inhibit P-glycoprotein(P-gp),
In in vitro studies, perampanel did not compete with AMPA for binding to the AMPA receptor,
An endometrial thickness(EMT) of less than 7 mm decreases the pregnancy rate in in vitro fertilization by an odds ratio of approximately 0.4 compared to an EMT of over 7 mm.
No evidence of mutagenicity or genotoxicity was observed in in vitro microbial mutagenesis(Ames) tests, in vitro alkaline
Stavudine was genotoxic in in vitro tests in human lymphocytes possessing triphosphorylating activity(in which no no-effect level was established),
No signs of genotoxicity were identified in in vitro assays(bacterial mutation[AMES Assay],
was mutagenic in in vitro tests and was clastogenic in vitro(chromosome aberrations
but consistent with other nucleoside analogues, they inhibit cellular DNA replication in in vitro mammalian tests such as the mouse lymphoma assay.
In in vitro bio-assays, fluralaner is not affected by proven field resistances against amidines(tick),
The active substance was not genotoxic in in vitro assays.
a weak clastogenic activity was observed in in vitro studies.
In in vitro assays asenapine acts as an antagonist at these receptors.
In in vitro studies, the protein binding of amprenavir is approximately 90.
Fosaprepitant was rapidly converted to aprepitant in in vitro incubations with liver preparations from humans.
Sodium oxybate was non-mutagenic and non-clastogenic in in vitro and in vivo assays.
In in vitro studies, no antagonism has been observed between tigecycline
relevant clastogenic activity in in vitro studies and no.
In in vitro studies in human hepatic microsomes, minor inhibition of CYP1A2 and CYP2B6 was observed.
In in vitro studies, lixisenatide did not affect the activity of cytochrome P450 isozymes
In in vitro studies, regadenoson has been shown to have little binding affinity for the A2B and A3 adenosine receptors.