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mutagenesis
mutagenees

mutagenesis:
hiirte ja koertega teostatud kartsinogeensusuuringutes sarnaseid neerukahjustuse leide ei täheldatud.

carcinogenesis, mutagenesis
kartsinogenees, mutagenees

carcinogenesis and mutagenesis
kantserogenees ja mutagenees

mutagenesis 35, 191-201.
mutagenesis 35, 191–201.

carcinogenesis, mutagenesis, reproductive toxicity
kartsinogenees, mutagenees, reproduktsioonitoksilisus

carcinogenesis, mutagenesis, impairment of fertility
kartsinogeensus, mutageensus ja reproduktsioonitoksilisus

limited but relevant mutagenesis tests have been carried out.
mutagenees: läbi on viidud olulised, ent piiratud arv mutageneesi teste.

teratogenesis, carcinogenesis, and mutagenesis, 4, p. 181-188.
teratogenesis, carcinogenesis, and mutagenesis 4; 181-188.

carcinogenesis, mutagenesis, impairment of fertility: bexarotene is not genotoxic.
kartsinogenees, mutagenees, viljakuse halvenemine: beksaroteen ei ole genotoksiline.

mutagenesis: tolcapone was shown not to be genotoxic in a complete series of mutagenicity studies.
mutagenees: mutageensustestides ei ole ilmnenud tolkapooni genotoksilist toimet.

eribulin was positive in the mouse lymphoma mutagenesis assay and was clastogenic in the in vivo rat micronucleus assay.
eribuliin andis positiivse tulemuse hiire lümfoomi mutageneesi testis ning oli klastogeenne in vivo roti mikrotuumade testis.

carcinogenesis, mutagenesis, impairment of fertility studies have not been performed to determine the carcinogenic potential of alitretinoin.
kartsinogenees, mutagenees, viljakuse häired uuringuid alitretinoiini võimaliku kartsinogeensuse määramiseks ei ole läbi viidud.

two intermediates of the manufacturing process, which are also present in the final product, are positive for mutagenesis in the ames assay.
kaks tootmisprotsessi vaheprodukti, mida leidub ka lõpptootes, osutusid amesi testis mutageenseteks.

mutagenesis and carcinogenesis studies can generally be dispensed with if the chemical composition, practical experience, or other considerations do not indicate the likelihood of changes.
mutageneesi ja kantserogeneesi uuringutest võib üldiselt loobuda, kui keemiline koostis, praktilised kogemused või muud kaalutlused ei osuta muutuste võimalusele.

in a cell-based accelerated mutagenesis assay, no mutation in bcr-abl was detected that could confer resistance to 40 nm ponatinib.
rakupõhises kiirendatud mutageneesi analüüsis ei leitud bcr-abl-i mutatsiooni, mis võiks anda edasi resistentsust 40 nm ponatiniibile.

, an investigation into the activation and deactivation of chlorinated hydrocarbons to genotoxins in metabolically competent human cells, mutagenesis, 11, 247-274.
, an investigation into the activation and deactivation of chlorinated hydrocarbons to genotoxins in metabolically competent human cells, mutagenesis, 11, 247–274.

(eds), in vitro metabolic activation in mutagenesis testing, elsevier, north-holland, pp. 85-88.
(eds), in vitro metabolic activation in mutagenesis testing, elsevier, north-holland, pp. 85–88.

, the use of fluorescence in-situ hybridisation for the detection of aneugens in cytokinesis-blocked mouse splenocytes, mutagenesis, 8, 329-334.
, the use of fluorescence in-situ hybridisation for the detection of aneugens in cytokinesis-blocked mouse splenocytes, mutagenesis, 8, 329–334.

, classification of micronuclei in murine erythrocytes: immunofluorescent staining using crest antibodies compared to in situ hybridization with biotinylated gamma satellite dna, mutagenesis, 6, 297-302.
, classification of micronuclei in murine erythrocytes: immunofluorescent staining using crest antibodies compared to in situ hybridization with biotinylated gamma satellite dna, mutagenesis, 6, 297–302.