1973
DOI: 10.1016/0027-5107(73)90035-3
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A rapid in vivo test for chromosomal damage☆

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Cited by 705 publications
(228 citation statements)
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“…1) [1][2][3][4][5][6] . The cytokinesis-block micronucleus (CBMN) assay is the preferred method for measuring MNi in cultured human and/or mammalian cells because scoring is specifically restricted to once-divided BN cells, which are the cells that can express MNi [3][4][5][6] .…”
Section: Introductionmentioning
confidence: 99%
See 1 more Smart Citation
“…1) [1][2][3][4][5][6] . The cytokinesis-block micronucleus (CBMN) assay is the preferred method for measuring MNi in cultured human and/or mammalian cells because scoring is specifically restricted to once-divided BN cells, which are the cells that can express MNi [3][4][5][6] .…”
Section: Introductionmentioning
confidence: 99%
“…The ''cytome'' concept implies that every cell in the system studied is scored cytologically for its viability status (necrosis, apoptosis), its mitotic status (mononucleated, BN, multinucleated) and its chromosomal damage or instability status (presence of MNi, NPBs, NBUDs and number of centromere probe signals among nuclei or MNi of BN cell if such molecular tools are used in combination with the assay) (Figs. [1][2][3][4][5]. For these reasons, it is now appropriate to refer to this technique as the cytokinesisblock MN cytome (CBMN Cyt) assay.…”
Section: Introductionmentioning
confidence: 99%
“…The occurrence of micronuclei is increased following exposure to clastogenic agents that cause double-strand DNA breaks and also by aneugens that disrupt chromosomal segregation [1][2]. The in vivo rodent micronucleus (MN) test is widely used to identify or otherwise study chemicals with genotoxic potential [3][4][5].…”
Section: Introductionmentioning
confidence: 99%
“…Genotoxic effects can result by micronuclei (MN) induction. Micronuclei are cytoplasmic chromatin-containing bodies formed during the metaphase/anaphase transition of mitosis (cell division) either from a whole lagging chromosome (aneugenic event) or lagging acentric chromosome fragments caused by chromosomal breakage (clastogenic event) which do not integrate in the daughter cell nuclei following anaphase (Heddle, 1973;Schmidt, 1975;Miller et al, 1998).…”
mentioning
confidence: 99%