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Clarification of some aspects related to genotoxicity assessment
The European Commission requested EFSA to provide advice on the following: (1) the suitability of the unscheduled DNA synthesis (UDS) in vivo assay to follow‐up positive results in in vitro gene mutation tests; (2) the adequacy to demonstrate target tissue exposure in in vivo studies, particularly i...
Tallennettuna:
| Julkaisussa: | EFSA J |
|---|---|
| Päätekijät: | , , , , , , , , , , , , , , , , , , , , , , , , , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
John Wiley and Sons Inc.
2017
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7009892/ https://ncbi.nlm.nih.gov/pubmed/32625393 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2903/j.efsa.2017.5113 |
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