دورية أكاديمية

In vitro genotoxicity studies: n-Butyl acrylate L5178Y mouse lymphoma (TK+/− locus assay), 2-Ethylhexyl acrylate gene mutation assay in Chinese hamster V79 cells, and 2-Ethylhexyl acrylate micronucleus test in human lymphocytes

التفاصيل البيبلوغرافية
العنوان: In vitro genotoxicity studies: n-Butyl acrylate L5178Y mouse lymphoma (TK+/− locus assay), 2-Ethylhexyl acrylate gene mutation assay in Chinese hamster V79 cells, and 2-Ethylhexyl acrylate micronucleus test in human lymphocytes
المؤلفون: Sandra Murphy, Robert Ellis-Hutchings, Lavorgie Finch, Stefanie Welz, Karin Wiench
المصدر: Data in Brief, Vol 20, Iss , Pp 316-325 (2018)
بيانات النشر: Elsevier, 2018.
سنة النشر: 2018
المجموعة: LCC:Computer applications to medicine. Medical informatics
LCC:Science (General)
مصطلحات موضوعية: Computer applications to medicine. Medical informatics, R858-859.7, Science (General), Q1-390
الوصف: Available point mutation tests have shown inconsistent results with various acrylates. Most of those tests were performed prior to OECD guidelines and appropriate data regarding cytotoxicity are not given. Data from three current OECD guideline compliant experiments conducted under GLP are provided. They include (a) an in vitro mouse lymphoma (TK+/−) assay (OECD 490) [3], (b) an in vitro HPRT locus gene mutation assay utilizing cultures of Chinese hamster V79 cells (OECD 476) [1], and (c) an in vitro micronucleus test in human lymphocytes (OECD 487) [2]. Test materials were not mutagenic under these experimental conditions, adding to the weight-of-evidence of non-genotoxicity for this group of chemicals.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 2352-3409
Relation: http://www.sciencedirect.com/science/article/pii/S2352340918306590; https://doaj.org/toc/2352-3409
DOI: 10.1016/j.dib.2018.06.008
URL الوصول: https://doaj.org/article/c9c97b9439b44c678de851291883a961
رقم الأكسشن: edsdoj.9c97b9439b44c678de851291883a961
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:23523409
DOI:10.1016/j.dib.2018.06.008