Suppr超能文献

小鼠淋巴瘤胸苷激酶基因突变试验:2005年于旧金山召开的遗传毒性测试国际研讨会会议,关于24小时处理的建议

Mouse lymphoma thymidine kinase gene mutation assay: meeting of the International Workshop on Genotoxicity Testing, San Francisco, 2005, recommendations for 24-h treatment.

作者信息

Moore Martha M, Honma Masamitsu, Clements Julie, Bolcsfoldi George, Burlinson Brian, Cifone Maria, Clarke Jane, Clay Philip, Doppalapudi Rupa, Fellows Michael, Gollapudi Bhaskar, Hou Saimei, Jenkinson Peter, Muster Wolfgang, Pant Kamala, Kidd Darren A, Lorge Elisabeth, Lloyd Melvyn, Myhr Brian, O'Donovan Michael, Riach Colin, Stankowski Leon F, Thakur Ajit K, Van Goethem Freddy

机构信息

National Center for Toxicological Research, Food and Drug Administration, Jefferson, AR 72079, USA.

出版信息

Mutat Res. 2007 Feb 3;627(1):36-40. doi: 10.1016/j.mrgentox.2006.08.013. Epub 2006 Dec 6.

Abstract

The Mouse Lymphoma Assay (MLA) Workgroup of the International Workshop on Genotoxicity Testing (IWGT), comprised of experts from Japan, Europe and the United States, met on September 9, 2005, in San Francisco, CA, USA. This meeting of the MLA Workgroup was devoted to reaching a consensus on issues involved with 24-h treatment. Recommendations were made concerning the acceptable values for the negative/solvent control (mutant frequency, cloning efficiency and suspension growth) and the criteria to define an acceptable positive control response. Consensus was also reached concerning the use of the global evaluation factor (GEF) and appropriate statistical trend analysis to define positive and negative responses for the 24-h treatment. The Workgroup agreed to continue their support of the International Committee on Harmonization (ICH) recommendation that the MLA assay should include a 24-h treatment (without S-9) in those situations where the short treatment (3-4 h) gives negative results.

摘要

由来自日本、欧洲和美国的专家组成的国际遗传毒性测试研讨会(IWGT)小鼠淋巴瘤试验(MLA)工作组于2005年9月9日在美国加利福尼亚州旧金山举行会议。MLA工作组的这次会议致力于就与24小时处理相关的问题达成共识。针对阴性/溶剂对照的可接受值(突变频率、克隆效率和悬浮生长)以及定义可接受阳性对照反应的标准提出了建议。还就使用全局评估因子(GEF)和适当的统计趋势分析以定义24小时处理的阳性和阴性反应达成了共识。工作组同意继续支持国际协调会议(ICH)的建议,即在短时间处理(3 - 4小时)得出阴性结果的情况下,MLA试验应包括24小时处理(无S - 9)。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验