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Statistical analysis of the lacI transgenic mouse mutagenicity assay.

机译:lacI转基因小鼠诱变分析的统计分析。

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摘要

The transgenic mouse assay is now widely used to test chemicals for genotoxic potential. In this article, we consider statistical tests for increasing trend in mutant frequency with increasing dose, along with statistical models that may be used to describe the observed dose-response relationships. The application of these methods is illustrated using data on 2-acetylaminofluorene, di(2-ethylhexyl)phthalate, heptachlor, and sodium phenobarbital. No strong evidence of extra-binomial variation was detected at the plate level, but greater evidence was noted when the data were aggregated to the package or animal level in liver, necessitating the use of statistical methods that allow for overdispersion relative to binomial variation. Clear increase on mutant frequency induced by 2-acetylaminofluorene was detected in both liver and bladder, but no apparent trends were noted with di(2-ethylhexyl)phthalate, heptachlor, and sodium phenobarbital. The exponential model provides a good fit to the observed dose-response relationship in liver, whereas a Weibull model provides a better fit for bladder.
机译:现在,转基因小鼠测定法已广泛用于测试化学品的遗传毒性潜力。在本文中,我们考虑了随着剂量增加突变频率增加趋势的统计测试,以及可以用来描述观察到的剂量反应关系的统计模型。使用关于2-乙酰氨基芴,邻苯二甲酸二(2-乙基己基)酯,七氯和苯巴比妥钠的数据说明了这些方法的应用。在板水平上没有检测到有明显的二项式外变异的证据,但是当将数据汇总到肝脏中的包装或动物水平时,注意到了更多的证据,因此需要使用允许相对于二项式变异过度分散的统计方法。在肝脏和膀胱中均检测到2-乙酰氨基芴诱导的突变体频率明显增加,但是邻苯二甲酸二(2-乙基己基)酯,七氯和苯巴比妥钠未见明显趋势。指数模型可以很好地拟合肝脏中观察到的剂量反应关系,而韦伯模型则可以更好地拟合膀胱。

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