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Genetically Modified Rat Models for Pharmacokinetics

机译:基因修饰的大鼠药代动力学模型

摘要

The present invention provides a desired rat or a rat cell which contains a predefined, specific and desired alteration rendering the rat or rat cell predisposed to drug transport sensitivity or resistance drug transport resistance or sensitivity. Specifically, the invention pertains to a genetically altered rat, or a rat cell in culture, that is defective in at least one of two alleles of a drug transporter gene such as the Slc7a11 (NC_005101.2) gene, the Abcb1 (NC_005103.2) gene, etc. The present invention also provides a desired rat or a rat cell which contains a predefined, specific and desired alteration rendering the rat or rat cell predisposed to drug transport sensitivity or resistance drug transport resistance or sensitivity. Specifically, the invention pertains to a genetically altered rat, or a rat cell in culture, that is defective in at least one of two alleles of a drug transporter gene.
机译:本发明提供了一种期望的大鼠或大鼠细胞,其包含预定义的,特异性的和期望的改变,使得该大鼠或大鼠细胞易受药物转运敏感性或耐药性的影响。具体而言,本发明涉及在药物转运蛋白基因如Slc7a11(NC_005101.2)基因Abcb1(NC_005103.2)的两个等位基因的至少一个等位基因中有缺陷的转基因大鼠或培养中的大鼠细胞。本发明还提供了一种期望的大鼠或大鼠细胞,其包含预定的,特异性的和期望的改变,使得该大鼠或大鼠细胞易于发生药物转运敏感性或耐药性。具体地,本发明涉及在药物转运蛋白基因的两个等位基因中的至少一个等位基因中有缺陷的遗传改变的大鼠或培养中的大鼠细胞。

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