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PXR基因多态性的研究现状及其对环孢素A的药物相互作用的预测意义 被引量:2

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摘要 环孢素A作为广泛应用于器官移植术后的免疫抑制剂,狭窄的治疗窗、显著的药动学个体差异,尤其是药物联用情况下的初始剂量选择是众多学者关注的问题.CYP3A4显著的表型差异是造成环孢素A药动学差异的主要原因.核受体PXR作为CYP3A4以及P糖蛋白编码基因的上游调控关键因子,其自身基因序列的突变可能是导致下游基因转录活性发生改变的分子机制.因此,从PXR的基因入手,探索环孢素A的最佳初始剂量,将为器官移植患者提供更加准确的治疗方案.
作者 曾勇 周宏灏
出处 《第四军医大学学报》 北大核心 2009年第11期1051-1054,共4页 Journal of the Fourth Military Medical University
基金 国家自然科学基金(30300428)
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参考文献26

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同被引文献49

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