Methods The cell-free system was prepared by ultracentrifugation of Xenopus eggs and activated by cytochrome C.

方法超离心制备非洲爪蟾卵无细体系,用细C激活为凋亡体系。

A method for the cytochrome C-catalyzed fluorescence determination of artemisinin was developed using pyronine B(PB) as substrate.

在细C催化下,吡啰红B青蒿反应导致荧光降低,细C青蒿的反应为酶-底物模型。

Many of the drugs used in angina pectoris are the substrate of cytochrome P450, drug interactions are easily to occur when antianginal drugs co-administrated with other drugs and foods.

本文综述用抗心绞痛药物相关的药动学方面的相互作用研究进展,为临床用药提供参考。

Methods The cell-free system was prepared by ultracentrifugation of Xenopus eggs and activated by cytochrome C.

方法超离心制备非洲爪蟾卵无细胞系,用细胞色素C激活为凋亡系。

A method for the cytochrome C-catalyzed fluorescence determination of artemisinin was developed using pyronine B(PB) as substrate.

在细胞色素C催化下,吡啰红B与青蒿素反应导降低,细胞色素C与青蒿素反应为-底物模型。

Many of the drugs used in angina pectoris are the substrate of cytochrome P450, drug interactions are easily to occur when antianginal drugs co-administrated with other drugs and foods.

本文综述了与常用抗心绞痛药物相关药动学方面相互作用研究进展,为临床用药提供参考。

Methods The cell-free system was prepared by ultracentrifugation of Xenopus eggs and activated by cytochrome C.

方法超离心制备非洲爪细胞体系,用细胞色素C激活为凋亡体系。

A method for the cytochrome C-catalyzed fluorescence determination of artemisinin was developed using pyronine B(PB) as substrate.

在细胞色素C催下,吡啰红B与青蒿素反应导致荧光降低,细胞色素C与青蒿素的反应为-底物模型。

Many of the drugs used in angina pectoris are the substrate of cytochrome P450, drug interactions are easily to occur when antianginal drugs co-administrated with other drugs and foods.

本文综述了与常用抗心绞痛药物相关的药动学方面的相互作用研究进展,为临床用药提供参考。

Methods The cell-free system was prepared by ultracentrifugation of Xenopus eggs and activated by cytochrome C.

方法超离心制备非洲爪蟾卵无细胞系,用细胞色素C激活为凋亡系。

A method for the cytochrome C-catalyzed fluorescence determination of artemisinin was developed using pyronine B(PB) as substrate.

在细胞色素C催化下,吡啰红B与青蒿素反应导降低,细胞色素C与青蒿素反应为-底物模型。

Many of the drugs used in angina pectoris are the substrate of cytochrome P450, drug interactions are easily to occur when antianginal drugs co-administrated with other drugs and foods.

本文综述了与常用抗心绞痛药物相关药动学方面相互作用研究进展,为临床用药提供参考。

Methods The cell-free system was prepared by ultracentrifugation of Xenopus eggs and activated by cytochrome C.

方法超离心制备非洲爪蟾卵无细胞系,用细胞色素C激活为系。

A method for the cytochrome C-catalyzed fluorescence determination of artemisinin was developed using pyronine B(PB) as substrate.

在细胞色素C催化下,吡啰B与青蒿素反应导致荧光降低,细胞色素C与青蒿素反应为酶-底物模型。

Many of the drugs used in angina pectoris are the substrate of cytochrome P450, drug interactions are easily to occur when antianginal drugs co-administrated with other drugs and foods.

本文综述了与常用抗心绞痛药物相关药动学方面相互作用研究进展,为临床用药提供参考。

Methods The cell-free system was prepared by ultracentrifugation of Xenopus eggs and activated by cytochrome C.

方法超离心制备非洲爪蟾卵无细胞体系,用细胞色C激活为凋亡体系。

A method for the cytochrome C-catalyzed fluorescence determination of artemisinin was developed using pyronine B(PB) as substrate.

在细胞色C下,吡啰红B与青蒿反应导致荧光降低,细胞色C与青蒿的反应为-底物模型。

Many of the drugs used in angina pectoris are the substrate of cytochrome P450, drug interactions are easily to occur when antianginal drugs co-administrated with other drugs and foods.

本文综述了与常用抗心绞痛药物相关的药动学方面的相互作用研究进展,为临床用药提供参考。

Methods The cell-free system was prepared by ultracentrifugation of Xenopus eggs and activated by cytochrome C.

方法超离心制备非洲爪蟾卵无细胞体系,用细胞色素C激活凋亡体系。

A method for the cytochrome C-catalyzed fluorescence determination of artemisinin was developed using pyronine B(PB) as substrate.

在细胞色素C催化下,吡啰红B与青蒿素反应导致荧光降低,细胞色素C与青蒿素的反应-物模型。

Many of the drugs used in angina pectoris are the substrate of cytochrome P450, drug interactions are easily to occur when antianginal drugs co-administrated with other drugs and foods.

本文综述了与常用抗心绞痛药物相关的药动学方面的相互作用研究进展,临床用药提供参考。

Methods The cell-free system was prepared by ultracentrifugation of Xenopus eggs and activated by cytochrome C.

方法超离心制备非洲爪蟾卵无细胞体系,用细胞色素C激活为凋亡体系。

A method for the cytochrome C-catalyzed fluorescence determination of artemisinin was developed using pyronine B(PB) as substrate.

在细胞色素C催化下,吡啰红B与青蒿素反应导致荧光降低,细胞色素C与青蒿素的反应为-模型。

Many of the drugs used in angina pectoris are the substrate of cytochrome P450, drug interactions are easily to occur when antianginal drugs co-administrated with other drugs and foods.

本文综述了与常用抗心绞痛药相关的药动学方面的相互作用研究进展,为临床用药提供参考。

Methods The cell-free system was prepared by ultracentrifugation of Xenopus eggs and activated by cytochrome C.

方法超离心制备蟾卵无细胞体系,用细胞色素C激活为凋亡体系。

A method for the cytochrome C-catalyzed fluorescence determination of artemisinin was developed using pyronine B(PB) as substrate.

在细胞色素C催化下,吡啰红B与青蒿素反应导致荧光降低,细胞色素C与青蒿素的反应为酶-底物模型。

Many of the drugs used in angina pectoris are the substrate of cytochrome P450, drug interactions are easily to occur when antianginal drugs co-administrated with other drugs and foods.

本文综述了与常用抗心绞痛药物相关的药动学方面的相互作用研究进展,为临床用药提供参考。

Methods The cell-free system was prepared by ultracentrifugation of Xenopus eggs and activated by cytochrome C.

方法超离心制备非洲爪蟾卵无细胞体系,用细胞色素C激活为凋亡体系。

A method for the cytochrome C-catalyzed fluorescence determination of artemisinin was developed using pyronine B(PB) as substrate.

在细胞色素C催化下,吡B青蒿素反应导致荧光降低,细胞色素C青蒿素的反应为酶-底物模型。

Many of the drugs used in angina pectoris are the substrate of cytochrome P450, drug interactions are easily to occur when antianginal drugs co-administrated with other drugs and foods.

本文综述了常用抗心绞痛药物相关的药动学方面的相互作用研究进展,为临床用药提供参考。