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-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C催化下,吡啰红B青蒿反应导致荧光降低,细胞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体系,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与青蒿反应导致荧光降低,细C与青蒿的反应为酶-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.

本文综述了与常抗心绞痛药物相关的药动学方面的相互作研究进展,为临床药提供参考。

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胞体系,用胞色素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.

在胞色素C催化下,吡啰红B与青蒿素反应导致荧光,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与青蒿反应导致荧光降低,细C与青蒿的反应为酶-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催下,吡啰红B与反应导致荧光降低,细胞色C与的反应为酶-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,吡啰红B与青蒿素导致荧光降低,细胞色素C与青蒿素为酶-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体系,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.

在素C催化下,吡啰红B青蒿素反应导致荧光降低,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.

本文综述了抗心绞痛药物相关的药动学方面的相互作研究进展,为临床药提供参考。