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阻断剂

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To investigated the relationship of the signal transduction pathway and other signal molucules, three signal transduction inhibitors were tested for their effects on L929 cell and the change of caspase activation. The inhitors include Staurosporine Quinacrine (PLA2 inhibitor) andVerapamil (Ca2+ channel blocker).

为了探讨γTNFβ和TNFβ诱导细胞凋亡的信号转导通路与其它信号分子的关系,我们检测了蛋白激酶C抑制剂Staurosporine、磷脂酶A2抑制剂Quinacrine和钙离子通道阻断剂Verapamil对γTNFβ及TNFβ杀伤L929细胞的影响及其伴随的Caspase8和Caspase3活性的变化。

Both mitochondrial Ca2+ channels are unaffected by blockers of other possibly Ca2+-conducting mitochondrial pores but were activated by spermine (1 mmol/L).

其他可能参与Ca2+转运的线粒体孔阻断剂对这2种钙通道没有作用,精胺(1 mmol/L)则可以激活二者。

By superfusion of ET-1,the hypoxia-induced decrease in RPF was remarkably potentiated and the occurrence of pacemaker arrest was shifted to an earlier time. The h3,poxia-induced effects could be effectively attenuated after pretreatment with BQ-123,implying the role of endogenous ET-1 release in hypoxia-induced effects.

ET-1可显著加重缺氧所致的RPF降低,使起搏细胞停跳时间前移;而以ET*受体阻断剂BQ-123预处理窦房结标本后,则能有效地缓解缺氧对起搏细胞的效应,提示内源性ET-1的释放在缺氧效应中的作用。

Carteolol Arteoptic(superscript is the only one non-selective Beta-blocker with ISA (Intrinsic Sympathomimetic Activity) now.

CarteololArteoptic(上标是目前唯一具有ISA的非选择性β阻断剂

Objective To investigate the therapeutic action of synthetic interleukin-1 blockers on uveitis in rats.

目的 观察人工合成的白细胞介素-1(interleukin-1,IL-1)受体阻断剂对大鼠葡萄膜炎的治疗作用。

This protocol was performed under placebo and -2 adrenergic (ADRA2) blockade with yohimbine in counterbalanced order to test for the influence of ADRA2 mechanisms.

这项记录在安慰剂组和α-2肾上腺素受体阻断剂育亨宾组完成,来测试α-2肾上腺素受体机制的影响。

After therapy with adrenergic blockade, a repeat ECG revealed near complete resolution of the ischemic changes.

经过交感神经阻断剂的治疗后,再追踪心电图,显示心肌缺氧的异常几乎恢复正常。

In this laboratorystudy we sought to characterize the effect of epinephrine andconcomitant calcium channel blockade on postresuscitation myocardialperformance after brief asphyxial cardiac arrest.

本研究中,作者探究窒息后短暂心跳停止复苏后肾上腺素的作用和合并使用钙通道阻断剂对复苏后心肌的影响。

The ventilatory responses of peripheral chemoreflex following 0.1 m l microinjection within the NTS of either PTK inhibitor genistein(10 mol/L), AMPA glutamate receptor inhibitor CNQX (10 mol/L),or inactive PTK inhibitor daidzein (10 mol/L) were recorded.

在孤束核处分别微量注射蛋白酪氨酸激酶的抑制剂genistein和其非活动性抑制剂daidzein 以及 AMPA受体阻断剂CNQX,观察这些药物对外周化学感受性反射的影响。

Such epileptoid activities were not influenced by the synaptic receptor inhibitors, and were obviously related to tile persistent sodium current.

这种癫痫样放电的产生不受突触传递阻断剂的影响,但与持续性钠电流明显相关。

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