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inhibitor相关的网络例句

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与 inhibitor 相关的网络例句 [注:此内容来源于网络,仅供参考]

The absorption of thymosinα1 in rat colon and enhancement effect of different absorption enhancers or protease inhibitor (sodium desoxycholate, Carbomer 940, water-soluble chitosan and bacitracin) were investigated using in situ perfusion method.

考察了大鼠在体结肠对胸腺肽α1(1)及其在各吸收促进剂或酶抑制剂(去氧胆酸钠、卡波姆940、水溶性壳聚糖和杆菌肽)作用下的吸收情况。

We hypothesized that the use of a bacteriostatic protein synthesis inhibitor would improve outcomes by reducing the inflammatory response.

我们推测,应用具有抑菌作用的蛋白合成抑制剂会通过减轻炎症反应来改善结局。

A large quantity of evidence has showed that higher EO might be one of the pathogenic factors of hypertension. EO also referred to endogenous sodium pump inhibitor, endogenous digitalis-like substance or endogenous digoxin-like factor before, is a recently identified sterone hormone that might be secreted from adrenal cortex.

内源性哇巴因(endogenous ouabain, EO)是新近发现主要由肾上腺皮质所分泌的一种类固醇激素,大量证据表明,体内EO含量升高可能是高血压的发病因素之一。

On the basis of synthesis of the H+/K+-ATPase inhibitor omeprazole,seven benzimidazole derivatives were synthesized for the first time,and their structures were identified by 1H-NMR、MS and elementary analysis.

设计合成了7个未见文献报道的苯并咪唑类衍生物,经质谱、核磁共振氢谱和元素分析确定了结构。

K-ATPase is the last passageway of gastric acid secretion.On the basis of synthesis of the H+K-ATPase inhibitor pantoprazole,twelve benzimidazole derivatives were synthesized for the first time,and their structures were proved by IR,1H-NMR and elementary analysis.

摘 要 H+/K+-ATP酶是胃酸分泌的最后环节,在合成H+/K+-ATP酶抑制剂泮托拉唑的基础上,设计合成了12个未见文献报道的苯并咪唑类衍生物,经红外光谱、核磁共振氢谱和元素分析确定了结构。

3H]-TdR incorporation rate was used as an index of cell proliferation. Additionally, we investigated whether the ASMC proliferative responses to SP were modulated by preincubation for 2 h with GR71251, a specific antagonist of NK-1 receptor, and neomycin, a phospholipase C inhibitor, and nitrendipine, a blockader of Ca2+ channel, respectively.

细胞增殖实验研究:将平滑肌细胞以1×103/孔接种在96孔板内,含10% FCS-DMEM培养24 h,吸去上清,以无血清DMEM洗涤2次,加入该培养基培养48 h,同步化之后以无血清培养基继续培养48 h或分别加入含SP(10-7~10-5 mol/L)和NK-1受体激动剂[Sar9,Met(O2)11]-SP(10-7~10-5 mol/L)的无血清DMEM培养相同时间。

Objective:To investigate the ACE inhibitor of β-blocker treatment of chronic heart failure treatment.

目 的:探讨ACE抑制剂联合β受体阻滞剂治疗慢性心力衰竭的临床疗效。

Brachiation along the branches of such trees from structurally complex to simple scaffolds with retained yet varying bioactivity is feasible at high frequency for the five major pharmaceutically relevant target classes and allows for the identification of new inhibitor types for a given target.

结构上从复杂到简单的支架的树分枝而仍旧保留不同的生物活性的臂力摆荡,就五大主要药学相关靶分级而言是可行的,并且允许新的特定目标类型抑制剂识别。

Therefore, It is necessary to join the inhibitor in the butadiene extraction process to retard polymerization.

因此,在丁二烯抽提生产过程中需要加入阻聚剂,以阻滞丁二烯单体的聚合。

RESULTS: A LOX inhibitor clearly inhibited the effect of butyrate on TJ permeability, whereas COX inhibitors did not.

结果:使用LOX抑制剂能够明显的抑制丁酸盐所引起的紧密连接通透性的增加,而COX抑制剂则没有这种作用。

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