查询词典 inhibitor

These data strongly suggest that NYD-SP27 is a physiological inhibitor of PLC that acts as an intrinsic decapacitation factor in sperm to prevent premature capacitation and acrosome reaction.

这些数据有力的表明NYD-SP27是一种生理性的PLC抑制剂，它作为精子内的内源性的去获能因子发挥作用以阻止过早的获能和顶体反应的发生。

Objective: To investigate the effect of enzyme inhibitor of inducible nitric oxide synthase S-methylisothiourea in cervical intervertebral disc cataplasia of rats.

目的：研究诱导型一氧化氮合酶抑制剂S-甲基异硫脲(S-methylisothiourea， SMT)在大鼠颈椎间盘退变中的作用。

Selective cathepsin K inhibitor may be new drug for osteoporosis.

另外，选择性的组织蛋白酶K抑制剂可能成为治疗骨质疏松的新药。

Specific inhibitor of the Ca2+-dependent cysteine protease calpain I and of cathepsin B and L.

三肽醛。Ca2+依赖性半胱氨酸蛋白酶钙蛋白酶I和组织蛋白酶B和 L专属抑制剂

After careful studying their relative importance to immune response and the possibility of the match, seventeen sequences of interest were selected for further experiment, including ESTss analogous to 11.5KD antibacterial peptide, lysozyme, serine protease and its inhibitor, lectin, antifreeze protein, et al. Primers designed according to the sequences were used to amplify the corresponding ESTss from both blood and cephalothorax cDNA library.

在仔细分析了它们在免疫系统中的重要性和在对虾中出现的可能性之后，从中选出了17条可能编码抗菌肽，溶菌酶，凝集素、丝氨酸蛋白酶及其抑制剂，抗冻蛋白等蛋白质的序列，以此为依据设计引物，在中国对虾的血液和头胸部cDNA文库中扩增相应的序列。

The influence of acrylic acid and cetane alcohol,amount of catalyst and inhibitor,reaction temperature,reaction time were investigated.

实验结果表明，合成的最佳反应条件为：丙烯酸与十六酯的物质的量之比为1.2∶1，对甲苯磺酸的用量为0.6%，对苯二酚的用量为0.4%，反应温度为110℃，反应时间为5 h。

Results as bellows: AtSIRT1 was located in Mitochondrial as hSIRT4 of human, and maybe take part in respiration and electron transformation chain, AtSIRT2 was located in nucleolus as hSIRT6 of human, maybe play important role in extend lifespan;mutation in AtSIRT1 leaded to cotyledon of plant turn to yellow and caused short life span. Mutation in AtSIRT2 could make the color of leaf turn to purple and accumulate a lot of anthocyanin;Sirtinol, a inhibitor of SIRT which did not cause the same model of the mutation of AtSIRT1 and AtSIRT2 indicated that the mechanism of Sirtinol was different from other organism;the structure of AtSIRT1 and AtSIRT2 were similar to other known Sir2, which indicated that they maybe have the same function;AtSIRT2 was overexpressed and its activity was detected.

结果表明，1，拟南芥AtSIRT1与人的同源蛋白hSIRT4相同，定位于线粒体，可能参与呼吸作用和电子传递，SIRT2与人的同源蛋白hSIRT6相同，定位于细胞核，可能同它的功能类似，在延缓衰老及调节细胞寿命方面起作用。2，AtSIRT1突变，可引起幼苗和植株的子叶变黄和早衰；AtSIRT2突变，可引起叶片发紫，沉积大量花青素。3，SIRT蛋白的抑制剂Sirtinol不能表型模写AtSIRT1和AtSIRT2突变体，说明Sirtinol在拟南芥中的作用机制不同于其他生物。4，AtSIRT1和AtSIRT2蛋白质结构预测表明与已知的Sir2蛋白相似，揭示其功能的相似性。5，在大肠杆菌中过量表达了其中一个基因(AtSIRT2)，可体外检测其酶学活性，进一步证明其功能。

Objective: To investigate the effect of the inhibitor of PI3'K/Akt in inducing apoptosis of human gastric cancer cells interfered by chemotherapeutics.

目的：检测PI3'K/Akt通路抑制剂对抗肿瘤药物诱导人胃癌细胞凋亡过程的影响。

The inhibitor of PI3K/AKt can up-regulate the apoptosis level of gastric cells and enhance the effect of chemotherapeutics.

PI3K/AKT通路抑制剂能促进胃癌细胞凋亡，增强抗肿瘤化疗药物的疗效。

A cholinesterase inhibitor and immunosuppressive therapy were applied for treatment.

一种胆碱酯酶抑制剂和免疫抑制疗法用于治疗。

The objective is to subjugate and discourage the people, because that allows the elite to continue to rule unopposed.

其目的是压制和打击人民的积极性，因为这可以让实权派继续统治不会沦为反对派。

GOD,this is the second time you vanquished me!

天啊，这是第二次你打败了我！