合成因子

He TFPI/FXa complex then subsequently binds with TF/activated factor VII complex, ultimately inhibiting thrombin generation.

F/ FXa 合成物随后与 TF/活化因子 VII合成物结合，最终制凝血酶生成。

Pheromone traps; sex pheromone; anemotaxis; lures; disparlure; integrated control; attractants; chemical senses; chemoreception; chemoreceptors; infochemicals; semiochemicals; chemical stimuli; chemical communication; chemical cues; chemical perception; pheromones; pheromone receptors; pheromone biosynthesis-activating neuropeptide; pheromone biosynthesis; pheromone-binding protein; PBAN

信息素诱骗；性信息素趋风性；诱惑；舞毒蛾性引诱剂；综合防治；引诱剂；化学知觉；化学感受；化学接受体；信息化学；化学信息素；化学刺激物；化学通讯；化学因子；化学感觉；信息素；信息素受体；信息素生物合成-激活神经肽；信息素生物合成；信息素-结合蛋白；PBAN

Based on the generally accepted enol and carbide mechanismes of the FTS, the above model was derived, and the inhibition of water was interpreted in terms of the heat of adsorption for the combined term b in the denominator of the kinetic equation.

本文就是结合煤化所煤基合成液体燃料的过程开发，对已工业化的FT合成沉淀Fe/Cu/K催化剂进行反应动力学、有效因子的计算和管式固定床反应器数学模型的研究，结果可分述如下： 1。

Methods: In this paper, a quinazoline purine analogues for the parent nucleus, respectively, and four of its seven introduced to replace the structure of diverse and flexible side-chain amino-benzene, design a series of 4 - to replace the aniline-based -6 - methoxy --7 -(2 - hydroxy replace C oxy) quinazoline compounds.

目的：通过各种化学合成方法完成目标化合物4--6-甲氧基-7-(2-羟基取代丙氧基)喹唑啉的合成并对目标化合物进行结构修饰，以期获得高活性的表皮生长因子受体酪氨酸激酶抑制剂。

Objective: through various chemical synthesis target compounds 4 -- 6 - the - 7 -(2 - hydroxyl replace c oxygen radicals) quinazoline compounds were synthesized and the structure of the modified, so as to get high epidermal growth factor receptor tyrosine kinase inhibitor.

目的：通过各种化学合成方法完成目标化合物4--6-甲氧基-7-(2-羟基取代丙氧基)喹唑啉的合成并对目标化合物进行结构修饰，以期获得高活性的表皮生长因子受体酪氨酸激酶抑制剂。

Wenxin capsule can promote endolethial cells releasing CO and synthesing 〓, enhance activity of HO, induce angiectasis through activating guanylic cyclase and adenglate cyclate of intracellar of vessel smooth muscle cell to enhance content of intracellar cGMP and AMP. 3. Wenxin capsule can inhibit releasing of platelet activiting factor 〓 which inhibit platelet aggregation and have antithrombosis function. 4. Wenxin capsule can promote activity of t-PA, reduce activity of PAI-1, strengthen fibrinolytic function, therefore inhibit fibrin disposition. 5. Wenxin capsule can inhibit synthesis of smooth muscle cellular DNA. Its function don't kill it directly but prevent transformation from period Go to peried S. 6. Wenxin capsule is an effective prescription of anti-coronary atherosclerosis atherosis. The results of image pattern analysis tastifies that area of lipid plaque in treating group reduce 54% and 58% in contrast with that in control group. The results of light, electro- microscopy show that structure of endolethial cell and smooth muscle cell in treating group is more integral than that in control group.

其作用机制之一是由于该药具有良好的调脂降脂作用，其不仅能明显降低血清LDL-c及升高HDL-c含量，且能有效阻止TC沉积于血管壁，从而保护内皮细胞结构完整；此外，温心胶囊尚具有明显的抗氧化作用，该药不仅能明显降低血浆LPO含量，且能提高SOD活性，同时其对血红素在细胞内代谢的调节作用也参与了抗氧化过程。2 温心胶囊能明显促进内皮细胞释放CO及合成〓，提高HO活性，通过激活血管平滑肌细胞内鸟苷酸环化酶及腺苷酸环化酶引起细胞内cGMP、AMP浓度增加而引起血管舒张。3 温心胶囊能明显抑制血小板激活因子〓的释放，从而抑制血小板聚集，抗血栓形成。4 温心胶囊能明显提高t-PA活性，降低PAI-1活性，增强纤溶功能，从而抑制纤维蛋白沉积。5 温心胶囊能明显抑制平滑肌细胞DNA合成，其抑制作用不是直接杀伤抑制，而是阻止细胞由Go期向S期转化。6 温心胶囊是抗冠状动脉粥样硬化的有效制剂，图象分析结果证实，该药治疗组脂斑面积比对照组缩小了54％和58％，光电镜结果显示内皮细胞及平滑肌细胞结构较为完整。

A potential approach to this problem is to make use of a natural defense mechanism called " the stress response," which is characterized by a transient down - regulated synthesis of nonvital cellular proteins and increased production of endogenous protective factors known as heat shock proteins that act to allow proper refolding of proteins denatured by the incipient injury.

应激反应的特征是一过性下调细胞非必需蛋白的合成及增加被称为热休克蛋白的内源性保护因子的合成。热休克蛋白作用是促使损伤导致变性的蛋白适当地再折叠。HSP家族中HSP70被认为在细胞保护中发挥重要作用。

Since swines were a breed with high reproductivity, we have studied mechanism of acute regulation of piglet testosterone synthesis.

大量的研究表明，类固醇合成快速调节蛋白是调节类固醇合成的限速因子，因此，我们首先研究了StAR蛋白在仔猪睾丸中的表达。

The ammo acid sequences deduced from the other ESTs are homologous to glutamine synthetase, lipase-like protein, decarboxylase family protein, putative AUXl-like permease, HT-ATP synthetase, Proline-rich protein, RNA transporter binding protein and cation-transporting ATPase, respectively.

摘要其它ESTs的编码产物分别与谷氛酞胺合成酶、类似脂酶、脱数酶家族蛋白、H+- ATP合成酶、激素类渗透酶、阳离子运输ATPa se、RNA运输因子结合蛋白和富含脯氮酸的蛋白等同源。

The furthest along in development are the glucagon-like peptide-1 (GLP-1) drugs, which pack a triple whammy against the disease, stimulating insulin secretion, suppressing glucagon secretion, and inhibiting gastric emptying. The furthest along in its class is exenatide, a synthetic version of a GLP-1-like substance found in the saliva of the Gila monster. An open-label study reported at the meeting showed that about half of patients failing oral therapy achieved near-normal glycemic control when exenatide was added to their regimen.

最先进的研究是类高血糖因子胜-1（GLP-1）药物，这种药物对於疾病的药效高出三倍，可以刺激胰岛素分泌、抑制高血糖因子分泌和抑制胃清空，其中最先进的一类药物为exenatide，这是一种从希拉毒蜥的唾液所合成的类GLP-1物质，根据一项公开标示的研究显示，无法以口服治疗的患者中，有一半的患者在服用exenatide之后，其血糖接近正常值。

As she looked at Warrington's manly face, and dark, melancholy eyes, she had settled in her mind that he must have been the victim of an unhappy attachment.

每逢看到沃林顿那刚毅的脸，那乌黑、忧郁的眼睛，她便会相信，他一定作过不幸的爱情的受害者。

Maybe they'll disappear into a pothole.

也许他们将在壶穴里消失