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"By using hormone therapy in prostate cancer you can help enhance your T-cell response to where the cancer is in the prostate gland, and you are also more likely to achieve a better immune response," said Arlen.

"通过使用激素治疗前列腺癌的您可以帮助增强您的T细胞反应的地方，癌症是在前列腺，你也更有可能取得更好的免疫反应，说："阿伦。

In addition, intrarenal pelvic infusion of DADLE increased ARNA, but failed to alter the magnitude of ARNA response produced by stimulating chemoreceptor with infusion of hypertonic saline solution (600mM NaCl). Taken together, our study suggests that opioids stimulate the renal sensory function, especially in rats with UUO, but do not participate in the response to the stimulation of mechano- and chemo- receptors.

综观以上结果，类鸦片与肾脏肾脏反射的感觉传递路径不同，其可能经由其他未被发现的路径来调控肾脏的感觉弁遄A尤其在肾脏病态时。

In order to optimize enzymolysis technology for production of antioxidant peptides from chickpea protein, effect of ratio of enzyme to substrate, enzymolysis temperature, and hydrolysis time on the technology in which reducibility and superoxide anion radical capturing rate were taken as response values was analyzed with response surface methodology.

为优化Alcalase蛋白酶酶解鹰嘴豆蛋白制备抗氧化肽的工艺条件，采用响应面分析法，以还原能力、超氧阴离子捕获率为响应值，研究了酶与底物的比值、酶解温度和酶解时间对制备抗氧化肽工艺的影响。

There are usually several vibration modes participating in heliostat's response to wind induction. The complete quadratic combination method can take the modes' coupling effect into account. The result is precise, however the computation work is heavy. Therefore, the proper orthogonal decomposing stochastic wind field was proposed to be applied in computation of heliostat's response to wind induction.

定日镜结构风振响应中有多个振型参与，利用完全二次型组合法可以考虑各振型间的耦合作用，得到精确结果，但计算量很大，因此提出将随机风场本征正交分解技术运用到定日镜结构响应计算中。

The expressed protein concentrates were about 0.5-5mg/L. 3. Classification and functional annotation of kinases have been studied: according to the kinases Classification in PlantsP (http://plantsp.genomics.purdue.edu/), 27 kinases belong to 7 groups in the class 1 of Transmembrane Receptor Kinase and Related non-Transmembrane Kinases on PlantsP, namely Receptor like cytoplasmic kinaseⅦof group 1.2, CRPK1 Like Kinase of group 1.3, Crinkly 4_Like kinase of group 1.4, Plant Extemal Response Like Kinase of group 1.6, CRPK1 Like Kinase (Types 1 and ) and S-Domain Kinase (Type 2) of group 1.9, Legume Lectin Domain Kinase of group 1.11, Wall associate kinase of group 1.5, respectively. 4. 21 kinases expressed in S.

对获得的蛋白激酶进行了分类和功能预测：按照PlantsP网站(http：//plantsp.genomics.purdue.edu/)的激酶分类系统，本实验表达的激酶分别属于第一类跨膜受体激酶和无跨膜区的激酶中的7个不同组，即第2组的Receptor LikeCytoplasmic KinaseⅦ家族、第3组的CRPK1L(Type 1)家族、第4组的Crinkly 4_Likekinase家族、第6组的Plant External Response Like Kinase家族、第9组的CRPK1 LikeKinase(Types 1 and 2)和S-Domain Kinase(Type 2)家族、第11组的Legume LectinDomain Kinase家族和第17组的Wall Associated Kinase kinase家族； 4。

In order to investigate the hot destruction of explosive products,the temperature response test of TNT explosive products,including explosive experiments in free field response and the half-airtight space,is carried out by WRe5/26 thermocouple according to Seebeck effect and heat transfer theory principle.

为研究炸药爆炸产物的热毁伤作用，根据塞贝克效应和传热学原理，利用WRe5/26热电偶对TNT爆炸产物进行了温度响应测试，包括自由场实验和半密闭空间实验，获得了相应的温度曲线，分析了影响热电偶响应的因素。

To evaluate the vascular response in relation to baseline, adjusting for systemic effects and skewed data, we expressed the hyperemic response as the natural logarithm of the ratio of postdeflation to baseline pulse amplitude in the hyperemic finger divided by the same ratio in the contralateral finger that served as control.

为了评价血管反应性与基线血管反应的关系，校正全身性作用及偏离的数据，我们计算袖套排气后充血手指脉搏幅度与基线脉搏幅度的比率以及对侧作对照手指的脉搏幅度与基线脉搏幅度的比率，两比率之比取自然对数表示充血反应。

A commutation error is then considered in addition to the conventional residual error to generate the innovative residual error. Such an error is applied into cost functions to derive finite impulse response and infinite impulse response filter-based adaptive algorithms for ANC applications, referred to as FxRLS/CE and FuRLS/FRE+CE algorithms, respectively. Convergence analyses based on Lyapunov stability criteria for time-varying discrete-time systems can be carried out for the FxLMS/CE, FxRLS/CE and FuRLS/ FRE+CE algorithms to ensure stability. Computer simulations and experiments demonstrate that the innovative residual error-based adaptive algorithms can free the restriction of the slow-adaptation assumption in the conventional ANC approaches.

本文中也定义一交换误差并且加入到传统残留误差行形成新残留误差来改善适应性演算法的收敛速度，使用新残留误差推导出了有限脉冲响应滤波器与无限脉冲响应滤波器之适应演算法的新适应性演算法分别为： FxLMS/CE、 FxRLS/CE 和 FuRLS/FRE+CE 演算法，并且以离散时间的 Lyapunov 稳定性准则来证明演算法的收敛性，电脑模拟与实验也显示新演算法免除以往滤波器的参数必须缓慢更新的条件。

By use of site mutation strategy and PCR technology, we obtained the gene P12X3C that includes full length P1, 2A, 3C and a part of 2B and 3B and the gene P12X3C3D that includes full length P1, 2A, 3C, 3D and a part of 2B and 3B. After being digested by restriction enzyme respectively, the gene P12X3C and the gene P12X3C3D were cloned into the pcDNA3. 1 and pTARGET expression vector that were digested by the same enzyme. Recombinant plasmids were checked by restriction enzyme analysis and nucleic acid sequencing. Further more, recombinant plasmids were transfected into BHK-21 cells by using lipoid. The proteins of foot-and-mouth disease virus , which were expressed in BHK-21 cells, were confirmed by sandwich-ELISA and fluoroscopy, and the capsid of FMDV was tested by electron microscope. In order to evaluate enhanced immune response of guinea pigs against FMDV, DNA vaccines which were designed to produce viral capsids lacking infectious viral nucleic acid and contained the gene P12X3C and the gene P12X3C3D were injected respectively with FMDV 3D protein which was expressed in Pichia Pastoris Secreted expression System and purified or with pcDNA3. 1/IFN which includes the gene IFN-α of cattle. Subsequently, Recombinant plasmids were injected to cattles with or without pcDNA3. 1/IFN. Anti-FMDV antibodies were detected by ELISA, and the T lymphocyte proliferation response was tested by MTT assay, neutralization antibodies titers were analyzed by micro-neutralization assay.

为研制带有O型口蹄疫病毒(Foot-and-Mouth Disease Virus，FMDV)China99株结构蛋白基因及多个非结构蛋白基因的DNA疫苗，本研究通过定点突变方法和PCR扩增方法，获得包含有FMDV China99株结构蛋白P1、非结构蛋白2A、3C以及部分2B、3B编码基因的片段P12X3C和包含有FMDV China99株结构蛋白P1、非结构蛋白2A、3C、3D以及部分2B、3B编码基因的片段P12X3C3D，将获得的基因片段直接/酶切后与同样处理的真核表达质粒连接，分别得到重组质粒pcDNA3.1/P12X3C和pcDNA3.1/P12X3C3D、pTARGET/P12X3C3D；对重组质粒进行序列测定、分析，并将重组质粒分别转染BHK-21细胞，通过双抗体夹心ELISA方法和间接免疫荧光标记方法检测细胞中FMDV抗原的表达，用电子显微镜观察病毒空衣壳的组装；为评价重组质粒作为DNA疫苗对实验动物及本动物的免疫效果，将重组质粒经肌肉注射方法接种豚鼠，并与酵母表达的纯化FMDV China99株3D蛋白及带有牛α干扰素的真核表达质粒pcDNA3.1/IFN分别/同时免疫，第二次免疫后第三周豚鼠攻以1OOID〓或1000ID〓的O型FMDV China99株；随后将质粒pcDNA3.1/P12X3C、pcDNA3.1/P12X3C3D与带有牛α干扰素的真核表达质粒pcDNA3.1/IFN同时免疫牛，三周后经牛舌皮攻以10〓ID〓的O型FMDV China99株。

By use of site mutation strategy and PCR technology, we obtained the gene P12X3C that includes full length PI, 2A, 3C and a part of 2B and 3B and the gene P12X3C3D that includes full length PI, 2A, 3C, 3D and a part of 2B and 3B. After being digested by restriction enzyme respectively, the gene P12X3C and the gene P12X3C3D were cloned into the pcDNA3.1 and pTARGET expression vector that were digested by the same enzyme. Recombinant plasmids were checked by restriction enzyme analysis and nucleic acid sequencing. Further more, recombinant plasmids were transfected into BHK-21 cells by using lipoid. The proteins of foot-and-mouth disease virus, which were expressed in BHK-21 cells, were confirmed by sandwich-ELlSA and fluoroscopy, and the capsid of FMDV was tested by electron microscope. In order to evaluate enhanced immune response of guinea pigs against FMDV, DNA vaccines which were designed to produce viral capsids lacking infectious viral nucleic acid and contained the gene P12X3C and the gene P 12X3C3D were injected respectively with FMDV 3D protein which was expressed in Pichia Pastoris Secreted expression System and purified or with pcDNA3.1/lFN which includes the gene IFN-a of cattle. Subsequently, Recombinant plasmids were injected to catties with or without pcDNA3.1/IFN. Anti-FMDV antibodies were detected by ELISA, and the T lymphocyte proliferation response was tested by MTT assay, neutralization antibodies liters were analyzed by micro-neutralization assay.

为研制带有O型口蹄疫病毒(Foot-and-Mouth Disease Virus，FMDV)China99株结构蛋白基因及多个非结构蛋白基因的DNA疫曲，本研究通过定点突变方法和PCR扩增方法，获得包含有FMDV China99株结构蛋白P1、非结构蛋白2A、3C以及部分2B、3B编码基因的片段P12X3C和包含有FMDV China99株结构蛋白P1、非结构蛋白2A、3C、3D以及部分2B、3B编码基因的片段P12X3C3D，将获得的基因片段直接／酶切后与同样处理的真核表达质粒连接，分别得到重组质粒pcDNA3.1／P12X3C和pcDNA3.1／P12X3C3D、pTARGET／P12X3C3D；对重组质粒进行序列测定、分析，并将重组质粒分别转染BHK-21细胞，通过双抗体夹心ELISA方法和间接免疫荧光标记方法检测细胞中FMDV抗原的表达，用电子显微镜观察病毒空衣壳的组装；为评价重组质粒作为DNA疫苗对实验动物及本动物的免疫效果，将重组质粒经肌肉注射方法接种豚鼠，并与酵母表达的纯化FMDV China99株3D蛋白及带有牛α干扰素的真核表达质粒pcDNA3.1／IFN分别／同时免疫，第二次免疫后第三周豚鼠攻以100ID_(50)或1000ID_(50)的O型FMDV China99株：随后将质粒pcDNA3.1／P12X3C、pcDNA3.1／P12X3C3D与带有牛α干扰素的真核表达质粒pcDNA3.1／IFN同时免疫牛，三周后经牛舌皮攻以10~4ID_(50)的O型FMDV China99株。

In the United States, chronic alcoholism and hepatitis C are the most common ones.

在美国，慢性酒精中毒，肝炎是最常见的。

If you have any questions, you can contact me anytime.

如果有任何问题，你可以随时联系我。