小体内的

With Fluorescence humic acid and arsenic injection, 4 out of 7 animals developed symptoms; with Fluorescence humic acid injection alone, 2 out of 7 animals developed symptoms, but all symptoms disappeared in 4-12 days even injections were continued. It seems, animals have the ability to recovery by themself.

在注射萤光腐植酸加砷的一组，七只小白鼠中有四只产生症状，在只注射萤光腐植酸的一组，七只小白鼠中有两只产生症状，但是虽未停止投药，症状却在4-12天内完全消失，似乎小白鼠体内自有修复伤害的能力。

In this study, the classification of Chinese Babesia spp. infective to cattle were carried out by the classical methods and molecular biotechnology, and investigated the vector ticks of an unidentified Babesia sp. isolated from Xinjiang province by the experimental transmission, and observed the developmental forms of Babesia sp. in the engorged Hyalomma anatolicum anatolicum females;We developed the indirect hemoagglutination test for Babesia bigemina, and evaluated its effect in the sero-survey;We made slow-released injection of imidocarb, and estimated its efficacy on the treatment and prevention of Babesia bigemina infection by the laboratory work and the field tests. The major results were presented as following:1. Discovery of a bovine Babesia sp.

本研究以牛的巴贝斯虫为研究对象，采用传统技术与分子生物学技术相结合的方法对在我国已分离的牛巴贝斯虫病主要病原进行了分类学研究，在实验室内运用蜱传播试验对分离于我国新疆的牛的巴贝斯虫未定种的媒介蜱及其传播方式进行了详细的研究，采用组织抹片方法对牛的巴贝斯虫未定种在小亚璃眼蜱饱血雌虫体内的发育过程进行了观察；建立了间接血球凝集试验诊断方法，并对其在血清学调查中的应用效果进行了考察；研制了咪唑苯脲缓释注射剂，并通过实验室工作和田间试验对防治效果进行了评价。

A GFP-labeled Hela cell line and a mouse tumor model based on the cell line were established, and the animal model provides useful experimental materials for cervical cancer study. The in vivo fluorescence imaging system could be used to quantitatively evaluate the living tumor cell growth in vivo but not the size or volume of the tumor detected by slide caliper.

绿色荧光蛋白能够在人宫颈癌细胞Hela中长期稳定表达，用绿色荧光蛋白标记的人宫颈癌细胞Hela建立的裸鼠肿瘤模型可以为人宫颈癌研究提供理想的实验材料，应用小动物活体成像系统能够客观定量评价活的肿瘤细胞在动物体内的生长情况，而不是肿瘤体积的变化。

The stable clones are further identified by RT-PCR and Western blot; 6 MTT assay is used to investigate the effect of ZNRD1 on the cell growth of cells (AGS, SGC7901, MKN28, NIH3T3, GES-1); 7 Soft agar assay is used to investigate the effect of ZNRD1 on the clonality of cells (AGS, MKN28); 8 Nude mice assay is used to investigate the effect of ZNRD1 on the cell growth of gastric cancer cells (AGS, MKN28); 9 Flow cytometry is used to investigate the effect of ZNRD1 on the cell cycle distribution of cells (AGS, MKN28, NIH3T3, GES-1); 10 Flow cytometry is used to investigate the effect of ZNRD1 on the cell apoptosis of cells (AGS, MKN28, NIH3T3); 11 MTT assay is used to investigate the effect of ZNRD1 on the drug sensitivity of cancer cells (SGC7901, SGC7901/VCR, HL-60, HL-60/VCR) in vitro; 12 SRCA is used to investigate the effect of ZNRD1 on the drug sensitivity of gastric cancer cells (SGC7901, SGC7901/VCR) in vivo; 13 Flow cytometry is used to investigate the effect of ZNRD1 on adriamycin accumulation of cancer cells (SGC7901, SGC7901/VCR, HL-60, HL-60/VCR); 14 Transmission electron microscope is used to investigate the effect of ZNRD1 on the sensitivity of SGC7901 cells towards drug-induced apoptosis; 15 Flow cytometry and DNA ladder assay are used to investigate the effect of ZNRD1 on the sensitivity of cells (SGC7901, SGC7901/VCR, HL-60/VCR) towards drug-induced apoptosis; 16 Microarray is used to investigate the profiling of ZNRD1-responsive genes in gastric cancer cells (AGS, MKN28, SGC7901, SGC7901/VCR); 17 RT-PCR and Western blot are used to identify the results of microarray; 18 Reporter gene assay is used to investigate the effect of ZNRD1 on the transcriptional activity of cyclin D1; 19 Reporter gene assay is used to investigate the effect of ZNRD1 on the transcriptional activity of MDR1; 20 Kinase assay is used to investigate the effect of ZNRD1 on the activity of cyclin E-CDK2 kinase; 21 The antisensenucleic acids of p21 is used to inhibit the expression of p21, and flow cytometry is used to investigate the effect of p21 on ZNRD1-induced cell cycle arrest in gastric cancer cells; 22 The antisensenucleic acids of p27 is used to inhibit the expression of p27, and flow cytometry is used to investigate the effect of p27 on ZNRD1-induced cell cycle arrest in gastric cancer cells; 23 Liposome is used to up-regulate the expression of Skp2, and flow cytometry is used to investigate the effect of Skp2 on ZNRD1-induced cell cycle arrest in gastric cancer cells; 24 Western blot is used to investigate the effect of ZNRD1 on the stability of Skp2 and p27 in gastric cancer cells; 25 MVD assay is used to investigate the effect of ZNRD1 on the angiopoietic activity of gastric cancer cells; 26 ELISA is used to investigate the effect of ZNRD1 on the expression of VEGF165 in gastric cancer cells; 27 The roles of DARPP-32 in MDR of gastric cancer cells are investigated using gene transfection, MTT assay, SRCA, flow cytometry and DNA ladder assay.

应用杂交瘤技术制备ZNRD1的首个单克隆抗体；2）利用RT-PCR、Western blot和免疫组化检测ZNRD1在胃癌组织、胃炎组织、正常胃上皮组织、胃癌细胞和正常胃组织上皮细胞中的表达；3）构建ZNRD1的小干扰RNA载体，并测序鉴定；4）利用脂质体将ZNRD1的真核表达载体及其空载体转染胃癌细胞（AGS、SGC7901、MKN28）和小鼠成纤维细胞（NIH3T3），G418筛选后进行鉴定；5）利用脂质体将ZNRD1的小干扰RNA载体及其空载体转染药敏胃癌细胞（SGC7901）、正常胃组织上皮细胞（GES-1）、对长春新碱耐药的胃癌细胞（SGC7901/VCR）、药敏白血病细胞（HL-60）、对长春新碱耐药的白血病细胞（HL-60/VCR），G418筛选后进行鉴定；6）利用MTT实验检测ZNRD1高/低表达对细胞（AGS、SGC7901、MKN28、NIH3T3、GES-1）生长的影响；7）通过软琼脂克隆形成实验检测上调ZNRD1对AGS、MKN28细胞克隆形成能力的影响；8）通过裸鼠成瘤实验检测上调ZNRD1对AGS、MKN28细胞体内成瘤性的影响；9）通过流式细胞仪分析ZNRD1高/低表达对细胞（AGS、MKN28、NIH3T3、GES-1）的细胞周期的影响；10）通过流式细胞仪分析上调ZNRD1对细胞（AGS、MKN28、NIH3T3）的凋亡的影响；11）通过MTT实验检测ZNRD1高/低表达对细胞（SGC7901、SGC7901/VCR、HL-60、HL-60/VCR）体外药物敏感性的影响；12）通过肾包膜下移植法检测ZNRD1高/低表达对细胞（SGC7901、SGC7901/VCR）体内药物敏感性的影响；13）通过流式细胞仪分析ZNRD1高/低表达对细胞（SGC7901、SGC7901/VCR、HL-60、HL-60/VCR）内阿霉素蓄积和泵出的影响；14）通过透射电镜检测上调ZNRD1对SGC7901细胞凋亡敏感性的影响；15）通过流式细胞仪和DNA梯度试验检测ZNRD1高/低表达对细胞（SGC7901、SGC7901/VCR、HL-60）凋亡敏感性的影响；16）通过基因芯片检测ZNRD1高/低表达对胃癌细胞内基因表达谱的影响；17）利用RT-PCR、Western blot对基因芯片的结果进行鉴定；18）利用报告基因实验检测ZNRD1对cyclin D1的启动子活性的调节作用；19）利用报告基因实验检测ZNRD1高/低表达对MDR1的启动子活性的调节作用；20）利用激酶试验检测ZNRD1对cyclin E-CDK2 激酶活力的影响；21）利用反义核酸技术抑制p21的表达；通过流式细胞仪检测抑制p21对ZNRD1介导的细胞周期阻滞的影响；22）利用反义核酸技术抑制p27的表达；通过流式细胞仪检测抑制p27对ZNRD1介导的细胞周期阻滞的影响；23）利用脂质体转染法上调Skp2的表达；通过流式细胞仪检测上调Skp2对ZNRD1介导的细胞周期阻滞的影响；24）利用Western blot检测ZNRD1对p27和Skp2的蛋白稳定性的影响；25）利用微血管密度实验检测ZNRD1对AGS、MKN28细胞裸鼠移植瘤微血管形成的影响；26）利用ELISA检测ZNRD1对AGS、MKN28细胞培养上清和移植瘤匀浆中VEGF165含量的影响；27）利用脂质体转染法、MTT实验、肾包膜下移植法、流式细胞仪和DNA梯度试验检测新耐药相关分子DARPP-32对细胞（SGC7901、SGC7901/VCR、对阿霉素耐药的胃癌细胞SGC7901/ADR）多药耐药表型的影响；利用脂质体转染法和MTT实验检测下调ZNRD1对DARPP-32介导的胃癌多药耐药的调控作用。

Objective:To explore the changes of plasma Lysophatisic acid level in patients with transient ischemic attacks or cerebric infrction.

溶血磷脂酸是磷脂中的一种小分子物质，是磷脂生物合成早期阶段的关键性前体，在体内的信号传递中起着十分重要的作用，因此被称为多功能&磷脂信使&［1］。

Objective:To explore the changes of plasma Lysophatisic acid level in patients with transient ischemic attacks or cerebric infrction. And to value the effect of those in the formation and progress of those diseases.

溶血磷脂酸是磷脂中的一种小分子物质，是磷脂生物合成早期阶段的关键性前体，在体内的信号传递中起着十分重要的作用，因此被称为多功能&磷脂信使&［1］。

From theoretic tell, wave motion of the capacity inside the body in PD process is small, be opposite as a result of its again leftover kidney function has better protective effect, consequently, compare at blood dialytic , PD can maintain the stability of status of the size inside body better.

从理论上讲，PD过程中体内容量波动小，又由于其对残余肾功能有较好的保护功能，因而，相比于血液透析，PD能够更好地维持体内容量状态的稳定。

Degradation test in vitro was carried out in phosphate buffer solution (0.1M, pH7. 4) at 37 ℃. The buffer solution was changed daily. Degradation test in vivo was implanted the sample to subdermal in adult ICH rat in the scapular area lateral to the dorsal midline. At suitable time the samples were recovered. Molecular weight changes in surface layer and bulk of polymer sample were measured by GPC and weight loss was determined gravimetrically. It was found that the degradation behavior can be regulated by changing the composition of copolymers. The critical compositions from surface to bulk degradation behavior for PGCA, PLCA, PLMCA, PLDCA systems were 15-20, 20-30, 30- 40, 40 of mol percent GA or LA unit in copolymers, respectively. The degradation behavior of PGCA, PLCA, PLMCA, PLDCA systems were compared and analysed. Some factors influencing the degradation character, such as copolymer composition, hydrophobicity, crystallinity and enzyme affect etc. played important role.

体外实验中材料降解环境为37℃，0.1M，pH7.4磷酸缓冲溶液，每天换液，定期取样；体内实验中将聚合物试样埋置于ICH小白鼠背部肩胛骨皮下部位，定期处死小鼠，取样，将体内体外样品进行重量损失及试样内外层分子量变化测定，分析各聚合物试样降解行为特性，实验结果证明，改变共聚物组成，可以调节各聚合体系降解行为特性，对PGCA，PLCA，PLMCA，PLDCA共聚体系，交酯摩尔百分含量15-20％，20-30％，30-40％，40％分别为各体系内降解行为特性由表面降解型向本体降解型过渡的临界转折点，交酯含量较低的聚合物不同程度地表现表面降解行为特性，论文对各共聚体系体内外降解行为作了分析对照，例如共聚物组成对材料降解速度与降解行为的影响；生物体内酶对降解行为的影响；材料亲疏水性，聚合物链段结晶行为及碳酸酯结构对材料降解行为的影响等，得出交酯/环碳酸酯共聚体系降解行为一些共性和规律。

In addition, it must also evade immune clearance. Elimination of H. pylori by phagocytes is inefficient because H. pylori exhibits several virulence factors to evade opsonization, retard phagocytosis, and disrupt membrane trafficking and phagosome maturation after internalization of the microorganism.

为了增加存活与持续的依附在宿主体内，幽门螺旋杆菌发展出一些策略来抵御被免疫清除的命运，它可影响吞噬细胞的功能，包括避免受调理作用、抑制吞噬细胞的吞噬作用、影响细胞内的运输作用与吞噬小体的成熟。

The finite element model included two types of main element: beam element for concrete and truss element for internal unbonded or external tendon. The end nodes of main elements were connected with internal constraints named MPC in ABAQUS. Spring elements with very large stiffness were set up at the place of the deviators of externally prestressed beams, or along the span with relatively little space of unbonded internally prestressed beams. The modified Riks method is utilized to trace the entire structural response of beams prestressed with unbonded tendon from zero to ultimate loads. The reliability of the analysis model is verified by analytical results of typical test beams in comparison with experimental ones.

该有限元模型由两类主单元组成，即混凝土梁单元和体内无粘结或体外预应力筋桁架单元；主单元的端部节点用ABAQUS的内在约束MPC连接；在体外预应力梁的转向块处，或沿体内无粘结预应力梁全跨并以比较小的间隔设置刚度足够大的弹簧单元。

The concept of equivalent rotationally rigidity is offered and the formula of rotationally rigidity is obtained.

主要做了如下几个方面的工作：对伸臂位于顶部的单层框架—筒体模型进行分析，提出了等效转动约束的概念和转动约束刚度的表达式。

Male cats normally do not need aftercare with the exception of the night after the anesthetic.

男猫通常不需要善后除了晚上的麻醉。