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Result: Bidaweishu capsule has the obvious therapeutic action of treatment chronic superficial gastritis, at the same time.it can double regulate the disfunction of gastroenteric motive function, and it has the obvious function of antiinflammatory and analgetic.

结果：必达胃舒胶囊对慢性浅表性胃炎具有明显的治疗作用，对胃肠运动功能紊乱具有双向调节作用，具有明显的止痛抗炎作用。

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。

Background:The recent studies showed specific physiology protection mechanism of premanopausal women. The endogenous estrogen of physiology level in their bodies was helpful to regulate lipid metabolism , provent and delay artherosclerosis , protect blood vessel endothelium , inhibit vascular smooth muscle hyperplasing , dilat blood vessel , degrade angiotasis , improve blood rheology , improve insulin resistance , raise survival rate and quality of life of premanopausal women patients with coronary heart disease .

背景：目前研究显示由于绝经前女性特有的生理保护机制，其体内生理水平的内源性雌激素有助于调整脂质代谢，防止和延缓动脉粥样硬化，保护血管内皮，抑制血管平滑肌增殖，扩张血管，降低血管张力，改善血液流变学，改善胰岛素抵抗，提高绝经前女性冠心病患者生存率和生活质量。

Extracts of anthyllis, witch hazel and calendula combine with nurturing oils to stimulate natural oil production and regulate moisture balance.

黄苜蓿、金缕梅和金盏花提取物结合营养油激发自然油脂生成，调节滋润度的平衡。

In order to increase solar energy utilization ratio in mulberry gardens, mulberrytrees of different varieties were planted alternately to regulate the growth relationshipbetween individual trees and tree population,between arboreous and bush mulberries .

为提高桑园空间与光能利用率，在桑园采用不同的桑树品种搭配、进行高低立体交叉栽植，合理调整桑树单株与群体、乔木桑与灌木桑之间的生长关系

Small artery and arteriole are the main position of organism to regulate the organ blood flow and the redistribution of blood among apparatus.

小动脉和微动脉是机体调节器官血流量和器官之间血液重新分配的主要部位，其血管的口径受神经体液因素的调节。

Abstract〕 objective autogenetic and allogenous erythrocytes regulate the immunological reactions activated by antigens by means of natural isolated experimental system, to observe the changes of cytokines.

目的：运用系统血液免疫反应分离实验体系，探讨在抗原激活的情况下异体血细胞对反应体系中细胞因子含量水平影响的变化规律。

Abstract〕 Objective Autogenetic and allogenous erythrocytes regulate the immunological reactions activated by antigens by means of natural isolated experimental system, to observe the changes of cytokines.

红细胞在天然免疫防御网络中发挥着重要作用，红细胞在补体系统天然免疫反应的参与下有黏附和调理抗原、清除循环免疫复合物、调控淋巴细胞表达免疫分子和细胞因子等作用。

A piece of cartilage chip was cut from an adult rabbit patella in lateral border, and autogenic chondrocytes were isolated、culture、subcultured in medium complemented with bFGF and TGF-βin order to regulate their differentiation and proliferation.

在成年兔自体膝关节髌骨外侧缘取部分软骨，分离、传代培养软骨细胞，同时应用bFGF和TGF-β控制其分化和增殖。

In the process of root cutting, the root accumulated a lot of soluble sugar and soluble protein, which provided material and energy for the cell differentiation. As root differentiating, soluable protein was continuously used up. During 10 to 20 days, the content of soluble sugar and soluble protein in the basipetal top and end of rootkept comparatively stable, then declined as adventitious buds and roots growing. 40 days later, they kept invariable, because the newly formed bud can photosynthesize and the newly formed root can absorb nutrient from outside. The dynamic balances of endogenous hormone regulate adventitious buds and roots of the root. During callus growing and adventitious bud differentiating.

上部根段在细胞分化前期积累了大量的可溶性糖，为后期的分化提供能源物质，同时积累了大量的可溶性蛋白质，为愈伤组织的产生提供能源，而后随着分化，可溶性蛋白质不断被消耗。10～20d根段上部及下部的可溶性糖、可溶性蛋白质含量保持在相对稳定的水平变化不大，后期随着不定芽及不定根的生长下降较快。40d后，新形成的芽已经能够进行光合作用，新形成的根也可从外界吸收营养物质，可溶性糖、可溶性蛋白质含量基本保持不变。

Don not attempt to do something which you can not to do.

不要企图做那些办不到的事情。

The expression of CTGF and TNF-αweredetected by immunochemistry and the number of Clara Cells was calculated.

光镜下观察肺组织的病理变化，采用免疫组化染色观察肺组织中结缔组织生长因子和肿瘤坏死因子-α的表达和Clara细胞的数量。