后成

Industrial residue is combined with coke dust to produce granular materials that is transferred to liquation furnace for high - temperature processing after automatic computation and proportioning , and the melt is processed to be fiber by fiber machine , then after containing dust , floatation deslagging, shot separation and modification processing , whitening and dehydration , which the fiber is pressed to inorganic fiber for paper making in vacuum condition and the product is weighed,packaged and put in storage automatically .

工业废渣配焦炭粉造粒料，经自动计量配比后送熔化炉高温处理，熔化液经成纤机加工成纤维，再经集尘，气浮除渣，渣球分离及改性处理后，漂白脱水，真空压榨成造纸用无机纤维产品，自动称量包装入库。

Hero bonus -- seven dragon jamie had the most important one is the hero of the system, which led to the various attributes to force, in July 2008, the hero of the updated bonuses formula for every point: change attributes (ability and equipment which combined) increased leadership forces (including upgrades and VIP effect) 3%, no soldier endurance series.

英雄加成—七龙纪中最重要的系统之一，就是英雄各种属性对所带领的部队有加成作用，在2008年7月的更新后，英雄的属性加成公式更改为：每点属性增加所领导部队（含升级后和VIP的效果）的3%，无士兵级数限制。

And the production comprises that dissolving polyarylamide into organic solvent; mixing and adding alumina particles, disperser, holing agent to be vibrated via ultrasonic wave; putting into drying box to be aged and defoamed; irrigating into film; vaporizing it in drying box; putting into solidify liquid to be emerged; washing with distilled water, processing aminic acid solution, compressing and shaping.

分散剂0.6～8wt。％、成孔剂2～8wt。％组成，制备方法为：将芳香聚酰胺溶于有机溶剂中，在搅拌中加入氧化铝颗粒、分散剂、成孔剂超生震荡；放入干燥箱中熟化、脱泡；浇铸成膜；浇铸后的膜在干燥箱中蒸发，然后放入凝固液中浸泡，接着用蒸馏水漂洗干净后用甲酸溶液处理；最后预压成型。

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。

Methods There were 100 cases in normal group and 36 cases in group of chest injuries. All cases were performed in volume scan according to conventional chest scan by SIEMENS Sensation 4 MSCT , then performed in thin slice low and high contrast image reconstructions. After that, all the source images were input into CT 3D work stations,costicartilage were imaged by post process software such as multiplanar reconstructions, maximum intensity projection, surface shade display and volume rendering technique. All the pictures were observed and analyzed by two radiologists.

利用西门子Sensation 4 多层螺旋CT机按照胸部常规扫描条件对胸部外伤组36例和对照组100例患者进行容积扫描，然后进行薄层低对比及高对比图像重建，并将重建图像导入CT三维（3D）工作站，利用多平面重建成像、最大密度投影、表面遮盖法成像及容积成像技术对图像进行后处理，由2名CT诊断医生一起对各种后处理图像进行观察和分析。

They are most abundant in quartz of pegmatitic leucosomes and granitic rocks, and represent the fluid appearing in their cooling stage. The DL(H2O) of such fluid is 0.93～0.96g/cm3 corresponding to P≈0.6GPa which is compatible with condition when the rapid decompression in this region was ended. 3 CO2-H2O two or three phases inclusions. They are the most widespread, and more frequently in clusters and in intragranular tails in quartz. The relative content of CO2+CH4 and H2O is considerably variable. They are also characterized with lower density (0.6～0.8g/cm3) and low pressure about 0.3～0.4GPa, and may be originated by mixture of carbonic liquid from breaking of most inclusions of peak stage and aqueous liquid of magmatic source. After entrapment, the further decrease of temperature to lower than 330℃ made such fluid separated to two or three phases.

主要集中于伟晶质脉体和花岗岩中，是这期岩浆冷凝过程析出的流体相当时就被封闭所成，密度为0.93～0.96g/cm3，相应压力约0.6GPa，这与峰期后迅速减压过程结束时的条件相符。3CO2-H2O两相和多相包体，分布最广，成簇状和拖尾状包体群，碳质和H2O相对含量很不均匀，整体密度相对最低，一般为0.6～0.8g/cm3，相应压力为0.3～0.4GPa，它们可能是大幅度减压过程中第一类包体大量爆裂析出的碳质流体与第二类H2O溶液流体在各处以不同比例混溶所成，它们被封闭后在降温至330℃以下时分裂成两相或三相包体。

Methods:(1) The two-sided ovary of female animal and the two-sided testicle of male animal were excised. After the XLGBC to treat 28 days, the estradiol and the teststerone of serum were checked;(2) With intramuscular injection the Hydrocortisone,the Yangxu animals was made. After the XLGBC to treat 10 days, the testicle coefficient,the spermathecal gland coefficient and the ovary coefficient were observed;(3) With ig the Thyroid tablets and the Reserpine, the Yinxu animal was made. After the XLGBC to treat 10 days, the testicle coefficient,the spermathecal gland coefficient and the ovary coefficient were observed.

（1）雌性动物摘除双侧卵巢，雄性动物摘除双侧睾丸，复制成去势动物模型后予仙灵骨葆胶囊治疗28天，检测血清雌二醇和血清睾酮；（2）肌注氢化可的松，复制成阳虚动物模型后予仙灵骨葆胶囊治疗10天，观测并计算动物的睾丸系数、精囊腺系数和卵巢系数；（3）灌胃甲状腺片和利血平，复制成阴虚动物模型后予仙灵骨葆胶囊治疗10天，观测并计算动物的睾丸系数、精囊腺系数和卵巢系数。

Study of peripheral nerve lesions and the effects of the recipe of supplementing Qi and activating blood circulation on it in streptozotocin-induced diabetic rats: It was showed that the weight, MNCV and SNCV were significantly reduced, H reflex were significantly prolongated, the level of blood sugar were significantly increased in diabetic rats compared to normal rats at 1 week, 3 week and 5 week after STZ injection (p.05), some changes of the sciatic nerve structure were occurred after 5 weeks of the diabetic progress.

STZ大鼠周围神经功能变化及益气活血方对其影响的实验研究：STZ诱发的糖尿病大鼠，成模1W后体重减轻、血糖升高、SNCV、MNCV减慢、SNCVamp减小、SNCVlat及H反射延迟，以上各项指标与对照组相比差异显著（P均。05）：成模5W后上述改变更为明显。成模5W后大鼠坐骨神经纤维出现髓鞘变性、融合、部分神经纤维变性等形态改变。

In early days, there were two kinds of Old-fashioned Clear Ice. One is to sprinkle the syrup onto the shaved ice; the other kind is to shave the frozen ice brick, which is a mixture of boiling water, white sugar and banana oil, into snow-like tiny pieces.

老式清冰有两种，一种是将冰砖刨成雪花状后再淋上糖水；另一种则是将开水煮沸后加入白砂糖及香蕉油，搅拌后冷冻成冰砖状，再刨成雪花状的冰品，尝起来有股清新的果香与微甜口感。

B.c. and was later a Roman province. An independent state after a.d.1204, Epirus was conquered by the Turks in the15th ''.

世纪'。''''。'达到'。''全盛，后成罗马帝国一省，公元1204年成为一自由城邦，15''。

Do you know, i need you to come back

你知道吗，我需要你回来

Yang yinshu、Wang xiangsheng、Li decang,The first discovery of haemaphysalis conicinna.

1〕 杨银书，王祥生，李德昌。安徽省首次发现嗜群血蜱。