查询词典 group by group

Methods patients in 4 different groups including pulmonary acariasis group (n=35), scabies group (n=35), demodex group (n=38) and control group (n=30) were detected by the two methods, and the results were compared each other.

应用SPA -ELISA和Map-IFAT分别对肺螨病组(35例)、疮疮组(35例)、蠕形螨组(38例)、对照组(30例)进行血清抗体检测并对比分析。

During the following eight sessions in four weeks the subjects were randomly devided into four groups:(1) physical practice group, repeated physical practice twenty times per session,(2) alternating mental-physical practice group, alternating the techinques of physical and mental practice per session,(3) mental practice group, watching the film and listening to the instruction of badminton backhand lowservice,which was followed by five minutes in which the subjects were directed to practice the serve skills mentally for twenty repetitions per session, and (4) control group, no practice.

所有受试者接受羽球反手发短球之教学及练习后，隨机分派到下列四种不同练习组：22身体练习组：每天次练习羽球反手发短球二十次；4综合练习组：身体练习、心智练习间隔交替练习；3。心智练习组：提供羽球反手发短球击球动作录影带及指导语，受试者在五分钟內意像整个动作过程，共计二十次；6控制组：不练习。

Methods The target DNA sequence of yrdC was obtained from human spleen tissue by using RT-PCR,construct high titer recombinant adenovirus Ad-yrdC by using AdEasy adenovirus carrier system,detect yrdC protein expression by using Western blot and immunohistochemical method,set up control group and transfected Ad-Null group,and study the effects Ad-yrdC on BGC-823 cell line by drawing cell growth curve and MTT chromatometry.

方法用RT-PCR方法获取人脾脏组织yrdC基因序列，采用AdEasy腺病毒载体系统构建携带yrdC基因的高滴度重组腺病毒Ad-yrdC，将其转染胃癌BGC-823细胞，应用Western blot和免疫组织化学法检测yrdC蛋白表达，设对照组和转染Ad-Null组，并分别绘制细胞生长曲线和MTT比色法研究Ad-yrdC对BGC-823细胞的影响。

According to experimental results and etiopathogenisis and pathology of osteoporosis , and analyzing review investigation on hepcidin、associations of bone metabolism and iron metabolism and relations of ferri ion and calcium ion,we can make conclusions as follows: 1、We applied single manmade intervention approach to induce osteoporosis model in this study, there was no other influential factor. In the termination of test , rats bone density and bone histological anatomy indicated that osteoporosis model was creditable,meanwhile hepatic functional enzyme and hepatic microtome section demonstrated that hepatic function had noci-influence induced by medicinal herbs resource. Accordingly, we could believe that hepatic hepcidin gene expression and serum hepcidin contents can represent internal iron metabolism changes at selected test time. 2、In this investigation, different findings between test group and control group indicated that:according to changes of hepcidin gene expression measured by RT-PCR and changes of serum hepcidin contents determined by ELISA kit , there were correlations between hepcidin and rat osteoporosis model induced by retinoic acid. 3、Under the condition of this investigation,there was a interactive hypothesis as follows: Hepcidin iron metabolism←→ferriion←→calcium ion←→osteoporosis.

根据本次实验结果，对骨质疏松的病因病理的认识及铁代谢与铁调素、骨代谢与铁代谢关系、铁离子与钙离子的关系系列研究的回顾，经分析得出如下结论：1、本研究骨质疏松模型采用单一人工干预方法，没有其他影响因素；实验结束时大鼠骨密度、骨组织学检查表明骨质疏松形成，同时肝脏功能酶和HE切片显示肝脏功能未受药源性产生明显损伤性影响；因此，同期不同时间组大鼠肝脏铁调素基因表达、血清铁调素含量可以代表体内铁代谢不同时间的变化。2、在本研究中，模型组与对照组研究结果的差异表明：铁调素基因RT-PCR变化、血清铁调素ELISA测定含量变化与维甲酸制作的大鼠骨质疏松模型形成有实验相关性。3、在本研究平台下，形成了一个互相影响的假设图：铁调素←→铁代谢←→铁离子←→钙离子骨质疏松。

MethodsSolidtumorbearing mice were produced with Lewis lung cell and randomly divided into radiation group (n=18) and control group (n=17). The mice in the radiation group were irradiated by 30 Gy Xray. The expressions of Ecadherin and MMP9 were detected by immunohistochemical.ResultsAfter two weeks of therapy.

建立Lewis肺癌模型，将荷Lewis肺癌的C57BL/6 雄性小鼠35只随机分为照射组（n=18）和对照组（n=17），照射组接受30 Gy的X线肿瘤局部照射，对照组不接受照射，2周后采用免疫组化法检测瘤组织中E钙黏素蛋白和基质金属蛋白酶9(MMP9)蛋白的表达。

Methods: One thousand and one hundred patients with bladder tumors adjacent to the ureteral orifice who experienced obturator nerve blockade guided by PNS were randomly divided into group A guided by peripheral nerve stimulator and group B with anatomic positioning with 550 cases in each group.

膀胱肿瘤位于输尿管开口周围(0.5~2cm)患者1100例，随机分为A组（神经刺激仪引导定位下闭孔神经阻滞）和B组（传统解剖标志定位下闭孔神经阻滞）各550例。

Methods 76 patients (152 eyes) were divided into 2 groups (76 eyes in each group). The experimental group was treated by pearl clearsighted eye drops, and the control group was treated by 0.25% chloramphenicol. The period of treatment was 4 weeks.

将慢性结膜炎患者76例152眼随机分为2组，每组76眼，治疗组用珍珠明目滴眼液治疗，对照组用0.25%氯霉素滴眼液治疗，4周为一疗程。

All rats were administered by free drinking, the normal control group were treated by drinking water in 3 months, 45 d group was performed drinking water in 1.5 months and then revival liquid of quantum in 1.5 months, and the 90 d group was administrated the revival liquid of quantum in 3 months.

方法］ 取雌性Wistar大鼠36只，按体重随机分为对照组、量子复活液45 d组和90 d组；以自由饮用方式给药，给予对照组大鼠普通自来水喂养90 d，给予量子复活液45 d组大鼠普通自来水45 d后，再给予量子复活液喂养45 d，给予量子复活液90 d组大鼠量子复活液90 d。

METHODS: Human AMSCs were isolated in vitro sterilely. At the third passage, 0.5 mL single cell suspension at 1×109/L was obtained and transplanted by tail venous pathway in transplantation group mice, Mice in the control group were injected with an equal volume of saline. APP-gene mice in the normal group were left intact. 5'-bromo-2-deoxyuridine labeled third-generation AMSCs expression was detected in mice brain tissue by immunohistochemical method.

无菌条件下体外分离培养人羊膜间充质干细胞，传至第3代将细胞浓度调整为1×109 L-1，经尾静脉注入0.5 mL至细胞移植组转APP+基因小鼠体内；对照组经尾静脉注入同体积的生理盐水；正常组转APP-基因小鼠不给予任何干预措施。

Low dose Yiweitang group; 4. Diethylstilbestrol group; 5. Model control group. After 4 weeks intervention, get the left ovarie, a part of hypothalami and pituitary gland from head-off rat, and observe expression of ER, FSHR and GnRH by immune histochemistry method . Then extract RNA from the rihgt ovarie and the rest hypothalami and pituitary gland, so as to measure the expression of GnRHmRNA 、 ERmRNA 、 FSHRmRNA and P 16mRNA by RT-PCR. And the cerebrum were made to homogenate to examine SOD, GSH-PX and MDA.

各组实验动物灌药4周后，断头处死，取部分下丘脑、垂体及左侧卵巢组织固定切片，免疫组化法检测 ER 和 FSHR 表达、 GnRH ；取剩余部分下丘脑、垂体及右侧卵巢组织提取总 RNA ，用于 RT-PCR 检测下丘脑 GnRHmRNA ，下丘脑、垂体的 P 16mRNA 及下丘脑、垂体、卵巢的 ERmRNA 、 FSHRmRNA 基因表达；另外取部分大脑组织制作脑组织匀浆，用于 SOD 和 GSH-PX 酶活力以及 MDA 含量的测定。

The split between the two groups can hardly be papered over.

这两个团体间的分歧难以掩饰。

This approach not only encourages a greater number of responses, but minimizes the likelihood of stale groupthink.

这种做法不仅鼓励了更多的反应，而且减少跟风的可能性。