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group by group相关的网络例句

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与 group by group 相关的网络例句 [注:此内容来源于网络,仅供参考]

RESULTS: A total of 36 rabbit models, 6 in the 1-month therapy group and 8 in the 3-month therapy group were died from infection. In the 1-month therapy group, thick ureteric wall and smooth ureteric lumina developed without any contracture. Under the optical microscope, transitional epithelial cells covered throughout the inner walls and smooth muscle cells appeared sparsely in a mussy configuration. In addition, CKAE1/AE3 staining was positive butα-actin staining was very weak when checked by immunohistochemistry. In the 3-month therapy group, amnion-ureters were enclosed by their peripheral tissue and showed rich blood vessels and normal ureteric lumina without significant contracture, futher more, there had formed a well-arranged transitional epithelial layer and smooth muscular layer, the immunohistochemistry result showed that the expression of CKAE1/AE3 and α-actin were positive.

结果:36只大白兔中,1个月治疗组死亡6只,3个月治疗组死亡8只,死亡原因均为感染。1个月治疗组大白兔羊膜输尿管柔软,长4 cm,管壁变厚,无挛缩,移行上皮组织爬满内壁,平滑肌组织部分再生,但较稀疏,排列不规则;免疫组织化学检查提示CKAE1/AE3染色阳性,α-Actin染色微弱。3个月治疗组大白兔羊膜输尿管与周围粘连,有丰富的血运,无明显挛缩,管腔不缩小,已形成良好的移行上皮层和平滑肌层,免疫组织化学显示α-Actin和CKAE1/AE3染色均为阳性。

METHODS: In the experimental group, ADSCs were cultured with the scaffold and induced by CDMP1(50 μg/L) in basic medium for another 2 weeks. In the control group, SD rat cartilage cells were cultured with elementary nutrient liquid with scaffold for another 2 weeks. Twenty nude mice were imbedded the composite of cells-scaffold of the experimental group in their left armpits and the composites of cells-scaffold of the control group in right armpits. Every ten nude mice were killed at 8 and 12 weeks and were examined by safranine O-fast green and toluidine blue staining.

体外培养的脂肪干细胞复合于支架上,加入诱导液(基础培养液+ 50 μg/L软骨形态发生蛋白1)继续培养2周作为实验组;将SD仔鼠软骨细胞复合于支架上,常规培养2周作为对照组。20只裸小鼠,左侧腋窝皮下均植入实验组细胞-支架复合物,右侧腋窝皮下均植入对照组细胞-支架复合物。8, 12周各处死10只,行甲苯胺蓝和番红O-固绿染色。

Methods 110cases were randomly divided into treatment group and control group.56patients in the treatment group were treated by the therapy of combination of manual reduction and three edged needles and Chinese medicine.54patients in the control group were treated by the therapy of combi-nation of manual reduction and splintage and Chinese medicine.

将110例闭合性前臂双骨折随机分为两组,对照组56例采用手法复位经皮三棱针固定及中药三期施治治疗;对照组54例采用手法复位夹板固定及中药三期施治治疗。

Methods: SD female rats were divided randomly into 3 groups, 15 rats each group: sham-operation group, CHF model group, CHF model treated by Shengmai capsule group, preparing CHF rat models by constricting the suprarenal abdominal artery for 7 weeks.

将SD大鼠随机分为假手术组、心衰模型组和生脉胶囊组,采用腹主动脉缩窄7周复制大鼠慢性心力衰竭模型,分组灌胃治疗7周时,取大鼠心脏心尖部,运用Affymetrix大鼠全基因组表达谱芯片进行生脉胶囊组与心衰模型组心脏基因表达谱的差异性表达分析。

In group A, the model of allergosis was established by intravenous injection of horse serum twice at the interval of 3 weeks. In group B, the model of allergosis was also established by the same method as group A. After 2 weeks, group B was injected with prednisone at 45 mg·kg-1 for 3 days abdominally.

随机分单纯变态反应组和激素治疗变态反应组。A组采用分2次间隔3周给实验白兔iv马血清(10 ml·kg-1)建立变态反应疾病模型。B组采用与A组同样的方法,建立变态反应疾病模型,在模型建立后2周,连续3天腹腔内注射强的松龙(45 mg·kg-1)。

Methods: 50 normal Wistar male rats were randomly divided into five geoups: the sham operated group, injury model group, shenjindan capsule treat group, high dose and low dose group (duzhongyaotong pill treat, D and E)(n=10each). Autogenous nucleus pulposus was removed from the coccygeal vertebral and placed into the back of left L5~6 nerve root, The modle of the non-compressive nucleus pulposus protrusion was created by transplanting autogenous nucleus pulposus in the back of left L5~6 nerve roots. At tow weeks, the SP in dorsal root ganglion was determined by immunohistochemistry.

取健康Wistar大鼠50只,随机分为假手术组、模型组、对照组、高剂量组(D组、腰腿理痛散高剂量组)、低剂量组(E组、腰腿理痛散低剂量组),每组10只,将大鼠自身的尾椎髓核取出移植于左侧硬膜外腔L5、L6神经根背侧,造成非压迫性大鼠自体髓核移植硬膜外模型,通过免疫组化的方法测定大鼠2周时DRG中CGRP的变化。

Methods The chronic ocular hypertention rat model was made by cauterizating three episcleral veins.Rats were divided into control group,high level PROG group,middle level PROG group,low level PROG group according to different concentrations of PROG injected intraperitoneally.The left eye was model eye and the right eye was control eye.Three months later,the animals were executed and the eyeballs were enucleated.The RGCs were detected by HE staining and Thy-1.1 immunohistological staining.

通过烧灼3条巩膜上静脉制作慢性高眼压动物模型,此模型按腹腔注射不同浓度的孕酮而分为高、中、低浓度孕酮注射组及空白对照组,左眼为模型眼,右眼为自身对照眼,3个月后处死动物,取眼球制石蜡切片,行HE染色、Thy-1.1免疫组化染色及TUNEL原位凋亡检测。

To evaluate the efficacy of the recombinant fowlpox virus vaccine against the heterotype IBV, the chickens were challenged with the homotype IBV LX4 strain and the heterotype IBV LTJ95I strain after three weeks post vaccination. Antibodies against IBV were detected in vaccinated chickens one week post inoculation. The CD4+ T-lymphocytes in the peripheral blood increased rapidly in all groups challenged with IBV, except for the vaccinated group challenged by heterotype strain and the low level of CD4+ T-lymphocytes remained until end of the experiment. In all the groups, a high level of CD8+ T-lymphocytes only was observed in the vaccinated group after challenging with IBVhomotype strain. The morbidity and the mortality of this group were 21.43 % and 0 %, respectively, which showed significant difference with other groups. In addition, the lesions of chickens and virus shedding were less in the vaccinated group challenged by IBV homotype strain comparing with other groups, but there was no difference for the average body weight of chickens in all groups.

结果显示,重组疫苗接种1周后,免疫鸡产生抗IBV的抗体;而且外周血中CD4+和CD8+ T淋巴细胞的含量略高于非免疫对照组;攻毒后,异源强毒株攻毒的免疫组CD4+ T淋巴细胞呈下降趋势,并且该组低水平CD4+的状态一直持续到试验结束,而其他组CD4+ T淋巴细胞均迅速上升,峰值达到14.5 %;同源强毒株攻毒的免疫组CD8+ T淋巴细胞呈高水平的表达,而其他组攻毒后均无明显变化;保护率结果显示,同源强毒株攻毒免疫组的发病率和死亡率为21.43 %和0 %,与其他各组相比均有显著差异;另外同源强毒株攻毒的免疫组病理损伤与异源强毒株攻毒的试验组相比明显减轻,其排毒时间和排毒量也均有所减少;强毒攻毒后所有试验组体重无显著差异。

BMSCs and recombinant human GSF (50 μg/kg) were injected into models by tail vein and hypodermoclysis infusion respectively in the combination treatment group. Recombinant human GSF (50 μg/kg) was subcutaneously injected into models in the bone marrow stem cell autologous mobilization group. BMSCs were injected into rat models by tail vein in the BMSC group. Rat models in the heart failure group were intact.

造模后随机分成4组:联合治疗组尾静脉注射骨髓间充质细胞和皮下注入重组人粒细胞刺激因子50 μg/kg,自体骨髓干细胞动员组皮下注入重组人粒细胞刺激因子50 μg/kg,骨髓间充质干细胞组为尾静脉注射骨髓间充质细胞,心力衰竭组不给予任何干预。

Result: NO in injury group was high than that i n noninjury group and NO in group cultured by GS was less than that in group cul tured by common medium.

结果 :损伤组的NO含量比非损伤组高,损伤时人参皂苷培养组的NO含量比常规培养基组的含量低。

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