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break into groups相关的网络例句

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

Methods Eighty Kunming mice were equally randomized into 8 groups: normal group, model group, vitamin E (90mg.kg-1.d-1) group, highand lowdose RPM protein (20 and5 mg.kg-1.d-1 respectively) groups, high and lowdose RPM anthraquinone glycoside (28 and 7mg.kg-1.d-1 respectively) groups, combination (lowdose RPM protein and lowdose RPM anthraquinone glycosides)group. Except the normal group,the mice in other groups received subcutaneous injection of Dgalactose to indue the aging model.

选用昆明种小鼠80只,随机分为8组:正常组,模型组,维生素E组(剂量为90mg·kg-1·d-1),何首乌蛋白质高、低剂量组(剂量分别为20、5mg·kg-1·d-1),何首乌蒽醌苷高、低剂量组(剂量分别为28、7mg·kg-1·d-1),AGRPM与PRPM混合组(混合组,均取两者低剂量);除正常组外,其他组均采用长期(7周)皮下注射D半乳糖复制衰老小鼠模型。

Take the experimental rats into 8 groups including 3 groups for therapeutic dose,3 groups for toxic dose and 2 groups for lethiferous dose, with 10 rats for each group and male and female for half.

本实验研究是通过动物实验来考察伊曲康唑治疗儿童头癣的安全性。

In experiment one, male weanling Wistar rats were divided into 13 groups after being anemic; in hemoglobin repletion period, 5 groups were fed on standard diets (FeSO4 provided 0ppm, 6ppm, 12ppm, 18ppm and 35ppm of Fe), 3 groups were fed on milk A diets (milk A provided 6ppm, 12ppm, and 18ppm of Fe), 4 groups were pair-fed on milk A (daily supply of 2g, 3g, 4g and 6g of milk A powder), and one group was pair-fed on milk B (daily supply of 3g of milk B powder). The hemoglobin regeneration efficiency of milk A (19%-29%) was significantly lower than that of FeSO4 (69%-90%) and that of milk B (79%).

实验一采用雄性离乳Wistar大鼠,经耗铁贫血后,分为十三组,分别饲以标准饲料(以FeSO4供铁0ppm,6ppm,12ppm,18ppm,35ppm);奶粉饲料(以奶粉A提供铁6ppm,12ppm,18ppm);奶粉A对饲育组(每天供应2g,3g,4g,6g奶粉A);和奶粉B对饲育组(每天供应3公克奶粉B);两周的血红素再生期后,奶粉A与其对饲育组的血红素再生率(19%~29%)显著低於标准饲料(69%~90%)和奶粉B(79%)。

360 0-day-old AA broilers were randomly divided into eight treatments of three replicates each. Among these groups, two were control groups and the others treatment groups. These groups were offered with acidifiers of different levels. The aim was to study their effects on the pH value, the quantities of microbiology, and sift the suitable adding type and levels.

360只0日龄艾维茵肉鸡随机分为8组,每组3个重复,其中2组为对照组,6组为试验组,添加不同水平的自制复合酸化剂,观察各处理对肉鸡肠道pH及微生物数量的影响,并筛选适宜的添加类型和水平。

One hundred and eighty patients with acute exacerbation of COPD were randomized to divide into 3 groups, nebulised budesonide groups, oral prednisolone groups and placebo-controlled groups.

180例COPD急性加重期住院患者随机分为3组,分别给予布地奈德雾化和口服泼尼松龙与安慰剂进行对照治疗,观察3组患者肺功能、动脉血气及副反应情况。

one hundred and eighty patients with acute exacerbation of copd were randomized to divide into 3 groups, nebulised budesonide groups, oral prednisolone groups and placebo controlled groups. pulmonary function, arterial blood gases analysis and the adverse effects were measured.

180例copd急性加重期住院患者随机分为3组,分别给予布地奈德雾化和口服泼尼松龙与安慰剂进行对照治疗,观察3组患者肺功能、动脉血气及副反应情况。

Results:The results show that the survival rate of mammary epithelial cells were decreasing gradually with the increasing of the time of TGF-β1 treatment, and the survival rates of 24 h and 48 h groups were significantly lower than that of control group (p.05); the LDH activity of 6 h、12 h、24 h and 48 h groups were significantly higher than that of control group (p.05); the DNA degradation arisesed in 12 h, 24 h, and 48 h groups' mammary epithelial cells; the activity of Caspase-3 reach to a peak at 24 h, which was significantly higher than that of control group (p.05); the acinus of epithelial cells appears to break off and collapse with the increasing of treatment time, but the leydig structure keeps integrate;...

结果表明:1、5、10 ng/mL的TGF-β1均能抑制乳腺上皮细胞的增殖,且随浓度增加抑制作用加大,呈现剂量依赖性,其中10 ng/mL TGF-β1组与对照组差异显著(P.05);10 ng/mL TGF-β1作用于乳腺上皮细胞24 h,随作用时间延长细胞凋亡率逐渐增加,6 h、12 h和24 h组与对照组相比差异极显著(P.01);LDH活力也不断升高,6 h、12 h和24 h组与对照组差异显著(P.05);DNA随 TGF-β1作用时间的延长发生不同程度降解;TGF-β1作用2 h~6 h细胞大量表达HSP70,6 h达到高峰,而后下降,2~12 h的表达量均显著高于对照组(P.05)。结论:TGF-β1可以抑制奶牛乳腺上皮细胞的增殖,具有浓度依赖性。10 ng/mLTGF-β1。。。

METHODS: Sixty healthy Sprague-Dawley rats were randomly divided into 3 groups: 6 rats in normal control group, 6 rats in EGb treating normal IOP group, and the other 48 rats were established chronic high IOP models of rats by cauterizing two episcleral veins. The n 30 rats satisfying experimental level were selected and randomly divided into five groups: 6 rats in physiological brine treating group, and the other 24 rats were divided into four experimental groups according to the dose of EGb: group A, EGb 50mg/; group B, EGb 100mg/; group C, EGb 150mg/; and group D EGb 200mg/. After the treating time of 1 month, the rats were sacrificed on schedule.

取健康SD大鼠60只,正常对照组和正常银杏叶治疗组各6只,其余48只采用烧烙法,烙闭大鼠左眼2条浅层巩膜静脉,制作大鼠持续性高眼压模型,从中选出眼压稳定在实验要求水平的大鼠30只,随机分为生理盐水组,治疗A组(每日EGb 50mg/kg)、治疗B 组(每日EGb 100mg/kg)、治疗C 组(每日EGb 150mg/kg)、治疗D 组(每日EGb 200mg/kg),治疗时间为1mo,处死大鼠后做视网膜全层铺片,对RGCL神经元做特异性染色后行神经元计数分析来评估神经元的情况。

METHODS: Sixty healthy Sprague-Dawley rats were randomly divided into 3 groups: 6 rats in normal control group, 6 rats in EGb treating normal IOP group, and the other 48 rats were established chronic high IOP models of rats by cauterizing two episcleral veins. Then 30 rats satisfying experimental level were selected and randomly divided into five groups: 6 rats in physiological brine treating group, and the other 24 rats were divided into four experimental groups according to the dose of EGb: group A, EGb 50mg/; group B, EGb 100mg/; group C, EGb 150mg/; and group D EGb 200mg/. After the treating time of 1 month, the rats were sacrificed on schedule. Flat preparation of whole retinaes was stained distinctively and neuron counting in retinal ganglion cell layer from both eyes of each rat were performed to evaluate neuron situation.

取健康SD大鼠60只,正常对照组和正常银杏叶治疗组各6只,其余48只采用烧烙法,烙闭大鼠左眼2条浅层巩膜静脉,制作大鼠持续性高眼压模型,从中选出眼压稳定在实验要求水平的大鼠30只,随机分为生理盐水组,治疗A组(每日EGb 50mg/kg)、治疗B 组(每日EGb 100mg/kg)、治疗C 组(每日EGb 150mg/kg)、治疗D 组(每日EGb 200mg/kg),治疗时间为1mo,处死大鼠后做视网膜全层铺片,对RGCL神经元做特异性染色后行神经元计数分析来评估神经元的情况。

METHODS: Sixty healthy Sprague-Dawley rats were randomly divided into 3 groups: 6 rats in normal control group, 6 rats in EGb treating normal IOP group, and the other 48 rats were established chronic high IOP models of rats by cauterizing two episcleral veins. The n 30 rats satisfying experimental level were selected and randomly divided into five groups: 6 rats in physiological brine treating group, and the other 24 rats were divided into four experimental groups according to the dose of EGb: group A, EGb 50mg/; group B, EGb 100mg/; group C, EGb 150mg/; and group D EGb 200mg/. After the treating time of 1 month, the rats were sacrificed on schedule. Flat preparation of whole retinaes was stained distinctively and neuron counting in retinal ganglion cell layer from both eyes of each rat were performed to evaluate neuron situation.

取健康SD大鼠60只,正常对照组和正常银杏叶治疗组各6只,其余48只采用烧烙法,烙闭大鼠左眼2条浅层巩膜静脉,制作大鼠持续性高眼压模型,从中选出眼压稳定在实验要求水平的大鼠30只,随机分为生理盐水组,治疗A组(每日EGb 50mg/kg)、治疗B 组(每日EGb 100mg/kg)、治疗C 组(每日EGb 150mg/kg)、治疗D 组(每日EGb 200mg/kg),治疗时间为1mo,处死大鼠后做视网膜全层铺片,对RGCL神经元做特异性染色后行神经元计数分析来评估神经元的情况。

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