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maximum dose相关的网络例句

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

A small dose of a hormone, for example, can cause a woman to ovulate, while a larger dose can make her infertile.

例如,小剂量激素可致女性排卵,而更大剂量激素却可导致她不孕。

The changes of muscle protein content and pH values were observed. Results Thymus and spleen coefficients in high and low dosage group were 9.1±2.3, 6.3±1.1, respectively, and those of in the controll were 6.5±1.6, 3.4±0.5.The contents of muscle protein (g/100 g) in high, medium, and low dose groups were 24.68±0.55, 22.48±0.54, 21.22±1.25, respectively, lower than that of the control (31.83±2.36, P.05). Paramorphia of lymphocyte in high dose ciprofloxacin treated group was observed.

结果 对照组胸腺和脾脏系数分别为(9.1±2.3),(6.3±1.1)mg/g,高剂量组胸腺和脾脏系数分别为(6.5±1.6),(3.4±0.5)mg/g,与对照组比较,差异均有统计学意义(P.05或P.01);而中、低剂量组的脾脏指数与对照组比较,差异均有统计学意义(P.05);环丙沙星各剂量组与对照组比较,肌肉pH值变化不明显;环丙沙星高、中、低剂量肌肉蛋白质含量分别为(24.68±0.55),(22.48±0.54),(21.22±1.25)g/100 g,与对照组(31.83±2.36)g/100 g比较明显下降(P.05);与对照组比较,高剂量组脾淋巴细胞形态异常。

The character of hemagglutination of the virus could be inhibited by the antiserum of Newcastle disease virus.According to the international standard and method of virulence judgement of NDV, we measured the average death time、the minimal lethal dose and the median infective dose(EID50) of chicken embryos and the intracellular inoculation pathopoiesis index of 1-day-old chicks.

参照国际上规定的新城疫病毒毒力判定标准及其方法对分离毒株ZH1、ZH2进行了鸡胚最小致死量和平均死亡时间、鸡胚半数感染量(EID50)以及1日龄鸡脑内接种致病指数测定,结果ZH1、ZH2株的MDT为52h和44 h,EID50为106.4/ 0.1mL和108.64/ 0.1mL,ICPI为1.93和1.975。

Methods Seventy-five SD rats were randomized into five groups: normal, model, iodine glycerin (20 g/L), high-dose SP (200 g/L) and low-dose SP (100 g/L). The experimental periodontitis rat models were established by ligating molars with steel wire combined with intramuscularly injection of prednisolone (1.25mg, 8 times). Except that the model and normal groups were treated by applying saline, the other groups were treated by applying the corresponding drugs 0.5 mL to the peridentium, tid for 10 days. After treatment, debris index, probe depth and bleeding rate during probing were investigated and the pathological changes of periodontal tissues were also observed.

方法]SD大鼠随机分为正常组,模型组,碘甘油组(20g/L),舒口散高、低剂量组(200、100 g/L);采用钢丝结扎牙齿加肌注波尼松龙(l.25 mg/次,共8次)的方法复制大鼠实验性牙周炎模型;药物采用口腔局部涂搽,每次0.5mL,每日3次,10 d为1疗程,模型组与正常组给予等容积生理盐水;检测各组软垢指数、探诊深度、探诊出血阳性例数,并取牙周组织进行病理学检查。

Serum containing SSTG was obtained at different time after perorally administrated with different dose of SSTG.The cardiomyocytes were deprived of oxygen and glucose to mimic hypoxia reoxygenation injury and were treated by serum containing SSTG when reoxygenation.LDH content in supernatant was detected after reoxygenation.LDH release suppression rate was used to study the time-effect and dose-effect of serum containing SSTG.

以中药有效组分配伍方剂双参通冠方不同灌胃剂量、药后不同取血时间所得的药物血清为受试药物;培养心肌细胞,进行缺氧复氧实验,复氧同时给予不同双参通冠方药物血清处理,实验结束后取培养上清检测LDH值,以LDH释放抑制率为指标,观察含药血清药理作用强度与体内给药的量效、时效关系。

Results showed that the seed germination rate,emerged seedling rate and survival seedling rate of Platanus aceriflia Willd.decreased with dose increase at the dose of 50~400Gy,as well as the plant height,fresh weight and length of root.

结果表明,在50~400Gy辐射范围内,随着剂量的增加,悬铃木种子的萌发率、出苗率、成苗率降低,株高、鲜重、根长也明显下降。

Based on the data of seeding rate and root growth,it is concluded that the semi-lethal radiation dose of Platanus acerifolia Willd.dry seed was 50Gy,and the suitable dose range for radiation breeding was 50 to 250Gy.

通过对悬铃木辐射组与对照组成苗率和根长进行比较,初步推测悬铃木辐射的半致死剂量为50Gy,辐照诱变的适宜剂量为50至250Gy。

Patients with dental impaction received a presurgical dose 30 minutes before surgery and a postsurgical dose 3 hours later.

有牙科阻生的病人有手术前30分钟接受了一个手术前剂量,而在3小时后接受了一次手术后剂量。

Results:① large dose of piracetam(≧600mg/kg) significantly increased scores of praxiology(p.01)、decreased water content(p.05) and the expression of aquaporin( aqp4) in mcao.②all dose of piracetam decreased volume of ischemic (p.01) and remained relatively intact ultramicrostructure.

结果:吡拉西坦注射液剂量依赖性地降低侧大脑半球的含水量、改善其神经功能评分、下调水通道蛋白4(aop4)的表达、降低动物的脑梗死体积、改善缺血脑组织神经元细胞的超微结构。

In the preapproval clinical experience with a new medicinal product or its new usages, particularly as the therapeutic dose may not be established, all noxious and unintended responses to a medicinal product related to any dose should be considered adverse drug reactions.

指对于仍处于上市前临床研究的新医药产品或其新用法,尤其在其治疗剂量尚未建立以前,所有与药物任何剂量有关的有害或不期望的反应,均应认作为药品不良反应。

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