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1)  Cross-over trial
交叉试验
2)  Three-way crossover
三交叉试验
3)  cross matching test
交叉配合试验
1.
Objective To investigate the clinical efficacy of matched apheresis platelet by cross matching test.
目的探讨经血小板交叉配合试验的配合单采血小板的临床输注效果。
4)  Cross-neutralization test
交叉中和试验
1.
Four strain avian reovirus,CL(isolated from chicken),YH(isolated from muscovy duck),YB(isolated from muscovy duck) and S1133(standard strains) were examined in cross-neutralization tests using corresponding antiserum,and the antigen relationship of avian reovirus was analyzed.
采用血清学交叉中和试验方法,分析了4株禽呼肠孤病毒株CL(鸡源禽呼肠孤病毒)、YH和YB(鸭源禽呼肠孤病毒)及S1133(禽呼肠孤病毒标准株)之间抗原的相互关系;并对CL株的S3基因进行克隆测序,用DNAsis和Prosis等分析软件进行序列比较及推导氨基酸序列分析。
2.
Hyperimmune rabbit antisera against four field isolates from Guangxi and two commonly used vaccine strains of infectious bursal disease virus(IBDV) were prepared and used against heterogeneous and homogeneous IBDV strains in the virus cross-neutralization test.
应用兔制备的抗传染性法氏囊病病毒(IBDV)高免血清,在鸡胚成纤维细胞(CEF)上对从广西发病鸡群分离的4个IBDV代表性流行毒株和2个常用疫苗株进行交叉中和试验。
5)  crossover clinical trial
交叉临床试验
6)  cross design
交叉试验设计
1.
Of the red mature fruits of 12 tomato breeding lines,the dynamic analysis of multi-factor experiment from cross design including 3 factors was applied to study the rates of deterioration investigated through 21 days preservation,in condition of 4 treatment combinations of 2 environmental factors(temperature and cold injury).
采用3因子交叉试验设计对12个番茄育种品系红熟果实在2个环境因子(温度和冷害)4处理条件下贮藏21 d期间的变质率进行动态分析。
2.
Of the red mature fruits of 12 tomato breeding lines,the analysis of multi-factor experiment from cross design including 3 factors was applied to study the components of the rates of deterioration investigated through 21 days preservation,in condition of 4 treatment combinations of 2 environmental factors(temperature and cold injury).
本文采用3因子交叉试验设计对12个番茄育种品系红熟果实在2个环境因子(温度和冷害)4处理条件下贮藏21 d的变质率进行剖析,结果表明:总体情况,最适温(t=11~13℃)贮藏在受到冷害和无冷害情况下的变质率均低于常温(t=17~25℃)下的两个处理的变质率。
补充资料:交叉对照试验
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性质: 交叉对照试验可以在同一个体进行自身对照试验,也可在不同个体中进行组间交叉对照试验,当观察比较的药物多于2个时,可采用拉丁方设计。交叉对照试验适用于以下情况:(1)每种药物的药效都是短暂的;(2)延长总的治疗周期并不缩小各种药物治疗效应之间的差别;(3)所设计的交叉对照试验不致因先后两次或多次疗程而过量;(4)所用交叉设计无顺序影响或虽有顺序影响,但通过交叉试验这种顺序效应能得到平衡。

说明:补充资料仅用于学习参考,请勿用于其它任何用途。
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