1.The peak value of 78.5% reached at the ninth day in the CITE group versus 84.2 % at fourth day in the CPTE group.
CITE组扩张第 9天达到高峰 (78.5 % ) ,CPTE组扩张第 4天达到高峰 (84 .2 % )。
2.Methods Domestic pigs were chosen for CITE and CPTE models.
方法 用白色小家猪制作CITE和CPTE动物模型。
3.Firstly, the paper compares the differences of the current popular research information management softwares such as Reference Manager, Endnote and Pro - Cite, and then takes Reference Manager as a example to dissertate the process of constructing personal references library using manually inputing, importing from online searching and importing from Internet search through indirect methods.
本文首先比较了目前流行的信息管理软件Reference Manager、Endnote和Pro-Cite,接着以Reference Manager为例,论述了构建个人参考文献图书馆的多种方法:人工录入,联机检索导入和网络检索间接导入;
4.This examples uses the CITE element to render a citation in italic.
下面的例子使用了CITE元素将引文以斜体显示。
5.METHODS: Human TFPI-2 expression vector pBos-Cite-neo/TFPI-2 was transfected into pancreatic cancer cell line Panc-1. After being selected by G418, transfected and nontransfected cells were screened for TFPI-2 mRNA and protein by reverse transcription-polymerase chain reaction and Western blot analysis, respectively.
方法:脂质体介导人类TFPI-2真核表达载体pBos-Cite- neo/TFPI-2转染胰腺癌细胞系Panc-1,G418筛选阳性细胞,RT-PCR,Western blot技术检测转染前后胰腺癌细胞中TFPI-2 mRNA以及相应蛋白质的表达水平;
6.Methods: Human TFPI-2 expression vector pBos-Cite-neo/TFPI-2 was transfected into ovarian tumor cells line A2780. After the transfected cells were selected by G418, transfected and nontransfected cells were screened for TFPI-2 mRNA and protein by reverse transcription-polymerase chain reaction and Western blot analysis, respectively.
方法脂质体介导人类TFPI-2真核表达载体pBos-cite-neo／TFPI-2转染卵巢癌细胞系A：，8。 ，用G418筛选阳性细胞，经逆转录聚合酶链反应，Westernblot技术检测转染前后卵巢癌细胞中TFPI-2mRNA以及相应蛋白质表达水平；
7.METHODS: Human TFPI 2 expression vector pBos Cite neo/TFPI 2 was transfected into ovarian tumor cells line A2780. After the transfected cells were screened by G418, transfected and nontransfected cells were examined for TFPI 2 mRNA and protein by reverse transcription polymerase chain reaction (RT PCR) and Western blot analysis, respectively.
方法:脂质体介导人类TFPI-2真核表达载体pBos-Cite-neo/TFPI-2转染卵巢癌细胞株A2780,用G418筛选阳性细胞,经逆转录聚合酶链反应(reversetranscription-polymerasechainreaction,RT-PCR),Westernblot技术检测转染前后卵巢癌细胞中TFPI-2mRNA以及相应蛋白质表达水平;
8.Human TFPI-2 expression vector pBos-Cite-neo/TFPI-2 was transfected into keratocytes, transfected and nontransfected cells were screened for TFPI-2 mRNA and protein by reverse transcription-polymerase chain reaction and Western blot analysis, respectively.
脂质体介导人类TFPI- 2真核表达载体pBos -Cite -neo/TFPI- 2转染角膜基质细胞 ,RT -PCR ,Westernblot技术检测转染前后基质细胞中TFPI- 2mRNA及相应蛋白质的表达水平。
9.The cite situation of 220 treatises from 1985 to 1991 in journal of Luzhou medical college was analysed in terms of price index, and cite situation of 1991 year valume reference in the journal of the other medical college in Sichuan province and the National Medical Journal of China were compared with that of 1991 year valume reference in the journal of Luzhou Medical College.
用普赖斯指数分析泸州医学院学报1985～1991年220篇论著参考文献的引用情况,并用1991年学报与省内其他医学院校学报及中华医学杂志的同类情况比较,发现平均普赖斯指数为50.6％;
10.The function of forward link power control is to allocate power in cell cite and decrease the interference from cell cite to user.
前向链路控制用于分配小区基站功率、减小基站到用户的干扰;
