In this paper, by developing a transfer method, we study theoretically transport properties of 2DEGs through antiparallel magnetic-electric barrier structures.
本文中，我们发展了转移矩阵方法研究反平行磁电垒结构中二维电子气体的弹道输运特性，得到了弹道隧穿及共振分裂的一般性规律。
According to the manual, this binocular is immersible in 1.5m deep water for one hour and operational from -43 to+55 degs.
按照说明书的说法，该镜可以浸没于1.5m深的水下一小时，并且可以在-43 ~+55℃的温度条件下使用。
According to the manual, this binocular is immersible in 1.5m deep water for one hour and operational within -43 to +55 degs.
依据使用手册，该镜可浸入1.5米深水中1小时，可在-43-+55摄氏度下使用。
Expression patterns of phytohormone related DEGS supported that phytohormones are key factors for fruit setting.
在这些差异表达的基因中，与激素相关的基因表达模式支持植物激素是坐果关键因子的观点。
Britt. Methods: The chromatography condition was column packed with 15% of DEGS, column temperature was 182 ℃ using FID detector and heptadecanoic acid ethyl ester served as internal standard.
方法：色谱条件为15%丁二酸二乙二醇聚酯（DEGS）色谱柱，柱温182℃，FID检测器，内标为十七碳酸乙酯。
In the first step, significant analysis of microarrays (SAM) was used to select a subset of differentially expressed genes (DEGs).
第一步，采用基因表达差异显著性分析方法（SAM）筛选得到差异表达基因子集。
In contrast to PHA, the number of DEGs was similar between monkey and human.
不同于PHA，人和食蟹猴所产生的差异基因数目相似。
The dynamic changes in the differentially expressed genes (DEGs) and their relationship to stress were identified. Ten clusters of genes were found to be significantly co-expressed.
为了鉴定差异表达基因与胁迫之间的关系，对基因表达模式的动态变化进行了聚类分析，差异基因可以分为10类显著共表达的基因表达模式。
We performed an integrated-analysis of 4 LAD microarray datasets, encompassing 353 patients, to reveal differentially expressed genes (DEGs) between normal lung tissues and LAD of different stages.
我们筛选获得了4组芯片（353例样本），应用整合分析方法来寻找正常组织与肺腺癌各个期级之间的差异表达基因。
There were 420 up-regulated genes and 552 down-regulated genes in 2-fold DEGs, including 23 genes related to cytochrome P450;
2倍差异表达基因中，上调基因共420个，下调基因共552个，其中包括细胞色素P450相关基因23个；
It was observed that root-knot nematode infection increased with period after inoculation. As a result, stress of peanut roots and the total number of DEGs increased.
发现随着接种后时间的推移，根结线虫繁殖侵染增加，花生根部受到的胁迫增强，差异表达基因总数也随之增加。
We found 12 DEGs which had been confirmed as the pathogenicity-related factors in B. cinerea or in other plant pathogens. These genes may be involved in the pathogenesis process of B. cinerea.
其中，可能与灰葡萄孢菌和其它病原菌致病过程相关的差异表达基因有12个。
The interactions between DEGs and Ca2 + - target protein showed that they had close connections and were controlled by Ca2 +.
通过分析DEGs与钙靶蛋白的相互作用，发现DEGs与钙的靶蛋白有密切联系，说明也是受钙调控的。
METHODS: The separation was performed on 5% DEGS column with detector temperature at 220 ℃ and flow rate at 30ml/min, nitrogen gas was used as carrier.
方法色谱柱为5%DEGS柱，检测器温度为220℃，载气为氮气，流速为30ml/min。
SHIMADZU Model GA-14A gas chromatography. It is equipped with a flame ionization detector, and C-RA4 integrator. The column were 4.0mm×2.0m glass capillary columns coated with 15%DEGS/6201, 80-100 mesh solid phase.
色谱仪为日本岛津GA-14A气相色谱仪，氢离子火焰检测器，C-RA4数据处理机，色谱柱为4.0mm×2m玻璃柱，内填15%丁二酸二乙二醇聚酯/6201，80-100目固定相。