转

In this paper, the transfer data of address bus was determined by comparing of jump address and first address of circle program.

提出了一种通过跳转地址与循环首地址的比较确定跳转时刻地址数据编码方式的低功耗编码算法。

Affic light at the next corner turned red, but he whipped right at the corner without slowing.

下一个路角的交通信号灯转成了红色，但是他毫不减速在路角猛力右转。

Although it fills the same role, plain text editing, it has many advantages: 10-level undo, alphabetization, block indent/unindent, bookmark, case conversion, encoding conversion, file history, jump to line, jump to offset, keyboard macros, search and replace, spell checking, statistics, variable pitch font, and much more.

虽然它填补了同样的作用，纯文本编辑，它具有许多优点： 10级撤消， alphabetization ，座缩进/ unindent ，书签，案件的转换，编码转换，档案历史，跳转到线，跳转到抵销，键盘宏，搜索和替换，拼字检查，统计，变螺距的字体，以及更多。

In addition to the standard features, it offers many advantages including a 10-level undo system, alphabetization, block indent/unindent, bookmark, case conversion, encoding conversion, file history, jump to line, jump to offset, keyboard macros, search and replace, spell checker, statistics, variable pitch font, and more.

除了标准的功能之外，该软件还提供了包括10级取消操作系统，字母顺序排列，段落缩进/无缩进，书签，大写字母转换，编码转换，文件历史记录，跳转到行，跳转到偏移量，键槃宏，搜索和替换，拼写检查，统计表，可变倾斜度字体等在内的许多高级功能。

The influence of the substrate concentration, temperature, pH value, the concentration of certain inorganic ions(Mg, Mn, NH4 +), actinomycin D and α-amanitin on the polymera

观察了底物浓度、温度、pH等与转录活性的关系；探讨了Mg~、Mn~、NH_4~+等离子和放线菌素D、α-Amanitin对转录活性的影响。

We got the result: Bufo Raddei Strauch Tadpole (1) Bufo Raddei Strauch Tadpole was capable of lens regeneration, which originated from the epithelial cells at iris dorsal margin by dipigmentation.(2) Dipigmentation of Bufo Raddei Strauch by two methods: one was licked up by amoebocyte, the other one was flowed from the pigment cells.(3) In the lens regeneration cells of Bufo Raddei Strauch profiles of the mitochondria became complicated ribosome manifold, and the endoplasmic reticulum was cisternal dilation. During the process of deferentiation of lens fiber the cell nucleolus became little and chromatin shrinked.(4)The crystalline electrophoresis of Bufo Raddei Strauch Tadpole lens regeneration showed that during lens regeneration P-crystalline was expressed earliest then was γ-crystalline and α-crystallin, this result is consistent with newt.

结果表明：花背蟾蜍蝌蚪(1)具有晶状体再生的能力，其晶状体的再生来源于虹膜背缘的上皮细胞；(2)虹膜背缘去色素是转分化的前提，主要有两种方式：一种也是最主要的方式是在晶状体被摘除后虹膜外侧产生巨噬细胞，巨噬细胞吞噬虹膜色素上皮细胞中的色素颗粒；另一种方式是虹膜色素上皮细胞自身释放色素颗粒；(3)电镜观察发现虹膜色素上皮细胞转分化过程中线粒体有明显变化，核糖体增多，粗面内质网增多，晶状体纤维分化过程中细胞核逐渐凝聚；(4)SDS-PAGE电泳发现，花背蟾蜍蝌蚪晶状体再生中相关蛋白表达顺序与有尾类蝾螈相似，蛋白表达顺序依次是β-晶状体蛋白、γ-晶状体蛋白和α-晶状体蛋白，并且后两种蛋白几乎同时表达。

Using Pseudomonas syringae and Pantoea ananas , the dominant ice nucleation active bacteria strains from Yunnan province, as receptors of genetic engineering recombination, and Escherichia coli S17/pZJ25∶∶Tn5 as donator. By transposon Tn5 induced mutants method, the Tn5 was inserted and integrated into the genome of wild type INA + bacteria. INA + mutant as INA - when the linear continuous of INA + gene destroyed.

以云南省冰核细菌的优势种类丁香假单胞菌Pseudomonassyringae和菠萝泛菌Pantoeaananas为重组基因工程菌的受体菌，采用Tn5转座子诱变技术，以大肠杆菌EscherichiacoliS17/pZJ2 5∶∶Tn5作为转座子诱变的供体菌，使Tn5插入并整合到冰核细菌基因组中，使冰核基因的线性连续性被破坏，失去冰核活性。

NS equation ; rotation ; rolling moment ; roll angular velocity ; roll-damping moment coefficient derivative

NS方程；旋转；滚转力矩；滚转角速度；滚转阻尼力矩系数导数

When you pull out the lens, turn clockwise to lock it, when you want to push it back, always remember to turn the advance film knob first and after that press the button and turn the lens anticlockwise to keep it back and also to remember to pull out the lens when you want to rewind the film.

当你把镜头拉出来时，记得要顺时针转，当你要把镜头收回时，千万要记得过片先，然后按回收镜头键，在逆时针转，在收回去。还有，当回片时，千万计的要把镜头拉出来。

The parental BHK and the transfectants stably expressing human DR4, DR5, DcR1, or DcR2 were stained with control mouse IgG or murine antihuman DR4, DR5, DcR1, or DcR2 mAbs and analyzed by flow cytometry. Dotted and solid lines correspondent to control and specific stainings, respectiely. Cell surface staining with anti-DR4, anti-DR5 and anti-Fas mAbs.

抗人TRAIL受体的单克隆抗体的特异性：用小鼠IgG或鼠抗人DR4、DR5、DcR1及DcR2单克隆抗体对未转染的BHK细胞以及分别转染了人DR4、DR5、DcR1及DcR2并稳定表达的BHK细胞进行免疫组化染色，然后做流式细胞分析，点线和实线分别对应于对照及特异性染色。

The split between the two groups can hardly be papered over.

这两个团体间的分歧难以掩饰。

This approach not only encourages a greater number of responses, but minimizes the likelihood of stale groupthink.

这种做法不仅鼓励了更多的反应，而且减少跟风的可能性。