A binding mode of inositol monophosphate as a polar head group of the putative membrane phospholipid ligand to Cyt2Ca1 was presented using molecular docking. The residues of Leu9, Glu21, Tyr23 and Gln110 of the Cyt2Ca1 toxin are responsible for the interactions with inositol monophosphate via eight hydrogen bonds.
利用分子对接研究了以假定的膜磷脂的极性头部单磷酸肌醇作为配体与Cyt2Cal的结合模式，表明Cyt2Cal的氨基酸残基Leu9、Glu21、Tyr23和Gln110通过8个氢键与单磷酸肌醇发生作用。
There was no death caused by PN in STG, LCT and MCT/LCT groups. STG group reached positive nitrogen balance at day 4 prior to LCT and MCT/LCT groups. The nitrogen balance in STG group within 7 days was significantly higher than that in LCT and MCT/LCT groups, with higher nitrogen balance of MCT/LCT group than that of LCT group.
结果 与3种脂肪乳剂组相比，GLU组7 d内TG和LDLC逐渐升高，HDLC持续降低，7 d时呈负氮平衡，7 d动物死亡率为50%。7 d内3种脂肪乳剂组血清TG、TC、LDLC恢复正常水平，与SO组比较差异无统计学意义；HDLC水平持续升高，7 d内均达到正氮平衡；3种脂肪乳剂组均无PN所致死亡。4 d时STG组先于LCT、MCT/LCT两组转为正氮平衡，7 d内STG组氮平衡显著高于LCT、MCT/LCT两组，MCT/LCT组氮平衡高于LCT组。
Methods Fasting serum TG, TC, GLU, UA levels of 3828 college teachers were tested.
对3828名高校教师进行空腹血清中TG、TC、GLU和UA等指标检测。
Four kinds of mutation: CD8, CD8/9, CDs41/42 and IVS-Ⅰ-5 were revealed at the gene identification of 10 propositus of β-thalassemia.
其中的HbJ Tashikuergan［α19(AB1)Ala→Glu］系世界首次报道，CD8和CDs8/9为在中国人中首次发现。
objective to determine the influencing factors of urine test. methods the urine control and the patient fresh urine were compared in different temperature and using different soaked time in urine and exposed time in air. results soaked time and temperature influenced the results of glu, ubg, bil and ket, while exposed time changed the results of leu, giu, nit, ket and ubg. conclusion the correct test is important for clinical docˉtors to conclude the disease and make good treatment.
目的 探讨尿液检测过程中的影响因素。方法在不同室温，用不同的浸尿时间及在空气中暴露的尿试纸带分别对尿液质控品和患者的新鲜尿液进行测试比较。结果浸尿时间及不同室温对glu、ubg、bil、ket四个项目结果有影响；尿试纸带在空气中的暴露时间对leu、glu、nit、ket、ubg有影响。结论正确使用尿液试纸带的检测方法为医生判定病情及确定正确的治疗方案起重要的作用。
Results Soaked time and temperature influenced the results of GLU, UBG, BIL and KET, while exposed time changed the results of LEU, GIU, NIT, KET and UBG.
结果 浸尿时间及不同室温对GLU、UBG、BIL、KET四个项目结果有影响；尿试纸带在空气中的暴露时间对LEU、GLU、NIT、KET、UBG有影响。
If so, it can also be regarded as viscoelastic. An adequate amount of data useful for bioengineering has been obtained from one- and two-dimensional tensile tests for fresh pericardia of oxen and those fixed by glu-taraldehyde.
作者对新鲜的和戊二醛处理过的牛心包进行了一维和二维的拉伸，试验结果，得到一些可能对生物工程有用的数据。
Glutamate is the main neurotransmitter of excitatory synaptic transmission in afferent nerve system of cochlear.
谷氨酸(glutamate，Glu)是耳蜗传入神经系统兴奋性突触传递的主要神经递质，在介导突触兴奋性活动和突触可塑性方面起着重要作用。
To synthesize the octreotide, Phe-Leu-Glu-Glu-Leu and C_(15)H_(31)-CO-Lys-Thr -Thr-Lys-Ser peptides, the strategies are as followings: Fmoc- group as protective group for α-NH_2; TBTU, DIEA and HOBt as coupling reagent; and ethanedithiol -phenol - thioanisole - H_2O - TFA (2.5:5:5:5:82.5, V/V) as cleaving solution.
采用Fmoc固相合成法，以苯并三哗四甲基脲四氟硼酸盐、二异丙基乙胺和1-羟基苯骈三氮唑为缩合剂；苯酚—乙二硫醇—苯甲硫醚—水—三氟乙酸(5：5：2.5：5：82.5，V/V)为切割试剂，合成了奥曲肽、Phe-Leu-Glu-Glu-Leu及C_(15)H_(31)-CO-Lys-Thr-Thr-Lys-Ser三种小分子多肽，并对奥曲肽的合成规模进行了放大。
Modeling the objects in Max, scene setup and animation alternatives using the PWrapper function of Glu3D with the particle flow of Max, filling closed volumes with Glu3D particles and designing a fluid explosion are all thoroughly discussed.
在Max中建模，场景设置和动画使用Glu3D的PWrapper功能和Max的粒子流，填充体积使用Glu3D粒子，并且彻底地解释了如何设计流体爆炸。
Cetin also walks you through a production quality fluid simulation animation project, starting from the storyboards. Modeling the objects in Max, scene setup and animation alternatives using the PWrapper function of Glu3D with the particle flow of Max, filling closed volumes with Glu3D particles and designing a fluid explosion are all thoroughly discussed.
从storyboards 开始，cetin还带领您通过产品质量的流体模拟动画项目，对象建模，场景设置，动画选择，这些将使用Glu3D 中PWrapper 的作用，彻底讨论了粒子流，填充封闭容器，设计流体爆炸。
There are two isozymes in maize β-glycosidase, i. e. Glu1 and Glu2, which are controlled by two different genes.
玉米葡萄糖苷酶有两个同功酶即Glu1和Glu2分别由两个不同的基因控制。
Derect sequencing reveals that there is a G→C replacement in exon 3 of RDS gene, which results in a Gln substituted for a Glu in the 304th amino acid of the peripherin peptide.
经测序证实RDS基因第3外显子出现G→C突变，该突变导致RDS基因表达产物——盘膜边缘蛋白第304位氨基酸残基由谷氨酸变为谷氨酰胺（Glu304→Gln）。
There were no existence of association between any of the Glu192Arg and Leu54Met polymorphism and risk of PD. The relative risks were 1.041 (95%CI=0.922-1.177, p=0.434) for the Ang-allele and 0.992 (95%CI=0.962-1.023, P=0.611) for the Met-allele of the PONI. Further comparison of the genotypes and allelic frequencies of the PON1 in PD patients stratified both by gender and age at onset also revealed no significant associations. However, there was existence of a high dysequilibrium between the Gln192Arg and Leu54Met polymorphisms.
结果发现无论Glu192Arg或Leu54Met多形性都与PD的危险性并无以相关性存在，PON1中Arg对偶基因的相对危险为1.041(95%CI=0.922-1.177，p=0.434)，而Met对偶基因的相对危险为0.992(95% CI=0.962-1.023，P=0.611)，进一步以PD患者的性别及发病年龄来比较PONI的基因型与对偶基因频率，结果亦显示没有显著的相关陆，但发现在Glu192Arg与Leu54Met多型性之间有高度的不平衡性存在。
Therefore the determination of Glu content is the foundation to evaluate the neurotoxicities of xenobiotics.
因此测定兴奋性氨基酸含量的变化，是评定外来化合物神经毒性的基础。
The accordance rates of BLD, GLU, LEU and PRO by the 3 analyzers were all above 90
结果3种干化学分析仪测定结果隐血、葡萄糖、白细胞、蛋白的一般符合率都在90%以上
After BmK venom or BmK I was subcutaneously injected into rat hindpaw, glutamate and aspartate release could be evoked significantly within the initial 30 minutes.
同样，特异性钠通道调制剂BmK I经大鼠足底注射后，30分钟内也可观察到Asp和Glu的释放量较对照组明显升高，但增加幅度低于BmK粗毒诱导的兴奋性神经递质的释放，然而GABA的释放量在整个实验过程中无明显变化。
The nano-structures which were obtained by C20-2Glu assembly were used as template and proper chemical reactions were carried on. We successfully sysnthesized CuiS nanowires, CdS nanowires and nanotubes, Ag nanotubes and allthese nano-structures were observed by TEM. Electron diffraction analysis results proved that these nano-materials are muti-crystal nano-structures.
利用C20-2Glu所组装成的纳米结构作为模板，进行适当的化学反应，我们成功合成了硫化亚铜纳米线、硫化镉纳米线和纳米管、银的纳米管，这些纳米结构都是通过透射电子显微镜观察到的，电子衍射结果证明，这些纳米材料都具有多晶纳米结构。
The computered curvilinear regression and an auto-plotting were carried out in stead of a manual drawing.
大于生理浓度100倍和10，000倍的HGH、glu-cagon和ACTH对红细胞胰岛素结合率都无抑制作用。
Esculetin had the highest affinity toward the binding site of XO, and this was due to hydrogen bonding interactions. The hydroxyl group at C-6 formed hydrogen bonds with the carboxyl group Glu802 that played critical role on XO binding.
在8种香豆素衍生物中发现esculetin与黄嘌呤氧化酶的亲和力最高，因为在esculetin的结构上，C-6的OH基团可与麸胺酸802的COOH基团形成氢键，此键结对於抑制黄嘌伶氧化酶活性是很重要的，因而增加了两者结合的稳定性。