二基因的

Molecular genotyping is validated as a method to confirm a diagnosis of CHM by demonstrating androgenetic diploidy and to resolve p57-positive cases into diandric triploid PHMs, biparental diploid nonmolar specimens, and the rare CHM with aberrant p57 expression.

分子基因型检测显示父系二倍体能确诊CHM，并能将p57阳性病例分类确诊为雄性异型三倍体的PHMs、双亲二倍体的非胎块性病变和罕见p57异常表达的CHM。

A set of spelt monosomic lines as female parent were respectively crossed with wheat new variety SM96 and new line SM20005 to determine the chromosomal location of the gene conferring resistance to powdery mildew in both. Seeding of parents, F〓 and F〓 from monosomic F〓 were inoculated with race no. 15 of Blumeria graminis f. sp. tritici. Analysis of obtained data revealed that one major dominant resistant gene originating from wild Emmer in the variety SM96 and the line SM20005 was located on chromosome 4A.

为确定小麦新品种沈免96和新品系沈免20005含有的抗白粉病基因所在染色体，以一套斯卑尔脱单体系为母本分别与沈免96和沈免20005杂交，将亲本、F〓、单体F〓植株的F〓代群体在苗期用小麦白粉菌15号小种的单孢菌系接种鉴定，单体分析结果表明，沈免96及沈免20005所含源于野生二粒小麦的抗小麦白粉菌15号小种的1个显性主效基因位于4A染色体上。

In order to compare the homology of the gene encoding VP2 between MDPV-Q and MDPV which was registered in the GenBank, also in order to find out changes of the VP2 gene and the immuno-genicity between the wild-strain MDPV-Q and the attenuated strain MDPV-26 which derived by continued passage of virulent wild-type in muscovy duck embryo, a pair of primer (LHMP7/LHMP8) was designed. The upper one LHMP7 and the lower one LHMP8 corresponded to the MDPV-specific nucleotides sequence 2885-2900 and 4618-4604 respectively, according to the MDPV nucleotide sequence databases. The length of the sequence embraced by the primers was 1734bp.

为了获取这一基因片段与国外分离株进行同源性比较，同时也为了了解MDPV强、弱毒株VP2基因之间的异同关系，及其免疫原性的变化规律，通过DNA重组技术，设计了一对引物LHMP7／LHMP8，该对引物选取位于2885～2900及4618～4604的两段序列，跨幅为1734bp，并在这两条引物中分别加入两种限制性核酸内切酶SacⅡ和KpnⅠ的酶切位点，分别对MDPV-Q和由该株病毒经人工致弱后得到的MDPV-26株进行PCR扩增，并将PCR产物克隆到pMD18-T载体上，分别得到二个重组子：pMD18-T—M-Q VP2和pMD18-T-M-26 VP2。

It is concluded the result suggest that in the 569-764 nucleotides region of Ouabain combined sites of sodium pump α1 gene in Kazakans of Xinjiang might not exist gene variant or the frequency of variant might be extraordinary low.

钠泵 。1基因变异所致的钠离子转运障碍可能起着联系盐敏感与高血压的桥梁作用址'3二。目前针对钠泵基因与人类高血压关系的研究甚少。为探讨人类高血压的形成过程中

Yang E,Korsmeyer SJ.Molecular thanatopsis:a discourse on the BCL-2 family and cell death.Blood,1996,88:386[3] Campos L,Rouanlt JP,Salido O,et al.High expression of BCL-2 protein in acute myeloid leukemia cells is associated with poor response to chemotherapy.

BCL-2是新一类癌基因——凋亡调控基因BCL-2家族的代表，其编码26kd的蛋白存在于线粒体、核膜及内质网，与同家族的其它成员组成不同比例的同、异二聚体而影响凋亡启动[6]。

Results We can induce MSCs into osteoblasts which can express gene col Ⅰ and ALP. Through analysis growth curve, we demostrateed the diphosphonate or assemble flavone of drynaria rhizome with 10^(-4)~10^(-6)mmolL^(-1) had the inhibition on the osteomast; it with 10^(-8)mmolL^(-1) had a promotion on the osteoblast; it with 10^(-10)~10^(-12)mmolL^(-1) had a restraint on osteoblast. Conclusion Through gene analysis, we found the diphosphonate or assemble flavone of drynaria rhizome can have the promotion on the osteoblast.

结果 骨髓基质细胞经过4周诱导可转化为表达colⅠ和ALP的成骨细胞，经过生长曲线分析，二磷酸盐和骨碎补总黄酮10^(-4)~10^(-6)mmolL^(-1)时，对诱导后的成骨细胞有抑制作用；10^(-8)molL^(-1)有促进作用；10^(-10)~10^(-12)mmolL^(-1)不明显，其中10^(-8)mmolL^(-1)作用最强；基因分析后，发现二磷酸盐和骨碎补总黄酮促进成骨细胞表达colⅠ和ALP，且两者合用效果大于单独用药。

The multi-drug resistance rate of Salmonella and E.coli were 91.80% and 100%.According to the genes sequence published in Genbank ,we analysed the value of Tm ,content of G+C, oligonucleotide dimer by DNAStar and Primer 5.0 software, and according to the construction of I integron ,we designed 3 pairs of primers to amplify intIl gene ,variable segment ,3"-conserved segment for detectting Salmonella and E.coli"s I integron.As a result , aimed genes were amplified and sequenced;The detection rate of I integron of 61 Salmonella and 48 E.coli were 81.97% and 66.67%.

据文献报道及GenBank中注册的基因序列，运用DNAStar软件分析同源率及Primer5.0软件对Tm值、G+C含量、引物二聚体等进行分析，根据Ⅰ类整合子的结构设计了3对引物，对Ⅰ类整合子的intI1、可变区、3'保守端进行扩增，检测沙门氏菌和大肠杆菌Ⅰ类整合子；扩增出了相应基因片段并测序；61株沙门氏菌和48株大肠杆菌中分别有50株和32株菌检测出Ⅰ类整合子，Ⅰ类整合子的检测率分别为：81.97％和66.67％。

The body does not keep track of how it solves a problem , so it cannot pinpoint which genes to pump up the muscle on the blacksmith's biceps , or which genes regulate respiration and blood pressure .

身体并不记录自己是如何解决问题的，因此也就不能准确定位哪种基因是用来在铁匠的二头肌上给肌肉充血的，或者哪种基因是用来调节呼吸和血压的。

The body does not keep track of how it solves a problem , so it cannot pinpoint which genes to pump up the muscle on the blacksmith's biceps , or which genes regulate respiration and blood pressure .

身体并不明了自己是如何解决问题的，因此并不能准确定位哪种基因是用来在铁匠的二头肌上给肌肉充血的，或者哪种基因是用来调节呼吸和血压的。

The amplified fragment was inserted into pRSET-A to generate the first double repeat of the precursor gene. By utilizing a pair of isocaudamer BamH I and Bgl II sites, and another downstream Hind III site of plasmid pRSET-A, following a series of simple double digestions and ligation of the resulted products, a series of repeat (3, 4 and 6) precursor peptide fragment genes were derived.

本实验设计一对两侧含编码疏水性氨基酸密码子的引物，经过扩增前导序列10~34aa基因序列，并重新克隆入质粒pRSET-A构建串联二聚体后，再利用质粒pRSET-A的BamH I / Bgl II同尾酶克隆位点，经一系列简单的酶切和连接，快速构建这一前导肽中不含组氨酸标签序列的串联多聚体基因，并成功表达其六聚体重组蛋白。

However, as the name（read－only memory）implies, CD disks cannot be written onorchanged in any way.

然而，正如其名字所指出的那样，CD盘不能写，也不能用任何方式改变其内容。

Galvanizes steel pallet is mainly export which suits standard packing of European Union, the North America. galvanizes steel pallet is suitable to heavy rack. Pallet surface can design plate type, corrugated and the gap form, satisfies the different requirements.

镀锌钢托盘多用于出口，替代木托盘，免薰蒸，符合欧盟、北美各国对出口货物包装材料的法令要求；喷涂钢托盘适用于重载上货架之用，托盘表面根据需要制作成平板状、波纹状及间隔形式，满足不同的使用要求。