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The results of POPGENE analyze indicated that it was moderate level of the genetic diversity of Dipelta, mean PPB (percentage of polymorphic bands) h and I of 4 species of Dipelta as below: D.wenxianensis.(PPB=62.02%,h=0.1850,I=0.2826); D.yunnanensis (PPB=40.31%, h=0.1238, I=0.1874); D. floribunda (PPB=36.82%, h=0.1395,I=0.2045); D. elegans (PPB=15.51%, h=0.0583,I=0.0861). Genetic diversity in D.elegans is the lowest. It is possibly caused by the endemic distribution and local ecotope.

POPGENE分析结果表明，文县双盾木的多态位点百分率平均为62.02%，Nei&s基因多样性指数平均为0.1850，Shannon&s信息指数平均为0.2826；云南双盾木的PPB平均为40.31%；h值平均为0.1238；I值平均为0.1874；双盾木两个居群的PPB平均为36.82%；h值平均为0.1395；I值平均为0.2045；优美双盾木两个居群的PPB平均为15.51%，h值平均为0.0583；I值平均为0.0861；因此，我们认为双盾木属4个种的遗传多样性适中；而优美双盾木由于分布上的地理限制，居群的生境比较孤立，其遗传多样性较低。

All 21 exons with flanking intronic sequences, as well as a 263 bp fragment of the 5" flanking region, of GARS-AIRS-GART gene, were screened in the same five populations, by the method of PCR-SSCP analysis, combined with sequencing reactions. We detected 10 SNPs, C-179T from 5" flanking region, A5669G form exon 3, C6545Afrom exon 4, A7777G from intron 4, G10854T, C10867T, G10898T from intron 6, A16197G from intron 11, C21228T from intron 14, and C29686T from exon 21. These ten polymorphic sites were nominated as GARS1, GARS2, GARS3, GARS4, GARS5, GARS6, GARS7, GARS8, GARS9, and GARS 10, respectively. The mutation of C D A at GARS3 was a non-synonymous mutation, wh

其中外显子4中的6545处的c~A突变导致对应的氨基酸序列中的第173位氨基酸发生变异：天冬氨酸一谷氨酸；10个SNP位点依次命名为：GARSI、GARSZ、GARS3、GARS4、GARSS、GARS6、GARS7、GARSS、GARSg、GARS 10；(2)10个SN'P位点在不同的鸡种中的基因型分布差异显著(P.05)，进一步的方差分析显示，GASRI位点以及GARS3位点与肌肉肌昔酸含量之间存在着显著的关联；(3)在所检测的5个群体中GARsl位

In other words,163 sites in crested ibis genome were detected.The bands from 23 primers showed polymorphism.Minimurn of polymorphic ratio was 0,maximum was 85.71%,and average was 48.99%.In the population which was composed by 37 individuals, most of genetic distances between two arbitrary individuals were less than 0.1.The results showed that the degree of similarity among crested ibises was high while genetic diversity in thepopulation was low accordingly.

我们在对Operon公司OPG系列和OPA系列引物进行优化筛选的基础上，用24条随机引物共扩增出163条谱带，即检测了朱鹮基因组中的163个位点，其中23条引物的扩增结果具有多态性；谱带的多态比率最小为0，最大为85.71％，平均为48.99％；在由37只朱鹮组成的种群中，任意两个个体之间的遗传距离绝大多数在0.1以下。

Methods 34 patients genomic dna was amplified by polymorphic region in intron 16 of the ace gene.

54例冠心病患者的dna应用ace基因内含子16多态部位侧翼的前体进行pcr扩增。

It suggested the difference in salt tolerance of two groups maybe relate with SSR polymorphic loci on linkage groups between group A and B.

大豆应对盐胁迫的某个相关基因位点可能存在于这些差异区段中。

Torsades de pointes is a special form of polymorphic ventricular tachycardia. It is characterized by continuously changing morphology of the QRS complexes that seem to twist around an imaginary line, rate dependence, underlying QT prolongation and the so called "long-short initiation sequence".

Torsades de pointes是一种特殊形态的多形性心室频脉，其心电图的特徵包括：QRS波的形态会一直改变，彷佛缠绕著一条假想的线；另外它的发作常与心博过缓有关，合并有QT间距延长，及以所谓「长-短」的序列而开始。

RAPD(Random amplified polymorphic DNA) was used to detect the genetic diversity of Castanopsis eyrei populations in three forest communities at different succession stages in Tiantai mountain Zhejiang Province,namely,needle-leaved forest,needle/broad-leaved mixed forest and evergreen broad-leaved forest.

利用RAPD技术对甜槠种群在浙江省天台山不同演替阶段森林群落(针叶林、针阔混交林、常绿阔叶林)中的遗传多样性和遗传分化进行了分析。3个甜槠种群平均多态位点百分率为67.98%，总多态位点百分率为92.13%。

To investigate the methods to effectively and simply assess the CAG repeat size of HD gene which was necessary for gene diagnosis of Huntington disease, the sequence including polymorphic CAG repeat of HD gene was amplified by PCR with TaKaRa LA Taq DNA polymerase and GC buffer. PCR products were analyzed on polyacrylamide gel to distinguish normal alleles from HD alleles. The DNA fragments of affected alleles were recovered from polyacrylamide gel as templets for secondary PCR. The secondary PCR products were cloned into T vector for sequencing analysis to determine CAG repeat size. A total of 20 normal individuals and 3 members from a HD pedigree were included in this study.

为了简单高效检测HD基因开放阅读框5'端n三核苷酸重复序列，建立快速准确的亨廷顿病(Huntington disease， HD)基因诊断方法，应用TaKaRa LA Taq DNA聚合酶配合GC buffer扩增HD基因包含n重复序列的目的片段，非变性聚丙烯酰胺凝胶电泳检测后回收n拷贝数异常增多的目的片段，再次PCR扩增后将产物连接至T载体，进行DNA测序确定CAG的拷贝数。

Can detect and remove rootkits, mass-mailing worms, e-mail viruses, peer-to-peer viruses, Internet worms, file viruses, Trojans, stealth viruses, polymorphic viruses, bodiless viruses, macro viruses, MS Office viruses, script viruses, spyware, spybots, password stealers, keyloggers, paid dialers, adware, riskware, hacktools, backdoors, joke programs, malicious scripts and most other malware.

可以检测和删除的rootkit ，邮件群发蠕虫，电子邮件病毒，点对点病毒，互联网蠕虫病毒，文件病毒，木马，隐形病毒，多态病毒，脱胎病毒，宏病毒，病毒的MS Office ，脚本病毒，间谍软件， spybots ，密码盗取者，键盘记录程序，支付拨号，广告软件， riskware ， hacktools ，后门，玩笑程序，恶意脚本和其他大多数恶意软件。

Items, including almost all of the malware categories such as: Worms, Trojans, Backdoors, Macro Viruses, Dos Viruses, Boot Viruses, Polymorphic Viruses, Metamorphic viruses, Constructor Tools, Riskware, Flooders, Nukers, Sniffers, Spoofers, Droopers, Spam Tools, Adware, Rootkits, Malicious Scripts, Hack Tools, Exploits and other types of malware.

项目，其中包括几乎所有的恶意程序分类，如：蠕虫，特洛伊木马程序，后门，巨集病毒，多病毒，开机的病毒，多形性病毒，变质的病毒，构造器工具， riskware ， flooders ， nukers ，嗅探器， spoofers ， droopers ，垃圾邮件工具，广告软件， rootkit攻击，恶意脚本，黑客工具，攻击和其他类型的恶意软件。

Lugalbanda was a god and shepherd king of Uruk where he was worshipped for over a thousand years.

Lugalbanda 是神和被崇拜了一千年多 Uruk古埃及喜克索王朝国王。

I am coming just now,' and went on perfuming himself with Hunut, then he came and sat.

我来只是现在，'歼灭战perfuming自己与胡努特，那麼，他来到和SAT 。