等位性

Results:The major genotype of all groups in population case-control study and family study was homozygote CC genotype.

结果：人群病例对照研究和家系研究中，各组PTP-1B基因均以CC基因型为主，C等位基因频率差异无显著性。

Objective To explore the hereditary susceptibility of HLA-DRB1 and-DQB1 alleles of epidemic hemorrhagic fever at gene level and to further the features of their immunogenetics.

目的 从基因水平探讨HLA-DRB1、DQB1等位基因多态性与流行性出血热的相关性，以阐述其免疫遗传学特征。

All loci detected in the study showed polymorphism and the number of alleles ranged from 2 to 22 in total population.

在所检测的4个群体中，各群体均有较高的多态性，其杂合度都超过了0.55，各位点等位基因的数目为2~22。

Paternally inherited fetal alleles were detected in 23 of 30 plasma samples. including 6/10 cases in early pregnancy, 8/10 cases in middle pregnancy and 9/10 cases in late pregnancy respectively.

结果 10例孕妇均足月分娩，男婴3例，女婴7例。10例孕妇血浆中均检出胎儿父源性等位基因，即胎儿DNA.30份孕期血浆标本中有23份检出胎儿DNA，其中孕早期标本6份（6/10）；孕中期标本8份（8/10）；孕晚期标本9份（9/10）。7份标本未见到胎儿DNA。

The applicability of chicken microsatellite primers to peafowl population was analyzed in the present paper, and the results showed 14 of 29 pairs of microsatellite primers from chicken could amplify peafowl DNA and produce specific allele patterns. A mean of 1.71 alleles was found for each locus. Seven pairs were highly polymorphic, and MCW0080 and MCW0098 were ideal markers for peafowl.

利用29对鸡微卫星标记对孔雀基因组DNA进行种间扩增，发现14对引物能扩增出特异性条带，每对引物扩增的平均等位基因数为1.71，有7对引物具有较丰富的多态性，其中MCW0080和MCW0098最为理想。

Eczema, Urticaria and Atopic Dermatitis are clinic common irritability dermatosis but not easy to treat, which all possess symptom with skin flush, tumefaction, macula, canker, desquamation, and itchy.

摘要湿疹、蕁麻疹与异位性皮肤炎是临床常见又不容易治疗的过敏性皮肤病，三者都具有皮肤发红、肿胀、斑疹、溃烂、脱屑、瘙癢等症状。

The NAT2 slow acetylator genotypes of IBD patients had experienced side effects more frequently than the rapid acetylator genotypes of IBD patients in SASP treatment, but the result is not statistically significance .

结果NAT2等位基因型和基因型频率在IBD患者和正常人群中的分布无没有显著性差异。

No significant differences in AGT M235T genotypes and allelic frequencies among three groups.

三组间基因型分布与等位基因频率相比均无显著性差异。

TaqIB polymorphism possibly contributed to cerebrocardiac vascular disease.The accidents of cardiovascular disease in B1B1 type was the highest in three genotypes while the accidents of cerebrovascular disease in B1B2 type was the highest.B2 allel gene has probably protective effect on cerebrocardiac artery.

TaqIB基因多态性与心脑血管事件发生可能有关，B1B1型心血管事件发生率较高，B1B2型脑血管事件发生率较高，B2B2型心脑血管事件发生率均较低，B2等位基因可能具有心脑血管保护作用。

They identified 371 genes (nearly 10%) as monoallelically expressed in epigenetically stable patterns in at least one population of cells derived from a single B cell clone.

他们确认起源于一个单B细胞克隆种群的371个基因（近10％）以单等位基因性在后生遗传稳定模式中表达。

Plunder melds and run with this jewel!

掠夺melds和运行与此宝石！

My dream is to be a crazy growing tree and extend at the edge between the city and the forest.

此刻，也许正是在通往天国的路上，我体验着这白色的晕旋。