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MethodPICC was inserted from the cubital fossa,and the superior vena cava was at the end of the deep venous remote.

PICC是从肘窝静脉插入，其末端位于上腔静脉远端的深静脉置管。

Lenticels of young branchlets not obvious; floral disk thin, cupuliform; stamens inserted on margin of disk; fruit small, 6.5-10 mm wide, globose

幼枝的皮孔不明显；花的花盘薄，杯形；花盘的雄蕊着生于边缘；结果实小，6.5-10毫米宽， 3

The RT-PCR product was inserted into pTG19-T vector and transformed into E. coli successfully. By blastn, the sequence results of Kunming mus musculus were in complete accordance with the conservative sequence of Genbank NR_003278 (791bp-1153bp). By Blastn in NCBI, the sequence with little difference among animals was confirmed to be conservative. After Blastn, fourteen complete CDS coding for different animals were chosen. According to VECTOR NIT 9.0 software, the similarities between Kunming mus musculus and bos taurus, homo sapiens, erinaceus europaeus, cricetulus griseus, sus scrofa, dasypus novemcinctus, rattus norvegicus, rabbit, equus caballus, macaca fascicularis, didelphis virginiana, monodelphis domestica and vombatus ursinus was 67%, 100%, 100%, 36%, 100%, 100%, 67%, 100%, 100%, 92%, 99%, 99% and 99%. In the phylogenetic tress constructed with the forteen 18S rRNA by Treeview, the Kunming mus musculus clustered with cricetulus griseus, sus scrofa and rabbit, which was nearer to cricetulus griseus and was most far away from macaca fascicularis.(3) After sencodary structure analyses of 18S rRNA of mus musculus, an oligonucleotide fragment for RNAi was designed and synthesized, which was transformed into plasmid, and restriction enzyme analyses and sequencing results should the expression plasmid pGPH1/ GFP/Neo-mouse-sh 18S rRNA were constructed for RNAi successfully.

结果①通过RT-PCR检测显示18S rRNA基因在小鼠卵巢组织和单个GV期、MⅠ期卵母细胞中均有表达，且在未成熟卵母细胞中，MⅠ期的表达明显强于GV期的表达；②RT-PCR产物克隆测序结果显示：昆明小鼠18S rRNA基因保守区序列与基因库序列[NR_003278保守区部分(791bp～1153bp)]完全一致；Blastn比对结果发现：在不同物种中差异较小，选出14种生物18S rRNA全序列经VECTOR NIT 9.0软件分析，提示昆明小鼠18SrRNA与牛、人类、刺猬、中国仓鼠、猪、犰狳、褐鼠、兔子、马、食蟹猴、负鼠、短尾猊、袋熊的18S rRNA的相似率依次为67%，100%，100%，36%，100%，100%，67%，100%，100%，92%，99%，99%，99%；Clustal 1.81和Treeview构建出的分子进化树表明：在上述14种生物中昆明小鼠与中国仓鼠进化关系最近，与兔子、猪聚成一簇，与食蟹猴进化关系最远；③根据18S rRNA二级结构设计并合成RNA干扰寡核苷酸片段，重组质粒经过限制性内切酶及测序表明成功构建了pGPH1/GFP/Neo-mouse-sh 18S rRNA干扰表达质粒。

Stamens 5–10(–27), inserted at base of corolla, usually declinate; filaments linear to filiform, glabrous or pilose towards base; anthers without appendages, opening by terminal or oblique pores.

雄蕊5-10(-27)，花冠的着生的在基部，通常下倾；花丝线形到丝状，无毛或具柔毛向基部；花药没有附属物，通过顶生或者偏斜的孔开裂。

Filaments inserted at lower part of corolla tube, decurrent part oblong, not pubescent.

在花冠筒，下延的深裂的长圆形的下半部分着生的花丝，并非短柔毛。

Methods The IL17 cDNA and Thy1.1 fulllength cDNA were subcloned into MIT(MSCVIRESThy1.1) retrovirus vector, and the siRNAIL17, U6 promoter and Thy1.1 fulllength cDNA were also inserted into retrovirus vector of pMNDBANSHEE.The recombined vectors were transfected 293 packaging cells by DNA calcium phosphate coprecipitation. Virus supernatant which infected preactivated spleen cells from NOD/BDC mice was collected. After incubation, the IL17 expression in diabetogenic T cells was detected.

利用基因工程和细胞克隆技术分别将IL17的cDNA插入MSCVIRESThy1.1逆转录病毒载体，将Thy1.1、U6增强子(U6 promoter)基因和IL17的siRNA cDNA插入逆转录病毒载体pMNDBANSHEE，采用磷酸钙沉淀法将重组载体转染293包装细胞；收集病毒上清，转染预先活化的NOD/BDC小鼠脾细胞，测定致糖尿病性T细胞的IL17和siRNAIL17的表达。

Stamens 4, didynamous, inserted at middle of corolla tube, slightly exserted.

雄蕊4，花冠筒，稍外露的二强雄蕊，着生的在中部。

Stamens 4, didynamous, inserted on corolla tube, included.

雄蕊4，二强雄蕊，着生于花冠筒，包括。

Stamens 4, didynamous, inserted above middle of corolla tube, glabrous, included; anther locules distinct, divergent.

雄蕊4，花冠筒，无毛的二强雄蕊，着生的在中部以上，包括；药室离生，分叉。

Stamens 4, didynamous, inserted high in corolla tube; 1 anther cell fertile and ellipsoid, another caudate and appendagelike.

雄蕊4，在花冠筒里二强雄蕊，着生高； 1花药室能育和椭圆形，尾状的另一个和appendagelike。

Do you know, i need you to come back

你知道吗，我需要你回来

Yang yinshu、Wang xiangsheng、Li decang,The first discovery of haemaphysalis conicinna.

1〕 杨银书，王祥生，李德昌。安徽省首次发现嗜群血蜱。