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   navel vein 的翻译结果: 查询用时:0.008秒
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navel vein
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  脐静脉
     Results In human RPE cells, the expression of VEGF protein was more in recombinant plasmid pcDNA 3.1+-rho-VEGF 165 than that in plasmid pcDNA 3.1+-VEGF 165; in human navel vein endothelial cells, no obvious difference of the expression of VEGF protein between recombinant plasmid pcDNA 3.1+-rho-VEGF 165 and plasmid pcDNA 3.1+-VEGF 165 was found.
     结果 在人视网膜色素上皮细胞中 ,重组质粒pc DNA3.1 + - rho- VEGF1 6 5比质粒 pc DNA3.1 + - VEGF1 6 5的 VEGF蛋白表达强 ,在人脐静脉内皮细胞 ,两者的表达量无明显差别。
短句来源
     In the past experiment,we had found there is more CD40 on the breast cancer cell line MDA-MB-231 and navel vein endothelia cells.
     在我们的前期实验中发现,乳腺癌细胞系及脐静脉血管内皮细胞表面高表达CD40,因此我们设计并进行了如下的实验来观察CD40配基化对乳腺癌的治疗效果。
短句来源
     The navel vein bloods of infants were tested for HBVM when it was born.
     分娩时新生儿抽脐静脉血查乙肝病毒血清标志物(HBVM)。
短句来源
  “navel vein”译为未确定词的双语例句
     Nursing care of wear navel vein through mother′s belly
     经母腹胎儿脐静脉穿刺术的护理
短句来源
     After 30d's feeding liver injured mise groups with various dose of olive juice, the hepatic lobule structure of Mise with high dose was normal; Hepatic cord radially ranged as the center of navel vein. The cells were polyhedral, monocytic, occasionally dikaryocytes.
     ②用不同剂量橄榄汁喂养肝损伤模型组小鼠30d后,高剂量组橄榄汁喂养的小鼠,肝小叶结构正常,肝索以中央静脉为中心呈放射状排列,细胞呈多面体、单核,偶见双核,核大且圆,位于细胞中央;
短句来源
     Objective To observe effects of the third delivery stage and the prevention of postpartum hemorrhage in injecting Calcium Gluconate into the navel vein.
     目的 观察脐静脉注射葡萄糖酸钙预防产后出血及对第三产程的影响。
短句来源
     Methods In the study group of the cases of 100 patient,the navels were cut off from 5cm to the opening of vagina immediately,and injecting 10% Calcium Gluconate 10ml into the navel vein during five-ten minutes.
     方法 观察组 10 0例 ,在胎儿娩出后立即断脐 ,经脐静脉注射 10 %葡萄糖酸钙 10ml,时间 5~ 10min ;
短句来源
  相似匹配句对
     Vein
     脉
短句来源
     vein gen.
     vein gen.
短句来源
     The navel vein bloods of infants were tested for HBVM when it was born.
     分娩时新生儿抽脐静脉血查乙肝病毒血清标志物(HBVM)。
短句来源
     Nursing care of wear navel vein through mother′s belly
     经母腹胎儿脐静脉穿刺术的护理
短句来源
     Studies on Bagging of Navel
     脐橙果实套袋研究
短句来源
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Objective To observe effects of the third delivery stage and the prevention of postpartum hemorrhage in injecting Calcium Gluconate into the navel vein.Methods In the study group of the cases of 100 patient,the navels were cut off from 5cm to the opening of vagina immediately,and injecting 10% Calcium Gluconate 10ml into the navel vein during five-ten minutes.In the control group of the cases of 101 patients,20iu oxytocin was given by injecting-muscle(im)after the delivery of fetus.Results...

Objective To observe effects of the third delivery stage and the prevention of postpartum hemorrhage in injecting Calcium Gluconate into the navel vein.Methods In the study group of the cases of 100 patient,the navels were cut off from 5cm to the opening of vagina immediately,and injecting 10% Calcium Gluconate 10ml into the navel vein during five-ten minutes.In the control group of the cases of 101 patients,20iu oxytocin was given by injecting-muscle(im)after the delivery of fetus.Results Contrast to the control group,the amount of bleeding within two hours after delivery obviously decreased 64.76ml and the time of the third delivery stage reduced 2.03 minutes(P<0.01).Conclusion 10% Calcium Gluconate was injected into the navel vein,which made Caget into the vessel bed of placenta directly and made the uterus shrinked,placenta pelled off,its effect is obvious and reliable,suitable for wide-spread use.That is simple and easy.

目的 观察脐静脉注射葡萄糖酸钙预防产后出血及对第三产程的影响。方法 观察组 10 0例 ,在胎儿娩出后立即断脐 ,经脐静脉注射 10 %葡萄糖酸钙 10ml,时间 5~ 10min ;对照组 10 1例 ,胎儿娩出后即肌注催产素 2 0U。结果 实验组产后 2h出血量较对照组减少 64 .76ml,实验组第三产程时间较对照组减少 2 .0 3min(P <0 .0 1)。结论 脐静脉注射葡萄糖酸钙使钙离子直接到达胎盘血管床 ,促进子宫收缩、胎盘剥离 ,缩短第三产程 ,减少产后出血 ,疗效可靠 ,简便易行

Objective To construct specifically expressed vascular endothelial growth factor (VEGF) 165 gene in retina. Methods Rho promoter, specifically expressed in retina, was amplified by polymerase chain reaction (PCR) from the genomic DNA of a BLAB/C rat, then it was cut with restriction enzymes and cloned into the plasmid pcDNA 3.1+-VEGF 165 to form recombinant plasmid pcDNA 3.1+-rho-VEGF 165. The correct recombinant plasmid pcDNA 3.1+-rho-VEGF 165 was identified by restriction enzymes and...

Objective To construct specifically expressed vascular endothelial growth factor (VEGF) 165 gene in retina. Methods Rho promoter, specifically expressed in retina, was amplified by polymerase chain reaction (PCR) from the genomic DNA of a BLAB/C rat, then it was cut with restriction enzymes and cloned into the plasmid pcDNA 3.1+-VEGF 165 to form recombinant plasmid pcDNA 3.1+-rho-VEGF 165. The correct recombinant plasmid pcDNA 3.1+-rho-VEGF 165 was identified by restriction enzymes and PCR, and was transferred by jetPEI into cultured human navel vein endothelial cells and human retinal pigment epithelial (RPE) cells. The expression of VEGF protein in human navel vein endothelial and RPE cells was detected by immunocytochemical staining and protraction of the growth curve of the cells. Results In human RPE cells, the expression of VEGF protein was more in recombinant plasmid pcDNA 3.1+-rho-VEGF 165 than that in plasmid pcDNA 3.1+-VEGF 165; in human navel vein endothelial cells, no obvious difference of the expression of VEGF protein between recombinant plasmid pcDNA 3.1+-rho-VEGF 165 and plasmid pcDNA 3.1+-VEGF 165 was found. Conclusions The construction of pcDNA 3.1+-rho-VEGF 165 carrier may provide the basic material for the study of the nosogenesis of VEGF in retinal neovascularization, and establish the foundation to set up the model of transgenic mice with VEGF specific expressing in retina.

目的 构建在视网膜组织特异性表达的人血管内皮生长因子 (VEGF) 1 6 5基因。 方法 用聚合酶链反应 (PCR)方法从 BL AB/ C鼠全基因组扩增能在视网膜组织特异性表达的 rho启动子 ,经限制性内切酶纯化后克隆于质粒 pc DNA3.1 + - VEGF1 6 5中 ,建立重组质粒 pc DNA3.1 + - rho- VEGF1 6 5,通过限制性内切酶酶切分析及 PCR鉴定筛选出正确重组质粒 pc DNA3.1 + - rho- VEGF1 6 5,由 jet PEI介导转染人视网膜色素上皮细胞和人脐静脉内皮细胞 ,并通过免疫组织化学染色以及绘制细胞生长曲线检测在人视网膜色素上皮细胞和人脐静脉内皮细胞中 VEGF蛋白的表达。 结果 在人视网膜色素上皮细胞中 ,重组质粒pc DNA3.1 + - rho- VEGF1 6 5比质粒 pc DNA3.1 + - VEGF1 6 5的 VEGF蛋白表达强 ,在人脐静脉内皮细胞 ,两者的表达量无明显差别。 结论 载体 pc DNA3.1 + - rho- VEGF1 6 5的构建为进一步研究 VEGF在视网膜新生血管形成中的致病机理提供基础材料 ,并...

目的 构建在视网膜组织特异性表达的人血管内皮生长因子 (VEGF) 1 6 5基因。 方法 用聚合酶链反应 (PCR)方法从 BL AB/ C鼠全基因组扩增能在视网膜组织特异性表达的 rho启动子 ,经限制性内切酶纯化后克隆于质粒 pc DNA3.1 + - VEGF1 6 5中 ,建立重组质粒 pc DNA3.1 + - rho- VEGF1 6 5,通过限制性内切酶酶切分析及 PCR鉴定筛选出正确重组质粒 pc DNA3.1 + - rho- VEGF1 6 5,由 jet PEI介导转染人视网膜色素上皮细胞和人脐静脉内皮细胞 ,并通过免疫组织化学染色以及绘制细胞生长曲线检测在人视网膜色素上皮细胞和人脐静脉内皮细胞中 VEGF蛋白的表达。 结果 在人视网膜色素上皮细胞中 ,重组质粒pc DNA3.1 + - rho- VEGF1 6 5比质粒 pc DNA3.1 + - VEGF1 6 5的 VEGF蛋白表达强 ,在人脐静脉内皮细胞 ,两者的表达量无明显差别。 结论 载体 pc DNA3.1 + - rho- VEGF1 6 5的构建为进一步研究 VEGF在视网膜新生血管形成中的致病机理提供基础材料 ,并为进一步建立视网膜特异性表达 VEGF转基因鼠模型建立了基础。

Objective:Using HBIG to abscond the HBV intrauterine infection from the carrier-HBV pregnant women to their babies(Dissemination from father to bady.Dissemination from mother to bady).Methods:The carrier-HBV pregnant women were injected with HBIG 200 IU monthly form the 28 th week during pregnancy.The injection were 3 times totally(28 w,32 w,36 w).The navel vein bloods of infants were tested for HBVM when it was born.Results:Among the 83 babies whom born from the peoples HBV mothers,3 were infected by...

Objective:Using HBIG to abscond the HBV intrauterine infection from the carrier-HBV pregnant women to their babies(Dissemination from father to bady.Dissemination from mother to bady).Methods:The carrier-HBV pregnant women were injected with HBIG 200 IU monthly form the 28 th week during pregnancy.The injection were 3 times totally(28 w,32 w,36 w).The navel vein bloods of infants were tested for HBVM when it was born.Results:Among the 83 babies whom born from the peoples HBV mothers,3 were infected by HBV.The infection rate was 3.62%.The absconding rate of infection from mother to baby was 95.95%(71/74),and which from father to baby was 100%(9/9).Conclusion:By injection to the carrier-HBV pregnant women with HBIG 200 IU monthly(28 w,32 w,36 w)may prevent HBV intrauterine infection effectively.

目的:用乙肝免疫球蛋白(HBIG)阻断乙肝病毒携带者孕妇宫内感染(父婴、母婴垂直传播)。方法:对乙肝病毒携带者的孕妇自28周起每月肌注200IU的HBIG 1剂(28 W、32 W、36 W),产前共注射3剂。分娩时新生儿抽脐静脉血查乙肝病毒血清标志物(HBVM)。结果:83例乙肝病毒携带者所生的新生儿3例感染HBV,HBV宫内感染率为3.62%。母婴传播阻断率95.95%(71/74);父婴传播阻断率100.00(9/9)。结论:乙肝病毒携带者的孕妇在孕28 W、32W、36 W分别注射HBIG200IU 3剂,可有效预防胎儿HBV宫内感染。

 
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