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移植治疗组
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  transplant group
     Method:Thirty Wistar rats were respectively divided into three groups: semi-cut cavity injured group, D-Hanks control group and neural stem cells transplant group.
     方法:30只Wistar大鼠,分为半切洞损伤组、D-Hanks液对照组和神经干细胞移植治疗组
短句来源
     According to TAM standard: 48 tendons in autogenous fat particle purify transplant group,22 tendons were excellent,18 good,6 fair and no poor,the rate of excellent and good was 86.96%;
     采用自体脂肪颗粒纯化移植治疗组46条肌腱,优22条,良18条,中6条,差0条,优良率86.96%;
短句来源
  “移植治疗组”译为未确定词的双语例句
     RESULTS:The transplanted MSCs survived for more than four weeks in normal and infarcted tissues of brain,and the transplantation occurred. Until the third week,the range of transplantation was(3.626±1.831)mm2 in transplantation group,which was obvious larger than that in sham operation group(1.534±0.475) mm2, and it was significant difference(F=5.786 3, P< 0.05).
     结果:移植入脑的MSCs在正常脑组织与梗死区能存活至少4周以上,并发生迁移,至第3周移植治疗组迁移范围为(3.626±1.831)mm2,明显比假手术移植组(1.534±0.475)mm2大,差异有显著性意义(F=5.7863,P<0.05);
短句来源
     The overall 1- and 3-year survival rates were 94.7% and 52.6% in the patients receiving surgical treatment again and 71.9% and 7.1% in those not receiving the surgical treatment.
     尽管复发后的治疗方式大致相同,但复发病例中经再次切除和肝移植治疗组的1.3年生存率分别为94.7%和52.6%,而非手术治疗组的相应的生存率分别为71.9%和7.1%。
短句来源
     Group B and C underwent Wistar to SD transplantation,group B was untreated and group C was treated with Cyclosporine A(5 mg·kg~(-1)·d~(-1),i.p.×14 d).
     B组为Wistar-SD急性排斥组,移植前后未作处理; C组为Wistar-SD异基因移植治疗组,移植日开始给予环胞素A(CsA)5mg/kg/d腹腔注射×14d。
短句来源
     ③ SERCa2a mRNA greatly expressed in the SERCa2a gene treatment group and SERCa2a gene modified MSC transplantation group than that in the MSC transplantation group and the empty adenoviral vector control group.
     ③肌浆网钙离子ATP酶2a基因治疗组和肌浆网钙离子ATP酶2a基因修饰的骨髓干细胞移植治疗组心肌内肌浆网钙离子ATP酶2amRNA表达强度明显高于骨髓干细胞移植治疗组和腺病毒空载体对照组。
短句来源
     In group 2,the recurrent rate was 8.16%,corneal epithelia healed up in 1~6 days. The difference of recurrent rates in two groups was significant.
     羊膜移植治疗组复发率8.16%,角膜上皮修复时间1~6 d,平均(4.55±1.23)d,两组比较有显著性差异。
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  相似匹配句对
     ③Therapeutic group.
     (3)治疗
短句来源
     and no therapy was given to Group D;
     C为FST治疗 ;
短句来源
     Our study provides experimental support for clinical treatment of AMI by MSCs transplantation.
     移植
短句来源
     and group C,minipigs received pancreas autograft without immunosuppression.
     B为同种异体胰腺移植 ,使用免疫抑制治疗 ;
短句来源
     Cell transplantation in the treatment of diabetes
     糖尿病患者的细胞移植治疗
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  transplant group
The only significant change in the original transplant group was a decrease in Conscientiousness from baseline to 24 months.
      
Hypertension was the sole predictor of LVH in the transplant group.
      
The mRNA expression levels of IL-12, IL-15, IL-18 were increased obviously and those of IL-4, IL-10 were significantly decreased in the transplant group as compared with the control group (P>amp;lt;0.01).
      
In the TGF-β1 group, the mRNA expression levels of IL-12, IL-15, IL-18 were significantly decreased and those of IL-4, IL-10 were significantly increased as compared with the transplant group (P>amp;lt;0.01).
      
Data were assessed in terms of positive predictive value, and showed that conventional T-cell crossmatching is adequate for the primary transplant group, but more sensitive ancillary tests are indicated for regrafts.
      
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The results of treatment of 112 eyes with Mooren's ulcer were analysed.Conjunctivo- scleral excision was performed on 38 eyes and lamellar sclerokeratoplasty on 74 eyes.All patients had been followed up for at least 6 months.The cure and recurrent rates of the former group are 68.4% and 31.8% respectively,while those of the later

本文报告112眼蚕蚀性角膜溃疡,用结膜巩膜切除治疗38眼,板层角巩膜移植治疗74眼,治愈率前者为68.4%,后者97.3%。一次手术后,追踪6个月,结膜巩膜切除组复发率31.8%。板层角巩膜移植组复发率为13.5%。远期追踪,两组的复发率均较低。复发与年龄及单、双眼发病无明显关系,作者认为术后复发主要与病变组织及包含在其中的某些致病因素清除不够彻底有关。术后视力的恢复以板层角巩膜移植治疗组较满意。作者建议根据巩膜受累的轻重把此病分为轻症型与重证型,重症型有较高的复发倾向,但通过再次手术绝大多数可以获得治愈。文内还介绍了两种疗法的适应症。

The treatment and relapse of 51 cases with idiopathic nephrotic syndrome in children were studied. 25 of 51 cases receivied the long -term standard prednisone therapy(conarol group) and the others (26 ones) received the same long -term standard predisone therapy and transplantation of fetal thymus (treatmental group). The relapse of the disease after half a year, one year and three years was investigated. It was found that the relapse times and relapse rates of the treatmental group at different times were significatly...

The treatment and relapse of 51 cases with idiopathic nephrotic syndrome in children were studied. 25 of 51 cases receivied the long -term standard prednisone therapy(conarol group) and the others (26 ones) received the same long -term standard predisone therapy and transplantation of fetal thymus (treatmental group). The relapse of the disease after half a year, one year and three years was investigated. It was found that the relapse times and relapse rates of the treatmental group at different times were significatly lower than those of the control group, which indicated that transplantation of fetal thymus could reduce the relapse of this disease.

对51例原发性肾病综合征患儿进行了治疗效果和复发情况观察,其中25例原发性肾病综合征患儿采用标准泼尼松中长程疗法作为对照组,其它26例采用标准泼尼松中长程疗法加胚胎胸腺移植作为治疗组,观察两组治疗半年、1年和随访3年的复发情况。结果表明:加用胚胎胸腺移植的治疗组在各病期的复发次数,复发率均明显低于对照组(P<0.01),表明胚胎胸腺移植治疗,可减少该病的复发。

In order to study whether there was rejection in brain tissue transplantation, the embryonic cerebral neocortex from rat or mouse donors which were 16 to 18-day-old embryos was grafted into the neocortex of adult recipient rats. One group was treated with Cyclosporin A. At different thae after transplantation, the brain graft tissues were gtained immunocytochemically to examine the expression of MHC-class Ⅱ antigens and subsets of T-cells. The results indicated that the survival rate of treatment...

In order to study whether there was rejection in brain tissue transplantation, the embryonic cerebral neocortex from rat or mouse donors which were 16 to 18-day-old embryos was grafted into the neocortex of adult recipient rats. One group was treated with Cyclosporin A. At different thae after transplantation, the brain graft tissues were gtained immunocytochemically to examine the expression of MHC-class Ⅱ antigens and subsets of T-cells. The results indicated that the survival rate of treatment group with immunosuppressant was higher than that of nontreatment group. Immunocytochemical evaluation showed that a large number of T-cells appeared. A significant increase of the number of class Ⅱ major histocompatibility complexes (MHC) expressing cells was found within and around the allografts. We conclude that the CNS is not an "immunologically privileged site" and there is graft rejection existing in brain transplantation. It is necessary to treat brain transplant with immunosuppressant.

为了解脑组织移植是否存在排斥反应,将胎龄16~18天的同种及异种股脑皮质组织移植到Wistar大鼠预制脑腔内。术后给予环抱素A治疗。移植后动物在不同时间内分批处死,进行免疫组织化学染色,了解移植区局部T淋巴细胞亚群浸润情况及主要组织相容性复合物(MHC)Ⅱ类抗原的表达情况。结果显示同种移植治疗组的存活率明显高于同种移植未治疗组,在移植区发现大量T淋巴细胞表面抗原及MHCⅡ类抗原的表达,说明在移植区存在排斥反应。表明脑组织不是免疫特免器官,应用免疫抑制剂可有效增加移植物的存活率。

 
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