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   肾母细胞瘤 在 泌尿科学 分类中 的翻译结果: 查询用时:1.588秒
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肾母细胞瘤     
相关语句
  nephroblastoma
    Expression of Telomerase and Effect of Vitamin A in Development of Nephroblastoma
    肾母细胞瘤发生发展过程中端粒酶的表达和维生素A的影响
短句来源
    Cystic Partially Differentiated Nephroblastoma
    囊性部分分化性肾母细胞瘤
短句来源
    TREATMENT AND PROGNOSIS OF INFANT NEPHROBLASTOMA
    小儿肾母细胞瘤的治疗与预后
短句来源
    Diagnostic and Therapeutic Experiences of Nephroblastoma:An Analysis of 33 Cases
    肾母细胞瘤33例诊治经验
短句来源
    Adult nephroblastoma(report of 12 cases)
    成人肾母细胞瘤(附12例报告)
短句来源
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  wilms tumor
    Results According to National Wilms Tumor Study(NWTS) staging,there were 3 cases of stage Ⅰ,3 cases of stage Ⅱ,2 cases of stage Ⅲ,and 1 case of stage Ⅳ. Nephrectomy was performed in all patients.
    结果9例患者按照美国国家肾母细胞瘤研究组(National Wilms Tumor Study,NWTS)分期:Ⅰ期3例,Ⅱ期3例,Ⅲ期2例,Ⅳ期1例。
短句来源
    Deletion of WT_1 in wilms tumor.
    肾母细胞瘤WT_1基因缺失
短句来源
    The Relationship of Expression of Gene p16 and p53 with Biological Behavior and Prognosis of Wilms Tumor
    p16和p53抑癌基因在肾母细胞瘤中的表达及与预后关系
短句来源
    Expression of Survivin and Caspase-3 mRNA in Wilms tumor
    Survivin Caspase-3 mRNA在肾母细胞瘤中的表达及意义
短句来源
    Imaging Diagnosis of Adult Wilms Tumor (a Report 7 Cases)
    成人型肾母细胞瘤影像学诊断(附7例报告)
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  wilms ' tumor
    A study of correlation between of occurrence of Wilms' tumor with p53 tumor suppressor gene mutation
    小儿肾母细胞瘤的发生与p53抑癌基因突变关系的研究
短句来源
    Objective To investigate the methods of diagnosis and treatment of adult Wilms' tumor.
    目的探讨成人肾母细胞瘤的诊断和治疗方法。
短句来源
    Methods Retrospective analysis of clinical data of 9 cases of adult Wilms' tumor were conducted.
    方法回顾性分析9例成人肾母细胞瘤的临床表现、分期、治疗及预后。
短句来源
    Immunohistochemical study on P53 in Wilms' tumor
    肾母细胞瘤P53基因的免疫组化研究
短句来源
    The Treatment and Prognosis of Wilms' Tumor in 158 Cases
    158例肾母细胞瘤治疗与预后因素分析
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  wilms ' tumors
    Screening the WT1 Gene Mutations in 24 Cases of Wilms' Tumors
    24例肾母细胞瘤WT1基因突变筛查
短句来源
    The expression of Th1/Th2 cytokines in children with Wilms' tumors
    肾母细胞瘤Th1/Th2类细胞因子的表达
短句来源
    The gene expression of Th1/Th2 cytokines was detected by RT PCR and observed the expression and switch in postoperation of Th1/Th2 type cytokines in children with Wilms' tumors .
    采用逆转录聚合酶链反应 (RT- PCR)技术 ,检测正常儿及肾母细胞瘤患儿肿瘤组织、手术前后外周血Th1/ Th2类细胞因子的基因表达 ,观察肾母细胞瘤患儿手术前后 Th1/ Th2类细胞因子的表达和漂移情况。
短句来源
    Results Wilms' tumors appeared in solid masses in 34 cases (76%),cysticsolid masses in 9 cases(20%),cystic masses in 2 cases (4%),7 cases (15.6%)had thrombosis in renal vein or IVC.
    结果 肾母细胞瘤表现为实性肿块34例 (76 % )、囊实性 9例 (2 0 % )、囊性 2例 (4% )。
短句来源
    Objective To determine the WT2 gene among IGF2 , H19 and p57kip2 genes and to investigate the potential disease gene for Wilms' tumor by comparing the abnormal expressions of IGF2 , H19 , p57kip2 and WT1 genes in tumorigenesis of Wilms' tumors.
    目的 通过比较IFG2、H19、P5 7kip2及WT1基因在肾母细胞瘤中的表达 ,研究可能的WT2基因及与肾母细胞瘤发病相关的重要致病基因。
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      nephroblastoma
    The localization and development of nephroblastoma overexpressed gene (nov) protein-immunoreactive neurons in the brain of E8-P300 rats have been studied using immunocytochemistry and image analysis.
          
    Using human nov (nephroblastoma-overexpressed, nov) DNA as probe, hybridization to total cellular DNAs of tumor and normal cells digested by restriction enzymes BamHI or EcoRI respectively was carried out through Southern blot.
          
    Two large cooperative groups prospectively studied children with nephroblastoma: the National Wilms' Tumor Study Group, and the International Society of Paediatric Oncology.
          
    Advances in clinical management of children with nephroblastoma are also outlined.
          
    Clinical impact of histologic subtypes in localized non-anaplastic nephroblastoma treated according to the trial and study SIOP-
          
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      wilms tumor
    Other attractive targets are the Wilms' tumor 1 antigen and the PR1 epitope from proteinase 3, a granule protein overexpressed in CML.
          
    Recent progress in the biology and treatment of Wilms' tumor
          
    The survival rate of patients with Wilms' tumor has rapidly improved in the last few decades.
          
    As we enter into the new millennium, overall survival for all Wilms' tumor patients exceeds 80%.
          
    Two large cooperative groups prospectively studied children with nephroblastoma: the National Wilms' Tumor Study Group, and the International Society of Paediatric Oncology.
          
    更多          
      wilms ' tumor
    Other attractive targets are the Wilms' tumor 1 antigen and the PR1 epitope from proteinase 3, a granule protein overexpressed in CML.
          
    Recent progress in the biology and treatment of Wilms' tumor
          
    The survival rate of patients with Wilms' tumor has rapidly improved in the last few decades.
          
    As we enter into the new millennium, overall survival for all Wilms' tumor patients exceeds 80%.
          
    Two large cooperative groups prospectively studied children with nephroblastoma: the National Wilms' Tumor Study Group, and the International Society of Paediatric Oncology.
          
    更多          
      wilms ' tumors
    Although rare, renal side effects have also been documented, leading to acute renal failure and even Wilms' tumors in isolated cases.
          
    Rezidiv eines Wilms' Tumors nach 9j?hrigem krankheitsfreien Intervall
          
    An unusual case of rebound thymic hyperplasia is described, presenting five years after completion of chemotherapy for Wilms' tumors.
          
    This case of nephroblastomatosis demonstrates the whole spectrum of abnormalities from local regression to formation of true Wilms' tumors bilaterally over a 4-year period.
          
    Commentary: Imaging and staging of Wilms' tumors: Problems and controversies
          
    更多          


    Two cases of cystic partially differentiated nephroblastoma are reported, Grossly, the lesion is polycystic in appearance. Microscopically the cysts vary in size and are lined by cuboidal or flattened epithelial cells. Highly differentiated nephroblastoma elements can be seen in the septa of the cysts. This tumor may have its origin in the metanephrogenic blastoma, occurs frequently in children under 2 years of age, and is benign in nature. Quite a few terms have been applied to this disease, however in the...

    Two cases of cystic partially differentiated nephroblastoma are reported, Grossly, the lesion is polycystic in appearance. Microscopically the cysts vary in size and are lined by cuboidal or flattened epithelial cells. Highly differentiated nephroblastoma elements can be seen in the septa of the cysts. This tumor may have its origin in the metanephrogenic blastoma, occurs frequently in children under 2 years of age, and is benign in nature. Quite a few terms have been applied to this disease, however in the author's opinion, the term cystic partially differentiated nephroblastoma seems to be appropriate. It should be classified as a subgroup of nephroblastoma.

    本文报告2例罕见的儿童肾肿瘤。大体特征为多囊。镜下,囊大小不一,多由立方形到扁平上皮细胞衬覆;囊之间的间隔中,见典型肾母细胞瘤的某些成分,但分化较高、量较少。组织发生,可能与肾母细胞瘤相同,起源于后肾胚芽。该瘤多见于2岁以下儿童,绝大多数为良性。文献中名称甚多,以称囊性部分分化性肾母细胞瘤较为恰当,可列为肾母细胞瘤的亚型。

    Multilocular cystic nephroma(MCN)is a very rare renal tumor. Histogenesis of the tumor has not been clarified and the designation has been confused. Both the clinical and pathologic manifestations are similar to nephroblastoma and renal cystic diseases in some ways. The prognosis is very good.

    多房囊性肾瘤是十分罕见的肾脏肿瘤,其组织起源不清,命名混乱,临床表现和病理形态学与肾母细胞瘤以及多囊性肾脏病变有相似之处,而治疗和预后与Wilm’s瘤却有很大差别。本文报告1例,综合文献对其命名、组织发生和病变性质、病理特征、鉴别诊断、治疗及其预后进行讨论。

    Fifty cases of Wilm's tumor in children are analysed. Ninety per cent of the patients were children under the age of 5 years. According to NWTS-Ⅲ's classification, Ⅰ-Ⅱ stages accounted for 64%, Ⅲ-Ⅳ stages for 36%. Nephrectomy was performed in 43 eases. Thirty-eight cases were followed up for 4 months to 10 years. The over-all two-year survival rate was 57.7%, stage Ⅰ-Ⅱ was 82.6%. The diagnosis and treatment of Wilms' tumor are discussed in details. Early diagnosis andpostoperative individual therapy should be...

    Fifty cases of Wilm's tumor in children are analysed. Ninety per cent of the patients were children under the age of 5 years. According to NWTS-Ⅲ's classification, Ⅰ-Ⅱ stages accounted for 64%, Ⅲ-Ⅳ stages for 36%. Nephrectomy was performed in 43 eases. Thirty-eight cases were followed up for 4 months to 10 years. The over-all two-year survival rate was 57.7%, stage Ⅰ-Ⅱ was 82.6%. The diagnosis and treatment of Wilms' tumor are discussed in details. Early diagnosis andpostoperative individual therapy should be emphasized.

    本文总结了小儿肾母细胞瘤50例,获得随访38例,2年总存活率57.7%,其中Ⅰ~Ⅱ期2年存活率达82.6%。结合文献重点讨论了肾母细胞瘤的诊断和治疗。

     
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