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human genetic
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  人类遗传
     Research on Primary Application and Establishment of Chinese Human Genetic Resources Description Criteria
     我国人类遗传资源信息描述规范的研究制定与初步应用
短句来源
     The gene complex of Human Leukocyte Antigen (HLA) is located of chromosome 6p21, which is the most complicated dominant polymorphic genetic system. The HLA system has 108 genotypes. It is the best human genetic marker.
     人类白细胞抗原(Human Leukocyte Antigen,HLA)基因复合物定位于人类第6号染色体短臂上,是人类最复杂的显性多态遗传系统,基因型可达108种之多,是理想的人类遗传标记,已广泛应用于法医学亲子鉴定和个体识别。
短句来源
     In this article, after analyzing the question of gene patent, the author discusses the legal status of the donor of human genetic materials, and also give some suggestion on the protection of the donor and compensation of them.
     本文在分析基因专利这一问题的基础上,围绕着人类基因提供者的法律地位问题,就基因研究中的利益分配和个人基因信息的保护及利益补偿这两个方面,提出了笔者的看法:进而对我国《人类遗传资源管理暂行办法》进行评价并提出建议。
短句来源
     (HGRI) Methods: The description criteria of the human genetic resources (HGR) and standard coding system were maped out. It formed the basic system of description criteria and standard for HGR. At the same time, the study designed the project of HGRIS.
     方法:研究制定人类遗传资源描述规范,建立资源分类编码标准,形成人类遗传资源信息描述规范与标准的基本体系,设计人类遗传资源信息共享系统方案,整理、整合和分析我国重要人类遗传资源信息,并对其中部分信息资源进行应用研究;
短句来源
     Objective:Looking for the human phenotype blemish caused by injured DNA,collecting and storing the human genetic resources are necessary in order to study the structure and function of the human genes.
     目的寻找由DNA损伤引起的人类表型缺陷,为人类遗传资源的收集与保藏以及人类基因结构与功能的研究打下基础。
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  人类遗传性
     Rab27A is a unique member in the Rab family and has specific implications in human genetic diseases.
     Rab27A是这一家族中唯一一个明确涉及到人类遗传性疾病的成员。
短句来源
     Exploration of Connexin Gene mutations and Human Genetic Diseases
     连接蛋白基因突变与人类遗传性疾病关系的研究进展
短句来源
     The roles that the abnormal changes in genetic imprinting and its supervising mechanism play in the pathogenesis of human genetic disorders,especially in the carcinogenesis is getting more and more attention.
     印迹基因及其控制机制的异常(如 :印迹丢失、杂合性丢失、染色体单亲双体性以及突变失活等)在人类遗传性疾病尤其是肿瘤发生中的作用正引起越来越多的注意。
短句来源
     As far as human genetic syndrome is concerned,we have developed the study on the genetics of the syndrome.
     提出针对人类遗传性证候的出现 ,开展“证候遗传学”研究 ;
短句来源
     More and more researches showed that connexin genes mutations were closely associated with human genetic diseases.
     越来越多的研究表明,连接蛋白基因突变与人类遗传性疾病密切相关。
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  “human genetic”译为未确定词的双语例句
     Molecular cloning on(GCCT)_n·(CAGC)_n repeat sequences associated with human genetic diseases
     与人遗传病相关(GCCT)_n·(CAGG)_n重复序列的分子克隆
短句来源
     The Study of Association between the Human Genetic Mark (STR, HLA) and Longevity
     人类基因遗传标志物(STR,HLA)与男性长寿关联性的研究
短句来源
     Study on Family Collection,Gene Mapping,Gene Identification and Gene Function of Human Genetic Diseases
     人类遗传病的家系收集疾病基因定位克隆与疾病基因功能的研究
短句来源
     PRENATAL DIAGNOSIS OF HUMAN GENETIC DISEASES Ⅰ. REPORT ON RESULTS OF DIAGNOSIS OF 100 PREGNANCIES AMNIOTIC FLUID CULTURE
     遗传疾病的产前诊断——Ⅰ.羊水细胞培养和产前诊断一百例结果报道
短句来源
     MOLECULAR GENETIC STUDY ON HUMAN GENETIC SUSCEPTIBILITY TO STREPTOMYCININDUCED DEAFNESS
     人体对链霉素致聋遗传易感性的分子遗传学研究
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  human genetic
Duchenne dystrophy, one of the most widespread human genetic diseases, is at the same time the most extensively studied from the viewpoint of both genetic and histological changes leading to muscle fiber degeneration.
      
We discuss examples of the rare human genetic instability syndromes as they present themselves at the chromosome, telomere, and nuclear envelope level.
      
Mitochondrial disorders are human genetic diseases with extremely variable clinical and genetic features.
      
Definition of the problem:The frequency and scope of human genetic banking has increased significantly in recent years and is set to expand still further.
      
Collecting families: An institutional approach to human genetic biobanking in Indonesia
      
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In China, the research on prenatal diagnosis of human genetic diseases has just begun. The results of diagnosis of 100 pregnancies are presented in this report. Among these cases, 71% (71 out of 100 eases) were chromosome analysis. The remainders (29%) were neural tube defects (table 1). Four cases of neural tube defects, one case of balanced chromosomal translocation [i.e. 46, XY, t(4;5) (4pter →4q 35:: 5q 13→ 5qter; 5pter→5q 13:: 4q 3 5→4qter) ], and two cases of sex-linked diseases were aborted. The...

In China, the research on prenatal diagnosis of human genetic diseases has just begun. The results of diagnosis of 100 pregnancies are presented in this report. Among these cases, 71% (71 out of 100 eases) were chromosome analysis. The remainders (29%) were neural tube defects (table 1). Four cases of neural tube defects, one case of balanced chromosomal translocation [i.e. 46, XY, t(4;5) (4pter →4q 35:: 5q 13→ 5qter; 5pter→5q 13:: 4q 3 5→4qter) ], and two cases of sex-linked diseases were aborted. The prenatal diagnosis of balanced translocation and X-linked diseases were discussed.

遗传疾病的产前诊断技术在我国才刚刚开展。本文报道总结一百例染色体和甲胎蛋白宫内检查的结果。其中一例平衡易位、4例无脑畸形及两例性连锁遗传疾病,胎儿被流产。由此表明产前诊断是预防某些遗传疾病的有效措施之一。

Since the HLA system is one of the most complex human genetic polym- orphisms,its application in forensic medicine included disputed paternity and criminal identification,have been fairly recognized. The present paper reported the results of our study about the HLA typing in human blood stain,serum and saliva,it was concluded that:(1).The existed strong anti-complementary activity in human blood stain when the amount of complement used in microlym-phocytotoxicity inhibition test(MLIT) was incresed...

Since the HLA system is one of the most complex human genetic polym- orphisms,its application in forensic medicine included disputed paternity and criminal identification,have been fairly recognized. The present paper reported the results of our study about the HLA typing in human blood stain,serum and saliva,it was concluded that:(1).The existed strong anti-complementary activity in human blood stain when the amount of complement used in microlym-phocytotoxicity inhibition test(MLIT) was incresed to 10μl,it was found that the results of HLA-All,-B 5 typing in bloodstains were all correct,and the detectable period was at least 90 days; (2).The soluble HLA-A antigens in human serum could reliable detected with MLIT;(3).The soluble HLA-A antigens were also present in the human siliva.

HLA 是迄今人类最复杂的遗传多态性系统,其在法医学上的应用,包括亲子鉴定和个人识别的重要性日益被认识。作者等对血痕、血清和唾液的 HLA 测定的研究结果证明:(1)血痕中存在较强的抗补体作用。应用淋巴细胞毒抑制试验测定血痕的 HLA 时,增加补体用量可使测定的正确率达100%,经90天的血痕仍能完全正确检出 HLA 型。(2)血清的 HLA 测定是可行的,这对远道送检血清及尸体血清测定 HLA 有一定价值。(3)唾液中有可溶性 HLA 抗原存在。

Through discussing and and-lyesing the relation between human genetic quality and eugenics, The author points out the impr-ovent of human genetics depends opon envioment affection after being born, and also upou the guide of eugenics.The articl aims to aduance eugenics and increase human quality.

本文分析并讨论了人类遗传素质和优生之间的关系,旨在推动优生运动的深入开展,提高人口素质.

 
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