助手标题  
全文文献 工具书 数字 学术定义 翻译助手 学术趋势 更多
查询帮助
意见反馈
   fragile x 的翻译结果: 查询用时:0.007秒
图标索引 在分类学科中查询
所有学科
内分泌腺及全身性疾病
儿科学
妇产科学
精神病学
临床医学
神经病学
更多类别查询

图标索引 历史查询
 

fragile x
相关语句
  脆性x
     Fragile X Mental Retardation Protein Interacts with Human NDK/Nm23-H2
     脆性X智力低下蛋白与NDK/Nm23-H2的相互作用
短句来源
     Progress in research on FMR1 gene in fragile X syndrome
     脆性X综合征FMR1基因研究进展
短句来源
     Screening and Diagnosis of Fragile X Syndrome by PCR
     脆性X综合征的PCR筛查与诊断
短句来源
     The Study of the Variation of CGG Repeat in FMR - 1 Gene of Fragile X Syndrome.
     脆性X综合征FMR—1基因CGG重复数变异的研究
短句来源
     Comparison of Two Methods of DNA Extraction in Detecting Fragile X Syndrome FMR-I Gene
     两种方法提取的DNA在脆性X综合征基因FMR-I检测中的比较
短句来源
更多       
  脆性x染色体
     A clinical and EEG study of fragile X syndrome
     脆性X染色体综合征临床与脑电图的研究
短句来源
     The proband of pedigree A with highexpression of fragile X chromosome(35/273) was detected to be a full mutation patient of fragile X syndrome by the molecular genetic test.
     A家系先证者脆性X染色体高表达(35 273),分子遗传学检查证实为脆性X综合征全突变患者;
短句来源
     130 cases (53.9%) were found to have chromosomal aberrations. 120 cases of Down's Syndrome (Trisomy 21), 4cases of Turner's Syndrome and 6 cases of Fragile X Syndrome.
     染色体异常者130例(53.9%),其中先天愚型120例(49.8%),Turner综合征4例(1.7%),脆性X染色体综合征6例(2.5%)。
短句来源
     Objective To study the clinical and EEG characteristics of fragile X syndrome in pre puberty.
     目的研究青春期前脆性X染色体综合征临床和EEG表现特点。
短句来源
     The four patients all showed fragile X site at q27—28, ranging from 7—13%, The fragile X was found to be positive in one mother carrier.
     4例患者均检出脆性X染色体,频率为7~13%,且fra(x)在X染色体末端q27—28带区。
短句来源
更多       
  “fragile x”译为未确定词的双语例句
     The result shows that RPMI 1640 medium may replace TC199 for testing fragile X chromosome.
     结果表明RPMI1640培养基可代替TC199培养基用于Fra(X)染色体检测
短句来源
     The article is about autism and other related children development disorders,including Angelman syndrome,Asperger syndrome,fragile X syndrome,Landau-Kleffner syndrome,Prader-Willi syndrome,Rett syndrome and William syndrome.
     本文主要介绍自闭症和有关儿童发展障碍 ,包括 Angelman综合征、Asperger综合征、脆弱 X综合征、Landau- Kleffner综合征、Prader- Willi综合征、Rett综合征和 William综合征。
短句来源
     Molecular Mechanism and Cognitive Function of Fragile X Syndrome
     脆X综合征的分子基础及其认知研究进展
短句来源
     Fragile X syndrome (Fra(X)) is the most common form of inherited mental retardation and is associated with a fragile site at Xq27.3. A related gene named FMR1 was isolated and identified from the locus in 1991. FMR1 gene is involved in a large region extending at least 150 kb proximal and 34 kb distal to its 5' end, whose replication is delayed.
     1991年,在该位点克隆鉴定了Fra(X)的致病基因——FMR1。 FMR1基因存在迟复制现象,且与其共同迟复制的区域至少包含该基因5’上游150kb和下游34kb的范围。
短句来源
     The X chromosome disorders such as mutations of the human bone morphogenetic protein-15 gene,the zinc finger protein gene,the X-inactivation-specific transcript gene,the drosophila melanogaster diaphanous gene,the X 2 linked aminopeptidaseP enzyme gene,the fragile X mental retardation gene are associated with POF.
     某些基因(如人骨形成蛋白15基因、锌指蛋白基因、X染色体失活特异转录子基因、人黑色素透明基因、X-脯氨酰氨基肽酶2基因、家族性智力低下1基因、家族性智力低下2基因)可能与卵巢早衰发生有关。 对其发病机制的阐明有助预测可能发病人群,加深对卵巢功能维持机制的了解。
短句来源
更多       
查询“fragile x”译词为用户自定义的双语例句

    我想查看译文中含有:的双语例句
例句
为了更好的帮助您理解掌握查询词或其译词在地道英语中的实际用法,我们为您准备了出自英文原文的大量英语例句,供您参考。
  fragile x
Originally discovered in 1991 upon cloning the gene responsible for the fragile X syndrome, it has proved to be a general phenomenon responsible for a growing number of human neurological disorders.
      
The lab obtained priority results in devising and promoting methods of molecular diagnostics of the most common severe hereditary disorders such as cystic fibrosis, Duchenne muscular dystrophy, hemophilia A, and fragile X syndrome.
      
Fragile X mental retardation protein interacts with TDG
      
Fragile X syndrome is the most common form of inherited mental retardation disease, resulting from absent of expression of its disease geneFMR1.
      
To study the function of the fragile X mental retardation protein (FMRP) through protein/protein interaction, a mouse embryo cDNA library was screened by the yeast two-hybrid system.
      
更多          


A large kindred with fragile X syndrome is reported here. A phenotypicallyand cytogenetically normal male had transmitted the trait through eight ofhis daughters to sixteen of his grandsons and one great-grand son. No signof fragile X syndrome was present in his five sons and their offspring.Two deceased brothers of this man had been mentally retarded and one sisterwas an obligate carrier (with affected male offspring and carrier daughters).Incomplete penetrance appears to account for the normal...

A large kindred with fragile X syndrome is reported here. A phenotypicallyand cytogenetically normal male had transmitted the trait through eight ofhis daughters to sixteen of his grandsons and one great-grand son. No signof fragile X syndrome was present in his five sons and their offspring.Two deceased brothers of this man had been mentally retarded and one sisterwas an obligate carrier (with affected male offspring and carrier daughters).Incomplete penetrance appears to account for the normal phenotype andcytogenetic findings in this male. Unaffected male carriers seem to play animportant role in the transmission of the fragile X syndrome in some Kindred.Geneticists should pay special attention on the "normal" brothers of affectedindividuals. The history, clinical features, cytogenetic findings and preventionof the disease are discussed in this paper.

本文报告一个有24名患者的巨大家系。1例“正常”男性通过8个女儿将本病传递给16个外孙及1个曾外孙。不外显可能是造成这例正常表型与核型的原因。提示:在本病流行病学调查中,除注意男性患者及女性携带者外,对患者的表型正常的兄弟亦不应忽视,以期即时发现男性携带者,减少本病的扩延。

In this paper we have studied four mentally retarded men from a large family The study included clinical investigations and cytogenetic examinations of the patients and their mothers for the fragile X. The four patients all showed fragile X site at q27—28, ranging from 7—13%, The fragile X was found to be positive in one mother carrier. The discovery of fragile X is of paramount importance in prenatal diagnosis and prevention of X-linked mental retardation.

本文对来自同一家系的4例男性智力低下者进行了研究,分析了临床症状,并对患者及其母进行了有关脆性X染色体的细胞遗传学检查。4例患者均检出脆性X染色体,频率为7~13%,且fra(x)在X染色体末端q27—28带区。两例肯定携带者,fra(x)检出率分别为0%、1%。fra(x)的检出对产前诊断和预防X-连锁智力低下有重要意义。

Six families with fragile X syndrome were found from surveying the populations in three cities of Beijing,Shenyang and Qingdao.There are 15 patients with fragile X syndrome and 13 fragile X carriers in these families.Most of patients were moderate mental retardation and have macroorchidism.Half of fragile X female carreirs were mild mental retardation or dull.The frequencies of fragile X chromosome were 1-30% in male patients and 0-7% in female carriers.Three male patients with...

Six families with fragile X syndrome were found from surveying the populations in three cities of Beijing,Shenyang and Qingdao.There are 15 patients with fragile X syndrome and 13 fragile X carriers in these families.Most of patients were moderate mental retardation and have macroorchidism.Half of fragile X female carreirs were mild mental retardation or dull.The frequencies of fragile X chromosome were 1-30% in male patients and 0-7% in female carriers.Three male patients with fragile X syndrome have reproduced some offsprings.The incidence of fragile X syndrome was estimated to be 5.6/10,000 males in 45,498 subjects of Beijing suburb and 5.9/10,060 males in 6,696 children of Shenyang city.Prenatal diagnosis was performed on an indicative female carrier.No fragile X chromosome was found in amniotic fluid cells and a normal baby was born.

从北京、沈阳和青岛等城市的智能低下的群体调查和细胞遗传检查中发现6个脆性X综合征家庭。这些家庭中共有15个脆性X综合征病人,13个脆性X综合征女性携带者。在北京和沈阳两个城市的群体调查中,初步估算脆性X综合征的发病率分别为5.6/10,000男性和5.9/10,000男性。对一例适应症孕妇进行了脆性X综合征的产前诊断。

 
<< 更多相关文摘    
图标索引 相关查询

 


 
CNKI小工具
在英文学术搜索中查有关fragile x的内容
在知识搜索中查有关fragile x的内容
在数字搜索中查有关fragile x的内容
在概念知识元中查有关fragile x的内容
在学术趋势中查有关fragile x的内容
 
 

CNKI主页设CNKI翻译助手为主页 | 收藏CNKI翻译助手 | 广告服务 | 英文学术搜索
版权图标  2008 CNKI-中国知网
京ICP证040431号 互联网出版许可证 新出网证(京)字008号
北京市公安局海淀分局 备案号:110 1081725
版权图标 2008中国知网(cnki) 中国学术期刊(光盘版)电子杂志社