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1)  S-gene mutaion
S基因变异
2)  S gene mutant
S基因突变
3)  gene mutation
基因变异
1.
Investigation on pre-C and BCP gene mutation of hepatitis B virus DNA in patients with hepatocellullar carcinoma (HCC);
肝癌患者血清中乙型肝炎病毒前C和BCP区基因变异的临床研究
2.
Over the past 10 years, vigorous research has been done on mapping the POAG genes, showing that genetic factors and gene mutation play an important role in POAG.
原发性开角型青光眼(primary open angle glaucoma,POAG)是一种损伤视力及致盲性眼病,近年来越来越多的研究表明基因变异及遗传在POAG的发病中起重要作用。
3.
Objective: To isolate quinolone-resistant Uu (Ureaplasma urealyticum) from clinical isolates and further to determine the gene mutations in QRDRs (quinolone-resistant determining regions) in such resistant isolates.
目的:从临床分离的解脲脲原体中筛选出喹诺酮类药物耐药株,了解耐药株发生的比率,并研究耐药株中喹诺酮抗性决定区域(QRDR)出现基因变异的情况。
4)  Mutation [英][mju:'teɪʃn]  [美][mju'teʃən]
基因变异
1.
Cyclin A1 Mutation May Induce Specific Skin Lesions on the Head and Neck in Mice;
cyclin A1基因变异诱导小鼠发生头颈部皮肤病变
2.
Application of restriction fragment length polymorphism for genotyping in dynamic monitoring of genomic mutations of hepatitis B virus;
RFLP基因分型在动态监测乙型肝炎病毒基因变异中的应用
3.
Objective:To inve s tigate the Trp 64 Arg mutation rate in t he gene for the β 3adrenoceptor and to p robe into the relationship between the r ate and NIDDM and obesity in Chinese.
目的 :观察中国人群β3 肾上腺能受体 (β3 AR)基因 Trp 64Arg的变异频率 ,以及此基因变异与肥胖、胰岛素抵抗及非胰岛素依赖性糖尿病 ( NIDDM)的关系。
5)  genovariation
基因变异
1.
The Laboratory and Clinical Study of Enteroviral Genovariation and Children Central Nerve System Infection;
肠道病毒基因变异与小儿中枢感染的实验和临床研究
6)  Genetic variation
基因变异
1.
Research progress on the association between genetic variations in lipid metabolism and premature coronary artery disease;
脂质代谢相关基因变异在早发冠心病中作用的研究进展
2.
So the first aim of this study is to investigate the genetic variation of NS3 region of hepatitis C virus (HCV) and the role of variant epitope in HCV infection, the second is to find an con.
为此本课题主要从以下两个方面进行研究:一是研究HCV NS3区基因变异和细胞毒T细胞表位改变在HCV感染中的作用;二是寻找相对保守的T细胞表位和初步研究基因免疫在HCV感染防治中得作用,为丙型肝炎的防治打下基础。
3.
Objective To explore the relationship between genetic variations of prostasin gene and essential hypertension(EH) in Xinjiang Kazakhs.
目的探讨新疆哈萨克族prostasin基因变异与原发性高血压的关系。
补充资料:[3-(aminosulfonyl)-4-chloro-N-(2.3-dihydro-2-methyl-1H-indol-1-yl)benzamide]
分子式:C16H16ClN3O3S
分子量:365.5
CAS号:26807-65-8

性质:暂无

制备方法:暂无

用途:用于轻、中度原发性高血压。

说明:补充资料仅用于学习参考,请勿用于其它任何用途。
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