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- adenine nucleotide deaminase 腺苷酸脱氨酶
- nucleotide deaminase 核苷酸脱氨酶
- It also carries a specific nucleotide sequence, the anticodon. 它还带有特定的核苷酸序列即反密码子。
- Thymine or thymine nucleotide concentration was all disqulified. 胸腺嘧啶或胸腺嘧啶核苷均不合格。
- The smallest unit of DNA at which a mutation can occur; a nucleotide. 突变子能够产生巨变的脱氧核糖核酸的最小单位；一个核苷酸
- The smallest unit of DNA at which a mutation can occur;a nucleotide. 突变子能够产生巨变的脱氧核糖核酸的最小单位;一个核苷酸
- The nucleotide contents in erythrocytes of 8 diabetics were determined by HPLC. 本文采用HPLC法测定了8例糖尿病患者红细胞的核苷酸含量。
- A nucleotide molecule that consists of a combination of two nucleotide units. 二核苷酸两个单核苷酸结合而成的核苷酸分子
- The nucleotide sequence of this fragment is obtained by primer walking method. 通过引物步行法测定了该插入片段的核苷酸序列。
- Software solution that provides a visual interface to nucleotide mutations. 为核甘酸突变提供视觉介面的软件解决方案。
- Nucleotide takes part in the synthesis, and metabolism of genetic materials. 核苷酸可参与遗传物质的合成与代谢。
- A set of three nucleotide bases on an mRNA molecule is called a codon. 翻译是在细胞质中进行的。它是指以信使RNA为模板，合成具有一定氨基酸顺序的蛋白质的过程。）
- A group of 39 patients of advanced schistosomiasis were tested for serum monoamine oxidase (MAO) and another 72 for adenosine deaminase (ADA). 测定了39例晚期血吸虫病患者血清单胺氧化酶(MAO)及72例晚血患者血清的腺苷脱氨酶(ADA)。
- Objective To investigate the clinic value of serum adenosine deaminase(ADA)and cholinestetase(CHE)in liver diseases. 目的探讨血清腺苷脱氨酶(ADA)和胆碱酯酶(CHE)在肝病中的临床价值。
- The strain of Bacillus magterium AS1.127-NJU10 was firstly selected with high phenylalanine deaminase activity. 选育出一株具有较高苯丙氨酸脱氨酶活性的菌株巨大芽孢杆菌AS1.;127-NJU10。
- The ADEAMc domain is essential for the deaminase activity of the ADAR encoded protein. ADEAMc区域是ADAR蛋白发挥腺苷脱氨酶作用的重要区域,但目前尚未发现基因型和表型之间的明确相关性。
- Piras MA.Adenosine deaminase activity in pleural effusion aid to differential diagnosis[J].Br Med J,1978,2:1751. 费晓峰;黄祖荪;陈光伟;等.;腺苷脱氨酶活性测定对诊断结核性胸腹水价值的探讨[J]
- Objective To study the continuous monitoring method of adenosine deaminase (ADA) and its clinical application. 目的探讨应用连续监测法测定腺苷脱氨酶(ADA)及其临床应用价值。
- In non-coding region it shows mutation of single nucleotide deletion or substitution. 非编码区亦存在单个碱基缺失及置换突变。
- Kobaysahi F,Ikeda T,Marumo F,et al.Adenosine deaminase isoenzymes in liver disease. Am J Gastroenterol,1993（88）:266. 侯振江，张宗英，张淑敏.;腺苷脱氨酶测定的临床应用
