2) FOXL2
FOXL2基因
1.
The study on FOXL2 gene mutation in a pedigree affected by blepharophimosis ptosis epicanthus inversus syndrome
睑裂狭小综合征一家系的FOXL2基因突变研究
3) mutation
[英][mju:'teɪʃn] [美][mju'teʃən]
基因突变
1.
Detection of P53 gene mutations in 14 tumor cell lines;
14株肿瘤细胞P53基因突变的检测
2.
Aanlysis on acrR、marOR multi-drug regulated gene mutations in clinical isolates of Shigella;
志贺菌临床分离株耐多药与调控基因突变关系
3.
Relationship Between Mutation of Goosecoid Gene and Microtia;
Goosecoid基因突变与先天性小耳畸形的关系
4) Gene mutations
基因突变
1.
Effect of the gene mutations associated with knockdown resistance on sodium channel function in pest insects;
昆虫击倒抗性基因突变对钠通道功能的影响
2.
The structure of sodium channels and gene mutations associated with knockdown resistance in insects;
昆虫钠通道的结构和与击倒抗性有关的基因突变
3.
Objective To investigate the lamin A/C gene mutations in Chinese familial dilated cardiomyopathy.
目的 检测中国人家族性扩张型心肌病核纤层蛋白A/C(Lamin A/C)基因突变情况。
5) genetic mutation
基因突变
1.
Methods PCR technique was used to detect homozygous deletions of exon 1 and exon 2 of p16 gene and DNA sequencing technique was used to detect the genetic mutation.
方法PCR方法扩增p16基因外显子1(E1)及外显子2(E2)、检测等位基因纯合子缺失;紫外分光光度计检测DNA纯度浓度;应用DNA测序方法分析基因突变情况。
2.
This article reviews the genomic structure and genetic mutation of TPMT.
TPMT酶活性降低或缺乏与其基因突变密切相关。
3.
With no evidences,so does biological evolution caused by genetic mutation.
遗传变异不能产生新的物种,也没有证据表明基因突变导致生物进化产生了新物种。
6) genic mutation
基因突变
1.
Study of genic mutation and expression of β-catenin in endometrial carcinoma;
β-连环素表达及基因突变与子宫内膜癌发生发展相关性的研究
2.
Methods:PCR technique was used to detect homozygous deletions of exon 1 and exon 2 of p16 gene and single strand conformation polymorphism (SSCP) technique was used to detect the genic mutation.
方法 :PCR方法扩增p16基因外显子 1(E1)及外显子 2 (E2 ) ,检测等位基因纯合子缺失 ;应用单链构象多态性 (SSCP)方法分析基因突变情况。
3.
Two of the PTGMS lines with the characters, which were due to genic mutation, of complete sterile, stable fertility, lower critical temperature of the transformation and perfect multiplication had been selected and named as Zao 25S and Meixiang 851S,.
将在试验田亲本圃、杂交选育圃发现的雄性不育株进行不育度、不育稳定性、育性转换、起点温度、可繁性及测交恢复力鉴定 ,鉴定出两份不育度彻底、育性稳定、起点温度低、可繁性好的由基因突变引起的具有生产实用价值的两用核雄性不育材料 ,分别命名为早 2 5 S和美香 85 1S。
补充资料：操纵基因突变体
分子式：
CAS号：
性质：因操纵子的操纵基因突变而导致调节蛋白无法与之结合的细菌突变体。其特点是操纵子结构基因所编码的与代谢作用直接有关的酶为组成型表达。
CAS号：
性质：因操纵子的操纵基因突变而导致调节蛋白无法与之结合的细菌突变体。其特点是操纵子结构基因所编码的与代谢作用直接有关的酶为组成型表达。
说明：补充资料仅用于学习参考，请勿用于其它任何用途。
参考词条