1)NPM1 gene mutationNPM1基因突变
1.The NPM1 gene mutations were found in 7 out of 19 patients with normal karyotype and their incidence was significantly higher than that in patients with karyotypie abnormalities(1/14,7.本研究旨在探讨急性髓系白血病(AML)患者NPM1基因突变情况及临床特征。
英文短句/例句
1.Analysis of NPM1 Gene Mutations in Acute Myeloid Leukemia急性髓系白血病NPM1基因突变的研究
2.Research of NPM1 Gene Mutations in Adult Patients with Acute Myeloid Leukemia;成人急性髓系白血病患者NPM1基因突变的研究
3.Establishment and Clinical Application of the Detection of NPM1 Gene Mutations by Real Time Fluorescence Quantitative PCR实时荧光定量PCR检测NPM1基因突变及表达的方法学构建与临床应用
4.Research of NPM1 and FLT3-ITD Gene Mutations in Adult Patients with Acute Myeloid Leukemia成人急性髓细胞白血病NPM1与FLT3-ITD基因突变的研究
5.missense suppressor错义(突变)抑制基因,错义(突变)抑制因子
6.suppressor sensitive mutant抑制基因敏感突变型
7.Mutant Gene "Sparked Art and Culture"基因突变 文明曙光
8.ATP7A Genetic Analysis of Menkes Disease;Menkes病的ATP7A基因突变分析
9.Construction of Streptococcus mutans comE Mutant Strain Using In-frame Deletion System框内缺失突变法构建变形链球菌comE基因突变株
10.Mutation Analysis of Tumor Suppressor Genes (CDH1 and Ago Gene) Related with Gastric Carcinoma;胃癌相关抑癌基因CDH1、Ago基因突变分析
11.constitutive mutant组成性突变[使基因得到组成型表达的突变]
12.ENU-induced Mutagenesis in Mice and Mapping and Cloning Several Mutation Genes;ENU诱导小鼠突变及对部分突变基因的定位克隆
13.Screening Gene Mutations of XRCC4 by Denaturing High-performance Liquid Chromatography变性高效液相色谱法筛选XRCC4基因突变
14.Both frameshift and missense mutations can be suppressed by intragenic suppressors.移码突变和异义突变都能被基因内抑制基因所抑制。
15.Application of Mutation-sensitive Molecular Switch in the Detection of EGFR Mutations Associated with Lung Cancer;基因突变敏感性分子开关在肺癌EGFR基因突变检测中的应用研究
16.Study on OPTN Gene Mutation in Glaucoma Family with MYOC Gene T455K Mutation;MYOC基因T455K位点突变青光眼家系OPTN基因突变的研究
17.A30P and A53T Mutations of the SNCA Gene in α-synucleinopathiesα-突触核蛋白病SNCA基因A30P和A53T的突变筛查
18.Induction mutation of mustard gas at tk locus in L5178Y cellsL5178Y细胞tk基因突变试验评价芥子气致突性
相关短句/例句
NPM1 geneNPM1基因
1.The cDNA and fourth intron sequences of porcine NPM1 gene were cloned,and verified by bioinformatics method.克隆了猪NPM1基因的cDNA和第4内含子序列,并利用生物信息学方法进行验证。
3)mutation[英][mju:'te??n][美][mju'te??n]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。
延伸阅读
[3-(aminosulfonyl)-4-chloro-N-(2.3-dihydro-2-methyl-1H-indol-1-yl)benzamide]分子式:C16H16ClN3O3S分子量:365.5CAS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。
