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- A deletion mutation with frameshift of neurofibromatosis type 2 gene was detected by DNA sequencing. 以DNA序列分析出,在第二型纤维细胞瘤基因上发生染色体缺失造成移码突变。
- Objective:To understand large scale deletion mutation in mitochondrial DNA(mtDNA) and its significance. 目的:了解线粒体DNA大片段缺失突变及其意义。
- Recent researches indicate that the deletion mutation of MEF2A can attenuate the transcription activation,result in the dysplasia of blood vessel endothelium and stimulate the pathogenesis of coronary artery diseases. 近期研究表明,冠心病易感基因MEF2A的突变会影响其转录产物MEF2A蛋白的空间构象,减弱其在肌细胞信号介导的转录激活效能,进而导致血管内皮发育不良、单核细胞浸润,启动动脉粥样硬化斑块的形成。
- AML 1 gene abnormalities, including both chromosome translocation and mutation (point mutation, insertion, deletion mutation, et al), which lead to the lost of transcript activation, are general in acute leukemia. 在急性白血病中常见AML1基因结构异常,包括平衡易位及突变(如点突变、插入或缺失突变等),导致AML1的转录活性丧失,提示此基因功能缺失在急性白血病的发生及发展中起着重要作用。
- Deletion mutations in parkin gene can be detected both in patients with EOP and in patients with LOP. 无论是EOP还是LOP患者中均可检测到parkin基因突变。
- The detected ratios of pre-S2 start codon and pre-S deletion mutations were significantly higher in genotype C than in genotype B (43.04% vs 1.23%, 36.71% vs 19.75%, P < 0.05, respectively). C基因型前S2起始码变异的检出率为43.;04%25;高于B型的1
- According to sequence and aligning HBV BCP and PreC gene, we found the mutations of BCP were grouped in TA1 TA2 and TA3 of TATA-like boxes. There were no insertion or deletion mutations, which were different from the report of Dong jing in Beijing. 通过测序和比对分析HBV BCP和PreC基因序列,发现BCP变异主要集中在TATA样盒的TA1、TA2、TA3,未见插入和缺失突变,与北京董菁的报道显著不同。
- Our teacher has mutation of sounds suddenly. 我们的老师突然语音发生了变化。
- Study on a New Domain in Rat Ribosomal RNA and the Deletion Mutation of Cinnamomin A-chain 大鼠核糖体RNA一个新的结构域以及辛纳毒蛋白A链缺失突变的研究
- The Construction of pCMV-BD-ZNF424 and pCMV-Tag2-ZNF424 Deletion Mutation Recombinant Plasmids pCMV-BD-ZNF424和pCMV-Tag2-ZNF424缺失突变重组质粒的构建
- Keywords FKN;CX3CR1;Homonid;Old World Monkey;gene coevolution;negative selection sites;Darwinian positive selection sites;deletion mutation;structure and function; 人猿超科;旧大陆猴;基因协同进化;负选择位点;达尔文正选择位点;缺失突变;结构与功能;
- coli argS, a series of deletion mutations was constructed. 为了研究大肠杆菌argS的表达调控 ,构建了一系列的缺失突变。
- deletion mutations of Asp 95 ,Lys 96 ,Gly 97 ,Tyr 98 in CDR3; 在CDR3区缺少Asp95,Lys96,Gly97,Tyr98氨基酸残基。
- Formation or development of a mutation. 变异的形成或者发展
- To undergo or cause to undergo mutation. 经历变化或使经历变化
- Subdomain scheduled for deletion! 子域名计划删除!
- Mutation are produced by a number of chemicals. 许多化学试剂能产生突变。
- I think this section can the deletion. 我认为这一段可以删掉。
- To mark with a sign indicating deletion. 用删去符号标记出来
- Deletion of typed or printed matter. 注销删除打印的或印刷的内容