查询词典 mutations

PCR products of isolates that rpoB gene mutations were not found with PCR-SSCP were sequenced using double deoxidization chain terminating.

并对其中19株SSCP阴性的耐RFP株用双脱氧末端终止法进行测序分析。

PCR products of isolates that rpoB gene mutations were not found with PCR-SSCP were sequenced usˉing double deoxidization chain terminating.

并对其中19株SSCP阴性的耐RFP株用双脱氧末端终止法进行测序分析。

Secondly, we discuss the features of prediction models GM (1, 1) and SCGM (1, 1), and indicate that both are modeling methods for energy system, in which GM (1, 1) model requires a tiny develop coefficient while SCGM (1, 1) model not, while both are sensitive to disturbances and mutations.

讨论了GM（1，1）预测模型和SCGM（1，1）预测模型的特点，指出两者都是对能量系统建模的方法，其中GM（1，1）模型要求发展系数较小，而SCGM（1，1）模型则无此要求，两者对于扰动和突变都相当敏感。

These mutations will lead to potential variation in the secondary structure of TIR.

这些突变都可能造成TIR二级结构变化。

Background Slowly activating delayed rectifier potassium currentI_(Ks is important in therepolarization of human cardiomyocyte action potential,especially in forming andmaintaining plateau of action potential. I_ channel is combined byαandβsubunits,which are coded by KCNQ1 and KCNE1 respectively. Mutations ofhKCNQ1/hKCNE1 genes,chronic myocardial hypertrophy and chronic heartfailure will lead to dysfunction of I_ and ingenital or acquired LQTS which areimportant factor in hazardous ventricular arrhythmia such as Torsade depoints.

实验背景缓慢激活延迟整流钾电流I_(Ks是参与人心肌细胞动作电位复极，特别是平台期形成与维持的重要外向离子流。I_通道由KCNQ1基因编码的α亚单位及KCNE1基因编码的β亚单位组成。hKCNQ1/hKCNE1基因突变或慢性心肌肥厚、慢性心力衰竭等病理过程均可导致I_功能异常，引起遗传性或获得性长QT综合征，LQTS易引起尖端扭转型室性心动过速等心律失常，从而危及病人生命。

Mutations in treacle lead to Treacher Collins syndrome, an autosomal dominant disorder of craniofacial development.

Treacle蛋白突变会导致Treacher Collins症候群，此疾病是一种体染色体显性遗传的颅颜发育异常。

Lara made up imaginary records and pasts for a pair of nuclear researchers named Bert and Jennifer Kelly, neither of whom had mutations of their own, and explained to Alatan that her mutation was the result of a sperm cell failing to undergo meiotic division, which necessitated an in-depth discussion of chromosomes, DNA replication, and Alatan's own syndrome of triploidy.

资料似乎使 Alatan 失望--她绝望地想要相信她的父亲仍然是活著的向那边，和像她自己一样的一个突变异种，取而代之的是一个是死的正常人类当做

The other two were nonsense mutations that would also truncate the protein.

另2个为单碱基置换的无义突变。

Mutations in the cationic trypsinogen gene (PRSS1) have been detected in patients with hereditary pancreatitis.

阳离子胰蛋白酶原基因1突变在遗传性胰腺炎患者中被检测出来。

But when there are mutations in either molecule, they become uncoupled.

但是，当两个分子中任一发生突变，他们的作用就会分离。

This one mode pays close attention to network credence foundation of the businessman very much.

这一模式非常关注商人的网络信用基础。

Cell morphology of bacterial ghost of Pasteurella multocida was observed by scanning electron microscopy and inactivation ratio was estimated by CFU analysi.

扫描电镜观察多杀性巴氏杆菌细菌幽灵和菌落形成单位评价遗传灭活率。