突变的

Objective To explore parkin gene deletion mutations at exons 3 to 7 in Chinese familial patients with Parkinson's disease as well as the association with the clinical features.

目的 探讨中国家族性帕金森病患者parkin基因第 3～ 7外显子是否存在缺失突变，及其与该病临床特点的关系。

To detect the mutation of PINK1 gene in Chinese patients with early onset Parkinsonism by using DHPLC.

应用DHPLC技术对100例EOP患者进行PINK1基因突变筛查，对DHPLC筛查发现异常的PCR扩增片段进行DNA直接测序和分析。

Despite its dominant inheritance pattern, the phenotype is penetrant in only 60% of mutation carriers.

虽然它是显性遗传，但只有60%突变者的显型有穿透。

The half life of mutant A and B improved by 60% and 166% in comparison with parent PGA.

突变A和B在15%DMF中的半衰期分别比亲本PGA提高60%和166%。

These candidates affecting heart mutant phenotype are to be identified.

这些影响心脏突变表型的候选基因还需要进一步鉴定。

It is suggested that the in situ pistil transformation method can be used as a mutagenesis approach.

研究表明本文的转化方法可用于创建突变材料和新种质。

A pitman fractured at the position of abrupt change of cross-section in alignment after assembly.

某连杆在装配后的校直过程中在截面突变处发生断裂。

Results:Mutant CD59 cDNAs subcloned into the mammalian expression vector PLATER and transfected CHO together with the pcDNA,which confered resistance to G418. The positive clones were tested by FIH.

结果：运用阳离子脂质体导入法将重组pALTER质粒与pcDNA3质粒共转染CHO，成功筛选出的阳性克隆经FIH证明突变CD59可在CHO细胞表达。

These results demonstrate that deficiency in fatty acid biosynthesis has pleiotropic effects on plant growth and development, and causes premature cell death.

因此，mod1突变体是研究脂肪酸合成代谢调控及脂肪酸与细胞死亡关系的极好材料。

In addition, exposure to plumbum significantly repressed the LTM at 18, 36, and 48 h after training in both wild-type N2 and ncs-1 mutant animals.

而铅暴露可以显著抑制训练后18、36和48 h野生型和 ncs-1突变体动物在不同时间点下的IT百分数。

The split between the two groups can hardly be papered over.

这两个团体间的分歧难以掩饰。

This approach not only encourages a greater number of responses, but minimizes the likelihood of stale groupthink.

这种做法不仅鼓励了更多的反应，而且减少跟风的可能性。