突变的

Of the 150 patients screened for KRAS mutations, 26 (17.3%) patients were identified.

本研究中并未发现UGT1A7 基因多型性与KRAS 基因突变的发生具有显著之相关性。

Objective:Our aim was to study the relationship between factor v Leiden mutation and Chinese Budd-Chiari syndrome.

目的：探讨国人布-加综合征与凝血第Ⅴ因子Leiden突变的相关性。

Results Fifty-eight chronic liverish patients and 13 ASC persons were detected, in which HBV DNA levels with A83 mutations (log10) were (5.37±0.60),(4.02±0.51) copiesml^(-1) respectively. Ten blood donors were not found HBV A83 mutations.

结果 有HBV DNA前C区A83位点突变的58例慢性肝病患者血清中病毒变异株DNA水平为(5.37±0.60)copiesml^(-1)，13例无症状病毒携带者血清中病毒变异株DNA水平为(4.02±0.51)copiesml^(-1)，两者比较，t=7.54，P.001，差异有高度显著性；10例献血员血清中未检测到A83病毒变异株。

The PCR-SSP may be used for genotyping in mutational mononucleatide, and it has a good prospects.

PCR-SSP可对具有单核苷酸突变的基因分型，应用前景良好。

It is not factual or logical to deduce human evolution according to Neo-Darwinism s minority mutation.

按照小群突变的新达尔文主义来推断人类进化，既缺乏事实根据，也有悖于逻辑推理。

All available data suggest arg-13 plays a major role in mitochondrial ornithine transport.

已有报道arg-13为嘧啶合成代谢途径里pyr-3突变的部分抑制基因，序列分析表明arg-13编码一线粒体转运酶。

ObjectiveTo study the relationship between fluoroquinolone resistance in Neisseria gonorrhoeae and mutations in gyrA and/or parC genes.

目的研究淋病奈瑟球菌耐氟喹诺酮类药物与gyrA和parC基因突变的相关性。

Objective: To explore the characteristics of germline APC gene mutations in Chinese patients with familial adenomatous polyposis.

目的：探讨国人家族性腺瘤性息肉病患者APC基因胚系突变的特点。

There is always an element of presto chango in international relations.

国际关系总是存在着突变的因素。

Enzyme that directly reverses pyrimidine dimers, which usually are caused by UV light.

直接逆转嘧啶二聚体突变的酶。

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。