1·Conclusion GSTM1 gene deletion is not related to senile cataract formation.
结论GSTM 1基因缺失与老年性白内障的发生缺乏显著关系。
2·It is also improved M and NS genes by a site mutation and a gene deletion method.
通过点变异和基因删除方法对M和NS基因进行改进；
3·The PMP22 gene deletion detected by gene diagnosis is the golden criterion for the diagnosis of HNPP.
结论电生理检查对HNPP的诊断很重要，基因检测发现PMP22基因缺失是诊断HNPP的金标准。
4·Conclusion There is no difference in frequency of CYP2A6 gene deletion between lung cancer cases and controls.
结论CYP2A6突变基因在肺癌组及对照组中的频率分布没有差异。
5·Dual FISH technique provides specific, sensitive and direct evidence for molecular cytogenetic evaluation of gene deletion in tumors.
双色FISH技术为评估基因的缺失提供了特异、敏感、直观的分子细胞遗传学证据。
6·In the present study, we investigated whether gene deletion of AT2 receptor causes the compensatory chaos of renin-angiotensin system in mice.
依据上述论点，本研究利用AT2受体基因敲出小鼠，观察了AT2受体缺失后是否造成肾素-血管紧张素系统其它成分代偿性紊乱。
7·In all of the 24 bases of mutants, the base replacement occupies about 87.5% of the total mutants with only a small portion of gene deletion (12.5%).
在检测到的24个碱基突变中，主要是碱基的置换(87.5%)，碱基缺失的比例比较小(12.5%)。
8·they observed no instances in the subjects with bipolar illness of the chromosome 22 gene deletion implicated in schizophrenia and the velocardiofacial syndrome.
他们并未观察到22号染色体缺失的躁郁患者实例。这条染色体牵涉到精神分裂症、腭心面综合征。
9·Objective To investigate the relationship between the angiotensin converting enzyme (ACE) gene deletion polymorphism and cerebral infarction, hypertensive cerebral hemorrhage in Chinese.
目的探讨血管紧张素转化酶(ace)基因缺失多态性与中国人脑梗死、高血压性脑出血的关系。
10·The main methods used, or under investigation, for production of rumen gene engineering bacteria are:gene deletion technique, gene recombination technique and the application of promotor.
正在应用的或处于研究阶段的构建瘤胃基因工程菌的方式主要有基因缺失技术、基因复制性重组技术和启动子的应用技术。