RNA editing is the phenomenon of nucleotide insertion, deletion or replacement during RNA maturation, which is a post-transcriptional modification process, including complete editing, partial editing and silence editing.

Objective To investigate the relationship between angiotensin converting enzyme ( ACE) gene insertion/ deletion ( I/ D) polymorphism and the severe morbidity of neonates.

目的检测血管紧张素转化酶（angiotensin converting enzyme，ACE）基因型，探讨ACE基因插入或缺失多态性与新生儿危重症的关系。

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The Relationship between Insertion/ Deletion Polymorphism and Serum Enzyme Levels of the Angiotensin I-converting Enzyme Gene and N-terminal Pro-B-type Natriuretic Peptide in Acute Myocardial Infarction

急性心肌梗塞患者ACE基因插入/缺失多态性与血清ACE，氨基末端脑钠尿肽相关性的研究

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ACE gene was divided into II, DD and ID three genotypes for introne 16, and DD genotype was prominent in cardiovascular system.

ACE基因的16内含子插入或缺失使ACE基因存在3种基因型即II、DD、DI，而其DD型ACE水平最高，且心脏组织中的ACE水平在DD基因型中最高。

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Aim: To explore the polymorphism of angiotensin I converting enzyme gene insertion/ deletion in the patients with myocardial infarction ( MI).

目的：探讨心肌梗死患者（MI）血管紧张素转换酶（ACE）基因插入/缺失多态性。

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Relationship between Angiotension-Converting Enzyme Insertion/ Deletion ( I/ D) Polymorphism and Cerebral Hemorrhage among the Han Chinese Population: A Meta-Analysis

中国汉族人群脑出血患者血管紧张素转换酶基因插入/缺失多态性的Meta分析

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Screening of Rice Chlorophyll Deficient Mutants from T-DNA Insertion Pool and Isolation of Flanking Sequences of T-DNA

水稻T-DNA插入叶绿素缺失突变体筛选及侧翼序列分离

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Methods: I/ D polymorphism of ACE was determined by polymerase chain reaction ( PCR) in 72 normal controls, 78 patients with essential hypertension.

方法：应用聚合酶链反应（PCR）对78例新疆地区原发性高血压患者与72例正常血压对照者ACE基因第16内含子插入/缺失多态性进行鉴定。

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Objective The present study was performed to investigate the correlation between ACE genetic polymorphism and Low/ High-risk Group in acute coronary syndrome.

目的探讨ACE基因插入/缺失（I/D）多态性在急性冠状动脉综合征低/高危人群发病中的作用。

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Perhaps the ancestral role of guide RNAs that direct U insertion and deletion in the related kinetoplastid protozoa was to provide a template scaffold to link modules.

或许，与动基体目原生动物有亲缘关系的原生动物体内的引导尿嘧啶插入及缺失的指导RNA的古老作用就是为模块的连接提供一个模板支架。

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Analysis of insertion/ deletion polymorphisms and Y-SNPs with melting curve genotyping in forensic science

用熔解曲线法分析插入/缺失多态性和Y染色体SNPs多态性

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Meta-analysis on the association of the insertion/ deletion polymorphism of the angiotensin-converting enzyme gene and cerebral infarction in Chinese population

中国人脑梗死ACE基因插入/缺失多态性的Meta-分析

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Meta-analysis on the association between the insertion/ deletion polymorphism of ACE gene and diabetic nephropathy among Chinese population

中国汉族人ACE基因插入/缺失多态性与糖尿病肾病关联性Meta-分析

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Association of insertion/ deletion polymorphism in angiotensin-converting enzyme gene with hypertensive type 2 diabetes mellitus

ACE基因的插入/缺失多态性与2型糖尿病伴高血压的相互关系

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A Study on relationship between Insertion/ Deletion Polymorphism of Angiotensin-Converting Enzyme Gene and Cerebrovascular Disease

ACE基因插入/缺失多态性与脑血管病的关联性研究

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Multiple polymerase chain reaction ( PCR) was used to evaluate the ACE gene I/ D polymorphism.

应用聚合酶链反应（PCR）测定两组ACE基因插入/缺失多态性。

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A study of the I/ D polymorphism of angiotensin I converting enzyme gene in the Muslim and Han in Ningxia rural area and the relationship with essential hypertension

血管紧张素转换酶基因插入缺失多态性在宁夏农村回汉族人群中的分布及其与原发性高血压的关系

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Objective To investigate the relationship between the 4G/ 5G gene polymorphism of the plasminogen activator inhibitor 1 ( PAI 1) and myocardial and cerebrovascular infarctions.

目的研究我国汉族人纤溶酶原激活物抑制物1基因启动子区675位4G5G（单鸟嘌呤核苷酸插入缺失）基因多态性与心肌梗死和脑梗死的等位基因特异性的相关性。

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Simple indel coding plays a different role on the phylogenetic results when percentage of gaps is different.

空位含量不同，简单插入缺失编码对系统发育分析结果的影响力也不同。

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A total sequence of 599 nucleotide base pair was obtained by alignment with homologous sequences of another two Sardinella species in GenBank. There were 445 parsimony-informative sites and 154 variation sites, but no insertion/ deletions were observed.

与GenBank中另外2种小沙丁鱼的同源序列比对，去除部分端部序列后得到599bp同源序列，其中包括445个简约信息位点，154个变异位点，没有发现碱基的插入缺失。

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Among these SNPs, there were no SNPs, insertions or deletions found in the OTC biosynthesis cluster. While in S. rimosus 23383, some SNPs were identified in the primary metabolites related genes.

在这些SNPs之中，与OTC合成基因簇相关的基因中不存在任何SNP和插入缺失，然而在23383菌株中，发现一些初级代谢基因中存在着SNP，这些变化可能最终影响了OTC的生物合成。

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