gene insertion的例句大全

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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results: the gene insertion was proved correct using pcr and dna sequencing.

结果：PCR及序列分析显示融合基因插入载体正确；

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Conclusion: The ACE gene insertion/ deletion polymorphism is associated with left ventricular hypertrophy in hypertension patients. It is not completed by increasing plasma AT-ⅱ level.

结论：ACE基因插入缺失多态性与高血压左室肥厚有关，但并非通过升高血浆AT-Ⅱ水平实现的。

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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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Objective: To determine angiotension converting enzyme ( ACE) gene insertion/ deletion ( I/ D) polymorphism distribution in Chinese and its relation with serum ACE level.

目的：调查中国人血管紧张素转换酶（ACE）基因的插入／缺失多态性分布与及血清ACE水平的相关性。

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relationship between angiotensin i-converting enzyme gene insertion/ deletion polymorphism and mitral prolapse syndrome

原发性二尖瓣脱垂综合征与血管紧张素转换酶基因I/D多态性的相关性

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Objective To determine angiotension-converting enzyme ( ACE) gene insertion/ deletion ( I/ D) polymorphism distribution in Chinese Xinjiang Uighurs and its relation with serum ACE levels.

目的调查新疆维吾尔族血管紧张素转换酶（ACE）基因I/D多态性分布及其血清ACE水平的相关性。

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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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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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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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Objective: The relationship between the insertion/ deletion polymorphism of angiotensin converting enzyme ( ACE) gene and the susceptibility of kidney-deficiency asthma in children was investigated.

目的探讨血管紧张素转移酶（ACE）基因插入/缺失多态性与肾虚型哮喘病易感性的关系，为今后的连锁分析打下基础。

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Objective To identify the insertion/ deletion ( I/ D) polymorphism of angiotensin converting enzyme ( ACE) gene in Chinese hypertensives complicated with brain infarction.

目的探讨血管紧张素转化酶（ACE）基因插入／缺失（I／D）多态性与中国人高血压病合并脑梗塞的关系。

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Results of the mitochondrial COI gene sequence revealed that deletion/ insertion were detected among COI gene fragments.

结果表明，在COI基因片段中，存在碱基的插入或缺失。

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A lot of repeat sequences, including insert sequences, tandem repeat sequences and long terminal repeat, were predicted, which might be the result of adaption to new environment or the insertion and deletion of gene on a large scale.

预测发现该菌株具有大量的插入序列、串联重复序列和长末端重复序列，其中插入序列的存在暗示该菌株在进化过程中发生了大规模的基因片段插入与缺失。

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There are multiple molecular mechanisms that can cause genetic disorders such as point mutations, splicing site mutation, insertion/ deletion mutations, gene duplication, complex rearrangements and gene copy number abnormalities.

引起遗传性疾病的分子机制有多种，常见的有点突变、小片段插入/缺失突变、拼接位点突变、外显子缺失/重复突变、基因重复和复杂重排及基因拷贝数异常等。

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The study on the cellular and molecular mechanism of the citrus mutated characteristics is particularly introduced. The research on citrus bud mutation is focusing on retrotransposon insertion, DNA methylation and the difference of gene structure and expression.

阐述了部分柑橘芽变性状形成的细胞学机理和分子机理，指出目前对芽变的研究主要集中在反转录转座子的插入、DNA甲基化、基因结构和表达差异等方面。

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Genetic analysis showed that the mutant was controlled by a single recessive gene. The ts-ta mutant was not induced by T-DNA insertion though it was screened in T-DNA inserted mutant pools. Therefore, the mutant gene could not be isolated by T-DNA tagging method.

T1、T2及回交结果表明，该突变体能稳定遗传且受一对隐性单基因控制，共分离分析表明该突变性状不是由于T-DNA插入引起的，因此不能通过T-DNA标签法克隆该基因。

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the relationship between deletion/ insertion polymorphism of angiotensin-converting enzyme ( ace) gene and hypertrophic cardiomyopathy ( hcm) was investigated in 35 hcm patients.

为探讨血管紧张素转化酶（ACE）基因缺失／插入多态性与肥厚型心肌病（HCM）发病的关系，对35例HCM患者进行了检测。

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T-DNA insertion mutants library will provide a main resource to study gene function.

大规模T -DNA 标签库创建将成为高通量研究水稻基因功能的主要工具.

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A rolled-leaf mutant was obtained in a T-DNA ( containing bar gene and Ds element) insertion population, which consist of transgenic japonica rice Zhonghua 11 mediated by Agrobacterium tumefaciens.

在根癌农杆菌介导的T-DNA（携带有除草剂Basta抗性基因bar和Ds因子）转化中花11水稻群体中，获得了一个叶片发生明显内卷的突变体R1-A。

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