deletion

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。

Information must be stored so that it is secure from accidental deletion.

必须把资料保存起来，这样才不至于无意中删除。

There was a wide spectrum of mutation type including frame shift, nonsense, splice site mutation, in frame insertion or deletion and missense mutations.

突变类型包括移码突变、无义突变、剪接异常、框架内插入或缺失以及错义突变。

Conclusion GSTM 1 gene deletion is not related to senile cataract formation.

结论GSTM1基因缺失与老年性白内障的发生缺乏显著关系.

Any deletion or amendment must be initialed by the Customer.

3任何删除或修改必须由客户签署作实.

However, in each case the justification for the deletion shall be explained fully in writing.

每个机关还应备有现行的文件索引供公众查阅和复制.

Schema deletion failed: class is used as poss superior.

架构更新失败: 类别作为posssuperior使用.

The Work Deletion and Keystones of Short Message Chicane Casesin Our Country.

我国应对短信诈骗案件的工作缺失及重点.

Study on deletion of HHV 6 gene segment B 701 which can trans activate HIV 1 LTR

反式激活HIV-1LTR的HHV-6基因片段B701的缺失研究

What is more, deletion fitting method is not influenced by slight error of NMO correction velocity. This method can bring a fitted high-resolution P-wave section even though hyperbolae are not flattened thoroughly ( it is not sensitive to this.)

剔除拟合法的另一个优越性还在于它不受动校正速度的微小误差的影响，即使双曲线没有拉平，剔除拟合法对此也不敏感，照样能拟合出分辨率较高的P波剖面来。

The dependency service does not exist or has been marked for deletion.

依存服务不存在,或已被标记为删除.

Elegy of Female Getting Lost& On the Deletion of Female Subject Consciousness in the Film "Nuan"

女性失路的悲歌&论《暖》中女性主体意识的缺失

File shredding function for secure deletion of private, sensitive files and folders.

文件切碎功能,安全删除私人的, 敏感的文件和文件夹.

In this study Insertion/ Deletion molecular markers ( InDel) was first used in indica-japonica genetic differentiation of cultivated rice and identification of the degree of indica-japonica differentiation.

本研究首次采用高效精确鉴定籼-粳分化的插入-缺失分子标记（Insertion/Deletion，InDel），系统阐明栽培品种的籼-粳遗传分化，并定量地确定籼-粳遗传分化的程度。

Schema deletion failed: class is used as auxiliary class.

架构更新失败: 类别作为辅助类别使用.

In non-coding region It'shows mutation of single nucleotide deletion or substitution.

非编码区亦存在单个碱基缺失及置换突变.

Deletion and mutation of CTCF is associated with cancer.

CTCF的缺失和突变可能导致肿瘤的发生.

Administrator tool for secure shredding ( unrecoverable deletion ) of entire IDE disks.

管理员的工具,安全切碎 ( 不可删除 ) 整个IDE磁碟.

This involved the deletion of a great deal of irrelevant material.

这包括删除很大一部分不相关的内容。

We also found lots of insertion and deletion ( INDEL) and microsatellites in schistosome genes.

我们还在血吸虫基因中发现了大量的插入和缺失长度变化以及微卫星位点。

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。

Because of these deletion mutations, functional envelope protein could not be produced. S gene and HBV DNA polymerase gene are completely overlaps, but these variants were still predominant with mutated polymerase. The mechanism and significance were worth in-depth study.

由于复杂突变的变异株不能产生功能性包膜蛋白，S基因与HBV dna聚合酶基因完全重叠，而这类变异株为优势毒株，其机制和意义值得深入研究。

The processes of fingerprint verification, registration and deletion are simplified.

该进程的指纹验证, 登记,并删除简化.

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。

Conclusion The mtDNA deletion is considered to be an important cause of mitochondrial diseases.

结论mtDNA基因缺失是线粒体肌病和脑肌病的重要病因之一。

Folder deletion succeeded, but Netscape was unable to unsubscribe from the folder.

文件夹删除成功, 但netscape还无法撤消订阅这个文件夹.

There were deletion/ insertion variations as trinucleotide repeat sequence in the CAG-rich region of IRS-1 5' flanking region.

IRS-1基因5′调控序列CAG富含区存在以三核苷酸为单位的多种插入／缺失变异。

The most frequent structural variation occur in the chloroplast genome is insertion/ deletion. The probability of its occurrence decreased significantly as its length increases, together with bias of deletions.

叶绿体基因组中发生最多的微结构变化是插入和缺失，插入和缺失随着片段的增大，发生的概率明显下降，并且具有缺失的偏向性。

Through the application of deletion rule, generalization rule and combination rule, the microstructure of a text can be converted into the corresponding macrostructure.

通过运用删略规则、概括规则和组构规则可以将语篇的微观结构或微观命题转换成宏观结构。

Columns cannot be deleted. Column deletion protection is currently enabled.

不能删除列.列删除保护目前处于激活状态.