deletion的例句大全

α-Thalassemia major is a hereditary disease with a syndrome of hemolytic anemia, often caused bv the complete or partial deletion of a-globin genes.

α-地中海贫血是由于α-珠蛋白基因全部和部分缺失所致的一种遗传性溶血性贫血综合征。

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Objective To determine the karyotype of a case with a history of spontaneous abortion and terminal deletion by using of conventional G banding method and search the cause of insertional translocation of chromosomal terminal region.

目的确定一个有反复流产史且常规G显带发现有7q末端缺失病例的核型，探讨染色体末端区域插入易位的形成机理。

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Final results showed that the mutant with N terminal deletion of the first 7 amino acids maintained trace enzymatic activity ( less than 0.5%), while the mutant losing the first more than 8 amino acids was robbed of the enzymatic function completely.

结果表明，N末端缺失7个氨基酸的突变体几乎没有活性（小于天然活性的0.5%），N末端缺失8个以上氨基酸残基的突变体则完全丧失活性。

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Terminal 22q deletion syndrome: A newly recognized cause of speech and language dis-ability in the autism spectrum

22号染色体长臂末端缺失综合征：新发现的孤独症家系中语言功能障碍的病因

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Sequence analysis revealed that abnormally processed transcripts resulted in frame-shifts with premature termination by introducing stop codon, removal of translation initiation codon and deletion of functional domain.

经序列分析，CMO基因转录本的异常加工将导致移码后提前终止及翻译起始密码或功能结构域的丢失。

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China s criminal hearsay evidence rule deletion has five manifestations, causes include ideological and institutional reasons.

我国刑事传闻证据规则缺失有五大表现，原因包括思想上和制度上的原因。

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Construction of thymidine kinase deletion mutants of pseudorabies virus FA strain

伪狂犬病病毒Fa株胸苷激酶基因缺失株的构建

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In senior group, WT mice showed significant alveolar expansion and interstitial lung damage, by contrast, u-PA gene deletion had more complete alveolar wall structure and no significant increase of alveolar space.

相比之下，u-PA基因缺失小鼠肺泡壁结构较完整，肺泡腔无明显增大。

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The Effect of 30-Base Pair Deletion of Latent Membrane Protein 1 C Terminus of Epstein-Barr Virus on Cell Proliferation

EB病毒LMP1C-端序列缺失对细胞增殖的影响

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Thirty base pair ( 30 bp) deletion in latent membrane protein 1 oncogene in lymphoepithelial carcinoma of salivary glands

涎腺淋巴上皮癌中EB病毒潜伏膜抗原-1基因30碱基缺失的研究

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Detection of the 30 base pair deletion of Epstein-Barr virus latent membrane protein 1 in extranodal nasal type NK/ T-cell lymphoma and its prognostic significance

结外鼻型NK/T细胞淋巴瘤中EB病毒潜伏膜蛋白1基因30bp碱基缺失的检测意义及其与预后的关系

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Case had 1 base pair insertion TT → TAT in 85 codon and 1 base pair deletion GCA → GA, which may result in nonsense mutation.

1例85密码子第2、3碱基之间插入A，同时86密码子第2碱基缺失，即GCA→GA导致无义突变。

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Intravenous Thrombolysis by Tissue-type Plasminogen Activator Deletion Mutant in a Rabbit Model of Retinal Artery Occlusion

两种组织型纤溶酶原激活剂缺失突变体（r-PA）治疗实验性兔视网膜动脉阻塞

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Expression and activity of tissue-type plasminogen activator mutant reteplase with deletion of PAI-1 binding sites

抗PAI抑制作用的组织纤溶酶原激活剂在大肠杆菌中的表达

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In word processing, an editing feature in which the system automatically adjusts the right hand margin for insertion or deletion of copy during playback.

字（）理技术中的一种编辑特性，在此特性下，系统在副本中插入或删除后，右边自动对齐。

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Analysis and Application of MS-DOS Inner Deletion Command

MS-DOS内部删除命令解析及其应用

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A one base deletion is discovered in purA gene from inosine producing strain and guanosine producing strain, which will cause the open reading frame shift mutation.

分析结果表明两株生产菌的purA基因发生了1个碱基缺失，导致阅读框发生移码突变；

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Deletion of Rb gene in human gastric cancer cell lines

人胃癌细胞株Rb抗癌基因缺失的研究

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Using carbapenem antibiotic can induce the deletion of out membrance porin gene, thus increasing MIC values of carbapenem antibiotic.

碳青霉烯类药物的使用可以诱导外膜孔道蛋白基因缺失，从而增加对碳青霉烯类抗菌药物的MIC值。

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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。

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