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  deletion
    Establishment of an Oil Body-based Expression System and Deletion Analysis of a Vascular-specific Profilin2 Promoter
    植物油体表达体系的建立及Profilin2维管束特异表达启动子的区段缺失分析
短句来源
    Construction of Pseudorabies Virus SH Strain Mutant with gE-gI Gene Partial Deletion Inserting GFP-LacZ Reporter Gene and Primary Study Its Immunogenicity
    伪狂犬病病毒上海株gE~-/gI~-/GFP~+/LacZ~+缺失株的构建及其免疫原性初步研究
短句来源
    Study on a New Domain in Rat Ribosomal RNA and the Deletion Mutation of Cinnamomin A-chain
    大鼠核糖体RNA一个新的结构域以及辛纳毒蛋白A链缺失突变的研究
短句来源
    The Association Between the Infection of Mycobacterium Tuberculosis and the FHIT Gene Deletion of Lung Cancers with Pevious Pulmonary Tuberculosis
    结核杆菌感染与肺结核相关肺癌FHIT基因缺失的研究
短句来源
    Homozygous Deletion, Methylation, Expression and Microsatellite Instability of FHIT Gene in Laryngeal Squamous Cell Carcinoma
    喉鳞癌中FHIT基因纯合性缺失、甲基化、表达及其微卫星不稳定性研究
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  loss
    Study of Loss of Heterozygosity and Mutation as Well as Influencing Factors of Expression of ING1 in Human Gliomas
    胶质瘤ING1基因缺失突变及其表达影响因素的研究
短句来源
    Establishment of Murine Interstitial Cells of Cajal Loss Model and Study on SCF Promoting Its Restoration
    小鼠小肠Cajal间质细胞缺失模型的建立及SCF促其恢复研究
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    Loss of Market and CMEA during the Cold War
    市场缺失与冷战时期的经互会
短句来源
    Loss of Heterozygosity Analysis of Chromosome 9p13-23 in Microdissected Laryngeal Squamous Cell Carcinoma
    喉癌9p13-23区域微卫星DNA杂合性缺失的研究
短句来源
    Loss of Ha-ras Alleles in DNA from Gastric Carcinoma Tissue of Chinese Individuals
    在中国人胃癌组织DNA中发现癌基因Ha-ras等位基因缺失
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  lack
    The Shadow of Government and the Lack of Autonomous Brand
    政府蔽荫与自主品牌缺失
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    Lacking of inter-government money-transferring system is also an important resulting reason for the lack of rural compulsory education finance policy fairness.
    政府间转移支付制度缺乏规范性也是导致农村义务教育财政政策公平性缺失的重要原因。
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    It takes time for the campus culture to develop and settle in, but it doesn’t necessarily justify the lack of culture on university campus.
    大学校园文化需要漫长岁月的沉淀,但这并不是新建大学校园文化缺失的理由。
短句来源
    The gene of oprD2 was lack.
    oprD2基因扩增检测呈缺失型。
短句来源
    Furthermore,it was also revealed that individual in simultaneous lack of GSTT1 and GSTM1 would run 12 times as high risk as normal controls did(OR=12.338).
    GSTM1基因和GSTT1基因同时缺失的人群OR(95%CI)为12.338(3.621~22.042);
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  deletion
The case deletion model is equivalent to mean shift outlier model, as well as case weights model.
      
A diagnostic based on case-deletion approach in estimating equations is proposed.
      
It is shown that the case deletion model is equivalent to the mean shift outlier model.
      
By constructing an interval extension of adjustable entropy function and some region deletion test rules, a new interval algorithm is presented.
      
Differentiation of Indica-Japonica rice revealed by insertion/deletion (InDel) fragments obtained from the comparative genomic s
      
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