gene defect的例句大全

Application of Gene Knockout and Gene Defect Models in the Study of Drug Membrane Transport

基因敲除与基因突变动物模型在药物跨膜转运研究中的应用

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Objective To study gene defect of a hereditary coagulation factor XIII deficiency family.

目的研究一例遗传性凝血因子XIII（FXIII）缺陷症家系的基因缺陷。

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peanutsa gene defect that can triple the risk of a child developing an allergy to peanuts has been identified, scientists have said.

科学家称，他们明确了一个可导致儿童对花生过敏的风险增加三倍的基因缺陷。

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here, too, it is a gene defect that causes the molecules to misbehave.

在这，它是一种基因缺陷导致的分子做错事。

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construction of x-gene defect hbv expression plasmid and cells transfection study

X基因突变乙型肝炎病毒表达质粒的构建及细胞转染

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Study in mitochondrial gene defect of patients with mitochondrial myopathy and encephalomyopathy

线粒体肌病和脑肌病患者线粒体基因缺失的研究

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The repair of bone defect by bone marrow stromal cell transferred by retroviral vector mediated hBMP-7 gene

hBMP-7基因转染修复骨缺损的实验研究

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Objectives: To examine the frequency of exon 15 missense mutation ( D442G) and intron 14 splice defect ( I14A) in cholesteryl ester transfer protein gene in Chinese atherosclerotic subjects.

目的：检测中国人群动脉粥样硬化（AS）患者和正常人的胆固醇酯转运蛋白（CETP）基因15外显子D442G突变和14内含子I14A突变。

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Ventricular septal defect induced by mutation of mouse Fox C2 gene

小鼠叉头框C2基因变异致室间隔缺损

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Analysis of the GATA-4 Gene in Three Atrial Septal Defect Family

三个房间隔缺损家系的GATA-4基因分析

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Gene therapy in repairing the defect of articular cartilage: human insulin-like growth factor-I transfected chondrocytes and its expression in chondrocytes

关节软骨缺损修复的基因治疗实验&人胰岛素样生长因子I基因转染软骨细胞及其在软骨细胞中的表达

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Bone morphogenetic protein-2 released from carrier or gene could repair bone defect effectively.

载体或基因释放的骨形态发生蛋白2可有效修复骨缺损。

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Objective: To establish an experimental mandibular defect animal model and provide a template in gene therapy for the repair of mandibular defects.

目的：建立用于研究下颌骨骨缺损基因治疗的实验动物模型及基因导入方法。

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Conclusion The successful construction of ad5/ CMV-TGF-β 1 production in our experiment may lay foundation for the orthopaedic gene therapy such as in the treatment of the defect of bone, muscle tissue.

结论重组缺陷型腺病毒载体Ad5/CMV-TGF-β1的构建成功，为下一步进行基因疗法治疗骨骼、肌肉组织缺损提供基础。

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protein tyrosine kinase of focal adhesion kinase subfamily-a new related gene of ventricular septal defect

室间隔缺损新的相关基因-蛋白酪氨酸激酶的实验研究

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experimental study of gene therapy for colon cancer by replication-defective recombinant adenovirus harboring human endostatin

复制缺陷型重组腺病毒介导人内皮细胞抑制素基因治疗结肠癌的实验研究

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Gene therapy is one of the main directions of restoring bone defect.

基因治疗是修复骨缺损的主要研究方向之一.

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As a complex process, infiltration and metastasis of malignant tumor is associated with motility, motility factor with its receptor, signal transduction, hereditary defect, tumor metastasis-related gene and tumor suppressor gene.

肿瘤的浸润和转移是一个复杂的过程，与肿瘤细胞的能动性、能动性因子及其受体、转移的信号转导、肿瘤细胞的遗传性缺陷、肿瘤转移相关基因及肿瘤抑制基因等诸多因素相关。

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The defect of LpL gene is often associated with endogenous hypertriglyceridemia and coronary heart disease.

脂蛋白脂酶（LPL）是脂代谢的关键酶，其基因缺陷与内源性高甘油三脂血症（HTG）及冠心病等多种疾病有密切关系。

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In the process of identification of these genes found at least 250 embryos defective gene ( embryo-defective genes, EMBs) essential for the normal development of embryos.

在鉴定这些基因的过程中发现了至少250个胚缺陷基因（embryo-defective genes，EMBs）为胚正常发育所不可或缺。

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