• This research intended to construct a eukaryotic expression vector with a site-directed mutation of porcine MSTN propeptide gene.

    本研究旨在构建具有猪 MSTN 前肽基因定点突变的真核表达载体。

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  • "We already know that the over-expression or mutation of molecules known as NIK and TRAF3 in B cells is associated with human multiple myeloma," said Professor Mackay.

    “我们已经知道,在B细胞过度表达或突变的NIK和TRAF3分子是与人类多发性骨髓瘤相关,”麦凯教授说。

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  • The main application is in discovering new genes, analysis of gene expression, gene mutation, polymorphism and genetic sequence test.

    主要应用于新基因发现、基因表达分析、基因突变及多态性分析、基因测序等。

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  • Conclusion Construction of the eukaryotic expression vectors of wild type and mutant PRPF31 genes is basic work for research on the mechanisms of retinitis pigmentosa caused by PRPF31 mutation.

    结论野生型和突变型PRPF31基因真核表达载体的构建,为研究PRPF31基因突变引起视网膜色素变性的机制奠定了基础。

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  • Expression of the PTEN tumor suppressor is frequently lost in breast cancer in the absence of mutation or promoter methylation through as yet undetermined mechanisms.

    PTEN肿瘤抑制因子在乳腺癌中虽常呈失表达,但并不是通过基因突变或促进子甲基化而实现的,因此其失表达的机制还不清楚。

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  • So people will try and get some sort of gene-based test to measure the expression-mutation of these kinases.

    因此人们尝试着取得一些基因水平的测试蛋白激酶突变表达的方法。

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  • Objective: To analyse the significance and relationship between p53 gene mutation and the expression of mutant type p53 gene protein in the laryngeal carcinomas.

    目的:探讨喉癌P53基因突变与突变性P 53基因蛋白表达之间的相互关系及意义。

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  • The positive cells expression of P53 had an important relation to the appearance of EBL. B cells with P53 mutation strain might be a target cell to format tumors.

    EBL的发生与突变的P53蛋白过表达有重要关系,携带P53突变株的B淋巴细胞可能是形成肿瘤的靶细胞。

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  • That may be a common physiological mechanism which means organism can control the expression of genes and resist the virus infection, or the DNA mutation induced by during the period of evolution.

    在进化上,这可能是生物调控基因表达及抵御病毒侵染或转座子诱导DNA突变的一种共有的生理机制。

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  • The mutation or abnormal expression of CHD gene is thought to be related to some human diseases.

    CHD基因突变或表达异常与人类某些疾病有关。

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  • Because it has been realized that cancer is not only a disease of defects in gene expression or mutation but also a metabolic disease in that cells need nutrients to grow.

    因为人们已经认识到,癌症不仅仅是因一种基因表达或变异缺陷而导致的疾病,同时也似一种代谢性疾病,因为肿瘤细胞的生长需要营养物质。

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  • Consumptive mutation expression is the mutation that consumes a concept, consume the mutation of the object, consume the mutation of means.

    消费变异表现为消费理念的变异,消费对象的变异,消费方式的变异。

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  • The expression of mutation P53 protein was related closely to histopathologic grade, tumor size, metastasis and prognosis of tumor(P<0.05), but it was not related to histologic types(P>0.05).

    P53蛋白的阳性表达与组织学分级、肿瘤预后复发及肿瘤大小关系密切(P<0.05),但与组织学类型无相关性(P>0.05)。

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  • To study the relationships between the expression level of PTEN gene, gene mutation and occurrence and development of glioma.

    目的:探讨pten基因表达水平及其基因突变与脑胶质瘤的发生及恶性进展的关联性。

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  • By the mean time, the technique have reported in the gene expression analysis, new gene discovery, gene mutation detection, SNP analysis, DNA re-sequence and diagnosis.

    目前,该技术已用于基因表达谱分析、新基因发现、基因突变、基因多态性分析、药物筛选和基因测序及疾病的诊断。

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  • This research intended to construct eukaryotic expression vector with a site-directed mutation of porcine MSTN propeptide gene, and verify its expression efficacy in C2C12 cells.

    本研究旨在克隆通城猪含有第1个内含子的MSTN前肽基因,构建真核定点诱变载体,并通过转染C2C12细胞验证载体表达的有效性。

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  • OBJECTIVE: Purpose to study the expression of P53 mutation protein, estrin receptor (er) and progestin receptor (pr) in mammary cancer and their relativity.

    目的:探讨乳腺癌中P 5 3蛋白,雌激素受体(ER),孕激素受体(PR)的表达及相关性研究。

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  • Methods:Immunohistochemistry and PCR-SSCP were used to detect the expression of P53 protein and p53 gene mutation in 32 cases of TSCC and 10 cases of tongue leukoplakia.

    方法:应用免疫组织化学和聚合酶链反应—单链构象多态性分析(PCR-SSCP)检测10例舌白斑和32例舌癌,并结合临床资料进行分析。

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  • Methods:Immunohistochemistry and PCR-SSCP were used to detect the expression of P53 protein and p53 gene mutation in 32 cases of TSCC and 10 cases of tongue leukoplakia.

    方法:应用免疫组织化学和聚合酶链反应—单链构象多态性分析(PCR-SSCP)检测10例舌白斑和32例舌癌,并结合临床资料进行分析。

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