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- genetic gene mutation 遗传基因突变
- APC gene mutation is a critical genetic event in both the familial and sporadic forms of colorectal tumorigenesis. 结肠腺瘤性息肉基因的突变是家族型和散发型结肠癌的发生中危险的基因事件。
- As molecular genetic research proceeds, the molecular mechanism whereby HERG gene mutation causes long QT syndrome is being gradually revealed. 随着分子遗传学的进展,HERG基因突变如何导致长QT综合征的分子机制正逐步被揭示。
- Research of G6PD gene mutation types may provide some useful data for clinical diagnosis and prevention of G6PD deficiency , and for human genetic study. G6PD基因突变类型的研究,为该病的诊断和预防以及人类遗传学研究提供更多的资料和手段。
- There is K14 1A domain gene mutation in this DM-EBS pedigree. 本 DM-EBS家系存在 K14的基因突变。
- The FMR-1 gene mutation and Xq27.3 fragile site among 233 non-specific mentally retarded children were investigated in our genetic counseling department and two special educational schools by PCR, Southern Blot hybridization and cytogenetic methods. 采用PCR、Southern Blot印迹杂交及细胞遗传学方法;对233名原发性智力低下患儿进行了FMR-1基因的突变分析和Xq27.;3脆性位点检查。
- 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。
- Genetic Algorithm (GA) is a kind of highly paralel, stochastic, global probability search algorithm based on the evolutionism such as natural selection, genetic crossover and gene mutation. 遗传算法是一种基于自然选择、遗传杂效和基因变异等生物进化机制的高度并行、随机、全局性概率搜索算法。
- Ras gene mutation in childhood AML was mainly found in M2,M4,M5 subtypes. AML患儿中ras基因突变多见于M2、M4及M5型。
- GCH 1 gene mutation is only one of reasons to the DRD patients onset. GCH-1基因突变只是部分DRD患者的发病原因。
- It is the constitution with oneself is concerned above all, what act well among them is genetic gene. 首先是与本人的体质有关，其中起作用的是遗传基因。
- For instance, many primates cannot make vitamin C, because of a gene mutation. 例如，许多灵长类动物由于基因突变而不能制造维生素C。
- Gene mutations are alterations in the DNA code. 基因突变是指DNA 密码的改变。
- To investigate the relationship between isoniazid- resistance and Kat G gene mutation or deletion. 目的：探讨结核分枝杆菌异烟肼（INH）耐药与katG基因突变和缺失的关系。
- OBJECTIVE:To analyze the relationship between Chinese DRD onset and gene mutation of guanosine triphosphate cyclohydrolase 1(GCH 1). 目的:分析国人DRD患者发病与三磷酸鸟苷环化水解酶1(GCH-1)基因突变的关系。
- Cells with Ras gene mutation or transformed by Ras become resistant to p53 dependent apoptosis. Ras 基因转染或突变的细胞能够对DNA损伤引起的p53依赖性凋亡产生抗性。
- Study on tetrahydrobiopterin metabolism and gene mutation for dopa-responsive dystonia-a family report. 多巴反应性肌张力障碍一家系四氢生物蝶呤代谢与基因研究
- Abnormal genes mutating is the pathogeny of cancer. 癌症的病因就是反常的基因变异。
- A novel SCN5A gene mutation (del D1790) associated with congenital long QT syndrome. 遗传性长QT综合征SCN5A基因delD1790新突变
- Objective To identify the COL7A1 gene mutation in a family with dy strophic epidermolysis bullosa pruriginosa. 目的鉴定一痒疹样营养不良型大疱性表皮松解症家系的基因突变,为进一步开展基因诊断和基因治疗奠定基础。
