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- C gene mutation C区变异
- 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。
- A comparative study on p53 gene mutation in primary human Dukes C col on cancer with that in matched lymph node metastasis. Dukes C期大肠癌原发灶与淋巴结转移灶中p53基因突变的比较
- Objective To investigate the role of p53 and C myc gene mutation in carcinogenesis of cuteneous squamous cell carcinoma (SCC) and basal cell carcinoma(BCC). 目的 研究和探讨 p5 3和C myc基因突变在皮肤鳞状细胞癌 (SCC)和基底细胞癌 (BCC)的发生、发展中的作用。
- 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。
- 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。
- There is another protein with a different open reading frame from core protein within the HCV C gene. 除了核蛋白外，在丙型肝炎病毒核基因内，尚有一蛋白产生。
- Methods By means of PCR to detect polymorphism of pepsinogen C gene of the subjects. 方法采用PCR检测具不良生活习惯者中胃蛋白酶原C基因的多态性。
- 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。
- Ge C X, Chen G J, Huang J L.Amplification and cloning the full-length C gene and prM gene from dengue virus (NGC strain)[J].Chinese Journal of Zoonoses, 2002, 18(1): 5-7. [5]葛春喜; 陈观今; 黄炯烈.;登革病毒(NGC株)C与PrM全长基因的扩增与克隆[J]
- 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。
- 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。
- 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
- 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。
- Abnormal genes mutating is the pathogeny of cancer. 癌症的病因就是反常的基因变异。
- Fourteen of the Fifteen polymorphic probes and C gene (chromogen for pigmentation) were further used for the co-segregation analysis of heading date and RFLPs in the population of three-variety cross ( Pecos/Nanjing11//Akihikari). 进一步用14个多态性探针和形态标记色素原基因C分析三交群体Pecos/南京11//秋光中标记与抽穗日数的共分离.
