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- Objective: To study distribution rule of HBV gene mutation sites in chronical hepatitis B with Yin deficiency of liver and kidney syndrome. 摘要目的:研究慢性乙型肝炎肝肾阴虚证HBV基因突变点的分布规律。
- HBV gene mutation 基因变异
- 6.Objective To explore HBV gene polymorphism by detecting HBV gene mutation in pre-C/C、BCP andP regionwith DNA Chip,acquaint the relation between HBV gene polymorphism and treatment of lamivudine. 目的用芯片显色法检测HBVDNA在前C/C区、BCP区、P区基因突变来探讨拉米夫丁使用与HBV基因多态性关系。
- 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。
- Not only are ASON able to inhibit HBV gene expression with sequence specific but also clear HBV in the way of apoptosis. ASON不仅以序列特异性方式发挥抗病毒作用 ,而且可能以凋亡的方式清除HBV
- 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。
- Inhibition of HBV gene expression by a mixture of four different ASONs were not more effective than that by a single one. 4段ASON的联合用药并不能增强其对HBV的抑制作用。
- 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。
- Keywords HBV BCP;gene mutation;HCC; 基因变异;原发性肝癌;
- Detection of HBV gene polymorphism was carried out by using of enzyme coloration with digoxin-labeled primers in 63 cases of eAg(-) chronic HBV infections. 用地高辛标记引物酶显色法,检测了63例e抗原阴性慢性肝炎HBV基因多态性。
- 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。
- Nucleoside analogues are currently the main drug therapy against HBV infection.However, this type of therapy can cause gene mutations in HBV that result in drug resistance. 核苷类药物是目前抗乙型肝炎病毒(HBV)的主要药物,但它可引起HBV基因的变异,从而引起耐药。
- 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
- 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