...上游转录调控区的重组及表达 (期刊论文) 关键词:珠蛋白基因; 表达调控; 报告基因; 抑制子 [gap=1626]Key words β- globin gene ; expression regulation ; luciferase reporter gene ; silencer ..
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globin gene cluster 珠蛋白基因簇
like globin gene 族珠蛋白基因
beta-globin gene 珠蛋白基因
globin gene probe 珠蛋白基因探针
globin gene expression 珠蛋白基因表达
Vitreoscilla globin gene 透明颤菌血红蛋白基因
alpha globin gene 珠蛋白基因
e-globin gene 珠蛋白基因
human -globin gene 反转录病毒载体
The 5' breakpoint of the deletion is within the IVS II of Ar-globin gene. The 3' breakpoint is located in the distant downstream of β-globin gene, about 11 kb of upstream of the 3' breakpoint of HPFH-2.
限制性内切酶图谱分析证明了β-珠蛋白基因簇内的DNA顺序缺失,缺失的5′端点位于Aγ基因IVSⅡ内,3′端点在β-珠蛋白基因下游区远端,距HPFH-2的3′缺失端点上游区约11kb。
参考来源 - 与胎儿珠蛋白基因持续表达有关的(AMethods:PCR-ASO probe hybridization analysis, was used to scan 17 known types of beta-thalassemia mutation in Chinese. Using gene clone and DNA sequence analysis of the entire human beta-globin gene to identify the underlying causative mutation of the sample.
方法：采用PCR/ASO探针杂交法检测中国人常见17种β-地贫基因突变，β-珠蛋白基因全长DNA克隆测序技术分析其突变基因型。
参考来源 - β地中海贫血一个特殊基因突变的家系分析—《中国医药导报》—2008年第5期—龙源期刊网·2,447,543篇论文数据，部分数据来源于NoteExpress
Although advance has been made in the study on control of globin gene expression and switching, key factors of globin gene switching is still unknown till now.
虽然对于珠蛋白基因表达调控及开关的研究已取得许多进展，但至今对于调节这些开关的决定性调节因子仍不明确。
The globin gene types in G6PD deficiency children are multifarious, but there is no obvious relationship between G6PD deficiency and the different globin gene types.
合并地贫血的G6PD缺乏症患儿珠蛋白基因缺陷类型多样，但G6PD缺乏症与地贫不同基因型之间并无明显的相关性。
Validity oft his "non-DNA" principle was evaluated by amplification of globin gene from fresh tonsil tissues and plasmid gene on condition that gloves were contaminated by plasmid.
然后通过扩增新鲜扁桃体组织中珠蛋白基因及模拟手套被质粒污染的情况下扩增质粒基因，验证该无DNA操作过程对避免污染的有效性。
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