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- Keywords Ionizing radiation;Lymphoblastoid cell line;Mitochondrial DNA deletion; 电离辐射;淋巴细胞永生化细胞系;线粒体DNA缺失;
- Quantitative analysis of myocardial mitochondrial DNA deletion and its relationship with cardiac dysfunction in heart failure 心力衰竭患者心肌线粒体DNA缺失突变的定量分析及与心功能损害程度的关系
- Effect of Wuzi Yanzong Pill and Its Disassembled Prescription on Mitochondrial DNA Deletion, Respiratory Chain Complexes and ATP Synthesis in Aged Rats 五子衍宗丸及其拆方对老年大鼠心脑线粒体DNA缺失、线粒体呼吸链酶复合体及ATP合成的影响
- Effect of Wuzi Yanzong Pill on Mitochondrial DNA Deletion and Respiratory Chain Enzyme Complex Activity in Peripheral Leukocyte of Aged Male with Kidney Deficiency Syndrome 五子衍宗丸对男性老年肾虚者外周血白细胞线粒体DNA缺失及线粒体呼吸链酶复合体活力的影响
- Mitochondrial DNA deletion 线粒体DNA缺失
- Relationship between mitochondrial DNA deletions and noise-induced hearing loss 线粒体DNA缺失与噪声性听力损失关系的分析
- Objective:To understand large scale deletion mutation in mitochondrial DNA(mtDNA) and its significance. 目的：了解线粒体DNA大片段缺失突变及其意义。
- Objective To analyze mitochondrial DNA polymorphism of district of Lubunour at the Bronze Age in Xinjiang. 目的 :通过新疆罗布诺尔地区铜器时代古代居民 m t DNA多态性分析 ,探讨新疆境内古代欧洲人种成分的来源。
- Compared with the normals, the amount of the mitochondrial DNA were decreased universally in the patients with AD. （2）和正常老人相比，AD患者中线粒体DNA的数量普遍减少；
- Mammalian Mitochondrial DNA(mtDNA) control region consists of central domain, ETAS domain and CSB domain. 哺乳动物线粒体DNA(mitochondrialDNA,mtDNA)控制区由中央保守区、ETAS区和CSB区构成。
- Objective:To study the possible relationship between mitochondrial DNA point mutations and hereditary ataxia. 目的:探索线粒体DNA点突变与遗传性共济失调的关系。
- The strongest support that mitochondrial DNA offers for the African-origin hypothesis may not depend on trees. 线粒体DNA提供非洲起源说假设的最强而有力支持也许不是取决于族谱。
- Conclusion:The point mutation in this area of mitochondrial DNA might not be related hereditary ataxia. 结论:遗传性共济失调的发生、发展可能与该区域点突变无关。
- Ancient mutations in mitochondrial DNA are the same as those found in the cells of many tumors. 而在线粒体DNA中的远古突变和许多瘤细胞中发现的情况是一样的。
- Objective To simplify the DNA sequencing method and optimize the conditions for mitochondrial DNA (mtDNA) sequencing. 目的简化DNA测序方法，优化条件，以适用于线粒体DNA的测序。
- From our results,mitochondrial DNA mutation may be one of major factors in aminoglycoside antibiotic induced deafness. 提示线粒体DNA点突变是导致该家系致聋的主要因素之一。
- Mitochondrial DNA(mtDNA)and telomere are the primary DNA markers used in deducing individual age in recent years. 目前用于年龄推断研究的DNA标记主要是线粒体和端粒。
- Heteroplasmy is a common phenomenon in mitochondrial DNA somatic mutations of human tumors. 认为胞质异质性是人类肿瘤组织线粒体基因突变的普遍现象。
- People living near Medellin, Colombia, have almost exclusively Native American mitochondrial DNA and European--specifically, Spanish--Y chromosome DNA. 生活在哥伦比亚麦德林附近的人几乎是具有绝对单一的当地美洲人线粒体DNA和欧洲特别是西班牙的Y染色体DNA。
- One is the mitochondrial DNA which we all possess and which is passed down with only minor mutations through the female line. 你是的线粒体DNA我们全部拥有并且通过下来以唯一较小变化通过女性线。
