DNA deletion

Study on the mechanism of DNA deletion in the dystrophin gene

抗肌萎缩蛋白基因DNA缺失机制的探讨

PCR analysis of mitochondrial DNA deletion in children with neuromuscular diseases

神经肌肉性疾病的病理与血液PCR检测线粒体DNA缺失分析

A 13.1 kb mitochondrial DNA deletion mutation exist in various human tissues

人多种组织中线粒体DNA存在13.1kb片段缺失突变

Study on mitochondrial DNA deletion in aging mice

衰老小鼠线粒体DNA缺失突变的研究

Age-dependent increase of mitochondrial DNA deletion in myocardial cells and blood lymphocytes

心肌和淋巴细胞线粒体DNA缺失在衰老中的意义

Significance of mitochondrial DNA deletion in congestive heart failure

充血性心力衰竭患者线粒体DNA缺失的意义

Mitochondrial DNA deletion of the brain tissue of aged rats with learning and memory deficit

老年学习记忆减退大鼠脑线粒体DNA缺失

Effects of Aerobics and Aging on Myocardial Mitochondrial DNA Deletion and Mitochondrial Function in Mice

有氧运动和衰老对小鼠心肌线粒体DNA缺失及其功能的影响

Objective To explore the relationship between mitochondrial DNA deletion and malignant phenotypes of human lung cancer cells .

目的探讨线粒体DNA损伤对人肺癌细胞生长和侵袭能力的影响。

Results : One normal and one abnormal bands , corresponding to single mitochondrial DNA deletion were presented in 7 patients .

结果：11例中，7例除有一条正常大小杂交带外，还有一条异常的缺失型线粒体DNA杂交带。

Effect of anti-aging No. 1 on liver mitochondrial DNA deletion in aged Balb / c mice

抗衰1号对老年小鼠肝线粒体DNA缺失的影响

Mitochondrial DNA Deletion in the Cerebral Cortex , Hippocampus and Cerebellum of the Aged Rats

老年大鼠大脑皮质、海马和小脑的线粒体DNA缺失突变

Objective To study the mitochondrial DNA deletion of mitochondrial myopathy and mitochondrial encephalomyopathy .

目的为了检测线粒体肌病和脑肌病患者的骨骼肌细胞的线粒体DNA的缺失情况。

Mitochondrial DNA Deletion in Dilated Cardiomyopathy

扩张型心肌病与线粒体DNA缺失片段的研究

The reason that two flanking sequences is located on different Chromosomes may be due to DNA deletion or DNA recombination during REMI .

插入质粒两端的序列被定位于两个不同的染色体上，可能是由于在REMI转化过程中基因组DNA的缺失或重排造成的。

Effect of Herba Epimedii and Fructus Lycii on mitochondrial DNA deletion , activity of respiratory chain enzyme complexes and ATP synthesis in aged rats

淫羊藿、枸杞子对老年大鼠线粒体DNA缺失、线粒体呼吸链酶复合体和ATP合成的影响

Results : The main clinical characteristics of neuromuscular diseases was muscle weakness , the results of muscle pathologic checking were atrophy not particularly and variation of malnutrition . It was detected existing mt DNA deletion in 6 cases by PCR assay .

结果：神经肌肉性疾病主要表现为肌无力，肌肉病理检查多为非特异性的肌萎缩、肌营养不良改变，血PCR分析发现6例有mtDNA缺失。

The primary study on radiation damage induced by ionizing radiation with human peripheral blood mitochondrial DNA common deletion analysis

用人外周血线粒体DNA4977bp缺失检测辐射损伤初探

The results directly confirmed the fact that 60 Co gamma ray irradiation can induced a bigger DNA fragment deletion of plant genome DNA .

研究结果为60Coγ射线辐照导致植物基因组DNA缺失提供了一个最直接明确的证据。

Mutation of Mitochondrial DNA 4977 bp Deletion in Laryngeal Squamous Cell Cancer

喉鳞状细胞癌组织中线粒体基因4977bp缺失突变的检测

Construction and confirmation of the plasmid of human mitochondrial DNA 4977 bp deletion induced by ionizing radiation

电离辐射致线粒体DNA4977bp缺失质粒构建及其鉴定

Protective roles of vitamin E and coenzyme Q10 in the inner ear mitochondrial DNA 4834 bp deletion mutation of rats

维生素E和辅酶Q10对大鼠内耳组织线粒体DNA4834bp缺失突变的预防作用

This study is try to explore if the polymerase chain reaction ( PCR ) could be used to analyze the mitochondrial DNA 4977 bp deletion ( common deletion ) induced by ionizing radiation .

初步探索用聚合酶链反应（PCR）方法进行辐射诱导的线粒体DNA4977bp缺失分析的可行性。

A hypothesis for molecular mechanism for GT variation of rice is presented , that is DNA insertion , deletion or base substitution in coding sequence of alk contributes to GT variation of rice .

本研究同时提出了水稻稻米糊化温度调控的分子遗传假说，认为基因编码区内碱基插入、缺失或替换可能是GT改变的遗传基础。

This can occur through a mutation in the gene 's DNA sequence or through deletion of the gene .

这种缺失可能起源于基因的突变或者通过基因序列的缺失而产生。

Objective To investigate the effects of aerobics and aging on myocardial mitochondrial DNA ( mtDNA ) deletion and mitochondrial function in mice .

目的：观察和探讨有氧运动和衰老对心肌线粒体DNA（mtDNA）缺失和功能的影响。

Objective To explore the effect of anti-aging No. 1 on liver mitochondrial DNA ( mtDNA ) deletion in aged Balb / c mice .

目的研究抗衰1号对老年Balb/c小鼠肝线粒体DNA（mtDNA）缺失突变的影响。

AIM : To elucidate the role of mitochondrial DNA ( mtDNA ) deletion in the pathogenesis of viral myocarditis in mice .

目的：探讨线粒体DNA（mtDNA）缺失在病毒性心肌炎（VMC）发病机制中的作用。

AIM and METHODS : The ratio of mitochondrial DNA ( mtDNA ) deletion was measured to find the relationship between mtDNA deletion and aged learning and memory deficit .

目的和方法：测定老年大鼠脑mtDNA缺失型（以下简称缺失型），缺失mtDNA比例，探讨mtDNA缺失与老年性学习记忆减退的关系，为研究其分子机制提供基础资料。

Objective To study the myocardial mitochondrial DNA ( mtDNA ) deletion in the cases of sudden death due to primary cardiomyopathy ( PCM ) and its relationship with sudden death .

目的探讨原发性心肌病（PCM）猝死者心肌线粒体DNA（mtDNA4977）缺失情况及其与猝死的关系。