dystrophin

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

Western Blot analysis of dystrophin after transplantation : No dystrophin was detected in the blank control group ;

骨髓干细胞移植后抗肌萎缩蛋白westernblot免疫印迹分析结果：空白对照组无抗肌萎缩蛋白的表达；

Study on technical optimization of DNA microarray construction and application for Dystrophin gene analysis

Dystrophin基因缺失检测微阵列构建及应用中技术优化的研究

The Expression and Research of Dystrophin Gene in Dermal Fibroblast Cells

皮肤成纤维细胞中dystrophin基因的表达研究

There are high rate and different forms of mutations in the dystrophin gene .

DMD基因具有突变频率高且突变形式多样之特点。

Advances in the Research on the Mutation of Dystrophin Gene

dystrophin基因突变研究进展

Analysis of Deletion in Dystrophin Gene by Multiplex Polymerase Chain Reaction

多重聚合酶链反应分析Dystrophin基因缺失突变

Relationship of phenotype with type of deletion of dystrophin gene

不同表型肌营养不良症患者抗肌营养不良蛋白基因缺失类型的研究

Distributional characteristics of dystrophin gene deletion in Chinese population

中国人抗肌营养不良蛋白基因缺失的分布特点

Detection of dystrophin gene deletion by polymerase chain reaction

PCR扩增法检测DMD患者的基因缺失

Studying Dystrophin Gene Deletion in the Northeast of China and Applicating

东北地区抗肌营养不良蛋白基因缺失的研究及应用

The full sequence of intron 51 of dystrophin gene and its characteristic of sequence

Dystrophin基因第51内含子全序列的测序及序列特点分析

Preparation of specific antiserum anti 5 - 7 against dystrophin

抗Dystrophin特异性抗血清Anti5－7的制备

Strategy of localizing the deletion mutation point in large introns of Dystrophin gene

在Dystrophin基因大内含子上定位缺失突变位点的策略

Objective To understand the expression of dystrophin glycoprotein complex at neuronal cholinergic synapses .

目的了解dystrophinglycoproteincomplex（DGC）在神经元性胆碱能突触中的表达。

Dystrophin levels rose to near-normal , and the disease almost vanished .

Dystrophin升高到接近正常水平，故而症状几乎消失。

In the dystrophin gene , and in most of human genes , this genetic information is not contiguous .

在肌营养不良蛋白基因，在人类基因大多数，这种遗传信息不连续的。

Conclusion The absence or abnormal expression of dystrophin was the specific change for DMD / BMD .

结论肌营养不良蛋白的缺失或异常表达，是DMD/BMD型较为特异的改变。

Objective To investigate the significance on the expression of dystrophin in muscle tissue of the patients with myodystrophy .

目的探讨肌营养不良蛋白在肌营养不良症患者肌组织中表达的意义。

Cloning and Sequencing of Junction Fragment with Exon 51 Deletion of Dystrophin Gene

Dystrophin基因51号外显子缺失连接片段的克隆和测序

Protein . Diagnotic significance on the expression of dystrophin to myodystrophy

肌营养不良蛋白表达对肌营养不良症的诊断意义

Dystrophin expression in muscle tissues of DMD model-mdx mouse after myoblast transfer therapy

成肌细胞移植治疗DMD模型-mdx鼠骨骼肌Dystrophin表达的实验研究

Comparison and analysis of the molecular character of breakpoints in introns of deletion hotspots of dystrophin gene

缺失型杜氏肌营养不良症缺失热区内含子断裂点分子结构特点的对比分析

Observation of Bone Marrow Reconstitution and Dystrophin Expression after Bone Marrow Transplantation to Treat Duchenne Muscular Dystrophy

骨髓移植治疗DMD模型鼠后骨髓重建和目的蛋白的表达

DMD is caused by a mutation of the gene for dystrophin , a protein in the muscles .

DMD源于肌肉中一种称为肌营养不良蛋白的基因突变。

AIM : To study the methods of accurately localizing the deletion mutation point in the large introns of dystrophin gene .

目的：探讨在Dystrophin基因大内含子上准确定位缺失突变位点的方法。

The dystrophin gene is found on the X chromosome and passed on to children through a mother who is a carrier .

肌营养不良卵白基因位于人类X染色体，携带基因突变的母亲会遗传给婴儿。

Intron 44 is not the most unstable intron in the central deletion hot spot of dystrophin gene

44号内含子并非是dystrophin基因中央缺失热区最不稳定的内含子

It would not be suitable for treating different mutations in the dystrophin gene , or diseases not caused by nonsense mutations .

它对肌营养不良基因的其他类型的变异或非无意突变导致的疾病无效。

Objective To detect dystrophin expressions in muscle tissues of the patients with Duchenne Becker muscular dystrophy .

目的检测假肥大肌营养不良症肌组织中肌营养不良蛋白（dystrophin）的表达。