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- The behavioral investigation on Duchenne muscular dystrophy animal model after marrow transplantation. 型肌营养不良模型鼠骨髓移植后的行为学观察。
- Objective To detect dystrophin gene deletion of Duchenne muscular dystrophy (DMD) and make DMD gene diagnosis. 目的探讨Duchenne型肌营养不良症(DMD)患者基因缺失的突变特点并进行基因诊断。
- Objective To investigate the effects of Duchenne muscular dystrophy mice(mdx) treated with stem cells transplantation. 目的 研究骨髓干细胞移植治疗Duchenne型肌营养不良鼠 (mdx鼠 )的效果。
- Detection deleted Duchenne muscular dystrophy carriers by fluorescence quantitative polymerase chain reaction. 应用荧光定量PCR检测缺失型DMD携带者的研究
- To explore the application of freeze etching electrom microscopy in the study of Duchenne muscular dystrophy(DMD). 目的:探讨电镜冷冻蚀刻技术在Duchenne 型肌营养不良症( DMD) 研究中的应用。
- Duchenne muscular dystrophy (DMD): A quantitative study of type 2C fibers and muscle satellite cells. Duchenne型肌营养不良症:2c型纤维与肌卫星细胞的定量研究
- Duchenne muscular dystrophy(DMD) takes up 75%(12 cases) in 16 PMD cases,which slightly higher than reference reported. 本组16例PMD中DMD占75%25(12/16),比文献报道稍高[2];
- AVI's lead drug candidate, AVI-4658, is in clinical development for Duchenne Muscular Dystrophy. 阿维的领先候选药物,阿维- 4658,是在杜氏肌营养不良症的临床开发。
- Objective This paper was designed to investigate the feasibility of non invasive prenetal diagnosis of Duchenne muscular dystrophy(DMD). 目的 探讨杜氏肌营养不良症 (Duchenne muscular dystrophy,DMD)的无创性产前基因诊断的可行性。
- Objective To establish a normative procedure for clinical prenatal gene diagnosis of Duchenne and Becker muscular dystrophy(DMD/BMD). 目的 建立规范的假肥大型肌营养不良症 (DMD/BMD)产前基因诊断程序。
- Objective To study affected muscle selectivity and main laboratorial examination value of duchenne muscular dystrophy(DMD). 目的 探讨Duchenne型肌营养不良症(DMD)受累肌肉的选择性及各项实验室检查的诊断价值。
- Objective To study prenatal gene diagnosis in high danger pregnant wo men with Duchenne muscular dystrophy (DMD) families. 目的研究Duchenne肌营养不良症(DMD)家系中高风险孕妇的产前基因诊断。
- Objective:To observe bone marrow rebuilding after bone marrow transplantation (BMT) to treat Duchenne muscular dystrophy (DMD). 目的:观察在骨髓移植(bonemarrowtransplantation,BMT)治疗Duchenne型肌营养不良症(DMD)模 型鼠mdx鼠后,骨髓重建过程及目的蛋白的表达情况。
- The abnormal distribution and significance of lectin receptors in skeletal muscle of the patients with duchenne mys-cular dystrophy (DMD). Duchenne型肌营养不良症骨骼肌凝集素受体异常分布及其意义
- In addition, the charities Muscular Dystrophy Campaign (MDC), Action Duchenne and Duchenne Family Support Group also participate in the Consortium. 此外,肌肉萎缩症慈善运动(MDC),行动和裘馨裘馨家庭支援组也参加了联盟。
- First of all, mutation analysis of Duchenne muscular dystrophy (DMD) gene was carried out by CE coupled with multi-PCR technique. 在医学领域主要表现为以基因突变检测,基因家系连锁分析,特定基因的PCR产物直接检测为基础的基因诊断。
- Approximately one in every 3,500 boys worldwide is afflicted with Duchenne muscular dystrophy with 20,000 new cases reported each year. 大约每3500男孩全世界患有杜氏肌营养不良的20000新病例每年报告。
- Dystrophin, the protein missing in Duchenne muscular dystrophy patients, conducts this energy across the muscle cell's membrane, protecting the fiber. 但肌节产生的力量,如果没有向外引导的话,也会伤害肌纤维,DMD患者所缺乏的肌肉萎缩蛋白,能将这股力量传导到肌肉细胞膜上,而保护肌纤维。
- Objective To investigate the clinical and lab features of sibling brother and sister both with Duchenne muscular dystrophy(DMD). 目的探讨同患假肥大型肌营养不良症(DMD)兄妹的临床以及实验室检查特点。
- Duchenne Muscular Dystrophy (DMD) is one of the most common fatal genetic disorders to affect children around the world. 杜氏肌营养不良(DMD)是最常见的致命的遗传疾病之一,影响到世界各地的儿童。