Background Duchenne Muscular Dystrophy is an X-linked recessive lethal inherited disease, which involves skeletal and cardi...
Duchenne型肌营养不良症(Duchenne muscular dystrophy，DMD)是一种以骨骼肌进行性变性、坏死为主要表现的致死性X-连锁隐性遗传病。
The single cell 3-plex nested PCR established in our study is reliable, effective and sensitive technique for dystrophin and SRY gene, and is suitable for PGD in deleted DMD/BMD families with history.
首次深入研究中国南方DMD/BMD家系成员的dystrophin基因5个STR位点的多态性，发现部分多态性片段与西方DMD/BMD家系成员不同。
Methods Immunohistochemical stains using anti-Dystrophin monoclonal antibodies of three diffcrent domains(Dystrophin-N, -C, -R) were procedured for 11 patients with DMD, 5 patients with BMD and 3 other patients with neuromyopathies.
用肌营养不良蛋白三个不同区域的单克隆抗体(Dystrophin-N、-C、-R)对11例DMD患者，5例BMD患者和3例其他神经肌病患者同时行活检骨骼肌、皮肤免疫组织化学染色分析。
Creatase, electromyogram and muscle biopsy are important supplementary diagnostic methods. For patients with neuropathy in electromyogram and inflammatory cell infiltrate in biopsy, determination of gene and dystrophin should be performed.
结论血清肌酶、肌电图及肌活检是DMD重要的辅助诊断指标，对于肌电图有神经源性损害和肌活检病理检查有炎性细胞浸润者，应进行基因检测和dystrophin蛋白检测。
It can transmit 36 to 96 channels DMD layers digit al television
传输质量可以和光纤电视相
Polymerase chain reactionassay was employed to amplity DYZ-1 gene on the Y chromosome for determining fetal sex in 228 amniotic fluid cells, including 4 fetuses at risk for DMD/BMD and 1 fetus at risk for hemophilia A.
作者采用PCR技术扩增Y染色体长臂上的DYZ－1基因，对228例羊水进行了产前胎儿性别鉴定，其中4例为DMD／BMD的高危患儿，1例为甲型血友病的高危患儿。
Methods The clinical and laboratory data was analyzed in 40 children with confirmed diagnosis of Duchenne muscular dystrophy by dystrophin detection.
方法对40例经dystrophin蛋白检测确诊的DMD患儿的临床特征及实验室检查资料进行分析。
OBJECTIVE:To construct a simple DNA microarray for the measurement of the DMD gene common exon deletion, to grope for a methodology of new technique, and to prepare for the exploration of perfect DMD gene diagnosis chip.
目的：制备简易DNA微阵列检测DMD基因常见外显子缺失，作为一项新技术的方法学摸索，为开发更完善的DMD基因诊断芯片做准备。
Duchenne/Becker muscular dystrophy is an X-linked lethal recessive disease caused by mutation in the DMD gene.
假肥大性肌营养不良(Duchenne/Becker muscular dystrophy，DMD/BMD)是一种由于 DMD 基因突变导致的X连锁隐性致死性遗传病。
Objective To study the changes of isoforms of CK MM in children with DMD for early diagnosis and evaluation. Methods A discontinuous buffer system was used.
目的探讨假肥大型肌营养不良患儿肌型肌酸激酶同工酶亚型的变化在早期诊断和评价病情上的价值。
B-dystroglycan expression was detected by Western blot. Results A mutation C→T in 3202 of Dmd gene in model mice was found, and expression of b-dystroglycan was up-regulated in C57BL/10ScSn-Dmd/J.
结果 模型小鼠基因编码抗肌萎缩蛋白基因的第3202位点出现C→T的自发突变，模型小鼠β-dystroglycan的表达比正常鼠有显著性升高。
As stepping motor, it`s torque-frequency characteristic consists with the load of the let-off, this article adopted DM5676A type stepping motor and it`s driver of DMD402 type and designed the electric let-off, so that the system has adapted the need of the work of the air jet loom better.
而步进电机，由于其矩频特性正好与送经的负载特点相适应，基于此，本文采用DM5676A型步进电机及与之配套的DMD402型步进电机驱动器设计了送经驱动系统，以更好的适应喷气织机的工作要求。
The experimental results have also been demonstrated. 2. Intensity transfer function of DMD has been introduced, ITF is important for the quantity of projected sinusoidal fringe and the accuracy of phase measurement.
数字微镜器件及数字光处理技术作为实时空间光调制器在光学信息处理和光学三维传感领域具有广泛的应用前景。
Genes related to myogenesis, stem cells and apoptosis were detected at high levels in normal human EOMs, suggesting that efficient and continuous regeneration and/or myogenesis may be a mechanism by which the EOMs remain clinically and pathologically spared in diseases such as DMD.
与肌肉形成、干细胞和凋亡有关的基因在正常眼外肌中有较高表达，提示眼外肌中有充分的肌肉再生或形成，可能可以解释为何在杜兴型肌营养不良症中为何不受累。
Genes related to myogenesis, stem cells and apoptosis were detected at high leels in normal human EOMs, suggesting that efficient and continuous regeneration and/or myogenesis may be a mechanism by which the EOMs remain clinically and pathologically spared in diseases such as DMD.
与肌肉形成、干细胞和凋亡有关的基因在正常眼外肌中有较高表达，提示眼外肌中有充分的肌肉再生或形成，可能可以解释为何在杜兴型肌营养不良症中为何不受累。
The company was founded in the early days of 2003.5.4 is building a dedicated glass tempered glass, plastic folder for the main products of glass, since 2005 the introduction of new products - LCD dimming glass, produced in 2006 has 600 square meters, and widely used in Guangzhou Metro, Beijing Tsinghua University and Beijing Fortune Center and other key projects, the company with excellent processing capability, a complete packaging, transportation and installation won the customers, is an internationally renowned manufacturer of liquid crystal film transfer DMD Japan Korea UMU in mainland China's fixed-point processing enterprises.
本公司成立于2003.5.4之初是以建筑专用玻璃钢化玻璃，夹胶玻璃为主营产品的，自2005年起推出新产品-液晶调光玻璃，2006年已经生产了600平方米，并广泛应用于广州地铁，北京清华大学和北京财富中心等重点工程，公司以优良的加工能力，完备的包装，运输和安装赢得了客户的好评，是国际知名液晶调光膜生产厂家日本DMD韩国UMU在中国大陆的定点加工企业。
Results The small regenerating fibers, central location of nucelus and basophilia endochylema were observed under HE stain both in the patients with DMD and PM. Anachromasis of antiNCAM monoclonal immunohistochemistry stain was found in the regenerating muscle fibers. Positive Ezrin expression was also detected in the regenerating fibers. However, this expression tapered gradually as the mature process of skeletal muscle. The expression of Ezrin was negative in the mature fibers.
结果 DMD、PM患者被检肌HE染色所见再生肌纤维直径较小、核位于中央、胞浆嗜碱性；NCAM染色再生肌纤维深染；再生肌纤维Ezrin呈阳性表达，伴随肌纤维成熟Ezrin表达逐渐减弱，成熟肌纤维无Ezrin表达；成肌细胞Ezrin呈阳性表达。
These findings may help the design of interventions to develop family hardiness in families of children with DMD.
研究发现有助於设计介入措施目标增强发展杜显型肌失养症儿童之家庭的优势。
Objective:WT5BZUsing dinucleotide repeat polymorphism in the dystrophin gene as markers, we intended to improve prenatal diagnosis for Duchenne muscular dystroph families and to evaluate its feasibility.
目的：应用二核苷酸重复多态Duchenne型肌营养不良症基因诊断，探讨DMD产前基因诊断方案及其可行性。
The mirror in this case is part of an optical semiconductor called a digital micromirror device, or DMD.
在这里，镜子是被称做数字微镜器件的光半导体的一部分。