1) Dystroglycan
肌萎缩蛋白
1.
Dystroglycan participates in the activation of lymphocytes and formation of synapse;
肌萎缩蛋白参与淋巴细胞的活化及免疫突触的形成
2) dystrophin
抗肌萎缩蛋白
1.
Changes of dystrophin expression in muscle of patients with DMD and its relevance to clinical pathology;
DMD患者骨骼肌抗肌萎缩蛋白表达与临床病理改变
2.
Methods We conducted comprehensive clinical and lab investigations including the test of serum enzymes,electromyography(EMG),electrocardiography,color Doppler echocardiography,HE staining of skeletal muscles,immunohistochemical study of dystrophin and utrophin,multiple ligation probe amplification(MLPA)on exon 1-79 of dystrophin gene,and short tandem repeat-poly-merase chain reacti.
方法对患者进行临床观察、血清酶、肌电图、心电图及心脏彩色超声检查、肌肉病理HE染色,免疫组织化学染色检测肌肉组织抗肌萎缩蛋白、utrophin的表达,用多重连接探针扩增法对抗肌萎缩蛋白基因1～79号外显子进行缺失和/或重复突变检测,利用抗肌萎缩蛋白基因的CA短串联重复序列(STR)对该家系进行STR-PCR连锁分析。
3.
Duchenne muscular dystrophy(DMD)is X-linked recessive genetic disease caused by the complex mutations of the gigantic dystrophin gene.
随着分子生物学的研究进展,对DMD的基因和其编码的抗肌萎缩蛋白(dystrophin)及抗肌萎缩蛋白相关蛋白(utrophin)的认识不断深入。
3) dystrophinopathy
抗肌萎缩蛋白病
1.
Objective To investigate the clinical and pathological features of Turner syndrome with dystrophinopathy.
目的探讨Turner综合征合并抗肌萎缩蛋白病(dystrophinopathy)的临床表现、病理学特点。
4) utrophin
抗肌萎缩蛋白相关蛋白
1.
As the research of these mutations goes on,more and more propertities of dystrophin and utrophin,the genes responsible for DMD,have been uncovered.
随着分子生物学的研究进展,对DMD的基因和其编码的抗肌萎缩蛋白(dystrophin)及抗肌萎缩蛋白相关蛋白(utrophin)的认识不断深入。
5) microdystrophin gene
微小抗肌萎缩蛋白基因
1.
Transfection and in vitro expression of human microdystrophin gene in rat mesenchymal stem cells;
人微小抗肌萎缩蛋白基因转染大鼠骨髓间充质干细胞及其基因表达
6) Dystrophin gene
抗肌萎缩蛋白基因
补充资料：肌萎缩
肌萎缩
myoatrophy
肌肉体积缩小，肌纤维变细的一种表现。多由肌肉本身疾患或神经系统功能障碍所致。部分因肢体活动减少所致者称为废用性萎缩。本病常伴有肌纤维数目减少和肌张力减弱。
说明：补充资料仅用于学习参考，请勿用于其它任何用途。
参考词条