1) wilting proteins
致萎峰蛋白
2) 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
3) Dystrophin
抗肌萎蛋白
1.
Clinical and Pathological Analysis on 25 Children with Muscular Dystrophy Caused by Deficiency of Dystrophin;
抗肌萎蛋白缺陷型肌营养不良症25例临床和病理研究
4) allergic protein
致敏蛋白
1.
Effect of extraction and processing methods on allergic proteins of peanut;
提取及加工方法对花生致敏蛋白的影响
2.
Study on the mechanisim of IgE-binding to soybean allergic proteins;
大豆致敏蛋白致敏机制研究
3.
5 kD allergic proteins of soybean products and 18.
本实验采用酶联免疫印迹和竞争性抑制实验识别大豆制品中的致敏蛋白。
5) 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。
6) 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。
补充资料：萎萎衰衰
1.犹萎靡不振。
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