干细胞移植治疗假肥大型肌营养不良症的文献分析

X Yang - 中国神经再生研究(英文版), 2012 - sjzsyj.com.cn
… for treating Duchenne muscular dystrophy using a bibliometric … transplantation for treating
Duchenne muscular dystrophy from … Nucleofection of muscle-derived stem cells and myoblasts

[PDF][PDF] Duchenne 肌营养不良(DMD) 发病机制及治疗研究进展

刘延波, 徐乃军, 贾飞勇 - 生命科学, 2012 - lifescience.sinh.ac.cn
… 成肌细胞移植(myoblast transfer therapy, MTT): 在1987年,Partrige等[7]首先提出将MTT…
Duchenne muscular dystrophy with long-term corticosteroid treatment: implications for management

杆状病毒转导抗肌萎缩蛋白基因及抗肌萎缩蛋白相关蛋白双敲除小鼠脂肪干细胞的转基因表达和分化

Q Li, Q Zhai, J Geng, H Zheng, F Chen… - 中国神经再生研究 …, 2012 - sjzsyj.com.cn
… contribute to induce adipose-derived stem cell differentiation into myoblasts, in a broader
attempt to promote autologous stem cell transplantation for Duchenne muscular dystrophy. …

间充质干细胞治疗杜氏肌营养不良症: 如何优化移植方案?

朱慧, 庞荣清, 潘兴华, 阮光萍 - 中国组织工程研究, 2015 - cjter.com
Treatment of Duchenne muscular dystrophy is not ideal. In recent years, more and more
scientists try to treat Duchenne muscular dystrophytreatment for Duchenne muscular dystrophy

脂肪干细胞通过旁分泌改善肌营养不良的成肌分化

J Cao, Y Liang, Y Li, H Zhang, Y Zhu, J Geng… - 中国神经再生研究 …, 2016 - sjzsyj.com.cn
Duchenne muscular dystrophy (DMD) is a recessive X-linked form of muscular dystrophy
might have therapeutic potential for the treatment of muscular dystrophy in humans as well. …

[HTML][HTML] Duchenne 型肌营养不良基因治疗研究进展

董奇超 - Chinese Journal of Contemporary Pediatrics, 2018 - ncbi.nlm.nih.gov
Duchenne型肌营养不良(duchenne muscular dystrophy, DMD)是进行性肌营养不良中最常见
的类型,以进行性、致死性为主要特点。世界上每3 500~6 000个新生男婴中就有一名DMD患儿 […

[PDF][PDF] TAL 效应核酸酶的应用和发展

A Juillerat, P Duchateau, T Cathomen… - 基因 …, 2016 - everestgene.wordpress.com
… editing restores dystrophin expression in cells from Duchenne muscular dystrophy patients.
Mol … The status of exon skipping as a therapeutic approach to Duchenne muscular dystrophy. …

失神经支配快肌和慢肌萎缩早期的miRNA 靶向信号通路

G Li, Q Li, W Li, J Wei, W Chang, Z Chen… - 中国神经再生研究 …, 2016 - sjzsyj.com.cn
… We assumed that denervated fast muscle atrophy might share characteristics with
primary muscle disorders such as Duchenne muscular dystrophy, Miyoshi myopathy, and …

脑源性神经营养因子rs6265 (Val66Met) 单核苷酸多态性作为人类病理生理学的主要修饰因子

BH Van Thuan Nguyen, N Sims, A Heck… - 中国神经再生研究 …, 2023 - sjzsyj.com.cn
… (2016) Translating golden retriever muscular dystrophy microarray findings to novel
biomarkers for cardiac/skeletal muscle function in Duchenne muscular dystrophy. Pediatr Res 79:…

[PDF][PDF] 大鼠肌源性干细胞的分离, 纯化和培养☆

叶锦, 靳风烁, 陈锦, 王鹏, 梁培禾, 聂志林… - Journal of Clinical …, 2010 - cjter.com
… of a putative pathway for the muscle homing of stem cells in a muscular dystrophy model.
J … Skeletal myoblast transplantation for repair of myocardial necrosis.J Clin Invest. 1996;98(11)…