arrow
V

Vincent Mouly

Centre de Recherche en Myologie
H指数:68
被引数:1.3万

个人简介

暂无内容

教育背景

暂无内容

工作经历

暂无内容

荣誉奖项

暂无内容

Niclosamide reprograms macrophages and improves muscle integrity in Duchenne muscular dystrophy models

氯硝柳胺重编程巨噬细胞并改善杜氏肌营养不良模型中的肌肉完整性

2026-07-280
OAAI
Biallelic PAX7 variants cause a novel Satellite Cell-opathy with progressive muscle involvement resembling facioscapulohumeral muscular dystrophy
2026-01-290
OAAI
Obestatin Treatment Counteracts Muscle Wasting by Reactivation of Autophagy in Duchenne Muscular Dystrophy

奥贝斯坦汀治疗通过重新激活自噬来对抗杜氏肌营养不良症中的肌肉萎缩

MedComm
IF10.7
2026-01-140
OAAI
An Isogenic Human Myoblast Cell Model for Cystinosis Myopathy Reveals Alteration of Key Myogenic Regulatory Proteins

同源人肌成纤维细胞模型用于胱氨酸贮积症肌病研究,揭示了关键肌源性调控蛋白的异常变化

2025-11-100
OAAI
Generation Using Phage-Display of pH-Dependent Antibodies Against the Tumor-Associated Antigen AXL

通过噬菌体展示技术生成针对肿瘤相关抗原AXL的pH依赖性抗体

2025-10-010
OAAI
Immortalized human myotonic dystrophy type 1 muscle cell lines to address patient heterogeneity (vol 27, 109930, 2024)

永生性人类肌强直性营养不良1型肌细胞系用于解决患者异质性 (vol 27, 109930, 2024)

2024-12-010
OAAI
Cell-mediated exon skipping normalizes dystrophin expression and muscle function in a new mouse model of Duchenne Muscular Dystrophy (vol 16, 927, 2024)
2024-09-060
OAAI
Different outcomes of endurance and resistance exercise in skeletal muscles of Oculopharyngeal muscular dystrophy

眼咽型肌营养不良的骨骼肌耐力和抗阻运动的不同结果

2024-08-070
OA
Cell-mediated exon skipping normalizes dystrophin expression and muscle function in a new mouse model of Duchenne Muscular Dystrophy
2024-03-041
OAAI