日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

The role of dystrophin isoforms and interactors in the brain

肌营养不良蛋白亚型及其相互作用蛋白在大脑中的作用

Tetorou, Konstantina; Aghaeipour, Artadokht; Singh, Simran; Morgan, Jennifer E; Muntoni, Francesco

Engineered human myogenic cells in hydrogels generate innervated vascularized myofibers within dystrophic mouse muscle on long-term engraftment.

水凝胶中的工程化人类成肌细胞在长期移植后可在营养不良小鼠肌肉内生成有神经支配的血管化肌纤维

Kowala Anna, Boot James, Meng Jinhong, Mein Charles A, Pourquié Olivier, Connelly John T, Morgan Jennifer E, Lin Yung-Yao

Regional Expression of Dystrophin Gene Transcripts and Proteins in the Mouse Brain.

小鼠脑内肌营养不良蛋白基因转录本和蛋白质的区域表达。

Tetorou Konstantina, Aghaeipour Artadokht, Ma Shunyi, Gileadi Talia, Saoudi Amel, Perdomo Quinteiro Pablo, Aragón Jorge, van Putten Maaike, Spitali Pietro, Montanez Cecilia, Vaillend Cyrille, Morgan Jennifer E, Montanaro Federica, Muntoni Francesco

Investigating the Impact of Delivery Routes for Exon Skipping Therapies in the CNS of DMD Mouse Models

研究外显子跳跃疗法递送途径对DMD小鼠模型中枢神经系统的影响

Saoudi, Amel; Fergus, Claire; Gileadi, Talia; Montanaro, Federica; Morgan, Jennifer E; Kelly, Vincent P; Tensorer, Thomas; Garcia, Luis; Vaillend, Cyrille; Muntoni, Francesco; Goyenvalle, Aurélie

Effects of Mini-Dystrophin on Dystrophin-Deficient, Human Skeletal Muscle-Derived Cells

迷你肌营养不良蛋白对缺乏肌营养不良蛋白的人类骨骼肌衍生细胞的影响

Meng, Jinhong; Counsell, John; Morgan, Jennifer E

Publisher Correction: Necroptosis mediates myofibre death in dystrophin-deficient mice

出版商更正:坏死性凋亡介导肌营养不良蛋白缺陷小鼠的肌纤维死亡

Morgan, Jennifer E; Prola, Alexandre; Mariot, Virginie; Pini, Veronica; Meng, Jinhong; Hourde, Christophe; Dumonceaux, Julie; Conti, Francesco; Relaix, Frederic; Authier, Francois-Jerôme; Tiret, Laurent; Muntoni, Francesco; Bencze, Maximilien

Genome Editing and Muscle Stem Cells as a Therapeutic Tool for Muscular Dystrophies

基因组编辑和肌肉干细胞作为治疗肌营养不良症的工具

Pini, Veronica; Morgan, Jennifer E; Muntoni, Francesco; O'Neill, Helen C

Loss-of-function mutations in SCN4A cause severe foetal hypokinesia or 'classical' congenital myopathy

SCN4A基因功能缺失突变会导致严重的胎儿运动减少症或“经典”先天性肌病。

Zaharieva, Irina T; Thor, Michael G; Oates, Emily C; van Karnebeek, Clara; Hendson, Glenda; Blom, Eveline; Witting, Nanna; Rasmussen, Magnhild; Gabbett, Michael T; Ravenscroft, Gianina; Sframeli, Maria; Suetterlin, Karen; Sarkozy, Anna; D'Argenzio, Luigi; Hartley, Louise; Matthews, Emma; Pitt, Matthew; Vissing, John; Ballegaard, Martin; Krarup, Christian; Slørdahl, Andreas; Halvorsen, Hanne; Ye, Xin Cynthia; Zhang, Lin-Hua; Løkken, Nicoline; Werlauff, Ulla; Abdelsayed, Mena; Davis, Mark R; Feng, Lucy; Phadke, Rahul; Sewry, Caroline A; Morgan, Jennifer E; Laing, Nigel G; Vallance, Hilary; Ruben, Peter; Hanna, Michael G; Lewis, Suzanne; Kamsteeg, Erik-Jan; Männikkö, Roope; Muntoni, Francesco

Autologous skeletal muscle derived cells expressing a novel functional dystrophin provide a potential therapy for Duchenne Muscular Dystrophy

表达新型功能性肌营养不良蛋白的自体骨骼肌衍生细胞为杜氏肌营养不良症提供了一种潜在疗法

Meng, Jinhong; Counsell, John R; Reza, Mojgan; Laval, Steven H; Danos, Olivier; Thrasher, Adrian; Lochmüller, Hanns; Muntoni, Francesco; Morgan, Jennifer E

Matrix Metalloproteinases and Tissue Inhibitor of Metalloproteinases in Inflammation and Fibrosis of Skeletal Muscles

基质金属蛋白酶和金属蛋白酶组织抑制剂在骨骼肌炎症和纤维化中的作用

Alameddine, Hala S; Morgan, Jennifer E