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

Development of a split-toxin CRISPR screening platform to systematically identify regulators of human myoblast fusion.

开发分裂毒素 CRISPR 筛选平台,以系统地鉴定人类成肌细胞融合的调节因子。

Zhang Haifeng, Shang Renjie, Zhang Zheng, Zhou Min, Bigot Anne, Cai Yanqing, Zhao Yanran, Wang Yushu, Deshmukh Aaryahi, Kudryashova Elena, Kudryashov Dmitri S, He Cuiyu, Mouly Vincent, Bi Pengpeng

Tet2 deficiency promotes IgG1+ B-cell expansion and differentiation blockade through deregulation of the Nfkbia-c-Rel axis

Tet2 缺陷通过 Nfkbia-c-Rel 轴的失调促进 IgG1+ B 细胞扩增和分化阻滞

Ghamlouch, Hussein; Degaud, Michaël; Della-Valle, Veronique; Eeckhoutte, Alexandre; Armand, Marine; Joudat, Amina; Decaudin, Camille; Dominguez, Pilar M; Rosikiewicz, Wojciech; Pawlikowska, Patrycja; Darwiche, Walaa; Mouly, Enguerran; Li, Sheng; Melnick, Ari M; Aoufouchi, Said; Bernard, Olivier A

Obestatin Treatment Counteracts Muscle Wasting by Reactivation of Autophagy in Duchenne Muscular Dystrophy

奥贝斯汀治疗通过重新激活杜氏肌营养不良症患者的自噬来对抗肌肉萎缩

Santos-Zas, Icía; Costas-Abalde, Silvia; Lodeiro, Andrea C; Fernández-Barreiro, Fátima; Cid-Díaz, Tania; Leal-López, Saúl; González-Sánchez, Jessica; García-Lamela, Mar; Debasa-Corral, Lucía; Mosteiro, Carlos S; Mamchaoui, Kamel; Mouly, Vincent; Casabiell, Xesús; Gallego, Rosalía; Relova, José Luis; Pazos, Yolanda; Camiña, Jesus P

Biallelic PAX7 variants cause a novel Satellite Cell-opathy with progressive muscle involvement resembling facioscapulohumeral muscular dystrophy.

双等位基因 PAX7 变异体引起一种新型卫星细胞病,伴有进行性肌肉受累,类似于面肩肱型肌营养不良症。

Ganassi Massimo, Strafella Claudia, Savarese Marco, Heher Philipp, Engquist Elise N, McGuire Liam, Johari Mridul, De Nicola Gian F, Bigot Anne, Mouly Vincent, Bortolani Sara, Torchia Eleonora, Monforte Mauro, Megalizzi Domenica, Sabino Andrea, Ricci Enzo, Giardina Emiliano, Zammit Peter S, Tasca Giorgio

Best reference genes for unbiased normalized transcript expression in normal and dystrophic human cell models of myogenesis

肌生成正常和肌营养不良的人类细胞模型中,用于无偏标准化转录表达的最佳参考基因

Quarta, Raffaella; Boccanegra, Brigida; Cristiano, Enrica; Ladisa, Alberto; Conte, Elena; Ohana, Jessica; Mouly, Vincent; De Luca, Annamaria; Hildyard, John; Cappellari, Ornella

Maternal High-Fat Diet and Neonatal LPS Exposure Prolong USV Sequences and Shift Call-Type Repertoires in Neonatal Rats

母体高脂饮食和新生儿LPS暴露延长新生大鼠的超声波发声序列并改变其鸣叫类型库

Purohit, Mansi Kamlesh; Woo, Ingrid; Rahman, Mouly; Abuaish, Sameera; McGowan, Patrick O

Small nucleolar RNAs promote the restoration of muscle differentiation defects in cells from myotonic dystrophy type 1.

小核仁RNA促进1型强直性肌营养不良细胞肌肉分化缺陷的恢复

Bogard Baptiste, Bonnet Hélène, Boyarchuk Ekaterina, Tellier Gilles, Furling Denis, Mouly Vincent, Francastel Claire, Hubé Florent

Obestatin treatment links mitochondrial homeostasis and skeletal muscle repair in Duchenne muscle dystrophy.

奥贝斯汀治疗将杜氏肌营养不良症的线粒体稳态与骨骼肌修复联系起来。

Lodeiro Andrea C, Costas-Abalde Silvia, Cid-Díaz Tania, Debasa-Corral Lucía, Leal-López Saúl, Mamchaoui Kamel, Mouly Vincent, Casabiell Xesús, Gallego Rosalía, Relova José Luis, Pazos Yolanda, Santos-Zas Icía, Camiña Jesus P

Role of Peptides in Skeletal Muscle Wasting: A Scoping Review

肽在骨骼肌萎缩中的作用:一项范围综述

Naumovski, Petar; De Spiegeleer, Bart; Wakjira, Aster; Van De Wiele, Christophe; Mouly, Vincent; Goljanek-Whysall, Katarzyna; da Costa, Kauê Santana; de Oliveira, Ewerton Cristhian Lima; Wynendaele, Evelien; De Spiegeleer, Anton

An Isogenic Human Myoblast Cell Model for Cystinosis Myopathy Reveals Alteration of Key Myogenic Regulatory Proteins

胱氨酸病肌病同源人成肌细胞模型揭示关键肌源性调节蛋白的改变

Medaer, Louise; Mora, Roger; Zhou, Zhuoheng; Giarratana, Nefele; Yedigaryan, Laura; La Rovere, Rita; Levtchenko, Elena; Mouly, Vincent; Verhoeyen, Els; Eeltink, Sebastiaan; Treumann, Achim; Vervliet, Tim; Sampaolesi, Maurilio; Gijsbers, Rik