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

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

Transcriptional adaptation upregulates utrophin in Duchenne muscular dystrophy.

转录适应上调杜氏肌营养不良症中的肌营养不良蛋白

Falcucci Lara, Dooley Christopher M, Adamoski Douglas, Juan Thomas, Martinez Justin, Georgieva Angelina M, Mamchaoui Kamel, Cirzi Cansu, Stainier Didier Y R

Micro-Scale Topography Triggers Dynamic 3D Nuclear Deformations.

微观地形引发动态三维核形变

Leclech Claire, Cardillo Giulia, Roellinger Bettina, Zhang Xingjian, Frederick Joni, Mamchaoui Kamel, Coirault Catherine, Barakat Abdul I

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

Allele-specific RNAi therapy corrects an extracellular matrix defect in Schuurs-Hoeijmakers syndrome.

等位基因特异性 RNAi 疗法可纠正 Schuurs-Hoeijmakers 综合征的细胞外基质缺陷。

Mekzine Lylia, Pinzón Natalia, Mamchaoui Kamel, Kondili Maria, Cadot Bruno, Bitoun Marc, Trochet Delphine

Human Laminin-111-Derived AG73 Increases Proliferation, Migration, and Differentiation of Human Myoblasts: A Promising Candidate in Regenerative Medicine

人层粘连蛋白-111衍生的AG73可促进人成肌细胞的增殖、迁移和分化:再生医学领域中一种有前景的候选药物

Horita, Samuel Iwao Maia; Bensalah, Mona; Bigot, Anne; Mamchaoui, Kamel; Butler Browne, Gillian S; Beghini, Daniela Gois; Savino, Wilson; Trollet, Capucine; Mouly, Vincent; Negroni, Elisa; Henriques Pons, Andrea; Riederer, Ingo

The Emerging TNNT3 Spectrum: From Distal Arthrogryposis to Congenital Myopathy

TNNT3 疾病谱的演变:从远端关节挛缩症到先天性肌病

Altin, Nami; Mamchaoui, Kamel; Ohana, Jessica; Bigot, Anne; Corradi, Beatrice; Maragliano, Luca; Madia, Francesca; Ognibene, Marzia; Nosrati, Mohammad Sadegh Shams; Paladini, Dario; Iacomino, Michele; Rashid, Asma; Bodamer, Olaf; Quijano-Roy, Susana; Punetha, Jaya; Capra, Valeria; Zara, Federico; Trollet, Capucine; Scala, Marcello

A Novel Assay Reveals the Early Setting-Up of Membrane Repair Machinery in Human Skeletal Muscle Cells

一种新型检测方法揭示了人类骨骼肌细胞中膜修复机制的早期建立

d'Agata, Léna; Rassinoux, Phoebe; Gounou, Céline; Bouvet, Flora; Bouragba, Dounia; Mamchaoui, Kamel; Bouter, Anthony

Characterization of DMPK and MBNL1 expression in cell models of myotonic dystrophy: a platform for drug screening

肌强直性营养不良细胞模型中DMPK和MBNL1表达的特征分析:药物筛选平台

López-Martínez, Andrea; Martín-González, Sergio; Torres-Conde, Noemi; Alcalá-Manso, Nahia; Al-Ani, Abdullah; López de Munain, Adolfo; Bigot, Anne; Mamchaoui, Kamel; Nogales-Gadea, Gisela; Arechavala-Gomeza, Virginia

Functional benefit of CRISPR-Cas9-induced allele deletion for RYR1 dominant mutation

CRISPR-Cas9诱导的等位基因缺失对RYR1显性突变的功能益处

Beaufils, Mathilde; Melka, Margaux; Brocard, Julie; Benoit, Clement; Debbah, Nagi; Mamchaoui, Kamel; Romero, Norma B; Dalmas-Laurent, Anne Frédérique; Quijano-Roy, Susana; Fauré, Julien; Rendu, John; Marty, Isabelle