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

Simtuzumab Attenuates Loxl2-Mediated Extracellular Matrix Remodeling and Preserves Cardiac Function in LMNA Mutation-Induced Dilated Cardiomyopathy

Simtuzumab 可减轻 Loxl2 介导的细胞外基质重塑,并在 LMNA 突变诱发的扩张型心肌病中维持心脏功能。

Kervella, Marie; Behrens, Charlotta S; Peccate, Cécile; Guesmia, Zoheir; Grandi, Fiorella; Mougenot, Nathalie; Forand, Anne; Charrabi, Azzouz; Brochier, Guy; Andriantsitohaina, Ramaroson; Singh, Sonia R; Eschenhagen, Thomas; Meli, Albano C; Muchir, Antoine

Long-Term Dystrophin Replacement Therapy in Duchenne Muscular Dystrophy Causes Cardiac Inflammation.

杜氏肌营养不良症长期肌营养不良蛋白替代疗法会导致心脏炎症

Forand Anne, Moog Sophie, Mougenot Nathalie, Lemaitre Mégane, Sevoz-Couche Caroline, Guesmia Zoheir, Virtanen Laura, Giordani Lorenzo, Muchir Antoine, Pietri-Rouxel France

Fighting for every beat: cardiac therapies in Duchenne muscular dystrophy

为每一次心跳而战:杜氏肌营养不良症的心脏治疗

Muchir, Antoine

Genome organization in cardiomyocytes expressing mutated A-type lamins

表达突变型A型核纤层蛋白的心肌细胞的基因组组织

Kervella, Marie; Jahier, Maureen; Meli, Albano C; Muchir, Antoine

Author Correction: Loss of MTX2 causes mandibuloacral dysplasia and links mitochondrial dysfunction to altered nuclear morphology

作者更正:MTX2 缺失导致下颌肢端发育不良,并将线粒体功能障碍与核形态改变联系起来

Elouej, Sahar; Harhouri, Karim; Mao, Morgane Le; Baujat, Genevieve; Nampoothiri, Sheela; Kayserili, Hϋlya; Menabawy, Nihal Al; Selim, Laila; Paneque, Arianne Llamos; Kubisch, Christian; Lessel, Davor; Rubinsztajn, Robert; Charar, Chayki; Bartoli, Catherine; Airault, Coraline; Deleuze, Jean-François; Rötig, Agnes; Bauer, Peter; Pereira, Catarina; Loh, Abigail; Escande-Beillard, Nathalie; Muchir, Antoine; Martino, Lisa; Gruenbaum, Yosef; Lee, Song-Hua; Manivet, Philippe; Lenaers, Guy; Reversade, Bruno; Lévy, Nicolas; De Sandre-Giovannoli, Annachiara

Combined Treatment with Peptide-Conjugated Phosphorodiamidate Morpholino Oligomer-PPMO and AAV-U7 Rescues the Severe DMD Phenotype in Mice

肽偶联磷酰二胺吗啉寡聚体(PPMO)与AAV-U7联合治疗可挽救小鼠的严重DMD表型

Forand, Anne; Muchir, Antoine; Mougenot, Nathalie; Sevoz-Couche, Caroline; Peccate, Cécile; Lemaitre, Mégane; Izabelle, Charlotte; Wood, Matthew; Lorain, Stéphanie; Piétri-Rouxel, France

An Omics View of Emery-Dreifuss Muscular Dystrophy

从组学角度看埃默里-德雷福斯肌营养不良症

Vignier, Nicolas; Muchir, Antoine

Emery-Dreifuss muscular dystrophy: focal point nuclear envelope

埃默里-德雷福斯肌营养不良症:核膜焦点

Muchir, Antoine; Worman, Howard J

The Pathogenesis and Therapies of Striated Muscle Laminopathies

横纹肌层粘连蛋白病的病理机制和治疗方法

Brull, Astrid; Morales Rodriguez, Blanca; Bonne, Gisèle; Muchir, Antoine; Bertrand, Anne T

ERK1/2 directly acts on CTGF/CCN2 expression to mediate myocardial fibrosis in cardiomyopathy caused by mutations in the lamin A/C gene

ERK1/2 直接作用于 CTGF/CCN2 的表达,从而介导由层粘蛋白 A/C 基因突变引起的心肌病中的心肌纤维化。

Chatzifrangkeskou, Maria; Le Dour, Caroline; Wu, Wei; Morrow, John P; Joseph, Leroy C; Beuvin, Maud; Sera, Fusako; Homma, Shunichi; Vignier, Nicolas; Mougenot, Nathalie; Bonne, Gisèle; Lipson, Kenneth E; Worman, Howard J; Muchir, Antoine