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Spine|May 7, 2004
Effects of functional restoration versus 3 hours per week physical therapy: a randomized controlled studyNathalie Jousset, Serge Fanello, Luc Bontoux, et al.
The Journal of Cell Biology|March 10, 2021
Endoplasmic reticulum maintains ion homeostasis required for plasma membrane repairGoutam Chandra, Sen Chandra Sreetama, Davi A G Mázala, et al.
Biochemistry|August 12, 2008
Calpain 1 binding capacities of the N1-line region of titin are significantly enhanced by physiological concentrations of calciumGerald Coulis, Samira Becila, Carlos H Herrera-Mendez, et al.
Human Molecular Genetics|May 16, 2019
Loss of Cajal bodies in motor neurons from patients with novel mutations in VRK1Lara El-Bazzal, Khalil Rihan, Nathalie Bernard-Marissal, et al.
Plos Genetics|June 21, 2013
Deregulation of the protocadherin gene FAT1 alters muscle shapes: implications for the pathogenesis of facioscapulohumeral dystrophyNathalie Caruso, Balàzs Herberth, Marc Bartoli, et al.
Human Mutation|July 27, 2017
Molecular combing reveals complex 4q35 rearrangements in Facioscapulohumeral dystrophyKarine Nguyen, Francesca Puppo, Stéphane Roche, et al.
Human Molecular Genetics|February 8, 2017
Exploiting the CRISPR/Cas9 system to study alternative splicing in vivo: application to titinKarine Charton, Laurence Suel, Sara F Henriques, et al.
The Journal of Biological Chemistry|July 17, 2010
Interactions with M-band titin and calpain 3 link myospryn (CMYA5) to tibial and limb-girdle muscular dystrophiesJaakko Sarparanta, Gaëlle Blandin, Karine Charton, et al.
Human Molecular Genetics|September 22, 2010
Removal of the calpain 3 protease reverses the myopathology in a mouse model for titinopathiesKarine Charton, Nathalie Danièle, Anna Vihola, et al.
Scientific Reports|September 11, 2024
Correction of exon 2, exon 2-9 and exons 8-9 duplications in DMD patient myogenic cells by a single CRISPR/Cas9 systemJuliette Lemoine, Auriane Dubois, Alan Dorval, et al.
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