
About
Our team aims to understand, in the model of skeletal muscle fibers, mechanisms controlling genome expression, cytoskeleton rearrangements and nuclear domain establishment and their implication in pathological contexts such as genetic disorders (Emery-Dreifuss Muscular Dystrophy and Centronuclear myopathies) or physiological aging (Sarcopenia). We also aim, in the model of cardiomyocyte, decipher implication of mutations identified in cardiomyopathies such as inherited hypertrophic cardiomyopathies (HCM), Atrial fibrillation (AF) or Arrhythmogenic right ventricular cardiomyopathy (ARVC).

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Projects
The nuclei actively position themselves throughout muscle development. Extensive data support a direct connection between the regulation of nuclear domains, […]

The function of skeletal muscle tissue relies on the maintenance and regeneration of myofibers through a finely regulated process. It […]

The functioning of the muscle fiber (myofiber) is supported by precise positioning of its organelles and nuclei. The contractile force […]

Secretory protein transport is necessary to fulfil essential cellular functions, enabling communication between cells, tissue maintenance and specialized functions. Differentiated […]

Cardiac arrhythmias are cardiomyopathies that regroup different pathophysiological syndromes such as atrial fibrillation, tachycardia and ventricular fibrillation. Deciphering molecular mechanisms […]



