Identify the genetic basis of myopathies
Subgroup Leader : Valérie BIANCALANA
We study rare and severe neuromuscular disorders caused by mutations in proteins controlling intracellular organization and dynamics. We aim to tackle the three main bottlenecks in this field:
Identify the genetic basis of myopathies, myalgia and high athletic performances
Project leaders : Valérie BIANCALANA, Johann BOHM, Jocelyn LAPORTE
Understand and cure myotubular/centronuclear myopathies through gene modulation and pharmacology
Project leader : Jocelyn LAPORTE
Understand and cure tubular aggregates myopathy and Stormorken syndrome through gene modulation and pharmacology
Project leader : Johann BOHM
Subgroup Leader : Valérie BIANCALANA
Subgroup Leader : Jocelyn LAPORTE
Advances in Biological Regulation ; Volume: 52 ; Page: 98-107
European Journal of Human Genetics ; Volume: 20 ; Page: 1101--1101
PLoS Genetics ; Volume: 8 ; Page: e1002965
Acta Neuropathologica ; Volume: 124 ; Page: 273 - 283
Skeletal Muscle ; Volume: 1 ; Page: 26
Neuromuscular Disorders ; Volume: 21 ; Page: 379-386
Nature Medicine ; Volume: 17 ; Page: 720-5
Médecine/Sciences ; Volume: 27 ; Page: 458-460
American Journal of Pathology ; Volume: 178 ; Page: 2224-2235
Journal of Clinical Investigation ; Volume: 121 ; Page: 70 - 85
Current fundings:
On February 27, the IGBMC opened its doors to several members of the Unistra Alumni Network, led by Agnès Villanueva (Director of Alumni Relations),…
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Follow our publications and latest research on Researchgate : www.researchgate.net/profile/Jocelyn-Laporte
Raw data for our study on Multi-omics comparisons of different forms of centronuclear myopathies and the effects of several therapeutic strategies. Mol Ther. 2021 Apr 30:S1525-0016(21)00247-1.
www.ncbi.nlm.nih.gov/geo/query/acc.cgi
www.sciencedirect.com/science/article/abs/pii/S1525001621002471
In the press: