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
European Journal of Human Genetics ; Volume: 21 ; Page: 637-342
PLoS ONE ; Volume: 8 ; Page: e67527
PLoS Genetics ; Volume: 9, online ; Page: Non paginé
American Journal of Human Genetics ; Volume: 92 ; Page: 271-278
Phosphoinositides and Disease ; Volume: 362 ; Page: 209-233
Acta Neuropathologica ; Volume: 124 ; Page: 575-581
Trends in Molecular Medicine ; Volume: 18 ; Page: 317-327
Human Mutation ; Volume: 33 ; Page: 949 - 959
PLoS Genetics ; Volume: 8 ; Page: e1002595
European Journal of Human Genetics ; Volume: 20 ; Page: 701-704
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: