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: 12 ; Page: 181-186
Growth Hormone and IGF Research ; Volume: 14 Suppl A ; Page: S158-165
Molecular Endocrinology -Baltimore- ; Volume: 17 ; Page: 2448-2460
Human Molecular Genetics ; Volume: 12 ; Page: R285-R292
Proceedings of the National Academy of Sciences of the United States of America ; Volume: 100 ; Page: 8660-8665
American Journal of Human Genetics ; Volume: 72 ; Page: 1141-1153
American Journal of Human Genetics ; Volume: 72 ; Page: 454-464
Human Genetics ; Volume: 112 ; Page: 135-142
Human Genetics ; Volume: 112 ; Page: 135-142
Neuromuscular Disorders ; Volume: 12 ; Page: 939-946
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: