Camille Loret
5PUBLICATIONS
23CO-AUTHORS
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Publications (5)
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|Aug 01, 2025
Nationwide Phenotypic and Genotypic Characterisation of 103 Patients With SH3TC2 Gene-Related Demyelinating Peripheral Neuropathy.Pauline Jaubert, Camille Loret, Tanya Stojkovic
|Mar 13, 2025
From in vivo models to in vitro bioengineered neuromuscular junctions for the study of Charcot-Marie-Tooth disease.Camille Scherrer, Camille Loret, Nicolas Védrenne
|Jul 27, 2024
CRISPR Base Editing to Create Potential Charcot-Marie-Tooth Disease Models with High Editing Efficiency: Human Induced Pluripotent Stem Cell Harboring SH3TC2 Variants.Camille Loret, Amandine Pauset, Pierre-Antoine Faye
|Mar 28, 2024
Readthrough Activators and Nonsense-Mediated mRNA Decay Inhibitor Molecules: Real Potential in Many Genetic Diseases Harboring Premature Termination Codons.Nesrine Benslimane, Camille Loret, Pauline Chazelas
|Jul 29, 2023
Amlexanox: Readthrough Induction and Nonsense-Mediated mRNA Decay Inhibition in a Charcot-Marie-Tooth Model of hiPSCs-Derived Neuronal Cells Harboring a Nonsense Mutation in GDAP1 Gene.Nesrine Benslimane, Federica Miressi, Camille Loret
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Frequent Collaborators
4 joint publications
Pierre-Antoine Faye
4 joint publications
Frédéric Favreau
3 joint publications
Anne-Sophie Lia
2 joint publications
Nesrine Benslimane
2 joint publications
Ioanna Pyromali
2 joint publications
Fabrice Lejeune
2 joint publications
Franck Sturtz
1 joint publications
Valérie Prouzet-Mauleon
1 joint publications
Federica Miressi
1 joint publications
Béatrice Turcq
