Marc Bartoli

12PUBLICATIONS
33CO-AUTHORS
Microelectromechanical systems (MEMS)Medical biochemistry - amino acids and metabolitesGenetically modified animalsNeurology and neuromuscular diseasesMedical molecular engineering of nucleic acids and proteins
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Publications (12)

|Jun 16, 2026
Restoring the interplay between the endoplasmic reticulum and mitochondria by gene therapy improves Charcot-Marie-Tooth type 2A disease.

|May 16, 2024
System-level analysis of genes mutated in muscular dystrophies reveals a functional pattern associated with muscle weakness distribution.

Ozan Ozisik, Svetlana Gorokhova, Mathieu Cerino

|May 27, 2023
A Dysferlin Exon 32 Nonsense Mutant Mouse Model Shows Pathological Signs of Dysferlinopathy.

Océane Ballouhey, Marie Chapoton, Benedicte Alary

|Oct 31, 2022
Imbalance of NRG1-ERBB2/3 signalling underlies altered myelination in Charcot-Marie-Tooth disease 4H.

Lara El-Bazzal, Adeline Ghata, Clothilde Estève

|Aug 12, 2022
Objective Evaluation of Clinical Actionability for Genes Involved in Myopathies: 63 Genes with a Medical Value for Patient Care.

Maude Vecten, Emmanuelle Pion, Marc Bartoli

|Jul 27, 2022
Novel Exon-Skipping Therapeutic Approach for the DMD Gene Based on Asymptomatic Deletions of Exon 49.

Mario Abaji, Svetlana Gorokhova, Nathalie Da Silva

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Frequent Collaborators

5 joint publications

Svetlana Gorokhova

2 joint publications

Mathieu Cerino

2 joint publications

Nathalie Bernard-Marissal

2 joint publications

Nathalie Bonello-Palot