Florian Barthélémy

Affiliations: 
2009-2013 Myologie Translationnelle AIx-Marseille Universités, Marseille, Provence-Alpes-Côte d'Azur, France 
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"Florian Barthélémy"
Mean distance: 17.58 (cluster 32)
 
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Publications

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Bartoli M, Bailey RM, Meyer K, et al. (2023) Editorial: Personalized medicine for neuromuscular disorders. Frontiers in Cell and Developmental Biology. 11: 1329048
Barthélémy F, Santoso JW, Rabichow L, et al. (2022) Modeling Patient-Specific Muscular Dystrophy Phenotypes and Therapeutic Responses in Reprogrammed Myotubes Engineered on Micromolded Gelatin Hydrogels. Frontiers in Cell and Developmental Biology. 10: 830415
Barthélémy F, Wang RT, Hsu C, et al. (2019) Targeting RyR Activity Boosts Antisense Exon 44 and 45 Skipping in Human DMD Skeletal or Cardiac Muscle Culture Models. Molecular Therapy. Nucleic Acids. 18: 580-589
Gibbs EM, Barthélémy F, Douine ED, et al. (2019) Large in-frame 5' deletions in DMD associated with mild Duchenne muscular dystrophy: Two case reports and a review of the literature. Neuromuscular Disorders : Nmd
Barthélémy F, Wein N. (2018) Personalized gene and cell therapy for Duchenne Muscular Dystrophy. Neuromuscular Disorders : Nmd
Barthélémy F, Courrier S, Lévy N, et al. (2018) Dysferlin Exon 32 Skipping in Patient Cells. Methods in Molecular Biology (Clifton, N.J.). 1828: 489-496
Barthelemy F, Wang D, Nelson SF, et al. (2018) Validation and Detection of Exon Skipping Boosters in DMD Patient Cell Models and mdx Mouse. Methods in Molecular Biology (Clifton, N.J.). 1828: 309-326
Wang RT, Barthelemy F, Martin AS, et al. (2018) DMD genotype correlations from duchenneConnect: Endogenous exon skipping is a factor in prolonged ambulation for individuals with a defined mutation sub-type. Human Mutation
Barthélémy F, Defour A, Lévy N, et al. (2018) Muscle Cells Fix Breaches by Orchestrating a Membrane Repair Ballet. Journal of Neuromuscular Diseases. 5: 21-28
Barthélémy F, Blouin C, Wein N, et al. (2015) Exon 32 Skipping of Dysferlin Rescues Membrane Repair in Patients' Cells. Journal of Neuromuscular Diseases. 2: 281-290
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