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Capsid-specific removal of circulating antibodies to adeno-associated virus vectors
Bertin B, Veron P, Leborgne C, et al.
Scientific Reports, 2020, 10, 1, p 864
Titin splicing regulates cardiotoxicity associated with calpain 3 gene therapy for limb-girdle muscular dystrophy type 2A
Lostal W, Roudaut C, Faivre M, et al.
Science translational medicine, 2019, 11, 520
Vascular Delivery of Allogeneic MuStem Cells in Dystrophic Dogs Requires Only Short-Term Immunosuppression to Avoid Host Immunity and Generate Clinical/Tissue Benefits
Lorant J, Larcher T, Jaulin N, et al.
Cell transplantation, 2018
Long-term microdystrophin gene therapy is effective in a canine model of Duchenne muscular dystrophy
Le Guiner C, Servais L, Montus M, et al.
Nature communications, 2017, 8
Differential Gene Expression Profiling of Dystrophic Dog Muscle after MuStem Cell Transplantation
Robriquet F, Lardenois A, Babarit C, et al.
PLoS ONE, 2015, 10, 5
Forelimb Treatment in a Large Cohort of Dystrophic Dogs Supports Delivery of a Recombinant AAV for Exon Skipping in Duchenne Patients
Le Guiner C, Montus M, Servais L, et al.
Molecular therapy : the journal of the American Society of Gene Therapy, 2014, 22, 11, p 1923
Restoration of vsion in the pde6beta-deficient dog, a large animal model of rod-cone dystrophy
Petit L, Lheriteau E, Weber M, et al.
Molecular therapy, 2012, 20, 11, p. 2019-2030
Restoration of vision in the pde6Beta-deficient dog, a large animal model of rod-cone dystrophy
Petit L, Lheriteau E, Weber M, et al.
Molecular therapy : the journal of the American Society of Gene Therapy, 2012, 20, 11, p 2019
Gene transfer of human CD40Ig does not prevent rejection in a non-human primate kidney allotransplantation model
Angin M, Poirier N, Dilek N, et al.
Transplant immunology, 2012, 27, 4, p 139
Fatal overdose after ingestion of a transdermal fentanyl patch in two non-human primates
Deschamps JY, Gaulier JM, Podevin G, et al.
Veterinary anaesthesia and analgesia, 2012, 39, 6, p 653
Systemic delivery of allogenic muscle stem (MuStem) cells induces long-term muscle repair and clinical efficacy in Duchenne muscular dystrophy dogs
Rouger K, Larcher T, Dubreil L, et al.
American journal of pathology (The), 2011, 179,5, p. 2501-2518
Dystrophin expression after locoregional injection of RAAV8-U7 SNRNA vectors in the forelimb of GRMD dogs
Cherel Y, Larcher T, François V, et al.
Congrès : 4th International Congress of Myology, 4ème colloque international de Myologie (9-13 mai 2011; Lille (France))
2011, p. 78
Intra-muscular distribution of dystrophin positive fibers after locoregional injection of RAAV8-U7 SNRNA vectors in thefore limb of GRMD dogs
Cherel Y, Larcher T, Deschamps JY, et al.
Congrès : 4th International Congress of Myology, 4ème colloque international de Myologie (9-13 mai 2011; Lille (France))
2011, p. 38
Long-term muscle repair and clinical efficacy in duchenne muscular dystrophy dogs induced by systemic delivery of allogenic muscle stem (mustem) cells
Rouger K, Larcher T, Dubreil L, et al.
Congrès : 4th International Congress of Myology, 4ème colloque international de Myologie (9-13 mai 2011; Lille (France))
2011, p. 107
Systemic delivery of allogenic muscle stem cells induces long-term muscle repair and clinical efficacy in Duchenne muscular dystrophy dogs
Rouger K, Larcher T, Dubreil L, et al.
The American journal of pathology, 2011, 179, 5, p 2501
Lack of immunotoxicity after regional intravenous (RI) delivery of rAAV to nonhuman primate skeletal muscle
Toromanoff A, Adjali O, Larcher T, et al.
Molecular therapy : the journal of the American Society of Gene Therapy, 2010, 18, 1, p 151
Regulation of retinal function but nonrescue of vision in RPE65-deficient dogs treated with doxycycline-regulatable AAV vectors
Lheriteau E, Libeau L, Mendes-Madeira A, et al.
Molecular therapy : the journal of the American Society of Gene Therapy, 2010, 18, 6, p 1085
Tolerogenic dendritic cells actively inhibit T cells through heme oxygenase-1 in rodents and in nonhuman primates
Moreau A, Hill M, Thebault P, et al.
FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 2009, 23, 9, p 3070
Detection of intact rAAV particles up to 6 years after successful gene transfer in the retina of dogs and primates
Stieger K, Schroeder J, Provost N, et al.
Molecular therapy : the journal of the American Society of Gene Therapy, 2009, 17, 3, p 516
Efficient intrathymic gene transfer following in situ administration of a rAAV serotype 8 vector in mice and nonhuman primates
Moreau A, Vicente R, Dubreil L, et al.
Molecular therapy : the journal of the American Society of Gene Therapy, 2009, 17, 3, p 472
Subretinal delivery of recombinant AAV serotype 8 vector in dogs results in gene transfer to neurons in the brain
Stieger K, Colle MA, Dubreil L, et al.
Molecular therapy : the journal of the American Society of Gene Therapy, 2008, 16, 5, p 916
Safety and efficacy of regional intravenous (r.i.) versus intramuscular (i.m.) delivery of rAAV1 and rAAV8 to nonhuman primate skeletal muscle
Toromanoff A, Cherel Y, Guilbaud M, et al.
Molecular therapy : the journal of the American Society of Gene Therapy, 2008, 16, 7, p 1291
Muscle regeneration potential of canine muscle-derived stem cells in GRMD dog model
Rouger K, Dubreil L, Fornasari B, et al.
Congrès : Congrès international de myologie 2008 (International Congress of Myology 2008; 26-30 mai 2008; Marseille, France)
2008, p. 460
Safety and efficacy of regional intravenous (RI) versus intramuscular (IM) delivery of RAAV1 and RAAV8 to nonhuman primate skeletal muscle
Toromanoff A, Cherel Y, Guilbaud M, et al.
Congrès : Congrès international de myologie 2008 (International Congress of Myology 2008; 26-30 mai 2008; Marseille, France)
2008, p. 613
Safety and efficacy of regional intravenous (RI) versus intramuscular (IM) delivery of RAAV1 and RAAV8 to nonhuman primate skeletal muscle (P 89)
Toromanoff A, Cherel Y, Guilbaud M, et al.
Congrès : Colloque jeunes chercheurs (7 mars 2008; EVRY - Centre conférence Génocentre Evry)
2008, p. 12
