Détail de l'auteur
Auteur Deschamps JY |
Documents disponibles écrits par cet auteur



![]()
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
Revue : Scientific Reports, 10, 1 Titre : Capsid-specific removal of circulating antibodies to adeno-associated virus vectors Type de document : Article Auteurs : Bertin B ; Veron P ; Leborgne C ; Deschamps JY ; Moullec S ; Fromes Y ; Collaud F ; Boutin S ; Latournerie V ; Van Wittenberghe L ; Delache B ; Le Grand R ; Dereuddre-Bosquet N ; Benveniste O ; Moullier P ; Masurier C ; Merten O ; Mingozzi F Editeur : England Année de publication : 01/2020 Pages : p 864 Langues : Anglais (eng) Mots-clés : plasmaphérèse ; RECHERCHE ; réponse immunitaire ; singe ; souris ; stratégie thérapeutique ; thérapie génique ; vecteur adénoassocié Pubmed / DOI : Pubmed : 31965041 / DOI : 10.1038/s41598-020-57893-z
N° Profil MNM : 2020013 En ligne : http://www.ncbi.nlm.nih.gov/pubmed/31965041 Voir aussiAvis des lecteurs Aucun avis, ajoutez le vôtre !
(mauvais) 15 (excellent)
![]()
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
Revue : Science translational medicine, 11, 520 Titre : Titin splicing regulates cardiotoxicity associated with calpain 3 gene therapy for limb-girdle muscular dystrophy type 2A Type de document : Article Auteurs : Lostal W ; Roudaut C ; Faivre M ; Charton K ; Suel L ; Bourg N ; Best H ; Smith JE ; Gohlke J ; Corre G ; Li X ; Elbeck Z ; Knöll R ; Deschamps JY ; Granzier H ; Richard I Editeur : United States Année de publication : 11/2019 Langues : Anglais (eng) Mots-clés : calpaïne ; calpaïne 3 ; calpaïne 3 (maladie liée à) ; dystrophie musculaire des ceintures ; effet indésirable ; essai préclinique ; LGMDR1 ; maladie neuromusculaire ; Primates ; souris ; thérapie génique ; vecteur adénoassocié Pubmed / DOI : Pubmed : 31776291 / DOI : 10.1126/scitranslmed.aat6072
N° Profil MNM : 2019121 En ligne : http://www.ncbi.nlm.nih.gov/pubmed/31776291 Avis des lecteurs Aucun avis, ajoutez le vôtre !
(mauvais) 15 (excellent)
![]()
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
Revue : Cell transplantation Titre : Vascular Delivery of Allogeneic MuStem Cells in Dystrophic Dogs Requires Only Short-Term Immunosuppression to Avoid Host Immunity and Generate Clinical/Tissue Benefits Type de document : Article Auteurs : Lorant J, Auteur ; Larcher T ; Jaulin N ; Hedan B ; Lardenois A ; Leroux I ; Dubreil L ; Ledevin M ; Goubin H ; Moullec S ; Deschamps JY ; Thorin C ; André C ; Adjali O ; Rouger K Année de publication : 01/01/2018 Langues : Anglais (eng) Pubmed / DOI : DOI : 10.1177/0963689718776306 / Pubmed : 29871519
N° Profil MNM : 2018061 En ligne : http://www.ncbi.nlm.nih.gov/pubmed/29871519 Avis des lecteurs Aucun avis, ajoutez le vôtre !
(mauvais) 15 (excellent)
![]()
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
Avis des lecteurs Aucun avis, ajoutez le vôtre !
(mauvais) 15 (excellent)
![]()
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
Revue : PLoS ONE, 10, 5 Titre : Differential Gene Expression Profiling of Dystrophic Dog Muscle after MuStem Cell Transplantation Type de document : Article Auteurs : Robriquet F, Auteur ; Lardenois A ; Babarit C ; Larcher T ; Dubreil L ; Leroux I ; Zuber C ; Ledevin M ; Deschamps JY ; Fromes Y ; Cherel Y ; Guevel L ; Rouger K Année de publication : 2015 Langues : Anglais (eng) Mots-clés : chien grmd ; dystrophie musculaire de Duchenne ; expression génique ; muscle squelettique ; myoblaste ; transplantation cellulaire Pubmed / DOI : Pubmed : 25955839 / DOI : 10.1371/journal.pone.0123336
Avis des lecteurs Aucun avis, ajoutez le vôtre !
(mauvais) 15 (excellent)
![]()
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
Permalink![]()
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
Permalink![]()
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
Permalink![]()
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
Permalink![]()
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
Permalink![]()
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
Permalink![]()
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
Permalink![]()
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
Permalink![]()
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
Permalink![]()
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
Permalink![]()
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
Permalink![]()
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
Permalink![]()
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
Permalink![]()
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
Permalink![]()
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
Permalink![]()
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
Permalink![]()
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
Permalink![]()
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
Permalink![]()
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
Permalink![]()
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
Permalink