Zobrazeno 1 - 10
of 39
pro vyhledávání: '"Bodvael, Fraysse"'
Autor:
Audrey Bourdon, Virginie François, Liwen Zhang, Aude Lafoux, Bodvael Fraysse, Gilles Toumaniantz, Thibaut Larcher, Tiphaine Girard, Mireille Ledevin, Cyrielle Lebreton, Agnès Hivonnait, Anna Creismeas, Marine Allais, Basile Marie, Justine Guguin, Véronique Blouin, Séverine Remy, Ignacio Anegon, Corinne Huchet, Alberto Malerba, Betty Kao, Anita Le Heron, Philippe Moullier, George Dickson, Linda Popplewell, Oumeya Adjali, Federica Montanaro, Caroline Le Guiner
Publikováno v:
Gene Therapy. 29:520-535
Autor:
Bodvael Fraysse, Jean-François Desaphy, Jean-François Rolland, Sabata Pierno, Antonella Liantonio, Viviana Giannuzzi, Claudia Camerino, M. Paola Didonna, Daniela Cocchi, Annamaria De Luca, Diana Conte Camerino
Publikováno v:
Neurobiology of Disease, Vol 21, Iss 2, Pp 372-380 (2006)
The mechanisms by which aging induces muscle impairment are not well understood yet. We studied the impact of aging on Ca2+ homeostasis in the slow-twitch soleus and the fast-twitch extensor digitorum longus (EDL) muscles of aged rats by using the fu
Externí odkaz:
https://doaj.org/article/c42dff5a571d4982875704381ee8a59d
Autor:
Bodvael Fraysse, Antonella Liantonio, Michela Cetrone, Rosa Burdi, Sabata Pierno, Antonio Frigeri, Michela Pisoni, Claudia Camerino, Annamaria De Luca
Publikováno v:
Neurobiology of Disease, Vol 17, Iss 2, Pp 144-154 (2004)
Chronic exercise in vivo aggravates dystrophy in mdx mice. Calcium homeostasis was evaluated ex vivo by micro-spectrofluorometry on tendon-to-tendon dissected extensor digitorum longus (EDL) muscle fibers. Resting cytosolic calcium ([Ca2+]i) and sarc
Externí odkaz:
https://doaj.org/article/8d171f21b90c4bc7a7a342ce607293eb
Autor:
Audrey, Bourdon, Virginie, François, Liwen, Zhang, Aude, Lafoux, Bodvael, Fraysse, Gilles, Toumaniantz, Thibaut, Larcher, Tiphaine, Girard, Mireille, Ledevin, Cyrielle, Lebreton, Agnès, Hivonnait, Anna, Creismeas, Marine, Allais, Basile, Marie, Justine, Guguin, Véronique, Blouin, Séverine, Remy, Ignacio, Anegon, Corinne, Huchet, Alberto, Malerba, Betty, Kao, Anita, Le Heron, Philippe, Moullier, George, Dickson, Linda, Popplewell, Oumeya, Adjali, Federica, Montanaro, Caroline, Le Guiner
Publikováno v:
Gene therapy. 29(9)
Duchenne muscular dystrophy (DMD) is a muscle wasting disorder caused by mutations in the gene encoding dystrophin. Gene therapy using micro-dystrophin (MD) transgenes and recombinant adeno-associated virus (rAAV) vectors hold great promise. To overc
Autor:
Oumeya Adjali, Bodvael Fraysse, Mireille Ledevin, M. Allais, C. Le Guiner, V. Le Razavet, Corinne Huchet, C. Gazaille, A. Bourdon, G. Toumanianz, Ignacio Anegon, A. Lafoux, A. Creisméas, Thibaut Larcher
Publikováno v:
Neuromuscular Disorders. 31:S76
Gait characterization in golden retriever muscular dystrophy dogs using linear discriminant analysis
Autor:
Stéphane Blot, Jean-Yves Hogrel, El Mostafa Qannari, Chantal Thorin, Caroline Le Guiner, Inès Barthélémy, Yan Cherel, Karl Rouger, Bodvael Fraysse
Publikováno v:
BMC Musculoskeletal Disorders
BMC Musculoskeletal Disorders, BioMed Central, 2017, 18 (1), ⟨10.1186/s12891-017-1494-4⟩
BMC Musculoskeletal Disorders, Vol 18, Iss 1, Pp 1-9 (2017)
BMC Musculoskeletal Disorders 1 (18), . (2017)
BMC Musculoskeletal Disorders, BioMed Central, 2017, 18 (1), ⟨10.1186/s12891-017-1494-4⟩
BMC Musculoskeletal Disorders, Vol 18, Iss 1, Pp 1-9 (2017)
BMC Musculoskeletal Disorders 1 (18), . (2017)
Background Accelerometric analysis of gait abnormalities in golden retriever muscular dystrophy (GRMD) dogs is of limited sensitivity, and produces highly complex data. The use of discriminant analysis may enable simpler and more sensitive evaluation
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::105de050fd708b0b6e39e7695819832d
https://hal.archives-ouvertes.fr/hal-01702256
https://hal.archives-ouvertes.fr/hal-01702256
Long-term microdystrophin gene therapy is effective in a canine model of Duchenne muscular dystrophy
Autor:
Virginie François, Oumeya Adjali, Jean-Yves Hogrel, George Dickson, Thibaut Larcher, Maeva Dutilleul, Taeyoung Koo, Marie Montus, Stéphane Ederhy, Stéphane Blot, M. Allais, Carole Masurier, Alberto Malerba, Marie Devaux, B. Matot, Karim Wahbi, Sophie Moullec, Bernard Gjata, Bodvael Fraysse, Laurent Servais, Fulvio Mavilio, Inès Barthélémy, Pierre G. Carlier, Takis Athanasopoulos, Isabelle Testault, Samia Martin, Jack-Yves Deschamps, Philippe Moullier, Federico Mingozzi, Philippe Veron, Christophe Georger, Johanne Le Duff, Caroline Le Guiner, Thomas Voit, Jean-Laurent Thibaut
Publikováno v:
Nature Communications
Nature Communications, 2017, 8 (1), pp.16105. ⟨10.1038/ncomms16105⟩
Nature communications (8), 16105. (2017)
Nature Communications, Nature Publishing Group, 2017, 8 (1), pp.16105. ⟨10.1038/ncomms16105⟩
Nature Communications, Vol 8, Iss 1, Pp 1-15 (2017)
Nature Communications, 2017, 8 (1), pp.16105. ⟨10.1038/ncomms16105⟩
Nature communications (8), 16105. (2017)
Nature Communications, Nature Publishing Group, 2017, 8 (1), pp.16105. ⟨10.1038/ncomms16105⟩
Nature Communications, Vol 8, Iss 1, Pp 1-15 (2017)
Duchenne muscular dystrophy (DMD) is an incurable X-linked muscle-wasting disease caused by mutations in the dystrophin gene. Gene therapy using highly functional microdystrophin genes and recombinant adeno-associated virus (rAAV) vectors is an attra
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4c348d77df95e4b68a2b7f4ada280b2b
https://univ-evry.hal.science/hal-02179396
https://univ-evry.hal.science/hal-02179396
Autor:
C. Le Guiner, Thibaut Larcher, D. Caudal, Ignacio Anegon, A. Lafoux, Corinne Huchet, M. Allais, Bodvael Fraysse, E. Amosse, Séverine Remy, Gilles Toumaniantz
Publikováno v:
Neuromuscular Disorders
22nd International Annual Congress of the World-Muscle-Society (WMS)
22nd International Annual Congress of the World-Muscle-Society (WMS), Oct 2017, Saint Malo, France. pp.1, ⟨10.1016/j.nmd.2017.06.546⟩
22nd International Annual Congress of the World-Muscle-Society (WMS)
22nd International Annual Congress of the World-Muscle-Society (WMS), Oct 2017, Saint Malo, France. pp.1, ⟨10.1016/j.nmd.2017.06.546⟩
National audience
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cb41ac907576cb2f529d9a50963a0c7b
https://hal.inrae.fr/hal-02736526
https://hal.inrae.fr/hal-02736526
Autor:
Giulia Maria Camerino, Diana Conte Camerino, Maria Cannone, Bodvael Fraysse, Domenico Tricarico, Antonia Scaramuzzi, Elena Conte, Antonella Liantonio, Sabata Pierno, Michela De Bellis
Publikováno v:
The American Journal of Pathology. 184:2803-2815
Hypertension is often associated with skeletal muscle pathological conditions related to function and metabolism. The mechanisms underlying the development of these pathological conditions remain undefined. Because calcium homeostasis is a biomarker
Autor:
Gillian Butler-Browne, Daniel Metzger, Arnaud Ferry, Alban Vignaud, Bourama Fane, Mélanie Schuh, Bodvael Fraysse
Publikováno v:
Steroids
Steroids, 2014, 87, pp.6-11. ⟨10.1016/j.steroids.2014.05.005⟩
Steroids, 2014, 87, pp.6-11. ⟨10.1016/j.steroids.2014.05.005⟩
International audience; As androgens might have rapid androgen-receptor (AR) independent action on muscle cells, we analysed the in vivo acute effect of androgens on maximal force generation capacity and electrically evoked calcium transient responsi