Zobrazeno 1 - 10
of 245
pro vyhledávání: '"A. Oumeya"'
Autor:
Magalie Penaud-Budloo, Emilie Lecomte, Quentin Lecomte, Simon Pacouret, Frédéric Broucque, Aurélien Guy-Duché, Jean-Baptiste Dupont, Laurence Jeanson-Leh, Cécile Robin, Véronique Blouin, Eduard Ayuso, Oumeya Adjali
Publikováno v:
Molecular Therapy: Methods & Clinical Development, Vol 32, Iss 3, Pp 101305- (2024)
With more than 130 clinical trials and 8 approved gene therapy products, adeno-associated virus (AAV) stands as one of the most popular vehicles to deliver therapeutic DNA in vivo. One critical quality attribute analyzed in AAV batches is the presenc
Externí odkaz:
https://doaj.org/article/042640a504cc42909af1d623d410fa67
Autor:
Penaud-Budloo, Magalie, Lecomte, Emilie, Lecomte, Quentin, Pacouret, Simon, Broucque, Frédéric, Guy-Duché, Aurélien, Dupont, Jean-Baptiste, Jeanson-Leh, Laurence, Robin, Cécile, Blouin, Véronique, Ayuso, Eduard, Adjali, Oumeya
Publikováno v:
In Molecular Therapy - Methods & Clinical Development 12 September 2024 32(3)
Autor:
Mozin, Elise, Massouridès, Emmanuelle, Mournetas, Virginie, Lièvre, Clémence, Bourdon, Audrey, Jackson, Dana L., Packer, Jonathan S., Seong, Juyoung, Trapnell, Cole, Le Guiner, Caroline, Adjali, Oumeya, Pinset, Christian, Mack, David L., Dupont, Jean-Baptiste
Publikováno v:
In iScience 19 July 2024 27(7)
Autor:
Anais Defois, Nina Bon, Mathieu Mével, David Deniaud, Yves Maugars, Jérôme Guicheux, Oumeya Adjali, Claire Vinatier
Publikováno v:
Journal of Cartilage & Joint Preservation, Vol 4, Iss 2, Pp 100186- (2024)
Introduction: Osteoarthritis (OA), the most common form of joint disease, affects more than 500 million people worldwide. This painful and debilitating disease imposes a huge socioeconomic cost worldwide. Despite years of promising research, no etiol
Externí odkaz:
https://doaj.org/article/88140a72be4d4f7b9fc8ae02b09f9ce1
Autor:
Defois, Anais, Bon, Nina, Mével, Mathieu, Deniaud, David, Maugars, Yves, Guicheux, Jérôme, Adjali, Oumeya, Vinatier, Claire
Publikováno v:
In Journal of Cartilage & Joint Preservation June 2024 4(2)
Autor:
Mével, Mathieu, Pichard, Virginie, Bouzelha, Mohammed, Alvarez-Dorta, Dimitri, Lalys, Pierre-Alban, Provost, Nathalie, Allais, Marine, Mendes, Alexandra, Landagaray, Elodie, Ducloyer, Jean-Baptiste, Toublanc, Estelle, Galy, Anne, Brument, Nicole, Lefevre, Gaëlle M., Gouin, Sébastien G., Isiegas, Carolina, Le Meur, Guylène, Cronin, Thérèse, Le Guiner, Caroline, Weber, Michel, Moullier, Philippe, Ayuso, Eduard, Deniaud, David, Adjali, Oumeya
Publikováno v:
In Molecular Therapy - Methods & Clinical Development 14 March 2024 32(1)
Autor:
Leray, Aurélien, Lalys, Pierre-Alban, Varin, Juliette, Bouzelha, Mohammed, Bourdon, Audrey, Alvarez-Dorta, Dimitri, Pavageau, Karine, Depienne, Sébastien, Marchand, Maia, Mellet, Anthony, Demilly, Joanna, Ducloyer, Jean-Baptiste, Girard, Tiphaine, Fraysse, Bodvaël, Ledevin, Mireille, Guilbaud, Mickaël, Gouin, Sébastien G., Ayuso, Eduard, Adjali, Oumeya, Larcher, Thibaut, Cronin, Thérèse, Le Guiner, Caroline, Deniaud, David, Mével, Mathieu
Publikováno v:
In Biomedicine & Pharmacotherapy February 2024 171
Autor:
Caroline Le Guiner, Xiao Xiao, Thibaut Larcher, Aude Lafoux, Corinne Huchet, Gilles Toumaniantz, Oumeya Adjali, Ignacio Anegon, Séverine Remy, Josh Grieger, Juan Li, Vahid Farrokhi, Hendrik Neubert, Jane Owens, Maritza McIntyre, Philippe Moullier, R. Jude Samulski
Publikováno v:
Molecular Therapy: Methods & Clinical Development, Vol 30, Iss , Pp 30-47 (2023)
Duchenne muscular dystrophy (DMD) is an X-linked disease caused by loss-of-function mutations in the dystrophin gene and is characterized by muscle wasting and early mortality. Adeno-associated virus-mediated gene therapy is being investigated as a t
Externí odkaz:
https://doaj.org/article/7a89e1515ecf4452944c4318d3851f25
Autor:
Mathieu Mével, Virginie Pichard, Mohammed Bouzelha, Dimitri Alvarez-Dorta, Pierre-Alban Lalys, Nathalie Provost, Marine Allais, Alexandra Mendes, Elodie Landagaray, Jean-Baptiste Ducloyer, Estelle Toublanc, Anne Galy, Nicole Brument, Gaëlle M. Lefevre, Sébastien G. Gouin, Carolina Isiegas, Guylène Le Meur, Thérèse Cronin, Caroline Le Guiner, Michel Weber, Philippe Moullier, Eduard Ayuso, David Deniaud, Oumeya Adjali
Publikováno v:
Molecular Therapy: Methods & Clinical Development, Vol 32, Iss 1, Pp 101187- (2024)
Inherited retinal diseases are a leading and untreatable cause of blindness and are therefore candidate diseases for gene therapy. Recombinant vectors derived from adeno-associated virus (rAAV) are currently the most promising vehicles for in vivo th
Externí odkaz:
https://doaj.org/article/1edecadd12924319b147b4cab1a426f8
Autor:
Le Guiner, Caroline, Xiao, Xiao, Larcher, Thibaut, Lafoux, Aude, Huchet, Corinne, Toumaniantz, Gilles, Adjali, Oumeya, Anegon, Ignacio, Remy, Séverine, Grieger, Josh, Li, Juan, Farrokhi, Vahid, Neubert, Hendrik, Owens, Jane, McIntyre, Maritza, Moullier, Philippe, Samulski, R. Jude
Publikováno v:
In Molecular Therapy - Methods & Clinical Development 14 September 2023 30:30-47