Zobrazeno 1 - 10
of 674
pro vyhledávání: '"A. Lafoux"'
We investigate the impact of confinement density (i.e the number of individuals in a group per unit area of available space) on transitions from polarized to milling state, using groups of rummy-nose tetra fish (\textit{Hemigrammus rhodostomus}) unde
Externí odkaz:
http://arxiv.org/abs/2401.01850
Serotonin reuptake inhibitors improve muscle stem cell function and muscle regeneration in male mice
Autor:
Mylène Fefeu, Michael Blatzer, Anita Kneppers, David Briand, Pierre Rocheteau, Alexandre Haroche, David Hardy, Mélanie Juchet-Martin, Anne Danckaert, François Coudoré, Abdulkarim Tutakhail, Corinne Huchet, Aude Lafoux, Rémi Mounier, Olivier Mir, Raphaël Gaillard, Fabrice Chrétien
Publikováno v:
Nature Communications, Vol 15, Iss 1, Pp 1-15 (2024)
Abstract Serotonin reuptake inhibitor antidepressants such as fluoxetine are widely used to treat mood disorders. The mechanisms of action include an increase in extracellular level of serotonin, neurogenesis, and growth of vessels in the brain. We i
Externí odkaz:
https://doaj.org/article/e38e2d2ee87c4271aef118d9c4f7a763
We experimentally investigate the role of illumination on the collective dynamics of a large school (ca. 50 individuals) of Hemigrammus rhodostomus. The structure of the group, defined using two order parameters, is quantified while progressively alt
Externí odkaz:
http://arxiv.org/abs/2301.09577
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
Publikováno v:
Communications Biology, Vol 6, Iss 1, Pp 1-6 (2023)
Abstract We experimentally investigate the role of illumination on the collective dynamics of a large school (ca. 50 individuals) of Hemigrammus rhodostomus. The structure of the group, defined using two order parameters, is quantified while progress
Externí odkaz:
https://doaj.org/article/4f1ea0c0372b4d698b59cd579daad9aa
Autor:
Lafoux, Blaise, Baillet, Nicolas, Picard, Caroline, Fourcaud, Gustave, Borges-Cardoso, Virginie, Reynard, Stéphanie, Journeaux, Alexandra, Germain, Clara, Perthame, Emeline, Mateo, Mathieu, Hortion, Jimmy, Carnec, Xavier, Pietrosemoli, Natalia, Moroso, Marie, Lacroix, Orianne, Jourjon, Ophélie, Barron, Stéphane, Vallve, Audrey, Duthey, Aurélie, Jacquot, Frédéric, Barrot, Laura, Dirheimer, Manon, Raoul, Hervé, Nougier, Christophe, Baize, Sylvain
Publikováno v:
In Blood 14 December 2023 142(24):2092-2104
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
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Autor:
Jérôme Montnach, Laila Ananda Blömer, Ludivine Lopez, Luiza Filipis, Hervé Meudal, Aude Lafoux, Sébastien Nicolas, Duong Chu, Cécile Caumes, Rémy Béroud, Chris Jopling, Frank Bosmans, Corinne Huchet, Céline Landon, Marco Canepari, Michel De Waard
Publikováno v:
Nature Communications, Vol 13, Iss 1, Pp 1-13 (2022)
Photoactivable toxins targeting ion channels have great potential to control cell activity. Here the authors report HwTxIV-Nvoc, a UV light-cleavable and photoactivatable peptide that targets voltage-gated sodium channels; they validate this in cells
Externí odkaz:
https://doaj.org/article/423c1529d3814c50834a3cc0ac0261d0
Autor:
Anna Creisméas, Claire Gazaille, Audrey Bourdon, Marc-Antoine Lallemand, Virginie François, Marine Allais, Mireille Ledevin, Thibaut Larcher, Gilles Toumaniantz, Aude Lafoux, Corinne Huchet, Ignacio Anegon, Oumeya Adjali, Caroline Le Guiner, Bodvaël Fraysse
Publikováno v:
Journal of Translational Medicine, Vol 19, Iss 1, Pp 1-17 (2021)
Abstract Background Duchenne muscular dystrophy (DMD) is an X-linked inherited disease caused by mutations in the gene encoding dystrophin that leads to a severe and ultimately life limiting muscle-wasting condition. Recombinant adeno-associated vect
Externí odkaz:
https://doaj.org/article/df4837365a234a57b360f01bc60d2a4d