Zobrazeno 1 - 10
of 243
pro vyhledávání: '"Chaffiol, A."'
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
Berling, David, Baroni, Luca, Chaffiol, Antoine, Gauvain, Gregory, Picaud, Serge, Antolík, Ján
Publikováno v:
Journal of Neuroscience; 12/4/2024, Vol. 44 Issue 49, p1-13, 13p
Autor:
Chaffiol, Antoine, Provansal, Matthieu, Joffrois, Corentin, Blaize, Kévin, Labernede, Guillaume, Goulet, Ruben, Burban, Emma, Brazhnikova, Elena, Duebel, Jens, Pouget, Pierre, Sahel, José Alain, Picaud, Serge, Arcizet, Fabrice, Gauvain, Gregory
Publikováno v:
In Molecular Therapy - Methods & Clinical Development 10 March 2022 24:1-10
Autor:
Antoine Chaffiol, Matthieu Provansal, Corentin Joffrois, Kévin Blaize, Guillaume Labernede, Ruben Goulet, Emma Burban, Elena Brazhnikova, Jens Duebel, Pierre Pouget, José Alain Sahel, Serge Picaud, Fabrice Arcizet, Gregory Gauvain
Publikováno v:
Molecular Therapy: Methods & Clinical Development, Vol 24, Iss , Pp 1-10 (2022)
Over the last 15 years, optogenetics has changed fundamental research in neuroscience and is now reaching toward therapeutic applications. Vision restoration strategies using optogenetics are now at the forefront of these new clinical opportunities.
Externí odkaz:
https://doaj.org/article/3539475107dc44d68426b97714ec967c
Autor:
Simmons, Tabatha R., Vetter, Tatyana A., Huang, Nianyuan, Vulin-Chaffiol, Adeline, Wein, Nicolas, Flanigan, Kevin M.
Publikováno v:
In Molecular Therapy - Methods & Clinical Development 11 June 2021 21:325-340
Autor:
Tabatha R. Simmons, Tatyana A. Vetter, Nianyuan Huang, Adeline Vulin-Chaffiol, Nicolas Wein, Kevin M. Flanigan
Publikováno v:
Molecular Therapy: Methods & Clinical Development, Vol 21, Iss , Pp 325-340 (2021)
Duchenne muscular dystrophy (DMD) is an X-linked progressive disease characterized by loss of dystrophin protein that typically results from truncating mutations in the DMD gene. Current exon-skipping therapies have sought to treat deletion mutations
Externí odkaz:
https://doaj.org/article/6912488c4ecd404facb01ca8c3e269ec
Autor:
M. Provansal, G. Labernède, C. Joffrois, A. Rizkallah, R. Goulet, M. Valet, W. Deschamps, U. Ferrari, A. Chaffiol, D. Dalkara, J. A. Sahel, M. Tanter, S. Picaud, G. Gauvain, F. Arcizet
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-12 (2021)
Abstract Optogenetics has revolutionized neurosciences by allowing fine control of neuronal activity. An important aspect for this control is assessing the activation and/or adjusting the stimulation, which requires imaging the entire volume of optog
Externí odkaz:
https://doaj.org/article/1dd37e80ffb447ca9a7dfd8e7970b325
Autor:
Gregory Gauvain, Himanshu Akolkar, Antoine Chaffiol, Fabrice Arcizet, Mina A. Khoei, Mélissa Desrosiers, Céline Jaillard, Romain Caplette, Olivier Marre, Stéphane Bertin, Claire-Maelle Fovet, Joanna Demilly, Valérie Forster, Elena Brazhnikova, Philippe Hantraye, Pierre Pouget, Anne Douar, Didier Pruneau, Joël Chavas, José-Alain Sahel, Deniz Dalkara, Jens Duebel, Ryad Benosman, Serge Picaud
Publikováno v:
Communications Biology, Vol 4, Iss 1, Pp 1-15 (2021)
Gauvain et al demonstrate that optogenetic therapy using the AAV2.7m8- ChR-tdT construct can partially restore vision in non-human primates to levels above those considered legally-blind. This study enables the identification of the most suitable con
Externí odkaz:
https://doaj.org/article/0b4ca90d06f64da69afaff7c49d68f90
Autor:
Tournier, Marie, Neumann, Anke, Pambrun, Elodie, Weill, Alain, Chaffiol, Jean-Philippe, Alla, François, Bégaud, Bernard, Maura, Géric, Verdoux, Hélène
Publikováno v:
In Journal of Affective Disorders 1 October 2019 257:412-420
Autor:
Pouzat, Christophe, Chaffiol, Antoine
After an elementary derivation of the "time transformation", mapping a counting process onto a homogeneous Poisson process with rate one, a brief review of Ogata's goodness of fit tests is presented and a new test, the "Wiener process test", is propo
Externí odkaz:
http://arxiv.org/abs/0909.2785
