Seguir
serge picaud
serge picaud
Institut de la vision
Dirección de correo verificada de inserm.fr
Título
Citado por
Citado por
Año
Genetic reactivation of cone photoreceptors restores visual responses in retinitis pigmentosa
V Busskamp, J Duebel, D Balya, M Fradot, TJ Viney, S Siegert, AC Groner, ...
science 329 (5990), 413-417, 2010
7432010
Light-emitting diodes (LED) for domestic lighting: any risks for the eye?
F Behar-Cohen, C Martinsons, F Viénot, G Zissis, A Barlier-Salsi, ...
Progress in retinal and eye research 30 (4), 239-257, 2011
5232011
Partial recovery of visual function in a blind patient after optogenetic therapy
JA Sahel, E Boulanger-Scemama, C Pagot, A Arleo, F Galluppi, JN Martel, ...
Nature medicine 27 (7), 1223-1229, 2021
4292021
Cellular retinol‐binding protein I is essential for vitamin A homeostasis
NB Ghyselinck, C Båvik, V Sapin, M Mark, D Bonnier, C Hindelang, ...
The EMBO journal, 1999
3831999
Retinitis pigmentosa: rod photoreceptor rescue by a calcium-channel blocker in the rd mouse
M Frasson, JA Sahel, M Fabre, M Simonutti, H Dreyfus, S Picaud
Nature medicine 5 (10), 1183-1187, 1999
2941999
A spike sorting toolbox for up to thousands of electrodes validated with ground truth recordings in vitro and in vivo
P Yger, GLB Spampinato, E Esposito, B Lefebvre, S Deny, C Gardella, ...
Elife 7, e34518, 2018
2882018
Glial cell line–derived neurotrophic factor induces histologic and functional protection of rod photoreceptors in the rd/rd mouse
M Frasson, S Picaud, T Léveillard, M Simonutti, S Mohand–Said, ...
Investigative ophthalmology & visual science 40 (11), 2724-2734, 1999
2841999
Optogenetic therapy for retinitis pigmentosa
V Busskamp, S Picaud, JA Sahel, B Roska
Gene therapy 19 (2), 169-175, 2012
2802012
Optimized allotopic expression of the human mitochondrial ND4 prevents blindness in a rat model of mitochondrial dysfunction
S Ellouze, S Augustin, A Bouaita, C Bonnet, M Simonutti, V Forster, ...
The American Journal of Human Genetics 83 (3), 373-387, 2008
2402008
Emerging therapies for inherited retinal degeneration
HPN Scholl, RW Strauss, MS Singh, D Dalkara, B Roska, S Picaud, ...
Science translational medicine 8 (368), 368rv6-368rv6, 2016
2292016
Functional cone rescue by RdCVF protein in a dominant model of retinitis pigmentosa
Y Yang, S Mohand-Said, A Danan, M Simonutti, V Fontaine, E Clerin, ...
Molecular therapy 17 (5), 787-795, 2009
2102009
Targeting channelrhodopsin-2 to ON-bipolar cells with vitreally administered AAV restores ON and OFF visual responses in blind mice
E Macé, R Caplette, O Marre, A Sengupta, A Chaffiol, P Barbe, ...
Molecular Therapy 23 (1), 7-16, 2015
2052015
Expanded polyglutamines induce neurodegeneration and trans-neuronal alterations in cerebellum and retina of SCA7 transgenic mice
G Yvert, KS Lindenberg, S Picaud, GB Landwehrmeyer, JA Sahel, ...
Human molecular genetics 9 (17), 2491-2506, 2000
2012000
Glutamine-expanded ataxin-7 alters TFTC/STAGA recruitment and chromatin structure leading to photoreceptor dysfunction
D Helmlinger, S Hardy, G Abou-Sleymane, A Eberlin, AB Bowman, ...
PLoS biology 4 (3), e67, 2006
1872006
Phototoxic action spectrum on a retinal pigment epithelium model of age-related macular degeneration exposed to sunlight normalized conditions
E Arnault, C Barrau, C Nanteau, P Gondouin, K Bigot, F Viénot, E Gutman, ...
PloS one 8 (8), e71398, 2013
1862013
Red‐shifted channelrhodopsin stimulation restores light responses in blind mice, macaque retina, and human retina
A Sengupta, A Chaffiol, E Macé, R Caplette, M Desrosiers, M Lampič, ...
EMBO molecular medicine 8 (11), 1248-1264, 2016
1772016
Human Usher 1B/Mouse shaker-1 : The Retinal Phenotype Discrepancy Explained By The Presence/Absence of Myosin VIIA in The Photoreceptor …
A El-Amraoui, I Sahly, S Picaud, J Sahel, M Abitbol, C Petit
Human molecular genetics 5 (8), 1171-1178, 1996
1711996
Bilateral visual improvement with unilateral gene therapy injection for Leber hereditary optic neuropathy
P Yu-Wai-Man, NJ Newman, V Carelli, ML Moster, V Biousse, AA Sadun, ...
Science translational medicine 12 (573), eaaz7423, 2020
1632020
Inherited retinal degenerations: therapeutic prospects
MN Delyfer, T Léveillard, S Mohand-Saïd, D Hicks, S Picaud, JA Sahel
Biology of the Cell 96 (4), 261-269, 2004
1592004
Microglial changes occur without neural cell death in diabetic retinopathy
D Gaucher, JA Chiappore, M Pâques, M Simonutti, C Boitard, JA Sahel, ...
Vision research 47 (5), 612-623, 2007
1572007
El sistema no puede realizar la operación en estos momentos. Inténtalo de nuevo más tarde.
Artículos 1–20