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Different pharmacological profile of two closely related endocannabinoid ester analogs. [electronic resource] by
- Bobrov, Mikhail
- Gretskaya, Natalia
- Payet, Olivier
- Bezuglov, Vladimir
- Durand, Thierry
- Maurin, Laurence
- Tourrel, Frank
- Adjali, Oumeya
- Rinaldi-Carmona, Murielle
- Muller, Agnès
Producer: 20050818
In:
Life sciences vol. 77
Availability: No items available.
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14.
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OPA1 gene therapy prevents retinal ganglion cell loss in a Dominant Optic Atrophy mouse model. [electronic resource] by
- Sarzi, Emmanuelle
- Seveno, Marie
- Piro-Mégy, Camille
- Elzière, Lucie
- Quilès, Mélanie
- Péquignot, Marie
- Müller, Agnès
- Hamel, Christian P
- Lenaers, Guy
- Delettre, Cécile
Producer: 20181211
In:
Scientific reports vol. 8
Availability: No items available.
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15.
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The ocular anomalies in a cystinosis animal model mimic disease pathogenesis. [electronic resource] by
- Kalatzis, Vasiliki
- Serratrice, Nicolas
- Hippert, Claire
- Payet, Olivier
- Arndt, Carl
- Cazevieille, Chantal
- Maurice, Tangui
- Hamel, Christian
- Malecaze, François
- Antignac, Corinne
- Müller, Agnes
- Kremer, Eric J
Producer: 20070919
In:
Pediatric research vol. 62
Availability: No items available.
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16.
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Increased steroidogenesis promotes early-onset and severe vision loss in females with OPA1 dominant optic atrophy. [electronic resource] by
- Sarzi, Emmanuelle
- Seveno, Marie
- Angebault, Claire
- Milea, Dan
- Rönnbäck, Cecilia
- Quilès, Melanie
- Adrian, Mathias
- Grenier, Joanna
- Caignard, Angélique
- Lacroux, Annie
- Lavergne, Christian
- Reynier, Pascal
- Larsen, Michael
- Hamel, Christian P
- Delettre, Cécile
- Lenaers, Guy
- Müller, Agnès
Producer: 20170714
In:
Human molecular genetics vol. 25
Availability: No items available.
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17.
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Increased steroidogenesis promotes early-onset and severe vision loss in females with OPA1 dominant optic atrophy. [electronic resource] by
- Sarzi, Emmanuelle
- Seveno, Marie
- Angebault, Claire
- Milea, Dan
- Rönnbäck, Cecilia
- Quilès, Melanie
- Adrian, Mathias
- Grenier, Joanna
- Caignard, Angélique
- Lacroux, Annie
- Lavergne, Christian
- Reynier, Pascal
- Larsen, Michael
- Hamel, Christian P
- Delettre, Cécile
- Lenaers, Guy
- Müller, Agnès
Publication details: Human molecular genetics 12 2017
In:
Human molecular genetics vol. 26
Availability: No items available.
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18.
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Reversible optic neuropathy with OPA1 exon 5b mutation. [electronic resource] by
- Cornille, Karen
- Milea, Dan
- Amati-Bonneau, Patrizia
- Procaccio, Vincent
- Zazoun, Lydie
- Guillet, Virginie
- El Achouri, Ghizlane
- Delettre, Cécile
- Gueguen, Naïg
- Loiseau, Dominique
- Muller, Agnès
- Ferré, Marc
- Chevrollier, Arnaud
- Wallace, Douglas C
- Bonneau, Dominique
- Hamel, Christian
- Reynier, Pascal
- Lenaers, Guy
Producer: 20080610
In:
Annals of neurology vol. 63
Availability: No items available.
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19.
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Dominant mutations in mtDNA maintenance gene SSBP1 cause optic atrophy and foveopathy. [electronic resource] by
- Piro-Mégy, Camille
- Sarzi, Emmanuelle
- Tarrés-Solé, Aleix
- Péquignot, Marie
- Hensen, Fenna
- Quilès, Mélanie
- Manes, Gaël
- Chakraborty, Arka
- Sénéchal, Audrey
- Bocquet, Béatrice
- Cazevieille, Chantal
- Roubertie, Agathe
- Müller, Agnès
- Charif, Majida
- Goudenège, David
- Lenaers, Guy
- Wilhelm, Helmut
- Kellner, Ulrich
- Weisschuh, Nicole
- Wissinger, Bernd
- Zanlonghi, Xavier
- Hamel, Christian
- Spelbrink, Johannes N
- Sola, Maria
- Delettre, Cécile
Producer: 20200724
In:
The Journal of clinical investigation vol. 130
Availability: No items available.
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