Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Sophie Lourdel"'
Autor:
Juliette Bitard, Elodie-Kim Grellier, Sophie Lourdel, Helena Prior Filipe, Annaïg Hamon, François Fenaille, Florence Anne Castelli, Emeline Chu-Van, Jérôme E. Roger, Morgane Locker, Muriel Perron
Publikováno v:
Cell Death Discovery, Vol 10, Iss 1, Pp 1-14 (2024)
Abstract Glaucoma is a multifactorial neurodegenerative disease characterized by the progressive and irreversible degeneration of the optic nerve and retinal ganglion cells. Despite medical advances aiming at slowing degeneration, around 40% of treat
Externí odkaz:
https://doaj.org/article/5094564ec34949d59e846b3ed1d20852
Autor:
Karine Parain, Sophie Lourdel, Alicia Donval, Albert Chesneau, Caroline Borday, Odile Bronchain, Morgane Locker, Muriel Perron
Publikováno v:
Cells, Vol 11, Iss 5, p 807 (2022)
Retinitis pigmentosa is an inherited retinal dystrophy that ultimately leads to blindness due to the progressive degeneration of rod photoreceptors and the subsequent non-cell autonomous death of cones. Rhodopsin is the most frequently mutated gene i
Externí odkaz:
https://doaj.org/article/34b9309b04e5467f96c918c127021bd6
Autor:
César García-Cruz, Jorge Aragón, Sophie Lourdel, Ahrmad Annan, Jérôme E Roger, Cecilia Montanez, Cyrille Vaillend
Publikováno v:
Human molecular genetics.
The large DMD gene encodes a group of dystrophin proteins in brain and retina, produced from multiple promoters and alternative splicing events. Dystrophins are core components of different scaffolding complexes in distinct cell types. Their absence
Autor:
Juliette Bitard, Elodie-Kim Grellier, Sophie Lourdel, Helena Prior Filipe, Annaïg Hamon, François Fenaille, Florence Anne Castelli, Emeline Chu-Van, Jérôme E. Roger, Morgane Locker, Muriel Perron
Glaucoma is an optic neuropathy often referred to as “the silent thief of sight”, due to its late diagnosis, which is generally made when degeneration of the optic nerve and retinal ganglion cells is already well under way. It is thus of utmost i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1e45c9aaabd8247762f0d7707214a161
https://doi.org/10.1101/2022.05.16.492143
https://doi.org/10.1101/2022.05.16.492143
Autor:
Karine, Parain, Sophie, Lourdel, Alicia, Donval, Albert, Chesneau, Caroline, Borday, Odile, Bronchain, Morgane, Locker, Muriel, Perron
Publikováno v:
Cells. 11(5)
Retinitis pigmentosa is an inherited retinal dystrophy that ultimately leads to blindness due to the progressive degeneration of rod photoreceptors and the subsequent non-cell autonomous death of cones.
Autor:
Jerome E. Roger, Parth Shah, Muriel Perron, Anand Swaroop, Sophie Lourdel, Catherine Hottin, Elena Kisseleff, Leah Thomas, Robin J. Vigouroux, Alain Chédotal
Publikováno v:
eNeuro
Glycogen synthase kinase 3 (GSK3) proteins (GSK3α and GSK3β) are key mediators of signaling pathways, with crucial roles in coordinating fundamental biological processes during neural development. Here we show that the complete loss of GSK3 signali