Jerome E Roger
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Explore the profile of Jerome E Roger including associated specialties, affiliations and a list of published articles.
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31
Citations
739
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Recent Articles
1.
Zanetti A, Dujardin G, Fares-Taie L, Amiel J, Roger J, Audo I, et al.
Nat Commun
. 2024 Nov;
15(1):10096.
PMID: 39572588
Here we conduct a study involving 12 individuals with retinal dystrophy, neurological impairment, and skeletal abnormalities, with special focus on GPATCH11, a lesser-known G-patch domain-containing protein, regulator of RNA metabolism....
2.
Garcia-Garcia D, Vidal-Gil L, Parain K, Lun J, Audic Y, Chesneau A, et al.
Sci Adv
. 2024 Oct;
10(40):eadp7916.
PMID: 39356769
Unlike mammals, some nonmammalian species recruit Müller glia for retinal regeneration after injury. Identifying the underlying mechanisms may help to foresee regenerative medicine strategies. Using a model of retinitis pigmentosa,...
3.
Gonzalez-Reyes M, Aragon J, Sanchez-Trujillo A, Rodriguez-Martinez G, Duarte K, Eleftheriou E, et al.
Mol Neurobiol
. 2024 May;
61(12):10883-10900.
PMID: 38802640
Dystrophin Dp71 is the major product of the Duchenne muscular dystrophy (DMD) gene in the brain, and its loss in DMD patients and mouse models leads to cognitive impairments. Dp71...
4.
Bitard J, Grellier E, Lourdel S, Filipe H, Hamon A, Fenaille F, et al.
Cell Death Discov
. 2024 Jan;
10(1):48.
PMID: 38272861
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%...
5.
Gozlan S, Batoumeni V, Fournier T, Nanteau C, Potey A, Clemencon M, et al.
Commun Biol
. 2023 Jul;
6(1):762.
PMID: 37479765
Retinal progenitor cells (RPCs) are the source of all retinal cell types during retinogenesis. Until now, the isolation and expansion of RPCs has been at the expense of their multipotency....
6.
Zeitz C, Roger J, Audo I, Michiels C, Sanchez-Farias N, Varin J, et al.
Prog Retin Eye Res
. 2023 Jan;
93:101155.
PMID: 36669906
Myopia is the most common eye disorder, caused by heterogeneous genetic and environmental factors. Rare progressive and stationary inherited retinal disorders are often associated with high myopia. Genes implicated in...
7.
Hottin C, Perron M, Roger J
Cells
. 2022 Sep;
11(18).
PMID: 36139472
Glycogen synthase kinase 3 (GSK3) is a key regulator of many cellular signaling processes and performs a wide range of biological functions in the nervous system. Due to its central...
8.
Garcia-Cruz C, Aragon J, Lourdel S, Annan A, Roger J, Montanez C, et al.
Hum Mol Genet
. 2022 Sep;
32(4):659-676.
PMID: 36130212
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...
9.
Rodrigues A, Slembrouck-Brec A, Nanteau C, Terray A, Tymoshenko Y, Zagar Y, et al.
NPJ Regen Med
. 2022 Aug;
7(1):39.
PMID: 35974011
Mutations in the ubiquitously expressed pre-mRNA processing factor (PRPF) 31 gene, one of the most common causes of dominant form of Retinitis Pigmentosa (RP), lead to a retina-specific phenotype. It...
10.
Kisseleff E, Vigouroux R, Hottin C, Lourdel S, Thomas L, Shah P, et al.
eNeuro
. 2021 Sep;
8(5).
PMID: 34518365
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...