Celine GONTHIER
Assistant Ingénieur
GONTHIER
Celine
Assistant Ingénieur
AI
Publications
The Long Non-Coding RNA HOXA-AS2 Promotes Proliferation of Glioma Stem Cells and Modulates Their Inflammation Pathway Mainly through Post-Transcriptional Regulation.
Publié le 25 Avr 2022 dans International journal of molecular sciences , vol. 23
Le Boiteux E , Guichet PO, Masliantsev K, Montibus B , Vaurs-Barriere C, Gonthier-Gueret C, Chautard E, Verrelle P, Karayan-Tapon L, Fogli A , Court F , Arnaud P
TET3 controls the expression of the H3K27me3 demethylase Kdm6b during neural commitment.
Publié le 30 Jan 2021 dans Cellular and molecular life sciences : CMLS , vol. 78 - pp 757-768
Montibus B , Cercy J , Bouschet T, Charras A, Maupetit-Méhouas S , Nury D , Gonthier-Guéret C, Chauveau S , Allegre N , Chariau C, Hong CC, Vaillant I , Marques CJ, Court F , Arnaud P
Automated 3D bio-imaging analysis of nuclear organization by NucleusJ 2.0.
Publié le 30 Déc 2020 dans Nucleus (Austin, Tex.) , vol. 11 - pp 315-329
Dubos T , Poulet A , Gonthier-Gueret C, Mougeot G , Vanrobays E , Li Y , Tutois S , Pery E, Chausse F, Probst AV , Tatout C , Desset S
Oxidative stress and mitochondrial dynamics malfunction are linked in Pelizaeus-Merzbacher disease.
Publié le 30 Sep 2018 dans Brain pathology (Zurich, Switzerland) , vol. 28 - pp 611-630
Ruiz M, Bégou M, Launay N, Ranea-Robles P, Bianchi P, López-Erauskin J, Morató L, Guilera C, Petit B, Vaurs-Barriere C , Guéret-Gonthier C, Bonnet-Dupeyron MN, Fourcade S, Auwerx J, Boespflug-Tanguy O, Pujol A
Relevance of GJC2 promoter mutation in Pelizaeus-Merzbacher-like disease.
Publié le 30 Jan 2012 dans Annals of neurology , vol. 71 - pp 146-8
Combes P, Kammoun N, Monnier A, Gonthier-Guéret C, Giraud G , Bertini E, Chahnez T, Fakhfakh F, Boespflug-Tanguy O, Vaurs-Barrière C
Eukaryotic initiation factor 2B (eIF2B) GEF activity as a diagnostic tool for EIF2B-related disorders.
Publié le 15 Déc 2009 dans PloS one , vol. 4 - pp e8318
Horzinski L, Huyghe A, Cardoso MC, Gonthier C , Ouchchane L, Schiffmann R, Blanc P , Boespflug-Tanguy O, Fogli A
Exon deletion in the non-catalytic domain of eIF2Bepsilon due to a splice site mutation leads to infantile forms of CACH/VWM with severe decrease of eIF2B GEF activity.
Publié le 30 Mai 2008 dans Annals of human genetics , vol. 72 - pp 410-5
Horzinski L, Gonthier C , Rodriguez D, Scherer C, Boespflug-Tanguy O, Fogli A
