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Mechanisms of Ageing and Development|June 3, 2008
HGPS and related premature aging disorders: from genomic identification to the first therapeutic approachesSandrine Pereira, Patrice Bourgeois, Claire Navarro, et al.
Physiological Reports|September 9, 2022
Heterozygous expression of Cre recombinase in podocytes has no impact on the anti-glomerular basement membrane glomerulonephritis model in C57BL/6J miceCyril Mousseaux, Tiffany Migeon, Perrine Frère, et al.
Bioinformatics (Oxford, England)|July 19, 2018
Random walk with restart on multiplex and heterogeneous biological networksAlberto Valdeolivas, Laurent Tichit, Claire Navarro, et al.
Genetic Testing and Molecular Biomarkers|July 15, 2009
Identification of different genomic deletions and one duplication in the dysferlin gene using multiplex ligation-dependent probe amplification and genomic quantitative PCRMartin Krahn, Ana Borges, Claire Navarro, et al.
EMBO Molecular Medicine|July 5, 2017
MG132-induced progerin clearance is mediated by autophagy activation and splicing regulationKarim Harhouri, Claire Navarro, Danielle Depetris, et al.
Seminars in Cell & Developmental Biology|April 2, 2014
WITHDRAWN: Nuclear matrix, nuclear envelope and premature aging syndromes in a translational research perspectivePierre Cau, Claire Navarro, Karim Harhouri, et al.
Seminars in Cell & Developmental Biology|March 26, 2014
Nuclear matrix, nuclear envelope and premature aging syndromes in a translational research perspectivePierre Cau, Claire Navarro, Karim Harhouri, et al.
Cell Reports|July 31, 2012
Unique preservation of neural cells in Hutchinson- Gilford progeria syndrome is due to the expression of the neural-specific miR-9 microRNAXavier Nissan, Sophie Blondel, Claire Navarro, et al.
Experimental Cell Research|April 3, 2012
Absence of T and B lymphocytes modulates dystrophic features in dysferlin deficient animal modelAndrea Farini, Clementina Sitzia, Claire Navarro, et al.
NPJ Aging and Mechanisms of Disease|July 20, 2017
Metformin decreases progerin expression and alleviates pathological defects of Hutchinson-Gilford progeria syndrome cellsAnne-Laure Egesipe, Sophie Blondel, Alessandra Lo Cicero, et al.
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