The MFN2 gene is responsible for mitochondrial DNA instability and optic atrophy 'plus' phenotype von Rouzier, Cécile, Bannwarth, Sylvie, Chaussenot, Annabelle, Chevrollier, Arnaud, Verschueren, Annie, Bonello-Palot, Nathalie, Fragaki, Konstantina, Cano, Aline, Pouget, Jean, Pellissier, Jean-François, Procaccio, Vincent, Chabrol, Brigitte, Paquis-Flucklinger, Véronique

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STochastic Optical Reconstruction Microscopy (STORM) reveals the nanoscale organization of pathological aggregates in human brain von Codron, P., Letournel, F., Marty, S., Renaud, L., Bodin, A., Duchesne, M., Verny, C., Lenaers, G., Duyckaerts, C., Julien, J.‐P., Cassereau, J., Chevrollier, A.

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Perspectives of drug-based neuroprotection targeting mitochondria von Procaccio, V., Bris, C., Chao de la Barca, J.M., Oca, F., Chevrollier, A., Amati-Bonneau, P., Bonneau, D., Reynier, P.

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Phenotypic spectrum of MFN2 mutations in the Spanish population von Casasnovas, C, Banchs, I, Cassereau, J, Gueguen, N, Chevrollier, A, Martínez-Matos, J A, Bonneau, D, Volpini, V

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SIMULTANEOUS MFN2 AND GDAP1 MUTATIONS CAUSE MAJOR MITOCHONDRIAL DEFECTS IN A PATIENT WITH CMT von CASSEREAU, J, CASASNOVAS, C, PROCACCIO, V, CHEVROLLIER, A, GUEGUEN, N, MALINGE, M.-C, GUILLET, V, REYNIER, P, BONNEAU, D, AMATI-BONNEAU, P, BANCHS, I, VOLPINI, V

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Microdosimetry in 3D realistic mitochondria phantoms: Geant4 Monte Carlo tracking of 250 keV photons in phantoms reconstructed from microscopic images von Zein, S., Francis, Z., Montarou, G., Chandez, F., Kane, M.S., Chevrollier, A.

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MULTIPLE SCLEROSIS-LIKE DISORDER IN OPA1-RELATED AUTOSOMAL DOMINANT OPTIC ATROPHY von VERNY, C, LOISEAU, D, BONNEAU, D, SCHERER, C, LEJEUNE, P, CHEVROLLIER, A, GUEGUEN, N, GUILLET, V, DUBAS, F, REYNIER, P, AMATI-BONNEAU, P

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Novel pathophysiological mechanisms in dominant optic atrophy beyond the mitochondrial dynamics equilibrium von Lenaers, G., Charif, M., Amati‐Bonneau, P., la Barca, J. Chao, Procaccio, V., Chevrollier, A., Leruez, S., Bonneau, D., Reynier, P.

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Microdosimetry in 3D realistic mitochondria phantoms: Geant4 Monte Carlo tracking of 250keV photons in phantoms reconstructed from microscopic images von Zein, S., Francis, Z., Montarou, G., Chandez, F., Kane, M.S., Chevrollier, A.

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Mitochondrial Activity in XTC.UC1 Cells Derived from Thyroid Oncocytoma von Savagner, F., Chevrollier, A., Loiseau, D., Morgan, C., Reynier, P., Clark, O., Stepien, G., Malthiery, Y.

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Idebenone increases mitochondrial complex I activity in fibroblasts from LHON patients while producing contradictory effects on respiration von Angebault, Claire, Gueguen, Naïg, Desquiret-Dumas, Valérie, Chevrollier, Arnaud, Guillet, Virginie, Verny, Christophe, Cassereau, Julien, Ferre, Marc, Milea, Dan, Amati-Bonneau, Patrizia, Bonneau, Dominique, Procaccio, Vincent, Reynier, Pascal, Loiseau, Dominique

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OPA1 R445H mutation in optic atrophy associated with sensorineural deafness von Amati-Bonneau, Patrizia, Guichet, Agnès, Olichon, Aurélien, Chevrollier, Arnaud, Viala, Frédérique, Miot, Stéphanie, Ayuso, Carmen, Odent, Sylvie, Arrouet, Catherine, Verny, Christophe, Calmels, Marie-Noelle, Simard, Gilles, Belenguer, Pascale, Wang, Jing, Puel, Jean-Luc, Hamel, Christian, Malthièry, Yves, Bonneau, Dominique, Lenaers, Guy, Reynier, Pascal

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ANT2 isoform required for cancer cell glycolysis von Chevrollier, Arnaud, Loiseau, Dominique, Chabi, Béatrice, Renier, Gilles, Douay, Olivier, Malthièry, Yves, Stepien, Georges

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LPS-enriched small extracellular vesicles from metabolic syndrome patients trigger endothelial dysfunction by activation of TLR4 von Ali, S., Malloci, M., Safiedeen, Z., Soleti, R., Vergori, L., Vidal-Gomez, X., Besnard, C., Dubois, S., Le Lay, S., Jerome, B., Chevrollier, A., Gagnadoux, F., Simard, G., Andriantsitohaina, R., Martinez, C.

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Induction of ANT2 gene expression in liver of patients with mitochondrial DNA depletion von Bonod-Bidaud, Christelle, Chevrollier, Arnaud, Bourasseau, Ingrid, Lachaux, Alain, Mousson de Camaret, Bénédicte, Stepien, Georges

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Reply: MFN2 mutations cause compensatory mitochondrial DNA proliferation von Rouzier, C., Bannwarth, S., Chaussenot, A., Chevrollier, A., Verschueren, A., Bonello-Palot, N., Fragaki, K., Cano, A., Pouget, J., Pellissier, J.-F., Procaccio, V., Chabrol, B., Paquis-Flucklinger, V.

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Reply: MFN2, a new gene responsible for mitochondrial DNA depletion von Rouzier, C., Serre, V., Chaussenot, A., Bannwarth, S., Chevrollier, A., Verschueren, A., Bonello-Palot, N., Fragaki, K., Cano, A., Pouget, J., Pellissier, J.-F., Procaccio, V., Munnich, A., Chabrol, B., Paquis-Flucklinger, V.

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ANT2 expression under hypoxic conditions produces opposite cell-cycle behavior in 143B and HepG2 cancer cells von Chevrollier, Arnaud, Loiseau, Dominique, Gautier, Fabien, Malthièry, Yves, Stepien, Georges

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Random mtDNA deletions and functional consequence in aged human skeletal muscle von Chabi, Béatrice, de Camaret, Bénédicte Mousson, Chevrollier, Arnaud, Boisgard, Stéphane, Stepien, Georges

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Perspectives of drug-based neuroprotection targeting mitochondria: Mitochondrial diseases von PROCACCIO, V, BRIS, C, CHAO DE LA BARCA, J. M, OCA, F, CHEVROLLIER, A, AMATI-BONNEAU, P, BONNEAU, D, REYNIER, P

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