Arnaud CHEVROLLIER

Identifiants chercheurs

IdHAL :

arnaud-chevrollier

ORCID :

0000-0002-5135-6643

IdRef :

083154116

ResearcherID :

http://www.researcherid.com/rid/K-2853-2015

Publications

Article dans une revue (72)

Mitofusin MFN2 acts as a molecular sensor preventing protein aggregation and mitophagy, with a protective effect against apoptosis in Charcot–Marie–Tooth type 2A disease Mariana Joaquim,Maike Dohrn,Arnaud Chevrollier,Mafalda Escobar-Henriques Autophagy Reports, 2026, 5 (1), pp.2629624. ⟨10.1080/27694127.2026.2629624⟩ Article dans une revue hal-05606162v1
Charcot–Marie–Tooth type 2A variants of mitofusin 2 sensitize cells to apoptotic cell death Mariana Joaquim,Maria-Bianca Bulimaga,Marie Mohn,Solenn Plouzennec,Leon Osinskiet al. Journal of Cell Science, 2025, 138 (18), pp.jcs263691. ⟨10.1242/jcs.263691⟩ Article dans une revue hal-05606159v1
BI-ALLELIC VARIANTS IN TM2D3 CAUSE A SEVERE SYNDROMIC NEURODEVELOPMENTAL DISORDER ASSOCIATED WITH ENDOPLASMIC RETICULUM AND MITOCHONDRIAL ABNORMALITIES. Claudie Gabillard-Lefort,Caroline Silveira Martinez,Naïg Gueguen,Valérie Desquiret-Dumas,Méline Weryet al. American Journal of Human Genetics, 2025, 112 (7), pp.1711-1721. ⟨10.1016/j.ajhg.2025.05.004⟩ Article dans une revue hal-05283235v1
An Apparently Isolated Optic Neuropathy Associated with Biallelic Variants in SLC25A46 Gene Encoding the Mitochondrial Ugo1-Like Protein Pascal Reynier,Patrizia Amati-Bonneau,Valérie Desquiret-Dumas,Marc Ferré,Naïg Gueguenet al. Neuro-Ophthalmology, 2025, 50 (1), pp.96-100. ⟨10.1080/01658107.2025.2581675⟩ Article dans une revue hal-05606176v1
Mitofusin 2 displays fusion-independent roles in proteostasis surveillance Mariana Joaquim,Selver Altin,Maria-Bianca Bulimaga,Tânia Simões,Hendrik Nolteet al. Nature Communications, 2025, 16 (1), pp.1501. ⟨10.1038/s41467-025-56673-5⟩ Article dans une revue hal-05606165v1
The Role of Phospholipids in Mitochondrial Dynamics and Associated Diseases Solenn Plouzennec,Juan Manuel Chao de la Barca,Arnaud Chevrollier Frontiers in Bioscience-Landmark, 2025, 30 (8), pp.27634. ⟨10.31083/FBL27634⟩ Article dans une revue hal-05606168v1
Mitochondrial F0F1-ATP synthase governs the induction of mitochondrial fission Charlène Lhuissier,Valérie Desquiret-Dumas,Anaïs Girona,Jennifer Alban,Justine Faureet al. iScience, 2024, 27 (5), pp.109808. ⟨10.1016/j.isci.2024.109808⟩ Article dans une revue hal-04622662v1
Food perception induces fast fragmentation of hepatic mitochondria Arnaud Chevrollier,Jérome Boursier,Valérie Desquiret-Dumas Trends in Endocrinology and Metabolism = Trends in Endocrinology & Metabolism , 2024, 35 (8), pp.680-682. ⟨10.1016/j.tem.2024.06.002⟩ Article dans une revue hal-05606173v1
Super-resolution microscopies, technological breakthrough to decipher mitochondrial structure and dynamic. Pauline Teixeira,Rémi Galland,Arnaud Chevrollier Seminars in Cell and Developmental Biology, 2024, 159-160, pp.38 - 51. ⟨10.1016/j.semcdb.2024.01.006⟩ Article dans une revue hal-04657389v1
Super-resolution microscopies, technological breakthrough to decipher mitochondrial structure and dynamic. Pauline Teixeira,Rémi Galland,Arnaud Chevrollier Seminars in Cell and Developmental Biology, 2024, 159-160, pp.38-51. ⟨10.1016/j.semcdb.2024.01.006⟩ Article dans une revue hal-04455163v1
Homozygous MFN2 variants causing severe antenatal encephalopathy with clumped mitochondria Arnaud Chevrollier,Adeline Alice Bonnard,Lyse Ruaud,Naïg Gueguen,Laurence Perrinet al. Brain - A Journal of Neurology , 2024, 147 (1), pp.91 - 99. ⟨10.1093/brain/awad347⟩ Article dans une revue inserm-04410829v1
Homozygous MFN2 variants causing severe antenatal encephalopathy with clumped mitochondria Arnaud Chevrollier,Adeline Alice Bonnard,Lyse Ruaud,Naïg Gueguen,Laurence Perrinet al. Brain - A Journal of Neurology , 2024, 147 (1), pp.91-99. ⟨10.1093/brain/awad347⟩ Article dans une revue hal-04454759v1
Transactive response DNA-binding protein 43 is enriched at the centrosome in human cells Alexia Bodin,Logan Greibill,Julien Gouju,Franck Letournel,Silvia Pozziet al. Brain - A Journal of Neurology , 2023, 146 (9), pp.3624-3633. ⟨10.1093/brain/awad228⟩ Article dans une revue hal-04254654v1
Next generation sequencing identifies novel PMPCA variants in patients with dominant optic atrophy Majida Charif,Arnaud Chevrollier,Naïg Gueguen,Selma Kane,Céline Briset al. Genes, 2022, 13 (7), pp.1202. ⟨10.3390/genes13071202⟩ Article dans une revue hal-03861086v1
Cancer/Testis Antigen 55 is required for cancer cell proliferation and mitochondrial DNA maintenance Jade Aurrière,David Goudenege,Simone Baechler,Shar-Yin Huang,Naig Gueguenet al. Mitochondrion, 2022, 64, pp.19-26. ⟨10.1016/j.mito.2022.02.005⟩ Article dans une revue hal-03771509v1
Case report: Thirty-year progression of an EMPF1 encephalopathy due to defective mitochondrial and peroxisomal fission caused by a novel de novo heterozygous DNM1L variant Charlène Lhuissier,Bart Wagner,Amy Vincent,Gaëtan Garraux,Olivier Hougrandet al. Frontiers in Neurology, 2022, 13, ⟨10.3389/fneur.2022.937885⟩ Article dans une revue hal-03861074v1
Glutamate-Induced Deregulation of Krebs Cycle in Mitochondrial Encephalopathy Lactic Acidosis Syndrome Stroke-Like Episodes (MELAS) Syndrome Is Alleviated by Ketone Body Exposure Sophie Belal,David Goudenège,Cinzia Bocca,Florent Dumont,Juan Manuel Chao de la Barcaet al. Biomedicines, 2022, 10 (7), pp.1665. ⟨10.3390/biomedicines10071665⟩ Article dans une revue hal-03861087v1
Protective role of the mitochondrial fusion protein OPA1 in hypertension Pauline Robert,Phuc Minh Chau Nguyen,Alexis Richard,Céline Grenier,Arnaud Chevrollieret al. FASEB Journal, 2021, 35, ⟨10.1096/fj.202000238rrr⟩ Article dans une revue hal-03379614v1
The Long Non-Coding RNA SAMMSON Is a Regulator of Chemosensitivity and Metabolic Orientation in MCF-7 Doxorubicin-Resistant Breast Cancer Cells Charlotte Orre,Xavier Dieu,Jordan Guillon,Naïg Gueguen,Seyedeh Tayebeh Ahmadpouret al. Biology, 2021, 10 (11), pp.1156. ⟨10.3390/biology10111156⟩ Article dans une revue inserm-03546999v1
LPS-enriched small extracellular vesicles from metabolic syndrome patients trigger endothelial dysfunction by activation of TLR4 Sakina Ali,Marine Malloci,Zainab Safiedeen,Raffaella Soleti,Luisa Vergoriet al. Metabolism, 2021, 118, pp.154727. ⟨10.1016/j.metabol.2021.154727⟩ Article dans une revue hal-03284090v1
Dominant ACO2 mutations are a frequent cause of isolated optic atrophy Majida Charif,Naïg Gueguen,Marc Ferré,Zouhair Elkarhat,Salim Khiatiet al. Brain Communications, 2021, 3 (2), ⟨10.1093/braincomms/fcab063⟩ Article dans une revue hal-03873017v1
Oxidative stress contributes differentially to the pathophysiology of Charcot-Marie-Tooth disease type 2K Julien Cassereau,Arnaud Chevrollier,Philippe Codron,Cyril Goizet,Naïg Gueguenet al. Experimental Neurology, 2020, 323, pp.113069. ⟨10.1016/j.expneurol.2019.113069⟩ Article dans une revue hal-02388209v1
Mutations in the m-AAA proteases AFG3L2 and SPG7 are causing isolated dominant optic atrophy Majida Charif,Arnaud Chevrollier,Naïg Gueguen,Céline Bris,David Goudenègeet al. Neurology Genetics, 2020, 6 (3), ⟨10.1212/NXG.0000000000000428⟩ Article dans une revue hal-04960357v1
Mutations in the m-AAA proteases AFG3L2 and SPG7 are causing isolated dominant optic atrophy Majida Charif,Arnaud Chevrollier,Naïg Gueguen,Céline Bris,David Goudenègeet al. Neurology Genetics, 2020, 6 (3), pp.e428. ⟨10.1212/NXG.0000000000000428⟩ Article dans une revue hal-02942795v1
Étude du cerveau humain à l’échelle nanoscopique par microscopie Super-Résolutive STORM Philippe Codron,Franck Letournel,Serge Marty,Mathilde Duchesne,Christophe Vernyet al. Revue Neurologique, 2020, 176, pp.S105. ⟨10.1016/j.neurol.2020.01.296⟩ Article dans une revue hal-02942785v1
Lipidomics Reveals Triacylglycerol Accumulation Due to Impaired Fatty Acid Flux in Opa1 -Disrupted Fibroblasts Cinzia Bocca,Mariame Selma Kane,Charlotte Veyrat-Durebex,Judith Kouassi Nzoughet,Juan Manuel Chao de La Barcaet al. Journal of Proteome Research, 2019, 18 (7), pp.2779-2790. ⟨10.1021/acs.jproteome.9b00081⟩ Article dans une revue hal-02388215v1
Warburg-like effect is a hallmark of complex I assembly defects Valerie Desquiret-Dumas,Geraldine Leman,Celine Wetterwald,Stephanie Chupin,Anaïs Lebertet al. Biochimica et Biophysica Acta - Molecular Basis of Disease, 2019, 1865 (9), pp.2475-2489. ⟨10.1016/j.bbadis.2019.05.011⟩ Article dans une revue hal-02942827v1
Is multidetector CT-scan able to detect T3a renal tumor before surgery? Marie Caillaud,Mickaël Laisney,Alexandre Bejanin,Clarisse Scherer-Gagou,Harmony Ducloset al. Scandinavian Journal of Urology and Nephrology Supplements, 2019, 53 (5), pp.350-355. ⟨10.1080/21681805.2019.1675756⟩ Article dans une revue hal-02975277v1
The Metabolomic Bioenergetic Signature of Opa1-Disrupted Mouse Embryonic Fibroblasts Highlights Aspartate Deficiency Cinzia Bocca,Mariame Selma Kane,Charlotte Veyrat-Durebex,Stéphanie Chupin,Jennifer Albanet al. Scientific Reports, 2018, 8 (1), ⟨10.1038/s41598-018-29972-9⟩ Article dans une revue hal-02388227v1
Current mechanistic insights into the CCCP-induced cell survival response Mariame Kane,Aurelien Paris,Philippe Codron,Julien Cassereau,Vincent Procaccioet al. Biochemical Pharmacology, 2018, 148, pp.100-110. ⟨10.1016/j.bcp.2017.12.018⟩ Article dans une revue istex hal-01964494v1
A Plasma Metabolomic Signature Involving Purine Metabolism in Human Optic Atrophy 1 (OPA1)-Related Disorders Cinzia Bocca,Judith Nzoughet,Stéphanie Leruez,Patrizia Amati-Bonneau,Marc Ferréet al. Investigative Ophthalmology & Visual Science, 2018, 59, pp.185-195. ⟨10.1167/iovs.17-23027⟩ Article dans une revue hal-01964499v1
Primary fibroblasts derived from sporadic amyotrophic lateral sclerosis patients do not show ALS cytological lesions Philippe Codron,Julien Cassereau,Patrick Vourc'H,Charlotte Veyrat-Durebex,Hélène Blascoet al. Amyotrophic lateral sclerosis & frontotemporal degeneration, 2018, 19 (5-6), pp.446-456. ⟨10.1080/21678421.2018.1431787⟩ Article dans une revue hal-01964500v1
Reply: The expanding neurological phenotype of DNM1L-related disorders Sylvie Gerber,Majida Charif,Arnaud Chevrollier,Tanguy Chaumette,Claire Angebaultet al. Brain - A Journal of Neurology , 2018, 141 (4), pp.e29-e29. ⟨10.1093/brain/awy027⟩ Article dans une revue hal-02388229v1
CLUH couples mitochondrial distribution to the energetic and metabolic status Jamal Wakim,David Goudenege,Rodolphe Perrot,Naig Gueguen,Valerie Desquiret-Dumaset al. Journal of Cell Science, 2017, 130 (11), pp.1940 - 1951. ⟨10.1242/jcs.201616⟩ Article dans une revue hal-01601889v1
Targeted Metabolomics Reveals Early Dominant Optic Atrophy Signature in Optic Nerves of Opa1 delTTAG/+ Mice Juan Manuel Chao de la Barca,Gilles Simard,Emmanuelle Sarzi,Tanguy Chaumette,Guillaume Rousseauet al. Investigative Ophthalmology & Visual Science, 2017, 58 (2), pp.812-820. ⟨10.1167/iovs.16-21116⟩ Article dans une revue hal-01784466v1
The addition of ketone bodies alleviates mitochondrial dysfunction by restoring complex I assembly in a MELAS cellular model Samuel Frey,Guillaume Geffroy,Valérie Desquiret-Dumas,Naig Guegen,Celine Briset al. Biochimica et Biophysica Acta - Molecular Basis of Disease, 2016, 1863 (1), pp.284-291. ⟨10.1016/j.bbadis.2016.10.028⟩ Article dans une revue hal-01396751v1
Increase in Cardiac Ischemia-Reperfusion Injuries in Opa1+/- Mouse Model Sophie Le Page,Marjorie Niro,J. Fauconnier,Laura Cellier,Sophie Tamareilleet al. PLoS ONE, 2016, 11 (10), pp.e0164066. ⟨10.1371/journal.pone.0164066⟩ Article dans une revue hal-01818418v1
Increased mitochondrial fusion in a autosomal recessive CMT2A family with mitochondrial GTPase mitofusin 2 mutations Philippe Codron,Arnaud Chevrollier,Mariame-Selma Kane,Andoni Echaniz-Laguna,Philippe Latouret al. J Peripher Nerv Syst, 2016, 21 (4), pp.365-369. ⟨10.1111/jns.12192⟩ Article dans une revue istex hal-02104500v1
The metabolomic signature of Leber's hereditary optic neuropathy reveals endoplasmic reticulum stress Juan Manuel Chao de La Barca,Gilles Simard,Patrizia Amati-Bonneau,Zainab Safiedeen,Delphine Mirebeau-Prunieret al. Brain - A Journal of Neurology , 2016, 139 (11), pp.2864-2876. ⟨10.1093/brain/aww222⟩ Article dans une revue hal-02103390v1
Assembly defects induce oxidative stress in inherited mitochondrial complex I deficiency Géraldine Leman,Naig Guegen,Valérie Desquiret-Dumas,Mariame Kane,Céline Wetterwaldet al. International Journal of Biochemistry and Cell Biology, 2015, 65, pp.91-103. ⟨10.1016/j.biocel.2015.05.017⟩ Article dans une revue istex hal-01399131v1
OPA1-related disorders: Diversity of clinical expression, modes of inheritance and pathophysiology Juan Manuel Chao de La Barca,Delphine Mirebeau-Prunier,Patrizia Amati-Bonneau,Marc Ferré,Emmanuelle Sarziet al. Neurobiology of Disease, 2015, pp.20-26. ⟨10.1016/j.nbd.2015.08.015⟩ Article dans une revue istex hal-01392230v1
Loss-of-Function Mutations in WDR73 Are Responsible for Microcephaly and Steroid-Resistant Nephrotic Syndrome: Galloway-Mowat Syndrome Estelle Colin,Huynh Cong,G. Mollet,Agnés Guichet,O. Gribouvalet al. American Journal of Human Genetics, 2014, 95 (6), pp.637 - 48. ⟨10.1016/j.ajhg.2014.10.011⟩ Article dans une revue hal-03404021v1
Early-onset Behr syndrome due to compound heterozygous mutations in OPA1 Dominique Bonneau,Estelle Colin,Florine Oca,Marc Ferré,Arnaud Chevrollieret al. Brain - A Journal of Neurology , 2014, Non spécifié. ⟨10.1093/brain/awu184⟩ Article dans une revue hal-03403967v1
Perspectives of drug-based neuroprotection targeting mitochondria Vincent Procaccio,Céline Bris,Juan Manuel Chao de La Barca,Florine Oca,Arnaud Chevrollieret al. Revue Neurologique, 2014, 170 (5), pp.390 - 400. ⟨10.1016/j.neurol.2014.03.005⟩ Article dans une revue hal-03404068v1
Experimental determination of organelle targeting peptide cleavage sites using transient expression of GFP translational fusions Adrien Candat,Pauline Poupart,Jean-Pierre Andrieu,Arnaud Chevrollier,Pascal Reynieret al. Analytical Biochemistry, 2013, 434 (1), pp.44-51. ⟨10.1016/j.ab.2012.10.040⟩ Article dans une revue istex hal-01209902v1
Is ABCC6 a genuine mitochondrial protein? Marc Ferré,Pascal Reynier,Arnaud Chevrollier,Delphine Prunier-Mirebeau,Georges Lefthériotiset al. BMC Research Notes, 2013, 6 (1), pp.427. ⟨10.1186/1756-0500-6-427⟩ Article dans une revue inserm-00877607v1
Resveratrol induces a mitochondrial complex I-dependent increase in NADH oxidation responsible for sirtuin activation in liver cells Valérie Desquiret-Dumas,Naïg Gueguen,Géraldine Leman,Stephanie Baron,Valerie Nivet-Antoineet al. Journal of Biological Chemistry, 2013, 288 (51), pp.36662 - 75. ⟨10.1074/jbc.M113.466490⟩ Article dans une revue hal-03404098v1
Standardized mitochondrial analysis gives new insights into mitochondrial dynamics and OPA1 function Arnaud Chevrollier,Julien Cassereau,Marc Ferré,Jennifer Alban,Valérie Desquiret-Dumaset al. International journal of biochemistry & cell biology, 2012, 44 (6), pp.980 - 8. ⟨10.1016/j.biocel.2012.03.006⟩ Article dans une revue istex hal-03404105v1
Metabolically induced heteroplasmy shifting and l-arginine treatment reduce the energetic defect in a neuronal-like model of MELAS Valérie Desquiret-Dumas,Naïg Gueguen,Magalie Barth,Arnaud Chevrollier,S. Hancocket al. BBA - Biochimica et Biophysica Acta, 2012, 1822 (6), pp.1019 - 29. ⟨10.1016/j.bbadis.2012.01.010⟩ Article dans une revue hal-03404030v1
The MFN2 gene is responsible for mitochondrial DNA instability and optic atrophy 'plus' phenotype C. Rouzier,Sylvie Bannwarth,A. Chaussenot,Arnaud Chevrollier,A. Verschuerenet al. Brain - A Journal of Neurology , 2011, 135 (Pt 1), pp.23 - 34. ⟨10.1093/brain/awr323⟩ Article dans une revue hal-03408506v1
Mitochondrial dysfunction and pathophysiology of Charcot-Marie-Tooth disease involving GDAP1 mutations Julien Cassereau,Arnaud Chevrollier,Naïg Gueguen,Valérie Desquiret-Dumas,Christophe Vernyet al. Experimental Neurology, 2011, 227 (1), pp.31 - 41. ⟨10.1016/j.expneurol.2010.09.006⟩ Article dans une revue istex hal-03408479v1
Simultaneous MFN2 and GDAP1 mutations cause major mitochondrial defects in a patient with CMT Julien Cassereau,C. Casasnovas,Naïg Gueguen,Marie-Claire Malinge,Virginie Guilletet al. Neurology, 2011, 76 (17), pp.1524 - 6. ⟨10.1212/WNL.0b013e318217e77d⟩ Article dans une revue hal-03408522v1
Bioenergetic defect associated with mKATP channel opening in a mouse model carrying a mitofusin 2 mutation Virginie Guillet,Naïg Gueguen,R. Cartoni,Arnaud Chevrollier,Valérie Desquiret-Dumaset al. FASEB Journal, 2011, 25 (5), pp.1618 - 27. ⟨10.1096/fj.10-173609⟩ Article dans une revue hal-03408441v1
Idebenone increases mitochondrial complex I activity in fibroblasts from LHON patients while producing contradictory effects on respiration. Claire Angebault,Naïg Gueguen,Valérie Desquiret-Dumas,Arnaud Chevrollier,Virginie Guilletet al. BMC Research Notes, 2011, 4 (1), pp.557. ⟨10.1186/1756-0500-4-557⟩ Article dans une revue inserm-00673659v1
Adenine nucleotide translocase 2 is a key mitochondrial protein in cancer metabolism Arnaud Chevrollier,Dominique Loiseau,Pascal Reynier,Georges Stepien Biochimica biophysica acta (BBA) - Bioenergetics, 2011, 1807 (6), pp.562 - 567. ⟨10.1016/j.bbabio.2010.10.008⟩ Article dans une revue hal-02645378v1
A locus-specific database for mutations in GDAP1 allows analysis of genotype-phenotype correlations in Charcot-Marie-Tooth diseases type 4A and 2K. Julien Cassereau,Arnaud Chevrollier,Dominique Bonneau,Christophe Verny,Vincent Procaccioet al. Orphanet Journal of Rare Diseases, 2011, 6 (1), pp.87. ⟨10.1186/1750-1172-6-87⟩ Article dans une revue inserm-00683147v1
Phenotypic spectrum of MFN2 mutations in the Spanish population C. Casasnovas,I. Banchs,Julien Cassereau,Naïg Gueguen,Arnaud Chevrollieret al. Journal of Medical Genetics, 2010, 47 (4), pp.249 - 56. ⟨10.1136/jmg.2009.072488⟩ Article dans une revue istex hal-03408512v1
Ethambutol-induced optic neuropathy linked to OPA1 mutation and mitochondrial toxicity Virginie Guillet,Arnaud Chevrollier,Julien Cassereau,Franck Letournel,Naïg Gueguenet al. Mitochondrion, 2010, 10 (2), pp.115 - 124. ⟨10.1016/j.mito.2009.11.004⟩ Article dans une revue istex hal-03403265v1
Adenine nucleotide translocase is involved in a mitochondrial coupling defect in MFN2-related Charcot–Marie–Tooth type 2A disease Virginie Guillet,Naïg Gueguen,Christophe Verny,Marc Ferré,Chadi Homedanet al. neurogenetics, 2010, 11 (1), pp.127 - 133. ⟨10.1007/s10048-009-0207-z⟩ Article dans une revue istex hal-03406912v1
De la levure aux maladies neurodégénératives : Dix ans d’exploration des pathologies de la dynamique mitochondriale Guy Lenaers,Patrizia Amati-Bonneau,Cécile Delettre,Arnaud Chevrollier,Christophe Vernyet al. Médecine/Sciences, 2010, 26 (10), pp.836 - 841. ⟨10.1051/medsci/20102610836⟩ Article dans une revue hal-03408444v1
Hereditary spastic paraplegia-like disorder due to a mitochondrial ATP6 gene point mutation Christophe Verny,Naïg Gueguen,Valérie Desquiret-Dumas,Arnaud Chevrollier,Adriana Prundeanet al. Mitochondrion, 2010, 11 (1), pp.70 - 75. ⟨10.1016/j.mito.2010.07.006⟩ Article dans une revue istex hal-03408492v1
Mitochondrial complex I deficiency in GDAP1-related autosomal dominant Charcot-Marie-Tooth disease (CMT2K) Julien Cassereau,Arnaud Chevrollier,Naïg Gueguen,Marie-Claire Malinge,Franck Letournelet al. neurogenetics, 2009, 10 (2), pp.145 - 150. ⟨10.1007/s10048-008-0166-9⟩ Article dans une revue istex hal-03403277v1
Acute and late-onset optic atrophy due to a novel OPA1 mutation leading to a mitochondrial coupling defect Yannick Nochez,Sophie Arsene,Naïg Gueguen,Arnaud Chevrollier,Marc Ferréet al. Molecular Vision, 2009, 15, pp.598 - 608 Article dans une revue hal-03406919v1
OPA1-associated disorders: Phenotypes and pathophysiology Patrizia Amati-Bonneau,Dan Milea,Dominique Bonneau,Arnaud Chevrollier,Marc Ferréet al. International Journal of Biochemistry and Cell Biology, 2009, 41 (10), pp.1855 - 1865. ⟨10.1016/j.biocel.2009.04.012⟩ Article dans une revue istex hal-03406909v1
OPA1-related dominant optic atrophy is not strongly influenced by mitochondrial DNA background. Denis Pierron,Marc Ferré,Christophe Rocher,Arnaud Chevrollier,Pascal Murailet al. BMC Medical Genetics, 2009, 10 (1), pp.70. ⟨10.1186/1471-2350-10-70⟩ Article dans une revue inserm-00663623v1
Mitochondrial bioenergetic background confers a survival advantage to HepG2 cells in response to chemotherapy Dominique Loiseau,Daniel Morvan,Arnaud Chevrollier,Aicha Demidem,Olivier Douayet al. Molecular Carcinogenesis, 2009, 48 (8), pp.733-741. ⟨10.1002/mc.20539⟩ Article dans une revue istex hal-02655649v1
Molecular screening of 980 cases of suspected hereditary optic neuropathy with a report on 77 novel OPA1 mutations. Marc Ferré,Dominique Bonneau,Dan Milea,Arnaud Chevrollier,Christophe Vernyet al. Human Mutation, 2009, 30 (7), pp.E692-705. ⟨10.1002/humu.21025⟩ Article dans une revue inserm-00372261v1
Reversible optic neuropathy with OPA1 exon 5b mutation. Karen Cornille,Dan Milea,Patrizia Amati-Bonneau,Vincent Procaccio,Lydie Zazounet al. Annals of Neurology, 2008, 63 (5), pp.667-71. ⟨10.1002/ana.21376⟩ Article dans une revue istex inserm-00287509v1
Multiple Sclerosis–Like Disorder in Opa1-Related Autosomal Dominant Optic Atrophy Christophe Verny,Dominique Loiseau,Clarisse Scherer,P. Lejeune,Arnaud Chevrollieret al. Neurology, 2008, 70 (13 Part 2), pp.1152 - 1153. ⟨10.1212/01.wnl.0000289194.89359.a1⟩ Article dans une revue hal-03419056v1
Hereditary optic neuropathies share a common mitochondrial coupling defect. Arnaud Chevrollier,Virginie Guillet,Dominique Loiseau,Naïg Gueguen,Marie-Anne Pou de Crescenzoet al. Annals of Neurology, 2008, 63 (6), pp.794-8. ⟨10.1002/ana.21385⟩ Article dans une revue istex hal-00282865v1
ANT2 isoform required for cancer cell glycolysis Arnaud Chevrollier,Dominique Loiseau,Béatrice Chabi,Gilles Renier,Olivier Douayet al. Journal of Bioenergetics and Biomembranes, 2005, 37 (5), pp.307-316. ⟨10.1007/s10863-005-8642-5⟩ Article dans une revue istex hal-02679782v1
Random mtDNA deletions and functional consequence in aged human skeletal muscle Béatrice Chabi,Bénédicte de Camaret,Arnaud Chevrollier,Stéphane Boisgard,Georges Stepien Biochemical and Biophysical Research Communications, 2005, 332 (2), pp.542-549. ⟨10.1016/j.bbrc.2005.04.153⟩ Article dans une revue istex hal-02682861v1

Communication dans un congrès (1)

Human Brain Imaging with STochastic Optical Reconstruction Microscopy (STORM) Philippe Codron,Franck Letourneur,Guy Lenaers,Arnaud Chevrollier 63eme congress of the french neuropathological society, Dec 2021, Pparis, France Communication dans un congrès hal-03455529v1

Poster de conférence (2)

Expression de l'isoforme 2 de la translocase des nucléotides adényliques mitochondriale et métabolisme de la cellule cancéreuse Arnaud Chevrollier,Dominique Loiseau,Béatrice Chabi,Georges Stepien Congrès international de Biochimie – Forum des Jeunes Chercheurs, May 2004, Marrakech, Maroc. 1 p., 2004 Poster de conférence hal-02831407v1
Expression de l'isoforme 2 de la translocase des nucléotides adényliques mitochondriale et métabolisme de la cellule cancéreuse Arnaud Chevrollier,Dominique Loiseau,Béatrice Chabi,Georges Stepien 2. Assises de Génétique Humaine et Médicale, Jan 2004, Angers, France. 1 p., 2004 Poster de conférence hal-02831378v1

Pré-publication, Document de travail (1)

Encoding of the colorectal cancer metabolic program through MICU2 Alison Robert,David Crottès,Jérôme Bourgeais,Naïg Gueguen,Arnaud Chevrollieret al. 2026 Pré-publication, Document de travail hal-05448690v1