Arnaud CHEVROLLIER

55%

Libre accès

Documents

Affiliations actuelles

511702
484896

Identifiants chercheurs

arnaud-chevrollier
ResearcherId : K-2853-2015
0000-0002-5135-6643
IdRef : 083154116
ResearcherId : http://www.researcherid.com/rid/K-2853-2015

Contact

Domaines de recherche

Bio-Informatique, Biologie Systémique [q-bio.QM] Génétique humaine

Compétences

Publications

	Homozygous MFN2 variants causing severe antenatal encephalopathy with clumped mitochondria Arnaud Chevrollier , Adeline Alice Bonnard , Lyse Ruaud , Naïg Gueguen , Laurence Perrin Brain - A Journal of Neurology , 2024, 147 (1), pp.91-99. ⟨10.1093/brain/awad347⟩ Article dans une revue hal-04454759v1
	Homozygous MFN2 variants causing severe antenatal encephalopathy with clumped mitochondria Arnaud Chevrollier , Adeline Alice Bonnard , Lyse Ruaud , Naïg Gueguen , Laurence Perrin Brain - A Journal of Neurology , 2024, 147 (1), pp.91 - 99. ⟨10.1093/brain/awad347⟩ Article dans une revue inserm-04410829v1
	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
	Transactive response DNA-binding protein 43 is enriched at the centrosome in human cells Alexia Bodin , Logan Greibill , Julien Gouju , Franck Letournel , Silvia Pozzi 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 Bris Genes, 2022, 13 (7), pp.1202. ⟨10.3390/genes13071202⟩ Article dans une revue hal-03861086v1
	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 Barca Biomedicines, 2022, 10 (7), pp.1665. ⟨10.3390/biomedicines10071665⟩ Article dans une revue hal-04436403v1
	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 Hougrand Frontiers in Neurology, 2022, 13, ⟨10.3389/fneur.2022.937885⟩ Article dans une revue hal-03861074v1
	MELAS syndrome causes glutamate and tricarboxylic acid cycle dysfunctions alleviated by ketone body treatment Sophie Belal , David Goudenège , Cinzia Bocca , Florent Dumont , Juan Manuel Chao de la Barca Biomedicines, 2022, 10 (7), pp.1665. ⟨10.3390/biomedicines10071665⟩ Article dans une revue hal-03861087v1
	Cancer/Testis Antigen 55 is required for cancer cell proliferation and mitochondrial DNA maintenance Jade Aurrière , David Goudenege , Simone Baechler , Shar-Yin Huang , Naig Gueguen Mitochondrion, 2022, 64, pp.19-26. ⟨10.1016/j.mito.2022.02.005⟩ Article dans une revue hal-03771509v1
	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 Vergori 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 Khiati Brain Communications, 2021, 3 (2), ⟨10.1093/braincomms/fcab063⟩ Article dans une revue hal-03873017v1
	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 Ahmadpour Biology, 2021, 10 (11), pp.1156. ⟨10.3390/biology10111156⟩ Article dans une revue inserm-03546999v1
	Protective role of the mitochondrial fusion protein OPA1 in hypertension Pauline Robert , Phuc Minh Chau Nguyen , Alexis Richard , Céline Grenier , Arnaud Chevrollier FASEB Journal, 2021, 35, ⟨10.1096/fj.202000238rrr⟩ Article dans une revue hal-03379614v1
	Mutations in the m-AAA proteases AFG3L2 and SPG7 are causing isolated dominant optic atrophy Majida Charif , Arnaud Chevrollier , Naïg Gueguen , Céline Bris , David Goudenège 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 Verny Revue Neurologique, 2020, 176, pp.S105. ⟨10.1016/j.neurol.2020.01.296⟩ Article dans une revue hal-02942785v1
	Oxidative stress contributes differentially to the pathophysiology of Charcot-Marie-Tooth disease type 2K Julien Cassereau , Arnaud Chevrollier , Philippe Codron , Cyril Goizet , Naïg Gueguen Experimental Neurology, 2020, 323, pp.113069. ⟨10.1016/j.expneurol.2019.113069⟩ Article dans une revue hal-02388209v1
	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 Barca 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 Lebert 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 Duclos Scandinavian Journal of Urology and Nephrology Supplements, 2019, 53 (5), pp.350-355. ⟨10.1080/21681805.2019.1675756⟩ Article dans une revue hal-02975277v1
	Reply: The expanding neurological phenotype of DNM1L-related disorders Sylvie Gerber , Majida Charif , Arnaud Chevrollier , Tanguy Chaumette , Claire Angebault Brain - A Journal of Neurology , 2018, 141 (4), pp.e29-e29. ⟨10.1093/brain/awy027⟩ Article dans une revue hal-02388229v1
	The Metabolomic Bioenergetic Signature of Opa1-Disrupted Mouse Embryonic Fibroblasts Highlights Aspartate Deficiency Cinzia Bocca , Mariame Selma Kane , Charlotte Veyrat-Durebex , Stéphanie Chupin , Jennifer Alban Scientific Reports, 2018, 8 (1), ⟨10.1038/s41598-018-29972-9⟩ Article dans une revue hal-02388227v1
	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 Ferré Investigative Ophthalmology & Visual Science, 2018, 59, pp.185-195. ⟨10.1167/iovs.17-23027⟩ Article dans une revue hal-01964499v1
	Current mechanistic insights into the CCCP-induced cell survival response Mariame Kane , Aurelien Paris , Philippe Codron , Julien Cassereau , Vincent Procaccio Biochemical Pharmacology, 2018, 148, pp.100-110. ⟨10.1016/j.bcp.2017.12.018⟩ Article dans une revue hal-01964494v1
	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 Blasco Amyotrophic lateral sclerosis & frontotemporal degeneration, 2018, 19 (5-6), pp.446-456. ⟨10.1080/21678421.2018.1431787⟩ Article dans une revue hal-01964500v1
	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 Rousseau Investigative Ophthalmology & Visual Science, 2017, 58 (2), pp.812-820. ⟨10.1167/iovs.16-21116⟩ Article dans une revue hal-01784466v1
	CLUH couples mitochondrial distribution to the energetic and metabolic status Jamal Wakim , David Goudenege , Rodolphe Perrot , Naig Gueguen , Valerie Desquiret-Dumas Journal of Cell Science, 2017, 130 (11), pp.1940 - 1951. ⟨10.1242/jcs.201616⟩ Article dans une revue hal-01601889v1
	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 Latour J Peripher Nerv Syst, 2016, 21 (4), pp.365-369. ⟨10.1111/jns.12192⟩ Article dans une revue hal-02104500v1
	Increase in Cardiac Ischemia-Reperfusion Injuries in Opa1+/- Mouse Model Sophie Le Page , Marjorie Niro , J. Fauconnier , Laura Cellier , Sophie Tamareille PLoS ONE, 2016, 11 (10), pp.e0164066. ⟨10.1371/journal.pone.0164066⟩ Article dans une revue hal-01818418v1
	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 Bris 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
	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-Prunier Brain - A Journal of Neurology , 2016, 139 (11), pp.2864-2876. ⟨10.1093/brain/aww222⟩ Article dans une revue hal-02103390v1
	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 Sarzi Neurobiology of Disease, 2015, pp.20-26. ⟨10.1016/j.nbd.2015.08.015⟩ Article dans une revue hal-01392230v1
	Assembly defects induce oxidative stress in inherited mitochondrial complex I deficiency Géraldine Leman , Naig Guegen , Valérie Desquiret-Dumas , Mariame Kane , Céline Wetterwald International Journal of Biochemistry and Cell Biology, 2015, 65, pp.91-103. ⟨10.1016/j.biocel.2015.05.017⟩ Article dans une revue hal-01399131v1
	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. Gribouval 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 Chevrollier 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 Chevrollier 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 Reynier Analytical Biochemistry, 2013, 434 (1), pp.44-51. ⟨10.1016/j.ab.2012.10.040⟩ Article dans une revue hal-01209902v1
	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-Antoine Journal of Biological Chemistry, 2013, 288 (51), pp.36662 - 75. ⟨10.1074/jbc.M113.466490⟩ Article dans une revue hal-03404098v1
	Is ABCC6 a genuine mitochondrial protein? Marc Ferré , Pascal Reynier , Arnaud Chevrollier , Delphine Prunier-Mirebeau , Georges Lefthériotis BMC Research Notes, 2013, 6 (1), pp.427. ⟨10.1186/1756-0500-6-427⟩ Article dans une revue inserm-00877607v1
	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. Hancock BBA - Biochimica et Biophysica Acta, 2012, 1822 (6), pp.1019 - 29. ⟨10.1016/j.bbadis.2012.01.010⟩ Article dans une revue hal-03404030v1
	Standardized mitochondrial analysis gives new insights into mitochondrial dynamics and OPA1 function Arnaud Chevrollier , Julien Cassereau , Marc Ferré , Jennifer Alban , Valérie Desquiret-Dumas International journal of biochemistry & cell biology, 2012, 44 (6), pp.980 - 8. ⟨10.1016/j.biocel.2012.03.006⟩ Article dans une revue hal-03404105v1
	Simultaneous MFN2 and GDAP1 mutations cause major mitochondrial defects in a patient with CMT Julien Cassereau , C. Casasnovas , Naïg Gueguen , Marie-Claire Malinge , Virginie Guillet 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-Dumas FASEB Journal, 2011, 25 (5), pp.1618 - 27. ⟨10.1096/fj.10-173609⟩ Article dans une revue hal-03408441v1
	Mitochondrial dysfunction and pathophysiology of Charcot-Marie-Tooth disease involving GDAP1 mutations Julien Cassereau , Arnaud Chevrollier , Naïg Gueguen , Valérie Desquiret-Dumas , Christophe Verny Experimental Neurology, 2011, 227 (1), pp.31 - 41. ⟨10.1016/j.expneurol.2010.09.006⟩ Article dans une revue hal-03408479v1
	The MFN2 gene is responsible for mitochondrial DNA instability and optic atrophy 'plus' phenotype C. Rouzier , Sylvie Bannwarth , A. Chaussenot , Arnaud Chevrollier , A. Verschueren Brain - A Journal of Neurology , 2011, 135 (Pt 1), pp.23 - 34. ⟨10.1093/brain/awr323⟩ Article dans une revue hal-03408506v1
	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 Procaccio Orphanet Journal of Rare Diseases, 2011, 6 (1), pp.87. ⟨10.1186/1750-1172-6-87⟩ Article dans une revue inserm-00683147v1
	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
	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 Guillet BMC Research Notes, 2011, 4 (1), pp.557. ⟨10.1186/1756-0500-4-557⟩ Article dans une revue inserm-00673659v1
	Hereditary spastic paraplegia-like disorder due to a mitochondrial ATP6 gene point mutation Christophe Verny , Naïg Gueguen , Valérie Desquiret-Dumas , Arnaud Chevrollier , Adriana Prundean Mitochondrion, 2010, 11 (1), pp.70 - 75. ⟨10.1016/j.mito.2010.07.006⟩ Article dans une revue hal-03408492v1
	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 Homedan neurogenetics, 2010, 11 (1), pp.127 - 133. ⟨10.1007/s10048-009-0207-z⟩ Article dans une revue hal-03406912v1
	Phenotypic spectrum of MFN2 mutations in the Spanish population C. Casasnovas , I. Banchs , Julien Cassereau , Naïg Gueguen , Arnaud Chevrollier Journal of Medical Genetics, 2010, 47 (4), pp.249 - 56. ⟨10.1136/jmg.2009.072488⟩ Article dans une revue hal-03408512v1
	Ethambutol-induced optic neuropathy linked to OPA1 mutation and mitochondrial toxicity Virginie Guillet , Arnaud Chevrollier , Julien Cassereau , Franck Letournel , Naïg Gueguen Mitochondrion, 2010, 10 (2), pp.115 - 124. ⟨10.1016/j.mito.2009.11.004⟩ Article dans une revue hal-03403265v1
	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 Verny Médecine/Sciences, 2010, 26 (10), pp.836 - 841. ⟨10.1051/medsci/20102610836⟩ Article dans une revue hal-03408444v1
	Mitochondrial bioenergetic background confers a survival advantage to HepG2 cells in response to chemotherapy Dominique Loiseau , Daniel Morvan , Arnaud Chevrollier , Aicha Demidem , Olivier Douay Molecular Carcinogenesis, 2009, 48 (8), pp.733-741. ⟨10.1002/mc.20539⟩ Article dans une revue hal-02655649v1
	Mitochondrial complex I deficiency in GDAP1-related autosomal dominant Charcot-Marie-Tooth disease (CMT2K) Julien Cassereau , Arnaud Chevrollier , Naïg Gueguen , Marie-Claire Malinge , Franck Letournel neurogenetics, 2009, 10 (2), pp.145 - 150. ⟨10.1007/s10048-008-0166-9⟩ Article dans une revue 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 Ferré 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 Ferré International Journal of Biochemistry and Cell Biology, 2009, 41 (10), pp.1855 - 1865. ⟨10.1016/j.biocel.2009.04.012⟩ Article dans une revue hal-03406909v1
	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 Verny Human Mutation, 2009, 30 (7), pp.E692-705. ⟨10.1002/humu.21025⟩ Article dans une revue inserm-00372261v1
	OPA1-related dominant optic atrophy is not strongly influenced by mitochondrial DNA background. Denis Pierron , Marc Ferré , Christophe Rocher , Arnaud Chevrollier , Pascal Murail BMC Medical Genetics, 2009, 10 (1), pp.70. ⟨10.1186/1471-2350-10-70⟩ Article dans une revue inserm-00663623v1
	Reversible optic neuropathy with OPA1 exon 5b mutation. Karen Cornille , Dan Milea , Patrizia Amati-Bonneau , Vincent Procaccio , Lydie Zazoun Annals of Neurology, 2008, 63 (5), pp.667-71. ⟨10.1002/ana.21376⟩ Article dans une revue inserm-00287509v1
	Multiple Sclerosis–Like Disorder in Opa1-Related Autosomal Dominant Optic Atrophy Christophe Verny , Dominique Loiseau , Clarisse Scherer , P. Lejeune , Arnaud Chevrollier 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 Crescenzo Annals of Neurology, 2008, 63 (6), pp.794-8. ⟨10.1002/ana.21385⟩ Article dans une revue hal-00282865v1
	ANT2 isoform required for cancer cell glycolysis Arnaud Chevrollier , Dominique Loiseau , Béatrice Chabi , Gilles Renier , Olivier Douay Journal of Bioenergetics and Biomembranes, 2005, 37 (5), pp.307-316. ⟨10.1007/s10863-005-8642-5⟩ Article dans une revue 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 hal-02682861v1

	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

	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

Arnaud CHEVROLLIER

Domaines de recherche

Compétences

Publications

Homozygous MFN2 variants causing severe antenatal encephalopathy with clumped mitochondria

Homozygous MFN2 variants causing severe antenatal encephalopathy with clumped mitochondria

Super-resolution microscopies, technological breakthrough to decipher mitochondrial structure and dynamic.

Transactive response DNA-binding protein 43 is enriched at the centrosome in human cells

Next generation sequencing identifies novel PMPCA variants in patients with dominant optic atrophy

Glutamate-Induced Deregulation of Krebs Cycle in Mitochondrial Encephalopathy Lactic Acidosis Syndrome Stroke-Like Episodes (MELAS) Syndrome Is Alleviated by Ketone Body Exposure

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

MELAS syndrome causes glutamate and tricarboxylic acid cycle dysfunctions alleviated by ketone body treatment

Cancer/Testis Antigen 55 is required for cancer cell proliferation and mitochondrial DNA maintenance

LPS-enriched small extracellular vesicles from metabolic syndrome patients trigger endothelial dysfunction by activation of TLR4

Dominant ACO2 mutations are a frequent cause of isolated optic atrophy

The Long Non-Coding RNA SAMMSON Is a Regulator of Chemosensitivity and Metabolic Orientation in MCF-7 Doxorubicin-Resistant Breast Cancer Cells

Protective role of the mitochondrial fusion protein OPA1 in hypertension

Mutations in the m-AAA proteases AFG3L2 and SPG7 are causing isolated dominant optic atrophy

Étude du cerveau humain à l’échelle nanoscopique par microscopie Super-Résolutive STORM

Oxidative stress contributes differentially to the pathophysiology of Charcot-Marie-Tooth disease type 2K

Lipidomics Reveals Triacylglycerol Accumulation Due to Impaired Fatty Acid Flux in Opa1 -Disrupted Fibroblasts

Warburg-like effect is a hallmark of complex I assembly defects

Is multidetector CT-scan able to detect T3a renal tumor before surgery?

Reply: The expanding neurological phenotype of DNM1L-related disorders

The Metabolomic Bioenergetic Signature of Opa1-Disrupted Mouse Embryonic Fibroblasts Highlights Aspartate Deficiency

A Plasma Metabolomic Signature Involving Purine Metabolism in Human Optic Atrophy 1 (OPA1)-Related Disorders

Current mechanistic insights into the CCCP-induced cell survival response

Primary fibroblasts derived from sporadic amyotrophic lateral sclerosis patients do not show ALS cytological lesions

Targeted Metabolomics Reveals Early Dominant Optic Atrophy Signature in Optic Nerves of Opa1 delTTAG/+ Mice

CLUH couples mitochondrial distribution to the energetic and metabolic status

Increased mitochondrial fusion in a autosomal recessive CMT2A family with mitochondrial GTPase mitofusin 2 mutations

Increase in Cardiac Ischemia-Reperfusion Injuries in Opa1+/- Mouse Model

The addition of ketone bodies alleviates mitochondrial dysfunction by restoring complex I assembly in a MELAS cellular model

The metabolomic signature of Leber's hereditary optic neuropathy reveals endoplasmic reticulum stress

OPA1-related disorders: Diversity of clinical expression, modes of inheritance and pathophysiology

Assembly defects induce oxidative stress in inherited mitochondrial complex I deficiency

Loss-of-Function Mutations in WDR73 Are Responsible for Microcephaly and Steroid-Resistant Nephrotic Syndrome: Galloway-Mowat Syndrome

Early-onset Behr syndrome due to compound heterozygous mutations in OPA1

Perspectives of drug-based neuroprotection targeting mitochondria

Experimental determination of organelle targeting peptide cleavage sites using transient expression of GFP translational fusions

Resveratrol induces a mitochondrial complex I-dependent increase in NADH oxidation responsible for sirtuin activation in liver cells

Is ABCC6 a genuine mitochondrial protein?

Metabolically induced heteroplasmy shifting and l-arginine treatment reduce the energetic defect in a neuronal-like model of MELAS

Standardized mitochondrial analysis gives new insights into mitochondrial dynamics and OPA1 function

Simultaneous MFN2 and GDAP1 mutations cause major mitochondrial defects in a patient with CMT

Bioenergetic defect associated with mKATP channel opening in a mouse model carrying a mitofusin 2 mutation

Mitochondrial dysfunction and pathophysiology of Charcot-Marie-Tooth disease involving GDAP1 mutations

The MFN2 gene is responsible for mitochondrial DNA instability and optic atrophy 'plus' phenotype

A locus-specific database for mutations in GDAP1 allows analysis of genotype-phenotype correlations in Charcot-Marie-Tooth diseases type 4A and 2K.

Adenine nucleotide translocase 2 is a key mitochondrial protein in cancer metabolism

Idebenone increases mitochondrial complex I activity in fibroblasts from LHON patients while producing contradictory effects on respiration.

Hereditary spastic paraplegia-like disorder due to a mitochondrial ATP6 gene point mutation

Adenine nucleotide translocase is involved in a mitochondrial coupling defect in MFN2-related Charcot–Marie–Tooth type 2A disease

Phenotypic spectrum of MFN2 mutations in the Spanish population

Ethambutol-induced optic neuropathy linked to OPA1 mutation and mitochondrial toxicity

De la levure aux maladies neurodégénératives : Dix ans d’exploration des pathologies de la dynamique mitochondriale

Mitochondrial bioenergetic background confers a survival advantage to HepG2 cells in response to chemotherapy

Mitochondrial complex I deficiency in GDAP1-related autosomal dominant Charcot-Marie-Tooth disease (CMT2K)

Acute and late-onset optic atrophy due to a novel OPA1 mutation leading to a mitochondrial coupling defect

OPA1-associated disorders: Phenotypes and pathophysiology

Molecular screening of 980 cases of suspected hereditary optic neuropathy with a report on 77 novel OPA1 mutations.

OPA1-related dominant optic atrophy is not strongly influenced by mitochondrial DNA background.

Reversible optic neuropathy with OPA1 exon 5b mutation.

Multiple Sclerosis–Like Disorder in Opa1-Related Autosomal Dominant Optic Atrophy

Hereditary optic neuropathies share a common mitochondrial coupling defect.

ANT2 isoform required for cancer cell glycolysis

Random mtDNA deletions and functional consequence in aged human skeletal muscle

Human Brain Imaging with STochastic Optical Reconstruction Microscopy (STORM)

Expression de l'isoforme 2 de la translocase des nucléotides adényliques mitochondriale et métabolisme de la cellule cancéreuse

Expression de l'isoforme 2 de la translocase des nucléotides adényliques mitochondriale et métabolisme de la cellule cancéreuse