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Papers authored by Chevrollier A

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OPA1-associated disorders: phenotypes and pathophysiology.

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Amati-Bonneau P, Milea D, Bonneau D, Chevrollier A, Ferré M, Guillet V, Gueguen N, Loiseau D, de Crescenzo MA, Verny C, Procaccio V, Lenaers G, and Reynier P

The international journal of biochemistry & cell biology 41(10):1855-65, 2009 Oct - Who cited this? | PubMed ID: 19389487 | Fulltext

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

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Loiseau D, Morvan D, Chevrollier A, Demidem A, Douay O, Reynier P, and Stepien G

Molecular carcinogenesis 48(8):733-41, 2009 Aug - Who cited this? | PubMed ID: 19347860 | Fulltext

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

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Ferré M, Bonneau D, Milea D, Chevrollier A, Verny C, Dollfus H, Ayuso C, Defoort S, Vignal C, Zanlonghi X, Charlin JF, Kaplan J, Odent S, Hamel CP, Procaccio V, Reynier P,

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Human mutation 30(7):E692-705, 2009 Jul - Who cited this? | PubMed ID: 19319978 | Fulltext

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

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Cassereau J, Chevrollier A, Gueguen N, Malinge MC, Letournel F, Nicolas G, Richard L, Ferre M, Verny C, Dubas F, Procaccio V, Amati-Bonneau P, Bonneau D, and Reynier P

Neurogenetics 10(2):145-50, 2009 Apr - Who cited this? | PubMed ID: 19089472 | Fulltext

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

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Nochez Y, Arsene S, Gueguen N, Chevrollier A, Ferré M, Guillet V, Desquiret V, Toutain A, Bonneau D, Procaccio V, Amati-Bonneau P, Pisella PJ, and Reynier P

Molecular vision 15:598-608, 2009 - Who cited this? | PubMed ID: 19325939 | Fulltext

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

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Pierron D, Ferré M, Rocher C, Chevrollier A, Murail P, Thoraval D, Amati-Bonneau P, Reynier P, and Letellier T

BMC medical genetics 10:70, 2009 - Who cited this? | PubMed ID: 19619285 | Fulltext

Hereditary optic neuropathies share a common mitochondrial coupling defect.

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Chevrollier A, Guillet V, Loiseau D, Gueguen N, de Crescenzo MA, Verny C, Eng MF, Dollfus H, Odent S, Milea D, Goizet C, Amati-Bonneau P, Procaccio V, Bonneau D, and Reynier P

Annals of neurology 63(6):794-8, 2008 Jun - Who cited this? | PubMed ID: 18496845 | Fulltext

Reversible optic neuropathy with OPA1 exon 5b mutation.

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Cornille K, Milea D, Amati-Bonneau P, Procaccio V, Zazoun L, Guillet V, El Achouri G, Delettre C, Gueguen N, Loiseau D, Muller A, Ferré M, Chevrollier A, Wallace DC, Bonneau D, Hamel C,

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Annals of neurology 63(5):667-71, 2008 May - Who cited this? | PubMed ID: 18360822 | Fulltext

Multiple sclerosis-like disorder in opa1-related autosomal dominant optic atrophy.

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Verny C, Loiseau D, Scherer C, Lejeune P, Chevrollier A, Gueguen N, Guillet V, Dubas F, Reynier P, Amati-Bonneau P, and Bonneau D

Neurology 70(13 Pt 2):1152-3, 2008 Mar 25 - Who cited this? | PubMed ID: 18287570 | Fulltext

Mitochondrial coupling defect in Charcot-Marie-Tooth type 2A disease.

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Loiseau D, Chevrollier A, Verny C, Guillet V, Gueguen N, Pou de Crescenzo MA, Ferré M, Malinge MC, Guichet A, Nicolas G, Amati-Bonneau P, Malthièry Y, Bonneau D, and Reynier P

Annals of neurology 61(4):315-23, 2007 Apr - Who cited this? | PubMed ID: 17444508 | Fulltext

mtDNA controls expression of the Death Associated Protein 3.

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Jacques C, Chevrollier A, Loiseau D, Lagoutte L, Savagner F, Malthièry Y, and Reynier P

Experimental cell research 312(6):737-45, 2006 Apr 1 - Who cited this? | PubMed ID: 16413536 | Fulltext

OPA1 R445H mutation in optic atrophy associated with sensorineural deafness.

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Amati-Bonneau P, Guichet A, Olichon A, Chevrollier A, Viala F, Miot S, Ayuso C, Odent S, Arrouet C, Verny C, Calmels MN, Simard G, Belenguer P, Wang J, Puel JL, Hamel C,

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Annals of neurology 58(6):958-63, 2005 Dec - Who cited this? | PubMed ID: 16240368 | Fulltext

ANT2 isoform required for cancer cell glycolysis.

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Chevrollier A, Loiseau D, Chabi B, Renier G, Douay O, Malthièry Y, and Stepien G

Journal of bioenergetics and biomembranes 37(5):307-16, 2005 Oct - Who cited this? | PubMed ID: 16341775 | Fulltext

Random mtDNA deletions and functional consequence in aged human skeletal muscle.

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Chabi B, de Camaret BM, Chevrollier A, Boisgard S, and Stepien G

Biochemical and biophysical research communications 332(2):542-9, 2005 Jul 1 - Who cited this? | PubMed ID: 15896715 | Fulltext

[What is the specific role of ANT2 in cancer cells?].

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Chevrollier A, Loiseau D, and Stepien G

Medecine sciences : M/S 21(2):156-61, 2005 Feb - Who cited this? | PubMed ID: 15691486 | Fulltext

ANT2 expression under hypoxic conditions produces opposite cell-cycle behavior in 143B and HepG2 cancer cells.

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Chevrollier A, Loiseau D, Gautier F, Malthièry Y, and Stepien G

Molecular carcinogenesis 42(1):1-8, 2005 Jan - Who cited this? | PubMed ID: 15486956 | Fulltext

Oxygen consumption and expression of the adenine nucleotide translocator in cells lacking mitochondrial DNA.

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Loiseau D, Chevrollier A, Douay O, Vavasseur F, Renier G, Reynier P, Malthièry Y, and Stepien G

Experimental cell research 278(1):12-8, 2002 Aug 1 - Who cited this? | PubMed ID: 12126953 | Fulltext

Induction of ANT2 gene expression in liver of patients with mitochondrial DNA depletion.

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Bonod-Bidaud C, Chevrollier A, Bourasseau I, Lachaux A, Mousson de Camaret B, and Stepien G

Mitochondrion 1(3):217-24, 2001 Oct - Who cited this? | PubMed ID: 16120279 | Fulltext

Mitochondrial activity in XTC.UC1 cells derived from thyroid oncocytoma.

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Savagner F, Chevrollier A, Loiseau D, Morgan C, Reynier P, Clark O, Stepien G, and Malthiery Y

Thyroid : official journal of the American Thyroid Association 11(4):327-33, 2001 Apr - Who cited this? | PubMed ID: 11349830 | Fulltext

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