Angebault C - Search Results

1

LIX1-mediated changes in mitochondrial metabolism control the fate of digestive mesenchyme-derived cells.

Guérin A, Angebault C, Kinet S, Cazevieille C, Rojo M, Fauconnier J, Lacampagne A, Mourier A, Taylor N, de Santa Barbara P, Faure S. Guérin A, et al. Among authors: angebault c. Redox Biol. 2022 Oct;56:102431. doi: 10.1016/j.redox.2022.102431. Epub 2022 Aug 13. Redox Biol. 2022. PMID: 35988446 Free PMC article.

2

ER-mitochondria cross-talk is regulated by the Ca²⁺ sensor NCS1 and is impaired in Wolfram syndrome.

Angebault C, Fauconnier J, Patergnani S, Rieusset J, Danese A, Affortit CA, Jagodzinska J, Mégy C, Quiles M, Cazevieille C, Korchagina J, Bonnet-Wersinger D, Milea D, Hamel C, Pinton P, Thiry M, Lacampagne A, Delprat B, Delettre C. Angebault C, et al. Sci Signal. 2018 Oct 23;11(553):eaaq1380. doi: 10.1126/scisignal.aaq1380. Sci Signal. 2018. PMID: 30352948 Free article.

3

Metformin Reverses the Enhanced Myocardial SR/ER-Mitochondria Interaction and Impaired Complex I-Driven Respiration in Dystrophin-Deficient Mice.

Angebault C, Panel M, Lacôte M, Rieusset J, Lacampagne A, Fauconnier J. Angebault C, et al. Front Cell Dev Biol. 2021 Jan 25;8:609493. doi: 10.3389/fcell.2020.609493. eCollection 2020. Front Cell Dev Biol. 2021. PMID: 33569379 Free PMC article.

4

Mitochondrial oxidative stress induces leaky ryanodine receptor during mechanical ventilation.

Dridi H, Yehya M, Barsotti R, Reiken S, Angebault C, Jung B, Jaber S, Marks AR, Lacampagne A, Matecki S. Dridi H, et al. Among authors: angebault c. Free Radic Biol Med. 2020 Jan;146:383-391. doi: 10.1016/j.freeradbiomed.2019.11.019. Epub 2019 Nov 19. Free Radic Biol Med. 2020. PMID: 31756525 Free article.

5

The human OPA1delTTAG mutation induces premature age-related systemic neurodegeneration in mouse.

Sarzi E, Angebault C, Seveno M, Gueguen N, Chaix B, Bielicki G, Boddaert N, Mausset-Bonnefont AL, Cazevieille C, Rigau V, Renou JP, Wang J, Delettre C, Brabet P, Puel JL, Hamel CP, Reynier P, Lenaers G. Sarzi E, et al. Among authors: angebault c. Brain. 2012 Dec;135(Pt 12):3599-613. doi: 10.1093/brain/aws303. Brain. 2012. PMID: 23250881

6

Light action spectrum on oxidative stress and mitochondrial damage in A2E-loaded retinal pigment epithelium cells.

Marie M, Bigot K, Angebault C, Barrau C, Gondouin P, Pagan D, Fouquet S, Villette T, Sahel JA, Lenaers G, Picaud S. Marie M, et al. Among authors: angebault c. Cell Death Dis. 2018 Feb 19;9(3):287. doi: 10.1038/s41419-018-0331-5. Cell Death Dis. 2018. PMID: 29459695 Free PMC article.

7

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

Guillet V, Gueguen N, Cartoni R, Chevrollier A, Desquiret V, Angebault C, Amati-Bonneau P, Procaccio V, Bonneau D, Martinou JC, Reynier P. Guillet V, et al. Among authors: angebault c. FASEB J. 2011 May;25(5):1618-27. doi: 10.1096/fj.10-173609. Epub 2011 Feb 1. FASEB J. 2011. PMID: 21285398 Free article.

8

Recessive Mutations in RTN4IP1 Cause Isolated and Syndromic Optic Neuropathies.

Angebault C, Guichet PO, Talmat-Amar Y, Charif M, Gerber S, Fares-Taie L, Gueguen N, Halloy F, Moore D, Amati-Bonneau P, Manes G, Hebrard M, Bocquet B, Quiles M, Piro-Mégy C, Teigell M, Delettre C, Rossel M, Meunier I, Preising M, Lorenz B, Carelli V, Chinnery PF, Yu-Wai-Man P, Kaplan J, Roubertie A, Barakat A, Bonneau D, Reynier P, Rozet JM, Bomont P, Hamel CP, Lenaers G. Angebault C, et al. Am J Hum Genet. 2015 Nov 5;97(5):754-60. doi: 10.1016/j.ajhg.2015.09.012. Epub 2015 Oct 22. Am J Hum Genet. 2015. PMID: 26593267 Free PMC article.

9

Increased steroidogenesis promotes early-onset and severe vision loss in females with OPA1 dominant optic atrophy.

Sarzi E, Seveno M, Angebault C, Milea D, Rönnbäck C, Quilès M, Adrian M, Grenier J, Caignard A, Lacroux A, Lavergne C, Reynier P, Larsen M, Hamel CP, Delettre C, Lenaers G, Müller A. Sarzi E, et al. Among authors: angebault c. Hum Mol Genet. 2016 Jun 15;25(12):2539-2551. doi: 10.1093/hmg/ddw117. Epub 2016 Jun 3. Hum Mol Genet. 2016. PMID: 27260406

10

Mutation in NDUFA13/GRIM19 leads to early onset hypotonia, dyskinesia and sensorial deficiencies, and mitochondrial complex I instability.

Angebault C, Charif M, Guegen N, Piro-Megy C, Mousson de Camaret B, Procaccio V, Guichet PO, Hebrard M, Manes G, Leboucq N, Rivier F, Hamel CP, Lenaers G, Roubertie A. Angebault C, et al. Hum Mol Genet. 2015 Jul 15;24(14):3948-55. doi: 10.1093/hmg/ddv133. Epub 2015 Apr 21. Hum Mol Genet. 2015. PMID: 25901006

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