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Items: 12

1.

OPA1 haploinsufficiency induces a BNIP3-dependent decrease in mitophagy in neurons: relevance to Dominant Optic Atrophy.

Moulis MF, Millet AM, Daloyau M, Miquel MC, Ronsin B, Wissinger B, Arnauné-Pelloquin L, Belenguer P.

J Neurochem. 2017 Feb;140(3):485-494. doi: 10.1111/jnc.13894. Epub 2016 Dec 20.

2.

Loss of Msp1p in Schizosaccharomyces pombe induces a ROS-dependent nuclear mutator phenotype that affects mitochondrial fission genes.

Delerue T, Khosrobakhsh F, Daloyau M, Emorine LJ, Dedieu A, Herbert CJ, Bonnefoy N, Arnauné-Pelloquin L, Belenguer P.

FEBS Lett. 2016 Oct;590(20):3544-3558. doi: 10.1002/1873-3468.12432. Epub 2016 Oct 11.

3.

Mitochondrial fusion/fission dynamics in neurodegeneration and neuronal plasticity.

Bertholet AM, Delerue T, Millet AM, Moulis MF, David C, Daloyau M, Arnauné-Pelloquin L, Davezac N, Mils V, Miquel MC, Rojo M, Belenguer P.

Neurobiol Dis. 2016 Jun;90:3-19. doi: 10.1016/j.nbd.2015.10.011. Epub 2015 Oct 19. Review.

PMID:
26494254
4.

Barth syndrome: cellular compensation of mitochondrial dysfunction and apoptosis inhibition due to changes in cardiolipin remodeling linked to tafazzin (TAZ) gene mutation.

Gonzalvez F, D'Aurelio M, Boutant M, Moustapha A, Puech JP, Landes T, Arnauné-Pelloquin L, Vial G, Taleux N, Slomianny C, Wanders RJ, Houtkooper RH, Bellenguer P, Møller IM, Gottlieb E, Vaz FM, Manfredi G, Petit PX.

Biochim Biophys Acta. 2013 Aug;1832(8):1194-206. doi: 10.1016/j.bbadis.2013.03.005. Epub 2013 Mar 20.

5.

Inner-membrane proteins PMI/TMEM11 regulate mitochondrial morphogenesis independently of the DRP1/MFN fission/fusion pathways.

Rival T, Macchi M, Arnauné-Pelloquin L, Poidevin M, Maillet F, Richard F, Fatmi A, Belenguer P, Royet J.

EMBO Rep. 2011 Mar;12(3):223-30. doi: 10.1038/embor.2010.214. Epub 2011 Jan 28.

6.

[Mitochondrial morphology and dynamics: actors, mechanisms and functions].

Sauvanet C, Arnauné-Pelloquin L, David C, Belenguer P, Rojo M.

Med Sci (Paris). 2010 Oct;26(10):823-9. doi: 10.1051/medsci/20102610823. Review. French.

7.

Processing of the dynamin Msp1p in S. pombe reveals an evolutionary switch between its orthologs Mgm1p in S. cerevisiae and OPA1 in mammals.

Leroy I, Khosrobakhsh F, Diot A, Daloyau M, Arnauné-Pelloquin L, Cavelier C, Emorine LJ, Belenguer P.

FEBS Lett. 2010 Jul 16;584(14):3153-7. doi: 10.1016/j.febslet.2010.05.060. Epub 2010 Jun 1.

8.

The BH3-only Bnip3 binds to the dynamin Opa1 to promote mitochondrial fragmentation and apoptosis by distinct mechanisms.

Landes T, Emorine LJ, Courilleau D, Rojo M, Belenguer P, Arnauné-Pelloquin L.

EMBO Rep. 2010 Jun;11(6):459-65. doi: 10.1038/embor.2010.50. Epub 2010 Apr 30.

9.

OPA1 (dys)functions.

Landes T, Leroy I, Bertholet A, Diot A, Khosrobakhsh F, Daloyau M, Davezac N, Miquel MC, Courilleau D, Guillou E, Olichon A, Lenaers G, Arnauné-Pelloquin L, Emorine LJ, Belenguer P.

Semin Cell Dev Biol. 2010 Aug;21(6):593-8. doi: 10.1016/j.semcdb.2009.12.012. Epub 2010 Jan 4. Review.

PMID:
20045077
10.

Transmembrane segments of the dynamin Msp1p uncouple its functions in the control of mitochondrial morphology and genome maintenance.

Diot A, Guillou E, Daloyau M, Arnauné-Pelloquin L, Emorine LJ, Belenguer P.

J Cell Sci. 2009 Aug 1;122(Pt 15):2632-9. doi: 10.1242/jcs.040139. Epub 2009 Jun 30.

11.

Effects of OPA1 mutations on mitochondrial morphology and apoptosis: relevance to ADOA pathogenesis.

Olichon A, Landes T, Arnauné-Pelloquin L, Emorine LJ, Mils V, Guichet A, Delettre C, Hamel C, Amati-Bonneau P, Bonneau D, Reynier P, Lenaers G, Belenguer P.

J Cell Physiol. 2007 May;211(2):423-30.

PMID:
17167772
12.

Mitochondrial dynamics and disease, OPA1.

Olichon A, Guillou E, Delettre C, Landes T, Arnauné-Pelloquin L, Emorine LJ, Mils V, Daloyau M, Hamel C, Amati-Bonneau P, Bonneau D, Reynier P, Lenaers G, Belenguer P.

Biochim Biophys Acta. 2006 May-Jun;1763(5-6):500-9. Epub 2006 Apr 20. Review.

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