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13 results
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Role of mitofusin 2 mutations in the physiopathology of Charcot-Marie-Tooth disease type 2A.
Cartoni R, Martinou JC. Cartoni R, et al. Exp Neurol. 2009 Aug;218(2):268-73. doi: 10.1016/j.expneurol.2009.05.003. Epub 2009 May 8. Exp Neurol. 2009. PMID: 19427854 Review.
Mitofusins 1/2 and ERRalpha expression are increased in human skeletal muscle after physical exercise.
Cartoni R, Léger B, Hock MB, Praz M, Crettenand A, Pich S, Ziltener JL, Luthi F, Dériaz O, Zorzano A, Gobelet C, Kralli A, Russell AP. Cartoni R, et al. J Physiol. 2005 Aug 15;567(Pt 1):349-58. doi: 10.1113/jphysiol.2005.092031. Epub 2005 Jun 16. J Physiol. 2005. PMID: 15961417 Free PMC article.
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: cartoni r. FASEB J. 2011 May;25(5):1618-27. doi: 10.1096/fj.10-173609. Epub 2011 Feb 1. FASEB J. 2011. PMID: 21285398
Expression of mitofusin 2(R94Q) in a transgenic mouse leads to Charcot-Marie-Tooth neuropathy type 2A.
Cartoni R, Arnaud E, Médard JJ, Poirot O, Courvoisier DS, Chrast R, Martinou JC. Cartoni R, et al. Brain. 2010 May;133(Pt 5):1460-9. doi: 10.1093/brain/awq082. Brain. 2010. PMID: 20418531
PLEKHG5 deficiency leads to an intermediate form of autosomal-recessive Charcot-Marie-Tooth disease.
Azzedine H, Zavadakova P, Planté-Bordeneuve V, Vaz Pato M, Pinto N, Bartesaghi L, Zenker J, Poirot O, Bernard-Marissal N, Arnaud Gouttenoire E, Cartoni R, Title A, Venturini G, Médard JJ, Makowski E, Schöls L, Claeys KG, Stendel C, Roos A, Weis J, Dubourg O, Leal Loureiro J, Stevanin G, Said G, Amato A, Baraban J, LeGuern E, Senderek J, Rivolta C, Chrast R. Azzedine H, et al. Among authors: cartoni r. Hum Mol Genet. 2013 Oct 15;22(20):4224-32. doi: 10.1093/hmg/ddt274. Epub 2013 Jun 17. Hum Mol Genet. 2013. PMID: 23777631 Free PMC article.
Disruption of skeletal muscle mitochondrial network genes and miRNAs in amyotrophic lateral sclerosis.
Russell AP, Wada S, Vergani L, Hock MB, Lamon S, Léger B, Ushida T, Cartoni R, Wadley GD, Hespel P, Kralli A, Soraru G, Angelini C, Akimoto T. Russell AP, et al. Among authors: cartoni r. Neurobiol Dis. 2013 Jan;49:107-17. doi: 10.1016/j.nbd.2012.08.015. Epub 2012 Sep 4. Neurobiol Dis. 2013. PMID: 22975021
Akt signalling through GSK-3beta, mTOR and Foxo1 is involved in human skeletal muscle hypertrophy and atrophy.
Léger B, Cartoni R, Praz M, Lamon S, Dériaz O, Crettenand A, Gobelet C, Rohmer P, Konzelmann M, Luthi F, Russell AP. Léger B, et al. Among authors: cartoni r. J Physiol. 2006 Nov 1;576(Pt 3):923-33. doi: 10.1113/jphysiol.2006.116715. Epub 2006 Aug 17. J Physiol. 2006. PMID: 16916907 Free PMC article.
The Mammalian-Specific Protein Armcx1 Regulates Mitochondrial Transport during Axon Regeneration.
Cartoni R, Norsworthy MW, Bei F, Wang C, Li S, Zhang Y, Gabel CV, Schwarz TL, He Z. Cartoni R, et al. Neuron. 2016 Dec 21;92(6):1294-1307. doi: 10.1016/j.neuron.2016.10.060. Neuron. 2016. PMID: 28009275 Free PMC article.
The Mammalian-Specific Protein Armcx1 Regulates Mitochondrial Transport during Axon Regeneration.
Cartoni R, Norsworthy MW, Bei F, Wang C, Li S, Zhang Y, Gabel CV, Schwarz TL, He Z. Cartoni R, et al. Neuron. 2017 May 3;94(3):689. doi: 10.1016/j.neuron.2017.04.028. Neuron. 2017. PMID: 28472662 Free article. No abstract available.
Differential effects of unfolded protein response pathways on axon injury-induced death of retinal ganglion cells.
Hu Y, Park KK, Yang L, Wei X, Yang Q, Cho KS, Thielen P, Lee AH, Cartoni R, Glimcher LH, Chen DF, He Z. Hu Y, et al. Among authors: cartoni r. Neuron. 2012 Feb 9;73(3):445-52. doi: 10.1016/j.neuron.2011.11.026. Neuron. 2012. PMID: 22325198 Free PMC article.
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