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Mizushima N, Komatsu M. Autophagy: renovation of cells and tissues. Cell. 2011; 147:728–41.MizushimaNKomatsuMAutophagy: renovation of cells and tissues20111477284110.1016/j.cell.2011.10.026Search in Google Scholar
Tai HC, Schuman EM. Ubiquitin, the proteasome and protein degradation in neuronal function and dysfunction. Nat Rev Neurosci. 2008; 9:826–38.TaiHCSchumanEMUbiquitin, the proteasome and protein degradation in neuronal function and dysfunction200898263810.1038/nrn2499Search in Google Scholar
Marino G, Madeo F, Kroemer G. Autophagy for tissue homeostasis and neuroprotection. Curr Opin Cell Biol. 2011; 23:198–206.MarinoGMadeoFKroemerGAutophagy for tissue homeostasis and neuroprotection20112319820610.1016/j.ceb.2010.10.001Search in Google Scholar
Ghavami S, Shojaei S, Yeganeh B, Ande SR, Jangamreddy JR, Mehrpour M, et al. Autophagy and apoptosis dysfunction in neurodegenerative disorders. Prog Neurobiol. 2014; 112:24–49.GhavamiSShojaeiSYeganehBAndeSRJangamreddyJRMehrpourMAutophagy and apoptosis dysfunction in neurodegenerative disorders2014112244910.1016/j.pneurobio.2013.10.004Search in Google Scholar
Dennissen FJ, Kholod N, van Leeuwen FW. The ubiquitin proteasome system in neurodegenerative diseases: culprit, accomplice or victim? Prog Neurobiol. 2012; 96:190–207.DennissenFJKholodNvan LeeuwenFWThe ubiquitin proteasome system in neurodegenerative diseases: culprit, accomplice or victim?20129619020710.1016/j.pneurobio.2012.01.003Search in Google Scholar
Ying Z, Wang H, Wang G. The ubiquitin proteasome system as a potential target for the treatment of neurodegenerative diseases. Curr Pharm Des. 2013; 19:3305–14.YingZWangHWangGThe ubiquitin proteasome system as a potential target for the treatment of neurodegenerative diseases20131933051410.2174/1381612811319180013Search in Google Scholar
Diskin T, Tal-Or P, Erlich S, Mizrachy L, Alexandrovich A, Shohami E, et al. Closed head injury induces upregulation of Beclin 1 at the cortical site of injury. J Neurotrauma. 2005; 22:750–62.DiskinTTal-OrPErlichSMizrachyLAlexandrovichAShohamiEClosed head injury induces upregulation of Beclin 1 at the cortical site of injury2005227506210.1089/neu.2005.22.750Search in Google Scholar
Lai Y, Hickey RW, Chen Y, Bayir H, Sullivan ML, Chu CT, et al. Autophagy is increased after traumatic brain injury in mice and is partially inhibited by the antioxidant gamma-glutamylcysteinyl ethyl ester. J Cereb Blood Flow Metab. 2008; 28:540–50.LaiYHickeyRWChenYBayirHSullivanMLChuCTAutophagy is increased after traumatic brain injury in mice and is partially inhibited by the antioxidant gamma-glutamylcysteinyl ethyl ester2008285405010.1038/sj.jcbfm.9600551Search in Google Scholar
Liu CL, Chen S, Dietrich D, Hu BR. Changes in autophagy after traumatic brain injury. J Cereb Blood Flow Metab. 2008; 28:674–83.LiuCLChenSDietrichDHuBRChanges in autophagy after traumatic brain injury2008286748310.1038/sj.jcbfm.9600587Search in Google Scholar
Kanno H, Ozawa H, Sekiguchi A, Itoi E. The role of autophagy in spinal cord injury. Autophagy. 2009; 5:390–2.KannoHOzawaHSekiguchiAItoiEThe role of autophagy in spinal cord injury20095390210.4161/auto.5.3.7724Search in Google Scholar
Rodriguez-Muela N, Boya P. Axonal damage, autophagy and neuronal survival. Autophagy. 2012; 8:286–8.Rodriguez-MuelaNBoyaPAxonal damage, autophagy and neuronal survival20128286810.4161/auto.8.2.18982Search in Google Scholar
Egami Y, Kiryu-Seo S, Yoshimori T, Kiyama H. Induced expressions of Rab24 GTPase and LC3 in nerve-injured motor neurons. Biochem Biophys Res Commun. 2005; 337:1206–13.EgamiYKiryu-SeoSYoshimoriTKiyamaHInduced expressions of Rab24 GTPase and LC3 in nerve-injured motor neurons200533712061310.1016/j.bbrc.2005.09.171Search in Google Scholar
Huang HC, Chen L, Zhang HX, Li SF, Liu P, Zhao TY, et al. Autophagy promotes peripheral nerve regeneration and motor recovery following sciatic nerve crush injury in rats. J Mol Neurosci. 2016; 58:416–23.HuangHCChenLZhangHXLiSFLiuPZhaoTYAutophagy promotes peripheral nerve regeneration and motor recovery following sciatic nerve crush injury in rats2016584162310.1007/s12031-015-0672-9Search in Google Scholar
Savedia S, Kiernan JA. Increased production of ubiquitin mRNA in motor neurons after axotomy. Neuropathol Appl Neurobiol. 1994; 20:577–86.SavediaSKiernanJAIncreased production of ubiquitin mRNA in motor neurons after axotomy1994205778610.1111/j.1365-2990.1994.tb01012.xSearch in Google Scholar
Lee HK, Shin YK, Jung J, Seo SY, Baek SY, Park HT. Proteasome inhibition suppresses Schwann cell dedifferentiation in vitro and in vivo. Glia. 2009; 57:1825–34.LeeHKShinYKJungJSeoSYBaekSYParkHTProteasome inhibition suppresses Schwann cell dedifferentiation in vitro and in vivo20095718253410.1002/glia.20894Search in Google Scholar
Hu J, Fink D, Mata M. Microarray analysis suggests the involvement of proteasomes, lysosomes, and matrix metalloproteinases in the response of motor neurons to root avulsion. Eur J Neurosci. 2002; 16:1409–16.HuJFinkDMataMMicroarray analysis suggests the involvement of proteasomes, lysosomes, and matrix metalloproteinases in the response of motor neurons to root avulsion20021614091610.1046/j.1460-9568.2002.02218.xSearch in Google Scholar
Yang Y, Xie Y, Chai H, Fan M, Liu S, Liu H, et al. Microarray analysis of gene expression patterns in adult spinal motoneurons after different types of axonal injuries. Brain Res. 2006; 1075:1–12.YangYXieYChaiHFanMLiuSLiuHMicroarray analysis of gene expression patterns in adult spinal motoneurons after different types of axonal injuries2006107511210.1016/j.brainres.2005.12.060Search in Google Scholar
Agthong S, Kaewsema A, Tanomsridejchai N, Chentanez V. Activation of MAPK ERK in peripheral nerve after injury. BMC Neurosci. 2006; 7:45.AgthongSKaewsemaATanomsridejchaiNChentanezVActivation of MAPK ERK in peripheral nerve after injury200674510.1186/1471-2202-7-45Search in Google Scholar
Bramhall S, Noack N, Wu M, Loewenberg JR. A simple colorimetric method for determination of protein. Anal Biochem. 1969; 31:146–8.BramhallSNoackNWuMLoewenbergJRA simple colorimetric method for determination of protein196931146810.1016/0003-2697(69)90251-6Search in Google Scholar
Berliocchi L, Russo R, Maiaru M, Levato A, Bagetta G, Corasaniti MT. Autophagy impairment in a mouse model of neuropathic pain. Mol Pain. 2011; 7:83.BerliocchiLRussoRMaiaruMLevatoABagettaGCorasanitiMTAutophagy impairment in a mouse model of neuropathic pain201178310.1186/1744-8069-7-83Search in Google Scholar
Zhang E, Yi MH, Ko Y, Kim HW, Seo JH, Lee YH, et al. Expression of LC3 and Beclin 1 in the spinal dorsal horn following spinal nerve ligation-induced neuropathic pain. Brain Res. 2013; 1519:31–9.ZhangEYiMHKoYKimHWSeoJHLeeYHExpression of LC3 and Beclin 1 in the spinal dorsal horn following spinal nerve ligation-induced neuropathic pain2013151931910.1016/j.brainres.2013.04.055Search in Google Scholar
Maday S. Mechanisms of neuronal homeostasis: Autophagy in the axon. Brain Res. 2016; 1649:143–50.MadaySMechanisms of neuronal homeostasis: Autophagy in the axon201616491435010.1016/j.brainres.2016.03.047Search in Google Scholar
Jang SY, Shin YK, Park SY, Park JY, Lee HJ, Yoo YH, et al. Autophagic myelin destruction by Schwann cells during Wallerian degeneration and segmental demyelination. Glia. 2016; 64:730–42.JangSYShinYKParkSYParkJYLeeHJYooYHAutophagic myelin destruction by Schwann cells during Wallerian degeneration and segmental demyelination2016647304210.1002/glia.22957Search in Google Scholar