Parkin Regulation and Neurodegenerative Disorders

Parkin is a unique, multifunctional ubiquitin ligase whose various roles in the cell, particularly in neurons, are widely thought to be protective. The pivotal role that Parkin plays in maintaining neuronal survival is underscored by our current recognition that Parkin dysfunction represents not onl...

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Published inFrontiers in aging neuroscience Vol. 7; p. 248
Main Authors Zhang, Cheng-Wu, Hang, Liting, Yao, Tso-Pang, Lim, Kah-Leong
Format Journal Article
LanguageEnglish
Published Switzerland Frontiers Research Foundation 12.01.2016
Frontiers Media S.A
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Abstract Parkin is a unique, multifunctional ubiquitin ligase whose various roles in the cell, particularly in neurons, are widely thought to be protective. The pivotal role that Parkin plays in maintaining neuronal survival is underscored by our current recognition that Parkin dysfunction represents not only a predominant cause of familial parkinsonism but also a formal risk factor for the more common, sporadic form of Parkinson's disease (PD). Accordingly, keen research on Parkin over the past decade has led to an explosion of knowledge regarding its physiological roles and its relevance to PD. However, our understanding of Parkin is far from being complete. Indeed, surprises emerge from time to time that compel us to constantly update the paradigm of Parkin function. For example, we now know that Parkin's function is not confined to mere housekeeping protein quality control (QC) roles but also includes mitochondrial homeostasis and stress-related signaling. Furthermore, emerging evidence also suggest a role for Parkin in several other major neurodegenerative diseases including Alzheimer's disease (AD) and Amyotrophic Lateral Sclerosis (ALS). Yet, it remains truly amazing to note that a single enzyme could serve such multitude of functions and cellular roles. Clearly, its activity has to be tightly regulated. In this review, we shall discuss this and how dysregulated Parkin function may precipitate neuronal demise in various neurodegenerative disorders.
AbstractList Parkin is a unique, multifunctional ubiquitin ligase whose various roles in the cell, particularly in neurons, are widely thought to be protective. The pivotal role that Parkin plays in maintaining neuronal survival is underscored by our current recognition that Parkin dysfunction represents not only a predominant cause of familial parkinsonism but also a formal risk factor for the more common, sporadic form of Parkinson’s disease. Accordingly, keen research on Parkin over the past decade has led to an explosion of knowledge regarding its physiological roles and its relevance to PD. However, our understanding of Parkin is far from being complete. Indeed, surprises emerge from time to time that compel us to constantly update the paradigm of Parkin function. For example, we now know that Parkin’s function is not confined to mere housekeeping protein quality control roles but also includes mitochondrial homeostasis and stress-related signalling. Furthermore, emerging evidence also suggest a role for Parkin in several other major neurodegenerative diseases including Alzheimer’s disease and Amyotrophic Lateral Sclerosis. Yet, it remains truly amazing to note that a single enzyme could serve such multitude of functions and cellular roles. Clearly, its activity has to be tightly regulated. In this review, we shall discuss this and how dysregulated Parkin function may precipitate neuronal demise in various neurodegenerative disorders.
Parkin is a unique, multifunctional ubiquitin ligase whose various roles in the cell, particularly in neurons, are widely thought to be protective. The pivotal role that Parkin plays in maintaining neuronal survival is underscored by our current recognition that Parkin dysfunction represents not only a predominant cause of familial parkinsonism but also a formal risk factor for the more common, sporadic form of Parkinson’s disease (PD). Accordingly, keen research on Parkin over the past decade has led to an explosion of knowledge regarding its physiological roles and its relevance to PD. However, our understanding of Parkin is far from being complete. Indeed, surprises emerge from time to time that compel us to constantly update the paradigm of Parkin function. For example, we now know that Parkin’s function is not confined to mere housekeeping protein quality control (QC) roles but also includes mitochondrial homeostasis and stress-related signaling. Furthermore, emerging evidence also suggest a role for Parkin in several other major neurodegenerative diseases including Alzheimer’s disease (AD) and Amyotrophic Lateral Sclerosis (ALS). Yet, it remains truly amazing to note that a single enzyme could serve such multitude of functions and cellular roles. Clearly, its activity has to be tightly regulated. In this review, we shall discuss this and how dysregulated Parkin function may precipitate neuronal demise in various neurodegenerative disorders.
Author Zhang, Cheng-Wu
Lim, Kah-Leong
Yao, Tso-Pang
Hang, Liting
AuthorAffiliation 2 Institute of Advanced Materials, Nanjing Tech University Nanjing, People’s Republic of China
5 Duke-NUS Graduate Medical School, National University of Singapore Singapore, Singapore
3 Department of Physiology, National University of Singapore Singapore, Singapore
4 Departments of Pharmacology and Cancer Biology, Duke University Medical Center Durham, NC, USA
1 Neurodegeneration Research Laboratory, National Neuroscience Institute Singapore, Singapore
AuthorAffiliation_xml – name: 3 Department of Physiology, National University of Singapore Singapore, Singapore
– name: 2 Institute of Advanced Materials, Nanjing Tech University Nanjing, People’s Republic of China
– name: 4 Departments of Pharmacology and Cancer Biology, Duke University Medical Center Durham, NC, USA
– name: 5 Duke-NUS Graduate Medical School, National University of Singapore Singapore, Singapore
– name: 1 Neurodegeneration Research Laboratory, National Neuroscience Institute Singapore, Singapore
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  organization: Neurodegeneration Research Laboratory, National Neuroscience InstituteSingapore, Singapore; Institute of Advanced Materials, Nanjing Tech UniversityNanjing, People's Republic of China
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  givenname: Liting
  surname: Hang
  fullname: Hang, Liting
  organization: Department of Physiology, National University of Singapore Singapore, Singapore
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  surname: Yao
  fullname: Yao, Tso-Pang
  organization: Departments of Pharmacology and Cancer Biology, Duke University Medical Center Durham, NC, USA
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  givenname: Kah-Leong
  surname: Lim
  fullname: Lim, Kah-Leong
  organization: Neurodegeneration Research Laboratory, National Neuroscience InstituteSingapore, Singapore; Institute of Advanced Materials, Nanjing Tech UniversityNanjing, People's Republic of China; Department of Physiology, National University of SingaporeSingapore, Singapore; Duke-NUS Graduate Medical School, National University of SingaporeSingapore, Singapore
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Cites_doi 10.15252/embj.201592237
10.1212/wnl.56.4.555
10.1073/pnas.0931262100
10.1073/pnas.1006083107
10.1038/nrm3028
10.1074/jbc.m504994200
10.1111/j.1365-2362.2010.02354.x
10.1016/j.molcel.2015.08.016
10.1091/mbc.e03-02-0078
10.1016/j.bbr.2008.01.017
10.1074/jbc.M707494200
10.1038/ncb2012
10.1074/jbc.m512649200
10.1111/j.1582-4934.2008.00443.x
10.1523/jneurosci.4474-04.2005
10.1080/15548627.2015.1034408
10.1074/jbc.m407724200
10.1093/hmg/ddl131
10.1093/hmg/ddi413
10.1159/000354307
10.1093/hmg/ddt501
10.1074/jbc.m111.299990
10.1016/j.molcel.2013.08.016
10.1016/j.cub.2011.11.057
10.1093/hmg/ddp258
10.1073/pnas.0500346102
10.1093/hmg/ddr091
10.1074/jbc.m806245200
10.1038/nature13418
10.1111/jnc.12630
10.1074/jbc.m212235200
10.1038/nature04779
10.1016/s0197-4580(02)00065-9
10.1196/annals.1427.006
10.1038/nbt849
10.1091/mbc.e05-11-1027
10.1074/jbc.m510393200
10.1093/hmg/ddr048
10.1038/nn.3230
10.1038/srep01002
10.1523/JNEUROSCI.23-08-03316.2003
10.1093/hmg/ddh012
10.1517/14728222.2013.827173
10.15252/embj.201592337
10.1016/j.yexcr.2007.04.016
10.1111/j.1471-4159.2007.04911.x
10.1038/sj.emboj.7600774
10.1074/jbc.m609466200
10.1016/j.celrep.2014.10.046
10.1371/journal.pone.0010054
10.15252/embr.201540514
10.1111/j.1471-4159.2007.04762.x
10.1002/jnr.22178
10.1038/nature14879
10.1016/j.neurobiolaging.2005.07.023
10.1096/fj.04-1493fje
10.1093/hmg/ddm320
10.1158/0008-5472.CAN-11-3060
10.1126/science.1237908
10.1074/jbc.M110.101469
10.1074/jbc.m110.108241
10.1093/brain/awg136
10.1074/jbc.M113.515940
10.1083/jcb.201401070
10.1016/j.neuron.2014.12.007
10.1093/hmg/ddu244
10.1073/pnas.0913485107
10.1038/77060
10.1073/pnas.240347797
10.1074/jbc.m409282200
10.1038/emboj.2013.125
10.1074/jbc.m306889200
10.1073/pnas.0737556100
10.1111/j.1471-4159.2005.03023.x
10.1074/jbc.c000447200
10.1016/j.neuron.2004.11.026
10.1038/nm1314
10.1016/s0169-328x(03)00318-8
10.1038/ncomms2016
10.1038/srep04874
10.1016/s0962-8924(00)01852-3
10.1016/j.febslet.2008.12.055
10.1098/rsob.120080
10.1038/ncomms2623
10.1371/journal.pone.0073235
10.1074/jbc.m413591200
10.1038/nature09966
10.1038/nm1001-1144
10.4161/auto.5444
10.1093/hmg/ddi292
10.1111/j.1471-4159.2005.03442.x
10.1093/brain/awh572
10.15252/embj.201489729
10.1083/jcb.201402104
10.1038/cddis.2014.581
10.1371/journal.pbio.1000298
10.1074/jbc.c600041200
10.1056/NEJM200005253422103
10.1093/hmg/ddn210
10.1523/jneurosci.2172-05.2005
10.1371/journal.pone.0052830
10.1002/ana.74.abs
10.3389/fneur.2013.00033
10.1016/j.brainres.2009.05.039
10.1016/j.cell.2011.10.018
10.1371/journal.pone.0019720
10.4161/auto.6.8.13426
10.1128/MCB.00535-13
10.1016/j.nbd.2003.08.011
10.1074/jbc.m306769200
10.1002/mds.20232
10.1074/jbc.M114.634063
10.1038/nature04788
10.1038/42166
10.3233/JAD-2002-4506
10.1074/jbc.M110.144238
10.1111/j.1471-4159.2008.05261.x
10.1073/pnas.1221132110
10.1073/pnas.1405752111
10.1093/hmg/ddg328
10.1016/s0896-6273(03)00084-9
10.1126/science.1060627
10.1038/nature14893
10.1083/jcb.200809125
10.1038/ncomms2982
10.1083/jcb.200611128
10.1093/hmg/ddn407
10.15252/embj.201488104
10.1038/33416
10.1093/hmg/ddh089
10.1074/jbc.m408955200
10.1038/ncb1441
10.1002/emmm.201302771
10.1038/emboj.2011.204
10.1016/j.cub.2007.12.038
10.1016/j.molcel.2015.08.011
10.1073/pnas.0911187107
10.1016/j.cell.2011.02.010
10.1038/nature08971
10.1016/j.expneurol.2006.09.009
10.1083/jcb.200910140
10.1074/jbc.m608243200
10.1101/gad.262758.115
10.1523/jneurosci.5537-06.2007
10.1093/hmg/ddg159
10.1038/nature13392
10.1083/jcb.201001039
10.1074/jbc.M110.209338
10.1093/hmg/ddv059
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Copyright © 2016 Zhang, Hang, Yao and Lim. 2016 Zhang, Hang, Yao and Lim
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Keywords proteasome
mitophagy
autophagy
mitochondria
protein misfolding
neurodegeneration
Parkinson’s disease
ubiquitin
Language English
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PublicationTitle Frontiers in aging neuroscience
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References 19966284 - Proc Natl Acad Sci U S A. 2010 Jan 5;107(1):378-83
21179058 - Nat Rev Mol Cell Biol. 2011 Jan;12(1):9-14
23661642 - Science. 2013 Jun 21;340(6139):1451-5
23256036 - Sci Rep. 2012;2:1002
12498954 - Neurobiol Aging. 2003 Mar-Apr;24(2):197-211
11431533 - Science. 2001 Jul 13;293(5528):263-9
9560156 - Nature. 1998 Apr 9;392(6676):605-8
26161729 - Nature. 2015 Aug 20;524(7565):370-4
11078524 - Proc Natl Acad Sci U S A. 2000 Nov 21;97(24):13354-9
20457763 - J Cell Biol. 2010 May 17;189(4):671-9
26254304 - EMBO J. 2015 Oct 14;34(20):2506-21
19464273 - Brain Res. 2009 Jul 24;1281:91-100
12719539 - Proc Natl Acad Sci U S A. 2003 May 13;100(10 ):5956-61
25611507 - Neuron. 2015 Jan 21;85(2):257-73
25456142 - Cell Rep. 2014 Nov 20;9(4):1538-53
20823226 - Proc Natl Acad Sci U S A. 2010 Sep 21;107(38):16691-6
22431710 - Cancer Res. 2012 May 15;72 (10 ):2543-53
21694720 - EMBO J. 2011 Jun 21;30(14 ):2853-67
18362144 - J Biol Chem. 2008 May 16;283(20):13771-9
12783850 - Hum Mol Genet. 2003 Jun 15;12 (12 ):1427-37
12972409 - J Biol Chem. 2003 Nov 28;278(48):48120-8
10973942 - J Biol Chem. 2000 Nov 17;275(46):35661-4
23930597 - Expert Opin Ther Targets. 2013 Oct;17 (10 ):1133-44
14976155 - Hum Mol Genet. 2004 Apr 1;13 Spec No 1:R127-33
23770887 - Nat Commun. 2013;4:1982
16714300 - Hum Mol Genet. 2006 Jul 1;15(13):2059-75
24105468 - Hum Mol Genet. 2014 Feb 15;23 (4):1056-72
10888878 - Nat Genet. 2000 Jul;25(3):302-5
20194754 - Proc Natl Acad Sci U S A. 2010 Mar 16;107(11):5018-23
20404107 - J Cell Biol. 2010 Apr 19;189(2):211-21
21532592 - Nature. 2011 Jun 2;474(7349):105-8
15947065 - Brain. 2005 Oct;128(Pt 10):2281-90
16517603 - J Biol Chem. 2006 May 5;281(18):12809-16
15603737 - Neuron. 2004 Dec 16;44(6):931-45
25995186 - Genes Dev. 2015 May 15;29(10 ):989-99
24515116 - J Biol Chem. 2014 Apr 11;289(15):10769-84
24029689 - Neurodegener Dis. 2014;13(2-3):69-71
15718234 - J Biol Chem. 2005 Apr 29;280(17 ):16619-24
20428114 - Nature. 2010 May 13;465(7295):223-6
15132984 - FASEB J. 2004 Jul;18(10 ):1135-7
24298989 - J Neurochem. 2014 Apr;129(2):350-61
16135753 - J Neurosci. 2005 Aug 31;25(35):7968-78
19074146 - J Biol Chem. 2009 Feb 6;284(6):4009-17
23737459 - EMBO Mol Med. 2013 Aug;5(8):1247-62
15728840 - J Neurosci. 2005 Feb 23;25(8):2002-9
24784582 - Nature. 2014 Jun 5;510(7503):162-6
12628165 - Neuron. 2003 Mar 6;37(5):735-49
16227987 - Nat Med. 2005 Nov;11(11):1214-21
22226745 - Curr Biol. 2012 Jan 24;22(2):135-41
18671761 - J Cell Mol Med. 2009 Sep;13(9B):3061-8
24035499 - Mol Cell. 2013 Sep 26;51(6):819-28
25294927 - Proc Natl Acad Sci U S A. 2014 Oct 21;111(42):E4439-48
17512523 - Exp Cell Res. 2007 Aug 1;313(13):2858-74
21625422 - PLoS One. 2011;6(5):e19720
11261512 - Ann Neurol. 2001 Mar;49(3):367-76
14519684 - Hum Mol Genet. 2003 Nov 15;12 (22):2957-65
15632191 - J Biol Chem. 2005 Mar 11;280(10 ):9425-30
23300790 - PLoS One. 2012;7(12):e52830
9278044 - Nature. 1997 Aug 28;388(6645):839-40
14678753 - Neurobiol Dis. 2003 Dec;14 (3):357-64
17981811 - Hum Mol Genet. 2008 Feb 1;17 (3):431-9
25915564 - Autophagy. 2015 Apr 3;11(4):595-606
16672220 - J Biol Chem. 2006 Jun 16;281(24):16193-6
22761419 - J Biol Chem. 2012 Aug 17;287(34):28576-85
20098416 - Nat Cell Biol. 2010 Feb;12 (2):119-31
12446971 - J Alzheimers Dis. 2002 Oct;4(5):399-404
22910362 - Nat Commun. 2012;3:1016
25861987 - J Biol Chem. 2015 May 29;290(22):13862-74
17327227 - J Biol Chem. 2007 Apr 27;282(17 ):12842-50
17883392 - J Neurochem. 2007 Dec;103(6):2354-68
17314283 - J Neurosci. 2007 Feb 21;27(8):1868-78
21376232 - Cell. 2011 Mar 4;144(5):689-702
18640988 - Hum Mol Genet. 2008 Oct 15;17 (20):3128-43
16096643 - EMBO J. 2006 Jan 11;25(1):211-21
23535647 - Nat Commun. 2013;4:1626
20735469 - Eur J Clin Invest. 2010 Nov;40(11):1048-60
12764050 - Brain. 2003 Jun;126(Pt 6):1271-8
16672981 - Nature. 2006 Jun 29;441(7097):1162-6
14645198 - Hum Mol Genet. 2004 Jan 1;13(1):117-35
11121744 - Trends Cell Biol. 2000 Dec;10(12):524-30
25611391 - Cell Death Dis. 2015 Jan 22;6:e1617
16672980 - Nature. 2006 Jun 29;441(7097):1157-61
15816865 - J Neurochem. 2005 Apr;93(2):422-31
20890124 - Autophagy. 2010 Nov;6(8):1090-106
16278233 - Hum Mol Genet. 2005 Dec 15;14 (24):3885-97
24023840 - PLoS One. 2013 Sep 02;8(9):e73235
24751536 - J Cell Biol. 2014 Apr 28;205(2):143-53
18346797 - Behav Brain Res. 2008 Jun 3;189(2):350-6
15557340 - J Biol Chem. 2005 Feb 4;280(5):3390-9
17553932 - Mol Biol Cell. 2007 Aug;18(8):3105-18
19029340 - J Cell Biol. 2008 Dec 1;183(5):795-803
20889974 - J Biol Chem. 2010 Dec 3;285(49):38214-23
12642658 - Proc Natl Acad Sci U S A. 2003 Apr 1;100(7):4078-83
22078885 - Cell. 2011 Nov 11;147(4):893-906
18207745 - Curr Biol. 2008 Jan 22;18(2):102-8
23509287 - Proc Natl Acad Sci U S A. 2013 Apr 16;110(16):6400-5
25107473 - EMBO J. 2014 Oct 1;33(19):2142-56
16339143 - J Biol Chem. 2006 Feb 10;281(6):3204-9
12972428 - J Biol Chem. 2003 Nov 21;278(47):47199-208
16862145 - Nat Cell Biol. 2006 Aug;8(8):834-42
19610108 - J Neurosci Res. 2010 Jan;88(1):167-78
21292769 - J Biol Chem. 2011 Apr 1;286(13):11649-58
19050041 - Hum Mol Genet. 2009 Mar 1;18(5):809-23
26365381 - Mol Cell. 2015 Oct 1;60(1):7-20
16002472 - Proc Natl Acad Sci U S A. 2005 Jul 19;102(29):10345-50
26266977 - Nature. 2015 Aug 20;524(7565):309-14
24852371 - Hum Mol Genet. 2014 Oct 1;23 (19):5227-42
11222808 - Neurology. 2001 Feb 27;56(4):555-7
12716939 - J Neurosci. 2003 Apr 15;23 (8):3316-24
24786396 - Sci Rep. 2014 May 02;4:4874
12937272 - Mol Biol Cell. 2003 Nov;14 (11):4541-56
22724072 - Open Biol. 2012 May;2(5):120080
23023293 - Nat Neurosci. 2012 Nov;15(11):1488-97
17097639 - Exp Neurol. 2007 Feb;203(2):531-41
17329252 - J Biol Chem. 2007 Apr 20;282(16):12310-8
17623040 - J Neurochem. 2007 Oct;103(1):98-114
16332688 - J Biol Chem. 2006 Feb 10;281(6):3595-603
21378096 - Hum Mol Genet. 2011 Jun 1;20(11):2091-102
15390070 - Mov Disord. 2004 Dec;19(12 ):1445-9
21296869 - Hum Mol Genet. 2011 May 1;20(9):1726-37
16150055 - J Neurochem. 2005 Dec;95(5):1259-76
20630868 - J Biol Chem. 2010 Sep 17;285(38):29231-8
20383334 - PLoS One. 2010 Apr 07;5(4):e10054
16213628 - Neurobiol Aging. 2006 Apr;27(4):524-9
26254305 - EMBO J. 2015 Oct 14;34(20):2492-505
26162776 - EMBO Rep. 2015 Sep;16(9):1114-30
25687137 - Hum Mol Genet. 2015 Jun 1;24(11):3058-81
16049031 - Hum Mol Genet. 2005 Sep 1;14 (17 ):2571-86
24896179 - Nature. 2014 Jun 19;510(7505):370-5
23727886 - EMBO J. 2013 Jul 31;32(15):2099-112
20126261 - PLoS Biol. 2010 Jan 26;8(1):e1000298
12872131 - Nat Biotechnol. 2003 Aug;21(8):921-6
19483198 - Hum Mol Genet. 2009 Sep 1;18(17 ):3206-16
17846173 - J Cell Biol. 2007 Sep 10;178(6):1025-38
23858059 - Mol Cell Biol. 2013 Sep;33(18):3627-43
23580245 - Front Neurol. 2013 Apr 08;4:33
19146857 - FEBS Lett. 2009 Feb 4;583(3):521-5
25216678 - EMBO J. 2014 Nov 3;33(21):2473-91
15492001 - J Biol Chem. 2004 Dec 24;279(52):54380-6
11590439 - Nat Med. 2001 Oct;7(10 ):1144-50
25154397 - J Cell Biol. 2014 Sep 1;206(5):655-70
26387737 - Mol Cell. 2015 Oct 1;60(1):21-34
19076454 - Ann N Y Acad Sci. 2008 Dec;1147:321-34
18248624 - J Neurochem. 2008 Jun;105(5):1806-19
14559152 - Brain Res Mol Brain Res. 2003 Oct 7;117(2):179-89
12676955 - J Biol Chem. 2003 Jun 13;278(24):22044-55
21454557 - J Biol Chem. 2011 Jun 3;286(22):19630-40
10824074 - N Engl J Med. 2000 May 25;342(21):1560-7
Lee (B64) 2015; 60
Schlehe (B107) 2008; 283
Lazarou (B62) 2015; 524
Greene (B32) 2003; 100
Khalil (B48) 2015; 6
Ko (B51) 2006; 281
Ren (B94) 2009; 284
Neuspiel (B83) 2008; 18
Vives-Bauza (B128) 2010; 107
Cookson (B18) 2003; 12
Dawson (B22) 2014; 13
Carroll (B9) 2014; 9
Rubio de la Torre (B101) 2009; 18
Avraham (B3) 2007; 282
Henn (B37) 2007; 27
Vandiver (B126) 2013; 4
Rosen (B99) 2010; 88
Kumar (B58) 2015; 34
Youle (B145) 2011; 12
Corsetti (B20) 2015; 24
Wong (B141) 2014; 111
Lim (B67) 2005; 25
Yoshii (B144) 2011; 286
Lee (B63) 2010; 189
Park (B87) 2006; 441
Peng (B89) 2003; 21
Chung (B210) 2001; 7
Narendra (B79) 2010a; 8
Joch (B44) 2007; 18
Kondapalli (B54) 2012; 2
Wenzel (B138) 2011; 474
Hebron (B36) 2014; 129
Zhang (B146) 2000; 97
Soubannier (B113) 2012b; 7
Stribl (B117) 2014; 289
Norris (B84) 2015; 290
Pickrell (B92) 2015; 85
Muqit (B77) 2004; 13
Moore (B76) 2008; 105
Lim (B65) 2013; 8
Ashrafi (B2) 2014; 206
Tay (B121) 2010; 285
Soubannier (B112) 2012a; 22
Durcan (B25) 2015; 29
Kane (B46) 2014; 205
Periquet (B90) 2005; 95
Lücking (B71) 2000; 342
Sauvé (B105) 2015; 34
Yeo (B143) 2012; 72
Hao (B35) 2013; 51
Wang (B134) 2011b; 147
Yamamoto (B142) 2005; 280
Rosen (B100) 2006; 281
Imai (B42) 2000; 275
Heo (B38) 2015; 60
Wang (B133) 2012; 287
Tan (B119) 2008a; 4
Khandelwal (B49) 2011; 20
LaVoie (B61) 2005; 11
Sánchez (B103) 2002; 4
Karuppagounder (B47) 2014; 4
Rodríguez-Navarro (B97) 2007; 103
Ren (B95) 2003; 23
Rubio (B102) 2009; 1281
Mata (B73) 2004; 13
Winklhofer (B139) 2003; 278
Shimura (B109) 2000; 25
Braak (B5) 2003; 24
Ko (B53) 2005; 25
Fallon (B28) 2006; 8
Wang (B131) 2005b; 93
Cesari (B10) 2003; 100
Fukae (B30) 2009; 583
Lim (B69) 2007; 313
Nemes (B82) 2004; 18
Ziviani (B148) 2010; 107
Maruyama (B72) 2010; 465
Sato (B104) 2006; 25
Olzmann (B86) 2007; 178
Zhong (B147) 2005; 280
Burns (B8) 2009; 18
Navarro (B81) 2008; 189
Scarpulla (B106) 2008; 1147
Wauer (B137) 2015; 524
LaVoie (B60) 2007; 103
Geisler (B31) 2010; 12
Cha (B11) 2005; 102
Shiba-Fukushima (B108) 2012; 2
Choi (B16) 2003; 117
Poole (B93) 2010; 5
van de Warrenburg (B125) 2001; 56
Wang (B132) 2011a; 286
Okatsu (B85) 2012; 3
Sriram (B115) 2005; 14
Wauer (B136) 2013; 32
Ardley (B1) 2003; 14
Lagier-Tourenne (B59) 2012; 15
Chaugule (B13) 2011; 30
Doss-Pepe (B24) 2005; 280
Kopito (B55) 2000; 10
Gu (B33) 2003; 14
Walter (B129) 2004; 19
Fiesel (B29) 2015; 16
Vincow (B127) 2013; 110
Dehvari (B23) 2009; 13
Matsuda (B74) 2006; 281
Periquet (B91) 2003; 126
Bingol (B4) 2014; 510
Huynh (B41) 2007; 203
Lonskaya (B70) 2013; 5
Matsuda (B75) 2010; 189
Hilker (B39) 2001; 49
Lim (B66) 2013; 4
Rodríguez-Navarro (B98) 2008; 17
Tsai (B123) 2003; 278
Narendra (B78) 2008; 183
Burbulla (B7) 2010; 40
Jiang (B43) 2004; 279
Cornelissen (B19) 2014; 23
Wang (B130) 2005a; 14
Wong (B140) 2007; 282
Kitada (B50) 1998; 392
Shin (B111) 2011; 144
Trempe (B122) 2013; 340
Sugiura (B118) 2014; 33
Narendra (B80) 2010b; 6
Um (B124) 2006; 281
Lim (B68) 2006; 27
Shimura (B110) 2001; 293
Kalia (B45) 2004; 44
Ekholm-Reed (B27) 2013; 33
Hampe (B34) 2006; 15
Corti (B21) 2003; 12
Kubo (B57) 2013; 17
Durcan (B26) 2014; 33
Riley (B96) 2013; 4
Staropoli (B116) 2003; 37
Clark (B17) 2006; 441
Hong (B40) 2014; 23
Wang (B135) 2015; 11
Chen (B14) 2010; 285
Chew (B15) 2011; 6
Buhmann (B6) 2005; 128
Chan (B12) 2011; 20
Tan (B120) 2008b; 17
Pawlyk (B88) 2003; 278
Koyano (B56) 2014; 510
Ko (B52) 2010; 107
Spillantini (B114) 1997; 388
References_xml – volume: 34
  start-page: 2492
  year: 2015
  ident: B105
  article-title: A Ubl/ubiquitin switch in the activation of Parkin
  publication-title: EMBO J.
  doi: 10.15252/embj.201592237
  contributor:
    fullname: Sauvé
– volume: 56
  start-page: 555
  year: 2001
  ident: B125
  article-title: Clinical and pathologic abnormalities in a family with parkinsonism and parkin gene mutations
  publication-title: Neurology
  doi: 10.1212/wnl.56.4.555
  contributor:
    fullname: van de Warrenburg
– volume: 100
  start-page: 5956
  year: 2003
  ident: B10
  article-title: Parkin, a gene implicated in autosomal recessive juvenile parkinsonism, is a candidate tumor suppressor gene on chromosome 6q25-q27
  publication-title: Proc. Natl. Acad. Sci. U S A
  doi: 10.1073/pnas.0931262100
  contributor:
    fullname: Cesari
– volume: 107
  start-page: 16691
  year: 2010
  ident: B52
  article-title: Phosphorylation by the c-Abl protein tyrosine kinase inhibits parkin’s ubiquitination and protective function
  publication-title: Proc. Natl. Acad. Sci. U S A
  doi: 10.1073/pnas.1006083107
  contributor:
    fullname: Ko
– volume: 12
  start-page: 9
  year: 2011
  ident: B145
  article-title: Mechanisms of mitophagy
  publication-title: Nat. Rev. Mol. Cell Biol.
  doi: 10.1038/nrm3028
  contributor:
    fullname: Youle
– volume: 281
  start-page: 3595
  year: 2006
  ident: B124
  article-title: Parkin ubiquitinates and promotes the degradation of RanBP2
  publication-title: J. Biol. Chem.
  doi: 10.1074/jbc.m504994200
  contributor:
    fullname: Um
– volume: 40
  start-page: 1048
  year: 2010
  ident: B7
  article-title: Balance is the challenge—the impact of mitochondrial dynamics in Parkinson’s disease
  publication-title: Eur. J. Clin. Invest.
  doi: 10.1111/j.1365-2362.2010.02354.x
  contributor:
    fullname: Burbulla
– volume: 60
  start-page: 7
  year: 2015
  ident: B38
  article-title: The PINK1-PARKIN mitochondrial ubiquitylation pathway drives a program of OPTN/NDP52 recruitment and TBK1 activation to promote mitophagy
  publication-title: Mol. Cell
  doi: 10.1016/j.molcel.2015.08.016
  contributor:
    fullname: Heo
– volume: 14
  start-page: 4541
  year: 2003
  ident: B1
  article-title: Inhibition of proteasomal activity causes inclusion formation in neuronal and non-neuronal cells overexpressing Parkin
  publication-title: Mol. Biol. Cell
  doi: 10.1091/mbc.e03-02-0078
  contributor:
    fullname: Ardley
– volume: 189
  start-page: 350
  year: 2008
  ident: B81
  article-title: Memory and exploratory impairment in mice that lack the Park-2 gene and that over-express the human FTDP-17 mutant Tau
  publication-title: Behav. Brain Res.
  doi: 10.1016/j.bbr.2008.01.017
  contributor:
    fullname: Navarro
– volume: 283
  start-page: 13771
  year: 2008
  ident: B107
  article-title: Aberrant folding of pathogenic Parkin mutants: aggregation versus degradation
  publication-title: J. Biol. Chem.
  doi: 10.1074/jbc.M707494200
  contributor:
    fullname: Schlehe
– volume: 12
  start-page: 119
  year: 2010
  ident: B31
  article-title: PINK1/Parkin-mediated mitophagy is dependent on VDAC1 and p62/SQSTM1
  publication-title: Nat. Cell Biol.
  doi: 10.1038/ncb2012
  contributor:
    fullname: Geisler
– volume: 281
  start-page: 12809
  year: 2006
  ident: B100
  article-title: Parkin protects against mitochondrial toxins and beta-amyloid accumulation in skeletal muscle cells
  publication-title: J. Biol. Chem.
  doi: 10.1074/jbc.m512649200
  contributor:
    fullname: Rosen
– volume: 13
  start-page: 3061
  year: 2009
  ident: B23
  article-title: Parkin-mediated ubiquitination regulates phospholipase C-γ1
  publication-title: J. Cell. Mol. Med.
  doi: 10.1111/j.1582-4934.2008.00443.x
  contributor:
    fullname: Dehvari
– volume: 25
  start-page: 2002
  year: 2005
  ident: B67
  article-title: Parkin mediates nonclassical, proteasomal-independent ubiquitination of synphilin-1: implications for Lewy body formation
  publication-title: J. Neurosci.
  doi: 10.1523/jneurosci.4474-04.2005
  contributor:
    fullname: Lim
– volume: 11
  start-page: 595
  year: 2015
  ident: B135
  article-title: Deubiquitinating enzymes regulate PARK2-mediated mitophagy
  publication-title: Autophagy
  doi: 10.1080/15548627.2015.1034408
  contributor:
    fullname: Wang
– volume: 280
  start-page: 3390
  year: 2005
  ident: B142
  article-title: Parkin phosphorylation and modulation of its E3 ubiquitin ligase activity
  publication-title: J. Biol. Chem.
  doi: 10.1074/jbc.m407724200
  contributor:
    fullname: Yamamoto
– volume: 15
  start-page: 2059
  year: 2006
  ident: B34
  article-title: Biochemical analysis of Parkinson’s disease-causing variants of Parkin, an E3 ubiquitin-protein ligase with monoubiquitylation capacity
  publication-title: Hum. Mol. Genet.
  doi: 10.1093/hmg/ddl131
  contributor:
    fullname: Hampe
– volume: 14
  start-page: 3885
  year: 2005a
  ident: B130
  article-title: Stress-induced alterations in parkin solubility promote parkin aggregation and compromise parkin’s protective function
  publication-title: Hum. Mol. Genet.
  doi: 10.1093/hmg/ddi413
  contributor:
    fullname: Wang
– volume: 13
  start-page: 69
  year: 2014
  ident: B22
  article-title: Parkin plays a role in sporadic Parkinson’s disease
  publication-title: Neurodegener. Dis.
  doi: 10.1159/000354307
  contributor:
    fullname: Dawson
– volume: 23
  start-page: 1056
  year: 2014
  ident: B40
  article-title: Parkin overexpression ameliorates hippocampal long-term potentiation and beta-amyloid load in an Alzheimer’s disease mouse model
  publication-title: Hum. Mol. Genet.
  doi: 10.1093/hmg/ddt501
  contributor:
    fullname: Hong
– volume: 287
  start-page: 28576
  year: 2012
  ident: B133
  article-title: Ataxin-3 regulates aggresome formation of copper-zinc superoxide dismutase (SOD1) by editing K63-linked polyubiquitin chains
  publication-title: J. Biol. Chem.
  doi: 10.1074/jbc.m111.299990
  contributor:
    fullname: Wang
– volume: 51
  start-page: 819
  year: 2013
  ident: B35
  article-title: Proteasomes activate aggresome disassembly and clearance by producing unanchored ubiquitin chains
  publication-title: Mol. Cell
  doi: 10.1016/j.molcel.2013.08.016
  contributor:
    fullname: Hao
– volume: 22
  start-page: 135
  year: 2012a
  ident: B112
  article-title: A vesicular transport pathway shuttles cargo from mitochondria to lysosomes
  publication-title: Curr. Biol.
  doi: 10.1016/j.cub.2011.11.057
  contributor:
    fullname: Soubannier
– volume: 18
  start-page: 3206
  year: 2009
  ident: B8
  article-title: Parkin promotes intracellular Abet a1–42 clearance
  publication-title: Hum. Mol. Genet.
  doi: 10.1093/hmg/ddp258
  contributor:
    fullname: Burns
– volume: 102
  start-page: 10345
  year: 2005
  ident: B11
  article-title: Parkin negatively regulates JNK pathway in the dopaminergic neurons of Drosophila
  publication-title: Proc. Natl. Acad. Sci. U S A
  doi: 10.1073/pnas.0500346102
  contributor:
    fullname: Cha
– volume: 20
  start-page: 2091
  year: 2011
  ident: B49
  article-title: Parkin mediates beclin-dependent autophagic clearance of defective mitochondria and ubiquitinated Abeta in AD models
  publication-title: Hum. Mol. Genet.
  doi: 10.1093/hmg/ddr091
  contributor:
    fullname: Khandelwal
– volume: 284
  start-page: 4009
  year: 2009
  ident: B94
  article-title: Parkin protects dopaminergic neurons against microtubule-depolymerizing toxins by attenuating microtubule-associated protein kinase activation
  publication-title: J. Biol. Chem.
  doi: 10.1074/jbc.m806245200
  contributor:
    fullname: Ren
– volume: 510
  start-page: 370
  year: 2014
  ident: B4
  article-title: The mitochondrial deubiquitinase USP30 opposes parkin-mediated mitophagy
  publication-title: Nature
  doi: 10.1038/nature13418
  contributor:
    fullname: Bingol
– volume: 129
  start-page: 350
  year: 2014
  ident: B36
  article-title: Parkin reverses TDP-43-induced cell death and failure of amino acid homeostasis
  publication-title: J. Neurochem.
  doi: 10.1111/jnc.12630
  contributor:
    fullname: Hebron
– volume: 278
  start-page: 22044
  year: 2003
  ident: B123
  article-title: Parkin facilitates the elimination of expanded polyglutamine proteins and leads to preservation of proteasome function
  publication-title: J. Biol. Chem.
  doi: 10.1074/jbc.m212235200
  contributor:
    fullname: Tsai
– volume: 441
  start-page: 1162
  year: 2006
  ident: B17
  article-title: Drosophila pink1 is required for mitochondrial function and interacts genetically with parkin
  publication-title: Nature
  doi: 10.1038/nature04779
  contributor:
    fullname: Clark
– volume: 24
  start-page: 197
  year: 2003
  ident: B5
  article-title: Staging of brain pathology related to sporadic Parkinson’s disease
  publication-title: Neurobiol. Aging
  doi: 10.1016/s0197-4580(02)00065-9
  contributor:
    fullname: Braak
– volume: 1147
  start-page: 321
  year: 2008
  ident: B106
  article-title: Nuclear control of respiratory chain expression by nuclear respiratory factors and PGC-1-related coactivator
  publication-title: Ann. N Y Acad. Sci.
  doi: 10.1196/annals.1427.006
  contributor:
    fullname: Scarpulla
– volume: 21
  start-page: 921
  year: 2003
  ident: B89
  article-title: A proteomics approach to understanding protein ubiquitination
  publication-title: Nat. Biotechnol.
  doi: 10.1038/nbt849
  contributor:
    fullname: Peng
– volume: 18
  start-page: 3105
  year: 2007
  ident: B44
  article-title: Parkin-mediated Monoubiquitination of the PDZ Protein PICK1 regulates the activity of acid-sensing ion channels
  publication-title: Mol. Biol. Cell
  doi: 10.1091/mbc.e05-11-1027
  contributor:
    fullname: Joch
– volume: 281
  start-page: 3204
  year: 2006
  ident: B74
  article-title: Diverse effects of pathogenic mutations of Parkin that catalyze multiple monoubiquitylation in vitro
  publication-title: J. Biol. Chem.
  doi: 10.1074/jbc.m510393200
  contributor:
    fullname: Matsuda
– volume: 20
  start-page: 1726
  year: 2011
  ident: B12
  article-title: Broad activation of the ubiquitin-proteasome system by Parkin is critical for mitophagy
  publication-title: Hum. Mol. Genet.
  doi: 10.1093/hmg/ddr048
  contributor:
    fullname: Chan
– volume: 15
  start-page: 1488
  year: 2012
  ident: B59
  article-title: Divergent roles of ALS-linked proteins FUS/TLS and TDP-43 intersect in processing long pre-mRNAs
  publication-title: Nat. Neurosci.
  doi: 10.1038/nn.3230
  contributor:
    fullname: Lagier-Tourenne
– volume: 2
  start-page: 1002
  year: 2012
  ident: B108
  article-title: PINK1-mediated phosphorylation of the Parkin ubiquitin-like domain primes mitochondrial translocation of Parkin and regulates mitophagy
  publication-title: Sci. Rep.
  doi: 10.1038/srep01002
  contributor:
    fullname: Shiba-Fukushima
– volume: 23
  start-page: 3316
  year: 2003
  ident: B95
  article-title: Parkin binds to alpha/beta tubulin and increases their ubiquitination and degradation
  publication-title: J. Neurosci.
  doi: 10.1523/JNEUROSCI.23-08-03316.2003
  contributor:
    fullname: Ren
– volume: 13
  start-page: 117
  year: 2004
  ident: B77
  article-title: Parkin is recruited into aggresomes in a stress-specific manner: over-expression of parkin reduces aggresome formation but can be dissociated from parkin’s effect on neuronal survival
  publication-title: Hum. Mol. Genet.
  doi: 10.1093/hmg/ddh012
  contributor:
    fullname: Muqit
– volume: 17
  start-page: 1133
  year: 2013
  ident: B57
  article-title: Can parkin be a target for future treatment of Parkinson’s disease?
  publication-title: Expert Opin. Ther Targets
  doi: 10.1517/14728222.2013.827173
  contributor:
    fullname: Kubo
– volume: 34
  start-page: 2506
  year: 2015
  ident: B58
  article-title: Disruption of the autoinhibited state primes the E3 ligase parkin for activation and catalysis
  publication-title: EMBO J.
  doi: 10.15252/embj.201592337
  contributor:
    fullname: Kumar
– volume: 313
  start-page: 2858
  year: 2007
  ident: B69
  article-title: Parkin interacts with LIM Kinase 1 and reduces its cofilin-phosphorylation activity via ubiquitination
  publication-title: Exp. Cell Res.
  doi: 10.1016/j.yexcr.2007.04.016
  contributor:
    fullname: Lim
– volume: 103
  start-page: 2354
  year: 2007
  ident: B60
  article-title: The effects of oxidative stress on parkin and other E3 ligases
  publication-title: J. Neurochem.
  doi: 10.1111/j.1471-4159.2007.04911.x
  contributor:
    fullname: LaVoie
– volume: 25
  start-page: 211
  year: 2006
  ident: B104
  article-title: 14–3-3eta is a novel regulator of parkin ubiquitin ligase
  publication-title: EMBO J.
  doi: 10.1038/sj.emboj.7600774
  contributor:
    fullname: Sato
– volume: 282
  start-page: 12310
  year: 2007
  ident: B140
  article-title: Relative sensitivity of parkin and other cysteine-containing enzymes to stress-induced solubility alterations
  publication-title: J. Biol. Chem.
  doi: 10.1074/jbc.m609466200
  contributor:
    fullname: Wong
– volume: 9
  start-page: 1538
  year: 2014
  ident: B9
  article-title: Parkin sensitizes toward apoptosis induced by mitochondrial depolarization through promoting degradation of Mcl-1
  publication-title: Cell Rep.
  doi: 10.1016/j.celrep.2014.10.046
  contributor:
    fullname: Carroll
– volume: 5
  start-page: e10054
  year: 2010
  ident: B93
  article-title: The mitochondrial fusion-promoting factor mitofusin is a substrate of the PINK1/parkin pathway
  publication-title: PLoS One
  doi: 10.1371/journal.pone.0010054
  contributor:
    fullname: Poole
– volume: 16
  start-page: 1114
  year: 2015
  ident: B29
  article-title: (Patho-)physiological relevance of PINK1-dependent ubiquitin phosphorylation
  publication-title: EMBO Rep.
  doi: 10.15252/embr.201540514
  contributor:
    fullname: Fiesel
– volume: 103
  start-page: 98
  year: 2007
  ident: B97
  article-title: Mortality, oxidative stress and tau accumulation during ageing in parkin null mice
  publication-title: J. Neurochem.
  doi: 10.1111/j.1471-4159.2007.04762.x
  contributor:
    fullname: Rodríguez-Navarro
– volume: 88
  start-page: 167
  year: 2010
  ident: B99
  article-title: Parkin reverses intracellular beta-amyloid accumulation and its negative effects on proteasome function
  publication-title: J. Neurosci. Res.
  doi: 10.1002/jnr.22178
  contributor:
    fullname: Rosen
– volume: 524
  start-page: 370
  year: 2015
  ident: B137
  article-title: Mechanism of phospho-ubiquitin-induced PARKIN activation
  publication-title: Nature
  doi: 10.1038/nature14879
  contributor:
    fullname: Wauer
– volume: 27
  start-page: 524
  year: 2006
  ident: B68
  article-title: Parkin-mediated lysine 63-linked polyubiquitination: a link to protein inclusions formation in Parkinson’s and other conformational diseases?
  publication-title: Neurobiol. Aging
  doi: 10.1016/j.neurobiolaging.2005.07.023
  contributor:
    fullname: Lim
– volume: 18
  start-page: 1135
  year: 2004
  ident: B82
  article-title: Cross-linking of ubiquitin, HSP27, parkin and alpha-synuclein by gamma-glutamyl-epsilon-lysine bonds in Alzheimer’s neurofibrillary tangles
  publication-title: FASEB J.
  doi: 10.1096/fj.04-1493fje
  contributor:
    fullname: Nemes
– volume: 17
  start-page: 431
  year: 2008b
  ident: B120
  article-title: Lysine 63-linked ubiquitination promotes the formation and autophagic clearance of protein inclusions associated with neurodegenerative diseases
  publication-title: Hum. Mol. Genet.
  doi: 10.1093/hmg/ddm320
  contributor:
    fullname: Tan
– volume: 72
  start-page: 2543
  year: 2012
  ident: B143
  article-title: Parkin pathway activation mitigates glioma cell proliferation and predicts patient survival
  publication-title: Cancer Res.
  doi: 10.1158/0008-5472.CAN-11-3060
  contributor:
    fullname: Yeo
– volume: 340
  start-page: 1451
  year: 2013
  ident: B122
  article-title: Structure of parkin reveals mechanisms for ubiquitin ligase activation
  publication-title: Science
  doi: 10.1126/science.1237908
  contributor:
    fullname: Trempe
– volume: 285
  start-page: 38214
  year: 2010
  ident: B14
  article-title: Parkin Mono-ubiquitinates Bcl-2 and regulates autophagy
  publication-title: J. Biol. Chem.
  doi: 10.1074/jbc.M110.101469
  contributor:
    fullname: Chen
– volume: 285
  start-page: 29231
  year: 2010
  ident: B121
  article-title: Parkin enhances the expression of cyclin-dependent kinase 6 and negatively regulates the proliferation of breast cancer cells
  publication-title: J. Biol. Chem.
  doi: 10.1074/jbc.m110.108241
  contributor:
    fullname: Tay
– volume: 126
  start-page: 1271
  year: 2003
  ident: B91
  article-title: Parkin mutations are frequent in patients with isolated early-onset parkinsonism
  publication-title: Brain
  doi: 10.1093/brain/awg136
  contributor:
    fullname: Periquet
– volume: 289
  start-page: 10769
  year: 2014
  ident: B117
  article-title: Mitochondrial dysfunction and decrease in body weight of a transgenic knock-in mouse model for TDP-43
  publication-title: J. Biol. Chem.
  doi: 10.1074/jbc.M113.515940
  contributor:
    fullname: Stribl
– volume: 206
  start-page: 655
  year: 2014
  ident: B2
  article-title: Mitophagy of damaged mitochondria occurs locally in distal neuronal axons and requires PINK1 and Parkin
  publication-title: J. Cell Biol.
  doi: 10.1083/jcb.201401070
  contributor:
    fullname: Ashrafi
– volume: 85
  start-page: 257
  year: 2015
  ident: B92
  article-title: The roles of PINK1, parkin and mitochondrial fidelity in Parkinson’s disease
  publication-title: Neuron
  doi: 10.1016/j.neuron.2014.12.007
  contributor:
    fullname: Pickrell
– volume: 23
  start-page: 5227
  year: 2014
  ident: B19
  article-title: The deubiquitinase USP15 antagonizes Parkin-mediated mitochondrial ubiquitination and mitophagy
  publication-title: Hum. Mol. Genet.
  doi: 10.1093/hmg/ddu244
  contributor:
    fullname: Cornelissen
– volume: 107
  start-page: 5018
  year: 2010
  ident: B148
  article-title: Drosophila parkin requires PINK1 for mitochondrial translocation and ubiquitinates mitofusin
  publication-title: Proc. Natl. Acad. Sci. U S A
  doi: 10.1073/pnas.0913485107
  contributor:
    fullname: Ziviani
– volume: 25
  start-page: 302
  year: 2000
  ident: B109
  article-title: Familial Parkinson disease gene product, parkin, is a ubiquitin-protein ligase
  publication-title: Nat. Genet.
  doi: 10.1038/77060
  contributor:
    fullname: Shimura
– volume: 97
  start-page: 13354
  year: 2000
  ident: B146
  article-title: Parkin functions as an E2-dependent ubiquitin- protein ligase and promotes the degradation of the synaptic vesicle-associated protein, CDCrel-1
  publication-title: Proc. Natl. Acad. Sci. U S A
  doi: 10.1073/pnas.240347797
  contributor:
    fullname: Zhang
– volume: 279
  start-page: 54380
  year: 2004
  ident: B43
  article-title: Parkin increases dopamine uptake by enhancing the cell surface expression of dopamine transporter
  publication-title: J. Biol. Chem.
  doi: 10.1074/jbc.m409282200
  contributor:
    fullname: Jiang
– volume: 32
  start-page: 2099
  year: 2013
  ident: B136
  article-title: Structure of the human Parkin ligase domain in an autoinhibited state
  publication-title: EMBO J.
  doi: 10.1038/emboj.2013.125
  contributor:
    fullname: Wauer
– volume: 278
  start-page: 48120
  year: 2003
  ident: B88
  article-title: Novel monoclonal antibodies demonstrate biochemical variation of brain parkin with age
  publication-title: J. Biol. Chem.
  doi: 10.1074/jbc.m306889200
  contributor:
    fullname: Pawlyk
– volume: 100
  start-page: 4078
  year: 2003
  ident: B32
  article-title: Mitochondrial pathology and apoptotic muscle degeneration in Drosophila parkin mutants
  publication-title: Proc. Natl. Acad. Sci. U S A
  doi: 10.1073/pnas.0737556100
  contributor:
    fullname: Greene
– volume: 93
  start-page: 422
  year: 2005b
  ident: B131
  article-title: Alterations in the solubility and intracellular localization of parkin by several familial Parkinson’s disease-linked point mutations
  publication-title: J. Neurochem.
  doi: 10.1111/j.1471-4159.2005.03023.x
  contributor:
    fullname: Wang
– volume: 275
  start-page: 35661
  year: 2000
  ident: B42
  article-title: Parkin suppresses unfolded protein stress-induced cell death through its E3 ubiquitin-protein ligase activity
  publication-title: J. Biol. Chem.
  doi: 10.1074/jbc.c000447200
  contributor:
    fullname: Imai
– volume: 44
  start-page: 931
  year: 2004
  ident: B45
  article-title: BAG5 inhibits parkin and enhances dopaminergic neuron degeneration
  publication-title: Neuron
  doi: 10.1016/j.neuron.2004.11.026
  contributor:
    fullname: Kalia
– volume: 11
  start-page: 1214
  year: 2005
  ident: B61
  article-title: Dopamine covalently modifies and functionally inactivates parkin
  publication-title: Nat. Med.
  doi: 10.1038/nm1314
  contributor:
    fullname: LaVoie
– volume: 117
  start-page: 179
  year: 2003
  ident: B16
  article-title: SEPT5_v2 is a parkin-binding protein
  publication-title: Brain Res. Mol. Brain Res.
  doi: 10.1016/s0169-328x(03)00318-8
  contributor:
    fullname: Choi
– volume: 3
  start-page: 1016
  year: 2012
  ident: B85
  article-title: PINK1 autophosphorylation upon membrane potential dissipation is essential for Parkin recruitment to damaged mitochondria
  publication-title: Nat. Commun.
  doi: 10.1038/ncomms2016
  contributor:
    fullname: Okatsu
– volume: 4
  start-page: 4874
  year: 2014
  ident: B47
  article-title: The c-Abl inhibitor, nilotinib, protects dopaminergic neurons in a preclinical animal model of Parkinson’s disease
  publication-title: Sci. Rep.
  doi: 10.1038/srep04874
  contributor:
    fullname: Karuppagounder
– volume: 10
  start-page: 524
  year: 2000
  ident: B55
  article-title: Aggresomes, inclusion bodies and protein aggregation
  publication-title: Trends Cell Biol.
  doi: 10.1016/s0962-8924(00)01852-3
  contributor:
    fullname: Kopito
– volume: 583
  start-page: 521
  year: 2009
  ident: B30
  article-title: Programmed cell death-2 isoform1 is ubiquitinated by parkin and increased in the substantia nigra of patients with autosomal recessive Parkinson’s disease
  publication-title: FEBS Lett.
  doi: 10.1016/j.febslet.2008.12.055
  contributor:
    fullname: Fukae
– volume: 2
  start-page: 120080
  year: 2012
  ident: B54
  article-title: PINK1 is activated by mitochondrial membrane potential depolarization and stimulates Parkin E3 ligase activity by phosphorylating Serine 65
  publication-title: Open Biol.
  doi: 10.1098/rsob.120080
  contributor:
    fullname: Kondapalli
– volume: 4
  start-page: 1626
  year: 2013
  ident: B126
  article-title: Sulfhydration mediates neuroprotective actions of parkin
  publication-title: Nat. Commun.
  doi: 10.1038/ncomms2623
  contributor:
    fullname: Vandiver
– volume: 8
  start-page: e73235
  year: 2013
  ident: B65
  article-title: Proteasome inhibition promotes Parkin-Ubc13 interaction and lysine 63-linked ubiquitination
  publication-title: PLoS One
  doi: 10.1371/journal.pone.0073235
  contributor:
    fullname: Lim
– volume: 280
  start-page: 16619
  year: 2005
  ident: B24
  article-title: Alpha-synuclein and parkin contribute to the assembly of ubiquitin lysine 63-linked multiubiquitin chains
  publication-title: J. Biol. Chem.
  doi: 10.1074/jbc.m413591200
  contributor:
    fullname: Doss-Pepe
– volume: 474
  start-page: 105
  year: 2011
  ident: B138
  article-title: UBCH7 reactivity profile reveals parkin and HHARI to be RING/HECT hybrids
  publication-title: Nature
  doi: 10.1038/nature09966
  contributor:
    fullname: Wenzel
– volume: 7
  start-page: 1144
  year: 2001
  ident: B210
  article-title: Parkin ubiquitinates the α-synuclein-interacting protein, synphilin-1: implications for Lewy-body formation in Parkinson disease
  publication-title: Nat. Med.
  doi: 10.1038/nm1001-1144
  contributor:
    fullname: Chung
– volume: 4
  start-page: 251
  year: 2008a
  ident: B119
  article-title: Lysine 63-linked polyubiquitin potentially partners with p62 to promote the clearance of protein inclusions by autophagy
  publication-title: Autophagy
  doi: 10.4161/auto.5444
  contributor:
    fullname: Tan
– volume: 14
  start-page: 2571
  year: 2005
  ident: B115
  article-title: Familial-associated mutations differentially disrupt the solubility, localization, binding and ubiquitination properties of parkin
  publication-title: Hum. Mol. Genet.
  doi: 10.1093/hmg/ddi292
  contributor:
    fullname: Sriram
– volume: 95
  start-page: 1259
  year: 2005
  ident: B90
  article-title: Proteomic analysis of parkin knockout mice: alterations in energy metabolism, protein handling and synaptic function
  publication-title: J. Neurochem.
  doi: 10.1111/j.1471-4159.2005.03442.x
  contributor:
    fullname: Periquet
– volume: 128
  start-page: 2281
  year: 2005
  ident: B6
  article-title: Motor reorganization in asymptomatic carriers of a single mutant Parkin allele: a human model for presymptomatic parkinsonism
  publication-title: Brain
  doi: 10.1093/brain/awh572
  contributor:
    fullname: Buhmann
– volume: 33
  start-page: 2473
  year: 2014
  ident: B26
  article-title: USP8 regulates mitophagy by removing K6-linked ubiquitin conjugates from parkin
  publication-title: EMBO J.
  doi: 10.15252/embj.201489729
  contributor:
    fullname: Durcan
– volume: 205
  start-page: 143
  year: 2014
  ident: B46
  article-title: PINK1 phosphorylates ubiquitin to activate Parkin E3 ubiquitin ligase activity
  publication-title: J. Cell Biol.
  doi: 10.1083/jcb.201402104
  contributor:
    fullname: Kane
– volume: 6
  start-page: e1617
  year: 2015
  ident: B48
  article-title: PINK1-induced mitophagy promotes neuroprotection in Huntington’s disease
  publication-title: Cell Death Dis.
  doi: 10.1038/cddis.2014.581
  contributor:
    fullname: Khalil
– volume: 8
  start-page: e1000298
  year: 2010a
  ident: B79
  article-title: PINK1 is selectively stabilized on impaired mitochondria to activate Parkin
  publication-title: PLoS Biol.
  doi: 10.1371/journal.pbio.1000298
  contributor:
    fullname: Narendra
– volume: 281
  start-page: 16193
  year: 2006
  ident: B51
  article-title: Identification of far upstream element-binding protein-1 as an authentic parkin substrate
  publication-title: J. Biol. Chem.
  doi: 10.1074/jbc.c600041200
  contributor:
    fullname: Ko
– volume: 342
  start-page: 1560
  year: 2000
  ident: B71
  article-title: Association between early-onset Parkinson’s disease and mutations in the parkin gene. French Parkinson’s disease genetics study group
  publication-title: N. Engl. J. Med.
  doi: 10.1056/NEJM200005253422103
  contributor:
    fullname: Lücking
– volume: 17
  start-page: 3128
  year: 2008
  ident: B98
  article-title: Parkin deletion causes cerebral and systemic amyloidosis in human mutated tau over-expressing mice
  publication-title: Hum. Mol. Genet.
  doi: 10.1093/hmg/ddn210
  contributor:
    fullname: Rodríguez-Navarro
– volume: 25
  start-page: 7968
  year: 2005
  ident: B53
  article-title: Accumulation of the authentic parkin substrate aminoacyl-tRNA synthetase cofactor, p38/JTV-1, leads to catecholaminergic cell death
  publication-title: J. Neurosci.
  doi: 10.1523/jneurosci.2172-05.2005
  contributor:
    fullname: Ko
– volume: 7
  start-page: e52830
  year: 2012b
  ident: B113
  article-title: Reconstitution of mitochondria derived vesicle formation demonstrates selective enrichment of oxidized cargo
  publication-title: PLoS One
  doi: 10.1371/journal.pone.0052830
  contributor:
    fullname: Soubannier
– volume: 49
  start-page: 367
  year: 2001
  ident: B39
  article-title: Positron emission tomographic analysis of the nigrostriatal dopaminergic system in familial parkinsonism associated with mutations in the parkin gene
  publication-title: Ann. Neurol.
  doi: 10.1002/ana.74.abs
  contributor:
    fullname: Hilker
– volume: 4
  start-page: 33
  year: 2013
  ident: B66
  article-title: Molecular events underlying Parkinson’s disease - an interwoven tapestry
  publication-title: Front. Neurol.
  doi: 10.3389/fneur.2013.00033
  contributor:
    fullname: Lim
– volume: 1281
  start-page: 91
  year: 2009
  ident: B102
  article-title: Effects of partial suppression of parkin on huntingtin mutant R6/1 mice
  publication-title: Brain Res.
  doi: 10.1016/j.brainres.2009.05.039
  contributor:
    fullname: Rubio
– volume: 147
  start-page: 893
  year: 2011b
  ident: B134
  article-title: PINK1 and Parkin target Miro for phosphorylation and degradation to arrest mitochondrial motility
  publication-title: Cell
  doi: 10.1016/j.cell.2011.10.018
  contributor:
    fullname: Wang
– volume: 6
  start-page: e19720
  year: 2011
  ident: B15
  article-title: Parkin mediates apparent E2-independent monoubiquitination in vitro and contains an intrinsic activity that catalyzes polyubiquitination
  publication-title: PLoS One
  doi: 10.1371/journal.pone.0019720
  contributor:
    fullname: Chew
– volume: 6
  start-page: 1090
  year: 2010b
  ident: B80
  article-title: p62/SQSTM1 is required for Parkin-induced mitochondrial clustering but not mitophagy; VDAC1 is dispensable for both
  publication-title: Autophagy
  doi: 10.4161/auto.6.8.13426
  contributor:
    fullname: Narendra
– volume: 33
  start-page: 3627
  year: 2013
  ident: B27
  article-title: Parkin-dependent degradation of the F-box protein Fbw7beta promotes neuronal survival in response to oxidative stress by stabilizing Mcl-1
  publication-title: Mol. Cell. Biol.
  doi: 10.1128/MCB.00535-13
  contributor:
    fullname: Ekholm-Reed
– volume: 14
  start-page: 357
  year: 2003
  ident: B33
  article-title: The C289G and C418R missense mutations cause rapid sequestration of human Parkin into insoluble aggregates
  publication-title: Neurobiol. Dis.
  doi: 10.1016/j.nbd.2003.08.011
  contributor:
    fullname: Gu
– volume: 278
  start-page: 47199
  year: 2003
  ident: B139
  article-title: Inactivation of parkin by oxidative stress and C-terminal truncations: a protective role of molecular chaperones
  publication-title: J. Biol. Chem.
  doi: 10.1074/jbc.m306769200
  contributor:
    fullname: Winklhofer
– volume: 19
  start-page: 1445
  year: 2004
  ident: B129
  article-title: Brain parenchyma sonography detects preclinical parkinsonism
  publication-title: Mov. Disord.
  doi: 10.1002/mds.20232
  contributor:
    fullname: Walter
– volume: 290
  start-page: 13862
  year: 2015
  ident: B84
  article-title: Convergence of Parkin, PINK1 and alpha-Synuclein on stress-induced mitochondrial morphological remodeling
  publication-title: J. Biol. Chem.
  doi: 10.1074/jbc.M114.634063
  contributor:
    fullname: Norris
– volume: 441
  start-page: 1157
  year: 2006
  ident: B87
  article-title: Mitochondrial dysfunction in Drosophila PINK1 mutants is complemented by parkin
  publication-title: Nature
  doi: 10.1038/nature04788
  contributor:
    fullname: Park
– volume: 388
  start-page: 839
  year: 1997
  ident: B114
  article-title: Alpha-synuclein in Lewy bodies
  publication-title: Nature
  doi: 10.1038/42166
  contributor:
    fullname: Spillantini
– volume: 4
  start-page: 399
  year: 2002
  ident: B103
  article-title: Progressive supranuclear palsy and tau hyperphosphorylation in a patient with a C212Y parkin mutation
  publication-title: J. Alzheimers Dis.
  doi: 10.3233/JAD-2002-4506
  contributor:
    fullname: Sánchez
– volume: 286
  start-page: 11649
  year: 2011a
  ident: B132
  article-title: Parkin ubiquitinates Drp1 for proteasome-dependent degradation: implication of dysregulated mitochondrial dynamics in Parkinson’s disease
  publication-title: J. Biol. Chem.
  doi: 10.1074/jbc.M110.144238
  contributor:
    fullname: Wang
– volume: 105
  start-page: 1806
  year: 2008
  ident: B76
  article-title: Parkin mediates the degradation-independent ubiquitination of Hsp70
  publication-title: J. Neurochem.
  doi: 10.1111/j.1471-4159.2008.05261.x
  contributor:
    fullname: Moore
– volume: 110
  start-page: 6400
  year: 2013
  ident: B127
  article-title: The PINK1-Parkin pathway promotes both mitophagy and selective respiratory chain turnover in vivo
  publication-title: Proc. Natl. Acad. Sci. U S A
  doi: 10.1073/pnas.1221132110
  contributor:
    fullname: Vincow
– volume: 111
  start-page: E4439
  year: 2014
  ident: B141
  article-title: Optineurin is an autophagy receptor for damaged mitochondria in parkin-mediated mitophagy that is disrupted by an ALS-linked mutation
  publication-title: Proc. Natl. Acad. Sci. U S A
  doi: 10.1073/pnas.1405752111
  contributor:
    fullname: Wong
– volume: 12
  start-page: 2957
  year: 2003
  ident: B18
  article-title: RING finger 1 mutations in Parkin produce altered localization of the protein
  publication-title: Hum. Mol. Genet.
  doi: 10.1093/hmg/ddg328
  contributor:
    fullname: Cookson
– volume: 37
  start-page: 735
  year: 2003
  ident: B116
  article-title: Parkin is a component of an SCF-like ubiquitin ligase complex and protects postmitotic neurons from kainate excitotoxicity
  publication-title: Neuron
  doi: 10.1016/s0896-6273(03)00084-9
  contributor:
    fullname: Staropoli
– volume: 293
  start-page: 263
  year: 2001
  ident: B110
  article-title: Ubiquitination of a new form of alpha -synuclein by parkin from human brain: implications for Parkinson’s disease
  publication-title: Science
  doi: 10.1126/science.1060627
  contributor:
    fullname: Shimura
– volume: 524
  start-page: 309
  year: 2015
  ident: B62
  article-title: The ubiquitin kinase PINK1 recruits autophagy receptors to induce mitophagy
  publication-title: Nature
  doi: 10.1038/nature14893
  contributor:
    fullname: Lazarou
– volume: 183
  start-page: 795
  year: 2008
  ident: B78
  article-title: Parkin is recruited selectively to impaired mitochondria and promotes their autophagy
  publication-title: J. Cell Biol.
  doi: 10.1083/jcb.200809125
  contributor:
    fullname: Narendra
– volume: 4
  start-page: 1982
  year: 2013
  ident: B96
  article-title: Structure and function of Parkin E3 ubiquitin ligase reveals aspects of RING and HECT ligases
  publication-title: Nat. Commun.
  doi: 10.1038/ncomms2982
  contributor:
    fullname: Riley
– volume: 178
  start-page: 1025
  year: 2007
  ident: B86
  article-title: Parkin-mediated K63-linked polyubiquitination targets misfolded DJ-1 to aggresomes via binding to HDAC6
  publication-title: J. Cell Biol.
  doi: 10.1083/jcb.200611128
  contributor:
    fullname: Olzmann
– volume: 18
  start-page: 809
  year: 2009
  ident: B101
  article-title: Combined kinase inhibition modulates parkin inactivation
  publication-title: Hum. Mol. Genet.
  doi: 10.1093/hmg/ddn407
  contributor:
    fullname: Rubio de la Torre
– volume: 33
  start-page: 2142
  year: 2014
  ident: B118
  article-title: A new pathway for mitochondrial quality control: mitochondrial-derived vesicles
  publication-title: EMBO J.
  doi: 10.15252/embj.201488104
  contributor:
    fullname: Sugiura
– volume: 392
  start-page: 605
  year: 1998
  ident: B50
  article-title: Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism
  publication-title: Nature
  doi: 10.1038/33416
  contributor:
    fullname: Kitada
– volume: 13
  start-page: R127
  year: 2004
  ident: B73
  article-title: Parkin genetics: one model for Parkinson’s disease
  publication-title: Hum. Mol. Genet.
  doi: 10.1093/hmg/ddh089
  contributor:
    fullname: Mata
– volume: 280
  start-page: 9425
  year: 2005
  ident: B147
  article-title: RING finger ubiquitin-protein isopeptide ligase Nrdp1/FLRF regulates parkin stability and activity
  publication-title: J. Biol. Chem.
  doi: 10.1074/jbc.m408955200
  contributor:
    fullname: Zhong
– volume: 8
  start-page: 834
  year: 2006
  ident: B28
  article-title: A regulated interaction with the UIM protein Eps15 implicates parkin in EGF receptor trafficking and PI(3)K-Akt signalling
  publication-title: Nat. Cell Biol.
  doi: 10.1038/ncb1441
  contributor:
    fullname: Fallon
– volume: 5
  start-page: 1247
  year: 2013
  ident: B70
  article-title: Tyrosine kinase inhibition increases functional parkin-Beclin-1 interaction and enhances amyloid clearance and cognitive performance
  publication-title: EMBO Mol. Med.
  doi: 10.1002/emmm.201302771
  contributor:
    fullname: Lonskaya
– volume: 30
  start-page: 2853
  year: 2011
  ident: B13
  article-title: Autoregulation of Parkin activity through its ubiquitin-like domain
  publication-title: EMBO J.
  doi: 10.1038/emboj.2011.204
  contributor:
    fullname: Chaugule
– volume: 18
  start-page: 102
  year: 2008
  ident: B83
  article-title: Cargo-selected transport from the mitochondria to peroxisomes is mediated by vesicular carriers
  publication-title: Curr. Biol.
  doi: 10.1016/j.cub.2007.12.038
  contributor:
    fullname: Neuspiel
– volume: 60
  start-page: 21
  year: 2015
  ident: B64
  article-title: Parkin regulates mitosis and genomic stability through Cdc20/Cdh1
  publication-title: Mol. Cell
  doi: 10.1016/j.molcel.2015.08.011
  contributor:
    fullname: Lee
– volume: 107
  start-page: 378
  year: 2010
  ident: B128
  article-title: PINK1-dependent recruitment of Parkin to mitochondria in mitophagy
  publication-title: Proc. Natl. Acad. Sci. U S A
  doi: 10.1073/pnas.0911187107
  contributor:
    fullname: Vives-Bauza
– volume: 144
  start-page: 689
  year: 2011
  ident: B111
  article-title: PARIS (ZNF746) repression of PGC-1alpha contributes to neurodegeneration in Parkinson’s disease
  publication-title: Cell
  doi: 10.1016/j.cell.2011.02.010
  contributor:
    fullname: Shin
– volume: 465
  start-page: 223
  year: 2010
  ident: B72
  article-title: Mutations of optineurin in amyotrophic lateral sclerosis
  publication-title: Nature
  doi: 10.1038/nature08971
  contributor:
    fullname: Maruyama
– volume: 203
  start-page: 531
  year: 2007
  ident: B41
  article-title: Parkin is an E3 ubiquitin-ligase for normal and mutant ataxin-2 and prevents ataxin-2-induced cell death
  publication-title: Exp. Neurol.
  doi: 10.1016/j.expneurol.2006.09.009
  contributor:
    fullname: Huynh
– volume: 189
  start-page: 211
  year: 2010
  ident: B75
  article-title: PINK1 stabilized by mitochondrial depolarization recruits Parkin to damaged mitochondria and activates latent Parkin for mitophagy
  publication-title: J. Cell Biol.
  doi: 10.1083/jcb.200910140
  contributor:
    fullname: Matsuda
– volume: 282
  start-page: 12842
  year: 2007
  ident: B3
  article-title: Phosphorylation of Parkin by the cyclin-dependent kinase 5 at the linker region modulates its ubiquitin-ligase activity and aggregation
  publication-title: J. Biol. Chem.
  doi: 10.1074/jbc.m608243200
  contributor:
    fullname: Avraham
– volume: 29
  start-page: 989
  year: 2015
  ident: B25
  article-title: The three ’P’s of mitophagy: PARKIN, PINK1 and post-translational modifications
  publication-title: Genes Dev.
  doi: 10.1101/gad.262758.115
  contributor:
    fullname: Durcan
– volume: 27
  start-page: 1868
  year: 2007
  ident: B37
  article-title: Parkin mediates neuroprotection through activation of IkappaB kinase/nuclear factor-kappaB signaling
  publication-title: J. Neurosci.
  doi: 10.1523/jneurosci.5537-06.2007
  contributor:
    fullname: Henn
– volume: 12
  start-page: 1427
  year: 2003
  ident: B21
  article-title: The p38 subunit of the aminoacyl-tRNA synthetase complex is a Parkin substrate: linking protein biosynthesis and neurodegeneration
  publication-title: Hum. Mol. Genet.
  doi: 10.1093/hmg/ddg159
  contributor:
    fullname: Corti
– volume: 510
  start-page: 162
  year: 2014
  ident: B56
  article-title: Ubiquitin is phosphorylated by PINK1 to activate parkin
  publication-title: Nature
  doi: 10.1038/nature13392
  contributor:
    fullname: Koyano
– volume: 189
  start-page: 671
  year: 2010
  ident: B63
  article-title: Disease-causing mutations in parkin impair mitochondrial ubiquitination, aggregation and HDAC6-dependent mitophagy
  publication-title: J. Cell Biol.
  doi: 10.1083/jcb.201001039
  contributor:
    fullname: Lee
– volume: 286
  start-page: 19630
  year: 2011
  ident: B144
  article-title: Parkin mediates proteasome-dependent protein degradation and rupture of the outer mitochondrial membrane
  publication-title: J. Biol. Chem.
  doi: 10.1074/jbc.M110.209338
  contributor:
    fullname: Yoshii
– volume: 24
  start-page: 3058
  year: 2015
  ident: B20
  article-title: NH2-truncated human tau induces deregulated mitophagy in neurons by aberrant recruitment of Parkin and UCHL-1: implications in Alzheimer’s disease
  publication-title: Hum. Mol. Genet.
  doi: 10.1093/hmg/ddv059
  contributor:
    fullname: Corsetti
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Snippet Parkin is a unique, multifunctional ubiquitin ligase whose various roles in the cell, particularly in neurons, are widely thought to be protective. The pivotal...
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SubjectTerms Amyotrophic lateral sclerosis
Autophagy
Basal ganglia
Binding sites
Central nervous system diseases
Enzymes
Homeostasis
Insects
Kinases
Mitochondria
mitophagy
Movement disorders
Mutation
Neurodegenerative Diseases
Neuroscience
Parkin protein
Parkinson Disease
Parkinson's disease
Phosphorylation
Proteins
Quality control
Risk factors
Ubiquitin
Ubiquitin-protein ligase
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Title Parkin Regulation and Neurodegenerative Disorders
URI https://www.ncbi.nlm.nih.gov/pubmed/26793099
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