References analysis of the Wikipedia article "Parkin (protein)" in the English version

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Kitada T, Asakawa S, Hattori N, Matsumine H, Yamamura Y, Minoshima S, Yokochi M, Mizuno Y, Shimizu N (April 1998). "Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism". Nature. 392 (6676): 605–8. Bibcode:1998Natur.392..605K. doi:10.1038/33416. PMID 9560156. S2CID 4432261.

Matsumine H, Yamamura Y, Hattori N, Kobayashi T, Kitada T, Yoritaka A, Mizuno Y (April 1998). "A microdeletion of D6S305 in a family of autosomal recessive juvenile parkinsonism (PARK2)". Genomics. 49 (1): 143–6. doi:10.1006/geno.1997.5196. PMID 9570960.

Pickart CM, Eddins MJ (November 2004). "Ubiquitin: structures, functions, mechanisms". Biochimica et Biophysica Acta (BBA) - Molecular Cell Research. 1695 (1–3): 55–72. doi:10.1016/j.bbamcr.2004.09.019. PMID 15571809.

Seirafi M, Kozlov G, Gehring K (June 2015). "Parkin structure and function". The FEBS Journal. 282 (11): 2076–88. doi:10.1111/febs.13249. PMC 4672691. PMID 25712550.

Dawson TM, Dawson VL (2014). "The role of parkin in familial and sporadic Parkinson's disease". Movement Disorders. 25 (Suppl 1): S32-9. doi:10.1002/mds.22798. PMC 4115293. PMID 20187240.

Zhang C, Lin M, Wu R, Wang X, Yang B, Levine AJ, Hu W, Feng Z (2011). "Parkin, a p53 target gene, mediates the role of p53 in glucose metabolism and the Warburg effect". Proceedings of the National Academy of Sciences of the United States of America. 108 (39): 16259–64. Bibcode:2011PNAS..10816259Z. doi:10.1073/pnas.1113884108. PMC 3182683. PMID 21930938.

Trempe JF, Sauvé V, Grenier K, Seirafi M, Tang MY, Ménade M, Al-Abdul-Wahid S, Krett J, Wong K, Kozlov G, Nagar B, Fon EA, Gehring K (June 2013). "Structure of parkin reveals mechanisms for ubiquitin ligase activation". Science. 340 (6139): 1451–5. Bibcode:2013Sci...340.1451T. doi:10.1126/science.1237908. PMID 23661642. S2CID 206548928.

Riley BE, Lougheed JC, Callaway K, Velasquez M, Brecht E, Nguyen L, Shaler T, Walker D, Yang Y, Regnstrom K, Diep L, Zhang Z, Chiou S, Bova M, Artis DR, Yao N, Baker J, Yednock T, Johnston JA (2013). "Structure and function of Parkin E3 ubiquitin ligase reveals aspects of RING and HECT ligases". Nature Communications. 4: 1982. Bibcode:2013NatCo...4.1982R. doi:10.1038/ncomms2982. PMC 3709503. PMID 23770887.

Koyano F, Okatsu K, Kosako H, Tamura Y, Go E, Kimura M, Kimura Y, Tsuchiya H, Yoshihara H, Hirokawa T, Endo T, Fon EA, Trempe JF, Saeki Y, Tanaka K, Matsuda N (June 2014). "Ubiquitin is phosphorylated by PINK1 to activate parkin". Nature. 510 (7503): 162–6. Bibcode:2014Natur.510..162K. doi:10.1038/nature13392. PMID 24784582. S2CID 4390259.

Iguchi M, Kujuro Y, Okatsu K, Koyano F, Kosako H, Kimura M, Suzuki N, Uchiyama S, Tanaka K, Matsuda N (July 2013). "Parkin-catalyzed ubiquitin-ester transfer is triggered by PINK1-dependent phosphorylation". The Journal of Biological Chemistry. 288 (30): 22019–32. doi:10.1074/jbc.M113.467530. PMC 3724655. PMID 23754282.

Wauer T, Komander D (July 2013). "Structure of the human Parkin ligase domain in an autoinhibited state". The EMBO Journal. 32 (15): 2099–112. doi:10.1038/emboj.2013.125. PMC 3730226. PMID 23727886.

Olszewska DA, Lynch T (2015). "Will Crystal Parkin Help in Understanding the Future of Parkinson's Disease?". Frontiers in Neurology. 6: 35. doi:10.3389/fneur.2015.00035. PMC 4338761. PMID 25759682.

Durcan TM, Fon EA (May 2015). "The three 'P's of mitophagy: PARKIN, PINK1, and post-translational modifications". Genes & Development. 29 (10): 989–99. doi:10.1101/gad.262758.115. PMC 4441056. PMID 25995186.

Youle RJ, van der Bliek AM (August 2012). "Mitochondrial fission, fusion, and stress". Science. 337 (6098): 1062–5. Bibcode:2012Sci...337.1062Y. doi:10.1126/science.1219855. PMC 4762028. PMID 22936770.

Twig G, Elorza A, Molina AJ, Mohamed H, Wikstrom JD, Walzer G, Stiles L, Haigh SE, Katz S, Las G, Alroy J, Wu M, Py BF, Yuan J, Deeney JT, Corkey BE, Shirihai OS (January 2008). "Fission and selective fusion govern mitochondrial segregation and elimination by autophagy". The EMBO Journal. 27 (2): 433–46. doi:10.1038/sj.emboj.7601963. PMC 2234339. PMID 18200046.

Sarraf SA, Raman M, Guarani-Pereira V, Sowa ME, Huttlin EL, Gygi SP, Harper JW (April 2013). "Landscape of the PARKIN-dependent ubiquitylome in response to mitochondrial depolarization". Nature. 496 (7445): 372–6. Bibcode:2013Natur.496..372S. doi:10.1038/nature12043. PMC 3641819. PMID 23503661.

Narendra D, Walker JE, Youle R (November 2012). "Mitochondrial quality control mediated by PINK1 and Parkin: links to parkinsonism". Cold Spring Harbor Perspectives in Biology. 4 (11): a011338. doi:10.1101/cshperspect.a011338. PMC 3536340. PMID 23125018.

Shlevkov E, Kramer T, Schapansky J, LaVoie MJ, Schwarz TL (October 2016). "Miro phosphorylation sites regulate Parkin recruitment and mitochondrial motility". Proceedings of the National Academy of Sciences of the United States of America. 113 (41): E6097 – E6106. Bibcode:2016PNAS..113E6097S. doi:10.1073/pnas.1612283113. PMC 5068282. PMID 27679849.

Geisler S, Holmström KM, Skujat D, Fiesel FC, Rothfuss OC, Kahle PJ, Springer W (February 2010). "PINK1/Parkin-mediated mitophagy is dependent on VDAC1 and p62/SQSTM1". Nature Cell Biology. 12 (2): 119–31. doi:10.1038/ncb2012. PMID 20098416. S2CID 26096413.

Aleksaniants GD (2013). "[Use of balneo-, peloid- and centimeter-wave therapy in the complex treatment of patients with circumscribed scleroderma]". Vestnik Dermatologii I Venerologii. 32 (6): 58–60. doi:10.1038/emboj.2013.70. PMC 3630365. PMID 23531882.

Müller-Rischart AK, Pilsl A, Beaudette P, Patra M, Hadian K, Funke M, Peis R, Deinlein A, Schweimer C, Kuhn PH, Lichtenthaler SF, Motori E, Hrelia S, Wurst W, Trümbach D, Langer T, Krappmann D, Dittmar G, Tatzelt J, Winklhofer KF (March 2013). "The E3 ligase parkin maintains mitochondrial integrity by increasing linear ubiquitination of NEMO". Molecular Cell. 49 (5): 908–21. doi:10.1016/j.molcel.2013.01.036. PMID 23453807.

da Costa CA, Sunyach C, Giaime E, West A, Corti O, Brice A, Safe S, Abou-Sleiman PM, Wood NW, Takahashi H, Goldberg MS, Shen J, Checler F (November 2009). "Transcriptional repression of p53 by parkin and impairment by mutations associated with autosomal recessive juvenile Parkinson's disease". Nature Cell Biology. 11 (11): 1370–5. doi:10.1038/ncb1981. PMC 2952934. PMID 19801972.

Matoba S, Kang JG, Patino WD, Wragg A, Boehm M, Gavrilova O, Hurley PJ, Bunz F, Hwang PM (June 2006). "p53 regulates mitochondrial respiration". Science. 312 (5780): 1650–3. Bibcode:2006Sci...312.1650M. doi:10.1126/science.1126863. PMID 16728594. S2CID 36668814.

Poorkaj P, Nutt JG, James D, Gancher S, Bird TD, Steinbart E, Schellenberg GD, Payami H (August 2004). "parkin mutation analysis in clinic patients with early-onset Parkinson [corrected] disease". American Journal of Medical Genetics. Part A. 129A (1): 44–50. doi:10.1002/ajmg.a.30157. PMID 15266615. S2CID 85058092.

Lohmann E, Periquet M, Bonifati V, Wood NW, De Michele G, Bonnet AM, Fraix V, Broussolle E, Horstink MW, Vidailhet M, Verpillat P, Gasser T, Nicholl D, Teive H, Raskin S, Rascol O, Destée A, Ruberg M, Gasparini F, Meco G, Agid Y, Durr A, Brice A (August 2003). "How much phenotypic variation can be attributed to parkin genotype?". Annals of Neurology. 54 (2): 176–85. doi:10.1002/ana.10613. PMID 12891670. S2CID 6411438.

Ishikawa A, Takahashi H (November 1998). "Clinical and neuropathological aspects of autosomal recessive juvenile parkinsonism". Journal of Neurology. 245 (11 Suppl 3): 4–9. doi:10.1007/pl00007745. PMID 9808334. S2CID 28670790.

Keeney PM, Xie J, Capaldi RA, Bennett JP (May 2006). "Parkinson's disease brain mitochondrial complex I has oxidatively damaged subunits and is functionally impaired and misassembled". The Journal of Neuroscience. 26 (19): 5256–64. doi:10.1523/JNEUROSCI.0984-06.2006. PMC 6674236. PMID 16687518.

Bender A, Krishnan KJ, Morris CM, Taylor GA, Reeve AK, Perry RH, Jaros E, Hersheson JS, Betts J, Klopstock T, Taylor RW, Turnbull DM (May 2006). "High levels of mitochondrial DNA deletions in substantia nigra neurons in aging and Parkinson disease". Nature Genetics. 38 (5): 515–7. doi:10.1038/ng1769. PMID 16604074. S2CID 13956928.

Shimura H, Hattori N, Kubo S, Mizuno Y, Asakawa S, Minoshima S, Shimizu N, Iwai K, Chiba T, Tanaka K, Suzuki T (July 2000). "Familial Parkinson disease gene product, parkin, is a ubiquitin-protein ligase". Nature Genetics. 25 (3): 302–5. doi:10.1038/77060. PMID 10888878. S2CID 8135537.

Chung KK, Zhang Y, Lim KL, Tanaka Y, Huang H, Gao J, Ross CA, Dawson VL, Dawson TM (October 2001). "Parkin ubiquitinates the alpha-synuclein-interacting protein, synphilin-1: implications for Lewy-body formation in Parkinson disease". Nature Medicine. 7 (10): 1144–50. doi:10.1038/nm1001-1144. PMID 11590439. S2CID 12487644.

Tan JM, Wong ES, Kirkpatrick DS, Pletnikova O, Ko HS, Tay SP, Ho MW, Troncoso J, Gygi SP, Lee MK, Dawson VL, Dawson TM, Lim KL (February 2008). "Lysine 63-linked ubiquitination promotes the formation and autophagic clearance of protein inclusions associated with neurodegenerative diseases". Human Molecular Genetics. 17 (3): 431–9. doi:10.1093/hmg/ddm320. PMID 17981811.

Corti O, Hampe C, Koutnikova H, Darios F, Jacquier S, Prigent A, Robinson JC, Pradier L, Ruberg M, Mirande M, Hirsch E, Rooney T, Fournier A, Brice A (June 2003). "The p38 subunit of the aminoacyl-tRNA synthetase complex is a Parkin substrate: linking protein biosynthesis and neurodegeneration". Human Molecular Genetics. 12 (12): 1427–37. doi:10.1093/hmg/ddg159. PMID 12783850.

Ko HS, Kim SW, Sriram SR, Dawson VL, Dawson TM (June 2006). "Identification of far upstream element-binding protein-1 as an authentic Parkin substrate". The Journal of Biological Chemistry. 281 (24): 16193–6. doi:10.1074/jbc.C600041200. PMID 16672220.

Hattori N, Matsumine H, Asakawa S, Kitada T, Yoshino H, Elibol B, Brookes AJ, Yamamura Y, Kobayashi T, Wang M, Yoritaka A, Minoshima S, Shimizu N, Mizuno Y (August 1998). "Point mutations (Thr240Arg and Gln311Stop) [correction of Thr240Arg and Ala311Stop] in the Parkin gene". Biochemical and Biophysical Research Communications. 249 (3): 754–8. doi:10.1006/bbrc.1998.9134. PMID 9731209.

Veeriah S, Taylor BS, Meng S, Fang F, Yilmaz E, Vivanco I, Janakiraman M, Schultz N, Hanrahan AJ, Pao W, Ladanyi M, Sander C, Heguy A, Holland EC, Paty PB, Mischel PS, Liau L, Cloughesy TF, Mellinghoff IK, Solit DB, Chan TA (January 2010). "Somatic mutations of the Parkinson's disease-associated gene PARK2 in glioblastoma and other human malignancies". Nature Genetics. 42 (1): 77–82. doi:10.1038/ng.491. PMC 4002225. PMID 19946270.

Letessier A, Garrido-Urbani S, Ginestier C, Fournier G, Esterni B, Monville F, Adélaïde J, Geneix J, Xerri L, Dubreuil P, Viens P, Charafe-Jauffret E, Jacquemier J, Birnbaum D, Lopez M, Chaffanet M (January 2007). "Correlated break at PARK2/FRA6E and loss of AF-6/Afadin protein expression are associated with poor outcome in breast cancer". Oncogene. 26 (2): 298–307. doi:10.1038/sj.onc.1209772. PMID 16819513.

Poulogiannis G, McIntyre RE, Dimitriadi M, Apps JR, Wilson CH, Ichimura K, Luo F, Cantley LC, Wyllie AH, Adams DJ, Arends MJ (August 2010). "PARK2 deletions occur frequently in sporadic colorectal cancer and accelerate adenoma development in Apc mutant mice". Proceedings of the National Academy of Sciences of the United States of America. 107 (34): 15145–50. Bibcode:2010PNAS..10715145P. doi:10.1073/pnas.1009941107. PMC 2930574. PMID 20696900.

Choi P, Golts N, Snyder H, Chong M, Petrucelli L, Hardy J, Sparkman D, Cochran E, Lee JM, Wolozin B (September 2001). "Co-association of parkin and alpha-synuclein". NeuroReport. 12 (13): 2839–43. doi:10.1097/00001756-200109170-00017. PMID 11588587. S2CID 83941655.

Kawahara K, Hashimoto M, Bar-On P, Ho GJ, Crews L, Mizuno H, Rockenstein E, Imam SZ, Masliah E (March 2008). "alpha-Synuclein aggregates interfere with Parkin solubility and distribution: role in the pathogenesis of Parkinson disease". The Journal of Biological Chemistry. 283 (11): 6979–87. doi:10.1074/jbc.M710418200. PMID 18195004.

Fallon L, Moreau F, Croft BG, Labib N, Gu WJ, Fon EA (January 2002). "Parkin and CASK/LIN-2 associate via a PDZ-mediated interaction and are co-localized in lipid rafts and postsynaptic densities in brain". The Journal of Biological Chemistry. 277 (1): 486–91. doi:10.1074/jbc.M109806200. PMID 11679592.

Staropoli JF, McDermott C, Martinat C, Schulman B, Demireva E, Abeliovich A (March 2003). "Parkin is a component of an SCF-like ubiquitin ligase complex and protects postmitotic neurons from kainate excitotoxicity". Neuron. 37 (5): 735–49. doi:10.1016/s0896-6273(03)00084-9. PMID 12628165. S2CID 17024826.

Imai Y, Soda M, Hatakeyama S, Akagi T, Hashikawa T, Nakayama KI, Takahashi R (July 2002). "CHIP is associated with Parkin, a gene responsible for familial Parkinson's disease, and enhances its ubiquitin ligase activity". Molecular Cell. 10 (1): 55–67. doi:10.1016/s1097-2765(02)00583-x. PMID 12150907.

Imai Y, Soda M, Inoue H, Hattori N, Mizuno Y, Takahashi R (June 2001). "An unfolded putative transmembrane polypeptide, which can lead to endoplasmic reticulum stress, is a substrate of Parkin". Cell. 105 (7): 891–902. doi:10.1016/s0092-8674(01)00407-x. PMID 11439185. S2CID 721363.

Fukae J, Sato S, Shiba K, Sato K, Mori H, Sharp PA, Mizuno Y, Hattori N (February 2009). "Programmed cell death-2 isoform1 is ubiquitinated by parkin and increased in the substantia nigra of patients with autosomal recessive Parkinson's disease". FEBS Letters. 583 (3): 521–5. doi:10.1016/j.febslet.2008.12.055. hdl:1721.1/96274. PMID 19146857. S2CID 7121769.

Choi P, Snyder H, Petrucelli L, Theisler C, Chong M, Zhang Y, Lim K, Chung KK, Kehoe K, D'Adamio L, Lee JM, Cochran E, Bowser R, Dawson TM, Wolozin B (October 2003). "SEPT5_v2 is a parkin-binding protein". Brain Research. Molecular Brain Research. 117 (2): 179–89. doi:10.1016/s0169-328x(03)00318-8. PMID 14559152.

Liu M, Aneja R, Sun X, Xie S, Wang H, Wu X, Dong JT, Li M, Joshi HC, Zhou J (December 2008). "Parkin regulates Eg5 expression by Hsp70 ubiquitination-dependent inactivation of c-Jun NH2-terminal kinase". The Journal of Biological Chemistry. 283 (51): 35783–8. doi:10.1074/jbc.M806860200. PMID 18845538.

Huynh DP, Scoles DR, Nguyen D, Pulst SM (October 2003). "The autosomal recessive juvenile Parkinson disease gene product, parkin, interacts with and ubiquitinates synaptotagmin XI". Human Molecular Genetics. 12 (20): 2587–97. doi:10.1093/hmg/ddg269. PMID 12925569.

Yu F, Zhou J (July 2008). "Parkin is ubiquitinated by Nrdp1 and abrogates Nrdp1-induced oxidative stress". Neuroscience Letters. 440 (1): 4–8. doi:10.1016/j.neulet.2008.05.052. PMID 18541373. S2CID 2169911.

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Seirafi M, Kozlov G, Gehring K (June 2015). "Parkin structure and function". The FEBS Journal. 282 (11): 2076–88. doi:10.1111/febs.13249. PMC 4672691. PMID 25712550.

Dawson TM, Dawson VL (2014). "The role of parkin in familial and sporadic Parkinson's disease". Movement Disorders. 25 (Suppl 1): S32-9. doi:10.1002/mds.22798. PMC 4115293. PMID 20187240.

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Parkin (protein) (English Wikipedia)