Familial Parkinson disease gene product, parkin, is a ubiquitin-protein ligase
Shimura, Hideki, Hattori, Nobutaka, Kubo, Shin-ichiro, Mizuno, Yoshikuni, Asakawa, Shuichi, Minoshima, Shinsei, Shimizu, Nobuyoshi, Iwai, Kazuhiro +3 more·2000·Nature Genetics
DOI 10.1038/77060
Cited by (1,004)
Items 201–300 of 1,004
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- The centrosome in human genetic diseaseJosé Luis Badano, Tanya M. Teslovich, Nicholas Katsanis · 2005 · Nature Reviews Genetics
- Accumulation of the Authentic Parkin Substrate Aminoacyl-tRNA Synthetase Cofactor, p38/JTV-1, Leads to Catecholaminergic Cell DeathHan Seok Ko, Rainer von Coelln, Sathya R. Sriram, Seong Who Kim, Kenny K. K. Chung, Olga Pletniková, Juan Carlos Troncoso, B. Lamar Johnson, Roya Saffary, Eyleen L. K. Goh et al. · 2005 · Journal of Neuroscience
- Role and Function of the 26S Proteasome in Proliferation and ApoptosisCord Naujokat, Stephan Hoffmann · 2002 · Laboratory Investigation
- Convergence of miRNA Expression Profiling, α-Synuclein Interacton and GWAS in Parkinson's DiseaseMadalena Martins, Alexandra Rosa, Leonor Correia Guedes, Benedita V. Fonseca, Kristina Gotovac, Sara Nunes Violante, Tiago Mestre, Miguel M Coelho, Mário Miguel Rosa, Eden R. Martin et al. · 2011 · PLoS ONE
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- Association of DJ-1 and parkin mediated by pathogenic DJ-1 mutations and oxidative stressDarren J. Moore, Li Zhang, Juan Carlos Troncoso, Michael K. Lee, Nobutaka Hattori, Yoshikuni Mizuno, Ted M. Dawson, Valina Lynn Dawson · 2004 · Human Molecular Genetics
- Cooperation of molecular chaperones with the ubiquitin/proteasome systemClaudia Esser, Simon Alberti, Jörg Höhfeld · 2004 · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research
- Parkin binds the Rpn10 subunit of 26S proteasomes through its ubiquitin‐like domainEri Sakata, Yoshiki Yamaguchi, Eiji Kurimoto, Jun Kikuchi, Shigeyuki Yokoyama, Shingo Yamada, Hiroyuki Kawahara, Hideyoshi Yokosawa, Nobutaka Hattori, Yoshikuni Mizuno et al. · 2003 · EMBO Reports
- The p38 subunit of the aminoacyl-tRNA synthetase complex is a Parkin substrate: linking protein biosynthesis and neurodegenerationOlga Corti · 2003 · Human Molecular Genetics
- Hsp90-Cdc37 Chaperone Complex Regulates Ulk1- and Atg13-Mediated MitophagyJoung Hyuck Joo, Frank Charles Dorsey, Aashish Joshi, Kristin M. Hennessy-Walters, Kristie Lindsey Rose, Kelly McCastlain, Ji Zhang, Rekha V. Iyengar, Chang Hwa Jung, Der‐Fen Suen et al. · 2011 · Molecular Cell
- Pathophysiological Roles of ASK1-MAP Kinase Signaling PathwaysHiroaki Nagai, Takuya Noguchi, Kohsuke Takeda, Hidenori Ichijo · 2007 · BMB Reports
- Parkin protects human dopaminergic neuroblastoma cells against dopamine-induced apoptosisJiang, Houbo, Ren, Yong, Zhao, Jinghui, Feng, Jian · 2004 · Human Molecular Genetics
- Endoplasmic reticulum dysfunction – a common denominator for cell injury in acute and degenerative diseases of the brain?Wulf Paschen, Aase Frandsen · 2001 · Journal of Neurochemistry
- Rare genetic mutations shed light on the pathogenesis of Parkinson diseaseTed M. Dawson, Valina Lynn Dawson · 2003 · Journal of Clinical Investigation
- Crystal Structures of Human DJ-1 and Escherichia coli Hsp31, Which Share an Evolutionarily Conserved DomainSun‐Joo Lee, So Jung Kim, In-Kwon Kim, Junsang Ko, Chang‐Sook Jeong, Gyung-Hwa Kim, Chankyu Park, Sa-Ouk Kang, Pann‐Ghill Suh, Heung-Soo Lee et al. · 2003 · Journal of Biological Chemistry
- Neuroprotective Strategies in Parkinson???s DiseaseSilvia A. Mandel, Edna Grünblatt, Peter Franz Riederer, Manfred Gerlach, Yona Levites, Moussa B. H. Youdim · 2003 · CNS Drugs
- The ubiquitin signal and autophagy: an orchestrated dance leading to mitochondrial degradationKoji Yamano, Noriyuki Matsuda, Keiji Tanaka · 2016 · EMBO Reports
- PARK2 deletions occur frequently in sporadic colorectal cancer and accelerate adenoma development in Apc mutant miceGeorge Poulogiannis, Rebecca E. McIntyre, Maria Dimitriadi, John Richard Apps, Catherine H. Wilson, Koichi Ichimura, Feijun Luo, Lewis C. Cantley, Andrew H. Wyllie, David J. Adams et al. · 2010 · Proceedings of the National Academy of Sciences
- L166P Mutant DJ-1, Causative for Recessive Parkinson's Disease, Is Degraded through the Ubiquitin-Proteasome SystemDavid W. Miller, Rili Ahmad, Stephen Hague, Melisa J. Baptista, Rosa Canet-Aviles, Chris McLendon, Donald M. Carter, Peng‐Peng Zhu, Julia Stadler, Jayanth S. Chandran et al. · 2003 · Journal of Biological Chemistry
- Are ubiquitination pathways central to Parkinson’s disease?Giasson, Benoit I, Lee, Virginia M.-Y · 2003 · Cell
- The diagnosis of manganese-induced parkinsonismMaria Graciela Cersosimo, William C. Koller · 2005 · NeuroToxicology
- iPS cell technologies: significance and applications to CNS regeneration and diseaseHideyuki Okano, Shinya Yamanaka · 2014 · Molecular Brain
- Parkin promotes the ubiquitination and degradation of the mitochondrial fusion factor mitofusin 1Glauser, Liliane, Sonnay, Sarah, Stafa, Klodjan, Moore, Darren J. · 2011 · Journal of Neurochemistry
- Evolving and Expanding the Roles of Mitophagy as a Homeostatic and Pathogenic ProcessÅsa B. Gustafsson, Gerald W. Dorn · 2018 · Physiological Reviews
- Recent advances in the genetics and pathogenesis of Parkinson diseaseM. Maral Mouradian · 2002 · Neurology
- Enhanced parkin levels favor ER-mitochondria crosstalk and guarantee Ca2+ transfer to sustain cell bioenergeticsTito Calí, Denis Ottolini, Alessandro Negro, Marisa Brini · 2013 · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease
- Biochemical analysis of Parkinson's disease-causing variants of Parkin, an E3 ubiquitin–protein ligase with monoubiquitylation capacityCornelia Hampe, Héctor Ardila-Osorio, Margot Fournier, Alexis Brice, Olga Corti · 2006 · Human Molecular Genetics
- Bcl-2 Family Proteins Participate in Mitochondrial Quality Control by Regulating Parkin/PINK1-Dependent MitophagyÉmilie Hollville, Richard G. Carroll, Sean P. Cullen, Séamus J. Martin · 2014 · Molecular Cell
- Familial-associated mutations differentially disrupt the solubility, localization, binding and ubiquitination properties of parkinSathya R. Sriram, Xiaojie Li, Han Seok Ko, Kenny K. K. Chung, Esther S.P. Wong, Kah Leong Lim, Valina Lynn Dawson, Ted M. Dawson · 2005 · Human Molecular Genetics
- The role of the ubiquitin-proteasomal pathway in Parkinson's disease and other neurodegenerative disordersKenny K. K. Chung, Valina Lynn Dawson, Ted M. Dawson · 2001 · Trends in Neurosciences
- Pathogenic mutations in Parkinson diseaseEng‐King Tan, Lisa M. Skipper · 2007 · Human Mutation
- The PARK8 Locus in Autosomal Dominant Parkinsonism: Confirmation of Linkage and Further Delineation of the Disease-Containing IntervalAlexander A. Zimprich, Bertram Müller-Myhsok, Matthew James Farrer, Petra Leitner, Manu Sharma, Mary Hulihan, Paul J. Lockhart, Audrey J. Strongosky, Jennifer M. Kachergus, Donald B. Calne et al. · 2004 · The American Journal of Human Genetics
- Parkin as a tumor suppressor gene for hepatocellular carcinomaM Fujiwara, Hiroyuki Marusawa, H-Q Wang, A Iwai, K Ikeuchi, Yuzuru Imai, Ayane Kataoka, Nobuyuki Nukina, Rei Takahashi, Tsutomu Chiba · 2008 · Oncogene
- Modeling Parkinson’s Disease in C. elegansJason F. Cooper, Jeremy M. Van Raamsdonk · 2018 · Journal of Parkinson s Disease
- CHIP: a quality-control E3 ligase collaborating with molecular chaperonesMurata, Shigeo, Chiba, Tomoki, Tanaka, Keiji · 2003 · The International Journal of Biochemistry & Cell Biology
- Andrographolide suppresses NLRP3 inflammasome activation in microglia through induction of parkin-mediated mitophagy in in-vitro and in-vivo models of Parkinson diseaseSahabuddin Ahmed, Mohit Kwatra, Samir Ranjan Panda, U.S.N Murty, V.G.M. Naidu · 2020 · Brain Behavior and Immunity
- Amyloid‐fibril formationEva Žerovnik · 2002 · European Journal of Biochemistry
- microRNAs in Parkinson’s Disease: From Pathogenesis to Novel Diagnostic and Therapeutic ApproachesLoredana Leggio, Silvia Vivarelli, Francesca L’Episcopo, Cataldo Tirolo, Salvatore Caniglia, Nunzio Testa, Bianca Marchetti, Nunzio Iraci · 2017 · International Journal of Molecular Sciences
- The genetic landscape of Parkinson's diseaseAriane Lunati, Suzanne Lesage, Alexis Brice · 2018 · Revue Neurologique
- The autosomal recessive juvenile Parkinson disease gene product, parkin, interacts with and ubiquitinates synaptotagmin XIDuong P. Huynh · 2003 · Human Molecular Genetics
- Parkin mutations and susceptibility alleles in late‐onset Parkinson's diseaseSofia A. Oliveira, William K. Scott, Eden R. Martin, MARTHA A. NANCE, Ray L. Watts, Jean Pintar Hubble, William C. Koller, Rajesh Pahwa, Matthew B. Stern, Bradley C. Hiner et al. · 2003 · Annals of Neurology
- Association of PINK1 and DJ-1 confers digenic inheritance of early-onset Parkinson's diseaseBeisha Tang, Hui Xiong, Ping Sun, Yuhu Zhang, Danling Wang, Zhengmao Hu, Zan-Hua Zhu, Hong Ma, Qian Pan, Jiahui Xia et al. · 2006 · Human Molecular Genetics
- Ubiquitin–proteasome system and Parkinson's diseaseC. Warren Olanow, Kevin St. P. McNaught · 2006 · Movement Disorders
- Parkin targets HIF-1α for ubiquitination and degradation to inhibit breast tumor progressionJuan Liu, Cen Zhang, Yuhan Zhao, Xuetian Yue, Hao Wu, SHAN HU HUANG, James Chen, Kyle Tomsky, Haiyang Xie, Christen A. Khella et al. · 2017 · Nature Communications
- Advancement in the modelling and therapeutics of Parkinson’s diseaseSachchida Nand, Payal Singh · 2020 · Journal of Chemical Neuroanatomy
- Novel regulation of parkin function through c-Abl-mediated tyrosine phosphorylation: implications for Parkinson’s diseaseImam, Syed Z., Zhou, Qing, Yamamoto, Ayako, Valente, Anthony J., Ali, Syed F., Bains, Mona, Roberts, James L., Kahle, Philipp J., Clark, Robert A., Li, Senlin · 2011 · The Journal of Neuroscience
- Transcriptional repression of p53 by parkin and impairment by mutations associated with autosomal recessive juvenile Parkinson's diseaseCristine Alvès da Costa, Claire Sunyach, Emilie Giaime, Andrew B. West, Olga Corti, Alexis Brice, Stephen H Safe, Patrick M. Abou‐Sleiman, Nicholas William Wood, Hitoshi Takahashi et al. · 2009 · Nature Cell Biology
- Mitophagy: Molecular Mechanisms, New Concepts on Parkin Activation and the Emerging Role of AMPK/ULK1 AxisRoberto Iorio, Giuseppe Celenza, Sabrina Petricca · 2021 · Cells
- Parkinson disease, 10 years after its genetic revolution: Multiple clues to a complex disorderChristine Klein, Michael G. Schlossmacher · 2007 · Neurology
- Parkin is a lipid-responsive regulator of fat uptake in mice and mutant human cellsKye‐Young Kim, Mark V. Stevens, M. Hasina Akter, Sarah E. Rusk, Robert J. Huang, Alexandra Cohen, Audrey C. Noguchi, Danielle Springer, Alexander V. Bocharov, Tomas L. Eggerman et al. · 2011 · Journal of Clinical Investigation
- Parkin-catalyzed Ubiquitin-Ester Transfer Is Triggered by PINK1-dependent PhosphorylationIguchi, Masahiro, Kujuro, Yuki, Okatsu, Kei, Koyano, Fumika, Kosako, Hidetaka, Kimura, Mayumi, Suzuki, Norihiro, Uchiyama, Shinichiro, Tanaka, Keiji, Matsuda, Noriyuki · 2013 · Journal of Biological Chemistry
- Dorfin Ubiquitylates Mutant SOD1 and Prevents Mutant SOD1-mediated NeurotoxicityJun-ichi Niwa, Shinsuke Ishigaki, Nozomi Hishikawa, Masahiko Yamamoto, Manabu Doyu, Shigeo Murata, Keiji Tanaka, Naoyuki Taniguchi, Gen Sobue · 2002 · Journal of Biological Chemistry
- Depletion of glial cell line-derived neurotrophic factor in substantia nigra neurons of Parkinson's disease brainNeelima B. Chauhan, George J. Siegel, John Michael Lee · 2001 · Journal of Chemical Neuroanatomy
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- Proteolytic stress: A unifying concept for the etiopathogenesis of Parkinson’s diseaseMcNaught, Kevin St. P., Olanow, C. Warren · 2003 · Annals of Neurology
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- Complex relationship between Parkin mutations and Parkinson diseaseAndrew B. West, Magali Periquet, Sarah Lincoln, Christoph B. Lücking, David Joseph Nicholl, Vincenzo Bonifati, Nina Rawal, Thomas Gasser, Ebba Lohmann, Jean‐François Deleuze et al. · 2002 · American Journal of Medical Genetics
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