A citation-based method for searching scientific literature

Justine Lebeau, T Kelly Rainbolt, R Luke Wiseman. Int Rev Cell Mol Biol 2018
Times Cited: 12







List of co-cited articles
77 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


ATP-dependent Lon protease controls tumor bioenergetics by reprogramming mitochondrial activity.
Pedro M Quirós, Yaiza Español, Rebeca Acín-Pérez, Francisco Rodríguez, Clea Bárcena, Kenta Watanabe, Enrique Calvo, Marta Loureiro, M Soledad Fernández-García, Antonio Fueyo,[...]. Cell Rep 2014
114
33

New roles for mitochondrial proteases in health, ageing and disease.
Pedro M Quirós, Thomas Langer, Carlos López-Otín. Nat Rev Mol Cell Biol 2015
284
33

Comparative Analysis of Mitochondrial N-Termini from Mouse, Human, and Yeast.
Sarah E Calvo, Olivier Julien, Karl R Clauser, Hongying Shen, Kimberli J Kamer, James A Wells, Vamsi K Mootha. Mol Cell Proteomics 2017
35
25

Defective PITRM1 mitochondrial peptidase is associated with Aβ amyloidotic neurodegeneration.
Dario Brunetti, Janniche Torsvik, Cristina Dallabona, Pedro Teixeira, Pawel Sztromwasser, Erika Fernandez-Vizarra, Raffaele Cerutti, Aurelio Reyes, Carmela Preziuso, Giulia D'Amati,[...]. EMBO Mol Med 2016
39
25

Cytosolic proteostasis through importing of misfolded proteins into mitochondria.
Linhao Ruan, Chuankai Zhou, Erli Jin, Andrei Kucharavy, Ying Zhang, Zhihui Wen, Laurence Florens, Rong Li. Nature 2017
218
25

Perrault syndrome is caused by recessive mutations in CLPP, encoding a mitochondrial ATP-dependent chambered protease.
Emma M Jenkinson, Atteeq U Rehman, Tom Walsh, Jill Clayton-Smith, Kwanghyuk Lee, Robert J Morell, Meghan C Drummond, Shaheen N Khan, Muhammad Asif Naeem, Bushra Rauf,[...]. Am J Hum Genet 2013
135
25

Mutations in LONP1, a mitochondrial matrix protease, cause CODAS syndrome.
Esra Dikoglu, Ali Alfaiz, Maria Gorna, Deborah Bertola, Jong Hee Chae, Tae-Joon Cho, Murat Derbent, Yasemin Alanay, Tulay Guran, Ok-Hwa Kim,[...]. Am J Med Genet A 2015
41
25

Global analysis of the mitochondrial N-proteome identifies a processing peptidase critical for protein stability.
F-Nora Vögtle, Stefanie Wortelkamp, René P Zahedi, Dorothea Becker, Claudia Leidhold, Kris Gevaert, Josef Kellermann, Wolfgang Voos, Albert Sickmann, Nikolaus Pfanner,[...]. Cell 2009
314
25

A mitochondrial protein compendium elucidates complex I disease biology.
David J Pagliarini, Sarah E Calvo, Betty Chang, Sunil A Sheth, Scott B Vafai, Shao-En Ong, Geoffrey A Walford, Canny Sugiana, Avihu Boneh, William K Chen,[...]. Cell 2008
25

CODAS syndrome is associated with mutations of LONP1, encoding mitochondrial AAA+ Lon protease.
Kevin A Strauss, Robert N Jinks, Erik G Puffenberger, Sundararajan Venkatesh, Kamalendra Singh, Iteen Cheng, Natalie Mikita, Jayapalraja Thilagavathi, Jae Lee, Stefan Sarafianos,[...]. Am J Hum Genet 2015
84
25


Structure of the mitochondrial inner membrane AAA+ protease YME1 gives insight into substrate processing.
Cristina Puchades, Anthony J Rampello, Mia Shin, Christopher J Giuliano, R Luke Wiseman, Steven E Glynn, Gabriel C Lander. Science 2017
107
25

AAA+ proteases: ATP-fueled machines of protein destruction.
Robert T Sauer, Tania A Baker. Annu Rev Biochem 2011
467
25

PINK1-dependent recruitment of Parkin to mitochondria in mitophagy.
Cristofol Vives-Bauza, Chun Zhou, Yong Huang, Mei Cui, Rosa L A de Vries, Jiho Kim, Jessica May, Maja Aleksandra Tocilescu, Wencheng Liu, Han Seok Ko,[...]. Proc Natl Acad Sci U S A 2010
25


Homozygous YME1L1 mutation causes mitochondriopathy with optic atrophy and mitochondrial network fragmentation.
Bianca Hartmann, Timothy Wai, Hao Hu, Thomas MacVicar, Luciana Musante, Björn Fischer-Zirnsak, Werner Stenzel, Ralph Gräf, Lambert van den Heuvel, Hans-Hilger Ropers,[...]. Elife 2016
62
16

Individuals with mutations in XPNPEP3, which encodes a mitochondrial protein, develop a nephronophthisis-like nephropathy.
John F O'Toole, Yangjian Liu, Erica E Davis, Christopher J Westlake, Massimo Attanasio, Edgar A Otto, Dominik Seelow, Gudrun Nurnberg, Christian Becker, Matti Nuutinen,[...]. J Clin Invest 2010
74
16

Deficiency of HTRA2/Omi is associated with infantile neurodegeneration and 3-methylglutaconic aciduria.
Hanna Mandel, Shotaro Saita, Simon Edvardson, Chaim Jalas, Avraham Shaag, Dorit Goldsher, Euvgeni Vlodavsky, Thomas Langer, Orly Elpeleg. J Med Genet 2016
22
16



Mutations in PMPCB Encoding the Catalytic Subunit of the Mitochondrial Presequence Protease Cause Neurodegeneration in Early Childhood.
F-Nora Vögtle, Björn Brändl, Austin Larson, Manuela Pendziwiat, Marisa W Friederich, Susan M White, Alice Basinger, Cansu Kücükköse, Hiltrud Muhle, Johanna A Jähn,[...]. Am J Hum Genet 2018
35
16

Autosomal recessive cerebellar ataxia caused by a homozygous mutation in PMPCA.
Karine Choquet, Olga Zurita-Rendón, Roberta La Piana, Sharon Yang, Marie-Josée Dicaire, Kym M Boycott, Jacek Majewski, Eric A Shoubridge, Bernard Brais, Martine Tétreault. Brain 2016
16
16

MIPEP recessive variants cause a syndrome of left ventricular non-compaction, hypotonia, and infantile death.
Mohammad K Eldomery, Zeynep C Akdemir, F-Nora Vögtle, Wu-Lin Charng, Patrycja Mulica, Jill A Rosenfeld, Tomasz Gambin, Shen Gu, Lindsay C Burrage, Aisha Al Shamsi,[...]. Genome Med 2016
26
16

PMPCA mutations cause abnormal mitochondrial protein processing in patients with non-progressive cerebellar ataxia.
Rebekah K Jobling, Mirna Assoum, Oleksandr Gakh, Susan Blaser, Julian A Raiman, Cyril Mignot, Emmanuel Roze, Alexandra Dürr, Alexis Brice, Nicolas Lévy,[...]. Brain 2015
38
16

Crystal structures of mitochondrial processing peptidase reveal the mode for specific cleavage of import signal sequences.
A B Taylor, B S Smith, S Kitada, K Kojima, H Miyaura, Z Otwinowski, A Ito, J Deisenhofer. Structure 2001
163
16


Silencing of mitochondrial Lon protease deeply impairs mitochondrial proteome and function in colon cancer cells.
Lara Gibellini, Marcello Pinti, Federica Boraldi, Valentina Giorgio, Paolo Bernardi, Regina Bartolomeo, Milena Nasi, Sara De Biasi, Sonia Missiroli, Gianluca Carnevale,[...]. FASEB J 2014
43
16


Targeting capacity and conservation of PreP homologues localization in mitochondria of different species.
Nyosha Alikhani, Anna-Karin Berglund, Tanja Engmann, Erika Spånning, F-Nora Vögtle, Pavel Pavlov, Chris Meisinger, Thomas Langer, Elzbieta Glaser. J Mol Biol 2011
31
16

Mitochondrial Quality Control Proteases in Neuronal Welfare.
Roman M Levytskyy, Edward M Germany, Oleh Khalimonchuk. J Neuroimmune Pharmacol 2016
20
16

Inhibition of the Mitochondrial Protease ClpP as a Therapeutic Strategy for Human Acute Myeloid Leukemia.
Alicia Cole, Zezhou Wang, Etienne Coyaud, Veronique Voisin, Marcela Gronda, Yulia Jitkova, Rachel Mattson, Rose Hurren, Sonja Babovic, Neil Maclean,[...]. Cancer Cell 2015
174
16

Multitasking in the mitochondrion by the ATP-dependent Lon protease.
Sundararajan Venkatesh, Jae Lee, Kamalendra Singh, Irene Lee, Carolyn K Suzuki. Biochim Biophys Acta 2012
109
16

Mutations in the mitochondrial protease gene AFG3L2 cause dominant hereditary ataxia SCA28.
Daniela Di Bella, Federico Lazzaro, Alfredo Brusco, Massimo Plumari, Giorgio Battaglia, Annalisa Pastore, Adele Finardi, Claudia Cagnoli, Filippo Tempia, Marina Frontali,[...]. Nat Genet 2010
210
16

Protein unfolding and degradation by the AAA+ Lon protease.
Eyal Gur, Marina Vishkautzan, Robert T Sauer. Protein Sci 2012
33
16

YME1L controls the accumulation of respiratory chain subunits and is required for apoptotic resistance, cristae morphogenesis, and cell proliferation.
Lukas Stiburek, Jana Cesnekova, Olga Kostkova, Daniela Fornuskova, Kamila Vinsova, Laszlo Wenchich, Josef Houstek, Jiri Zeman. Mol Biol Cell 2012
108
16

The crystal structure of apo-FtsH reveals domain movements necessary for substrate unfolding and translocation.
Christoph Bieniossek, Barbara Niederhauser, Ulrich M Baumann. Proc Natl Acad Sci U S A 2009
60
16


Substrate-engaged 26S proteasome structures reveal mechanisms for ATP-hydrolysis-driven translocation.
Andres H de la Peña, Ellen A Goodall, Stephanie N Gates, Gabriel C Lander, Andreas Martin. Science 2018
121
16

Reciprocal Degradation of YME1L and OMA1 Adapts Mitochondrial Proteolytic Activity during Stress.
T Kelly Rainbolt, Justine Lebeau, Cristina Puchades, R Luke Wiseman. Cell Rep 2016
87
16

Mechanical Protein Unfolding and Degradation.
Adrian O Olivares, Tania A Baker, Robert T Sauer. Annu Rev Physiol 2018
32
16

OPA1 processing controls mitochondrial fusion and is regulated by mRNA splicing, membrane potential, and Yme1L.
Zhiyin Song, Hsiuchen Chen, Maja Fiket, Christiane Alexander, David C Chan. J Cell Biol 2007
513
16

Ratchet-like polypeptide translocation mechanism of the AAA+ disaggregase Hsp104.
Stephanie N Gates, Adam L Yokom, JiaBei Lin, Meredith E Jackrel, Alexandrea N Rizo, Nathan M Kendsersky, Courtney E Buell, Elizabeth A Sweeny, Korrie L Mack, Edward Chuang,[...]. Science 2017
151
16

Control of mitochondrial biogenesis and function by the ubiquitin-proteasome system.
Piotr Bragoszewski, Michal Turek, Agnieszka Chacinska. Open Biol 2017
89
16

Mitochondrial division inhibitor-1 is neuroprotective in the A53T-α-synuclein rat model of Parkinson's disease.
Simone Bido, Federico N Soria, Rebecca Z Fan, Erwan Bezard, Kim Tieu. Sci Rep 2017
52
16

Drp1 inhibition attenuates neurotoxicity and dopamine release deficits in vivo.
Phillip M Rappold, Mei Cui, Jonathan C Grima, Rebecca Z Fan, Karen L de Mesy-Bentley, Linan Chen, Xiaoxi Zhuang, William J Bowers, Kim Tieu. Nat Commun 2014
116
16

Inhibition of Drp1 Ameliorates Synaptic Depression, Aβ Deposition, and Cognitive Impairment in an Alzheimer's Disease Model.
Seung Hyun Baek, So Jung Park, Jae In Jeong, Sung Hyun Kim, Jihoon Han, Jae Won Kyung, Sang-Ha Baik, Yuri Choi, Bo Youn Choi, Jin Su Park,[...]. J Neurosci 2017
96
16

Inhibition of mitochondrial fragmentation protects against Alzheimer's disease in rodent model.
Wenzhang Wang, Jun Yin, Xiaopin Ma, Fanpeng Zhao, Sandra L Siedlak, Zhenlian Wang, Sandy Torres, Hisashi Fujioka, Ying Xu, George Perry,[...]. Hum Mol Genet 2017
58
16

Mitophagy and Quality Control Mechanisms in Mitochondrial Maintenance.
Sarah Pickles, Pierre Vigié, Richard J Youle. Curr Biol 2018
584
16

Oxidative Stress in Neurodegenerative Diseases: From a Mitochondrial Point of View.
Giovanna Cenini, Ana Lloret, Roberta Cascella. Oxid Med Cell Longev 2019
147
16

Mutant huntingtin binds the mitochondrial fission GTPase dynamin-related protein-1 and increases its enzymatic activity.
Wenjun Song, Jin Chen, Alejandra Petrilli, Geraldine Liot, Eva Klinglmayr, Yue Zhou, Patrick Poquiz, Jonathan Tjong, Mahmoud A Pouladi, Michael R Hayden,[...]. Nat Med 2011
357
16


Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.