A citation-based method for searching scientific literature

Bojian Ding, Dwight W Martin, Anthony J Rampello, Steven E Glynn. Biochemistry 2018
Times Cited: 8







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



Times Cited
  Times     Co-cited
Similarity


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
75


Variable and tissue-specific subunit composition of mitochondrial m-AAA protease complexes linked to hereditary spastic paraplegia.
Mirko Koppen, Metodi D Metodiev, Giorgio Casari, Elena I Rugarli, Thomas Langer. Mol Cell Biol 2007
133
62


The m-AAA protease defective in hereditary spastic paraplegia controls ribosome assembly in mitochondria.
Mark Nolden, Sarah Ehses, Mirko Koppen, Andrea Bernacchia, Elena I Rugarli, Thomas Langer. Cell 2005
276
50

An intersubunit signaling network coordinates ATP hydrolysis by m-AAA proteases.
Steffen Augustin, Florian Gerdes, Sukyeong Lee, Francis T F Tsai, Thomas Langer, Takashi Tatsuta. Mol Cell 2009
74
50

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
50

Imbalanced OPA1 processing and mitochondrial fragmentation cause heart failure in mice.
Timothy Wai, Jaime García-Prieto, Michael J Baker, Carsten Merkwirth, Paule Benit, Pierre Rustin, Francisco Javier Rupérez, Coral Barbas, Borja Ibañez, Thomas Langer. Science 2015
238
50

m-AAA protease-driven membrane dislocation allows intramembrane cleavage by rhomboid in mitochondria.
Takashi Tatsuta, Steffen Augustin, Mark Nolden, Björn Friedrichs, Thomas Langer. EMBO J 2007
86
50

The i-AAA protease YME1L and OMA1 cleave OPA1 to balance mitochondrial fusion and fission.
Ruchika Anand, Timothy Wai, Michael J Baker, Nikolay Kladt, Astrid C Schauss, Elena Rugarli, Thomas Langer. J Cell Biol 2014
385
50

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
50

Metalloproteases of the Inner Mitochondrial Membrane.
Roman M Levytskyy, Iryna Bohovych, Oleh Khalimonchuk. Biochemistry 2017
26
37

SCA28, a novel form of autosomal dominant cerebellar ataxia on chromosome 18p11.22-q11.2.
Claudia Cagnoli, Caterina Mariotti, Franco Taroni, Marco Seri, Alessandro Brussino, Chiara Michielotto, Marina Grisoli, Daniela Di Bella, Nicola Migone, Cinzia Gellera,[...]. Brain 2006
82
37

Spinocerebellar ataxia type 28: a novel autosomal dominant cerebellar ataxia characterized by slow progression and ophthalmoparesis.
Caterina Mariotti, Alfredo Brusco, Daniela Di Bella, Claudia Cagnoli, Marco Seri, Cinzia Gellera, Stefano Di Donato, Franco Taroni. Cerebellum 2008
37
37

AFG3L2 supports mitochondrial protein synthesis and Purkinje cell survival.
Eva R Almajan, Ricarda Richter, Lars Paeger, Paola Martinelli, Esther Barth, Thorsten Decker, Nils-Göran Larsson, Peter Kloppenburg, Thomas Langer, Elena I Rugarli. J Clin Invest 2012
72
37


Electron cryomicroscopy structure of a membrane-anchored mitochondrial AAA protease.
Sukyeong Lee, Steffen Augustin, Takashi Tatsuta, Florian Gerdes, Thomas Langer, Francis T F Tsai. J Biol Chem 2011
43
37


The mitochondrial protease AFG3L2 is essential for axonal development.
Francesca Maltecca, Asadollah Aghaie, David G Schroeder, Laura Cassina, Benjamin A Taylor, Sandra J Phillips, Mariachiara Malaguti, Stefano Previtali, Jean-Louis Guénet, Angelo Quattrini,[...]. J Neurosci 2008
78
37

Haploinsufficiency of AFG3L2, the gene responsible for spinocerebellar ataxia type 28, causes mitochondria-mediated Purkinje cell dark degeneration.
Francesca Maltecca, Raffaella Magnoni, Federica Cerri, Gregory A Cox, Angelo Quattrini, Giorgio Casari. J Neurosci 2009
76
37

Membrane protein degradation by AAA proteases in mitochondria: extraction of substrates from either membrane surface.
K Leonhard, B Guiard, G Pellecchia, A Tzagoloff, W Neupert, T Langer. Mol Cell 2000
142
37

Multifunctional Mitochondrial AAA Proteases.
Steven E Glynn. Front Mol Biosci 2017
31
37

Spinocerebellar ataxia 28: a novel AFG3L2 mutation in a German family with young onset, slow progression and saccadic slowing.
Christine Zühlke, Barbara Mikat, Dagmar Timmann, Dagmar Wieczorek, Gabriele Gillessen-Kaesbach, Katrin Bürk. Cerebellum Ataxias 2015
15
37

A novel missense mutation in AFG3L2 associated with late onset and slow progression of spinocerebellar ataxia type 28.
Anna Mareike Löbbe, Jun-Suk Kang, Rüdiger Hilker, Holger Hackstein, Ulrich Müller, Dagmar Nolte. J Mol Neurosci 2014
18
37

The m-AAA Protease Associated with Neurodegeneration Limits MCU Activity in Mitochondria.
Tim König, Simon E Tröder, Kavya Bakka, Anne Korwitz, Ricarda Richter-Dennerlein, Philipp A Lampe, Maria Patron, Mareike Mühlmeister, Sergio Guerrero-Castillo, Ulrich Brandt,[...]. Mol Cell 2016
92
37


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
37



Evolutionary relationships and structural mechanisms of AAA+ proteins.
Jan P Erzberger, James M Berger. Annu Rev Biophys Biomol Struct 2006
516
37

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
37

Mechanism of DNA translocation in a replicative hexameric helicase.
Eric J Enemark, Leemor Joshua-Tor. Nature 2006
380
37

YME1L degradation reduces mitochondrial proteolytic capacity during oxidative stress.
T Kelly Rainbolt, Jaclyn M Saunders, R Luke Wiseman. EMBO Rep 2015
47
37

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
37

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
37

Structural basis of protein translocation by the Vps4-Vta1 AAA ATPase.
Nicole Monroe, Han Han, Peter S Shen, Wesley I Sundquist, Christopher P Hill. Elife 2017
74
37

Structure and function of the AAA+ nucleotide binding pocket.
Petra Wendler, Susanne Ciniawsky, Malte Kock, Sebastian Kube. Biochim Biophys Acta 2012
179
37

AAA+ proteases: ATP-fueled machines of protein destruction.
Robert T Sauer, Tania A Baker. Annu Rev Biochem 2011
467
37

The membrane scaffold SLP2 anchors a proteolytic hub in mitochondria containing PARL and the i-AAA protease YME1L.
Timothy Wai, Shotaro Saita, Hendrik Nolte, Sebastian Müller, Tim König, Ricarda Richter-Dennerlein, Hans-Georg Sprenger, Joaquin Madrenas, Mareike Mühlmeister, Ulrich Brandt,[...]. EMBO Rep 2016
87
25

Stress-regulated translational attenuation adapts mitochondrial protein import through Tim17A degradation.
T Kelly Rainbolt, Neli Atanassova, Joseph C Genereux, R Luke Wiseman. Cell Metab 2013
99
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
25

Presequence-dependent folding ensures MrpL32 processing by the m-AAA protease in mitochondria.
Florian Bonn, Takashi Tatsuta, Carmelina Petrungaro, Jan Riemer, Thomas Langer. EMBO J 2011
54
25

m-AAA proteases, mitochondrial calcium homeostasis and neurodegeneration.
Maria Patron, Hans-Georg Sprenger, Thomas Langer. Cell Res 2018
45
25

Whole-exome sequencing identifies homozygous AFG3L2 mutations in a spastic ataxia-neuropathy syndrome linked to mitochondrial m-AAA proteases.
Tyler Mark Pierson, David Adams, Florian Bonn, Paola Martinelli, Praveen F Cherukuri, Jamie K Teer, Nancy F Hansen, Pedro Cruz, James C Mullikin For The Nisc Comparative Sequencing Program, Robert W Blakesley,[...]. PLoS Genet 2011
137
25

Evidence for a pro-oxidant intermediate in the assembly of cytochrome oxidase.
Oleh Khalimonchuk, Amanda Bird, Dennis R Winge. J Biol Chem 2007
84
25


When, how and why? Regulated proteolysis by the essential FtsH protease in Escherichia coli.
Lisa-Marie Bittner, Jan Arends, Franz Narberhaus. Biol Chem 2017
39
25

Mechanisms Orchestrating Mitochondrial Dynamics for Energy Homeostasis.
Seungyoon B Yu, Gulcin Pekkurnaz. J Mol Biol 2018
60
25

Mitochondrial dynamics: overview of molecular mechanisms.
Lisa Tilokani, Shun Nagashima, Vincent Paupe, Julien Prudent. Essays Biochem 2018
323
25

Mitochondrial Tim9 protects Tim10 from degradation by the protease Yme1.
Michael P Spiller, Liang Guo, Qi Wang, Peter Tran, Hui Lu. Biosci Rep 2015
9
25


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.