A citation-based method for searching scientific literature

Takashi Tatsuta, Steffen Augustin, Mark Nolden, Björn Friedrichs, Thomas Langer. EMBO J 2007
Times Cited: 86







List of co-cited articles
1086 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


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
46

A novel two-step mechanism for removal of a mitochondrial signal sequence involves the mAAA complex and the putative rhomboid protease Pcp1.
Karlheinz Esser, Baris Tursun, Martin Ingenhoven, Georg Michaelis, Elke Pratje. J Mol Biol 2002
135
39

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

Processing of Mgm1 by the rhomboid-type protease Pcp1 is required for maintenance of mitochondrial morphology and of mitochondrial DNA.
Mark Herlan, Frank Vogel, Carsten Bornhovd, Walter Neupert, Andreas S Reichert. J Biol Chem 2003
285
37


Mitochondrial membrane remodelling regulated by a conserved rhomboid protease.
G Angus McQuibban, Saroj Saurya, Matthew Freeman. Nature 2003
298
33

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
33

Spastic paraplegia and OXPHOS impairment caused by mutations in paraplegin, a nuclear-encoded mitochondrial metalloprotease.
G Casari, M De Fusco, S Ciarmatori, M Zeviani, M Mora, P Fernandez, G De Michele, A Filla, S Cocozza, R Marconi,[...]. Cell 1998
600
31


Alternative topogenesis of Mgm1 and mitochondrial morphology depend on ATP and a functional import motor.
Mark Herlan, Carsten Bornhövd, Kai Hell, Walter Neupert, Andreas S Reichert. J Cell Biol 2004
180
27

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
44

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
25


Mitochondrial rhomboid PARL regulates cytochrome c release during apoptosis via OPA1-dependent cristae remodeling.
Sara Cipolat, Tomasz Rudka, Dieter Hartmann, Veronica Costa, Lutgarde Serneels, Katleen Craessaerts, Kristine Metzger, Christian Frezza, Wim Annaert, Luciano D'Adamio,[...]. Cell 2006
524
24


Axonal degeneration in paraplegin-deficient mice is associated with abnormal mitochondria and impairment of axonal transport.
Fatima Ferreirinha, Angelo Quattrini, Marinella Pirozzi, Valentina Valsecchi, Giorgia Dina, Vania Broccoli, Alberto Auricchio, Fiorella Piemonte, Giulia Tozzi, Laura Gaeta,[...]. J Clin Invest 2004
206
23

Regulation of mitochondrial morphology through proteolytic cleavage of OPA1.
Naotada Ishihara, Yuu Fujita, Toshihiko Oka, Katsuyoshi Mihara. EMBO J 2006
588
23

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
25

Loss of m-AAA protease in mitochondria causes complex I deficiency and increased sensitivity to oxidative stress in hereditary spastic paraplegia.
Luigia Atorino, Laura Silvestri, Mirko Koppen, Laura Cassina, Andrea Ballabio, Roberto Marconi, Thomas Langer, Giorgio Casari. J Cell Biol 2003
191
20

Chaperone-like activity of the AAA domain of the yeast Yme1 AAA protease.
K Leonhard, A Stiegler, W Neupert, T Langer. Nature 1999
162
20

Translocation of proteins into mitochondria.
Walter Neupert, Johannes M Herrmann. Annu Rev Biochem 2007
997
19



A new function in translocation for the mitochondrial i-AAA protease Yme1: import of polynucleotide phosphorylase into the intermembrane space.
Robert N Rainey, Jenny D Glavin, Hsiao-Wen Chen, Samuel W French, Michael A Teitell, Carla M Koehler. Mol Cell Biol 2006
76
21

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
20

Characterization of peptides released from mitochondria: evidence for constant proteolysis and peptide efflux.
Steffen Augustin, Mark Nolden, Stefan Müller, Olaf Hardt, Isabel Arnold, Thomas Langer. J Biol Chem 2005
78
19

Structure of the whole cytosolic region of ATP-dependent protease FtsH.
Ryoji Suno, Hajime Niwa, Daisuke Tsuchiya, Xiaodong Zhang, Masasuke Yoshida, Kosuke Morikawa. Mol Cell 2006
102
17

OPA1 processing reconstituted in yeast depends on the subunit composition of the m-AAA protease in mitochondria.
Stéphane Duvezin-Caubet, Mirko Koppen, Johannes Wagener, Michael Zick, Lars Israel, Andrea Bernacchia, Ravi Jagasia, Elena I Rugarli, Axel Imhof, Walter Neupert,[...]. Mol Biol Cell 2007
142
17

Autocatalytic processing of m-AAA protease subunits in mitochondria.
Mirko Koppen, Florian Bonn, Sarah Ehses, Thomas Langer. Mol Biol Cell 2009
37
40

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
34

Regulation of mitochondrial phospholipids by Ups1/PRELI-like proteins depends on proteolysis and Mdm35.
Christoph Potting, Claudia Wilmes, Tanja Engmann, Christof Osman, Thomas Langer. EMBO J 2010
117
17


Mitochondrial AAA proteases--towards a molecular understanding of membrane-bound proteolytic machines.
Florian Gerdes, Takashi Tatsuta, Thomas Langer. Biochim Biophys Acta 2012
86
16


AAA+ proteins: have engine, will work.
Phyllis I Hanson, Sidney W Whiteheart. Nat Rev Mol Cell Biol 2005
803
15



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
15


Mgr3p and Mgr1p are adaptors for the mitochondrial i-AAA protease complex.
Cory D Dunn, Yasushi Tamura, Hiromi Sesaki, Robert E Jensen. Mol Biol Cell 2008
41
31

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
15





Genetic interaction between the m-AAA protease isoenzymes reveals novel roles in cerebellar degeneration.
Paola Martinelli, Veronica La Mattina, Andrea Bernacchia, Raffaella Magnoni, Federica Cerri, Gregory Cox, Angelo Quattrini, Giorgio Casari, Elena I Rugarli. Hum Mol Genet 2009
41
29

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
15

Regulation of OPA1 processing and mitochondrial fusion by m-AAA protease isoenzymes and OMA1.
Sarah Ehses, Ines Raschke, Giuseppe Mancuso, Andrea Bernacchia, Stefan Geimer, Daniel Tondera, Jean-Claude Martinou, Benedikt Westermann, Elena I Rugarli, Thomas Langer. J Cell Biol 2009
372
13

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
16

Oma1, a novel membrane-bound metallopeptidase in mitochondria with activities overlapping with the m-AAA protease.
Michael Kaser, Melanie Kambacheld, Brigitte Kisters-Woike, Thomas Langer. J Biol Chem 2003
111
12


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.