A citation-based method for searching scientific literature

H Arlt, R Tauer, H Feldmann, W Neupert, T Langer. Cell 1996
Times Cited: 240







List of co-cited articles
1077 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
272
52

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
40


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
599
36

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
33


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
32

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
208
27

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
189
25

Chaperone-like activity of the AAA domain of the yeast Yme1 AAA protease.
K Leonhard, A Stiegler, W Neupert, T Langer. Nature 1999
162
25

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
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
204
22



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
77
25

Translocation of proteins into mitochondria.
Walter Neupert, Johannes M Herrmann. Annu Rev Biochem 2007
989
19

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
366
19


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
24

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
52
34

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
283
17

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
75
22

AAA+ proteins: have engine, will work.
Phyllis I Hanson, Sidney W Whiteheart. Nat Rev Mol Cell Biol 2005
798
16

Regulation of mitochondrial morphology through proteolytic cleavage of OPA1.
Naotada Ishihara, Yuu Fujita, Toshihiko Oka, Katsuyoshi Mihara. EMBO J 2006
580
16


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
40
40

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
75
21

Autocatalytic processing of m-AAA protease subunits in mitochondria.
Mirko Koppen, Florian Bonn, Sarah Ehses, Thomas Langer. Mol Biol Cell 2009
37
43

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
77
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
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
36


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

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



Importing mitochondrial proteins: machineries and mechanisms.
Agnieszka Chacinska, Carla M Koehler, Dusanka Milenkovic, Trevor Lithgow, Nikolaus Pfanner. Cell 2009
871
14

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
114
14

Proteomic analysis of mitochondrial protein turnover: identification of novel substrate proteins of the matrix protease pim1.
Tamara Major, Birgit von Janowsky, Thomas Ruppert, Axel Mogk, Wolfgang Voos. Mol Cell Biol 2006
81
16


Mitochondrial AAA proteases--towards a molecular understanding of membrane-bound proteolytic machines.
Florian Gerdes, Takashi Tatsuta, Thomas Langer. Biochim Biophys Acta 2012
83
15

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
18

The molecular architecture of the metalloprotease FtsH.
Christoph Bieniossek, Thomas Schalch, Mario Bumann, Markus Meister, Reto Meier, Ulrich Baumann. Proc Natl Acad Sci U S A 2006
109
12

A genomewide screen for petite-negative yeast strains yields a new subunit of the i-AAA protease complex.
Cory D Dunn, Marina S Lee, Forrest A Spencer, Robert E Jensen. Mol Biol Cell 2006
57
21

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
81
14

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
141
12

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
507
12

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
109
12

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
310
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.