A citation-based method for searching scientific literature

Florian Bonn, Takashi Tatsuta, Carmelina Petrungaro, Jan Riemer, Thomas Langer. EMBO J 2011
Times Cited: 55







List of co-cited articles
855 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
278
70

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
43

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
214
36

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
119
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
145
34


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
607
34

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
137
32

Translocation of proteins into mitochondria.
Walter Neupert, Johannes M Herrmann. Annu Rev Biochem 2007
32

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
385
32


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
323
30

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
138
29

Mitochondrial AAA proteases--towards a molecular understanding of membrane-bound proteolytic machines.
Florian Gerdes, Takashi Tatsuta, Thomas Langer. Biochim Biophys Acta 2012
87
29

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
287
27

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

Mitochondrial protein turnover: role of the precursor intermediate peptidase Oct1 in protein stabilization.
F-Nora Vögtle, Claudia Prinz, Josef Kellermann, Friedrich Lottspeich, Nikolaus Pfanner, Chris Meisinger. Mol Biol Cell 2011
83
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
140
25

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
533
25

Quality control of mitochondrial proteostasis.
Michael J Baker, Takashi Tatsuta, Thomas Langer. Cold Spring Harb Perspect Biol 2011
192
23

Importing mitochondrial proteins: machineries and mechanisms.
Agnieszka Chacinska, Carla M Koehler, Dusanka Milenkovic, Trevor Lithgow, Nikolaus Pfanner. Cell 2009
897
23

Inducible proteolytic inactivation of OPA1 mediated by the OMA1 protease in mammalian cells.
Brian Head, Lorena Griparic, Mandana Amiri, Shilpa Gandre-Babbe, Alexander M van der Bliek. J Cell Biol 2009
321
23

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
74
23


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
45
26


Chaperone-like activity of the AAA domain of the yeast Yme1 AAA protease.
K Leonhard, A Stiegler, W Neupert, T Langer. Nature 1999
164
21

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
21

Regulation of the mitochondrial dynamin-like protein Opa1 by proteolytic cleavage.
Lorena Griparic, Takayuki Kanazawa, Alexander M van der Bliek. J Cell Biol 2007
331
21

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
110
21

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
407
21

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
192
20

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
113
20

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
20

Mitochondrial membrane remodelling regulated by a conserved rhomboid protease.
G Angus McQuibban, Saroj Saurya, Matthew Freeman. Nature 2003
302
20

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
79
18




The proteome of Saccharomyces cerevisiae mitochondria.
Albert Sickmann, Jörg Reinders, Yvonne Wagner, Cornelia Joppich, René Zahedi, Helmut E Meyer, Birgit Schönfisch, Inge Perschil, Agnieszka Chacinska, Bernard Guiard,[...]. Proc Natl Acad Sci U S A 2003
658
18

Regulation of mitochondrial morphology through proteolytic cleavage of OPA1.
Naotada Ishihara, Yuu Fujita, Toshihiko Oka, Katsuyoshi Mihara. EMBO J 2006
601
18

The matrix peptide exporter HAF-1 signals a mitochondrial UPR by activating the transcription factor ZC376.7 in C. elegans.
Cole M Haynes, Yun Yang, Steven P Blais, Thomas A Neubert, David Ron. Mol Cell 2010
339
18

Processing of mitochondrial presequences.
Dirk Mossmann, Chris Meisinger, F-Nora Vögtle. Biochim Biophys Acta 2012
110
18

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
16


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
59
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
41
21

Mitochondrial processing peptidases.
Oleksandr Gakh, Patrizia Cavadini, Grazia Isaya. Biochim Biophys Acta 2002
284
16

Prohibitins interact genetically with Atp23, a novel processing peptidase and chaperone for the F1Fo-ATP synthase.
Christof Osman, Claudia Wilmes, Takashi Tatsuta, Thomas Langer. Mol Biol Cell 2007
104
16

Mitochondrial membrane potential regulates PINK1 import and proteolytic destabilization by PARL.
Seok Min Jin, Michael Lazarou, Chunxin Wang, Lesley A Kane, Derek P Narendra, Richard J Youle. J Cell Biol 2010
774
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.