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Tatsuta, T.; Augustin, S.; Nolden, M.; Friedrichs, B.; Langer, T.: m-AAA protease-driven membrane dislocation allows intramembrane cleavage by rhomboid in mitochondria. EMBO J 26 (2), pp. 325 - 35 (2007)

Osman, C.; Wilmes, C.; Tatsuta, T.; Langer, T.: Prohibitins interact genetically with Atp23, a novel processing peptidase and chaperone for the F1Fo-ATP synthase. Mol Biol Cell 18 (2), pp. 627 - 35 (2006)

Koppen, M.; Metodiev, M. D.; Casari, G.; Rugarli, E. I.; Langer, T.: Variable and tissue-specific subunit composition of mitochondrial m-AAA protease complexes linked to hereditary spastic paraplegia. Mol Cell Biol 27 (2), pp. 758 - 67 (2006)

Durr, M.; Escobar-Henriques, M.; Merz, S.; Geimer, S.; Langer, T.; Westermann, B.: Nonredundant roles of mitochondria-associated F-box proteins Mfb1 and Mdm30 in maintenance of mitochondrial morphology in yeast. Mol Biol Cell 17 (9), pp. 3745 - 55 (2006)

Escobar-Henriques, M.; Westermann, B.; Langer, T.: Regulation of mitochondrial fusion by the F-box protein Mdm30 involves proteasome-independent turnover of Fzo1. J Cell Biol 173 (5), pp. 645 - 50 (2006)

Escobar-Henriques, M.; Langer, T.: Mitochondrial shaping cuts. Biochim Biophys Acta 1763 (5-6), pp. 422 - 9 (2006)

Rugarli, E. I.; Langer, T.: Translating m-AAA protease function in mitochondria to hereditary spastic paraplegia. Trends Mol Med 12 (6), pp. 262 - 9 (2006)

Graef, M.; Langer, T.: Substrate specific consequences of central pore mutations in the i-AAA protease Yme1 on substrate engagement. J Struct Biol 156 (1), pp. 101 - 8 (2006)

Arnold, I.; Wagner-Ecker, M.; Ansorge, W.; Langer, T.: Evidence for a novel mitochondria-to-nucleus signalling pathway in respiring cells lacking i-AAA protease and the ABC-transporter Mdl1. Gene 367, pp. 74 - 88 (2006)

Nolden, M.; Kisters-Woike, B.; Langer, T.; Graef, M.: Quality control in the mitochondrion. Topics in Current Genetics 16, pp. 119 - 147 (2006)

Nolden, M.; Ehses, S.; Koppen, M.; Bernacchia, A.; Rugarli, E. I.; Langer, T.: The m-AAA protease defective in hereditary spastic paraplegia controls ribosome assembly in mitochondria. Cell 123 (2), pp. 277 - 89 (2005)

Kambacheld, M.; Augustin, S.; Tatsuta, T.; Muller, S.; Langer, T.: Role of the novel metallopeptidase Mop112 and saccharolysin for the complete degradation of proteins residing in different subcompartments of mitochondria. J Biol Chem 280 (20), pp. 20132 - 9 (2005)

Nolden, M.; Ehses, S.; Koppen, M.; Bernacchia, A.; Rugarli, E. I.; Langer, T.: The m-AAA Protease Defective in Hereditary Spastic Paraplegia Controls Ribosome Assembly in Mitochondria. Cell 123, pp. 277 - 289 (2005)

Augustin, S.; Nolden, M.; Muller, S.; Hardt, O.; Arnold, I.; Langer, T.: Characterization of peptides released from mitochondria: evidence for constant proteolysis and peptide efflux. J Biol Chem 280 (4), pp. 2691 - 9 (2004)

Tatsuta, T.; Model, K.; Langer, T.: Formation of membrane-bound ring complexes by prohibitins in mitochondria. Mol Biol Cell 16 (1), pp. 248 - 59 (2004)

Galluhn, D.; Langer, T.: Reversible assembly of the ATP-binding cassette transporter Mdl1 with the F1F0-ATP synthase in mitochondria. J Biol Chem 279 (37), pp. 38338 - 45 (2004)

Korbel, D.; Wurth, S.; Kaser, M.; Langer, T.: Membrane protein turnover by the m-AAA protease in mitochondria depends on the transmembrane domains of its subunits. EMBO Rep 5 (7), pp. 698 - 703 (2004)

Atorino, L.; Silvestri, L.; Koppen, M.; Cassina, L.; Ballabio, A.; Marconi, R.; Langer, T.; Casari, G.: Loss of m-AAA protease in mitochondria causes complex I deficiency and increased sensitivity to oxidative stress in hereditary spastic paraplegia. J Cell Biol 163 (4), pp. 777 - 87 (2003)

Kaser, M.; Kambacheld, M.; Kisters-Woike, B.; Langer, T.: Oma1, a novel membrane-bound metallopeptidase in mitochondria with activities overlapping with the m-AAA protease. J Biol Chem 278 (47), pp. 46414 - 23 (2003)