Publikationen

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), S. 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), S. 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, S. 277 - 289 (2005)