Publikationen

Lee, S.; Augustin, S.; Tatsuta, T.; Gerdes, F.; Langer, T.; Tsai, F. T.: Electron cryomicroscopy structure of a membrane-anchored mitochondrial AAA protease. J Biol Chem 286 (6), S. 4404 - 11 (2010)

Brüning, J.; Langer, T.; Trifunovic, A.: Highlight: The biology of aging: mechanisms and intervention. Biol Chem 391 (10), S. 1113 (2010)

Potting, C.; Wilmes, C.; Engmann, T.; Osman, C.; Langer, T.: Regulation of mitochondrial phospholipids by Ups1/PRELI-like proteins depends on proteolysis and Mdm35. EMBO J 29 (17), S. 2888 - 98 (2010)

Osman, C.; Haag, M.; Wieland, F. T.; Brugger, B.; Langer, T.: A mitochondrial phosphatase required for cardiolipin biosynthesis: the PGP phosphatase Gep4. EMBO J 29 (12), S. 1976 - 87 (2010)

Di Bella, D.; Lazzaro, F.; Brusco, A.; Plumari, M.; Battaglia, G.; Pastore, A.; Finardi, A.; Cagnoli, C.; Tempia, F.; Frontali, M. et al.; Veneziano, L.; Sacco, T.; Boda, E.; Brussino, A.; Bonn, F.; Castellotti, B.; Baratta, S.; Mariotti, C.; Gellera, C.; Fracasso, V.; Magri, S.; Langer, T.; Plevani, P.; Di Donato, S.; Muzi-Falconi, M.; Taroni, F.: Mutations in the mitochondrial protease gene AFG3L2 cause dominant hereditary ataxia SCA28. Nat Genet 42 (4), S. 313 - 21 (2010)

Bonn, F.; Pantakani, K.; Shoukier, M.; Langer, T.; Mannan, A. U.: Functional evaluation of paraplegin mutations by a yeast complementation assay. Hum Mutat 31 (5), S. 617 - 21 (2010)