Publikationen

Wang, S.; Jacquemyn, J.; Murru, S.; Martinelli, P.; Barth, E.; Langer, T.; Niessen, C. M.; Rugarli, E. I.: The Mitochondrial m-AAA Protease Prevents Demyelination and Hair Greying. PLoS Genet 12 (12), S. e1006463 (2016)

Wai, T.; Saita, S.; Nolte, H.; Muller, S.; Konig, T.; Richter-Dennerlein, R.; Sprenger, H.-G.; Madrenas, J.; Muhlmeister, M.; Brandt, U. et al.; Kruger, M.; Langer, T.: The membrane scaffold SLP2 anchors a proteolytic hub in mitochondria containing PARL and the i-AAA protease YME1L. EMBO Rep 17 (12), S. 1844 - 1856 (2016)

Koenig, T.; Troder, S. E.; Bakka, K.; Korwitz, A.; Richter-Dennerlein, R.; Lampe, P. A.; Patron, M.; Muhlmeister, M.; Guerrero-Castillo, S.; Brandt, U. et al.; Decker, T.; Lauria, I.; Paggio, A.; Rizzuto, R.; Rugarli, E. I.; De Stefani, D.; Langer, T.: The m-AAA Protease Associated with Neurodegeneration Limits MCU Activity in Mitochondria. Mol Cell 64 (1), S. 148 - 162 (2016)

Tatsuta, T.; Langer, T.: Intramitochondrial phospholipid trafficking. Biochim Biophys Acta 1862 (1), S. 81 - 89 (2016)

Hartmann, B.; Wai, T.; Hu, H.; MacVicar, T.; Musante, L.; Fischer-Zirnsak, B.; Stenzel, W.; Graf, R.; van den Heuvel, L.; Ropers, H. H. et al.; Wienker, T. F.; Hubner, C.; Langer, T.; Kaindl, A. M.: Homozygous YME1L1 mutation causes mitochondriopathy with optic atrophy and mitochondrial network fragmentation. Elife 5 (2016)

Aaltonen, M. J.; Friedman, J. R.; Osman, C.; Salin, B.; di Rago, J. P.; Nunnari, J.; Langer, T.; Tatsuta, T.: MICOS and phospholipid transfer by Ups2-Mdm35 organize membrane lipid synthesis in mitochondria. J Cell Biol 213 (5), S. 525 - 34 (2016)

Mandel, H.; Saita, S.; Edvardson, S.; Jalas, C.; Shaag, A.; Goldsher, D.; Vlodavsky, E.; Langer, T.; Elpeleg, O.: Deficiency of HTRA2/Omi is associated with infantile neurodegeneration and 3-methylglutaconic aciduria. J Med Genet 53 (10), S. 690 - 6 (2016)

MacVicar, T.; Langer, T.: OPA1 processing in cell death and disease - the long and short of it. J Cell Sci 129 (12), S. 2297 - 306 (2016)

Korwitz, A.; Merkwirth, C.; Richter-Dennerlein, R.; Troder, S. E.; Sprenger, H.-G.; Quiros, P. M.; Lopez-Otin, C.; Rugarli, E. I.; Langer, T.: Loss of OMA1 delays neurodegeneration by preventing stress-induced OPA1 processing in mitochondria. J Cell Biol 212 (2), S. 157 - 66 (2016)

Wai, T.; Garcia-Prieto, J.; Baker, M. J.; Merkwirth, C.; Benit, P.; Rustin, P.; Ruperez, F. J.; Barbas, C.; Ibanez, B.; Langer, T.: Imbalanced OPA1 processing and mitochondrial fragmentation cause heart failure in mice. Science 350 (6265), S. aad0116 (2016)

Wai, T.; Langer, T.: Mitochondrial Dynamics and Metabolic Regulation. Trends Endocrinol Metab 27 (2), S. 105 - 17 (2016)

Velazquez, A.; Tatsuta, T.; Ghillebert, R.; Drescher, I.; Graef, M.: Lipid droplet-mediated ER homeostasis regulates autophagy and cell survival during starvation. J Cell Biol 212 (6), S. 621 - 31 (2016)