Publikationen von N.G. Larsson

Bruton, J. D.; Place, N.; Yamada, T.; Silva, J. P.; Andrade, F. H.; Dahlstedt, A. J.; Zhang, S. J.; Katz, A.; Larsson, N.G.; Westerblad, H.: Reactive oxygen species and fatigue-induced prolonged low-frequency force depression in skeletal muscle fibres of rats, mice and SOD2 overexpressing mice. J Physiol 586 (1), S. 175 - 84 (2007)

Freyer, C.; Larsson, N.G.: Is energy deficiency good in moderation? Cell 131 (3), S. 448 - 50 (2007)

Niu, X.; Trifunovic, A.; Larsson, N.G.; Canlon, B.: Somatic mtDNA mutations cause progressive hearing loss in the mouse. Exp Cell Res 313 (18), S. 3924 - 34 (2007)

Park, C.B.; Asin-Cayuela, J.; Camara, Y.; Shi, Y.; Pellegrini, M.; Gaspari, M.; Wibom, R.; Hultenby, K.; Erdjument-Bromage, H.; Tempst, P. et al.; Falkenberg, M.; Gustafsson, C. M.; Larsson, N.G.: MTERF3 is a negative regulator of mammalian mtDNA transcription. Cell 130 (2), S. 273 - 85 (2007)

Falkenberg, M.; Larsson, N.G.; Gustafsson, C. M.: DNA replication and transcription in mammalian mitochondria. Annu Rev Biochem 76, S. 679 - 99 (2007)

Ekstrand, M. I.; Terzioglu, M.; Galter, D.; Zhu, S.; Hofstetter, C.; Lindqvist, E.; Thams, S.; Bergstrand, A.; Hansson, F. S.; Trifunovic, A. et al.; Hoffer, B.; Cullheim, S.; Mohammed, A. H.; Olson, L.; Larsson, N.G.: Progressive parkinsonism in mice with respiratory-chain-deficient dopamine neurons. Proc Natl Acad Sci U S A 104 (4), S. 1325 - 30 (2007)

Duvezin-Caubet, S.; Jagasia, R.; Wagener, J.; Hofmann, S.; Trifunovic, A.; Hansson, A.; Chomyn, A.; Bauer, M. F.; Attardi, G.; Larsson, N.G. et al.; Neupert, W.; Reichert, A. S.: Proteolytic processing of OPA1 links mitochondrial dysfunction to alterations in mitochondrial morphology. J Biol Chem 281 (49), S. 37972 - 9 (2006)

Wredenberg, A.; Freyer, C.; Sandstrom, M. E.; Katz, A.; Wibom, R.; Westerblad, H.; Larsson, N.G.: Respiratory chain dysfunction in skeletal muscle does not cause insulin resistance. Biochem Biophys Res Commun 350 (1), S. 202 - 7 (2006)

Silva, J. P.; Shabalina, I. G.; Dufour, E.; Petrovic, N.; Backlund, E. C.; Hultenby, K.; Wibom, R.; Nedergaard, J.; Cannon, B.; Larsson, N.G.: SOD2 overexpression: enhanced mitochondrial tolerance but absence of effect on UCP activity. Embo j 24 (23), S. 4061 - 70 (2005)

Linder, T.; Park, C. B.; Asin-Cayuela, J.; Pellegrini, M.; Larsson, N.G.; Falkenberg, M.; Samuelsson, T.; Gustafsson, C. M.: A family of putative transcription termination factors shared amongst metazoans and plants. Curr Genet 48 (4), S. 265 - 9 (2005)

Esteitie, N.; Hinttala, R.; Wibom, R.; Nilsson, H.; Hance, N.; Naess, K.; Tear-Fahnehjelm, K.; von Dobeln, U.; Majamaa, K.; Larsson, N.G.: Secondary metabolic effects in complex I deficiency. Ann Neurol 58 (4), S. 544 - 52 (2005)

Gaspari, M.; Larsson, N.G.; Gustafsson, C. M.: The transcription machinery in mammalian mitochondria. Biochim Biophys Acta 1659 (2-3), S. 148 - 52 (2004)

Gaspari, M.; Falkenberg, M.; Larsson, N.G.; Gustafsson, C. M.: The mitochondrial RNA polymerase contributes critically to promoter specificity in mammalian cells. Embo j 23 (23), S. 4606 - 14 (2004)

Esteitie, N.; Larsson, N.G.: Defective assembly of the respiratory chain. Acta Paediatr 93 (10), S. 1268 - 70 (2004)

Dufour, E.; Larsson, N.G.: Understanding aging: revealing order out of chaos. Biochim Biophys Acta 1658 (1-2), S. 122 - 32 (2004)

Ekstrand, M. I.; Falkenberg, M.; Rantanen, A.; Park, C. B.; Gaspari, M.; Hultenby, K.; Rustin, P.; Gustafsson, C. M.; Larsson, N.G.: Mitochondrial transcription factor A regulates mtDNA copy number in mammals. Hum Mol Genet 13 (9), S. 935 - 44 (2004)

Rantanen, A.; Gaspari, M.; Falkenberg, M.; Gustafsson, C. M.; Larsson, N.G.: Characterization of the mouse genes for mitochondrial transcription factors B1 and B2. Mamm Genome 14 (1), S. 1 - 6 (2003)

Graff, C.; Bui, T. H.; Larsson, N.G.: Mitochondrial diseases. Best Pract Res Clin Obstet Gynaecol 16 (5), S. 715 - 28 (2002)

Wredenberg, A.; Wibom, R.; Wilhelmsson, H.; Graff, C.; Wiener, H. H.; Burden, S. J.; Oldfors, A.; Westerblad, H.; Larsson, N.G.: Increased mitochondrial mass in mitochondrial myopathy mice. Proc Natl Acad Sci U S A 99 (23), S. 15066 - 71 (2002)

Larsson, N.G.: Leber hereditary optic neuropathy: a nuclear solution of a mitochondrial problem. Ann Neurol 52 (5), S. 529 - 30 (2002)