Publications

Kadkhodaei, B.; Ito, T.; Joodmardi, E.; Mattsson, B.; Rouillard, C.; Carta, M.; Muramatsu, S.; Sumi-Ichinose, C.; Nomura, T.; Metzger, D. et al.; Chambon, P.; Lindqvist, E.; Larsson, N.G.; Olson, L.; Bjorklund, A.; Ichinose, H.; Perlmann, T.: Nurr1 is required for maintenance of maturing and adult midbrain dopamine neurons. J Neurosci 29 (50), pp. 15923 - 32 (2009)

Edgar, D.; Larsson, N.G.; Trifunovic, A.: Point mutations are causing progeroid phenotypes in the mtDNA mutator mouse. Cell Metab 11 (1), p. 1 (2009)

Galter, D.; Pernold, K.; Yoshitake, T.; Lindqvist, E.; Hoffer, B.; Kehr, J.; Larsson, N.G.; Olson, L.: MitoPark mice mirror the slow progression of key symptoms and L-DOPA response in Parkinson's disease. Genes Brain Behav 9 (2), pp. 173 - 81 (2009)

Falkenberg, M.; Larsson, N.G.: Structure casts light on mtDNA replication. Cell 139 (2), pp. 231 - 3 (2009)

Edgar, D.; Shabalina, I.; Camara, Y.; Wredenberg, A.; Calvaruso, M. A.; Nijtmans, L.; Nedergaard, J.; Cannon, B.; Larsson, N.G.; Trifunovic, A.: Random point mutations with major effects on protein-coding genes are the driving force behind premature aging in mtDNA mutator mice. Cell Metab 10 (2), pp. 131 - 8 (2009)

Baranowska, I.; Jaderlund, K. H.; Nennesmo, I.; Holmqvist, E.; Heidrich, N.; Larsson, N.G.; Andersson, G.; Wagner, E. G.; Hedhammar, A.; Wibom, R. et al.; Andersson, L.: Sensory ataxic neuropathy in golden retriever dogs is caused by a deletion in the mitochondrial tRNATyr gene. PLoS Genet 5 (5), p. e1000499 (2009)

Pellegrini, M.; Asin-Cayuela, J.; Erdjument-Bromage, H.; Tempst, P.; Larsson, N.G.; Gustafsson, C. M.: MTERF2 is a nucleoid component in mammalian mitochondria. Biochim Biophys Acta 1787 (5), pp. 296 - 302 (2009)

Metodiev, M. D.; Lesko, N.; Park, C. B.; Camara, Y.; Shi, Y.; Wibom, R.; Hultenby, K.; Gustafsson, C. M.; Larsson, N.G.: Methylation of 12S rRNA is necessary for in vivo stability of the small subunit of the mammalian mitochondrial ribosome. Cell Metab 9 (4), pp. 386 - 97 (2009)

Larsson, N.G.: Introduction: Euromit VII--summarizing 50 years of research on mitochondrial disease. J Intern Med 265 (2), pp. 170 - 3 (2009)

Naess, K.; Freyer, C.; Bruhn, H.; Wibom, R.; Malm, G.; Nennesmo, I.; von Dobeln, U.; Larsson, N.G.: MONA mutations are a common cause of severe disease phenotypes in children with Leigh syndrome. SI 1787 (5), pp. 484 - 490 (2009)