Publikationen von N.G. Larsson

Gustafsson, C. M.; Larsson, N.G.: MTERF1 gives mtDNA an unusual twist. Cell Metab 12 (1), S. 3 - 4 (2010)

Freyer, C.; Park, C. B.; Ekstrand, M. I.; Shi, Y.; Khvorostova, J.; Wibom, R.; Falkenberg, M.; Gustafsson, C. M.; Larsson, N.G.: Maintenance of respiratory chain function in mouse hearts with severely impaired mtDNA transcription. Nucleic Acids Res 38 (19), S. 6577 - 88 (2010)

Larsson, N.G.: Somatic mitochondrial DNA mutations in mammalian aging. Annu Rev Biochem 79, S. 683 - 706 (2010)

Edgar, D.; Larsson, N.G.; Trifunovic, A.: Response: Point Mutations Are Causing Progeroid Phenotypes in the mtDNA Mutator Mouse. Cell Metab 11 (1), S. 93 (2010)

Lesko, N.; Naess, K.; Wibom, R.; Solaroli, N.; Nennesmo, I.; von Dobeln, U.; Karlsson, A.; Larsson, N.G.: Two novel mutations in thymidine kinase-2 cause early onset fatal encephalomyopathy and severe mtDNA depletion. Neuromuscul Disord 20 (3), S. 198 - 203 (2010)

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), S. 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), S. 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), S. 173 - 81 (2009)

Falkenberg, M.; Larsson, N.G.: Structure casts light on mtDNA replication. Cell 139 (2), S. 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), S. 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), S. 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), S. 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), S. 386 - 97 (2009)

Larsson, N.G.: Introduction: Euromit VII--summarizing 50 years of research on mitochondrial disease. J Intern Med 265 (2), S. 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), S. 484 - 490 (2009)

Naess, K.; Freyer, C.; Bruhn, H.; Wibom, R.; Malm, G.; Nennesmo, I.; von Dobeln, U.; Larsson, N.G.: MtDNA mutations are a common cause of severe disease phenotypes in children with Leigh syndrome. Biochim Biophys Acta 1787 (5), S. 484 - 90 (2008)

Aydin, J.; Andersson, D. C.; Hanninen, S. L.; Wredenberg, A.; Tavi, P.; Park, C. B.; Larsson, N.G.; Bruton, J. D.; Westerblad, H.: Increased mitochondrial Ca2+ and decreased sarcoplasmic reticulum Ca2+ in mitochondrial myopathy. Hum Mol Genet 18 (2), S. 278 - 88 (2008)

Stewart, J.; Freyer, C.; Elson, J. L.; Larsson, N.G.: Purifying selection of mtDNA and its implications for understanding evolution and mitochondrial disease. Nat Rev Genet 9 (9), S. 657 - 62 (2008)

Dufour, E.; Terzioglu, M.; Sterky, F. H.; Sorensen, L.; Galter, D.; Olson, L.; Wilbertz, J.; Larsson, N.G.: Age-associated mosaic respiratory chain deficiency causes trans-neuronal degeneration. Hum Mol Genet 17 (10), S. 1418 - 26 (2008)

Stewart, J.; Freyer, C.; Elson, J. L.; Wredenberg, A.; Cansu, Z.; Trifunovic, A.; Larsson, N.G.: Strong purifying selection in transmission of mammalian mitochondrial DNA. PLoS Biol 6 (1), S. e10 (2008)