Publications

External Member: Larsson Adjunct Group

Journal Article (7)

2010
Journal Article
Ross, J. M.; Oberg, J.; Brene, S.; Coppotelli, G.; Terzioglu, M.; Pernold, K.; Goiny, M.; Sitnikov, R.; Kehr, J.; Trifunovic, A. et al.; Larsson, N.G.; Hoffer, B. J.; Olson, L.: High brain lactate is a hallmark of aging and caused by a shift in the lactate dehydrogenase A/B ratio. Proc Natl Acad Sci U S A 107 (46), pp. 20087 - 92 (2010)
Journal Article
Sterky, F. H.; Ruzzenente, B.; Gustafsson, C. M.; Samuelsson, T.; Larsson, N.G.: LRPPRC is a mitochondrial matrix protein that is conserved in metazoans. Biochem Biophys Res Commun 398 (4), pp. 759 - 64 (2010)
Journal Article
Gustafsson, C. M.; Larsson, N.G.: MTERF1 gives mtDNA an unusual twist. Cell Metab 12 (1), pp. 3 - 4 (2010)
Journal Article
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), pp. 6577 - 88 (2010)
Journal Article
Larsson, N.G.: Somatic mitochondrial DNA mutations in mammalian aging. Annu Rev Biochem 79, pp. 683 - 706 (2010)
Journal Article
Edgar, D.; Larsson, N.G.; Trifunovic, A.: Response: Point Mutations Are Causing Progeroid Phenotypes in the mtDNA Mutator Mouse. Cell Metab 11 (1), p. 93 (2010)
Journal Article
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), pp. 198 - 203 (2010)
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