Larsson, N.G.; Tulinius, M. H.; Holme, E.; Oldfors, A.; Andersen, O.; Wahlstrom, J.; Aasly, J.: Segregation and manifestations of the mtDNA tRNA(Lys) A-->G(8344) mutation of myoclonus epilepsy and ragged-red fibers (MERRF) syndrome. Am J Hum Genet 51 (6), S. 1201 - 12 (1992)

Larsson, N.G.; Holme, E.: Multiple short direct repeats associated with single mtDNA deletions. Biochim Biophys Acta 1139 (4), S. 311 - 4 (1992)

Oldfors, A.; Larsson, N.G.; Holme, E.; Tulinius, M.; Kadenbach, B.; Droste, M.: Mitochondrial DNA deletions and cytochrome c oxidase deficiency in muscle fibres. J Neurol Sci 110 (1-2), S. 169 - 77 (1992)

Evers, M. E.; Langer, T.; Harder, W.; Hartl, F. U.; Veenhuis, M.: Formation and quantification of protein complexes between peroxisomal alcohol oxidase and GroEL. FEBS Lett 305 (1), S. 51 - 4 (1992)

Antebi, A.; Fink, G. R.: The yeast Ca(2+)-ATPase homologue, PMR1, is required for normal Golgi function and localizes in a novel Golgi-like distribution. Mol Biol Cell 3 (6), S. 633 - 54 (1992)

Langer, T.; Lu, C.; Echols, H.; Flanagan, J.; Hayer, M. K.; Hartl, F. U.: Successive action of DnaK, DnaJ and GroEL along the pathway of chaperone-mediated protein folding. Nature 356 (6371), S. 683 - 9 (1992)

Larsson, N.G.; Eiken, H. G.; Boman, H.; Holme, E.; Oldfors, A.; Tulinius, M. H.: Lack of transmission of deleted mtDNA from a woman with Kearns-Sayre syndrome to her child. Am J Hum Genet 50 (2), S. 360 - 3 (1992)

Larsson, N.G.; Andersen, O.; Holme, E.; Oldfors, A.; Wahlstrom, J.: Leber's hereditary optic neuropathy and complex I deficiency in muscle. Ann Neurol 30 (5), S. 701 - 8 (1991)

Martin, J.; Langer, T.; Boteva, R.; Schramel, A.; Horwich, A. L.; Hartl, F. U.: Chaperonin-mediated protein folding at the surface of groEL through a 'molten globule'-like intermediate. Nature 352 (6330), S. 36 - 42 (1991)

Langer, T.; Neupert, W.: Heat shock proteins hsp60 and hsp70: their roles in folding, assembly and membrane translocation of proteins. Curr Top Microbiol Immunol 167, S. 3 - 30 (1991)

Larsson, N.G.; Holme, E.; Kristiansson, B.; Oldfors, A.; Tulinius, M.: Progressive increase of the mutated mitochondrial DNA fraction in Kearns-Sayre syndrome. Pediatr Res 28 (2), S. 131 - 6 (1990)

Hecht, K.; Langer, T.; Wrba, A.; Jaenicke, R.: Lactate dehydrogenase from the extreme halophilic archaebacterium Halobacterium marismortui. Biol Chem Hoppe Seyler 371 (6), S. 515 - 9 (1990)

Oldfors, A.; Fyhr, I. M.; Holme, E.; Larsson, N.G.; Tulinius, M.: Neuropathology in Kearns-Sayre syndrome. Acta Neuropathol 80 (5), S. 541 - 6 (1990)

Larsson, N.G.; Holme, E.; Tulinius, M. H.: DNA diagnosis of mitochondrial diseases is now possible. Lakartidningen 86 (48), S. 4235 - 6 (1989)

Rudolph, H. K.; Antebi, A.; Fink, G. R.; Buckley, C. M.; Dorman, T. E.; LeVitre, J.; Davidow, L. S.; Mao, J. I.; Moir, D. T.: The yeast secretory pathway is perturbed by mutations in PMR1, a member of a Ca2+ ATPase family. Cell 58 (1), S. 133 - 45 (1989)

Welinder, C.; Larsson, N.G.; Szigeti, R.; Ehlin-Henriksson, B.; Henle, G.; Henle, W.; Klein, G.; Ricksten, A.; Rymo, L.; Sulitzeanu, D.: Stable transfection of a human lymphoma line by sub-genomic fragments of Epstein-Barr virus DNA to measure humoral and cellular immunity to the corresponding proteins. Int J Cancer 40 (3), S. 389 - 95 (1987)

Pasternack, R. F.; Gibbs, E. J.; Gaudemer, A.; Antebi, A.; Bassner, S.; De Poy, L.; Turner, D. H.; Williams, A.; Laplace, F.; Lansard, M. H. et al.; Merienne, C.; Perree-Fauvet, M.: Molecular complexes of nucleosides and nucleotides with a monomeric cationic porphyrin and some of its metal derivatives. J Am Chem Soc 107 (26), S. 8179 - 8186 (1985)

Graef, M.; Langer, T.; Engmann, T.: The recognition of substrates by AAA proteases in mitochondria. ATP-dependent proteases. (2007)

Dauben, H.; Matić, I.: Immunoprecipitation Using Mono-ADP-Ribosylation-Specific Antibodies. In: Poly(ADP-Ribose) Polymerase: Methods in Molecular Biology, Bd. 2609, S. 135 - 146 (Hg. Tulin, A. V.). Springer US, New York, NY (2023)

Misic, J.; Milenkovic, D.: Studying Mitochondrial Nucleic Acid Synthesis Utilizing Intact Isolated Mitochondria. In: Mitochondrial DNA: Methods in Molecular Biology, Bd. 2615, S. 219 - 228 (Hg. Nicholls, T. J.; Uhler, J. P.; Falkenberg, M.). Springer US, New York, NY (2023)