Journal Article (1341)

1993
Journal Article
Oldfors, A.; Larsson, N.G.; Lindberg, C.; Holme, E.: Mitochondrial DNA deletions in inclusion body myositis. Brain 116 ( Pt 2), pp. 325 - 36 (1993)
Journal Article
Holme, E.; Larsson, N.G.; Oldfors, A.; Tulinius, M.; Sahlin, P.; Stenman, G.: Multiple symmetric lipomas with high levels of mtDNA with the tRNA(Lys) A-->G(8344) mutation as the only manifestation of disease in a carrier of myoclonus epilepsy and ragged-red fibers (MERRF) syndrome. Am J Hum Genet 52 (3), pp. 551 - 6 (1993)
1992
Journal Article
Holme, E.; Greter, J.; Jacobson, C. E.; Larsson, N.G.; Lindstedt, S.; Nilsson, K. O.; Oldfors, A.; Tulinius, M.: Mitochondrial ATP-synthase deficiency in a child with 3-methylglutaconic aciduria. Pediatr Res 32 (6), pp. 731 - 5 (1992)
Journal Article
Langer, T.; Pfeifer, G.; Martin, J.; Baumeister, W.; Hartl, F. U.: Chaperonin-mediated protein folding: GroES binds to one end of the GroEL cylinder, which accommodates the protein substrate within its central cavity. EMBO J 11 (13), pp. 4757 - 65 (1992)
Journal Article
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), pp. 1201 - 12 (1992)
Journal Article
Larsson, N.G.; Holme, E.: Multiple short direct repeats associated with single mtDNA deletions. Biochim Biophys Acta 1139 (4), pp. 311 - 4 (1992)
Journal Article
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), pp. 169 - 77 (1992)
Journal Article
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), pp. 51 - 4 (1992)
Journal Article
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), pp. 633 - 54 (1992)
Journal Article
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), pp. 683 - 9 (1992)
Journal Article
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), pp. 360 - 3 (1992)
1991
Journal Article
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), pp. 701 - 8 (1991)
Journal Article
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), pp. 36 - 42 (1991)
Journal Article
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, pp. 3 - 30 (1991)
1990
Journal Article
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), pp. 131 - 6 (1990)
Journal Article
Hecht, K.; Langer, T.; Wrba, A.; Jaenicke, R.: Lactate dehydrogenase from the extreme halophilic archaebacterium Halobacterium marismortui. Biol Chem Hoppe Seyler 371 (6), pp. 515 - 9 (1990)
Journal Article
Oldfors, A.; Fyhr, I. M.; Holme, E.; Larsson, N.G.; Tulinius, M.: Neuropathology in Kearns-Sayre syndrome. Acta Neuropathol 80 (5), pp. 541 - 6 (1990)
1989
Journal Article
Larsson, N.G.; Holme, E.; Tulinius, M. H.: DNA diagnosis of mitochondrial diseases is now possible. Lakartidningen 86 (48), pp. 4235 - 6 (1989)
Journal Article
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), pp. 133 - 45 (1989)
1987
Journal Article
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), pp. 389 - 95 (1987)
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