Scientific Publications

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)

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)

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)

Larsson, N.G.; Holme, E.: Multiple short direct repeats associated with single mtDNA deletions. Biochim Biophys Acta 1139 (4), pp. 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), pp. 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), pp. 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), pp. 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), pp. 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), pp. 360 - 3 (1992)