Publikationen

Schmitt, M.; Neupert, W.; Langer, T.: Hsp78, a Clp homologue within mitochondria, can substitute for chaperone functions of mt-hsp70. EMBO J 14 (14), S. 3434 - 44 (1995)

Oldfors, A.; Moslemi, A. R.; Fyhr, I. M.; Holme, E.; Larsson, N.G.; Lindberg, C.: Mitochondrial DNA deletions in muscle fibers in inclusion body myositis. J Neuropathol Exp Neurol 54 (4), S. 581 - 7 (1995)

Holme, E.; Tulinius, M. H.; Larsson, N.G.; Oldfors, A.: Inheritance and expression of mitochondrial DNA point mutations. Biochim Biophys Acta 1271 (1), S. 249 - 52 (1995)

Walum, E.; Eriksson, G.; Peterson, A.; Holme, E.; Larsson, N.G.; Eriksson, C.; el-Shamy, W.: Use of primary cultures and continuous cell lines to study effects on astrocytic regulatory functions. Clin Exp Pharmacol Physiol 22 (4), S. 284 - 7 (1995)

Langer, T.; Pajic, A.; Wagner, I.; Neupert, W.: Proteolytic breakdown of membrane-associated polypeptides in mitochondria of Saccharomyces cerevisiae. Methods Enzymol 260, S. 495 - 503 (1995)

Larsson, N.G.; Clayton, D. A.: Molecular genetic aspects of human mitochondrial disorders. Annu Rev Genet 29, S. 151 - 78 (1995)

Larsson, N.G.; Tulinius, M. H.; Holme, E.; Oldfors, A.: Pathogenetic aspects of the A8344G mutation of mitochondrial DNA associated with MERRF syndrome and multiple symmetric lipomas. Muscle Nerve Suppl 3, S. S102 - 6 (1995)

Oldfors, A.; Holme, E.; Tulinius, M.; Larsson, N.G.: Tissue distribution and disease manifestations of the tRNA(Lys) A-->G(8344) mitochondrial DNA mutation in a case of myoclonus epilepsy and ragged red fibres. Acta Neuropathol 90 (3), S. 328 - 33 (1995)