Schmitt, M.; Neupert, W.; Langer, T.: Hsp78, a Clp homologue within mitochondria, can substitute for chaperone functions of mt-hsp70. EMBO J 14 (14), pp. 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), pp. 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), pp. 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), pp. 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, pp. 495 - 503 (1995)

Larsson, N.G.; Clayton, D. A.: Molecular genetic aspects of human mitochondrial disorders. Annu Rev Genet 29, pp. 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, pp. 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), pp. 328 - 33 (1995)

Wagner, I.; Arlt, H.; van Dyck, L.; Langer, T.; Neupert, W.: Molecular chaperones cooperate with PIM1 protease in the degradation of misfolded proteins in mitochondria. EMBO J 13 (21), pp. 5135 - 45 (1994)

Szabo, A.; Langer, T.; Schroder, H.; Flanagan, J.; Bukau, B.; Hartl, F. U.: The ATP hydrolysis-dependent reaction cycle of the Escherichia coli Hsp70 system DnaK, DnaJ, and GrpE. Proc Natl Acad Sci U S A 91 (22), pp. 10345 - 9 (1994)

Pajic, A.; Tauer, R.; Feldmann, H.; Neupert, W.; Langer, T.: Yta10p is required for the ATP-dependent degradation of polypeptides in the inner membrane of mitochondria. FEBS Lett 353 (2), pp. 201 - 6 (1994)

Tauer, R.; Mannhaupt, G.; Schnall, R.; Pajic, A.; Langer, T.; Feldmann, H.: Yta10p, a member of a novel ATPase family in yeast, is essential for mitochondrial function. FEBS Lett 353 (2), pp. 197 - 200 (1994)

Larsson, N.G.; Oldfors, A.; Holme, E.; Clayton, D. A.: Low levels of mitochondrial transcription factor A in mitochondrial DNA depletion. Biochem Biophys Res Commun 200 (3), pp. 1374 - 81 (1994)

Houshmand, M.; Larsson, N.G.; Holme, E.; Oldfors, A.; Tulinius, M. H.; Andersen, O.: Automatic sequencing of mitochondrial tRNA genes in patients with mitochondrial encephalomyopathy. Biochim Biophys Acta 1226 (1), pp. 49 - 55 (1994)

Cyr, D. M.; Langer, T.; Douglas, M. G.: DnaJ-like proteins: molecular chaperones and specific regulators of Hsp70. Trends Biochem Sci 19 (4), pp. 176 - 81 (1994)

Hartl, F. U.; Hlodan, R.; Langer, T.: Molecular chaperones in protein folding: the art of avoiding sticky situations. Trends Biochem Sci 19 (1), pp. 20 - 5 (1994)

Martin, J.; Mayhew, M.; Langer, T.; Hartl, F. U.: The reaction cycle of GroEL and GroES in chaperonin-assisted protein folding. Nature 366 (6452), pp. 228 - 33 (1993)

Hendrick, J. P.; Langer, T.; Davis, T. A.; Hartl, F. U.; Wiedmann, M.: Control of folding and membrane translocation by binding of the chaperone DnaJ to nascent polypeptides. Proc Natl Acad Sci U S A 90 (21), pp. 10216 - 20 (1993)

Schroder, H.; Langer, T.; Hartl, F. U.; Bukau, B.: DnaK, DnaJ and GrpE form a cellular chaperone machinery capable of repairing heat-induced protein damage. EMBO J 12 (11), pp. 4137 - 44 (1993)

Gambill, B. D.; Voos, W.; Kang, P. J.; Miao, B.; Langer, T.; Craig, E. A.; Pfanner, N.: A dual role for mitochondrial heat shock protein 70 in membrane translocation of preproteins. J Cell Biol 123 (1), pp. 109 - 17 (1993)