Publications of N.G. Larsson

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)

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)

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)

Oldfors, A.; Larsson, N.G.; Lindberg, C.; Holme, E.: Mitochondrial DNA deletions in inclusion body myositis. Brain 116 ( Pt 2), pp. 325 - 36 (1993)

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)

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)

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)

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)

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)

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)

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)

Larsson, N.G.; Holme, E.; Tulinius, M. H.: DNA diagnosis of mitochondrial diseases is now possible. Lakartidningen 86 (48), pp. 4235 - 6 (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), pp. 389 - 95 (1987)