Journal Article (1341)
1993
Journal Article
116 ( Pt 2), pp. 325 - 36 (1993)
Mitochondrial DNA deletions in inclusion body myositis. Brain
Journal Article
52 (3), pp. 551 - 6 (1993)
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 1992
Journal Article
32 (6), pp. 731 - 5 (1992)
Mitochondrial ATP-synthase deficiency in a child with 3-methylglutaconic aciduria. Pediatr Res
Journal Article
11 (13), pp. 4757 - 65 (1992)
Chaperonin-mediated protein folding: GroES binds to one end of the GroEL cylinder, which accommodates the protein substrate within its central cavity. EMBO J
Journal Article
51 (6), pp. 1201 - 12 (1992)
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
Journal Article
1139 (4), pp. 311 - 4 (1992)
Multiple short direct repeats associated with single mtDNA deletions. Biochim Biophys Acta
Journal Article
110 (1-2), pp. 169 - 77 (1992)
Mitochondrial DNA deletions and cytochrome c oxidase deficiency in muscle fibres. J Neurol Sci
Journal Article
305 (1), pp. 51 - 4 (1992)
Formation and quantification of protein complexes between peroxisomal alcohol oxidase and GroEL. FEBS Lett
Journal Article
3 (6), pp. 633 - 54 (1992)
The yeast Ca(2+)-ATPase homologue, PMR1, is required for normal Golgi function and localizes in a novel Golgi-like distribution. Mol Biol Cell
Journal Article
356 (6371), pp. 683 - 9 (1992)
Successive action of DnaK, DnaJ and GroEL along the pathway of chaperone-mediated protein folding. Nature
Journal Article
50 (2), pp. 360 - 3 (1992)
Lack of transmission of deleted mtDNA from a woman with Kearns-Sayre syndrome to her child. Am J Hum Genet 1991
Journal Article
30 (5), pp. 701 - 8 (1991)
Leber's hereditary optic neuropathy and complex I deficiency in muscle. Ann Neurol
Journal Article
352 (6330), pp. 36 - 42 (1991)
Chaperonin-mediated protein folding at the surface of groEL through a 'molten globule'-like intermediate. Nature
Journal Article
167, pp. 3 - 30 (1991)
Heat shock proteins hsp60 and hsp70: their roles in folding, assembly and membrane translocation of proteins. Curr Top Microbiol Immunol 1990
Journal Article
28 (2), pp. 131 - 6 (1990)
Progressive increase of the mutated mitochondrial DNA fraction in Kearns-Sayre syndrome. Pediatr Res
Journal Article
371 (6), pp. 515 - 9 (1990)
Lactate dehydrogenase from the extreme halophilic archaebacterium Halobacterium marismortui. Biol Chem Hoppe Seyler
Journal Article
80 (5), pp. 541 - 6 (1990)
Neuropathology in Kearns-Sayre syndrome. Acta Neuropathol 1989
Journal Article
86 (48), pp. 4235 - 6 (1989)
DNA diagnosis of mitochondrial diseases is now possible. Lakartidningen
Journal Article
58 (1), pp. 133 - 45 (1989)
The yeast secretory pathway is perturbed by mutations in PMR1, a member of a Ca2+ ATPase family. Cell 1987
Journal Article
40 (3), pp. 389 - 95 (1987)
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