Zeitschriftenartikel (1343)
1321.
Zeitschriftenartikel
12 (11), S. 4137 - 44 (1993)
DnaK, DnaJ and GrpE form a cellular chaperone machinery capable of repairing heat-induced protein damage. EMBO J 1322.
Zeitschriftenartikel
123 (1), S. 109 - 17 (1993)
A dual role for mitochondrial heat shock protein 70 in membrane translocation of preproteins. J Cell Biol 1323.
Zeitschriftenartikel
116 ( Pt 2), S. 325 - 36 (1993)
Mitochondrial DNA deletions in inclusion body myositis. Brain 1324.
Zeitschriftenartikel
52 (3), S. 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 1325.
Zeitschriftenartikel
32 (6), S. 731 - 5 (1992)
Mitochondrial ATP-synthase deficiency in a child with 3-methylglutaconic aciduria. Pediatr Res 1326.
Zeitschriftenartikel
11 (13), S. 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 1327.
Zeitschriftenartikel
51 (6), S. 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 1328.
Zeitschriftenartikel
1139 (4), S. 311 - 4 (1992)
Multiple short direct repeats associated with single mtDNA deletions. Biochim Biophys Acta 1329.
Zeitschriftenartikel
110 (1-2), S. 169 - 77 (1992)
Mitochondrial DNA deletions and cytochrome c oxidase deficiency in muscle fibres. J Neurol Sci 1330.
Zeitschriftenartikel
305 (1), S. 51 - 4 (1992)
Formation and quantification of protein complexes between peroxisomal alcohol oxidase and GroEL. FEBS Lett 1331.
Zeitschriftenartikel
3 (6), S. 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 1332.
Zeitschriftenartikel
356 (6371), S. 683 - 9 (1992)
Successive action of DnaK, DnaJ and GroEL along the pathway of chaperone-mediated protein folding. Nature 1333.
Zeitschriftenartikel
50 (2), S. 360 - 3 (1992)
Lack of transmission of deleted mtDNA from a woman with Kearns-Sayre syndrome to her child. Am J Hum Genet 1334.
Zeitschriftenartikel
30 (5), S. 701 - 8 (1991)
Leber's hereditary optic neuropathy and complex I deficiency in muscle. Ann Neurol 1335.
Zeitschriftenartikel
352 (6330), S. 36 - 42 (1991)
Chaperonin-mediated protein folding at the surface of groEL through a 'molten globule'-like intermediate. Nature 1336.
Zeitschriftenartikel
167, S. 3 - 30 (1991)
Heat shock proteins hsp60 and hsp70: their roles in folding, assembly and membrane translocation of proteins. Curr Top Microbiol Immunol 1337.
Zeitschriftenartikel
28 (2), S. 131 - 6 (1990)
Progressive increase of the mutated mitochondrial DNA fraction in Kearns-Sayre syndrome. Pediatr Res 1338.
Zeitschriftenartikel
371 (6), S. 515 - 9 (1990)
Lactate dehydrogenase from the extreme halophilic archaebacterium Halobacterium marismortui. Biol Chem Hoppe Seyler 1339.
Zeitschriftenartikel
80 (5), S. 541 - 6 (1990)
Neuropathology in Kearns-Sayre syndrome. Acta Neuropathol 1340.
Zeitschriftenartikel
86 (48), S. 4235 - 6 (1989)
DNA diagnosis of mitochondrial diseases is now possible. Lakartidningen