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200 (3), pp. 1374 - 81 (1994)
Low levels of mitochondrial transcription factor A in mitochondrial DNA depletion. Biochem Biophys Res Commun 1322.
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1226 (1), pp. 49 - 55 (1994)
Automatic sequencing of mitochondrial tRNA genes in patients with mitochondrial encephalomyopathy. Biochim Biophys Acta 1323.
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19 (4), pp. 176 - 81 (1994)
DnaJ-like proteins: molecular chaperones and specific regulators of Hsp70. Trends Biochem Sci 1324.
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19 (1), pp. 20 - 5 (1994)
Molecular chaperones in protein folding: the art of avoiding sticky situations. Trends Biochem Sci 1325.
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366 (6452), pp. 228 - 33 (1993)
The reaction cycle of GroEL and GroES in chaperonin-assisted protein folding. Nature 1326.
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90 (21), pp. 10216 - 20 (1993)
Control of folding and membrane translocation by binding of the chaperone DnaJ to nascent polypeptides. Proc Natl Acad Sci U S A 1327.
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12 (11), pp. 4137 - 44 (1993)
DnaK, DnaJ and GrpE form a cellular chaperone machinery capable of repairing heat-induced protein damage. EMBO J 1328.
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123 (1), pp. 109 - 17 (1993)
A dual role for mitochondrial heat shock protein 70 in membrane translocation of preproteins. J Cell Biol 1329.
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116 ( Pt 2), pp. 325 - 36 (1993)
Mitochondrial DNA deletions in inclusion body myositis. Brain 1330.
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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 1331.
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32 (6), pp. 731 - 5 (1992)
Mitochondrial ATP-synthase deficiency in a child with 3-methylglutaconic aciduria. Pediatr Res 1332.
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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 1333.
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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 1334.
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1139 (4), pp. 311 - 4 (1992)
Multiple short direct repeats associated with single mtDNA deletions. Biochim Biophys Acta 1335.
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110 (1-2), pp. 169 - 77 (1992)
Mitochondrial DNA deletions and cytochrome c oxidase deficiency in muscle fibres. J Neurol Sci 1336.
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305 (1), pp. 51 - 4 (1992)
Formation and quantification of protein complexes between peroxisomal alcohol oxidase and GroEL. FEBS Lett 1337.
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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 1338.
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356 (6371), pp. 683 - 9 (1992)
Successive action of DnaK, DnaJ and GroEL along the pathway of chaperone-mediated protein folding. Nature 1339.
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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 1340.
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30 (5), pp. 701 - 8 (1991)
Leber's hereditary optic neuropathy and complex I deficiency in muscle. Ann Neurol