Journal Article (1349)
1301.
Journal Article
134 (6), pp. 1375 - 86 (1996)
The molecular chaperone Hsp78 confers compartment-specific thermotolerance to mitochondria. J Cell Biol 1302.
Journal Article
15 (16), pp. 4218 - 29 (1996)
AAA proteases with catalytic sites on opposite membrane surfaces comprise a proteolytic system for the ATP-dependent degradation of inner membrane proteins in mitochondria. EMBO J 1303.
Journal Article
13 (3), pp. 296 - 302 (1996)
A single mouse gene encodes the mitochondrial transcription factor A and a testis-specific nuclear HMG-box protein. Nat Genet 1304.
Journal Article
85 (6), pp. 875 - 85 (1996)
The YTA10-12 complex, an AAA protease with chaperone-like activity in the inner membrane of mitochondria. Cell 1305.
Journal Article
271 (17), pp. 10137 - 42 (1996)
Substitution of PIM1 protease in mitochondria by Escherichia coli Lon protease. J Biol Chem 1306.
Journal Article
1 (1), pp. 5 - 12 (1996)
Chaperone function on Crete: a meeting report. Cell Stress Chaperones 1307.
Journal Article
97 (3), pp. 269 - 73 (1996)
Fatal mitochondrial myopathy, lactic acidosis, and complex I deficiency associated with a heteroplasmic A --> G mutation at position 3251 in the mitochondrial tRNALeu(UUR) gne. Hum Genet 1308.
Journal Article
380 (1-2), pp. 142 - 6 (1996)
Role of the mitochondrial DnaJ homologue, Mdj1p, in the prevention of heat-induced protein aggregation. FEBS Lett 1309.
Journal Article
14 (14), pp. 3434 - 44 (1995)
Hsp78, a Clp homologue within mitochondria, can substitute for chaperone functions of mt-hsp70. EMBO J 1310.
Journal Article
54 (4), pp. 581 - 7 (1995)
Mitochondrial DNA deletions in muscle fibers in inclusion body myositis. J Neuropathol Exp Neurol 1311.
Journal Article
1271 (1), pp. 249 - 52 (1995)
Inheritance and expression of mitochondrial DNA point mutations. Biochim Biophys Acta 1312.
Journal Article
22 (4), pp. 284 - 7 (1995)
Use of primary cultures and continuous cell lines to study effects on astrocytic regulatory functions. Clin Exp Pharmacol Physiol 1313.
Journal Article
260, pp. 495 - 503 (1995)
Proteolytic breakdown of membrane-associated polypeptides in mitochondria of Saccharomyces cerevisiae. Methods Enzymol 1314.
Journal Article
29, pp. 151 - 78 (1995)
Molecular genetic aspects of human mitochondrial disorders. Annu Rev Genet 1315.
Journal Article
3, pp. S102 - 6 (1995)
Pathogenetic aspects of the A8344G mutation of mitochondrial DNA associated with MERRF syndrome and multiple symmetric lipomas. Muscle Nerve Suppl 1316.
Journal Article
90 (3), pp. 328 - 33 (1995)
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 1317.
Journal Article
13 (21), pp. 5135 - 45 (1994)
Molecular chaperones cooperate with PIM1 protease in the degradation of misfolded proteins in mitochondria. EMBO J 1318.
Journal Article
91 (22), pp. 10345 - 9 (1994)
The ATP hydrolysis-dependent reaction cycle of the Escherichia coli Hsp70 system DnaK, DnaJ, and GrpE. Proc Natl Acad Sci U S A 1319.
Journal Article
353 (2), pp. 201 - 6 (1994)
Yta10p is required for the ATP-dependent degradation of polypeptides in the inner membrane of mitochondria. FEBS Lett 1320.
Journal Article
353 (2), pp. 197 - 200 (1994)
Yta10p, a member of a novel ATPase family in yeast, is essential for mitochondrial function. FEBS Lett