Zeitschriftenartikel (1347)
1301.
Zeitschriftenartikel
13 (3), S. 296 - 302 (1996)
A single mouse gene encodes the mitochondrial transcription factor A and a testis-specific nuclear HMG-box protein. Nat Genet 1302.
Zeitschriftenartikel
85 (6), S. 875 - 85 (1996)
The YTA10-12 complex, an AAA protease with chaperone-like activity in the inner membrane of mitochondria. Cell 1303.
Zeitschriftenartikel
271 (17), S. 10137 - 42 (1996)
Substitution of PIM1 protease in mitochondria by Escherichia coli Lon protease. J Biol Chem 1304.
Zeitschriftenartikel
1 (1), S. 5 - 12 (1996)
Chaperone function on Crete: a meeting report. Cell Stress Chaperones 1305.
Zeitschriftenartikel
97 (3), S. 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 1306.
Zeitschriftenartikel
380 (1-2), S. 142 - 6 (1996)
Role of the mitochondrial DnaJ homologue, Mdj1p, in the prevention of heat-induced protein aggregation. FEBS Lett 1307.
Zeitschriftenartikel
14 (14), S. 3434 - 44 (1995)
Hsp78, a Clp homologue within mitochondria, can substitute for chaperone functions of mt-hsp70. EMBO J 1308.
Zeitschriftenartikel
54 (4), S. 581 - 7 (1995)
Mitochondrial DNA deletions in muscle fibers in inclusion body myositis. J Neuropathol Exp Neurol 1309.
Zeitschriftenartikel
1271 (1), S. 249 - 52 (1995)
Inheritance and expression of mitochondrial DNA point mutations. Biochim Biophys Acta 1310.
Zeitschriftenartikel
22 (4), S. 284 - 7 (1995)
Use of primary cultures and continuous cell lines to study effects on astrocytic regulatory functions. Clin Exp Pharmacol Physiol 1311.
Zeitschriftenartikel
260, S. 495 - 503 (1995)
Proteolytic breakdown of membrane-associated polypeptides in mitochondria of Saccharomyces cerevisiae. Methods Enzymol 1312.
Zeitschriftenartikel
29, S. 151 - 78 (1995)
Molecular genetic aspects of human mitochondrial disorders. Annu Rev Genet 1313.
Zeitschriftenartikel
3, S. S102 - 6 (1995)
Pathogenetic aspects of the A8344G mutation of mitochondrial DNA associated with MERRF syndrome and multiple symmetric lipomas. Muscle Nerve Suppl 1314.
Zeitschriftenartikel
90 (3), S. 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 1315.
Zeitschriftenartikel
13 (21), S. 5135 - 45 (1994)
Molecular chaperones cooperate with PIM1 protease in the degradation of misfolded proteins in mitochondria. EMBO J 1316.
Zeitschriftenartikel
91 (22), S. 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 1317.
Zeitschriftenartikel
353 (2), S. 201 - 6 (1994)
Yta10p is required for the ATP-dependent degradation of polypeptides in the inner membrane of mitochondria. FEBS Lett 1318.
Zeitschriftenartikel
353 (2), S. 197 - 200 (1994)
Yta10p, a member of a novel ATPase family in yeast, is essential for mitochondrial function. FEBS Lett 1319.
Zeitschriftenartikel
200 (3), S. 1374 - 81 (1994)
Low levels of mitochondrial transcription factor A in mitochondrial DNA depletion. Biochem Biophys Res Commun 1320.
Zeitschriftenartikel
1226 (1), S. 49 - 55 (1994)
Automatic sequencing of mitochondrial tRNA genes in patients with mitochondrial encephalomyopathy. Biochim Biophys Acta