-
1
-
-
0033525773
-
Mitochondrial diseases in man and mouse
-
D.C. Wallace, Mitochondrial diseases in man and mouse, Science 283 (1999) 1482-1488.
-
(1999)
Science
, vol.283
, pp. 1482-1488
-
-
Wallace, D.C.1
-
3
-
-
0025807222
-
Maternally inherited myopathy and cardiomyopathy: Association with mutation in mitochondrial DNA tRNA-Leu (UUR)
-
M. Zeviani, C. Gellera, C. Antozzi, M. Rimoldi, L. Morandi, F. Villani, V. Tiranti, S. DiDonato, Maternally inherited myopathy and cardiomyopathy: Association with mutation in mitochondrial DNA tRNA-Leu (UUR), Lancet 338 (1991) 143-147.
-
(1991)
Lancet
, vol.338
, pp. 143-147
-
-
Zeviani, M.1
Gellera, C.2
Antozzi, C.3
Rimoldi, M.4
Morandi, L.5
Villani, F.6
Tiranti, V.7
Didonato, S.8
-
4
-
-
0026608057
-
MELAS mutation in mtDNA binding site for transcription termination factor causes defects in protein synthesis and in respiration but no change in levels of upstream and downstream mature transcripts
-
A. Chomyn, A. Martinuzzy, M. Yoneda, O. Hurko, D. Johns, S. Lai, I. Nonaka, G. Attardi, MELAS mutation in mtDNA binding site for transcription termination factor causes defects in protein synthesis and in respiration but no change in levels of upstream and downstream mature transcripts. Proc. Natl. Acad. Sci. USA 89 (1992) 4221-4225.
-
(1992)
Proc. Natl. Acad. Sci. USA
, vol.89
, pp. 4221-4225
-
-
Chomyn, A.1
Martinuzzy, A.2
Yoneda, M.O.3
Hurko4
Johns, D.5
Lai, S.6
Nonaka, I.7
Attardi, G.8
-
5
-
-
0029003333
-
Complementation and segregation behavior of disease-causing mitochondrial DNA mutations in cellular model systems
-
G. Attardi, M. Yoneda, A. Chomyn, Complementation and segregation behavior of disease-causing mitochondrial DNA mutations in cellular model systems, Bba-Mol Basis Dis 1271 (1995) 241-248.
-
(1995)
Bba-Mol Basis Dis
, vol.1271
, pp. 241-248
-
-
Attardi, G.1
Yoneda, M.2
Chomyn, A.3
-
6
-
-
0025836655
-
Introduction of disease-related mitochondrial DNA deletions into Hela cells lacking mitochondrial DNA results in mitochondrial dysfunction
-
J.H. Hayashi, S. Ohta, A. Kikuch, M. Takemitsu, Y.I. Goto, I. Nonaka, Introduction of disease-related mitochondrial DNA deletions into Hela cells lacking mitochondrial DNA results in mitochondrial dysfunction, Proc. Natl. Acad. Sci. USA 88 (1991) 10614-10618.
-
(1991)
Proc. Natl. Acad. Sci. USA
, vol.88
, pp. 10614-10618
-
-
Hayashi, J.H.1
Ohta, S.2
Kikuch, A.3
Takemitsu, M.4
Goto, Y.I.5
Nonaka, I.6
-
7
-
-
7344241008
-
Bioenergetic consequences of accumulating the common 4977-bp mitochondrial DNA deletion
-
W.K. Porteous, A.M. James, P.W. Sheard, C.M. Porteous, M.A. Packer, S.J. Hyslop, J.V. Melton, C.Y. Pang, Y.H. Wei, M.P. Murphy, Bioenergetic consequences of accumulating the common 4977-bp mitochondrial DNA deletion, Eur. J. Biochem. 257 (1998) 192-201.
-
(1998)
Eur. J. Biochem.
, vol.257
, pp. 192-201
-
-
Porteous, W.K.1
James, A.M.2
Sheard, P.W.3
Porteous, C.M.4
Packer, M.A.5
Hyslop, S.J.6
Melton, J.V.7
Pang, C.Y.8
Wei, Y.H.9
Murphy, M.P.10
-
8
-
-
0027467531
-
Control of oxidative phosphorylation in rat muscle mitochondria: Implications for mitochondrial myopathies
-
T. Letellier, M. Malgat, J.P. Mazat, Control of oxidative phosphorylation in rat muscle mitochondria: Implications for mitochondrial myopathies, Biochim. Biophys. Acta 1141 (1993) 58-64.
-
(1993)
Biochim. Biophys. Acta
, vol.1141
, pp. 58-64
-
-
Letellier, T.1
Malgat, M.2
Mazat, J.P.3
-
9
-
-
0027932783
-
The kinetic basis of threshold effects observed in mitochondrial diseases: A systemic approach
-
T. Letellier, R. Heinrich, M. Malgat, J.P. Mazat, The kinetic basis of threshold effects observed in mitochondrial diseases: A systemic approach, Biochem. J. 302 (1994) 171-174.
-
(1994)
Biochem. J.
, vol.302
, pp. 171-174
-
-
Letellier, T.1
Heinrich, R.2
Malgat, M.3
Mazat, J.P.4
-
10
-
-
0033584845
-
Threshold effect and tissue specificity. Implication for mitochondrial cytopathies
-
R. Rossignol, M. Malgat, J.P. Mazat, T. Letellier, Threshold effect and tissue specificity. Implication for mitochondrial cytopathies, J. Biol. Chem. 274 (1999) 33426-33432.
-
(1999)
J. Biol. Chem.
, vol.274
, pp. 33426-33432
-
-
Rossignol, R.1
Malgat, M.2
Mazat, J.P.3
Letellier, T.4
-
11
-
-
0034177951
-
Tissue variation in the control of oxidative phosphorylation: Implication for mitochondrial diseases
-
R. Rossignol, T. Letellier, M. Malgat, C. Rocher, J.P. Mazat, Tissue variation in the control of oxidative phosphorylation: Implication for mitochondrial diseases, Biochem. J. 347 (2000) 45-53.
-
(2000)
Biochem. J.
, vol.347
, pp. 45-53
-
-
Rossignol, R.1
Letellier, T.2
Malgat, M.3
Rocher, C.4
Mazat, J.P.5
-
12
-
-
0029873904
-
Threshold effects and control of oxidative phosphorylation in nonsynaptic rat brain mitochondria
-
G.P. Davey, J.B. Clark, Threshold effects and control of oxidative phosphorylation in nonsynaptic rat brain mitochondria, J. Neurochem. 66 (1996) 1617-1624.
-
(1996)
J. Neurochem.
, vol.66
, pp. 1617-1624
-
-
Davey, G.P.1
Clark, J.B.2
-
13
-
-
0030707553
-
Threshold effects in synaptosomal and nonsynaptic mitochondria from hippocampal CA1 and paramedian neocortex brain regions
-
G.P. Davey, L. Canevari, J.B. Clark, Threshold effects in synaptosomal and nonsynaptic mitochondria from hippocampal CA1 and paramedian neocortex brain regions, J. Neurochem. 69 (1997) 2564-2570.
-
(1997)
J. Neurochem.
, vol.69
, pp. 2564-2570
-
-
Davey, G.P.1
Canevari, L.2
Clark, J.B.3
-
14
-
-
0032557511
-
Energy thresholds in brain mitochondria. Potential involvement in neurodegeneration
-
G.P. Davey, S. Peuchen, J.B. Clark, Energy thresholds in brain mitochondria. Potential involvement in neurodegeneration, J. Biol. Chem. 273 (1998) 12753-12757.
-
(1998)
J. Biol. Chem.
, vol.273
, pp. 12753-12757
-
-
Davey, G.P.1
Peuchen, S.2
Clark, J.B.3
-
15
-
-
0027440565
-
Biochemical consequences of a large deletion in the mitochondrial genome of a Drosophila subobscura strain
-
R. Debise, S. Touraille, R. Durand, S. Alziari, Biochemical consequences of a large deletion in the mitochondrial genome of a Drosophila subobscura strain, Biochem. Biophys. Res. Commun. 196 (1993) 355-362.
-
(1993)
Biochem. Biophys. Res. Commun.
, vol.196
, pp. 355-362
-
-
Debise, R.1
Touraille, S.2
Durand, R.3
Alziari, S.4
-
16
-
-
1842412515
-
Biochemical and molecular consequences of massive mitochondrial gene loss in different tissues of a mutant strain of Drosophila subobscura
-
F. Beziat, S. Touraille, R. Debise, F. Morel, N. Petit, P. Lecher, S. Alziari, Biochemical and molecular consequences of massive mitochondrial gene loss in different tissues of a mutant strain of Drosophila subobscura, J. Biol. Chem. 272 (1997) 22583-22590.
-
(1997)
J. Biol. Chem.
, vol.272
, pp. 22583-22590
-
-
Beziat, F.1
Touraille, S.2
Debise, R.3
Morel, F.4
Petit, N.5
Lecher, P.6
Alziari, S.7
-
17
-
-
0036190166
-
The nuclear genome is involved in heteroplasmy control in a mitochondrial mutant strain of Drosophila subobscura
-
G. Farge, S. Touraille, S. Le Goff, N. Petit, M. Renoux, F. Morel, S. Alziari, The nuclear genome is involved in heteroplasmy control in a mitochondrial mutant strain of Drosophila subobscura, Eur. J. Biochem. 269 (2002) 998-1005.
-
(2002)
Eur. J. Biochem.
, vol.269
, pp. 998-1005
-
-
Farge, G.1
Touraille, S.2
Le Goff, S.3
Petit, N.4
Renoux, M.5
Morel, F.6
Alziari, S.7
-
18
-
-
0026437588
-
Stable heteroplasmy for a large-scale deletion in the coding region of Drosophila subobscura mitochondrial DNA
-
A. Volz-Lingenhöhl, M. Solignanc, D. Sperlich, Stable heteroplasmy for a large-scale deletion in the coding region of Drosophila subobscura mitochondrial DNA, Proc. Natl. Acad. Sci. USA 89 (1992) 11528-11532.
-
(1992)
Proc. Natl. Acad. Sci. USA
, vol.89
, pp. 11528-11532
-
-
Volz-Lingenhöhl, A.1
Solignanc, M.2
Sperlich, D.3
-
20
-
-
0017184389
-
Protein essay reagent
-
M. Bradford, Protein essay reagent, Anal. Biochem. 72 (1976) 248-251.
-
(1976)
Anal. Biochem.
, vol.72
, pp. 248-251
-
-
Bradford, M.1
-
21
-
-
0025087904
-
ATP production rate in mitochondria isolated from microsamples of human muscle
-
R. Wibom, E. Hultman, ATP production rate in mitochondria isolated from microsamples of human muscle, Am. J. Physiol. 259 (1990) 2004-2010.
-
(1990)
Am. J. Physiol.
, vol.259
, pp. 2004-2010
-
-
Wibom, R.1
Hultman, E.2
-
22
-
-
0018164454
-
Preparation and properties of NADH: Ubiquinone oxidoreductase (complex I) EC 1.6.5.3
-
in: S. Fleisher, L. Packer (Eds.); Academic Press, New York
-
Y. Hatefi, Preparation and properties of NADH: Ubiquinone oxidoreductase (complex I) EC 1.6.5.3, in: S. Fleisher, L. Packer (Eds.), Methods in Enzymology, vol. 53, Academic Press, New York, 1978, pp. 11-14.
-
(1978)
Methods in Enzymology
, vol.53
, pp. 11-14
-
-
Hatefi, Y.1
-
23
-
-
0018064984
-
Preparation and properties of dihydro-ubiquinone: Cytochrome c oxidoreductase (complex III)
-
in: S. Fleisher, L. Packer (Eds.); Academic Press, New York
-
Y. Hatefi, Preparation and properties of dihydro-ubiquinone: Cytochrome c oxidoreductase (complex III), in: S. Fleisher, L. Packer (Eds.), Methods in Enzymology, vol. 53, Academic Press, New York, 1978, pp. 35-40.
-
(1978)
Methods in Enzymology
, vol.53
, pp. 35-40
-
-
Hatefi, Y.1
-
24
-
-
0018176687
-
Preparation and properties of complex IV (ferrocytochrome c: oxygen oxidoreductase) EC 1.9.3.1
-
in: S. Fleisher, L. Packer (Eds.); Academic Press, New York
-
B. Errede, M.D. Kamen, Y. Kamen, Y. Hatefi, Preparation and properties of complex IV (ferrocytochrome c: oxygen oxidoreductase) EC 1.9.3.1, in: S. Fleisher, L. Packer (Eds.), Methods in Enzymology, vol. 53, Academic Press, New York, 1978, pp. 40-47.
-
(1978)
Methods in Enzymology
, vol.53
, pp. 40-47
-
-
Errede, B.1
Kamen, M.D.2
Kamen, Y.3
Hatefi, Y.4
-
25
-
-
77957011800
-
Citrate synthase from rat liver
-
in: J.M. Loweinstein (Ed.); Academic Press, New York
-
D. Sheperd, S. Garland, Citrate synthase from rat liver, in: J.M. Loweinstein (Ed.), Methods in Enzymology, vol. Academic Press, New York, 1969, pp. 11-16.
-
(1969)
Methods in Enzymology
, vol.13
, pp. 11-16
-
-
Sheperd, D.1
Garland, S.2
-
26
-
-
0024242545
-
Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy
-
D.C. Wallace, G. Singh, M.T. Lott, J.A. Hodge, T.G. Schurr, A.M. Lezza, L.J. Elsas, E.K. Nikoskelainen, Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy, Science 242 (1988) 1427-1430.
-
(1988)
Science
, vol.242
, pp. 1427-1430
-
-
Wallace, D.C.1
Singh, G.2
Lott, M.T.3
Hodge, J.A.4
Schurr, T.G.5
Lezza, A.M.6
Elsas, L.J.7
Nikoskelainen, E.K.8
-
27
-
-
0031745795
-
Inborn errors of metabolism in the light of metabolic control analysis
-
J.P. Mazat, T. Letellier, M. Malgat, R. Rossignol, B. Korzeniewski, F. Demaugre, J.P. Leroux, Inborn errors of metabolism in the light of metabolic control analysis, Biochem. Soc. Trans. 26 (1998) 141-145.
-
(1998)
Biochem. Soc. Trans.
, vol.26
, pp. 141-145
-
-
Mazat, J.P.1
Letellier, T.2
Malgat, M.3
Rossignol, R.4
Korzeniewski, B.5
Demaugre, F.6
Leroux, J.P.7
-
28
-
-
0027210867
-
Mitochondrial genome expression in a mutant strain of D. subobscura, an animal model for large scale mtDNA deletion
-
F. Béziat, F. Morel, A. Volz-Lingenhol, N. Saint-Paul, S. Alziari, Mitochondrial genome expression in a mutant strain of D. subobscura, an animal model for large scale mtDNA deletion, Nucleic Acids Res. 21 (1993) 387-392.
-
(1993)
Nucleic Acids Res.
, vol.21
, pp. 387-392
-
-
Béziat, F.1
Morel, F.2
Volz-Lingenhol, A.3
Saint-Paul, N.4
Alziari, S.5
-
29
-
-
0028107084
-
The control of mitochondrial oxidations by complex III in rat muscle and liver mitochondria-implications for our understanding of mitochondrial cytopathies in man
-
R.W. Taylor, M.A. Birchmachin, K. Bartlett, S.A. Lowerson, D.M. Turnbull, The control of mitochondrial oxidations by complex III in rat muscle and liver mitochondria-implications for our understanding of mitochondrial cytopathies in man, J. Biol. Chem. 269 (1994) 3523-3528.
-
(1994)
J. Biol. Chem.
, vol.269
, pp. 3523-3528
-
-
Taylor, R.W.1
Birchmachin, M.A.2
Bartlett, K.3
Lowerson, S.A.4
Turnbull, D.M.5
-
30
-
-
0028352261
-
Tissular distribution of heteroplasmy and ultrastructural studies of mitochondria from a Drosophila subobscura mitochondrial deletion mutant
-
P. Lecher, F. Beziat, S. Alziari, Tissular distribution of heteroplasmy and ultrastructural studies of mitochondria from a Drosophila subobscura mitochondrial deletion mutant, Biol. Cell 80 (1994) 25-33.
-
(1994)
Biol. Cell
, vol.80
, pp. 25-33
-
-
Lecher, P.1
Beziat, F.2
Alziari, S.3
-
31
-
-
0029910573
-
Localization by ultrastructural in situ hybridization of mitochondrial transcripts in epithelial cells of a Drosophila subobscura deletion mutant
-
P. Lecher, N. Petit, F. Beziat, S. Alziari, Localization by ultrastructural in situ hybridization of mitochondrial transcripts in epithelial cells of a Drosophila subobscura deletion mutant, Eur. J. Cell Biol. 71 (1996) 424-427.
-
(1996)
Eur. J. Cell Biol.
, vol.71
, pp. 424-427
-
-
Lecher, P.1
Petit, N.2
Beziat, F.3
Alziari, S.4
-
32
-
-
0033772366
-
Quantitative analysis, by ultrastructural in situ hybridization, of mitochondrial genomes and their expression in mid-gut and ovarian cells of a mutant strain of Drosophila subobscura
-
P. Lecher, N. Petit, S. Le Goff, S. Alziari, Quantitative analysis, by ultrastructural in situ hybridization, of mitochondrial genomes and their expression in mid-gut and ovarian cells of a mutant strain of Drosophila subobscura, Biol. Cell 92 (2000) 341-350.
-
(2000)
Biol. Cell
, vol.92
, pp. 341-350
-
-
Lecher, P.1
Petit, N.2
Le Goff, S.3
Alziari, S.4
-
33
-
-
0031834010
-
Developmental changes in heteroplasmy level and mitochondrial gene expression in a Drosophila subobscura mitochondrial deletion mutant
-
N. Petit, S. Touraille, R. Debise, F. Morel, M. Renoux, P. Lecher, S. Alziari, Developmental changes in heteroplasmy level and mitochondrial gene expression in a Drosophila subobscura mitochondrial deletion mutant, Curr. Genet. 33 (1998) 330-339.
-
(1998)
Curr. Genet.
, vol.33
, pp. 330-339
-
-
Petit, N.1
Touraille, S.2
Debise, R.3
Morel, F.4
Renoux, M.5
Lecher, P.6
Alziari, S.7
-
34
-
-
0034809484
-
Technical knockout, a Drosophila model of mitochondrial deafness
-
J.M. Toivonen, K.M. O'Dell, N. Petit, S.C. Irvin, G.K. Knight, M. Lehtonen, M. Longmuir, K. Luoto, S. Touraille, Z. Wang, S. Alziari, Z.H. Shah, H.T. Jacobs, Technical knockout, a Drosophila model of mitochondrial deafness, Genetics 159 (2001) 241-254.
-
(2001)
Genetics
, vol.159
, pp. 241-254
-
-
Toivonen, J.M.1
O'Dell, K.M.2
Petit, N.3
Irvin, S.C.4
Knight, G.K.5
Lehtonen, M.6
Longmuir, M.7
Luoto, K.8
Touraille, S.9
Wang, Z.10
Alziari, S.11
Shah, Z.H.12
Jacobs, H.T.13
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