-
1
-
-
84860840558
-
Mitochondrial diseases
-
Schapira, A.H. (2012) Mitochondrial diseases. Lancet, 379, 1825-1834.
-
(2012)
Lancet
, vol.379
, pp. 1825-1834
-
-
Schapira, A.H.1
-
2
-
-
82755161770
-
Mitochondrial DNA and disease
-
Greaves, L.C., Reeve, A.K., Taylor, R.W. and Turnbull, D.M. (2012) Mitochondrial DNA and disease. J. Pathol., 226, 274-286.
-
(2012)
J. Pathol.
, vol.226
, pp. 274-286
-
-
Greaves, L.C.1
Reeve, A.K.2
Taylor, R.W.3
Turnbull, D.M.4
-
3
-
-
84865405029
-
Therapies in inborn errors of oxidative metabolism
-
Schiff, M., Bénit, P., Jacobs, H.T., Vockley, J. and Rustin, P. (2012) Therapies in inborn errors of oxidative metabolism. Trends Endocrinol. Metab., 23, 488-495.
-
(2012)
Trends Endocrinol. Metab.
, vol.23
, pp. 488-495
-
-
Schiff, M.1
Bénit, P.2
Jacobs, H.T.3
Vockley, J.4
Rustin, P.5
-
4
-
-
70450253363
-
Respiratory chain alternative enzymes as tools to better understand and counteract respiratory chain deficiencies in human cells and animals
-
Rustin, P. and Jacobs, H.T. (2009) Respiratory chain alternative enzymes as tools to better understand and counteract respiratory chain deficiencies in human cells and animals. Physiol. Plant., 137, 362-370.
-
(2009)
Physiol. Plant.
, vol.137
, pp. 362-370
-
-
Rustin, P.1
Jacobs, H.T.2
-
5
-
-
68249124533
-
Alternative oxidase in animals: unique characteristics and taxonomic distribution
-
McDonald, A.E., Vanlerberghe, G.C. and Staples, J.F. (2009) Alternative oxidase in animals: unique characteristics and taxonomic distribution. J. Exp. Biol., 212, 2627-2634.
-
(2009)
J. Exp. Biol.
, vol.212
, pp. 2627-2634
-
-
McDonald, A.E.1
Vanlerberghe, G.C.2
Staples, J.F.3
-
6
-
-
33645769763
-
Allotopic expression of a mitochondrial alternative oxidase confers cyanide resistance to human cell respiration
-
Hakkaart, G.A., Dassa, E.P., Jacobs, H.T. and Rustin, P. (2006) Allotopic expression of a mitochondrial alternative oxidase confers cyanide resistance to human cell respiration. EMBO Rep., 7, 341-345.
-
(2006)
EMBO Rep.
, vol.7
, pp. 341-345
-
-
Hakkaart, G.A.1
Dassa, E.P.2
Jacobs, H.T.3
Rustin, P.4
-
7
-
-
70450247586
-
Expression of the alternative oxidase complements cytochrome c oxidase deficiency in human cells
-
Dassa, E.P., Dufour, E., Gonçalves, S., Paupe, V., Hakkaart, G.A., Jacobs, H.T. and Rustin, P. (2009) Expression of the alternative oxidase complements cytochrome c oxidase deficiency in human cells. EMBO Mol. Med., 1, 30-36.
-
(2009)
EMBO Mol. Med.
, vol.1
, pp. 30-36
-
-
Dassa, E.P.1
Dufour, E.2
Gonçalves, S.3
Paupe, V.4
Hakkaart, G.A.5
Jacobs, H.T.6
Rustin, P.7
-
8
-
-
65349167880
-
Expression of the Ciona intestinalis alternative oxidase (AOX) in Drosophila complements defects in mitochondrial oxidative phosphorylation
-
Fernandez-Ayala, D.J., Sanz, A., Vartiainen, S., Kemppainen, K.K., Babusiak, M., Mustalahti, E., Costa, R., Tuomela, T., Zeviani, M., Chung, J. et al. (2009) Expression of the Ciona intestinalis alternative oxidase (AOX) in Drosophila complements defects in mitochondrial oxidative phosphorylation. Cell Metab., 9, 449-460.
-
(2009)
Cell Metab.
, vol.9
, pp. 449-460
-
-
Fernandez-Ayala, D.J.1
Sanz, A.2
Vartiainen, S.3
Kemppainen, K.K.4
Babusiak, M.5
Mustalahti, E.6
Costa, R.7
Tuomela, T.8
Zeviani, M.9
Chung, J.10
-
9
-
-
84873498609
-
Alternative oxidase expression in the mouse enables bypassing cytochrome c oxidase blockade and limits mitochondrial ROS overproduction
-
El-Khoury, R., Dufour, E., Rak, M., Ramanantsoa, N., Grandchamp, N., Csaba, Z., Duvillie, B., Benit, P., Gallego, J., Gressens, P. et al. (2013) Alternative oxidase expression in the mouse enables bypassing cytochrome c oxidase blockade and limits mitochondrial ROS overproduction. PLoS Gemet., 9, e1003182.
-
(2013)
PLoS Gemet.
, vol.9
-
-
El-Khoury, R.1
Dufour, E.2
Rak, M.3
Ramanantsoa, N.4
Grandchamp, N.5
Csaba, Z.6
Duvillie, B.7
Benit, P.8
Gallego, J.9
Gressens, P.10
-
10
-
-
77952689461
-
Expression of the yeast NADH dehydrogenase Ndi1 in Drosophila confers increased lifespan independently of dietary restriction
-
Sanz, A., Soikkeli, M., Portero-Otín, M., Wilson, A., Kemppainen, E., McIlroy, G., Ellilä, S., Kemppainen, K.K., Tuomela, T., Lakanmaa, M. et al. (2010) Expression of the yeast NADH dehydrogenase Ndi1 in Drosophila confers increased lifespan independently of dietary restriction. Proc. Natl. Acad. Sci. USA, 107, 9105-9110.
-
(2010)
Proc. Natl. Acad. Sci. USA
, vol.107
, pp. 9105-9110
-
-
Sanz, A.1
Soikkeli, M.2
Portero-Otín, M.3
Wilson, A.4
Kemppainen, E.5
McIlroy, G.6
Ellilä, S.7
Kemppainen, K.K.8
Tuomela, T.9
Lakanmaa, M.10
-
11
-
-
84857923810
-
Structural studies on bovine heart cytochrome c oxidase
-
Yoshikawa, S., Muramoto, K., Shinzawa-Itoh, K. and Mochizuki, M. (2012) Structural studies on bovine heart cytochrome c oxidase. Biochim. Biophys. Acta, 1817, 579-589.
-
(2012)
Biochim. Biophys. Acta
, vol.1817
, pp. 579-589
-
-
Yoshikawa, S.1
Muramoto, K.2
Shinzawa-Itoh, K.3
Mochizuki, M.4
-
12
-
-
0032104133
-
Assembly of cytochrome-c oxidase in cultured human cells
-
Nijtmans, L.G., Taanman, J.W., Muijsers, A.O., Speijer, D. and Van den Bogert, C. (1998) Assembly of cytochrome-c oxidase in cultured human cells. Eur. J. Biochem., 254, 389-394.
-
(1998)
Eur. J. Biochem.
, vol.254
, pp. 389-394
-
-
Nijtmans, L.G.1
Taanman, J.W.2
Muijsers, A.O.3
Speijer, D.4
Van den Bogert, C.5
-
13
-
-
56149104649
-
Cytochrome c oxidase biogenesis: new levels of regulation
-
Fontanesi, F., Soto, I.C. and Barrientos, A. (2008) Cytochrome c oxidase biogenesis: new levels of regulation. IUBMB Life, 60, 557-568.
-
(2008)
IUBMB Life
, vol.60
, pp. 557-568
-
-
Fontanesi, F.1
Soto, I.C.2
Barrientos, A.3
-
14
-
-
84865771586
-
NDUFA4 is a subunit of complex IV of the mammalian electron transport chain
-
Balsa, E., Marco, R., Perales-Clemente, E., Szklarczyk, R., Calvo, E., Landázuri, M.O. and Enríquez, J.A. (2012) NDUFA4 is a subunit of complex IV of the mammalian electron transport chain. Cell Metab., 16, 378-386.
-
(2012)
Cell Metab.
, vol.16
, pp. 378-386
-
-
Balsa, E.1
Marco, R.2
Perales-Clemente, E.3
Szklarczyk, R.4
Calvo, E.5
Landázuri, M.O.6
Enríquez, J.A.7
-
15
-
-
84858061040
-
Rcf1 mediates cytochrome oxidase assembly and respirasome formation, revealing heterogeneity of the enzyme complex
-
Vukotic, M., Oeljeklaus, S., Wiese, S., Vögtle, F.N., Meisinger, C., Meyer, H.E., Zieseniss, A., Katschinski, D.M., Jans, D.C., Jakobs, S. et al. (2012) Rcf1 mediates cytochrome oxidase assembly and respirasome formation, revealing heterogeneity of the enzyme complex. Cell Metab., 15, 336-347.
-
(2012)
Cell Metab.
, vol.15
, pp. 336-347
-
-
Vukotic, M.1
Oeljeklaus, S.2
Wiese, S.3
Vögtle, F.N.4
Meisinger, C.5
Meyer, H.E.6
Zieseniss, A.7
Katschinski, D.M.8
Jans, D.C.9
Jakobs, S.10
-
16
-
-
84863229229
-
Identification of a protein mediating respiratory supercomplex stability
-
Chen, Y.C., Taylor, E.B., Dephoure, N., Heo, J.M., Tonhato, A., Papandreou, I., Nath, N., Denko, N.C., Gygi, S.P. and Rutter, J. (2012) Identification of a protein mediating respiratory supercomplex stability. Cell Metab., 15, 348-360.
-
(2012)
Cell Metab.
, vol.15
, pp. 348-360
-
-
Chen, Y.C.1
Taylor, E.B.2
Dephoure, N.3
Heo, J.M.4
Tonhato, A.5
Papandreou, I.6
Nath, N.7
Denko, N.C.8
Gygi, S.P.9
Rutter, J.10
-
17
-
-
84880387219
-
A stabilizing factor for mitochondrial respiratory supercomplex assembly regulates energy metabolism in muscle
-
Article number 2147
-
Ikeda, K., Shiba, S., Horie-Inoue, K., Shimokata, K. and Inoue, S. (2013) A stabilizing factor for mitochondrial respiratory supercomplex assembly regulates energy metabolism in muscle. Nat. Commun., 4. Article number 2147.
-
(2013)
Nat. Commun.
, vol.4
-
-
Ikeda, K.1
Shiba, S.2
Horie-Inoue, K.3
Shimokata, K.4
Inoue, S.5
-
18
-
-
84879617853
-
Supercomplex assembly determines electron flux in the mitochondrial electron transport chain
-
Lapuente-Brun, E., Moreno-Loshuertos, R., Acín-Pérez, R., Latorre-Pellicer, A., Colás, C., Balsa, E., Perales-Clemente, E., Quirós, P.M., Calvo, E., Rodríguez-Hernández, M.A. et al. (2013) Supercomplex assembly determines electron flux in the mitochondrial electron transport chain. Science, 340, 1567-1570.
-
(2013)
Science
, vol.340
, pp. 1567-1570
-
-
Lapuente-Brun, E.1
Moreno-Loshuertos, R.2
Acín-Pérez, R.3
Latorre-Pellicer, A.4
Colás, C.5
Balsa, E.6
Perales-Clemente, E.7
Quirós, P.M.8
Calvo, E.9
Rodríguez-Hernández, M.A.10
-
19
-
-
34250716562
-
Mutations in cytochrome c oxidase subunit VIa cause neurodegeneration and motor dysfunction in Drosophila
-
Liu, W., Gnanasambandam, R., Benjamin, J., Kaur, G., Getman, P.B., Siegel, A.J., Shortridge, R.D. and Singh, S. (2007) Mutations in cytochrome c oxidase subunit VIa cause neurodegeneration and motor dysfunction in Drosophila. Genetics, 176, 937-946.
-
(2007)
Genetics
, vol.176
, pp. 937-946
-
-
Liu, W.1
Gnanasambandam, R.2
Benjamin, J.3
Kaur, G.4
Getman, P.B.5
Siegel, A.J.6
Shortridge, R.D.7
Singh, S.8
-
20
-
-
84863746788
-
The many clinical faces of cytochrome c oxidase deficiency
-
DiMauro, S., Tanji, K. and Schon, E.A. (2012) The many clinical faces of cytochrome c oxidase deficiency. Adv. Exp. Med. Biol., 748, 341-357.
-
(2012)
Adv. Exp. Med. Biol.
, vol.748
, pp. 341-357
-
-
DiMauro, S.1
Tanji, K.2
Schon, E.A.3
-
21
-
-
71849115876
-
Cytochrome c oxidase deficiency: patients and animal models
-
Diaz, F. (2010) Cytochrome c oxidase deficiency: patients and animal models. Biochim. Biophys. Acta, 1802, 100-110.
-
(2010)
Biochim. Biophys. Acta
, vol.1802
, pp. 100-110
-
-
Diaz, F.1
-
22
-
-
0032470811
-
Mutations of SURF-1 in Leigh disease associated with cytochrome c oxidase deficiency
-
Tiranti, V., Hoertnagel, K., Carrozzo, R., Galimberti, C., Munaro, M., Granatiero, M., Zelante, L., Gasparini, P., Marzella, R., Rocchi, M. et al. (1999) Mutations of SURF-1 in Leigh disease associated with cytochrome c oxidase deficiency. Am. J. Hum. Genet., 63, 1609-1621.
-
(1999)
Am. J. Hum. Genet.
, vol.63
, pp. 1609-1621
-
-
Tiranti, V.1
Hoertnagel, K.2
Carrozzo, R.3
Galimberti, C.4
Munaro, M.5
Granatiero, M.6
Zelante, L.7
Gasparini, P.8
Marzella, R.9
Rocchi, M.10
-
23
-
-
17344362021
-
SURF1, encoding a factor involved in the biogenesis of cytochrome c oxidase, is mutated in Leigh syndrome
-
Zhu, Z., Yao, J., Johns, T., Fu, K., De Bie, I., Macmillan, C., Cuthbert, A.P., Newbold, R.F., Wang, J., Chevrette, M. et al. (1998) SURF1, encoding a factor involved in the biogenesis of cytochrome c oxidase, is mutated in Leigh syndrome. Nat. Genet., 20, 337-343.
-
(1998)
Nat. Genet.
, vol.20
, pp. 337-343
-
-
Zhu, Z.1
Yao, J.2
Johns, T.3
Fu, K.4
De Bie, I.5
Macmillan, C.6
Cuthbert, A.P.7
Newbold, R.F.8
Wang, J.9
Chevrette, M.10
-
24
-
-
79953683175
-
A mutation in C2orf64 causes impaired cytochrome c oxidase assembly and mitochondrial cardiomyopathy
-
Huigsloot, M., Nijtmans, L.G., Szklarczyk, R., Baars, M.J., van den Brand, M.A., Hendriksfranssen, M.G., van den Heuvel, L.P., Smeitink, J.A., Huynen, M.A. and Rodenburg, R.J. (2011) A mutation in C2orf64 causes impaired cytochrome c oxidase assembly and mitochondrial cardiomyopathy. Am. J. Hum. Genet., 88, 488-493.
-
(2011)
Am. J. Hum. Genet.
, vol.88
, pp. 488-493
-
-
Huigsloot, M.1
Nijtmans, L.G.2
Szklarczyk, R.3
Baars, M.J.4
van den Brand, M.A.5
Hendriksfranssen, M.G.6
van den Heuvel, L.P.7
Smeitink, J.A.8
Huynen, M.A.9
Rodenburg, R.J.10
-
25
-
-
0032699506
-
Fatal infantile cardioencephalomyopathy with COX deficiency and mutations SCO2in, a COX assembly gene
-
Papadopoulou, L.C., Sue, C.M., Davidson, M.M., Tanji, K., Nishino, I., Sadlock, J.E., Krishna, S., Walker, W., Selby, J., Glerum, D.M. et al. (1999) Fatal infantile cardioencephalomyopathy with COX deficiency and mutations SCO2in, a COX assembly gene. Nat Genet., 23, 333-337.
-
(1999)
Nat Genet.
, vol.23
, pp. 333-337
-
-
Papadopoulou, L.C.1
Sue, C.M.2
Davidson, M.M.3
Tanji, K.4
Nishino, I.5
Sadlock, J.E.6
Krishna, S.7
Walker, W.8
Selby, J.9
Glerum, D.M.10
-
26
-
-
0034192365
-
A mutation in the human heme A:farnesyltransferase gene (COX10) causes cytochrome c oxidase deficiency
-
Valnot, I., von Kleist-Retzow, J.C., Barrientos, A., Gorbatyuk, M., Taanman, J.-W., Mehaye, B., Rustin, P., Tzagoloff, A., Munnich, A. and Rotig, A. (2000) A mutation in the human heme A:farnesyltransferase gene (COX10) causes cytochrome c oxidase deficiency. Hum. Mol. Genet., 9, 1245-1249.
-
(2000)
Hum. Mol. Genet.
, vol.9
, pp. 1245-1249
-
-
Valnot, I.1
von Kleist-Retzow, J.C.2
Barrientos, A.3
Gorbatyuk, M.4
Taanman, J.-W.5
Mehaye, B.6
Rustin, P.7
Tzagoloff, A.8
Munnich, A.9
Rotig, A.10
-
27
-
-
45449121006
-
Severe infantile encephalomyopathy caused by a mutation in COX6B1, a nucleus-encoded subunit of cytochrome c oxidase
-
Massa, V., Fernandez-Vizarra, E., Alshahwan, S., Bakhsh, E., Goffrini, P., Ferrero, I., Mereghetti, P., D'Adamo, P., Gasparini, P. and Zeviani, M. (2008) Severe infantile encephalomyopathy caused by a mutation in COX6B1, a nucleus-encoded subunit of cytochrome c oxidase. Am. J. Hum. Genet., 82, 1281-1289.
-
(2008)
Am. J. Hum. Genet.
, vol.82
, pp. 1281-1289
-
-
Massa, V.1
Fernandez-Vizarra, E.2
Alshahwan, S.3
Bakhsh, E.4
Goffrini, P.5
Ferrero, I.6
Mereghetti, P.7
D'Adamo, P.8
Gasparini, P.9
Zeviani, M.10
-
28
-
-
84868366941
-
Mutations in COX7B cause microphthalmia with linear skin lesions, an unconventional mitochondrial disease
-
Indrieri, A., van Rahden, V.A., Tiranti, V., Morleo, M., Iaconis, D., Tammaro, R., D'Amato, I., Conte, I., Maystadt, I., Demuth, S. et al. (2012) Mutations in COX7B cause microphthalmia with linear skin lesions, an unconventional mitochondrial disease. Am. J. Hum. Genet., 91, 942-949.
-
(2012)
Am. J. Hum. Genet.
, vol.91
, pp. 942-949
-
-
Indrieri, A.1
van Rahden, V.A.2
Tiranti, V.3
Morleo, M.4
Iaconis, D.5
Tammaro, R.6
D'Amato, I.7
Conte, I.8
Maystadt, I.9
Demuth, S.10
-
29
-
-
28244461616
-
Mutations in mtDNA-encoded cytochrome c oxidase subunit genes causing isolated myopathy or severe encephalomyopathy
-
Horváth, R., Schoser, B.G., Müller-Höcker, J., Völpel, M., Jaksch, M. and Lochmüller, H. (2005) Mutations in mtDNA-encoded cytochrome c oxidase subunit genes causing isolated myopathy or severe encephalomyopathy. Neuromuscul. Disord., 15, 851-857.
-
(2005)
Neuromuscul. Disord.
, vol.15
, pp. 851-857
-
-
Horváth, R.1
Schoser, B.G.2
Müller-Höcker, J.3
Völpel, M.4
Jaksch, M.5
Lochmüller, H.6
-
30
-
-
0001411977
-
A missense mutation of cytochrome oxidase subunit II causes defective assembly and myopathy
-
Rahman, S., Taanman, J.W., Cooper, J.M., Nelson, I., Hargreaves, I., Meunier, B., Hanna, M.G., García, J.J., Capaldi, R.A., Lake, B.D. et al. (1999) A missense mutation of cytochrome oxidase subunit II causes defective assembly and myopathy. Am. J. Hum. Genet., 65, 1030-10939.
-
(1999)
Am. J. Hum. Genet.
, vol.65
, pp. 1030-10939
-
-
Rahman, S.1
Taanman, J.W.2
Cooper, J.M.3
Nelson, I.4
Hargreaves, I.5
Meunier, B.6
Hanna, M.G.7
García, J.J.8
Capaldi, R.A.9
Lake, B.D.10
-
31
-
-
14844288426
-
Mitochondrial myopathy and rhabdomyolysis associated with a novel nonsense mutation in the gene encoding cytochrome c oxidase subunit I
-
Kollberg, G., Moslemi, A.R., Lindberg, C., Holme, E. and Oldfors, A.J. (2005) Mitochondrial myopathy and rhabdomyolysis associated with a novel nonsense mutation in the gene encoding cytochrome c oxidase subunit I. Neuropathol. Exp. Neurol., 64, 123-128.
-
(2005)
Neuropathol. Exp. Neurol.
, vol.64
, pp. 123-128
-
-
Kollberg, G.1
Moslemi, A.R.2
Lindberg, C.3
Holme, E.4
Oldfors, A.J.5
-
32
-
-
0037458031
-
Identification of a gene causing human cytochrome c oxidase deficiency by integrative genomics
-
Mootha, V.K., Lepage, P., Miller, K., Bunkenborg, J., Reich, M., Hjerrild, M., Delmonte, T., Villeneuve, A., Sladek, R., Xu, F. et al. (2003) Identification of a gene causing human cytochrome c oxidase deficiency by integrative genomics. Proc. Natl. Acad. Sci. USA, 100, 605-610.
-
(2003)
Proc. Natl. Acad. Sci. USA
, vol.100
, pp. 605-610
-
-
Mootha, V.K.1
Lepage, P.2
Miller, K.3
Bunkenborg, J.4
Reich, M.5
Hjerrild, M.6
Delmonte, T.7
Villeneuve, A.8
Sladek, R.9
Xu, F.10
-
33
-
-
67649833762
-
Mutation in TACO1, encoding a translational activator of COXI, results in cytochrome c oxidase deficiency and late-onset Leigh syndrome
-
Weraarpachai, W., Antonicka, H., Sasarman, F., Seeger, J., Schrank, B., Kolesar, J.E., Lochmüller, H., Chevrette, M., Kaufman, B.A., Horvath, R. and Shoubridge, E.A. (2009) Mutation in TACO1, encoding a translational activator of COXI, results in cytochrome c oxidase deficiency and late-onset Leigh syndrome. Nat. Genet., 41, 833-837.
-
(2009)
Nat. Genet.
, vol.41
, pp. 833-837
-
-
Weraarpachai, W.1
Antonicka, H.2
Sasarman, F.3
Seeger, J.4
Schrank, B.5
Kolesar, J.E.6
Lochmüller, H.7
Chevrette, M.8
Kaufman, B.A.9
Horvath, R.10
Shoubridge, E.A.11
-
34
-
-
84865295946
-
Cytochrome c oxidase dysfunction in oxidative stress
-
Srinivasan, S. and Avadhani, N.G. (2012) Cytochrome c oxidase dysfunction in oxidative stress. Free Radic. Biol. Med., 53, 1252-1263.
-
(2012)
Free Radic. Biol. Med.
, vol.53
, pp. 1252-1263
-
-
Srinivasan, S.1
Avadhani, N.G.2
-
35
-
-
84863751490
-
Cytochrome c oxidase and its role in neurodegeneration and neuroprotection
-
Arnold, S. (2012) Cytochrome c oxidase and its role in neurodegeneration and neuroprotection. Adv. Exp. Med. Biol., 748, 305-339.
-
(2012)
Adv. Exp. Med. Biol.
, vol.748
, pp. 305-339
-
-
Arnold, S.1
-
36
-
-
70449433157
-
The role of cytochrome c oxidase deficiency in ROS and amyloid plaque formation
-
Pickrell, A.M., Fukui, H. and Moraes, C.T. (2009) The role of cytochrome c oxidase deficiency in ROS and amyloid plaque formation. J. Bioenerg. Biomembr., 41, 453-456.
-
(2009)
J. Bioenerg. Biomembr.
, vol.41
, pp. 453-456
-
-
Pickrell, A.M.1
Fukui, H.2
Moraes, C.T.3
-
37
-
-
33750347347
-
Mitochondrial dysfunction and oxidative stress in neurodegenerative diseases
-
Lin, M.T. and Beal, M.F. (2006) Mitochondrial dysfunction and oxidative stress in neurodegenerative diseases. Nature, 443, 787-795.
-
(2006)
Nature
, vol.443
, pp. 787-795
-
-
Lin, M.T.1
Beal, M.F.2
-
38
-
-
84876732347
-
Mitochondrial respiratory chain Complexes I and IV are impaired by b-amyloid via direct interaction and through complex I-dependent ROS production, respectively
-
Bobba, A., Amadoro, G., Valenti, D., Corsetti, V., Lassandro, R. and Atlante, A. (2013) Mitochondrial respiratory chain Complexes I and IV are impaired by b-amyloid via direct interaction and through complex I-dependent ROS production, respectively. Mitochondrion, 13, 298-311.
-
(2013)
Mitochondrion
, vol.13
, pp. 298-311
-
-
Bobba, A.1
Amadoro, G.2
Valenti, D.3
Corsetti, V.4
Lassandro, R.5
Atlante, A.6
-
39
-
-
84875920169
-
Dysfunctional mitochondrial respiration in the striatum of the Huntington's disease transgenic R6/2 mouse model
-
10.1371/currents.hd.d8917b4862929772c5a2f2a34ef1c201
-
Aidt, F.H., Nielsen, S.M., Kanters, J., Pesta, D., Nielsen, T.T., Nørremølle, A., Hasholt, L., Christiansen, M. and Hagen, C.M. (2013) Dysfunctional mitochondrial respiration in the striatum of the Huntington's disease transgenic R6/2 mouse model. PLoS Curr. 10.1371/currents.hd.d8917b4862929772c5a2f2a34ef1c201.
-
(2013)
PLoS Curr
-
-
Aidt, F.H.1
Nielsen, S.M.2
Kanters, J.3
Pesta, D.4
Nielsen, T.T.5
Nørremølle, A.6
Hasholt, L.7
Christiansen, M.8
Hagen, C.M.9
-
40
-
-
84857923094
-
Regulation of mitochondrial respiration and apoptosis through cell signaling: cytochrome c oxidase and cytochrome c in ischemia/reperfusion injury and inflammation
-
Hüttemann, M., Helling, S., Sanderson, T.H., Sinkler, C., Samavati, L., Mahapatra, G., Varughese, A., Lu, G., Liu, J., Ramzan, R. et al. (2012) Regulation of mitochondrial respiration and apoptosis through cell signaling: cytochrome c oxidase and cytochrome c in ischemia/reperfusion injury and inflammation. Biochim. Biophys. Acta, 1817, 598-609.
-
(2012)
Biochim. Biophys. Acta
, vol.1817
, pp. 598-609
-
-
Hüttemann, M.1
Helling, S.2
Sanderson, T.H.3
Sinkler, C.4
Samavati, L.5
Mahapatra, G.6
Varughese, A.7
Lu, G.8
Liu, J.9
Ramzan, R.10
-
41
-
-
84857922138
-
Cytochrome c oxidase: evolution of control via nuclear subunit addition
-
Pierron, D., Wildman, D.E., Hüttemann, M., Markondapatnaikuni, G.C., Aras, S. and Grossman, L.I. (2012) Cytochrome c oxidase: evolution of control via nuclear subunit addition. Biochim. Biophys. Acta, 1817, 590-597.
-
(2012)
Biochim. Biophys. Acta
, vol.1817
, pp. 590-597
-
-
Pierron, D.1
Wildman, D.E.2
Hüttemann, M.3
Markondapatnaikuni, G.C.4
Aras, S.5
Grossman, L.I.6
-
42
-
-
0033584845
-
Threshold effect and tissue specificity. Implication for mitochondrial cytopathies
-
Rossignol, R., Malgat, M., Mazat, J.P. and Letellier, T. (1999) Threshold effect and tissue specificity. Implication for mitochondrial cytopathies. J. Biol. Chem., 274, 33426-33432.
-
(1999)
J. Biol. Chem.
, vol.274
, pp. 33426-33432
-
-
Rossignol, R.1
Malgat, M.2
Mazat, J.P.3
Letellier, T.4
-
43
-
-
45549095853
-
Mitochondrial transcription factor B2 is essential for metabolic function in Drosophila melanogaster development
-
Adán, C., Matsushima, Y., Hernández-Sierra, R., Marco-Ferreres, R., Fernández-Moreno, M.A., González-Vioque, E., Calleja, M., Aragón, J.J., Kaguni, L.S. and Garesse, R.J. (2008) Mitochondrial transcription factor B2 is essential for metabolic function in Drosophila melanogaster development. J. Biol. Chem., 283, 12333-12342.
-
(2008)
J. Biol. Chem.
, vol.283
, pp. 12333-12342
-
-
Adán, C.1
Matsushima, Y.2
Hernández-Sierra, R.3
Marco-Ferreres, R.4
Fernández-Moreno, M.A.5
González-Vioque, E.6
Calleja, M.7
Aragón, J.J.8
Kaguni, L.S.9
Garesse, R.J.10
-
44
-
-
84863799820
-
Coiled coil domain-containing protein 56 (CCDC56) is a novel mitochondrial protein essential for cytochrome c oxidase function
-
Peralta, S., Clemente, P., Sánchez-Martínez, A., Calleja, M., Hernández-Sierra, R., Matsushima, Y., Adán, C., Ugalde, C., Fernández-Moreno, M.Á., Kaguni, L.S. and Garesse, R.J. (2012) Coiled coil domain-containing protein 56 (CCDC56) is a novel mitochondrial protein essential for cytochrome c oxidase function. J. Biol. Chem., 287, 24174-24185.
-
(2012)
J. Biol. Chem.
, vol.287
, pp. 24174-24185
-
-
Peralta, S.1
Clemente, P.2
Sánchez-Martínez, A.3
Calleja, M.4
Hernández-Sierra, R.5
Matsushima, Y.6
Adán, C.7
Ugalde, C.8
Fernández-Moreno, M.Á.9
Kaguni, L.S.10
Garesse, R.J.11
-
45
-
-
33847304164
-
Increased longevity and refractoriness to Ca(2+)-dependent neurodegeneration in Surf1 knockout mice
-
Dell'agnello, C., Leo, S., Agostino, A., Szabadkai, G., Tiveron, C., Zulian, A., Prelle, A., Roubertoux, P., Rizzuto, R. and Zeviani, M. (2007) Increased longevity and refractoriness to Ca(2+)-dependent neurodegeneration in Surf1 knockout mice. Hum. Mol. Genet., 16, 431-444.
-
(2007)
Hum. Mol. Genet.
, vol.16
, pp. 431-444
-
-
Dell'agnello, C.1
Leo, S.2
Agostino, A.3
Szabadkai, G.4
Tiveron, C.5
Zulian, A.6
Prelle, A.7
Roubertoux, P.8
Rizzuto, R.9
Zeviani, M.10
-
46
-
-
0035887745
-
Late-onset corticohippocampal neurodepletion attributable to catastrophic failure of oxidative phosphorylation in MILON mice
-
Sörensen, L., Ekstrand, M., Silva, J.P., Lindqvist, E., Xu, B., Rustin, P., Olson, L. and Larsson, N.G. (2001) Late-onset corticohippocampal neurodepletion attributable to catastrophic failure of oxidative phosphorylation in MILON mice. J. Neurosci., 21, 8082-8090.
-
(2001)
J. Neurosci.
, vol.21
, pp. 8082-8090
-
-
Sörensen, L.1
Ekstrand, M.2
Silva, J.P.3
Lindqvist, E.4
Xu, B.5
Rustin, P.6
Olson, L.7
Larsson, N.G.8
-
47
-
-
43049151118
-
Age-associated mosaic respiratory chain deficiency causes trans-neuronal degeneration
-
Dufour, E., Terzioglu, M., Sterky, F.H., Sörensen, L., Galter, D., Olson, L., Wilbertz, J. and Larsson, N.G. (2008) Age-associated mosaic respiratory chain deficiency causes trans-neuronal degeneration. Hum. Mol. Genet., 17, 1418-1426.
-
(2008)
Hum. Mol. Genet.
, vol.17
, pp. 1418-1426
-
-
Dufour, E.1
Terzioglu, M.2
Sterky, F.H.3
Sörensen, L.4
Galter, D.5
Olson, L.6
Wilbertz, J.7
Larsson, N.G.8
-
48
-
-
84862986470
-
Analysis of neural subtypes reveals selective mitochondrial dysfunction in dopaminergic neurons from parkin mutants
-
Burman, J.L., Yu, S., Poole, A.C., Decal, R.B. and Pallanck, L. (2012) Analysis of neural subtypes reveals selective mitochondrial dysfunction in dopaminergic neurons from parkin mutants. Proc. Natl. Acad. Sci.USA, 109, 10438-19443.
-
(2012)
Proc. Natl. Acad. Sci.USA
, vol.109
, pp. 10438-19443
-
-
Burman, J.L.1
Yu, S.2
Poole, A.C.3
Decal, R.B.4
Pallanck, L.5
-
49
-
-
84861749376
-
Alternative oxidase rescues mitochondria-mediated dopaminergic cell loss in Drosophila
-
Humphrey, D.M., Parsons, R.B., Ludlow, Z.N., Riemensperger, T., Esposito, G., Verstreken, P., Jacobs, H.T., Birman, S. and Hirth, F. (2012) Alternative oxidase rescues mitochondria-mediated dopaminergic cell loss in Drosophila. Hum. Mol. Genet., 21, 2698-2712.
-
(2012)
Hum. Mol. Genet.
, vol.21
, pp. 2698-2712
-
-
Humphrey, D.M.1
Parsons, R.B.2
Ludlow, Z.N.3
Riemensperger, T.4
Esposito, G.5
Verstreken, P.6
Jacobs, H.T.7
Birman, S.8
Hirth, F.9
-
50
-
-
77954102769
-
Exercise intolerance due to cytochrome b mutation
-
Massie, R., Wong, L.J. and Milone, M. (2010) Exercise intolerance due to cytochrome b mutation. Muscle Nerve, 42, 136-140.
-
(2010)
Muscle Nerve
, vol.42
, pp. 136-140
-
-
Massie, R.1
Wong, L.J.2
Milone, M.3
-
51
-
-
77953163811
-
MitochondrialROSproduction correlates with but does not directly regulate lifespan in Drosophila
-
Sanz, A., Fernández-Ayala, D.J., Stefanatos, R.K. and Jacobs, H.T. (2010) MitochondrialROSproduction correlates with but does not directly regulate lifespan in Drosophila. Aging, 2, 200-223.
-
(2010)
Aging
, vol.2
, pp. 200-223
-
-
Sanz, A.1
Fernández-Ayala, D.J.2
Stefanatos, R.K.3
Jacobs, H.T.4
-
52
-
-
33745242989
-
Respiratory chain supercomplexes set the threshold for respiration defects in human mtDNA mutant cybrids
-
D'Aurelio, M., Gajewski, C.D., Lenaz, G. and Manfredi, G. (2006) Respiratory chain supercomplexes set the threshold for respiration defects in human mtDNA mutant cybrids. Hum. Mol. Genet., 15, 2157-2169.
-
(2006)
Hum. Mol. Genet.
, vol.15
, pp. 2157-2169
-
-
D'Aurelio, M.1
Gajewski, C.D.2
Lenaz, G.3
Manfredi, G.4
-
53
-
-
79956032310
-
Mitochondrial complex I: a central regulator of the aging process
-
Stefanatos, R. and Sanz, A. (2011) Mitochondrial complex I: a central regulator of the aging process. Cell Cycle, 10, 1528-1532.
-
(2011)
Cell Cycle
, vol.10
, pp. 1528-1532
-
-
Stefanatos, R.1
Sanz, A.2
-
54
-
-
77953247010
-
Neuronal expression of a single-subunit yeast NADH-ubiquinone oxidoreductase (Ndi1) extends Drosophila lifespan
-
Bahadorani, S., Cho, J., Lo, T., Contreras, H., Lawal, H.O., Krantz, D.E., Bradley, T.J. and Walker, D.W. (2010) Neuronal expression of a single-subunit yeast NADH-ubiquinone oxidoreductase (Ndi1) extends Drosophila lifespan. Aging Cell, 9, 191-202.
-
(2010)
Aging Cell
, vol.9
, pp. 191-202
-
-
Bahadorani, S.1
Cho, J.2
Lo, T.3
Contreras, H.4
Lawal, H.O.5
Krantz, D.E.6
Bradley, T.J.7
Walker, D.W.8
-
55
-
-
0015415111
-
The α-glycerophosphate cycle in Drosophila melanogaster. I. Biochemical and developmental aspects
-
O'Brien, S.J. and MacIntyre, R.J. (1972) The α-glycerophosphate cycle in Drosophila melanogaster. I. Biochemical and developmental aspects. Biochem Genet., 7, 141-161.
-
(1972)
Biochem Genet.
, vol.7
, pp. 141-161
-
-
O'Brien, S.J.1
MacIntyre, R.J.2
-
56
-
-
0023806553
-
A Genetic analysis of the α-Glycerophosphate oxidase locus in Drosophila melanogaster
-
Davis, M.B. and MacIntyre, R.J. (1988) A Genetic analysis of the α-Glycerophosphate oxidase locus in Drosophila melanogaster. Genetics, 120, 755-766.
-
(1988)
Genetics
, vol.120
, pp. 755-766
-
-
Davis, M.B.1
MacIntyre, R.J.2
-
57
-
-
0032843441
-
stress sensitive B encodes an adenine nucleotide translocase in Drosophila melanogaster
-
Zhang, Y.Q., Roote, J., Brogna, S., Davis, A.W., Barbash, D.A., Nash, D. and Ashburner, M. (1999) stress sensitive B encodes an adenine nucleotide translocase in Drosophila melanogaster. Genetics, 153, 891-903.
-
(1999)
Genetics
, vol.153
, pp. 891-903
-
-
Zhang, Y.Q.1
Roote, J.2
Brogna, S.3
Davis, A.W.4
Barbash, D.A.5
Nash, D.6
Ashburner, M.7
-
58
-
-
0034809484
-
Technical knockout, a Drosophila model of mitochondrial deafness
-
Toivonen, J.M., O'Dell, K.M., Petit, N., Irvine, S.C., Knight, G.K., Lehtonen, M., Longmuir, M., Luoto, K., Touraille, S., Wang, Z. et al. (2001) technical knockout, a Drosophila model of mitochondrial deafness. Genetics, 159, 241-254.
-
(2001)
Genetics
, vol.159
, pp. 241-254
-
-
Toivonen, J.M.1
O'Dell, K.M.2
Petit, N.3
Irvine, S.C.4
Knight, G.K.5
Lehtonen, M.6
Longmuir, M.7
Luoto, K.8
Touraille, S.9
Wang, Z.10
-
59
-
-
0141684569
-
Genedosage and selective expression modify phenotype in a Drosophila model of human mitochondrial disease
-
Toivonen, J.M., Manjiry, S., Touraille, S., Alziari, S., O'Dell, K.M. and Jacobs, H.T. (2003) Genedosage and selective expression modify phenotype in a Drosophila model of human mitochondrial disease. Mitochondrion, 3, 83-96.
-
(2003)
Mitochondrion
, vol.3
, pp. 83-96
-
-
Toivonen, J.M.1
Manjiry, S.2
Touraille, S.3
Alziari, S.4
O'Dell, K.M.5
Jacobs, H.T.6
-
60
-
-
9644266769
-
Mitochondrial disease in flies
-
Jacobs, H.T., Fernández-Ayala, D.J., Manjiry, S., Kemppainen, E., Toivonen, J.M. and O'Dell, K.M. (2004) Mitochondrial disease in flies. Biochim. Biophys. Acta, 1659, 190-196.
-
(2004)
Biochim. Biophys. Acta
, vol.1659
, pp. 190-196
-
-
Jacobs, H.T.1
Fernández-Ayala, D.J.2
Manjiry, S.3
Kemppainen, E.4
Toivonen, J.M.5
O'Dell, K.M.6
-
61
-
-
77951243014
-
Neurologic dysfunction and male infertility in Drosophila porin mutants: a new model for mitochondrial dysfunction and disease
-
Graham, B.H., Li, Z., Alesii, E.P., Versteken, P., Lee, C., Wang, J. and Craigen, W.J. (2010) Neurologic dysfunction and male infertility in Drosophila porin mutants: a new model for mitochondrial dysfunction and disease. J. Biol. Chem., 285, 11143-11153.
-
(2010)
J. Biol. Chem.
, vol.285
, pp. 11143-11153
-
-
Graham, B.H.1
Li, Z.2
Alesii, E.P.3
Versteken, P.4
Lee, C.5
Wang, J.6
Craigen, W.J.7
-
62
-
-
0036042585
-
A genetic analysis of the porin gene encoding a voltage-dependent anion channel protein in Drosophila melanogaster
-
Oliva, M., De Pinto, V., Barsanti, P. and Caggese, C. (2002) A genetic analysis of the porin gene encoding a voltage-dependent anion channel protein in Drosophila melanogaster. Mol. Genet. Genomics, 267, 746-756.
-
(2002)
Mol. Genet. Genomics
, vol.267
, pp. 746-756
-
-
Oliva, M.1
De Pinto, V.2
Barsanti, P.3
Caggese, C.4
-
63
-
-
0035185070
-
Mutations at the mitochondrial DNA polymerase (POLG) locus associated with male infertility
-
Rovio, A.T., Marchington, D.R., Donat, S., Schuppe, H.C., Abel, J., Fritsche, E., Elliott, D.J., Laippala, P., Ahola, A.L., McNay, D. et al. (2001) Mutations at the mitochondrial DNA polymerase (POLG) locus associated with male infertility. Nat. Genet., 29, 261-262.
-
(2001)
Nat. Genet.
, vol.29
, pp. 261-262
-
-
Rovio, A.T.1
Marchington, D.R.2
Donat, S.3
Schuppe, H.C.4
Abel, J.5
Fritsche, E.6
Elliott, D.J.7
Laippala, P.8
Ahola, A.L.9
McNay, D.10
-
64
-
-
84861490270
-
The CAG repeat polymorphism of mitochondrial polymerase gamma (POLG) is associated with male infertility in Tunisia
-
Baklouti-Gargouri, S., Ghorbel, M., Chakroun, N., Sellami, A., Fakhfakh, F. and Ammar-Keskes, L. (2012) The CAG repeat polymorphism of mitochondrial polymerase gamma (POLG) is associated with male infertility in Tunisia. Andrologia, 44(Suppl. 1), 68-73.
-
(2012)
Andrologia
, vol.44
, Issue.SUPPL. 1
, pp. 68-73
-
-
Baklouti-Gargouri, S.1
Ghorbel, M.2
Chakroun, N.3
Sellami, A.4
Fakhfakh, F.5
Ammar-Keskes, L.6
-
65
-
-
0033842465
-
Human mtDNA haplogroups associated with high or reduced spermatozoa motility
-
Ruiz-Pesini, E., Lapeña, A.C., Díez-Sánchez, C., Pérez-Martos, A., Montoya, J., Alvarez, E., Díaz, M., Urriés, A., Montoro, L., López-Pérez, M.J. and Enríquez, J.A. (2000) Human mtDNA haplogroups associated with high or reduced spermatozoa motility. Am. J. Hum. Genet., 67, 682-689.
-
(2000)
Am. J. Hum. Genet.
, vol.67
, pp. 682-689
-
-
Ruiz-Pesini, E.1
Lapeña, A.C.2
Díez-Sánchez, C.3
Pérez-Martos, A.4
Montoya, J.5
Alvarez, E.6
Díaz, M.7
Urriés, A.8
Montoro, L.9
López-Pérez, M.J.10
Enríquez, J.A.11
-
66
-
-
84858277611
-
The role of mitochondria in energy production for human sperm motility
-
Piomboni, P., Focarelli, R., Stendardi, A., Ferramosca, A. and Zara, V. (2012) The role of mitochondria in energy production for human sperm motility. Int. J. Androl., 35, 109-124.
-
(2012)
Int. J. Androl.
, vol.35
, pp. 109-124
-
-
Piomboni, P.1
Focarelli, R.2
Stendardi, A.3
Ferramosca, A.4
Zara, V.5
-
67
-
-
1542290022
-
Cytochrome c oxidase subassemblies in fibroblast cultures from patients carrying mutations in COX10, SCO1, or SURF1
-
Williams, S.L., Valnot, I., Rustin, P. and Taanman, J.-W. (2004) Cytochrome c oxidase subassemblies in fibroblast cultures from patients carrying mutations in COX10, SCO1, or SURF1. J. Biol. Chem., 279, 7462-7469.
-
(2004)
J. Biol. Chem.
, vol.279
, pp. 7462-7469
-
-
Williams, S.L.1
Valnot, I.2
Rustin, P.3
Taanman, J.-W.4
-
68
-
-
0032568882
-
Drosophila synapse formation: regulation by transmembrane protein with Leu-rich repeats, CAPRICIOUS
-
Shishido, E., Takeichi, M. and Nose, A. (1998) Drosophila synapse formation: regulation by transmembrane protein with Leu-rich repeats, CAPRICIOUS. Science, 280, 2118-2121.
-
(1998)
Science
, vol.280
, pp. 2118-2121
-
-
Shishido, E.1
Takeichi, M.2
Nose, A.3
-
69
-
-
37749024370
-
Keap1/Nrf2 signaling regulates oxidative stress tolerance and lifespan in Drosophila
-
Sykiotis, G.P. and Bohmann, D. (2008) Keap1/Nrf2 signaling regulates oxidative stress tolerance and lifespan in Drosophila. Dev. Cell, 14, 76-85.
-
(2008)
Dev. Cell
, vol.14
, pp. 76-85
-
-
Sykiotis, G.P.1
Bohmann, D.2
-
70
-
-
33644780843
-
Post-transcriptional silencing and functional characterization of the Drosophila melanogaster homolog of human Surf1
-
Zordan, M.A., Cisotto, P., Benna, C., Agostino, A., Rizzo, G., Piccin, A., Pegoraro, M., Sandrelli, F., Perini, G., Tognon, G. et al. (2006) Post-transcriptional silencing and functional characterization of the Drosophila melanogaster homolog of human Surf1. Genetics, 172, 229-241.
-
(2006)
Genetics
, vol.172
, pp. 229-241
-
-
Zordan, M.A.1
Cisotto, P.2
Benna, C.3
Agostino, A.4
Rizzo, G.5
Piccin, A.6
Pegoraro, M.7
Sandrelli, F.8
Perini, G.9
Tognon, G.10
-
71
-
-
34447530305
-
A genome-wide transgenic RNAi library for conditional gene inactivation in Drosophila
-
Dietzl, G., Chen, D., Schnorrer, F., Su, K.C., Barinova, Y., Fellner, M., Gasser, B., Kinsey, K., Oppel, S., Scheiblauer, S. et al. (2007) A genome-wide transgenic RNAi library for conditional gene inactivation in Drosophila. Nature, 448, 151-156.
-
(2007)
Nature
, vol.448
, pp. 151-156
-
-
Dietzl, G.1
Chen, D.2
Schnorrer, F.3
Su, K.C.4
Barinova, Y.5
Fellner, M.6
Gasser, B.7
Kinsey, K.8
Oppel, S.9
Scheiblauer, S.10
-
72
-
-
0033782266
-
GFP and beta-galactosidase transformation vectors for promoter/enhancer analysis in Drosophila
-
Barolo, S., Carver, L.A. and Posakony, J.W. (2000) GFP and beta-galactosidase transformation vectors for promoter/enhancer analysis in Drosophila. Biotechniques, 29, 726-732.
-
(2000)
Biotechniques
, vol.29
, pp. 726-732
-
-
Barolo, S.1
Carver, L.A.2
Posakony, J.W.3
-
73
-
-
70149110198
-
Phenotypic suppression of the Drosophila mitochondrial disease-like mutant tko(25t)by duplication of the mutant gene in its natural chromosomal context
-
Kemppainen, E., Fernández-Ayala, D.J., Galbraith, L.C., O'Dell, K.M. and Jacobs, H.T. (2009) Phenotypic suppression of the Drosophila mitochondrial disease-like mutant tko(25t)by duplication of the mutant gene in its natural chromosomal context. Mitochondrion, 9, 353-363.
-
(2009)
Mitochondrion
, vol.9
, pp. 353-363
-
-
Kemppainen, E.1
Fernández-Ayala, D.J.2
Galbraith, L.C.3
O'Dell, K.M.4
Jacobs, H.T.5
-
74
-
-
0141526414
-
Superoxide and hydrogen peroxide production by Drosophila mitochondria
-
Miwa, S., St-Pierre, J., Partridge, L. and Brand, M.D. (2003) Superoxide and hydrogen peroxide production by Drosophila mitochondria. Free Radic. Biol. Med., 35, 938-948.
-
(2003)
Free Radic. Biol. Med.
, vol.35
, pp. 938-948
-
-
Miwa, S.1
St-Pierre, J.2
Partridge, L.3
Brand, M.D.4
-
75
-
-
84868030004
-
dj-1b regulates oxidative stress, insulin-like signaling and development in Drosophila melanogaster
-
Stefanatos, R., Sriram, A., Kiviranta, E., Mohan, A., Ayala, V., Jacobs, H.T., Pamplona, R. and Sanz, A. (2012) dj-1b regulates oxidative stress, insulin-like signaling and development in Drosophila melanogaster. Cell Cycle, 11, 3876-3886.
-
(2012)
Cell Cycle
, vol.11
, pp. 3876-3886
-
-
Stefanatos, R.1
Sriram, A.2
Kiviranta, E.3
Mohan, A.4
Ayala, V.5
Jacobs, H.T.6
Pamplona, R.7
Sanz, A.8
-
76
-
-
83455219227
-
Visualization of mitochondrial respiratory function using cytochrome c oxidase/succinate dehydrogenase (COX/SDH) double-labeling histochemistry
-
(2011)
-
Ross, J.M. (2011) Visualization of mitochondrial respiratory function using cytochrome c oxidase/succinate dehydrogenase (COX/SDH) double-labeling histochemistry. J. Vis. Exp. 2011;(57):e3266.
-
(2011)
J. Vis. Exp
, Issue.57
-
-
Ross, J.M.1
|