-
1
-
-
84896722928
-
The function of the respiratory supercomplexes: The plasticity model
-
R. Acin-Perez, and J.A. Enriquez The function of the respiratory supercomplexes: the plasticity model Biochim. Biophys. Acta 1837 2014 444 450
-
(2014)
Biochim. Biophys. Acta
, vol.1837
, pp. 444-450
-
-
Acin-Perez, R.1
Enriquez, J.A.2
-
2
-
-
12144291508
-
Respiratory complex III is required to maintain complex i in mammalian mitochondria
-
R. Acín-Pérez, M.P. Bayona-Bafaluy, P. Fernández-Silva, R. Moreno-Loshuertos, A. Pérez-Martos, C. Bruno, C.T. Moraes, and J.A. Enríquez Respiratory complex III is required to maintain complex I in mammalian mitochondria Mol. Cell 13 2004 805 815
-
(2004)
Mol. Cell
, vol.13
, pp. 805-815
-
-
Acín-Pérez, R.1
Bayona-Bafaluy, M.P.2
Fernández-Silva, P.3
Moreno-Loshuertos, R.4
Pérez-Martos, A.5
Bruno, C.6
Moraes, C.T.7
Enríquez, J.A.8
-
3
-
-
79953324327
-
Infantile cardioencephalopathy due to a COX15 gene defect: Report and review
-
M. Alfadhel, Y.P. Lillquist, P.J. Waters, G. Sinclair, E. Struys, D. McFadden, G. Hendson, L. Hyams, J. Shoffner, and H.D. Vallance Infantile cardioencephalopathy due to a COX15 gene defect: report and review Am. J. Med. Genet. A. 155A 2011 840 844
-
(2011)
Am. J. Med. Genet. A.
, vol.155 A
, pp. 840-844
-
-
Alfadhel, M.1
Lillquist, Y.P.2
Waters, P.J.3
Sinclair, G.4
Struys, E.5
McFadden, D.6
Hendson, G.7
Hyams, L.8
Shoffner, J.9
Vallance, H.D.10
-
4
-
-
84896264348
-
The i-AAA protease YME1L and OMA1 cleave OPA1 to balance mitochondrial fusion and fission
-
R. Anand, T. Wai, M.J. Baker, N. Kladt, A.C. Schauss, E. Rugarli, and T. Langer The i-AAA protease YME1L and OMA1 cleave OPA1 to balance mitochondrial fusion and fission J. Cell Biol. 204 2014 919 929
-
(2014)
J. Cell Biol.
, vol.204
, pp. 919-929
-
-
Anand, R.1
Wai, T.2
Baker, M.J.3
Kladt, N.4
Schauss, A.C.5
Rugarli, E.6
Langer, T.7
-
5
-
-
0037221950
-
Mutations in COX15 produce a defect in the mitochondrial heme biosynthetic pathway, causing early-onset fatal hypertrophic cardiomyopathy
-
H. Antonicka, A. Mattman, C.G. Carlson, D.M. Glerum, K.C. Hoffbuhr, S.C. Leary, N.G. Kennaway, and E.A. Shoubridge Mutations in COX15 produce a defect in the mitochondrial heme biosynthetic pathway, causing early-onset fatal hypertrophic cardiomyopathy Am. J. Hum. Genet. 72 2003 101 114
-
(2003)
Am. J. Hum. Genet.
, vol.72
, pp. 101-114
-
-
Antonicka, H.1
Mattman, A.2
Carlson, C.G.3
Glerum, D.M.4
Hoffbuhr, K.C.5
Leary, S.C.6
Kennaway, N.G.7
Shoubridge, E.A.8
-
6
-
-
84904890279
-
A proteomic screen with Drosophila Opa1-like identifies Hsc70-5/Mortalin as a regulator of mitochondrial morphology and cellular homeostasis
-
S. Banerjee, and B. Chinthapalli A proteomic screen with Drosophila Opa1-like identifies Hsc70-5/Mortalin as a regulator of mitochondrial morphology and cellular homeostasis Int. J. Biochem. Cell Biol. 54 2014 36 48
-
(2014)
Int. J. Biochem. Cell Biol.
, vol.54
, pp. 36-48
-
-
Banerjee, S.1
Chinthapalli, B.2
-
7
-
-
84886897974
-
The heme a synthase Cox15 associates with cytochrome c oxidase assembly intermediates during Cox1 maturation
-
B. Bareth, S. Dennerlein, D.U. Mick, M. Nikolov, H. Urlaub, and P. Rehling The heme a synthase Cox15 associates with cytochrome c oxidase assembly intermediates during Cox1 maturation Mol. Cell. Biol. 33 2013 4128 4137
-
(2013)
Mol. Cell. Biol.
, vol.33
, pp. 4128-4137
-
-
Bareth, B.1
Dennerlein, S.2
Mick, D.U.3
Nikolov, M.4
Urlaub, H.5
Rehling, P.6
-
8
-
-
0037051889
-
Regulation of the heme A biosynthetic pathway in Saccharomyces cerevisiae
-
M.H. Barros, and A. Tzagoloff Regulation of the heme A biosynthetic pathway in Saccharomyces cerevisiae FEBS Lett. 516 2002 119 123
-
(2002)
FEBS Lett.
, vol.516
, pp. 119-123
-
-
Barros, M.H.1
Tzagoloff, A.2
-
9
-
-
0035831217
-
Involvement of mitochondrial ferredoxin and Cox15p in hydroxylation of heme O
-
M.H. Barros, C.G. Carlson, D.M. Glerum, and A. Tzagoloff Involvement of mitochondrial ferredoxin and Cox15p in hydroxylation of heme O FEBS Lett. 492 2001 133 138
-
(2001)
FEBS Lett.
, vol.492
, pp. 133-138
-
-
Barros, M.H.1
Carlson, C.G.2
Glerum, D.M.3
Tzagoloff, A.4
-
10
-
-
9644275464
-
Clinical and molecular findings in children with complex i deficiency
-
M. Bugiani, F. Invernizzi, S. Alberio, E. Briem, E. Lamantea, F. Carrara, I. Moroni, L. Farina, M. Spada, and M.A. Donati Clinical and molecular findings in children with complex I deficiency Biochim. Biophys. Acta 1659 2004 136 147
-
(2004)
Biochim. Biophys. Acta
, vol.1659
, pp. 136-147
-
-
Bugiani, M.1
Invernizzi, F.2
Alberio, S.3
Briem, E.4
Lamantea, E.5
Carrara, F.6
Moroni, I.7
Farina, L.8
Spada, M.9
Donati, M.A.10
-
11
-
-
33645747992
-
Novel mutations in COX15 in a long surviving Leigh syndrome patient with cytochrome c oxidase deficiency
-
M. Bugiani, V. Tiranti, L. Farina, G. Uziel, and M. Zeviani Novel mutations in COX15 in a long surviving Leigh syndrome patient with cytochrome c oxidase deficiency J. Med. Genet. 42 2005 e28
-
(2005)
J. Med. Genet.
, vol.42
, pp. e28
-
-
Bugiani, M.1
Tiranti, V.2
Farina, L.3
Uziel, G.4
Zeviani, M.5
-
12
-
-
83455169110
-
Mitochondrial complex III stabilizes complex i in the absence of NDUFS4 to provide partial activity
-
M.A. Calvaruso, P. Willems, M. van den Brand, F. Valsecchi, S. Kruse, R. Palmiter, J. Smeitink, and L. Nijtmans Mitochondrial complex III stabilizes complex I in the absence of NDUFS4 to provide partial activity Hum. Mol. Genet. 21 2012 115 120
-
(2012)
Hum. Mol. Genet.
, vol.21
, pp. 115-120
-
-
Calvaruso, M.A.1
Willems, P.2
Van Den Brand, M.3
Valsecchi, F.4
Kruse, S.5
Palmiter, R.6
Smeitink, J.7
Nijtmans, L.8
-
14
-
-
84884909413
-
Mitochondrial cristae shape determines respiratory chain supercomplexes assembly and respiratory efficiency
-
S. Cogliati, C. Frezza, M.E. Soriano, T. Varanita, R. Quintana-Cabrera, M. Corrado, S. Cipolat, V. Costa, A. Casarin, and L.C. Gomes Mitochondrial cristae shape determines respiratory chain supercomplexes assembly and respiratory efficiency Cell 155 2013 160 171
-
(2013)
Cell
, vol.155
, pp. 160-171
-
-
Cogliati, S.1
Frezza, C.2
Soriano, M.E.3
Varanita, T.4
Quintana-Cabrera, R.5
Corrado, M.6
Cipolat, S.7
Costa, V.8
Casarin, A.9
Gomes, L.C.10
-
15
-
-
0035683581
-
Mutation spectrum and splicing variants in the OPA1 gene
-
C. Delettre, J.M. Griffoin, J. Kaplan, H. Dollfus, B. Lorenz, L. Faivre, G. Lenaers, P. Belenguer, and C.P. Hamel Mutation spectrum and splicing variants in the OPA1 gene Hum. Genet. 109 2001 584 591
-
(2001)
Hum. Genet.
, vol.109
, pp. 584-591
-
-
Delettre, C.1
Griffoin, J.M.2
Kaplan, J.3
Dollfus, H.4
Lorenz, B.5
Faivre, L.6
Lenaers, G.7
Belenguer, P.8
Hamel, C.P.9
-
16
-
-
34548349869
-
OPA1 processing reconstituted in yeast depends on the subunit composition of the m-AAA protease in mitochondria
-
S. Duvezin-Caubet, M. Koppen, J. Wagener, M. Zick, L. Israel, A. Bernacchia, R. Jagasia, E.I. Rugarli, A. Imhof, and W. Neupert OPA1 processing reconstituted in yeast depends on the subunit composition of the m-AAA protease in mitochondria Mol. Biol. Cell 18 2007 3582 3590
-
(2007)
Mol. Biol. Cell
, vol.18
, pp. 3582-3590
-
-
Duvezin-Caubet, S.1
Koppen, M.2
Wagener, J.3
Zick, M.4
Israel, L.5
Bernacchia, A.6
Jagasia, R.7
Rugarli, E.I.8
Imhof, A.9
Neupert, W.10
-
17
-
-
76149140917
-
Regulation of OPA1 processing and mitochondrial fusion by m-AAA protease isoenzymes and OMA1
-
S. Ehses, I. Raschke, G. Mancuso, A. Bernacchia, S. Geimer, D. Tondera, J.C. Martinou, B. Westermann, E.I. Rugarli, and T. Langer Regulation of OPA1 processing and mitochondrial fusion by m-AAA protease isoenzymes and OMA1 J. Cell Biol. 187 2009 1023 1036
-
(2009)
J. Cell Biol.
, vol.187
, pp. 1023-1036
-
-
Ehses, S.1
Raschke, I.2
Mancuso, G.3
Bernacchia, A.4
Geimer, S.5
Tondera, D.6
Martinou, J.C.7
Westermann, B.8
Rugarli, E.I.9
Langer, T.10
-
18
-
-
48349097445
-
Pathogenic mitochondrial DNA mutations are common in the general population
-
H.R. Elliott, D.C. Samuels, J.A. Eden, C.L. Relton, and P.F. Chinnery Pathogenic mitochondrial DNA mutations are common in the general population Am. J. Hum. Genet. 83 2008 254 260
-
(2008)
Am. J. Hum. Genet.
, vol.83
, pp. 254-260
-
-
Elliott, H.R.1
Samuels, D.C.2
Eden, J.A.3
Relton, C.L.4
Chinnery, P.F.5
-
19
-
-
84904003668
-
Coenzyme q and the respiratory chain: Coenzyme q pool and mitochondrial supercomplexes
-
J.A. Enriquez, and G. Lenaz Coenzyme q and the respiratory chain: coenzyme q pool and mitochondrial supercomplexes Mol. Syndromol. 5 2014 119 140
-
(2014)
Mol. Syndromol.
, vol.5
, pp. 119-140
-
-
Enriquez, J.A.1
Lenaz, G.2
-
20
-
-
0036024971
-
Isolation of biogenetically competent mitochondria from mammalian tissues and cultured cells
-
E. Fernández-Vizarra, M.J. López-Pérez, and J.A. Enriquez Isolation of biogenetically competent mitochondria from mammalian tissues and cultured cells Methods 26 2002 292 297
-
(2002)
Methods
, vol.26
, pp. 292-297
-
-
Fernández-Vizarra, E.1
López-Pérez, M.J.2
Enriquez, J.A.3
-
21
-
-
33745699393
-
OPA1 controls apoptotic cristae remodeling independently from mitochondrial fusion
-
C. Frezza, S. Cipolat, O. Martins de Brito, M. Micaroni, G.V. Beznoussenko, T. Rudka, D. Bartoli, R.S. Polishuck, N.N. Danial, B. De Strooper, and L. Scorrano OPA1 controls apoptotic cristae remodeling independently from mitochondrial fusion Cell 126 2006 177 189
-
(2006)
Cell
, vol.126
, pp. 177-189
-
-
Frezza, C.1
Cipolat, S.2
Martins De Brito, O.3
Micaroni, M.4
Beznoussenko, G.V.5
Rudka, T.6
Bartoli, D.7
Polishuck, R.S.8
Danial, N.N.9
De Strooper, B.10
Scorrano, L.11
-
22
-
-
34347236921
-
Organelle isolation: Functional mitochondria from mouse liver, muscle and cultured fibroblasts
-
C. Frezza, S. Cipolat, and L. Scorrano Organelle isolation: functional mitochondria from mouse liver, muscle and cultured fibroblasts Nat. Protoc. 2 2007 287 295
-
(2007)
Nat. Protoc.
, vol.2
, pp. 287-295
-
-
Frezza, C.1
Cipolat, S.2
Scorrano, L.3
-
23
-
-
0030802910
-
COX15 codes for a mitochondrial protein essential for the assembly of yeast cytochrome oxidase
-
D.M. Glerum, I. Muroff, C. Jin, and A. Tzagoloff COX15 codes for a mitochondrial protein essential for the assembly of yeast cytochrome oxidase J. Biol. Chem. 272 1997 19088 19094
-
(1997)
J. Biol. Chem.
, vol.272
, pp. 19088-19094
-
-
Glerum, D.M.1
Muroff, I.2
Jin, C.3
Tzagoloff, A.4
-
24
-
-
0034997256
-
The many shapes of mitochondrial membranes
-
L. Griparic, and A.M. van der Bliek The many shapes of mitochondrial membranes Traffic 2 2001 235 244
-
(2001)
Traffic
, vol.2
, pp. 235-244
-
-
Griparic, L.1
Van Der Bliek, A.M.2
-
25
-
-
34548313686
-
Regulation of the mitochondrial dynamin-like protein Opa1 by proteolytic cleavage
-
L. Griparic, T. Kanazawa, and A.M. van der Bliek Regulation of the mitochondrial dynamin-like protein Opa1 by proteolytic cleavage J. Cell Biol. 178 2007 757 764
-
(2007)
J. Cell Biol.
, vol.178
, pp. 757-764
-
-
Griparic, L.1
Kanazawa, T.2
Van Der Bliek, A.M.3
-
26
-
-
76149093590
-
Inducible proteolytic inactivation of OPA1 mediated by the OMA1 protease in mammalian cells
-
B. Head, L. Griparic, M. Amiri, S. Gandre-Babbe, and A.M. van der Bliek Inducible proteolytic inactivation of OPA1 mediated by the OMA1 protease in mammalian cells J. Cell Biol. 187 2009 959 966
-
(2009)
J. Cell Biol.
, vol.187
, pp. 959-966
-
-
Head, B.1
Griparic, L.2
Amiri, M.3
Gandre-Babbe, S.4
Van Der Bliek, A.M.5
-
27
-
-
84871819218
-
Control of protein synthesis in yeast mitochondria: The concept of translational activators
-
J.M. Herrmann, M.W. Woellhaf, and N. Bonnefoy Control of protein synthesis in yeast mitochondria: the concept of translational activators Biochim. Biophys. Acta 1833 2013 286 294
-
(2013)
Biochim. Biophys. Acta
, vol.1833
, pp. 286-294
-
-
Herrmann, J.M.1
Woellhaf, M.W.2
Bonnefoy, N.3
-
28
-
-
33746299692
-
Regulation of mitochondrial morphology through proteolytic cleavage of OPA1
-
N. Ishihara, Y. Fujita, T. Oka, and K. Mihara Regulation of mitochondrial morphology through proteolytic cleavage of OPA1 EMBO J. 25 2006 2966 2977
-
(2006)
EMBO J.
, vol.25
, pp. 2966-2977
-
-
Ishihara, N.1
Fujita, Y.2
Oka, T.3
Mihara, K.4
-
29
-
-
84890850876
-
MTOR inhibition alleviates mitochondrial disease in a mouse model of Leigh syndrome
-
S.C. Johnson, M.E. Yanos, E.B. Kayser, A. Quintana, M. Sangesland, A. Castanza, L. Uhde, J. Hui, V.Z. Wall, and A. Gagnidze mTOR inhibition alleviates mitochondrial disease in a mouse model of Leigh syndrome Science 342 2013 1524 1528
-
(2013)
Science
, vol.342
, pp. 1524-1528
-
-
Johnson, S.C.1
Yanos, M.E.2
Kayser, E.B.3
Quintana, A.4
Sangesland, M.5
Castanza, A.6
Uhde, L.7
Hui, J.8
Wall, V.Z.9
Gagnidze, A.10
-
30
-
-
84881348520
-
Mitochondrial complex i deficiency increases protein acetylation and accelerates heart failure
-
G. Karamanlidis, C.F. Lee, L. Garcia-Menendez, S.C. Kolwicz Jr., W. Suthammarak, G. Gong, M.M. Sedensky, P.G. Morgan, W. Wang, and R. Tian Mitochondrial complex I deficiency increases protein acetylation and accelerates heart failure Cell Metab. 18 2013 239 250
-
(2013)
Cell Metab.
, vol.18
, pp. 239-250
-
-
Karamanlidis, G.1
Lee, C.F.2
Garcia-Menendez, L.3
Kolwicz, Jr.S.C.4
Suthammarak, W.5
Gong, G.6
Sedensky, M.M.7
Morgan, P.G.8
Wang, W.9
Tian, R.10
-
31
-
-
84923685347
-
Mitochondria: From cell death executioners to regulators of cell differentiation
-
A. Kasahara, and L. Scorrano Mitochondria: from cell death executioners to regulators of cell differentiation Trends Cell Biol. 24 2014 761 770
-
(2014)
Trends Cell Biol.
, vol.24
, pp. 761-770
-
-
Kasahara, A.1
Scorrano, L.2
-
33
-
-
41449089840
-
Mice with mitochondrial complex i deficiency develop a fatal encephalomyopathy
-
S.E. Kruse, W.C. Watt, D.J. Marcinek, R.P. Kapur, K.A. Schenkman, and R.D. Palmiter Mice with mitochondrial complex I deficiency develop a fatal encephalomyopathy Cell Metab. 7 2008 312 320
-
(2008)
Cell Metab.
, vol.7
, pp. 312-320
-
-
Kruse, S.E.1
Watt, W.C.2
Marcinek, D.J.3
Kapur, R.P.4
Schenkman, K.A.5
Palmiter, R.D.6
-
34
-
-
0037458031
-
Identification of a gene causing human cytochrome c oxidase deficiency by integrative genomics
-
V.K. Mootha, P. Lepage, K. Miller, J. Bunkenborg, M. Reich, M. Hjerrild, T. Delmonte, A. Villeneuve, R. Sladek, and F. Xu Identification of a gene causing human cytochrome c oxidase deficiency by integrative genomics Proc. Natl. Acad. Sci. USA 100 2003 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
-
35
-
-
0036024975
-
Blue Native electrophoresis to study mitochondrial and other protein complexes
-
L.G. Nijtmans, N.S. Henderson, and I.J. Holt Blue Native electrophoresis to study mitochondrial and other protein complexes Methods 26 2002 327 334
-
(2002)
Methods
, vol.26
, pp. 327-334
-
-
Nijtmans, L.G.1
Henderson, N.S.2
Holt, I.J.3
-
36
-
-
0032534869
-
Identification and characterization of human cDNAs specific to BCS1, PET112, SCO1, COX15, and COX11, five genes involved in the formation and function of the mitochondrial respiratory chain
-
V. Petruzzella, V. Tiranti, P. Fernandez, P. Ianna, R. Carrozzo, and M. Zeviani Identification and characterization of human cDNAs specific to BCS1, PET112, SCO1, COX15, and COX11, five genes involved in the formation and function of the mitochondrial respiratory chain Genomics 54 1998 494 504
-
(1998)
Genomics
, vol.54
, pp. 494-504
-
-
Petruzzella, V.1
Tiranti, V.2
Fernandez, P.3
Ianna, P.4
Carrozzo, R.5
Zeviani, M.6
-
37
-
-
0035283150
-
A nonsense mutation in the NDUFS4 gene encoding the 18 kDa (AQDQ) subunit of complex i abolishes assembly and activity of the complex in a patient with Leigh-like syndrome
-
V. Petruzzella, R. Vergari, I. Puzziferri, D. Boffoli, E. Lamantea, M. Zeviani, and S. Papa A nonsense mutation in the NDUFS4 gene encoding the 18 kDa (AQDQ) subunit of complex I abolishes assembly and activity of the complex in a patient with Leigh-like syndrome Hum. Mol. Genet. 10 2001 529 535
-
(2001)
Hum. Mol. Genet.
, vol.10
, pp. 529-535
-
-
Petruzzella, V.1
Vergari, R.2
Puzziferri, I.3
Boffoli, D.4
Lamantea, E.5
Zeviani, M.6
Papa, S.7
-
38
-
-
77954638436
-
Complex i deficiency due to loss of Ndufs4 in the brain results in progressive encephalopathy resembling Leigh syndrome
-
A. Quintana, S.E. Kruse, R.P. Kapur, E. Sanz, and R.D. Palmiter Complex I deficiency due to loss of Ndufs4 in the brain results in progressive encephalopathy resembling Leigh syndrome Proc. Natl. Acad. Sci. USA 107 2010 10996 11001
-
(2010)
Proc. Natl. Acad. Sci. USA
, vol.107
, pp. 10996-11001
-
-
Quintana, A.1
Kruse, S.E.2
Kapur, R.P.3
Sanz, E.4
Palmiter, R.D.5
-
39
-
-
84865086994
-
Altered anesthetic sensitivity of mice lacking Ndufs4, a subunit of mitochondrial complex i
-
A. Quintana, P.G. Morgan, S.E. Kruse, R.D. Palmiter, and M.M. Sedensky Altered anesthetic sensitivity of mice lacking Ndufs4, a subunit of mitochondrial complex I PLoS ONE 7 2012 e42904
-
(2012)
PLoS ONE
, vol.7
, pp. e42904
-
-
Quintana, A.1
Morgan, P.G.2
Kruse, S.E.3
Palmiter, R.D.4
Sedensky, M.M.5
-
40
-
-
84875010856
-
Opa1 is required for proper mitochondrial metabolism in early development
-
J.J. Rahn, K.D. Stackley, and S.S. Chan Opa1 is required for proper mitochondrial metabolism in early development PLoS ONE 8 2013 e59218
-
(2013)
PLoS ONE
, vol.8
, pp. e59218
-
-
Rahn, J.J.1
Stackley, K.D.2
Chan, S.S.3
-
41
-
-
0242414752
-
Pathological mutations of the human NDUFS4 gene of the 18-kDa (AQDQ) subunit of complex i affect the expression of the protein and the assembly and function of the complex
-
S. Scacco, V. Petruzzella, S. Budde, R. Vergari, R. Tamborra, D. Panelli, L.P. van den Heuvel, J.A. Smeitink, and S. Papa Pathological mutations of the human NDUFS4 gene of the 18-kDa (AQDQ) subunit of complex I affect the expression of the protein and the assembly and function of the complex J. Biol. Chem. 278 2003 44161 44167
-
(2003)
J. Biol. Chem.
, vol.278
, pp. 44161-44167
-
-
Scacco, S.1
Petruzzella, V.2
Budde, S.3
Vergari, R.4
Tamborra, R.5
Panelli, D.6
Van Den Heuvel, L.P.7
Smeitink, J.A.8
Papa, S.9
-
43
-
-
0029875973
-
Cytochemistry and immunocytochemistry of mitochondria in tissue sections
-
M. Sciacco, and E. Bonilla Cytochemistry and immunocytochemistry of mitochondria in tissue sections Methods Enzymol. 264 1996 509 521
-
(1996)
Methods Enzymol.
, vol.264
, pp. 509-521
-
-
Sciacco, M.1
Bonilla, E.2
-
44
-
-
34548313688
-
OPA1 processing controls mitochondrial fusion and is regulated by mRNA splicing, membrane potential, and Yme1L
-
Z. Song, H. Chen, M. Fiket, C. Alexander, and D.C. Chan OPA1 processing controls mitochondrial fusion and is regulated by mRNA splicing, membrane potential, and Yme1L J. Cell Biol. 178 2007 749 755
-
(2007)
J. Cell Biol.
, vol.178
, pp. 749-755
-
-
Song, Z.1
Chen, H.2
Fiket, M.3
Alexander, C.4
Chan, D.C.5
-
45
-
-
84930607266
-
The Opa1-dependent mitochondrial cristae remodeling pathway controls atrophic, apoptotic and ischemic tissue damage
-
this issue
-
T. Varanita, M.E. Soriano, V. Romanello, T. Zaglia, and R. Quintana-Cabrera The Opa1-dependent mitochondrial cristae remodeling pathway controls atrophic, apoptotic and ischemic tissue damage Cell Met. 21 2015 834 844 this issue
-
(2015)
Cell Met.
, vol.21
, pp. 834-844
-
-
Varanita, T.1
Soriano, M.E.2
Romanello, V.3
Zaglia, T.4
Quintana-Cabrera, R.5
-
46
-
-
17344365132
-
Demonstration of a new pathogenic mutation in human complex i deficiency: A 5-bp duplication in the nuclear gene encoding the 18-kD (AQDQ) subunit
-
L. van den Heuvel, W. Ruitenbeek, R. Smeets, Z. Gelman-Kohan, O. Elpeleg, J. Loeffen, F. Trijbels, E. Mariman, D. de Bruijn, and J. Smeitink Demonstration of a new pathogenic mutation in human complex I deficiency: a 5-bp duplication in the nuclear gene encoding the 18-kD (AQDQ) subunit Am. J. Hum. Genet. 62 1998 262 268
-
(1998)
Am. J. Hum. Genet.
, vol.62
, pp. 262-268
-
-
Van Den Heuvel, L.1
Ruitenbeek, W.2
Smeets, R.3
Gelman-Kohan, Z.4
Elpeleg, O.5
Loeffen, J.6
Trijbels, F.7
Mariman, E.8
De Bruijn, D.9
Smeitink, J.10
-
47
-
-
84915761829
-
Architecture of mammalian respiratory complex i
-
K.R. Vinothkumar, J. Zhu, and J. Hirst Architecture of mammalian respiratory complex I Nature 515 2014 80 84
-
(2014)
Nature
, vol.515
, pp. 80-84
-
-
Vinothkumar, K.R.1
Zhu, J.2
Hirst, J.3
-
48
-
-
79959314684
-
In vivo correction of COX deficiency by activation of the AMPK/PGC-1α axis
-
C. Viscomi, E. Bottani, G. Civiletto, R. Cerutti, M. Moggio, G. Fagiolari, E.A. Schon, C. Lamperti, and M. Zeviani In vivo correction of COX deficiency by activation of the AMPK/PGC-1α axis Cell Metab. 14 2011 80 90
-
(2011)
Cell Metab.
, vol.14
, pp. 80-90
-
-
Viscomi, C.1
Bottani, E.2
Civiletto, G.3
Cerutti, R.4
Moggio, M.5
Fagiolari, G.6
Schon, E.A.7
Lamperti, C.8
Zeviani, M.9
-
49
-
-
59449101521
-
Regulation of the heme A biosynthetic pathway: Differential regulation of heme A synthase and heme O synthase in Saccharomyces cerevisiae
-
Z. Wang, Y. Wang, and E.L. Hegg Regulation of the heme A biosynthetic pathway: differential regulation of heme A synthase and heme O synthase in Saccharomyces cerevisiae J. Biol. Chem. 284 2009 839 847
-
(2009)
J. Biol. Chem.
, vol.284
, pp. 839-847
-
-
Wang, Z.1
Wang, Y.2
Hegg, E.L.3
|