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CeVO4 Nanozymes Catalyze the Reduction of Dioxygen to Water without Releasing Partially Reduced Oxygen Species
CeVO4 Nanozymes Catalyze the Reduction of Dioxygen to Water without Releasing Partially Reduced Oxygen Species
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CeVO4 Nanozymes Catalyze the Reduction of Dioxygen to Water without Releasing Partially Reduced Oxygen Species

Singh, Namrata ; Mugesh, Govindasamy

Angewandte Chemie (International ed.), 2019-06-03, Vol.58 (23), p.7797-7801 [Peer Reviewed Journal]

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2
Respiratory Chain Complex Disorganization Impairs Mitochondrial and Cellular Integrity: Phenotypic Variation in Cytochrome c Oxidase Deficiency
Respiratory Chain Complex Disorganization Impairs Mitochondrial and Cellular Integrity: Phenotypic Variation in Cytochrome c Oxidase Deficiency
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Respiratory Chain Complex Disorganization Impairs Mitochondrial and Cellular Integrity: Phenotypic Variation in Cytochrome c Oxidase Deficiency

Hatakeyama, Hideyuki ; Goto, Yu-Ichi

The American journal of pathology, 2017-01, Vol.187 (1), p.110-121 [Peer Reviewed Journal]

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3
A mitochondrial paradigm of metabolic and degenerative diseases, aging, and cancer: a dawn for evolutionary medicine
A mitochondrial paradigm of metabolic and degenerative diseases, aging, and cancer: a dawn for evolutionary medicine
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A mitochondrial paradigm of metabolic and degenerative diseases, aging, and cancer: a dawn for evolutionary medicine

Wallace, Douglas C

Annual review of genetics, 2005, Vol.39 (1), p.359-407 [Peer Reviewed Journal]

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4
Mutation in mitochondrial complex IV subunit COX5A causes pulmonary arterial hypertension, lactic acidemia, and failure to thrive
Mutation in mitochondrial complex IV subunit COX5A causes pulmonary arterial hypertension, lactic acidemia, and failure to thrive
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Mutation in mitochondrial complex IV subunit COX5A causes pulmonary arterial hypertension, lactic acidemia, and failure to thrive

Baertling, F ; Al-Murshedi, F ; Sanchez Caballero, L.M ; Al-Senaidi, K ; Joshi, N.P ; Venselaar, H ; Brand, M.A.M. van den ; Nijtmans, L.G.J ; Rodenburg, R.J.T

Human mutation, 2017, Vol.38 (6), p.692-703 [Peer Reviewed Journal]

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5
mTORC1 is required for expression of LRPPRC and cytochrome- c oxidase but not HIF-1α in Leigh syndrome French Canadian type patient fibroblasts
mTORC1 is required for expression of LRPPRC and cytochrome- c oxidase but not HIF-1α in Leigh syndrome French Canadian type patient fibroblasts
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mTORC1 is required for expression of LRPPRC and cytochrome- c oxidase but not HIF-1α in Leigh syndrome French Canadian type patient fibroblasts

Mukaneza, Yvette ; Cohen, Aaron ; Rivard, Marie-Ève ; Tardif, Jessica ; Deschênes, Sonia ; Ruiz, Matthieu ; Laprise, Catherine ; Des Rosiers, Christine ; Coderre, Lise

American Journal of Physiology: Cell Physiology, 2019-07-01, Vol.317 (1), p.C58-C67 [Peer Reviewed Journal]

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6
COX6A2 variants cause a muscle‐specific cytochrome c oxidase deficiency
COX6A2 variants cause a muscle‐specific cytochrome c oxidase deficiency
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COX6A2 variants cause a muscle‐specific cytochrome c oxidase deficiency

Inoue, Michio ; Uchino, Shumpei ; Iida, Aritoshi ; Noguchi, Satoru ; Hayashi, Shinichiro ; Takahashi, Tsutomu ; Fujii, Katsunori ; Komaki, Hirofumi ; Takeshita, Eri ; Nonaka, Ikuya ; Okada, Yukinori ; Yoshizawa, Takuya ; Van Lommel, Leentje ; Schuit, Frans ; Goto, Yu‐ichi ; Mimaki, Masakazu ; Nishino, Ichizo

Annals of neurology, 2019-08, Vol.86 (2), p.193-202 [Peer Reviewed Journal]

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7
Human COX20 cooperates with SCO1 and SCO2 to mature COX2 and promote the assembly of cytochrome c oxidase
Human COX20 cooperates with SCO1 and SCO2 to mature COX2 and promote the assembly of cytochrome c oxidase
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Human COX20 cooperates with SCO1 and SCO2 to mature COX2 and promote the assembly of cytochrome c oxidase

Bourens, Myriam ; Boulet, Aren ; Leary, Scot C ; Barrientos, Antoni

Human molecular genetics, 2014-06-01, Vol.23 (11), p.2901-2913 [Peer Reviewed Journal]

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8
Molecular basis of infantile reversible cytochrome c oxidase deficiency myopathy
Molecular basis of infantile reversible cytochrome c oxidase deficiency myopathy
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Molecular basis of infantile reversible cytochrome c oxidase deficiency myopathy

Horvath, Rita ; Kemp, John P ; Tuppen, Helen A. L ; Hudson, Gavin ; Oldfors, Anders ; Marie, Suely K. N ; Moslemi, Ali-Reza ; Servidei, Serenella ; Holme, Elisabeth ; Shanske, Sara ; Kollberg, Gittan ; Jayakar, Parul ; Pyle, Angela ; Marks, Harold M ; Holinski-Feder, Elke ; Scavina, Mena ; Walter, Maggie C ; Çoku, Jorida ; Günther-Scholz, Andrea ; Smith, Paul M ; McFarland, Robert ; Chrzanowska-Lightowlers, Zofia M. A ; Lightowlers, Robert N ; Hirano, Michio ; Lochmüller, Hanns ; Taylor, Robert W ; Chinnery, Patrick F ; Tulinius, Mar ; DiMauro, Salvatore

Brain (London, England : 1878), 2009-11, Vol.132 (11), p.3165-3174 [Peer Reviewed Journal]

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9
Beneficial effects of resveratrol on respiratory chain defects in patients' fibroblasts involve estrogen receptor and estrogen-related receptor alpha signaling
Beneficial effects of resveratrol on respiratory chain defects in patients' fibroblasts involve estrogen receptor and estrogen-related receptor alpha signaling
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Beneficial effects of resveratrol on respiratory chain defects in patients' fibroblasts involve estrogen receptor and estrogen-related receptor alpha signaling

Lopes Costa, Alexandra ; Le Bachelier, Carole ; Mathieu, Lise ; Rotig, Agnès ; Boneh, Avihu ; De Lonlay, Pascale ; Tarnopolsky, Mark A ; Thorburn, David R ; Bastin, Jean ; Djouadi, Fatima

Human molecular genetics, 2014-04-15, Vol.23 (8), p.2106-2119 [Peer Reviewed Journal]

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10
Multilevel heterogeneity of mitochondrial respiratory chain deficiency
Multilevel heterogeneity of mitochondrial respiratory chain deficiency
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Multilevel heterogeneity of mitochondrial respiratory chain deficiency

Vincent, Amy E ; Picard, Martin

The Journal of pathology, 2018-11, Vol.246 (3), p.261-265 [Peer Reviewed Journal]

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