These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
250 related articles for article (PubMed ID: 21965299)
1. Mitochondrial complex III stabilizes complex I in the absence of NDUFS4 to provide partial activity. Calvaruso MA; Willems P; van den Brand M; Valsecchi F; Kruse S; Palmiter R; Smeitink J; Nijtmans L Hum Mol Genet; 2012 Jan; 21(1):115-20. PubMed ID: 21965299 [TBL] [Abstract][Full Text] [Related]
2. Proteomic and metabolomic analyses of mitochondrial complex I-deficient mouse model generated by spontaneous B2 short interspersed nuclear element (SINE) insertion into NADH dehydrogenase (ubiquinone) Fe-S protein 4 (Ndufs4) gene. Leong DW; Komen JC; Hewitt CA; Arnaud E; McKenzie M; Phipson B; Bahlo M; Laskowski A; Kinkel SA; Davey GM; Heath WR; Voss AK; Zahedi RP; Pitt JJ; Chrast R; Sickmann A; Ryan MT; Smyth GK; Thorburn DR; Scott HS J Biol Chem; 2012 Jun; 287(24):20652-63. PubMed ID: 22535952 [TBL] [Abstract][Full Text] [Related]
4. NDUFS4 deletion triggers loss of NDUFA12 in Ndufs4 Adjobo-Hermans MJW; de Haas R; Willems PHGM; Wojtala A; van Emst-de Vries SE; Wagenaars JA; van den Brand M; Rodenburg RJ; Smeitink JAM; Nijtmans LG; Sazanov LA; Wieckowski MR; Koopman WJH Biochim Biophys Acta Bioenerg; 2020 Aug; 1861(8):148213. PubMed ID: 32335026 [TBL] [Abstract][Full Text] [Related]
5. Differences in assembly or stability of complex I and other mitochondrial OXPHOS complexes in inherited complex I deficiency. Ugalde C; Janssen RJ; van den Heuvel LP; Smeitink JA; Nijtmans LG Hum Mol Genet; 2004 Mar; 13(6):659-67. PubMed ID: 14749350 [TBL] [Abstract][Full Text] [Related]
6. Combined enzymatic complex I and III deficiency associated with mutations in the nuclear encoded NDUFS4 gene. Budde SM; van den Heuvel LP; Janssen AJ; Smeets RJ; Buskens CA; DeMeirleir L; Van Coster R; Baethmann M; Voit T; Trijbels JM; Smeitink JA Biochem Biophys Res Commun; 2000 Aug; 275(1):63-8. PubMed ID: 10944442 [TBL] [Abstract][Full Text] [Related]
8. Structural insights into respiratory complex I deficiency and assembly from the mitochondrial disease-related ndufs4 Yin Z; Agip AA; Bridges HR; Hirst J EMBO J; 2024 Jan; 43(2):225-249. PubMed ID: 38177503 [TBL] [Abstract][Full Text] [Related]
9. Disruption of a nuclear gene encoding a mitochondrial gamma carbonic anhydrase reduces complex I and supercomplex I + III2 levels and alters mitochondrial physiology in Arabidopsis. Perales M; Eubel H; Heinemeyer J; Colaneri A; Zabaleta E; Braun HP J Mol Biol; 2005 Jul; 350(2):263-77. PubMed ID: 15935378 [TBL] [Abstract][Full Text] [Related]
10. Effects of mitochondrial complex III disruption in the respiratory chain of Neurospora crassa. Duarte M; Videira A Mol Microbiol; 2009 Apr; 72(1):246-58. PubMed ID: 19239619 [TBL] [Abstract][Full Text] [Related]
11. 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 PM; Calvo E; Rodríguez-Hernández MA; Navas P; Cruz R; Carracedo Á; López-Otín C; Pérez-Martos A; Fernández-Silva P; Fernández-Vizarra E; Enríquez JA Science; 2013 Jun; 340(6140):1567-70. PubMed ID: 23812712 [TBL] [Abstract][Full Text] [Related]
12. Downregulation of the nuclear-encoded subunits of the complexes III and IV disrupts their respective complexes but not complex I in procyclic Trypanosoma brucei. Horváth A; Horáková E; Dunajcíková P; Verner Z; Pravdová E; Slapetová I; Cuninková L; Lukes J Mol Microbiol; 2005 Oct; 58(1):116-30. PubMed ID: 16164553 [TBL] [Abstract][Full Text] [Related]
13. Infantile mitochondrial encephalomyopathy with unusual phenotype caused by a novel BCS1L mutation in an isolated complex III-deficient patient. Blázquez A; Gil-Borlado MC; Morán M; Verdú A; Cazorla-Calleja MR; Martín MA; Arenas J; Ugalde C Neuromuscul Disord; 2009 Feb; 19(2):143-6. PubMed ID: 19162478 [TBL] [Abstract][Full Text] [Related]
14. Altered dopamine metabolism and increased vulnerability to MPTP in mice with partial deficiency of mitochondrial complex I in dopamine neurons. Sterky FH; Hoffman AF; Milenkovic D; Bao B; Paganelli A; Edgar D; Wibom R; Lupica CR; Olson L; Larsson NG Hum Mol Genet; 2012 Mar; 21(5):1078-89. PubMed ID: 22090423 [TBL] [Abstract][Full Text] [Related]
15. Complex I: a complex gateway to the powerhouse. Sterky FH; Larsson NG Cell Metab; 2008 Apr; 7(4):278-9. PubMed ID: 18396129 [TBL] [Abstract][Full Text] [Related]
16. COX7A2L Is a Mitochondrial Complex III Binding Protein that Stabilizes the III2+IV Supercomplex without Affecting Respirasome Formation. Pérez-Pérez R; Lobo-Jarne T; Milenkovic D; Mourier A; Bratic A; García-Bartolomé A; Fernández-Vizarra E; Cadenas S; Delmiro A; García-Consuegra I; Arenas J; Martín MA; Larsson NG; Ugalde C Cell Rep; 2016 Aug; 16(9):2387-98. PubMed ID: 27545886 [TBL] [Abstract][Full Text] [Related]
17. Partial loss of complex I due to NDUFS4 deficiency augments myocardial reperfusion damage by increasing mitochondrial superoxide/hydrogen peroxide production. Kuksal N; Gardiner D; Qi D; Mailloux RJ Biochem Biophys Res Commun; 2018 Mar; 498(1):214-220. PubMed ID: 29501746 [TBL] [Abstract][Full Text] [Related]