| scholarly article | Q13442814 |
| P50 | author | Alice Lepelley | Q56871875 |
| Flávia R G Carneiro | Q84113506 | ||
| P2093 | author name string | Sankar Ghosh | |
| Matthew S Hayden | |||
| John J Seeley | |||
| P2860 | cites work | PINK1 is selectively stabilized on impaired mitochondria to activate Parkin | Q21145802 |
| ECSIT is an evolutionarily conserved intermediate in the Toll/IL-1 signal transduction pathway | Q22010492 | ||
| Acyl-CoA dehydrogenase 9 is required for the biogenesis of oxidative phosphorylation complex I | Q24298522 | ||
| Cytosolic signaling protein Ecsit also localizes to mitochondria where it interacts with chaperone NDUFAF1 and functions in complex I assembly | Q24299292 | ||
| Mutations in PTEN-induced putative kinase 1 associated with recessive parkinsonism have differential effects on protein stability | Q24299939 | ||
| Mutant NDUFV2 subunit of mitochondrial complex I causes early onset hypertrophic cardiomyopathy and encephalopathy | Q24302105 | ||
| YME1L controls the accumulation of respiratory chain subunits and is required for apoptotic resistance, cristae morphogenesis, and cell proliferation | Q24302280 | ||
| TIMMDC1/C3orf1 functions as a membrane-embedded mitochondrial complex I assembly factor through association with the MCIA complex | Q24314040 | ||
| Parkin is recruited selectively to impaired mitochondria and promotes their autophagy | Q24317471 | ||
| The pathways of mitophagy for quality control and clearance of mitochondria | Q27009206 | ||
| Self and nonself: how autophagy targets mitochondria and bacteria | Q27012602 | ||
| Architecture of succinate dehydrogenase and reactive oxygen species generation | Q27640410 | ||
| Ubiquitin-dependent mitochondrial protein degradation | Q27692704 | ||
| The YTA10-12 complex, an AAA protease with chaperone-like activity in the inner membrane of mitochondria | Q27931009 | ||
| Isolated complex I deficiency in children: clinical, biochemical and genetic aspects | Q28143420 | ||
| Mitochondrial dysfunction and oxidative stress in neurodegenerative diseases | Q28269333 | ||
| Mitochondria and reactive oxygen species: physiology and pathophysiology | Q28397259 | ||
| Ecsit is required for Bmp signaling and mesoderm formation during mouse embryogenesis | Q28587816 | ||
| Intestinal epithelial autophagy is essential for host defense against invasive bacteria | Q30543790 | ||
| Respiratory chain complex I deficiency: an underdiagnosed energy generation disorder | Q33600939 | ||
| Oxidative stress and mitochondrial dysfunction across broad-ranging pathologies: toward mitochondria-targeted clinical strategies | Q33625254 | ||
| Low abundance of the matrix arm of complex I in mitochondria predicts longevity in mice | Q33626717 | ||
| A hyperactive piggyBac transposase for mammalian applications | Q33785567 | ||
| Mitochondrial reactive oxygen species (ROS) and ROS-induced ROS release | Q33913079 | ||
| High efficiency of ROS production by glycerophosphate dehydrogenase in mammalian mitochondria. | Q34014350 | ||
| Mitochondrial complex I activity suppresses inflammation and enhances bone resorption by shifting macrophage-osteoclast polarization | Q34143332 | ||
| TLR signalling augments macrophage bactericidal activity through mitochondrial ROS. | Q34180844 | ||
| A giant molecular proton pump: structure and mechanism of respiratory complex I. | Q34477041 | ||
| Mitochondrial ROS metabolism: modulation by uncoupling proteins. | Q34499078 | ||
| Mutations in human nuclear genes encoding for subunits of mitochondrial respiratory complex I: the NDUFS4 gene | Q34594206 | ||
| Regulating mitochondrial outer membrane proteins by ubiquitination and proteasomal degradation | Q35163362 | ||
| An update on complex I assembly: the assembly of players | Q35547747 | ||
| Kinases Mst1 and Mst2 positively regulate phagocytic induction of reactive oxygen species and bactericidal activity | Q36200269 | ||
| Natural disease course and genotype-phenotype correlations in Complex I deficiency caused by nuclear gene defects: what we learned from 130 cases. | Q36203487 | ||
| Mitochondrial respiratory-chain adaptations in macrophages contribute to antibacterial host defense. | Q37197479 | ||
| Biallelic Mutations in TMEM126B Cause Severe Complex I Deficiency with a Variable Clinical Phenotype | Q37218530 | ||
| Assembly factors for the membrane arm of human complex I. | Q37340668 | ||
| Mitochondrial complex I deficiency leads to increased production of superoxide radicals and induction of superoxide dismutase | Q37357532 | ||
| The ubiquitin ligase parkin mediates resistance to intracellular pathogens | Q37458253 | ||
| Assembly factors of human mitochondrial complex I and their defects in disease | Q37765531 | ||
| Ubiquitin-proteasome system and mitochondria - reciprocity | Q37776909 | ||
| Understanding mitochondrial complex I assembly in health and disease | Q37933572 | ||
| The role of mitochondrial OXPHOS dysfunction in the development of neurologic diseases | Q37994541 | ||
| The Assembly Pathway of Mitochondrial Respiratory Chain Complex I. | Q38741912 | ||
| A LON-ClpP Proteolytic Axis Degrades Complex I to Extinguish ROS Production in Depolarized Mitochondria. | Q39675106 | ||
| Mutations in the mitochondrial complex I assembly factor NDUFAF1 cause fatal infantile hypertrophic cardiomyopathy | Q39706072 | ||
| Parkin mediates proteasome-dependent protein degradation and rupture of the outer mitochondrial membrane | Q42235376 | ||
| Metformin Inhibits the Production of Reactive Oxygen Species from NADH:Ubiquinone Oxidoreductase to Limit Induction of Interleukin-1β (IL-1β) and Boosts Interleukin-10 (IL-10) in Lipopolysaccharide (LPS)-activated Macrophages. | Q42248604 | ||
| The contribution of mitochondrial respiratory complexes to the production of reactive oxygen species. | Q42514984 | ||
| A case of mitochondrial myopathy, lactic acidosis and complex I deficiency | Q43635325 | ||
| Generation of reactive oxygen species in the reaction catalyzed by alpha-ketoglutarate dehydrogenase. | Q45050762 | ||
| Mitochondrial alpha-ketoglutarate dehydrogenase complex generates reactive oxygen species. | Q45050765 | ||
| ELMO1 regulates the induction of autophagy and bacterial clearance during enteric infection. | Q46252758 | ||
| Recurrent ECSIT mutation encoding V140A triggers hyperinflammation and promotes hemophagocytic syndrome in extranodal NK/T cell lymphoma | Q47240802 | ||
| NDUFAF4 variants are associated with Leigh syndrome and cause a specific mitochondrial complex I assembly defect | Q47788849 | ||
| Loss of cytochrome c oxidase promotes RAS-dependent ROS production from the ER resident NADPH oxidase, Yno1p, in yeast | Q47818025 | ||
| Fatal mitochondrial myopathy, lactic acidosis, and complex I deficiency associated with a heteroplasmic A --> G mutation at position 3251 in the mitochondrial tRNALeu(UUR) gne. | Q49082669 | ||
| Complexome profiling identifies TMEM126B as a component of the mitochondrial complex I assembly complex. | Q50241308 | ||
| Afg3p, a mitochondrial ATP-dependent metalloprotease, is involved in degradation of mitochondrially-encoded Cox1, Cox3, Cob, Su6, Su8 and Su9 subunits of the inner membrane complexes III, IV and V | Q71103986 | ||
| P433 | issue | 10 | |
| P304 | page(s) | 2654-2666 | |
| P577 | publication date | 2018-03-01 | |
| P1433 | published in | Cell Reports | Q5058165 |
| P1476 | title | An Essential Role for ECSIT in Mitochondrial Complex I Assembly and Mitophagy in Macrophages | |
| P478 | volume | 22 |
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