| scholarly article | Q13442814 |
| P50 | author | Pierre Cardol | Q30524418 |
| P2093 | author name string | Bénédicte Mousson de Camaret | |
| Jean-Paul Issartel | |||
| Claire Ramus | |||
| Claire Remacle | |||
| Götz Hofhaus | |||
| Ingrid Bourges | |||
| Réjane Beugnot | |||
| P2860 | cites work | SURF1, encoding a factor involved in the biogenesis of cytochrome c oxidase, is mutated in Leigh syndrome | Q22008476 |
| Human complex I defects can be resolved by monoclonal antibody analysis into distinct subunit assembly patterns | Q24290607 | ||
| Efficient selection and characterization of mutants of a human cell line which are defective in mitochondrial DNA-encoded subunits of respiratory NADH dehydrogenase | Q40021624 | ||
| Lack of assembly of mitochondrial DNA-encoded subunits of respiratory NADH dehydrogenase and loss of enzyme activity in a human cell mutant lacking the mitochondrial ND4 gene product | Q40873588 | ||
| Coamplification of Nuclear Pseudogenes and Assessment of Heteroplasmy of Mitochondrial DNA Mutations | Q41031930 | ||
| Assessment of mitochondrial oxidative phosphorylation in patient muscle biopsies, lymphoblasts, and transmitochondrial cell lines | Q41244266 | ||
| Structure of the telomeric ends of mt DNA, transcriptional analysis and complex I assembly in the dum24 mitochondrial mutant of Chlamydomonas reinhardtii | Q43758583 | ||
| A novel, enzymatically active conformation of the Escherichia coli NADH:ubiquinone oxidoreductase (complex I). | Q43906933 | ||
| Impact of mutations affecting ND mitochondria-encoded subunits on the activity and assembly of complex I in Chlamydomonas. Implication for the structural organization of the enzyme | Q44038167 | ||
| Transmembrane topology of the NuoL, M and N subunits of NADH:quinone oxidoreductase and their homologues among membrane-bound hydrogenases and bona fide antiporters | Q44235462 | ||
| Characterization and Topology of the Membrane Domain Nqo10 Subunit of the Proton-Translocating NADH-Quinone Oxidoreductase of Paracoccus denitrificans | Q44402451 | ||
| Proteomics of the chloroplast envelope membranes from Arabidopsis thaliana. | Q44453314 | ||
| Identification and characterization of a common set of complex I assembly intermediates in mitochondria from patients with complex I deficiency | Q44588150 | ||
| Partial resolution of the enzymes catalyzing oxidative phosphorylation. XI. Stimulation of oxidative phosphorylation by coupling factors and oligomycin; inhibition by an antibody against coupling factor 1. | Q44903789 | ||
| Identification of the dicyclohexylcarbodiimide-binding subunit of NADH-ubiquinone oxidoreductase (Complex I). | Q46031854 | ||
| Immuno-purification of a dimeric subcomplex of the respiratory NADH-CoQ reductase of Rhodobacter capsulatus equivalent to the FP fraction of the mitochondrial complex I. | Q48051961 | ||
| Bilateral Striatal Necrosis and MELAS Associated with a New T3308C Mutation in the Mitochondrial ND1 Gene | Q48627434 | ||
| The mitochondrial DNA G13513A transition in ND5 is associated with a LHON/MELAS overlap syndrome and may be a frequent cause of MELAS | Q61797346 | ||
| Leigh disease associated with a novel mitochondrial DNA ND5 mutation | Q63952710 | ||
| Isolation and characterisation of subcomplexes of the mitochondrial NADH:ubiquinone oxidoreductase (complex I) | Q72797112 | ||
| Expression of mtDNA and nDNA encoded respiratory chain proteins in chemically and genetically-derived Rho0 human fibroblasts: a comparison of subunit proteins in normal fibroblasts treated with ethidium bromide and fibroblasts from a patient with mt | Q74439857 | ||
| CIA30 complex I assembly factor: a candidate for human complex I deficiency? | Q24293311 | ||
| The subunit composition of the human NADH dehydrogenase obtained by rapid one-step immunopurification | Q24296439 | ||
| Oxidative damage to mitochondrial complex I due to peroxynitrite: identification of reactive tyrosines by mass spectrometry | Q24307861 | ||
| Genomic structure of the human NDUFS8 gene coding for the iron–sulfur TYKY subunit of the mitochondrial NADH:ubiquinone oxidoreductase | Q24315917 | ||
| Mapping to 1q23 of the human gene (NDUFS2) encoding the 49-kDa subunit of the mitochondrial respiratory Complex I and immunodetection of the mature protein in mitochondria | Q24315960 | ||
| A mitochondrial DNA mutation at nucleotide pair 14459 of the NADH dehydrogenase subunit 6 gene associated with maternally inherited Leber hereditary optic neuropathy and dystonia | Q24561975 | ||
| Sequence and organization of the human mitochondrial genome | Q27860659 | ||
| Prohibitins act as a membrane-bound chaperone for the stabilization of mitochondrial proteins. | Q27934000 | ||
| Prohibitins regulate membrane protein degradation by the m-AAA protease in mitochondria | Q27934696 | ||
| The prohibitin family of mitochondrial proteins regulate replicative lifespan | Q27940160 | ||
| The nuclear encoded subunits of complex I from bovine heart mitochondria | Q28183992 | ||
| Respiratory chain complex I deficiency | Q28189572 | ||
| Human cells lacking mtDNA: repopulation with exogenous mitochondria by complementation | Q29614475 | ||
| An alternative strategy to determine the mitochondrial proteome using sucrose gradient fractionation and 1D PAGE on highly purified human heart mitochondria | Q30901111 | ||
| Three-dimensional structure of bovine NADH:ubiquinone oxidoreductase (complex I) at 22 å in ice | Q32065329 | ||
| Nuclear DNA origin of mitochondrial complex I deficiency in fatal infantile lactic acidosis evidenced by transnuclear complementation of cultured fibroblasts | Q33853426 | ||
| Structure and chromosomal distribution of human mitochondrial pseudogenes | Q33959798 | ||
| Leber hereditary optic neuropathy | Q34118893 | ||
| AAA proteases of mitochondria: quality control of membrane proteins and regulatory functions during mitochondrial biogenesis | Q34332387 | ||
| Toward a characterization of the connecting module of complex I | Q34429346 | ||
| Complex I: a chimaera of a redox and conformation-driven proton pump? | Q34429353 | ||
| On complex I and other NADH:ubiquinone reductases of Neurospora crassa mitochondria. | Q34429371 | ||
| Mitochondrial genetic control of assembly and function of complex I in mammalian cells | Q34429410 | ||
| Involvement of two novel chaperones in the assembly of mitochondrial NADH:ubiquinone oxidoreductase (complex I) 1 1Edited by A. R. Fersht | Q34474891 | ||
| The mitochondrial PHB complex: roles in mitochondrial respiratory complex assembly, ageing and degenerative disease | Q34536917 | ||
| The proton-translocating NADH-quinone oxidoreductase in the respiratory chain: the secret unlocked | Q35071327 | ||
| Large functional range of steady-state levels of nuclear and mitochondrial transcripts coding for the subunits of the human mitochondrial OXPHOS system | Q35806984 | ||
| Prohibitin, an evolutionarily conserved intracellular protein that blocks DNA synthesis in normal fibroblasts and HeLa cells | Q36958660 | ||
| The mitochondrial electron transport and oxidative phosphorylation system | Q39382891 | ||
| P433 | issue | Pt. 3 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | cell biology | Q7141 |
| mitochondrion | Q39572 | ||
| P304 | page(s) | 491-499 | |
| P577 | publication date | 2004-11-01 | |
| P1433 | published in | Biochemical Journal | Q864221 |
| P1476 | title | Structural organization of mitochondrial human complex I: role of the ND4 and ND5 mitochondria-encoded subunits and interaction with prohibitin | |
| P478 | volume | 383 |
| Q45788849 | A novel m.12908T>A mutation in the mitochondrial ND5 gene in patient with infantile-onset Pompe disease |
| Q28269042 | A novel prohibitin-binding compound induces the mitochondrial apoptotic pathway through NOXA and BIM upregulation |
| Q55027142 | A truncated PPAR gamma 2 localizes to mitochondria and regulates mitochondrial respiration in brown adipocytes. |
| Q38754109 | Accumulation of prohibitin is a common cellular response to different stressing stimuli and protects melanoma cells from ER stress and chemotherapy-induced cell death |
| Q24309072 | Alterations of the mitochondrial proteome caused by the absence of mitochondrial DNA: A proteomic view |
| Q38704797 | An unexpected role for the transcriptional coactivator isoform NT-PGC-1α in the regulation of mitochondrial respiration in brown adipocytes |
| Q35547747 | An update on complex I assembly: the assembly of players |
| Q55496547 | CDKN1B/p27 is localized in mitochondria and improves respiration-dependent processes in the cardiovascular system-New mode of action for caffeine. |
| Q37133567 | CFTR activity and mitochondrial function |
| Q50294526 | Complex I oxidises NADH to NAD+, reduces CoQ to QH2 |
| Q42511264 | Deficiency of PHB complex impairs respiratory supercomplex formation and activates mitochondrial flashes. |
| Q59795341 | Deoxynivalenol Affects Cell Metabolism and Increases Protein Biosynthesis in Intestinal Porcine Epithelial Cells (IPEC-J2): DON Increases Protein Biosynthesis |
| Q36525893 | Detection and analysis of protein-protein interactions in organellar and prokaryotic proteomes by native gel electrophoresis: (Membrane) protein complexes and supercomplexes |
| Q47972707 | Development and characterization of polyspecific anti-mitochondrion antibodies for proteomics studies on in toto tissue homogenates. |
| Q36200388 | Differential expression of proteins in fetal brains of alcohol-treated prenatally C57BL/6 mice: a proteomic investigation |
| Q33717303 | Disruption of interleukin-1β autocrine signaling rescues complex I activity and improves ROS levels in immortalized epithelial cells with impaired cystic fibrosis transmembrane conductance regulator (CFTR) function |
| Q39715625 | Five entry points of the mitochondrially encoded subunits in mammalian complex I assembly |
| Q41731725 | Flavaglines Ameliorate Experimental Colitis and Protect Against Intestinal Epithelial Cell Apoptosis and Mitochondrial Dysfunction |
| Q36495215 | Functional diversity of complex I subunits in Candida albicans mitochondria |
| Q38077447 | HCV and oxidative stress in the liver. |
| Q24338844 | Identification of mitochondrial complex I assembly intermediates by tracing tagged NDUFS3 demonstrates the entry point of mitochondrial subunits |
| Q28748900 | Increased phosphorylation of vimentin in noninfiltrative meningiomas |
| Q24298448 | Interleukin-6 transcriptionally regulates prohibitin expression in intestinal epithelial cells |
| Q24675030 | Kinetic properties of mutant deoxyguanosine kinase in a case of reversible hepatic mtDNA depletion |
| Q35842091 | LRP130 Protein Remodels Mitochondria and Stimulates Fatty Acid Oxidation |
| Q36243568 | Low Levels of Prohibitin in Substantia Nigra Makes Dopaminergic Neurons Vulnerable in Parkinson's Disease. |
| Q38337065 | Melatonin improves mitochondrial respiratory chain activity and liver morphology in ob/ob mice. |
| Q46359827 | Mitochondria and Angiogenesis |
| Q33358358 | Mitochondrial Band-7 family proteins: scaffolds for respiratory chain assembly? |
| Q48223189 | Mitochondrial Mutations in Cholestatic Liver Disease with Biliary Atresia. |
| Q36534792 | Mitochondrial complex I: structure, function and pathology |
| Q24305114 | Mitochondrial functions and estrogen receptor-dependent nuclear translocation of pleiotropic human prohibitin 2 |
| Q36444688 | Mitochondrial respiratory complex I: structure, function and implication in human diseases |
| Q39481814 | Mitochondrial–Nuclear Communication by Prohibitin Shuttling under Oxidative Stress |
| Q28087391 | Multifaceted role of prohibitin in cell survival and apoptosis |
| Q33404129 | Multiplex expression cloning of blood-brain barrier membrane proteins |
| Q24336408 | Mutation of C20orf7 disrupts complex I assembly and causes lethal neonatal mitochondrial disease |
| Q92214578 | Mutations in KARS cause a severe neurological and neurosensory disease with optic neuropathy |
| Q39210952 | Myocardium proteome remodelling after nutritional deprivation of methyl donors |
| Q36185450 | Nonsynonymous variants in mt-Nd2, mt-Nd4, and mt-Nd5 are linked to effects on oxidative phosphorylation and insulin sensitivity in rat conplastic strains |
| Q35581352 | Novel large-range mitochondrial DNA deletions and fatal multisystemic disorder with prominent hepatopathy |
| Q101216954 | Nuclear partitioning of Prohibitin 1 inhibits Wnt/β-catenin-dependent intestinal tumorigenesis |
| Q34036422 | Prohibitin 1 modulates mitochondrial function of Stat3. |
| Q38092225 | Prohibitin Ligands in Cell Death and Survival: Mode of Action and Therapeutic Potential |
| Q90169726 | Prohibitin S-nitrosylation is required for the neuroprotective effect of nitric oxide in neuronal cultures |
| Q38812131 | Prohibitin as the Molecular Binding Switch in the Retinal Pigment Epithelium. |
| Q37387991 | Prohibitin inhibits tumor necrosis factor alpha-induced nuclear factor-kappa B nuclear translocation via the novel mechanism of decreasing importin alpha3 expression |
| Q56394741 | Prohibitin is a positive modulator of mitochondrial function in PC12 cells under oxidative stress |
| Q41572511 | Prohibitin reduces mitochondrial free radical production and protects brain cells from different injury modalities |
| Q61813192 | Prohibitins: A Critical Role in Mitochondrial Functions and Implication in Diseases |
| Q92536112 | Proteomic Analysis of Placental Mitochondria Following Trophoblast Differentiation |
| Q39826756 | Proteomics analysis of mitochondrial proteins reveals overexpression of a mitochondrial protein chaperon, prohibitin, in cells expressing hepatitis C virus core protein |
| Q35613167 | Redefining the roles of mitochondrial DNA-encoded subunits in respiratory Complex I assembly |
| Q46804173 | Reduction of prohibitin expression contributes to left ventricular hypertrophy via enhancement of mitochondrial reactive oxygen species formation in spontaneous hypertensive rats |
| Q34110092 | Role of mitochondrial DNA damage in the development of diabetic retinopathy, and the metabolic memory phenomenon associated with its progression |
| Q38074717 | Signaling pathways of prohibitin and its role in diseases |
| Q35678495 | Simultaneous DNA and RNA Mapping of Somatic Mitochondrial Mutations across Diverse Human Cancers |
| Q42570026 | Structural and mutational analysis of band 7 proteins in the cyanobacterium Synechocystis sp. strain PCC 6803. |
| Q36451919 | Subunit-specific incorporation efficiency and kinetics in mitochondrial complex I homeostasis |
| Q33299162 | Supramolecular organization of the respiratory chain in Neurospora crassa mitochondria |
| Q39586047 | The expression of nicotinamide N-methyltransferase increases ATP synthesis and protects SH-SY5Y neuroblastoma cells against the toxicity of Complex I inhibitors |
| Q34489613 | The mitochondrial complex I activity is reduced in cells with impaired cystic fibrosis transmembrane conductance regulator (CFTR) function |
| Q37902119 | The molecular basis of human complex I deficiency. |
| Q41036551 | Unraveling the functions of type II-prohibitins in Arabidopsis mitochondria. |
Search more.