Human mitochondrial complex I assembly is mediated by NDUFAF1.
about
Mitochondrial translation and beyond: processes implicated in combined oxidative phosphorylation deficienciesNDUFB7 and NDUFA8 are located at the intermembrane surface of complex ICytosolic signaling protein Ecsit also localizes to mitochondria where it interacts with chaperone NDUFAF1 and functions in complex I assemblyA mutation in the human CBP4 ortholog UQCC3 impairs complex III assembly, activity and cytochrome b stabilityMutations in NDUFAF3 (C3ORF60), encoding an NDUFAF4 (C6ORF66)-interacting complex I assembly protein, cause fatal neonatal mitochondrial diseaseTIMMDC1/C3orf1 functions as a membrane-embedded mitochondrial complex I assembly factor through association with the MCIA complexHuman ind1, an iron-sulfur cluster assembly factor for respiratory complex IMutations in the UQCC1-interacting protein, UQCC2, cause human complex III deficiency associated with perturbed cytochrome b protein expressionCharacterization of mitochondrial FOXRED1 in the assembly of respiratory chain complex IIdentification of mitochondrial complex I assembly intermediates by tracing tagged NDUFS3 demonstrates the entry point of mitochondrial subunitsA mitochondrial protein compendium elucidates complex I disease biologyHuman CIA30 is involved in the early assembly of mitochondrial complex I and mutations in its gene cause diseaseAnalysis of the assembly profiles for mitochondrial- and nuclear-DNA-encoded subunits into complex IDynamics of Human Mitochondrial Complex I Assembly: Implications for Neurodegenerative DiseasesNDUFAF7 methylates arginine 85 in the NDUFS2 subunit of human complex INDUFAF5 Hydroxylates NDUFS7 at an Early Stage in the Assembly of Human Complex IHomozygous YME1L1 mutation causes mitochondriopathy with optic atrophy and mitochondrial network fragmentationAnalysis of 953 human proteins from a mitochondrial HEK293 fraction by complexome profilingSupramolecular organization of the respiratory chain in Neurospora crassa mitochondriaLow abundance of the matrix arm of complex I in mitochondria predicts longevity in mice.The C8ORF38 homologue Sicily is a cytosolic chaperone for a mitochondrial complex I subunit.Pioglitazone leads to an inactivation and disassembly of complex I of the mitochondrial respiratory chainA forward genetic screen identifies mutants deficient for mitochondrial complex I assembly in Chlamydomonas reinhardtii.Insights into the composition and assembly of the membrane arm of plant complex I through analysis of subcomplexes in Arabidopsis mutant lines.Genes associated with recurrence of hepatocellular carcinoma: integrated analysis by gene expression and methylation profilingHypothalamic mitochondrial dysfunction associated with anorexia in the anx/anx mouse.Identification of NDUFAF1 in mediating K-Ras induced mitochondrial dysfunction by a proteomic screening approach.Novel role for mitochondria: protein kinase Ctheta-dependent oxidative signaling organelles in activation-induced T-cell death.C7orf30 specifically associates with the large subunit of the mitochondrial ribosome and is involved in translationMitochondrial import and accumulation of alpha-synuclein impair complex I in human dopaminergic neuronal cultures and Parkinson disease brain.The iron-sulphur protein Ind1 is required for effective complex I assembly.Human NADH:ubiquinone oxidoreductase deficiency: radical changes in mitochondrial morphology?Ndufaf5 deficiency in the Dictyostelium model: new roles in autophagy and developmentRegulation of mitochondrial respiratory chain biogenesis by estrogens/estrogen receptors and physiological, pathological and pharmacological implications.Mitochondrial disorders caused by mutations in respiratory chain assembly factors.Mitochondria as oxidative signaling organelles in T-cell activation: physiological role and pathological implications.Mitochondrial disease associated with complex I (NADH-CoQ oxidoreductase) deficiency.A Mutation in the Flavin Adenine Dinucleotide-Dependent Oxidoreductase FOXRED1 Results in Cell-Type-Specific Assembly Defects in Oxidative Phosphorylation Complexes I and II.Characterization of T-DNA insertion mutants with decreased virulence in the entomopathogenic fungus Beauveria bassiana JEF-007.TNF-α mediates mitochondrial uncoupling and enhances ROS-dependent cell migration via NF-κB activation in liver cells.
P2860
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P2860
Human mitochondrial complex I assembly is mediated by NDUFAF1.
description
2005 nî lūn-bûn
@nan
2005 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2005 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
2005年の論文
@ja
2005年論文
@yue
2005年論文
@zh-hant
2005年論文
@zh-hk
2005年論文
@zh-mo
2005年論文
@zh-tw
2005年论文
@wuu
name
Human mitochondrial complex I assembly is mediated by NDUFAF1.
@ast
Human mitochondrial complex I assembly is mediated by NDUFAF1.
@en
Human mitochondrial complex I assembly is mediated by NDUFAF1.
@nl
type
label
Human mitochondrial complex I assembly is mediated by NDUFAF1.
@ast
Human mitochondrial complex I assembly is mediated by NDUFAF1.
@en
Human mitochondrial complex I assembly is mediated by NDUFAF1.
@nl
prefLabel
Human mitochondrial complex I assembly is mediated by NDUFAF1.
@ast
Human mitochondrial complex I assembly is mediated by NDUFAF1.
@en
Human mitochondrial complex I assembly is mediated by NDUFAF1.
@nl
P2093
P2860
P50
P1433
P1476
Human mitochondrial complex I assembly is mediated by NDUFAF1
@en
P2093
Henk-Jan Visch
Jan A M Smeitink
Leo G J Nijtmans
Massimo Zeviani
Melissa Grovenstein
Richard J Huijbens
Rolf J R J Janssen
Rutger O Vogel
P2860
P304
P356
10.1111/J.1742-4658.2005.04928.X
P407
P577
2005-10-01T00:00:00Z