NADH:ubiquinone oxidoreductase core subunit S3
NADH:ubiquinone oxidoreductase, 30kDa subunit superfamily
NADH:ubiquinone oxidoreductase, 30kDa subunit, protein family
NADH:ubiquinone oxidoreductase, 30kDa subunit
NADH:ubiquinone oxidoreductase, 30kDa subunit, conserved site
oxidoreductase activity, acting on NAD(P)H
negative regulation of intrinsic apoptotic signaling pathway
reactive oxygen species metabolic process
NADH:ubiquinone oxidoreductase, 30kDa subunit, conserved site, protein family
mitochondrial respiratory chain complex I
mitochondrial respiratory chain complex I assembly
Mutations in NDUFAF3 (C3ORF60), encoding an NDUFAF4 (C6ORF66)-interacting complex I assembly protein, cause fatal neonatal mitochondrial disease
DJ-1 binds to mitochondrial complex I and maintains its activity
TIMMDC1/C3orf1 functions as a membrane-embedded mitochondrial complex I assembly factor through association with the MCIA complex
Structural organization of mitochondrial human complex I: role of the ND4 and ND5 mitochondria-encoded subunits and interaction with prohibitin
LC-MS/MS as an alternative for SDS-PAGE in blue native analysis of protein complexes
cDNA Sequence and Chromosomal Localization of the Remaining Three Human Nuclear Encoded Iron Sulphur Protein (IP) Subunits of Complex I: The Human IP Fraction Is Completed
Coupling mitochondrial respiratory chain to cell death: an essential role of mitochondrial complex I in the interferon-beta and retinoic acid-induced cancer cell death
Human complex I defects can be resolved by monoclonal antibody analysis into distinct subunit assembly patterns
cDNA of eight nuclear encoded subunits of NADH:ubiquinone oxidoreductase: human complex I cDNA characterization completed
Identification of mitochondrial complex I assembly intermediates by tracing tagged NDUFS3 demonstrates the entry point of mitochondrial subunits
The subunit composition of the human NADH dehydrogenase obtained by rapid one-step immunopurification
Phylogenetic-based propagation of functional annotations within the Gene Ontology consortium
Quantitative Proteomic Analysis of Human Substantia Nigra in Alzheimer’s Disease, Huntington’s Disease and Multiple Sclerosis