Mitochondrial complex I: Structure, function and pathology

Journal of Inherited Metabolic Disease

Volumn 29, Issue 4, 2006, Pages 499-515

  Janssen, Rolf J R J ^a   Nijtmans, Leo G ^a   van den Heuvel, Lambert P ^a   Smeitink, Jan A M ^a  

^a RADBOUD UNIVERSITY MEDICAL CENTER   (Netherlands)

Author keywords

[No Author keywords available]

Indexed keywords

BACTERIAL COMPLEX 1; BACTERIAL ENZYME; CARDIOLIPIN; CHAPERONE; CYTOCHROME B; FRATAXIN; GENE ASSOCIATED WITH RETINOID INTERFERON INDUCED MORTALITY 19 PROTEIN; MEMBRANE PROTEIN; MITOCHONDRIAL DNA; MYC INDUCED MITOCHONDRIAL PROTEIN; REDUCED NICOTINAMIDE ADENINE DINUCLEOTIDE; REDUCED NICOTINAMIDE ADENINE DINUCLEOTIDE DEHYDROGENASE; REDUCED NICOTINAMIDE ADENINE DINUCLEOTIDE DEHYDROGENASE (UBIQUINONE); REDUCED NICOTINAMIDE ADENINE DINUCLEOTIDE PHOSPHATE; RIBOSOME RNA; TRANSFER RNA; UNCLASSIFIED DRUG;

ALZHEIMER DISEASE; ATAXIA; BIPOLAR DISORDER; BRAIN MITOCHONDRION; CARDIOMYOPATHY; CATALYSIS; COMPLEX I DEFICIENCY; CRYSTAL STRUCTURE; DEMETHYLATION; DNA REPLICATION; DOWN SYNDROME; DYSTONIA; ELECTRON TRANSPORT; ENZYME ACTIVITY; ENZYME CONFORMATION; ENZYME LOCALIZATION; ENZYME STRUCTURE; ENZYME SUBUNIT; EPIDEMIC MENINGITIS; FATTY ACID SYNTHESIS; GENE DISRUPTION; GENE MUTATION; GENETIC CONSERVATION; GENETIC HETEROGENEITY; GENETIC IDENTIFICATION; GENETIC REGULATION; GENOTYPE PHENOTYPE CORRELATION; GROWTH RETARDATION; HEART MITOCHONDRION; HEREDITARY MOTOR SENSORY NEUROPATHY; HUMAN; HUNTINGTON CHOREA; INBORN ERROR OF METABOLISM; LACTIC ACIDOSIS; LEBER HEREDITARY OPTIC NEUROPATHY; LEIGH DISEASE; LEUKODYSTROPHY; LEUKOENCEPHALOPATHY; MELAS SYNDROME; MITOCHONDRIAL ENCEPHALOPATHY; MITOCHONDRIAL ENERGY TRANSFER; MITOCHONDRIAL GENETICS; MYOCLONUS; NONHUMAN; NUCLEOTIDE BINDING SITE; NUCLEOTIDE SEQUENCE; OXIDATION REDUCTION REACTION; OXIDATIVE PHOSPHORYLATION; PARKINSON DISEASE; PROTEIN AGGREGATION; PROTEIN ASSEMBLY; PROTEIN DEGRADATION; PROTEIN FOLDING; PROTEIN FUNCTION; PROTEIN METHYLATION; PROTEIN PROTEIN INTERACTION; PROTEIN SYNTHESIS; PROTON TRANSPORT; REVIEW; SCHIZOPHRENIA; WILSON DISEASE;

ANIMALS; CATTLE; CELL NUCLEUS; ELECTRON TRANSPORT COMPLEX I; ELECTRONS; EVOLUTION, MOLECULAR; HUMANS; MITOCHONDRIAL DISEASES; MODELS, CHEMICAL; MODELS, MOLECULAR; NEUROSPORA CRASSA; OXIDATIVE PHOSPHORYLATION; PHOSPHORYLATION; PROTEIN STRUCTURE, TERTIARY;

EID: 33746878763     PISSN: 01418955     EISSN: 15732665     Source Type: Journal    
DOI: 10.1007/s10545-006-0362-4     Document Type: Review

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