Mitochondrial complex I mutations in Caenorhabditis elegans produce cytochrome c oxidase deficiency, oxidative stress and vitamin-responsive lactic acidosis.
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Mutation of C20orf7 disrupts complex I assembly and causes lethal neonatal mitochondrial diseaseA tissue-specific approach to the analysis of metabolic changes in Caenorhabditis elegansC. elegans ATAD-3 is essential for mitochondrial activity and developmentConservation of complete trimethylation of lysine-43 in the rotor ring of c-subunits of metazoan adenosine triphosphate (ATP) synthases.Bacteria, yeast, worms, and flies: exploiting simple model organisms to investigate human mitochondrial diseasesSubcomplex Ilambda specifically controls integrated mitochondrial functions in Caenorhabditis elegans.Identification and functional characterization of the Caenorhabditis elegans riboflavin transporters rft-1 and rft-2Supramolecular organization of the respiratory chain in Neurospora crassa mitochondriaEnvironmental exposure, obesity, and Parkinson's disease: lessons from fat and old worms.Caenorhabditis elegans: A useful model for studying metabolic disorders in which oxidative stress is a contributing factor.Mitochondrial DNA analysis in primary congenital glaucomaThe salt-responsive transcriptome of chickpea roots and nodules via deepSuperSAGE.Structure of a mitochondrial supercomplex formed by respiratory-chain complexes I and IIILack of heme synthesis in a free-living eukaryote.Mitochondrial fragmentation leads to intracellular acidification in Caenorhabditis elegans and mammalian cells.Novel interactions between mitochondrial superoxide dismutases and the electron transport chain.Acetaminophen dosing of humans results in blood transcriptome and metabolome changes consistent with impaired oxidative phosphorylationIntroduction of an additional pathway for lactate oxidation in the treatment of lactic acidosis and mitochondrial dysfunction in Caenorhabditis elegans.The paradox of mitochondrial dysfunction and extended longevity.New perspective in diagnostics of mitochondrial disorders: two years' experience with whole-exome sequencing at a national paediatric centre.A novel mitochondrial outer membrane protein, MOMA-1, that affects cristae morphology in Caenorhabditis elegansCaenorhabditis elegans expressing the Saccharomyces cerevisiae NADH alternative dehydrogenase Ndi1p, as a tool to identify new genes involved in complex I related diseases.AMP-Activated Protein Kinase Regulates Oxidative Metabolism in Caenorhabditis elegans through the NHR-49 and MDT-15 Transcriptional RegulatorsThe use of targeted genomic capture and massively parallel sequencing in diagnosis of Chinese LeukoencephalopathiesMitochondrial respiratory complex I: structure, function and implication in human diseases.Natural variation in Caenorhabditis briggsae mitochondrial form and function suggests a novel model of organelle dynamics.Metabolic pathway profiling of mitochondrial respiratory chain mutants in C. elegans.Mitochondrial complex I function modulates volatile anesthetic sensitivity in C. elegans.Caenorhabditis elegans: an emerging model in biomedical and environmental toxicology.Animal Mitochondrial DNA Replication.The pyruvate dehydrogenase complex as a therapeutic target for age-related diseases.Differential impact of environmental stresses on the pea mitochondrial proteome.Mitochondrial dysfunction, oxidative stress, and neurodegeneration elicited by a bacterial metabolite in a C. elegans Parkinson's model.Effects of TAT-conjugated platinum nanoparticles on lifespan of mitochondrial electron transport complex I-deficient Caenorhabditis elegans, nuo-1Neurospora strains harboring mitochondrial disease-associated mutations in iron-sulfur subunits of complex I.The effect of dichloroacetate on health- and lifespan in C. elegans.Cell Biology of the Mitochondrion.SLO2, a mitochondrial pentatricopeptide repeat protein affecting several RNA editing sites, is required for energy metabolism.Identification of homocysteine-suppressive mitochondrial ETC complex genes and tissue expression profile - Novel hypothesis establishment.The plant mitochondrial proteome and the challenge of defining the posttranslational modifications responsible for signalling and stress effects on respiratory functions
P2860
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P2860
Mitochondrial complex I mutations in Caenorhabditis elegans produce cytochrome c oxidase deficiency, oxidative stress and vitamin-responsive lactic acidosis.
description
2003 nî lūn-bûn
@nan
2003年の論文
@ja
2003年学术文章
@wuu
2003年学术文章
@zh-cn
2003年学术文章
@zh-hans
2003年学术文章
@zh-my
2003年学术文章
@zh-sg
2003年學術文章
@yue
2003年學術文章
@zh
2003年學術文章
@zh-hant
name
Mitochondrial complex I mutati ...... in-responsive lactic acidosis.
@en
Mitochondrial complex I mutati ...... in-responsive lactic acidosis.
@nl
type
label
Mitochondrial complex I mutati ...... in-responsive lactic acidosis.
@en
Mitochondrial complex I mutati ...... in-responsive lactic acidosis.
@nl
prefLabel
Mitochondrial complex I mutati ...... in-responsive lactic acidosis.
@en
Mitochondrial complex I mutati ...... in-responsive lactic acidosis.
@nl
P921
P356
P1476
Mitochondrial complex I mutati ...... in-responsive lactic acidosis.
@en
P2093
Bernard D Lemire
Leslie I Grad
P304
P356
10.1093/HMG/DDH027
P577
2003-12-08T00:00:00Z