Development and characterization of a conditional mitochondrial complex I assembly system.
about
Transcriptional profiling of MnSOD-mediated lifespan extension in Drosophila reveals a species-general network of aging and metabolic genesIdentification of mitochondrial complex I assembly intermediates by tracing tagged NDUFS3 demonstrates the entry point of mitochondrial subunitsAnalysis of the assembly profiles for mitochondrial- and nuclear-DNA-encoded subunits into complex IMAO-B elevation in mouse brain astrocytes results in Parkinson's pathologyThe mitochondrial disease associated protein Ndufaf2 is dispensable for Complex-1 assembly but critical for the regulation of oxidative stressMitochondrial function in Antarctic nototheniids with ND6 translocationNew MT-ND6 and NDUFA1 mutations in mitochondrial respiratory chain disorders.Comparative Analysis of the Mitochondrial Physiology of Pancreatic β CellsDownregulation of NDUFA1 and other oxidative phosphorylation-related genes is a consistent feature of basal cell carcinoma.Human mitochondrial complex I assembly is mediated by NDUFAF1.Mitochondrial dysfunction impairs tumor suppressor p53 expression/function.Insights into the composition and assembly of the membrane arm of plant complex I through analysis of subcomplexes in Arabidopsis mutant lines.An update on complex I assembly: the assembly of players.Redefining the roles of mitochondrial DNA-encoded subunits in respiratory Complex I assemblyHigh throughput gene complementation screening permits identification of a mammalian mitochondrial protein synthesis (ρ(-)) mutant.Proteomic investigations of complex I composition: how to define a subunit?Mitochondrial respiratory complex I: structure, function and implication in human diseases.Subunit-specific incorporation efficiency and kinetics in mitochondrial complex I homeostasisMechanism of neem limonoids-induced cell death in cancer: Role of oxidative phosphorylation.PPARα modulates gene expression profiles of mitochondrial energy metabolism in oral tumorigenesisThe 2-oxoacid dehydrogenase complexes in mitochondria can produce superoxide/hydrogen peroxide at much higher rates than complex IAIF deficiency compromises oxidative phosphorylation.Accessory subunits of mitochondrial complex I.Mitochondrial disease associated with complex I (NADH-CoQ oxidoreductase) deficiency.Mitochondrial DNA background modulates the assembly kinetics of OXPHOS complexes in a cellular model of mitochondrial disease.An assembled complex IV maintains the stability and activity of complex I in mammalian mitochondria.Genetic modification of human mesenchymal stem cells helps to reduce adiposity and improve glucose tolerance in an obese diabetic mouse modelTargeting the NAD7 subunit to mitochondria restores a functional complex I and a wild type phenotype in the Nicotiana sylvestris CMS II mutant lacking nad7.Identification of homocysteine-suppressive mitochondrial ETC complex genes and tissue expression profile - Novel hypothesis establishment.Mitochondrial network complexity and pathological decrease in complex I activity are tightly correlated in isolated human complex I deficiency.The decrease of glycolytic enzyme hexokinase 1 accelerates tumor malignancy via deregulating energy metabolism but sensitizes cancer cells to 2-deoxyglucose inhibition.
P2860
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P2860
Development and characterization of a conditional mitochondrial complex I assembly system.
description
2004 nî lūn-bûn
@nan
2004年の論文
@ja
2004年論文
@yue
2004年論文
@zh-hant
2004年論文
@zh-hk
2004年論文
@zh-mo
2004年論文
@zh-tw
2004年论文
@wuu
2004年论文
@zh
2004年论文
@zh-cn
name
Development and characterizati ...... ial complex I assembly system.
@en
type
label
Development and characterizati ...... ial complex I assembly system.
@en
prefLabel
Development and characterizati ...... ial complex I assembly system.
@en
P2093
P2860
P356
P1476
Development and characterizati ...... ial complex I assembly system.
@en
P2093
Immo E Scheffler
Nagendra Yadava
Prasanth Potluri
Toby Houchens
P2860
P304
12406-12413
P356
10.1074/JBC.M313588200
P407
P577
2004-01-13T00:00:00Z