Analysis of the assembly profiles for mitochondrial- and nuclear-DNA-encoded subunits into complex I - Wikidata - wikimedia - TriplyDB

Analysis of the assembly profiles for mitochondrial- and nuclear-DNA-encoded subunits into complex I

Analysis of the assembly profiles for mitochondrial- and nuclear-DNA-encoded subunits into complex I

http://www.wikidata.org/entity/Q24683107

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C6ORF66 is an assembly factor of mitochondrial complex I Proteomics analysis identifies phosphorylation-dependent alpha-synuclein protein interactions Mutations in NDUFAF3 (C3ORF60), encoding an NDUFAF4 (C6ORF66)-interacting complex I assembly protein, cause fatal neonatal mitochondrial disease TIMMDC1/C3orf1 functions as a membrane-embedded mitochondrial complex I assembly factor through association with the MCIA complex C11orf83, a mitochondrial cardiolipin-binding protein involved in bc1 complex assembly and supercomplex stabilization Characterization of mitochondrial FOXRED1 in the assembly of respiratory chain complex I Effects of the novel mitochondrial protein mimitin in insulin-secreting cells Mutation of C20orf7 disrupts complex I assembly and causes lethal neonatal mitochondrial disease Human CIA30 is involved in the early assembly of mitochondrial complex I and mutations in its gene cause disease Structural and Functional Requirements for Activity of the Tim9-Tim10 Complex in Mitochondrial Protein Import Dynamics of Human Mitochondrial Complex I Assembly: Implications for Neurodegenerative Diseases NDUFAF5 Hydroxylates NDUFS7 at an Early Stage in the Assembly of Human Complex I Proteomic and metabolomic analyses of mitochondrial complex I-deficient mouse model generated by spontaneous B2 short interspersed nuclear element (SINE) insertion into NADH dehydrogenase (ubiquinone) Fe-S protein 4 (Ndufs4) gene The mitochondrial disease associated protein Ndufaf2 is dispensable for Complex-1 assembly but critical for the regulation of oxidative stress Mitochondrial membrane potential regulates PINK1 import and proteolytic destabilization by PARL Recombinant human mitochondrial transcription factor A stimulates mitochondrial biogenesis and ATP synthesis, improves motor function after MPTP, reduces oxidative stress and increases survival after endotoxin Uncovering molecular biomarkers that correlate cognitive decline with the changes of hippocampus' gene expression profiles in Alzheimer's disease.Atomic structure of the entire mammalian mitochondrial complex I.Accessory subunits are integral for assembly and function of human mitochondrial complex I.Mimitin - a novel cytokine-regulated mitochondrial protein Analysis of the liver mitochondrial proteome in response to ethanol and S-adenosylmethionine treatments: novel molecular targets of disease and hepatoprotection.The p.M292T NDUFS2 mutation causes complex I-deficient Leigh syndrome in multiple families Inhibition of Bak activation by VDAC2 is dependent on the Bak transmembrane anchor Mutated NDUFS6 is the cause of fatal neonatal lactic acidemia in Caucasus Jews.A three-dimensional topology of complex I inferred from evolutionary correlations.Bax targets mitochondria by distinct mechanisms before or during apoptotic cell death: a requirement for VDAC2 or Bak for efficient Bax apoptotic function Subcomplexes of ancestral respiratory complex I subunits rapidly turn over in vivo as productive assembly intermediates in Arabidopsis Neuronal and astrocyte dysfunction diverges from embryonic fibroblasts in the Ndufs4fky/fky mouse.Mitochondrial cardiolipin involved in outer-membrane protein biogenesis: implications for Barth syndrome.Respiratory chain complex I deficiency caused by mitochondrial DNA mutations.Insights into the composition and assembly of the membrane arm of plant complex I through analysis of subcomplexes in Arabidopsis mutant lines.Mitochondrial Diseases Part I: mouse models of OXPHOS deficiencies caused by defects in respiratory complex subunits or assembly factors.Granzyme B-induced mitochondrial ROS are required for apoptosis An update on complex I assembly: the assembly of players.Accessory NUMM (NDUFS6) subunit harbors a Zn-binding site and is essential for biogenesis of mitochondrial complex I.Redefining the roles of mitochondrial DNA-encoded subunits in respiratory Complex I assembly Cells lacking Rieske iron-sulfur protein have a reactive oxygen species-associated decrease in respiratory complexes I and IV.Mitochondrial complex I plays an essential role in human respirasome assembly.Diabetes Susceptibility Genes Pdx1 and Clec16a Function in a Pathway Regulating Mitophagy in β-Cells.Mouse models of mitochondrial complex I dysfunction

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Analysis of the assembly profiles for mitochondrial- and nuclear-DNA-encoded subunits into complex I

http://www.wikidata.org/entity/Q24683107

description

2007 nî lūn-bûn

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2007 թուականի Յունիսին հրատարակուած գիտական յօդուած

@hyw

2007 թվականի հունիսին հրատարակված գիտական հոդված

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2007年の論文

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2007年論文

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2007年論文

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2007年論文

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2007年論文

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2007年論文

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2007年论文

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name

Analysis of the assembly profi ...... ncoded subunits into complex I

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Analysis of the assembly profi ...... ncoded subunits into complex I

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Analysis of the assembly profi ...... ncoded subunits into complex I

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type

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Analysis of the assembly profi ...... ncoded subunits into complex I

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Analysis of the assembly profi ...... ncoded subunits into complex I

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Analysis of the assembly profi ...... ncoded subunits into complex I

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Analysis of the assembly profi ...... ncoded subunits into complex I

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Analysis of the assembly profi ...... ncoded subunits into complex I

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Analysis of the assembly profi ...... ncoded subunits into complex I

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Molecular and Cellular Biology

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Analysis of the assembly profi ...... ncoded subunits into complex I

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Akira Ohtake

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Michael T Ryan

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P2860

Mitochondrial respiratory chain supercomplexes are destabilized in Barth Syndrome patients

NDUFS6 mutations are a novel cause of lethal neonatal mitochondrial complex I deficiency

Insertion and assembly of human tom7 into the preprotein translocase complex of the outer mitochondrial membrane

Differences in assembly or stability of complex I and other mitochondrial OXPHOS complexes in inherited complex I deficiency

Respiratory complex III is required to maintain complex I in mammalian mitochondria

Dissection of the mitochondrial import and assembly pathway for human Tom40

A molecular chaperone for mitochondrial complex I assembly is mutated in a progressive encephalopathy.

Tricine-sodium dodecyl sulfate-polyacrylamide gel electrophoresis for the separation of proteins in the range from 1 to 100 kDa

Mdm38 interacts with ribosomes and is a component of the mitochondrial protein export machinery.

Mba1, a membrane-associated ribosome receptor in mitochondria.

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4228-37

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scholarly article

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1547278

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10.1128/MCB.00074-07

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12

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27

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Michael Lazarou

Matthew McKenzie

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2007-06-01T00:00:00Z

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6390687

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17438127

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1900046

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