In vivo control of respiration by cytochrome c oxidase in wild-type and mitochondrial DNA mutation-carrying human cells. - Wikidata - wikimedia - TriplyDB

In vivo control of respiration by cytochrome c oxidase in wild-type and mitochondrial DNA mutation-carrying human cells.

In vivo control of respiration by cytochrome c oxidase in wild-type and mitochondrial DNA mutation-carrying human cells.

http://www.wikidata.org/entity/Q35990246

about

The mechanism of Intralipid®-mediated cardioprotection complex IV inhibition by the active metabolite, palmitoylcarnitine, generates reactive oxygen species and activates reperfusion injury salvage kinases Metabolic scaling: consensus or controversy?The multiple functions of cytochrome c and their regulation in life and death decisions of the mammalian cell: from respiration to apoptosis Respiratory complex III is required to maintain complex I in mammalian mitochondria Human mtDNA haplogroups associated with high or reduced spermatozoa motility Metabolic control analysis in a cellular model of elevated MAO-B: relevance to Parkinson's disease Evolution of the couple cytochrome c and cytochrome c oxidase in primates A role for Pet100p in the assembly of yeast cytochrome c oxidase: interaction with a subassembly that accumulates in a pet100 mutant.Mitochondrial membrane potential is dependent on the oligomeric state of F1F0-ATP synthase supracomplexes.Effect of 'binary mitochondrial heteroplasmy' on respiration and ATP synthesis: implications for mitochondrial diseases Early decrease in respiration and uncoupling event independent of cytochrome C release in PC12 cells undergoing apoptosis Phosphorylation of mammalian cytochrome c and cytochrome c oxidase in the regulation of cell destiny: respiration, apoptosis, and human disease Mitochondrial biogenesis drives a vicious cycle of metabolic insufficiency and mitochondrial DNA deletion mutation accumulation in aged rat skeletal muscle fibers Efficient repopulation of genetically derived rho zero cells with exogenous mitochondria Mitochondrial oxidative stress in mice lacking the glutathione peroxidase-1 gene Mitonuclear coevolution as the genesis of speciation and the mitochondrial DNA barcode gap Production of transmitochondrial cybrids containing naturally occurring pathogenic mtDNA variants.Lack of correlation between MYCN expression and the Warburg effect in neuroblastoma cell lines.A second mechanism of respiratory control.Tissue- and Condition-Specific Isoforms of Mammalian Cytochrome c Oxidase Subunits: From Function to Human Disease.Network clustering revealed the systemic alterations of mitochondrial protein expression.Allometric scaling of metabolic rate from molecules and mitochondria to cells and mammals.The myoclonic epilepsy and ragged-red fiber mutation provides new insights into human mitochondrial function and genetics.An mtDNA mutation in the initiation codon of the cytochrome C oxidase subunit II gene results in lower levels of the protein and a mitochondrial encephalomyopathy.New control of mitochondrial membrane potential and ROS formation--a hypothesis.Peroxisome proliferator-activated receptor-gamma coactivator 1-alpha (PGC1alpha) is a metabolic regulator of intestinal epithelial cell fate.Mitochondrial threshold effects.Normal levels of wild-type mitochondrial DNA maintain cytochrome c oxidase activity for two pathogenic mitochondrial DNA mutations but not for m.3243A-->G.Cytochrome c oxidase subunit 4 isoform 2-knockout mice show reduced enzyme activity, airway hyporeactivity, and lung pathology Expanding the functional human mitochondrial DNA database by the establishment of primate xenomitochondrial cybrids.Chronic hypoxia impairs cytochrome oxidase activity via oxidative stress in selected fetal Guinea pig organs Cosegregation of novel mitochondrial 16S rRNA gene mutations with the age-associated T414G variant in human cybrids.(-)-Epicatechin is associated with increased angiogenic and mitochondrial signalling in the hindlimb of rats selectively bred for innate low running capacity.Multiple phosphorylations of cytochrome c oxidase and their functions.Effects of aging on mitochondrial function in skeletal muscle of American American Quarter Horses.Computational prediction and in vitro analysis of potential physiological ligands of the bile acid binding site in cytochrome c oxidase Control of respiration by cytochrome c oxidase in intact cells: role of the membrane potential Low MT-CO1 in Monocytes and Microvesicles Is Associated With Outcome in Patients With Coronary Artery Disease.Cytochrome c oxidase: evolution of control via nuclear subunit addition.Mitochondrial DNA and functional investigations into the radiosensitivity of four mouse strains.

P2860

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P2860

In vivo control of respiration by cytochrome c oxidase in wild-type and mitochondrial DNA mutation-carrying human cells.

http://www.wikidata.org/entity/Q35990246

description

1997 nî lūn-bûn

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1997年の論文

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1997年論文

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1997年論文

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1997年論文

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1997年論文

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1997年論文

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1997年论文

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1997年论文

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1997年论文

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name

In vivo control of respiration ...... mutation-carrying human cells.

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In vivo control of respiration ...... mutation-carrying human cells.

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In vivo control of respiration ...... mutation-carrying human cells.

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In vivo control of respiration ...... mutation-carrying human cells.

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In vivo control of respiration ...... mutation-carrying human cells.

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Proceedings of the National Academy of Sciences of the United States of America

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In vivo control of respiration ...... mutation-carrying human cells.

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G Attardi

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P2860

A linear steady-state treatment of enzymatic chains. General properties, control and effector strength

Increase of flux control of cytochrome c oxidase in copper-deficient mottled brindled mice

Human cells lacking mtDNA: repopulation with exogenous mitochondria by complementation

Myoclonic epilepsy and ragged-red fiber disease (MERRF) is associated with a mitochondrial DNA tRNA(Lys) mutation.

Diseases of the mitochondrial DNA.

Use of transmitochondrial cybrids to assign a complex I defect to the mitochondrial DNA-encoded NADH dehydrogenase subunit 6 gene mutation at nucleotide pair 14459 that causes Leber hereditary optic neuropathy and dystonia.

Complementation of mutant and wild-type human mitochondrial DNAs coexisting since the mutation event and lack of complementation of DNAs introduced separately into a cell within distinct organelles.

In vitro genetic transfer of protein synthesis and respiration defects to mitochondrial DNA-less cells with myopathy-patient mitochondria.

Efficient selection and characterization of mutants of a human cell line which are defective in mitochondrial DNA-encoded subunits of respiratory NADH dehydrogenase

Biochemical evidence for nuclear gene involvement in phenotype of non-syndromic deafness associated with mitochondrial 12S rRNA mutation.

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1166-1171

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9037024

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mitochondrial DNA

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19762

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