Results 21 to 30 of about 129,488 (310)

Amyloid-β peptide binds to cytochrome C oxidase subunit 1.

open access: yesPLoS ONE, 2012
Extracellular and intraneuronal accumulation of amyloid-beta aggregates has been demonstrated to be involved in the pathogenesis of Alzheimer's disease (AD).
Luis Fernando Hernandez-Zimbron   +7 more
doaj   +1 more source

New insight into the mechanism of mitochondrial cytochrome c function. [PDF]

open access: yesPLoS ONE, 2017
We investigate functional role of the P76GTKMIFA83 fragment of the primary structure of cytochrome c. Based on the data obtained by the analysis of informational structure (ANIS), we propose a model of functioning of cytochrome c. According to this model,
Rita V Chertkova   +9 more
doaj   +1 more source

Data on cytochrome c oxidase assembly in mice and human fibroblasts or tissues induced by SURF1 defect

open access: yesData in Brief, 2016
This paper describes data related to a research article entitled “Tissue- and species-specific differences in cytochrome c oxidase assembly induced by SURF1 defects” [1].
Nikola Kovářová   +7 more
doaj   +1 more source

Serial femtosecond crystallography structure of cytochrome c oxidase at room temperature

open access: yesScientific Reports, 2017
Cytochrome c oxidase catalyses the reduction of molecular oxygen to water while the energy released in this process is used to pump protons across a biological membrane.
Rebecka Andersson   +15 more
doaj   +1 more source

Alterations of sirtuins in mitochondrial cytochrome c-oxidase deficiency. [PDF]

open access: yesPLoS ONE, 2017
Sirtuins are NAD+ dependent deacetylases, which regulate mitochondrial energy metabolism as well as cellular response to stress. The NAD/NADH-system plays a crucial role in oxidative phosphorylation linking sirtuins and the mitochondrial respiratory ...
Arne Björn Potthast   +3 more
doaj   +1 more source

Mitochondrial cytochrome c oxidase deficiency [PDF]

open access: yesClinical Science, 2016
As with other mitochondrial respiratory chain components, marked clinical and genetic heterogeneity is observed in patients with a cytochrome c oxidase deficiency. This constitutes a considerable diagnostic challenge and raises a number of puzzling questions. So far, pathological mutations have been reported in more than 30 genes, in both mitochondrial
Malgorzata, Rak   +7 more
openaire   +2 more sources

Loss of the RNA-binding protein TACO1 causes late-onset mitochondrial dysfunction in mice

open access: yesNature Communications, 2016
Mutations in the translational activator of cytochrome c oxidase subunit I (TACO1) causes cytochrome c oxidase deficiency and Leigh Syndrome in patients.
Tara R. Richman   +11 more
doaj   +1 more source

Mitochondrial CO1 genetic structure among breeding sites of Chinese egret (Egretta eulophotes) in South Korea

open access: yesJournal of Asia-Pacific Biodiversity, 2018
Chinese egret (Egretta eulophotes) is classified as an endangered species (VU, vulnerable) and is limited to Far East. This species breeds especially offshore in China, Russia, and the Korean peninsula.
Bo-Yeon Hwang   +4 more
doaj   +1 more source

Cytochrome c Oxidase Inhibition by ATP Decreases Mitochondrial ROS Production

open access: yesCells, 2022
This study addresses the eventual consequence of cytochrome c oxidase (CytOx) inhibition by ATP at high ATP/ADP ratio in isolated rat heart mitochondria. Earlier, it has been demonstrated that the mechanism of allosteric ATP inhibition of CytOx is one of
Rabia Ramzan   +6 more
doaj   +1 more source

Origin of Jordanian honeybees Apis mellifera (Hymenoptera: Apidae) using amplified mitochondrial DNA

open access: yesEuropean Journal of Entomology, 2008
The honeybee (Apis mellifera L.) has a large number of geographic subspecies distributed across Europe, Africa and Asia, many of which have been described. This identification is important for bee breeding and preserving honeybee biodiversity.
Shahera ZAITOUN   +2 more
doaj   +1 more source

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