Sentences with phrase «of cytochrome oxidase»

(1988) containing the papers presented at a meeting organized by the two of us and held in Rome and in the Convent of Santa Teresa (Caprarola) where the structure - function relationships and the physiopathology of cytochrome oxidase were discussed in depth.
Two haplotypes (genetic variants) of the Cytochrome Oxidase Type I sequence were detected: the «World haplotype» found in France, New Caledonia, French Polynesia, Singapore, Puerto Rico and Florida; and the «Australian haplotype» found in Australia.

Not exact matches

The terminal cytochrome oxidase is the main membrane enzyme responsible for the human mitochondrial respiration and was thought to be used for the breath of E. coli as well.
Each cell in our body «breathes» due to the work of only the cytochrome - c oxidase, others we have not.
However, the E. coli bacteria has two types of oxidase: bo - type cytochrome oxidase (analogue of «human» cytochrome - c oxidase) and completely different bd - type cytochromes.
Among the other genes she says play a role in thoroughbred performance are peroxisome proliferator - activated receptor - γ coactivator - 1 alpha (PGC - 1α), which is involved in skeletal muscle adaptation to exercise; pyruvate dehydrogenase kinase, isozyme 4 (PDK4), involved in glucose regulation, expression of which increased almost fourfold after sprints; and cytochrome c oxidase subunit 4 isoform 2 (COX 4I2), involved in respiration.
Adaptive evolution of cytochrome c oxidase: infrastructure for a carnivorous plant radiation.
Adaptive evolution of cytochrome c oxidase: infrastructure for a carnivorous plant radiation Jobson, R. W., R. Nielsen, L. Laakkonen, M. Wikström et al. 2004.
Chronic treatment with azide in situ leads to an irreversible loss of cytochrome c oxidase activity via holoenzyme dissociation.
Knockdown of human COX17 affects assembly and supramolecular organization of cytochrome c oxidase.
In recent years, Michel and his research group mainly studied two types of oxygen reductases: the so - called superfamily of «heme - copper oxidases», and the «cytochrome bd oxidase».
Cytochrome c oxidase is part of Complex IV.
This protein is one of the nuclear - coded polypeptide chains of cytochrome c oxidase, the terminal oxidase in mitochondrial electron transport.
Molecular evolution of the cytochrome c oxidase subunit 5A gene in primates.
DNA barcoding aims to provide an efficient method for species - level identifications using an array of species specific molecular tags derived from the 5 ′ region of the mitochondrial cytochrome c oxidase I (COI) gene.
Certain particle compounds may directly generate ROS in vivo because of their surface chemistry (eg, metals, organic compounds, and semiquinones) or after bioactivation by cytochrome P450 systems (eg, polycyclic aromatic hydrocarbon conversion to quinones).6, 290 a, 290 b A particle surface or anions present on otherwise more inert particles may disrupt iron homeostasis in the lung and thereby also generate ROS via Fenton reactions.291 Other PM constituents may do so indirectly by the upregulation of endogenous cellular sources (eg, nicotinamide adenine dinucleotide phosphate [NADPH]-RRB- oxidase) 292,293 or by perturbing organelle function (eg, mitochondria) by taken - up PM components.261 Particle stimulation of irritant and afferent ANS fibers may also play a role in local and systemic oxidative stress formation.294 Given the rich antioxidant defenses in the lung fluid, secondarily generated oxidization products of endogenous molecules (eg, oxidized phospholipids, proteins) or a reduction in endogenous antioxidants per se may be responsible at least in part for the state of oxidative stress in the lungs (along with instigating the subsequent cellular responses) rather than ROS derived directly from PM and its constituents.
Hybrid broadband NIRS / Diffuse correlation spectroscopy system for simultaneous monitoring of cerebral perfusion and cytochrome c oxidase
It's a function of the protein in the intermitochondrial membrane called uh — Cytochrome C Oxidase which I think most people know.
It is a cofactor in several oxidative enzymes vital to the function of hematopoietic, vascular and skeletal tissues, as well as the structure and function of the nervous system, including superoxide dismutase (oxygen radical scavenger), cytochrome - c oxidase (mitochondrial respiration), lysyl oxidase (collagen and elastin synthesis) and ceruloplasmin ferroxidase / haephestin (iron metabolism).
It helps to stimulate cytochrome c oxidase enzyme and increase ATP (adenosine triphosphate) in your tissue, which is your primary source of high energy production.
«By stimulating the cytochrome oxidase enzyme, we are utilizing that oxygen in the respiratory chain inside of the mitochondria, producing more ATP for that cell.
The copper - dependent enzyme cytochrome oxidase, when low in the brains of animal models, is the suspected cause of suppressed myelin formation.
Fatty Acid Oxidase, cytochrome oxidase, peroxidase, Catalase and Transhydrogenase are enzymes found in barley grass juice that help the decomposition of fats in the body proceed smoothly which also helps to promote correct body weight; without these enzymes, weight gain rOxidase, cytochrome oxidase, peroxidase, Catalase and Transhydrogenase are enzymes found in barley grass juice that help the decomposition of fats in the body proceed smoothly which also helps to promote correct body weight; without these enzymes, weight gain roxidase, peroxidase, Catalase and Transhydrogenase are enzymes found in barley grass juice that help the decomposition of fats in the body proceed smoothly which also helps to promote correct body weight; without these enzymes, weight gain results.
When cytochrome c - oxidase and NADH are activated by laser light they increase the synthesis of ATP, accelerating cellular function.
Below is a sequence of the barcode region Cytochrome oxidase subunit 1 (COI or COX1) from a member of the species.
Below is the sequence of the barcode region Cytochrome oxidase subunit 1 (COI or COX1) from a member of the species.
The heart of the innovation, as I understand it, lies in the choice of a particular and small region of DNA shared by many animals; to say it in technical terms: it's «a 648 base - pair region in the mitochondrial cytochrome c oxidase 1 gene («CO1»).»
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