Sentences with phrase «mitochondrial cytochrome»

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»).»
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.
The team looked at the DNA sequence of mitochondrial cytochrome b gene to gain more precise genetic information and gain insight into the history of the animals» migration routes.

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.
Jon Wetton and his co-workers at the Forensic Science Service believe that amplifying fragments of the cytochrome b gene of the tiger's mitochondrial DNA may fill the bill.
Indeed, the researchers determined that Inz - 1 targets the cytochrome B protein required for mitochondrial production of ATP.
Twelve percent encoded mitochondrial proteins such as succinate dehydrogenase complex, subunit B, iron sulfur (Ip)(τ statistic = — 0.76, P = 2.2 × 10 — 7), and ubiquinol — cytochrome c reductase subunit (τ statistic = — 0.65, P = 7.4 × 10 — 6)(Figure 1), and 6 % encoded lysosomal proteins (Supplemental Table 2, http://www.jci.org/cgi/content/full/112/12/1796/DC1).
Zuzana Kronekova (Roedel, TUD)-- «Assembly of mitochondrial ubiquinol - cytochrome c oxireductase complex in yeast Saccharomyces cerevisiae: The role of Cbp3p and Cbp4p assembly factors» (2005)
Chemical genetics unveils a key role of mitochondrial dynamics, cytochrome c release and IP3R activity in muscular dystrophy.
Kostmann syndrome: severe congenital neutropenia associated with defective expression of Bcl - 2, constitutive mitochondrial release of cytochrome c, and excessive apoptosis of myeloid progenitor cells.
All of this damage damages extremely precious mitochondrial DNA, which make the mitochondrias dysfunctional, clogging lysosome for mitophagy, and being incapable of keeping mitochondrial membrane potential (leading to Cytochrome C loss through mitochondrial permeability pores) and mitochondrial ATP OXPHOS respiration.
A famous example from the superfamily is cytochrome c oxidase, the last enzyme in the respiratory electron transport chain located in the mitochondrial membrane (see graph).
This protein is one of the nuclear - coded polypeptide chains of cytochrome c oxidase, the terminal oxidase in mitochondrial electron transport.
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).
Phylogenetics and Molecular Divergence of Tilapia Fish (Oreochromis Species) Using Mitochondrial D - Loop and Cytochrome b Regions
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