2014
DOI: 10.2174/15665240113136660081
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Animal Mitochondria: Evolution, Function, and Disease

Abstract: Mitochondria are sub-cellular organelles responsible for producing the majority of cellular energy through the process of oxidative phosphorylation (OXPHOS), and are found in nearly all eukaryotic cells. Mitochondria have a unique genetic system, mitochondrial DNA (mtDNA), which is a small, self-replicating and diverse genome. In the past 30 years, mtDNA has made significant contribution to molecular ecology and phylogeography. Mitochondria also represent a unique system of mitochondrial-nuclear genomic cooper… Show more

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Cited by 32 publications
(20 citation statements)
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“…Mt genomes have been extensively used as genetic markers in molecular phylogenetic studies due to it having several useful properties (i.e., haploidy, compactness, maternal inheritance, relatively high mutation rates, and the lack of recombination) [3]. To date, there are over 4000 complete mt genome sequences of metazoans available in GenBank, including some from parasites [4-10].…”
Section: Introductionmentioning
confidence: 99%
“…Mt genomes have been extensively used as genetic markers in molecular phylogenetic studies due to it having several useful properties (i.e., haploidy, compactness, maternal inheritance, relatively high mutation rates, and the lack of recombination) [3]. To date, there are over 4000 complete mt genome sequences of metazoans available in GenBank, including some from parasites [4-10].…”
Section: Introductionmentioning
confidence: 99%
“…Some properties of mitogenome, i.e. maternal inheritance, relatively high mutation rates, and the lack of recombination contribute to the broad consensus that mitogenome is widely regarded as genetic markers in molecular phylogenetic studies (Dermauw et al 2009;Gu et al 2014;Tao et al 2014).…”
mentioning
confidence: 99%
“…Los datos obtenidos muestran que a concentraciones mayores a 50μg/ml este metabolito puede afectar los complejos I, III y la ATPasa; y se ha establecido que deficiencias en el funcionamiento de estos complejos enzimáticos está asociados con varios síndromes clínicos como acidosis láctica, cardiomiopatía y cataratas (51)(52)(53). Igualmente, el aumento en las especies reactivas de oxígeno en la mitocondria, producto de deficiencias en el complejo I y III se han relacionado con el desarrollo y empeoramiento de enfermedades neurodegenerativas como Parkinson, enfermedad de Alzheimer, esclerosis lateral amiotrópica y enfermedad de Huntington (39,(54)(55)(56).…”
Section: Discussionunclassified