Results 11 to 20 of about 328,957 (317)

The Oxytricha trifallax mitochondrial genome [PDF]

open access: yesGenome Biology and Evolution, 2011
The Oxytricha trifallax mitochondrial genome contains the largest sequenced ciliate mitochondrial chromosome (;70 kb) plus a ;5-kb linear plasmid bearing mitochondrial telomeres.
Shum, J.   +21 more
core   +7 more sources

Complete Mitochondrial Genome and Phylogenetic Position of Chirolophis wui (Perciformes: Stichaeidae) [PDF]

open access: yes, 2023
The complete mitochondrial genome of Chirolophis wui (Wang and Wang, 1935) was sequenced using the Illumina platform. The genome sequence is 16,522 bp in length with 54% A+T content and contains 13 protein coding genes (PCGs), 22 transfer RNA genes ...
Yong-Suk Lee   +15 more
core   +1 more source

Modifying the Mitochondrial Genome [PDF]

open access: yesCell Metabolism, 2016
Human mitochondria produce ATP and metabolites to support development and maintain cellular homeostasis. Mitochondria harbor multiple copies of a maternally inherited, non-nuclear genome (mtDNA) that encodes for 13 subunit proteins of the respiratory chain.
Patananan, Alexander N   +3 more
openaire   +4 more sources

The ageing mitochondrial genome [PDF]

open access: yesNucleic Acids Research, 2007
The population of elderly individuals has increased significantly over the past century and is predicted to rise even more rapidly in the future. Ageing is a major risk factor for many diseases such as neurodegenerative disease, diabetes and cancer. This highlights the importance of understanding the mechanisms involved in the ageing process.
Krishnan, Kim J.   +3 more
openaire   +2 more sources

Lophotrochozoan mitochondrial genomes [PDF]

open access: yesIntegrative and Comparative Biology, 2006
Progress in both molecular techniques and phylogenetic methods has challenged many of the interpretations of traditional taxonomy. One example is in the recognition of the animal superphylum Lophotrochozoa (annelids, mollusks, echiurans, platyhelminthes, brachiopods, and other phyla), although the relationships within this group and the inclusion of ...
Valles, Yvonne, Boore, Jeffrey L.
openaire   +3 more sources

A Complete Mitochondrial Genome Sequence from a Mesolithic Wild Aurochs (Bos primigenius) [PDF]

open access: yes, 2010
Background The derivation of domestic cattle from the extinct wild aurochs (Bos primigenius) has been well-documented by archaeological and genetic studies.
Finlay Emma K.   +53 more
core   +1 more source

Mitochondrial helicases and mitochondrial genome maintenance [PDF]

open access: yesMechanisms of Ageing and Development, 2010
Helicases are essential enzymes that utilize the energy of nucleotide hydrolysis to drive unwinding of nucleic acid duplexes. Helicases play roles in all aspects of DNA metabolism including DNA repair, DNA replication and transcription. The subcellular locations and functions of several helicases have been studied in detail; however, the roles of ...
de Souza-Pinto, Nadja C   +4 more
openaire   +3 more sources

Mitochondrially-targeted APOBEC1 is a potent mtDNA mutator affecting mitochondrial function and organismal fitness in Drosophila

open access: yesNature Communications, 2019
The role of mitochondrial DNA mutations in organismal fitness and lifespan have been studied in mitochondrial mutator models with varying results. Here, the authors generate a new APOBEC1 expression-based Drosophila mutator model and show that it has ...
Simonetta Andreazza   +15 more
doaj   +1 more source

The mitochondrial genomes of sponges provide evidence for multiple invasions by Repetitive Hairpin-forming Elements (RHE) [PDF]

open access: yes, 2009
Background: The mitochondrial (mt) genomes of sponges possess a variety of features, which appear to be intermediate between those of Eumetazoa and non-metazoan opisthokonts.
Lavrov Dennis V   +11 more
core   +1 more source

Editing the Mitochondrial Genome

open access: yesNew England Journal of Medicine, 2020
Mending Mitochondrial Mutation For most patients with mitochondrial disorders, most of which are caused by mutations in genes in the mitochondrial genome, only symptomatic treatment is available.
Maria Falkenberg, Michio Hirano
openaire   +3 more sources

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