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Animal Mitochondrial DNA as We Do Not Know It: mt-Genome Organization and Evolution in Nonbilaterian Lineages
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1006/jmbi.1998.2523openalex-snapshot
Mitochondrial genes are found on minicircle DNA molecules in the mesozoan animal Dicyema
inferredcites →https://doi.org/10.1006/mpev.2001.1036openalex-snapshot
A Molecular Phylogenetic Framework for the Phylum Ctenophora Using 18S rRNA Genes
inferredcites →https://doi.org/10.1007/7171_2007_095openalex-snapshot
Linear Protein-Primed Replicating Plasmids in Eukaryotic Microbes
inferredcites →https://doi.org/10.1007/978-1-4614-1531-2_178openalex-snapshot
Mitochondrial Genomes in Unicellular Relatives of Animals
inferredcites →https://doi.org/10.1007/978-1-4614-6436-5_178-2openalex-snapshot
Mitochondrial Genomes in Unicellular Relatives of Animals
inferredcites →https://doi.org/10.1007/978-3-319-14753-6openalex-snapshot
Myxozoan Evolution, Ecology and Development
inferredcites →https://doi.org/10.1007/978-3-319-14753-6_5openalex-snapshot
Classification and Phylogenetics of Myxozoa
inferredcites →https://doi.org/10.1007/978-3-642-22380-8_13openalex-snapshot
Introns, Mobile Elements, and Plasmids
inferredcites →https://doi.org/10.1007/978-94-007-4688-6_2openalex-snapshot
No longer Demospongiae: Homoscleromorpha formal nomination as a fourth class of Porifera
inferredcites →https://doi.org/10.1007/978-94-011-5210-5_3openalex-snapshot
Deleterious mutation accumulation in organelle genomes
inferredcites →https://doi.org/10.1007/bf00389086openalex-snapshot
Laboratory culture of the lobate ctenophore Mnemiopsis mccradyi with notes on feeding and fecundity
inferredcites →https://doi.org/10.1007/bf02099755openalex-snapshot
The mitochondrial DNA molecule ofDrosophila yakuba: Nucleotide sequence, gene organization, and genetic code
inferredcites →https://doi.org/10.1007/s00239-004-0178-5openalex-snapshot
Single Nucleotide +1 Frameshifts in an Apparently FunctionalMitochondrial Cytochrome b Gene in Ants of the Genus Polyrhachis
inferredcites →https://doi.org/10.1007/s00239-006-0279-4openalex-snapshot
Novel Group I Introns Encoding a Putative Homing Endonuclease in the Mitochondrial cox1 Gene of Scleractinian Corals
inferredcites →https://doi.org/10.1007/s00239-007-9007-yopenalex-snapshot
Sequence and Characterization of Six Mitochondrial Subgenomes from Globodera rostochiensis: Multipartite Structure Is Conserved Among Close Nematode Relatives
inferredcites →https://doi.org/10.1007/s00239-007-9037-5openalex-snapshot
Structure and Evolution of the Atypical Mitochondrial Genome of Armadillidium vulgare (Isopoda, Crustacea)
inferredcites →https://doi.org/10.1007/s00239-007-9064-2openalex-snapshot
Poly(T) Variation Within Mitochondrial Protein-Coding Genes in Globodera (Nematoda: Heteroderidae)
inferredcites →https://doi.org/10.1007/s00239-009-9208-7openalex-snapshot
Evolution of the Mitochondrial Genome in Mammals Living at High Altitude: New Insights from a Study of the Tribe Caprini (Bovidae, Antilopinae)
inferredcites →https://doi.org/10.1007/s00239-010-9414-3openalex-snapshot
Poly(T) Variation in Heteroderid Nematode Mitochondrial Genomes is Predominantly an Artefact of Amplification
inferredcites →https://doi.org/10.1007/s00239-014-9653-9openalex-snapshot
A Mitochondrial Intron in a Verongid Sponge
inferredcites →https://doi.org/10.1007/s10126-005-0004-0openalex-snapshot
Complete Mitochondrial DNA Sequence of the Eastern Oyster Crassostrea virginica
inferredcites →https://doi.org/10.1007/s10750-011-0727-zopenalex-snapshot
Molecular phylogeny of glass sponges (Porifera, Hexactinellida): increased taxon sampling and inclusion of the mitochondrial protein-coding gene, cytochrome oxidase subunit I
inferredcites →https://doi.org/10.1007/s10750-011-0842-xopenalex-snapshot
No longer Demospongiae: Homoscleromorpha formal nomination as a fourth class of Porifera
inferredcites →https://doi.org/10.1007/s11692-012-9195-2openalex-snapshot
Biparental Inheritance Through Uniparental Transmission: The Doubly Uniparental Inheritance (DUI) of Mitochondrial DNA
inferredcites →https://doi.org/10.1016/0014-5793(84)81411-8openalex-snapshot
The Neutral Theory of Molecular Evolution
inferredcites →https://doi.org/10.1016/0092-8674(82)90049-6openalex-snapshot
Replication of animal mitochondrial DNA
inferredcites →https://doi.org/10.1016/0166-6851(92)90046-mopenalex-snapshot
The 6-kb element of Plasmodium falciparum encodes mitochondrial cytochrome genes
inferredcites →https://doi.org/10.1016/b978-0-12-282505-7.x5001-5openalex-snapshot
Reproduction of Marine Invertebrates
inferredcites →https://doi.org/10.1016/b978-0-12-387787-1.00007-6openalex-snapshot
Deep Phylogeny and Evolution of Sponges (Phylum Porifera)
inferredcites →https://doi.org/10.1016/b978-0-444-82235-2.50029-1openalex-snapshot
Mitochondrial Genomes of Anthozoa (Cnidaria)
inferredcites →https://doi.org/10.1016/j.biochi.2013.09.016openalex-snapshot
The plant mitochondrial genome: Dynamics and maintenance
inferredcites →https://doi.org/10.1016/j.cbd.2009.11.002openalex-snapshot
Complete mitochondrial genome sequences of the three pelagic chaetognaths Sagitta nagae, Sagitta decipiens and Sagitta enflata
inferredcites →https://doi.org/10.1016/j.cbd.2012.12.003openalex-snapshot
Complete mitochondrial DNA sequence of the ark shell Scapharca broughtonii: An ultra-large metazoan mitochondrial genome
inferredcites →https://doi.org/10.1016/j.cell.2015.07.016openalex-snapshot
An Essential Role of the Mitochondrial Electron Transport Chain in Cell Proliferation Is to Enable Aspartate Synthesis
inferredcites →https://doi.org/10.1016/j.compbiolchem.2016.04.007openalex-snapshot
Cryptic tRNAs in chaetognath mitochondrial genomes
inferredcites →https://doi.org/10.1016/j.cub.2006.06.054openalex-snapshot
Mitochondria: More Than Just a Powerhouse
inferredcites →https://doi.org/10.1016/j.cub.2015.09.066openalex-snapshot
Uncertainty in the Timing of Origin of Animals and the Limits of Precision in Molecular Timescales
inferredcites →https://doi.org/10.1016/j.cub.2015.11.043openalex-snapshot
Extensive Mitochondrial mRNA Editing and Unusual Mitochondrial Genome Organization in Calcaronean Sponges
inferredcites →https://doi.org/10.1016/j.cub.2016.03.053openalex-snapshot
A Eukaryote without a Mitochondrial Organelle
inferredcites →https://doi.org/10.1016/j.gde.2015.08.006openalex-snapshot
The evolution of animal genomes
inferredcites →https://doi.org/10.1016/j.gene.2006.06.021openalex-snapshot
Mitochondrial genome of the moon jelly Aurelia aurita (Cnidaria, Scyphozoa): A linear DNA molecule encoding a putative DNA-dependent DNA polymerase
inferredcites →https://doi.org/10.1016/j.gene.2007.12.002openalex-snapshot
The mitochondrial genome of Hydra oligactis (Cnidaria, Hydrozoa) sheds new light on animal mtDNA evolution and cnidarian phylogeny
inferredcites →https://doi.org/10.1016/j.gene.2010.12.009openalex-snapshot
Gene recruitment – A common mechanism in the evolution of transfer RNA gene families
inferredcites →https://doi.org/10.1016/j.gene.2013.10.041openalex-snapshot
Eight new mtDNA sequences of glass sponges reveal an extensive usage of + 1 frameshifting in mitochondrial translation
inferredcites →https://doi.org/10.1016/j.mito.2006.07.004openalex-snapshot
Comparison of chaetognath mitochondrial genomes and phylogenetical implications
inferredcites →https://doi.org/10.1016/j.tig.2004.09.002openalex-snapshot
Accelerated evolution of the electron transport chain in anthropoid primates
inferredcites →https://doi.org/10.1016/j.tig.2005.01.004openalex-snapshot
Transfer RNA gene recruitment in mitochondrial DNA
inferredcites →https://doi.org/10.1016/j.tig.2007.01.006openalex-snapshot
Mitochondrial introns: a critical view
inferredcites →https://doi.org/10.1016/j.tig.2007.03.008openalex-snapshot
Positive and negative selection on the mitochondrial genome
inferredcites →https://doi.org/10.1016/j.tig.2009.07.003openalex-snapshot
Group I-intron trans-splicing and mRNA editing in the mitochondria of placozoan animals
inferredcites →https://doi.org/10.1016/j.tig.2010.05.003openalex-snapshot
Evolution of the mutation rate
inferredcites →https://doi.org/10.1016/j.tig.2014.09.002openalex-snapshot
A resourceful genome: updating the functional repertoire and evolutionary role of animal mitochondrial DNAs
inferredcites →https://doi.org/10.1016/j.ympev.2005.07.015openalex-snapshot
The phylogeny of Mediterranean tortoises and their close relatives based on complete mitochondrial genome sequences from museum specimens
inferredcites →https://doi.org/10.1016/j.ympev.2006.08.016openalex-snapshot
The complete mitochondrial genome of the black coral Chrysopathes formosa (Cnidaria:Anthozoa:Antipatharia) supports classification of antipatharians within the subclass Hexacorallia
inferredcites →https://doi.org/10.1016/j.ympev.2011.12.009openalex-snapshot
Rapid evolution of the compact and unusual mitochondrial genome in the ctenophore, Pleurobrachia bachei
inferredcites →https://doi.org/10.1016/j.ympev.2013.05.002openalex-snapshot
A comprehensive analysis of bilaterian mitochondrial genomes and phylogeny
inferredcites →https://doi.org/10.1016/j.ympev.2013.07.016openalex-snapshot
Mitogenomics at the base of Metazoa
inferredcites →https://doi.org/10.1016/j.ympev.2014.02.016openalex-snapshot
Sea anemones possess dynamic mitogenome structures
inferredcites →https://doi.org/10.1016/j.ympev.2014.08.016openalex-snapshot
New phylogenomic and comparative analyses provide corroborating evidence that Myxozoa is Cnidaria
inferredcites →https://doi.org/10.1016/j.zool.2014.06.004openalex-snapshot
Exploring the potential of small RNA subunit and ITS sequences for resolving phylogenetic relationships within the phylum Ctenophora
inferredcites →https://doi.org/10.1016/s0014-5793(97)00357-8openalex-snapshot
RNA editing in metazoan mitochondria: staying fit without sex
inferredcites →https://doi.org/10.1016/s0074-7696(08)61635-6openalex-snapshot
Mitochondrial DNA: Physicochemical Properties, Replication, and Genetic Function
inferredcites →https://doi.org/10.1016/s0074-7696(08)62066-5openalex-snapshot
Animal Mitochondrial DNA: Structure and Evolution
inferredcites →https://doi.org/10.1016/s0140-6736(89)92145-4openalex-snapshot
MITOCHONDRIAL DNA MUTATIONS AS AN IMPORTANT CONTRIBUTOR TO AGEING AND DEGENERATIVE DISEASES
inferredcites →https://doi.org/10.1016/s0168-9525(99)01766-7openalex-snapshot
Why have organelles retained genomes?
inferredcites →https://doi.org/10.1016/s0378-1119(01)00807-1openalex-snapshot
Mitochondrial DNA in metazoa: degree of freedom in a frozen event
inferredcites →https://doi.org/10.1016/s0378-1119(97)00404-6openalex-snapshot
Mammalian mitochondrial D-loop region structural analysis: identification of new conserved sequences and their functional and evolutionary implications
inferredcites →https://doi.org/10.1016/s0959-437x(05)80116-9openalex-snapshot
Genetic novelties in mitochondrial genomes of multicellular animals
inferredcites →https://doi.org/10.1016/s1097-2765(03)00346-0openalex-snapshot
An RNA-Modifying Enzyme that Governs Both the Codon and Amino Acid Specificities of Isoleucine tRNA
inferredcites →https://doi.org/10.1017/s1355838202022021openalex-snapshot
tRNomics: Analysis of tRNA genes from 50 genomes of Eukarya, Archaea, and Bacteria reveals anticodon-sparing strategies and domain-specific features
inferredcites →https://doi.org/10.1017/s135583829999009xopenalex-snapshot
Insertional RNA editing in metazoan mitochondria: The cytochrome b gene in the nematode Teratocephalus lirellus
inferredcites →https://doi.org/10.1023/a:1017022522486openalex-snapshot
Deleterious mutation accumulation in organelle genomes
inferredcites →https://doi.org/10.1038/217624a0openalex-snapshot
Evolutionary Rate at the Molecular Level
inferredcites →https://doi.org/10.1038/246096a0openalex-snapshot
Slightly Deleterious Mutant Substitutions in Evolution
inferredcites →https://doi.org/10.1038/290457a0openalex-snapshot
Sequence and organization of the human mitochondrial genome
inferredcites →https://doi.org/10.1038/290470a0openalex-snapshot
tRNA punctuation model of RNA processing in human mitochondria
inferredcites →https://doi.org/10.1038/35047500openalex-snapshot
Rewiring the keyboard: evolvability of the genetic code
inferredcites →https://doi.org/10.1038/359412a0openalex-snapshot
Direct evidence for extensive paternal mitochondrial DNA inheritance in the marine mussel Mytilus
inferredcites →https://doi.org/10.1038/42696openalex-snapshot
Role of mutator alleles in adaptive evolution
inferredcites →https://doi.org/10.1038/nature01627openalex-snapshot
Humanin peptide suppresses apoptosis by interfering with Bax activation
inferredcites →https://doi.org/10.1038/nature12474openalex-snapshot
Germline mitochondrial DNA mutations aggravate ageing and can impair brain development
inferredcites →https://doi.org/10.1038/nature13400openalex-snapshot
The ctenophore genome and the evolutionary origins of neural systems
inferredcites →https://doi.org/10.1038/ng0497-363openalex-snapshot
A high observed substitution rate in the human mitochondrial DNA control region
inferredcites →https://doi.org/10.1038/nrg2158openalex-snapshot
Mutation rate variation in multicellular eukaryotes: causes and consequences
inferredcites →https://doi.org/10.1038/scientificamerican1179-98openalex-snapshot
The Neutral Theory of Molecular Evolution
inferredcites →https://doi.org/10.1038/srep06569openalex-snapshot
Maternally transmitted mitochondrial DNA mutations can reduce lifespan
inferredcites →https://doi.org/10.1038/srep07949openalex-snapshot
An integrated phylogenomic approach toward pinpointing the origin of mitochondria
inferredcites →https://doi.org/10.1042/bc20070037openalex-snapshot
Halting a cellular production line: responses to ribosomal pausing during translation
inferredcites →https://doi.org/10.1046/j.1365-294x.2003.02063.xopenalex-snapshot
The incomplete natural history of mitochondria
inferredcites →https://doi.org/10.1046/j.1365-2958.2000.02197.xopenalex-snapshot
Group II introns in the bacterial world
inferredcites →https://doi.org/10.1046/j.1420-9101.2002.00403.xopenalex-snapshot
Phylogeny of Medusozoa and the evolution of cnidarian life cycles
inferredcites →https://doi.org/10.1073/pnas.0336115100openalex-snapshot
Unique mitochondrial genome architecture in unicellular relatives of animals
inferredcites →https://doi.org/10.1073/pnas.0400941101openalex-snapshot
The mitochondrial genome of Paraspadella gotoi is highly reduced and reveals that chaetognaths are a sister group to protostomes
inferredcites →https://doi.org/10.1073/pnas.0407735101openalex-snapshot
The rate of DNA evolution: Effects of body size and temperature on the molecular clock
inferredcites →https://doi.org/10.1073/pnas.0602076103openalex-snapshot
Mitochondrial genome of Trichoplax adhaerens supports Placozoa as the basal lower metazoan phylum
inferredcites →https://doi.org/10.1073/pnas.0602444103openalex-snapshot
Naked corals: Skeleton loss in Scleractinia
inferredcites →https://doi.org/10.1073/pnas.0701256104openalex-snapshot
Accumulation of slightly deleterious mutations in mitochondrial protein-coding genes of large versus small mammals
inferredcites →https://doi.org/10.1073/pnas.0703359104openalex-snapshot
Metabolic rate does not calibrate the molecular clock
inferredcites →https://doi.org/10.1073/pnas.0912613107openalex-snapshot
Adaptive evolution of energy metabolism genes and the origin of flight in bats
inferredcites →https://doi.org/10.1073/pnas.1216223109openalex-snapshot
Drift-barrier hypothesis and mutation-rate evolution
inferredcites →https://doi.org/10.1073/pnas.1422049112openalex-snapshot
Mitochondrial and plastid genome architecture: Reoccurring themes, but significant differences at the extremes
inferredcites →https://doi.org/10.1073/pnas.1503453112openalex-snapshot
Error, signal, and the placement of Ctenophora sister to all other animals
inferredcites →https://doi.org/10.1073/pnas.1518127112openalex-snapshot
Genomic data do not support comb jellies as the sister group to all other animals
inferredcites →https://doi.org/10.1073/pnas.76.4.1967openalex-snapshot
Rapid evolution of animal mitochondrial DNA.
inferredcites →https://doi.org/10.1073/pnas.85.17.6465openalex-snapshot
Normal oxidative damage to mitochondrial and nuclear DNA is extensive.
inferredcites →https://doi.org/10.1073/pnas.89.18.8750openalex-snapshot
Class-level relationships in the phylum Cnidaria: evidence from mitochondrial genome structure.
inferredcites →https://doi.org/10.1073/pnas.90.9.4087openalex-snapshot
Body size, metabolic rate, generation time, and the molecular clock.
inferredcites →https://doi.org/10.1073/pnas.93.11.5619openalex-snapshot
Two mitochondrial group I introns in a metazoan, the sea anemone Metridium senile: one intron contains genes for subunits 1 and 3 of NADH dehydrogenase.
inferredcites →https://doi.org/10.1073/pnas.94.2.514openalex-snapshot
Mitochondrial DNA damage is more extensive and persists longer than nuclear DNA damage in human cells following oxidative stress
inferredcites →https://doi.org/10.1073/pnas.95.24.14226openalex-snapshot
Complete mitochondrial genome suggests diapsid affinities of turtles
inferredcites →https://doi.org/10.1073/pnas.96.24.13880openalex-snapshot
Recurrent invasion and extinction of a selfish gene
inferredcites →https://doi.org/10.1080/10635150701472164openalex-snapshot
Improvement of Phylogenies after Removing Divergent and Ambiguously Aligned Blocks from Protein Sequence Alignments
inferredcites →https://doi.org/10.1093/bfgp/elv027openalex-snapshot
The past, present and future of mitochondrial genomics: have we sequenced enough mtDNAs?
inferredcites →https://doi.org/10.1093/gbe/evr066openalex-snapshot
The Lower Bound to the Evolution of Mutation Rates
inferredcites →https://doi.org/10.1093/gbe/evr123openalex-snapshot
Evolution of Linear Mitochondrial Genomes in Medusozoan Cnidarians
inferredcites →https://doi.org/10.1093/gbe/evr127openalex-snapshot
First Complete Mitochondrial Genome Sequence from a Box Jellyfish Reveals a Highly Fragmented Linear Architecture and Insights into Telomere Evolution
inferredcites →https://doi.org/10.1093/gbe/evs074openalex-snapshot
The Mitochondrial Genome of Paraminabea aldersladei (Cnidaria: Anthozoa: Octocorallia) Supports Intramolecular Recombination as the Primary Mechanism of Gene Rearrangement in Octocoral Mitochondrial Genomes
inferredcites →https://doi.org/10.1093/gbe/evt008openalex-snapshot
Strikingly Bacteria-Like and Gene-Rich Mitochondrial Genomes throughout Jakobid Protists
inferredcites →https://doi.org/10.1093/gbe/evt081openalex-snapshot
Deep Sequencing of Mixed Total DNA without Barcodes Allows Efficient Assembly of Highly Plastic Ascidian Mitochondrial Genomes
inferredcites →https://doi.org/10.1093/gbe/evt094openalex-snapshot
Substantial Variation in the Extent of Mitochondrial Genome Fragmentation among Blood-Sucking Lice of Mammals
inferredcites →https://doi.org/10.1093/gbe/evu043openalex-snapshot
Chromera velia, Endosymbioses and the Rhodoplex Hypothesis—Plastid Evolution in Cryptophytes, Alveolates, Stramenopiles, and Haptophytes (CASH Lineages)
inferredcites →https://doi.org/10.1093/gbe/evu286openalex-snapshot
Octocoral Mitochondrial Genomes Provide Insights into the Phylogenetic History of Gene Order Rearrangements, Order Reversals, and Cnidarian Phylogenetics
inferredcites →https://doi.org/10.1093/gbe/evv124openalex-snapshot
Cytonuclear Interactions in the Evolution of Animal Mitochondrial tRNA Metabolism
inferredcites →https://doi.org/10.1093/gbe/evv224openalex-snapshot
The Utility of Genome Skimming for Phylogenomic Analyses as Demonstrated for Glycerid Relationships (Annelida, Glyceridae)
inferredcites →https://doi.org/10.1093/genetics/130.3.471openalex-snapshot
The mitochondrial genomes of two nematodes, Caenorhabditis elegans and Ascaris suum.
inferredcites →https://doi.org/10.1093/genetics/154.1.181openalex-snapshot
A Multipartite Mitochondrial Genome in the Potato Cyst Nematode Globodera pallida
inferredcites →https://doi.org/10.1093/genetics/156.1.385openalex-snapshot
Contrasting Patterns of Nonneutral Evolution in Proteins Encoded in Nuclear and Mitochondrial Genomes
inferredcites →https://doi.org/10.1093/genetics/157.2.621openalex-snapshot
Trichinella spiralismtDNA: A Nematode Mitochondrial Genome That Encodes a Putative ATP8 and Normally Structured tRNAs and Has a Gene Arrangement Relatable to Those of Coelomate Metazoans
inferredcites →https://doi.org/10.1093/icb/ict079openalex-snapshot
The Twin-Arginine Subunit C in Oscarella : Origin, Evolution, and Potential Functional Significance
inferredcites →https://doi.org/10.1093/jhered/est084openalex-snapshot
The Global Invertebrate Genomics Alliance (GIGA): Developing Community Resources to Study Diverse Invertebrate Genomes
inferredcites →https://doi.org/10.1093/molbev/msg018openalex-snapshot
Placozoa Are Not Derived Cnidarians: Evidence from Molecular Morphology
inferredcites →https://doi.org/10.1093/molbev/msg147openalex-snapshot
Estimating the Distribution of Selection Coefficients from Phylogenetic Data with Applications to Mitochondrial and Viral DNA
inferredcites →https://doi.org/10.1093/molbev/msh229openalex-snapshot
Identification of Chaetognaths as Protostomes Is Supported by the Analysis of Their Mitochondrial Genome
inferredcites →https://doi.org/10.1093/molbev/msi108openalex-snapshot
Mitochondrial Genomes of Two Demosponges Provide Insights into An Early Stage of Animal Evolution
inferredcites →https://doi.org/10.1093/molbev/msl154openalex-snapshot
Mitochondrial Diversity of Early-Branching Metazoa Is Revealed by the Complete mt Genome of a Haplosclerid Demosponge
inferredcites →https://doi.org/10.1093/molbev/msl167openalex-snapshot
Mitochondrial Genome of the Homoscleromorph Oscarella carmela (Porifera, Demospongiae) Reveals Unexpected Complexity in the Common Ancestor of Sponges and Other Animals
inferredcites →https://doi.org/10.1093/molbev/msm070openalex-snapshot
Glass Sponges and Bilaterian Animals Share Derived Mitochondrial Genomic Features: A Common Ancestry or Parallel Evolution?
inferredcites →https://doi.org/10.1093/molbev/msm248openalex-snapshot
Strong Variations of Mitochondrial Mutation Rate across Mammals--the Longevity Hypothesis
inferredcites →https://doi.org/10.1093/molbev/msn058openalex-snapshot
Two Circular Chromosomes of Unequal Copy Number Make Up the Mitochondrial Genome of the Rotifer Brachionus plicatilis
inferredcites →https://doi.org/10.1093/molbev/msp234openalex-snapshot
Hypervariability of Ascidian Mitochondrial Gene Order: Exposing the Myth of Deuterostome Organelle Genome Stability
inferredcites →https://doi.org/10.1093/molbev/msq112openalex-snapshot
Parallel Loss of Nuclear-Encoded Mitochondrial Aminoacyl-tRNA Synthetases and mtDNA-Encoded tRNAs in Cnidaria
inferredcites →https://doi.org/10.1093/molbev/msq244openalex-snapshot
A Phylogenetic Model for Investigating Correlated Evolution of Substitution Rates and Continuous Phenotypic Characters
inferredcites →https://doi.org/10.1093/molbev/msq345openalex-snapshot
Novel Protein Genes in Animal mtDNA: A New Sex Determination System in Freshwater Mussels (Bivalvia: Unionoida)?
inferredcites →https://doi.org/10.1093/molbev/msr113openalex-snapshot
Extensive and Evolutionarily Persistent Mitochondrial tRNA Editing in Velvet Worms (Phylum Onychophora)
inferredcites →https://doi.org/10.1093/molbev/msr243openalex-snapshot
High Mutation Rates in the Mitochondrial Genomes of Daphnia pulex
inferredcites →https://doi.org/10.1093/molbev/mss274openalex-snapshot
Mitochondrial DNA of Clathrina clathrus (Calcarea, Calcinea): Six Linear Chromosomes, Fragmented rRNAs, tRNA Editing, and a Novel Genetic Code
inferredcites →https://doi.org/10.1093/molbev/mst010openalex-snapshot
MAFFT Multiple Sequence Alignment Software Version 7: Improvements in Performance and Usability
inferredcites →https://doi.org/10.1093/molbev/msv021openalex-snapshot
Divergent Mitochondrial Respiratory Chains in Phototrophic Relatives of Apicomplexan Parasites
inferredcites →https://doi.org/10.1093/nar/14.11.4519openalex-snapshot
RNA mapping on Drosophila mitochondrial DNA: precursors and template strands
inferredcites →https://doi.org/10.1093/nar/gkt1152openalex-snapshot
Trans-splicing and RNA editing of LSU rRNA in Diplonema mitochondria
inferredcites →https://doi.org/10.1093/nar/gkv746openalex-snapshot
Towards a comprehensive picture of alloacceptor tRNA remolding in metazoan mitochondrial genomes
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a003854openalex-snapshot
Complete Sequence of the Mitochondrial Genome of the Tapeworm Hymenolepis diminuta: Gene Arrangements Indicate that Platyhelminths Are Eutrochozoans
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a025557openalex-snapshot
Mutation accumulation in transfer RNAs: molecular evidence for Muller's ratchet in mitochondrial genomes
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a025815openalex-snapshot
The mtDNA sequence of the ostrich and the divergence between paleognathous and neognathous birds
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a025884openalex-snapshot
An Extra Nucleotide is not Translated in Mitochondrial ND3 of Some Birds and Turtles
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a026393openalex-snapshot
Phylogenies Inferred from Mitochondrial Gene Orders—A Cautionary Tale from the Parasitic Flatworms
inferredcites →https://doi.org/10.1093/sysbio/syt022openalex-snapshot
PhyloBayes MPI: Phylogenetic Reconstruction with Infinite Mixtures of Profiles in a Parallel Environment
inferredcites →https://doi.org/10.1098/rstb.2013.0438openalex-snapshot
What cost mitochondria? The maintenance of functional mitochondrial DNA within and across generations
inferredcites →https://doi.org/10.1099/mic.0.038646-0openalex-snapshot
The mitochondrial genome of the pathogenic yeast Candida subhashii: GC-rich linear DNA with a protein covalently attached to the 5′ termini
inferredcites →https://doi.org/10.1101/gad.229724.113openalex-snapshot
Hallmarks of a new era in mitochondrial biochemistry
inferredcites →https://doi.org/10.1101/gr.161265.113openalex-snapshot
RNA–DNA differences in human mitochondria restore ancestral form of 16S ribosomal RNA
inferredcites →https://doi.org/10.1111/1462-2920.12881openalex-snapshot
A R ickettsiales symbiont of amoebae with ancient features
inferredcites →https://doi.org/10.1111/j.1550-7408.2001.tb00173.xopenalex-snapshot
Recent Advances in Our Knowledge of the Myxozoa
inferredcites →https://doi.org/10.1111/j.1755-0998.2010.02875.xopenalex-snapshot
Limitations of mitochondrial gene barcoding in Octocorallia
inferredcites →https://doi.org/10.1111/mec.13475openalex-snapshot
The rate of adaptive evolution in animal mitochondria
inferredcites →https://doi.org/10.1126/science.1056421openalex-snapshot
Costs and Benefits of High Mutation Rates: Adaptive Evolution of Bacteria in the Mouse Gut
inferredcites →https://doi.org/10.1126/science.1118884openalex-snapshot
Mutation Pressure and the Evolution of Organelle Genomic Architecture
inferredcites →https://doi.org/10.1126/science.1122033openalex-snapshot
Population Size Does Not Influence Mitochondrial Genetic Diversity in Animals
inferredcites →https://doi.org/10.1126/science.1180674openalex-snapshot
Hungry Codons Promote Frameshifting in Human Mitochondrial Ribosomes
inferredcites →https://doi.org/10.1126/science.1194167openalex-snapshot
Plasticity of Animal Genome Architecture Unmasked by Rapid Evolution of a Pelagic Tunicate
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Mitochondrial Genetics: A Paradigm for Aging and Degenerative Diseases?
inferredcites →https://doi.org/10.1126/science.283.5407.1476openalex-snapshot
Mitochondrial Evolution
inferredcites →https://doi.org/10.1126/science.289.5488.2342openalex-snapshot
High Direct Estimate of the Mutation Rate in the Mitochondrial Genome of Caenorhabditis elegans
inferredcites →https://doi.org/10.1128/genomea.00823-15openalex-snapshot
Mitochondrial Genome Sequence of the Glass Sponge Oopsacas minuta
inferredcites →https://doi.org/10.1128/mmbr.05024-11openalex-snapshot
Biochemistry and Evolution of Anaerobic Energy Metabolism in Eukaryotes
inferredcites →https://doi.org/10.1128/mmbr.54.1.66-74.1990openalex-snapshot
Invertrons, a class of structurally and functionally related genetic elements that includes linear DNA plasmids, transposable elements, and genomes of adeno-type viruses
inferredcites →https://doi.org/10.1139/z06-005openalex-snapshot
Phylogeny and evolution of calcareous sponges
inferredcites →https://doi.org/10.1146/annurev-biochem-060109-092838openalex-snapshot
Mitochondrial tRNA Import and Its Consequences for Mitochondrial Translation
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Somatic Mitochondrial DNA Mutations in Mammalian Aging
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The Neutral Theory of Molecular Evolution in the Genomic Era
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Why Do We Still Have a Maternally Inherited Mitochondrial DNA? Insights from Evolutionary Medicine
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FUNCTIONS AND MECHANISMS OF RNA EDITING
inferredcites →https://doi.org/10.1146/annurev.genet.37.110801.142526openalex-snapshot
Mitochondria of Protists
inferredcites →https://doi.org/10.11646/zootaxa.1668.1.11openalex-snapshot
The phylum Cnidaria: A review of phylogenetic patterns and diversity 300 years after Linnaeus*
inferredcites →https://doi.org/10.11646/zootaxa.3148.1.3openalex-snapshot
Animal biodiversity: An introduction to higher-level classification and taxonomic richness
inferredcites →https://doi.org/10.1186/1471-2148-10-288openalex-snapshot
Diversity of sponge mitochondrial introns revealed by cox 1sequences of Tetillidae
inferredcites →https://doi.org/10.1186/1471-2148-10-50openalex-snapshot
Mitochondrial phylogenomics of the Bivalvia (Mollusca): searching for the origin and mitogenomic correlates of doubly uniparental inheritance of mtDNA
inferredcites →https://doi.org/10.1186/1471-2148-11-228openalex-snapshot
A unique horizontal gene transfer event has provided the octocoral mitochondrial genome with an active mismatch repair gene that has potential for an unusual self-contained function
inferredcites →https://doi.org/10.1186/1471-2148-13-12openalex-snapshot
Comparative analysis of complete mitochondrial genome sequences confirms independent origins of plant-parasitic nematodes
inferredcites →https://doi.org/10.1186/1471-2148-13-5openalex-snapshot
Cnidarian phylogenetic relationships as revealed by mitogenomics
inferredcites →https://doi.org/10.1186/1471-2148-6-71openalex-snapshot
Putative cross-kingdom horizontal gene transfer in sponge (Porifera) mitochondria
inferredcites →https://doi.org/10.1186/1471-2148-8-139openalex-snapshot
Phylogenetic placement of the enigmatic parasite, Polypodium hydriforme, within the Phylum Cnidaria
inferredcites →https://doi.org/10.1186/1471-2148-9-54openalex-snapshot
The erratic mitochondrial clock: variations of mutation rate, not population size, affect mtDNA diversity across birds and mammals
inferredcites →https://doi.org/10.1186/1471-2164-10-534openalex-snapshot
Tunicate mitogenomics and phylogenetics: peculiarities of the Herdmania momus mitochondrial genome and support for the new chordate phylogeny
showing the first 200 of 240 · page through all 240
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Complete mitogenome and the phylogenetic status of Troglopedetes meridionalis Jantarit, Surakhamhaeng & Deharveng, 2020 (Collembola, Entomobryidae)
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Novel haplotypes of the COI-COII mtDNA region in the dark forest bee, Apis mellifera mellifera L., 1758
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Insights into phylogenetic relationships and gene rearrangements: complete mitogenomes of two sympatric species in the genus Rana (Anura, Ranidae)
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Evolutionary Biology and Mitochondrial Genomics: 50 000 Mitochondrial DNA Genomes and Counting
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When One Genome Is Not Enough: Organellar Heteroplasmy in Plants
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The enigmatic Placozoa part 2: Exploring evolutionary controversies and promising questions on earth and in space
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Ancient endosymbiont‐mediated transmission of a selfish gene provides a model for overcoming barriers to gene transfer into animal mitochondrial genomes
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Mitogenome evolution in ladybirds: Potential association with dietary adaptation
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Complete Mitochondrial Genome of Porites cylindrica From the Xisha Islands: Characterization and Comparative Mitogenomics of the Genus
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The phylogeny of the Anderson's White‐bellied Rat (Niviventer andersoni) based on complete mitochondrial genomes
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Does mitochondrial DNA evolution in metazoa drive the origin of new mitochondrial proteins?
inferred← citeshttps://doi.org/10.1002/iub.1961openalex-snapshot
Characterization of mitochondrial proteomes of nonbilaterian animals
inferred← citeshttps://doi.org/10.1007/978-1-0716-0834-0_10openalex-snapshot
High-Throughput Detection of mtDNA Mutations Leading to tRNA Processing Errors
inferred← citeshttps://doi.org/10.1007/978-1-0716-3642-8_1openalex-snapshot
Brief History of Ctenophora
inferred← citeshttps://doi.org/10.1007/978-1-0716-3642-8_10openalex-snapshot
Characterization of the Mitochondrial Proteome in the Ctenophore Mnemiopsis leidyi Using MitoPredictor
inferred← citeshttps://doi.org/10.1007/978-1-4939-9176-1_18openalex-snapshot
Assembly of Ancient Mitochondrial Genomes Without a Closely Related Reference Sequence
inferred← citeshttps://doi.org/10.1007/978-3-031-98584-3_10openalex-snapshot
Snapshots of Coral Reef Biodiversity
inferred← citeshttps://doi.org/10.1007/s00203-026-04784-yopenalex-snapshot
Host mitochondrial DNA in bacterial pathogenesis: Friend, Foe, or Both?
inferred← citeshttps://doi.org/10.1007/s00227-021-03887-yopenalex-snapshot
Toward a global reference database of COI barcodes for marine zooplankton
inferred← citeshttps://doi.org/10.1007/s10493-025-01066-yopenalex-snapshot
The first complete mitochondrial genome of Spinturnix psi (Dermanyssoidea, Spinturnicidae): gene content, composition, rearrangement and phylogenetic implications
inferred← citeshttps://doi.org/10.1007/s11033-024-09270-6openalex-snapshot
Comparative mitogenomics of Brachiopods reveals conservatism in articulate species and unusualness in inarticulate species
inferred← citeshttps://doi.org/10.1007/s12526-026-01642-4openalex-snapshot
Comparative mitogenomics and biodiversity studies of Nemertea
inferred← citeshttps://doi.org/10.1016/b978-0-12-820595-2.00009-6openalex-snapshot
Molecular markers and its application in animal breeding
inferred← citeshttps://doi.org/10.1016/b978-0-443-15750-9.00131-2openalex-snapshot
Coevolution Between the Mitochondrial and Nuclear Genomes
inferred← citeshttps://doi.org/10.1016/b978-0-443-27380-3.00044-0openalex-snapshot
Ctenophore neural systems: Independent origin(s) and “alien neurons”
inferred← citeshttps://doi.org/10.1016/j.biosystems.2017.10.004openalex-snapshot
On universal coding events in protein biogenesis
inferred← citeshttps://doi.org/10.1016/j.biosystems.2021.104426openalex-snapshot
Evolution of eukaryotes as a story of survival and growth of mitochondrial DNA over two billion years
inferred← citeshttps://doi.org/10.1016/j.cub.2019.01.068openalex-snapshot
Polyplacotoma mediterranea is a new ramified placozoan species
inferred← citeshttps://doi.org/10.1016/j.cub.2019.03.020openalex-snapshot
Selfish Mitonuclear Conflict
inferred← citeshttps://doi.org/10.1016/j.cub.2025.09.071openalex-snapshot
Natural and artificial variations of the standard genetic code
inferred← citeshttps://doi.org/10.1016/j.dnarep.2022.103273openalex-snapshot
Large dataset of octocoral mitochondrial genomes provides new insights into mt-mutS evolution and function
inferred← citeshttps://doi.org/10.1016/j.gene.2024.148999openalex-snapshot
One Ring does not rule them all: Linear mtDNA in Metazoa
inferred← citeshttps://doi.org/10.1016/j.genrep.2024.102111openalex-snapshot
Extensive mitochondrial genomic analyses reveal dynamic gene order rearrangements in the class Octocorallia (Cnidaria: Anthozoa)
inferred← citeshttps://doi.org/10.1016/j.genrep.2026.102663openalex-snapshot
Rethinking anthozoan mitogenomes: Extensive gene duplications in the tube anemone Ceriantheopsis lineata (Cnidaria: Anthozoa)
inferred← citeshttps://doi.org/10.1016/j.jembe.2024.152051openalex-snapshot
Mitochondrial DNA damage, repair and copy number dynamics of Sclerophytum sp. (Anthozoa: Octocorallia) in response to short-term abiotic oxidative stress
inferred← citeshttps://doi.org/10.1016/j.margen.2019.100703openalex-snapshot
Phylotranscriptomics confirms Alveopora is sister to Montipora within the family Acroporidae
inferred← citeshttps://doi.org/10.1016/j.mito.2020.02.007openalex-snapshot
Causes and consequences of mitochondrial proteome size variation in animals
inferred← citeshttps://doi.org/10.1016/j.mito.2020.03.007openalex-snapshot
Interchangeable parts: The evolutionarily dynamic tRNA population in plant mitochondria
inferred← citeshttps://doi.org/10.1016/j.mito.2020.06.002openalex-snapshot
Variation in protein gene and intron content among land plant mitogenomes
inferred← citeshttps://doi.org/10.1016/j.mito.2021.02.009openalex-snapshot
HERMES: An improved method to test mitochondrial genome molecular synapomorphies among clades
inferred← citeshttps://doi.org/10.1016/j.mrfmmm.2018.01.005openalex-snapshot
Replication stress in mitochondria
inferred← citeshttps://doi.org/10.1016/j.protis.2024.126048openalex-snapshot
Dinoflagellate chloroplasts as a model for extreme genome reduction and fragmentation in organelles – The COCOA principle for gene retention
inferred← citeshttps://doi.org/10.1016/j.pt.2021.01.010openalex-snapshot
Advances and Discoveries in Myxozoan Genomics
inferred← citeshttps://doi.org/10.1016/j.tig.2018.05.009openalex-snapshot
Mitochondrial DNA Transcription and Its Regulation: An Evolutionary Perspective
inferred← citeshttps://doi.org/10.1016/j.ympev.2019.106710openalex-snapshot
Hidden cases of tRNA gene duplication and remolding in mitochondrial genomes of amphipods
inferred← citeshttps://doi.org/10.1016/j.ympev.2022.107630openalex-snapshot
Evolution of mitochondrial and nuclear genomes in Pennatulacea
inferred← citeshttps://doi.org/10.1017/s0031182026102807openalex-snapshot
Characterization of the fragmented mitogenome of the European badger louse Trichodectes melis reveals conserved organization in non-coding regions
inferred← citeshttps://doi.org/10.1038/s41437-023-00650-5openalex-snapshot
Mitochondrially mediated RNA interference, a retrograde signaling system affecting nuclear gene expression
inferred← citeshttps://doi.org/10.1038/s41467-020-14725-yopenalex-snapshot
Relaxed sequence constraints favor mutational freedom in idiosyncratic metazoan mitochondrial tRNAs
inferred← citeshttps://doi.org/10.1038/s41467-023-42095-8openalex-snapshot
Mitogenomic evolutionary rates in bilateria are influenced by parasitic lifestyle and locomotory capacity
inferred← citeshttps://doi.org/10.1038/s41598-017-14286-zopenalex-snapshot
Keeping it complicated: Mitochondrial genome plasticity across diplonemids
inferred← citeshttps://doi.org/10.1038/s41598-018-25759-0openalex-snapshot
The bipartite mitochondrial genome of Ruizia karukerae (Rhigonematomorpha, Nematoda)
inferred← citeshttps://doi.org/10.1038/s41598-019-42621-zopenalex-snapshot
Linear Mitochondrial Genome in Anthozoa (Cnidaria): A Case Study in Ceriantharia
inferred← citeshttps://doi.org/10.1038/s41598-019-47145-0openalex-snapshot
Comparative mitogenomics of the Decapoda reveals evolutionary heterogeneity in architecture and composition
inferred← citeshttps://doi.org/10.1038/s41598-020-66287-0openalex-snapshot
Can Mitogenomes of the Northern Wheatear (Oenanthe oenanthe) Reconstruct Its Phylogeography and Reveal the Origin of Migrant Birds?
inferred← citeshttps://doi.org/10.1038/s41598-021-04077-yopenalex-snapshot
Recurrent erosion of COA1/MITRAC15 exemplifies conditional gene dispensability in oxidative phosphorylation
inferred← citeshttps://doi.org/10.1038/s41598-022-26970-wopenalex-snapshot
Low genetic diversity and predation threaten a rediscovered marine sponge
inferred← citeshttps://doi.org/10.1038/s41598-023-34059-1openalex-snapshot
Mito-nuclear discordance within Anthozoa, with notes on unique properties of their mitochondrial genomes
inferred← citeshttps://doi.org/10.1038/s41598-023-37425-1openalex-snapshot
Whole mitochondrial genomes reveal the relatedness of the browsing ant incursions in Australia
inferred← citeshttps://doi.org/10.1038/s41598-024-80695-6openalex-snapshot
A comprehensive study on the mitochondrial genome of Volva habei and exploring phylogenetic relationships in Littorinimorpha
inferred← citeshttps://doi.org/10.1038/s41598-026-57251-5openalex-snapshot
GARUDA: the first complete mitochondrial genome of the endangered Javan hawk-eagle (Nisaetus bartelsi) and its phylogenetic relationships within Accipitridae
inferred← citeshttps://doi.org/10.1038/s42003-023-04471-4openalex-snapshot
The metazoan landscape of mitochondrial DNA gene order and content is shaped by selection and affects mitochondrial transcription
inferred← citeshttps://doi.org/10.1042/bst20190238openalex-snapshot
Evolving mtDNA populations within cells
inferred← citeshttps://doi.org/10.1073/pnas.1909907117openalex-snapshot
A cnidarian parasite of salmon (Myxozoa: Henneguya ) lacks a mitochondrial genome
inferred← citeshttps://doi.org/10.1073/pnas.2317240121openalex-snapshot
Genome copy number predicts extreme evolutionary rate variation in plant mitochondrial DNA
inferred← citeshttps://doi.org/10.1079/9781789245547.0004openalex-snapshot
Molecular Biology of Stored-Product Psocids
inferred← citeshttps://doi.org/10.1080/14772000.2021.1915896openalex-snapshot
Hundreds of new DNA barcodes for South African sponges
inferred← citeshttps://doi.org/10.1080/15476286.2017.1279785openalex-snapshot
How tRNAs dictate nuclear codon reassignments: Only a few can capture non-cognate codons
inferred← citeshttps://doi.org/10.1080/24701394.2019.1634699openalex-snapshot
Novel diversity in mitochondrial genomes of deep-sea Pennatulacea (Cnidaria: Anthozoa: Octocorallia)
inferred← citeshttps://doi.org/10.1080/24701394.2026.2647326openalex-snapshot
The mitochondrial genome of Palythoa tuberculosa (Esper, 1805) contains a novel ORF with unknown function
inferred← citeshttps://doi.org/10.1093/femsle/fnz049openalex-snapshot
It's a small, small world: unravelling the role and evolution of small RNAs in organelle and endosymbiont genomes
inferred← citeshttps://doi.org/10.1093/gbe/evaa130openalex-snapshot
Revisiting Ceriantharian (Anthozoa) Mitochondrial Genomes: Casting Doubts about Their Structure and Size
inferred← citeshttps://doi.org/10.1093/gbe/evaa213openalex-snapshot
Mitochondrial Genome Evolution of Placozoans: Gene Rearrangements and Repeat Expansions
inferred← citeshttps://doi.org/10.1093/gbe/evab191openalex-snapshot
Multiple Losses of MSH1, Gain of mtMutS, and Other Changes in the MutS Family of DNA Repair Proteins in Animals
inferred← citeshttps://doi.org/10.1093/gbe/evac112openalex-snapshot
The Phylogenetic Position of the Enigmatic, Polypodium hydriforme (Cnidaria, Polypodiozoa): Insights from Mitochondrial Genomes
inferred← citeshttps://doi.org/10.1093/gbe/evac147openalex-snapshot
Long-read Sequencing Data Reveals Dynamic Evolution of Mitochondrial Genome Size and the Phylogenetic Utility of Mitochondrial DNA in Hercules Beetles (Dynastes; Scarabaeidae)
inferred← citeshttps://doi.org/10.1093/gbe/evad003openalex-snapshot
Myxozoans (Cnidaria) do not Retain Key Oxygen-Sensing and Homeostasis Toolkit Genes
inferred← citeshttps://doi.org/10.1093/gbe/evad219openalex-snapshot
ORFans in Mitochondrial Genomes of Marine Polychaete Polydora
inferred← citeshttps://doi.org/10.1093/gbe/evae048openalex-snapshot
Giants among Cnidaria: Large Nuclear Genomes and Rearranged Mitochondrial Genomes in Siphonophores
inferred← citeshttps://doi.org/10.1093/gbe/evae168openalex-snapshot
Mitochondrial DNA of the Demosponge Acanthella acuta: Linear Architecture and Other Unique Features
inferred← citeshttps://doi.org/10.1093/gbe/evae181openalex-snapshot
Evolutionary Insights from the Mitochondrial Genome of Oikopleura dioica : Sequencing Challenges, RNA Editing, Gene Transfers to the Nucleus, and tRNA Loss
inferred← citeshttps://doi.org/10.1093/gbe/evae220openalex-snapshot
The Highly Repetitive Genome of Myxobolus rasmusseni, an Emerging Myxozoan Parasite of Fathead Minnows
inferred← citeshttps://doi.org/10.1093/gbe/evaf020openalex-snapshot
Pervasive Mitochondrial tRNA Gene Loss in Clade B of Haplosclerid Sponges (Porifera, Demospongiae)
inferred← citeshttps://doi.org/10.1093/gbe/evaf209openalex-snapshot
Mitochondrial Gene Phylogenetic Incongruencies Are Linked to Chromosomal Position and Function
inferred← citeshttps://doi.org/10.1093/gbe/evag001openalex-snapshot
From Rigid Order to Radical Variation: Mitogenome Evolution in the Main Lineages of a Lesser-Known Animal Phylum (Gastrotricha)
inferred← citeshttps://doi.org/10.1093/gbe/evag019openalex-snapshot
Highlight: The “Wild West” of Mitochondrial Genome Evolution in the Gastrotricha
inferred← citeshttps://doi.org/10.1093/gbe/evag113openalex-snapshot
Genome of Facultatively Parthenogenetic Harvester (Opiliones) Indicates Frequent Mitonuclear Sequence Transfer and Novel Full-Length Insertions
inferred← citeshttps://doi.org/10.1093/gbe/evx010openalex-snapshot
Causes and Consequences of Rapidly Evolving mtDNA in a Plant Lineage
inferred← citeshttps://doi.org/10.1093/gbe/evx201openalex-snapshot
Comparative Genomics of Apomictic Root-Knot Nematodes: Hybridization, Ploidy, and Dynamic Genome Change
inferred← citeshttps://doi.org/10.1093/gbe/evx227openalex-snapshot
The First Mitochondrial Genomics and Evolution SMBE-Satellite Meeting: A New Scientific Symbiosis
inferred← citeshttps://doi.org/10.1093/genetics/iyab039openalex-snapshot
Detecting de novo mitochondrial mutations in angiosperms with highly divergent evolutionary rates
inferred← citeshttps://doi.org/10.1093/icb/icab057openalex-snapshot
Bivalve Molluscs as Model Systems for Studying Mitochondrial Biology
inferred← citeshttps://doi.org/10.1093/icb/icz124openalex-snapshot
Mitochondrial Ecophysiology: Assessing the Evolutionary Forces That Shape Mitochondrial Variation
inferred← citeshttps://doi.org/10.1093/jmammal/gyae144openalex-snapshot
Mitogenome comparative analysis of 3 Myotis species endemic to Mexico and detecting selection in OXPHOS genes
inferred← citeshttps://doi.org/10.1093/molbev/msab255openalex-snapshot
Rapid Shifts in Mitochondrial tRNA Import in a Plant Lineage with Extensive Mitochondrial tRNA Gene Loss
inferred← citeshttps://doi.org/10.1093/molbev/msad007openalex-snapshot
Single-molecule Sequencing of an Animal Mitochondrial Genome Reveals Chloroplast-like Architecture and Repeat-mediated Recombination
inferred← citeshttps://doi.org/10.1093/molbev/msx072openalex-snapshot
The Multipartite Mitochondrial Genome of Enteromyxum leei (Myxozoa): Eight Fast-Evolving Megacircles
inferred← citeshttps://doi.org/10.1093/molbev/msy176openalex-snapshot
High and Variable Rates of Repeat-Mediated Mitochondrial Genome Rearrangement in a Genus of Plants
inferred← citeshttps://doi.org/10.1093/nar/gkab901openalex-snapshot
A replication-linked mutational gradient drives somatic mutation accumulation and influences germline polymorphisms and genome composition in mitochondrial DNA
inferred← citeshttps://doi.org/10.1093/nar/gkag327openalex-snapshot
Frequent occurrence and predicted functions of tRNAs with 4-base-pair anticodon stems in bacteria: extended superwobble hypothesis
inferred← citeshttps://doi.org/10.1093/nargab/lqaa111openalex-snapshot
Hopeful monsters: unintended sequencing of famously malformed mite mitochondrial tRNAs reveals widespread expression and processing of sense–antisense pairs
inferred← citeshttps://doi.org/10.1098/rsbl.2022.0122openalex-snapshot
The longest mitochondrial protein in metazoans is encoded by the male-transmitted mitogenome of the bivalve Scrobicularia plana
inferred← citeshttps://doi.org/10.1098/rsbl.2022.0275openalex-snapshot
Confirmation of the first intronic sequence in the bivalvian mitochondrial genome of Macoma balthica (Linnaeus, 1758)
inferred← citeshttps://doi.org/10.1098/rsob.180267openalex-snapshot
A battle for transmission: the cooperative and selfish animal mitochondrial genomes
inferred← citeshttps://doi.org/10.1098/rsos.211550openalex-snapshot
Long-read sequencing reveals atypical mitochondrial genome structure in a New Zealand marine isopod
inferred← citeshttps://doi.org/10.1098/rspb.2018.0187openalex-snapshot
Mitochondrial genetic effects on reproductive success: signatures of positive intrasexual, but negative intersexual pleiotropy
inferred← citeshttps://doi.org/10.1098/rstb.2019.0176openalex-snapshot
Intracellular quality control of mitochondrial DNA: evidence and limitations
inferred← citeshttps://doi.org/10.1098/rstb.2019.0187openalex-snapshot
Mapping and editing animal mitochondrial genomes: can we overcome the challenges?
inferred← citeshttps://doi.org/10.1098/rstb.2020.0159openalex-snapshot
Molluscan mitochondrial genomes break the rules
inferred← citeshttps://doi.org/10.1098/rstb.2025.0074openalex-snapshot
The functional importance of mitochondrial sequences with dual functions: overlapping protein–protein and protein–RNA gene sequences as test cases
inferred← citeshttps://doi.org/10.1098/rstb.2025.0082openalex-snapshot
Extreme mitochondrial genome complexity in the calcaronean sponge Sycon ciliatum (Fabricius, 1780): fragmentation, gene duplication and mRNA editing
inferred← citeshttps://doi.org/10.1101/2020.05.09.085712openalex-snapshot
Evolutionary history of inversions in the direction of architecture-driven mutational pressures in crustacean mitochondrial genomes
inferred← citeshttps://doi.org/10.1101/2023.02.28.530434openalex-snapshot
Parasitism and locomotory capacity calibrate the mitogenomic evolutionary rates in Bilateria
inferred← citeshttps://doi.org/10.1101/2023.08.23.554511openalex-snapshot
Characterization of the mitochondrial proteome in the ctenophore Mnemiopsis leidyi using MitoPredictor
inferred← citeshttps://doi.org/10.1101/2024.01.10.575101openalex-snapshot
Acanthella acuta Mitochondrial DNA: Linear Architecture and Other Unique Features
inferred← citeshttps://doi.org/10.1101/2024.02.09.579586openalex-snapshot
The highly repetitive genome of Myxobolus sp., a myxozoan parasite of fathead minnows
inferred← citeshttps://doi.org/10.1101/2024.12.23.625590openalex-snapshot
Long-read sequencing reveals extensive size variation and suggests evolutionary patterns of expansion in bivalve mitogenomes
inferred← citeshttps://doi.org/10.1101/2025.04.29.651065openalex-snapshot
Convergent pathways of reductive mitochondrial evolution characterised with hypercubic inference
inferred← citeshttps://doi.org/10.1101/2025.07.08.663769openalex-snapshot
Hidden in Plain Sight: A Novel Symbiotic Haplosclerid Sponge Species Revealed by its Mitochondrial Genome
inferred← citeshttps://doi.org/10.1101/gr.280875.125openalex-snapshot
Nuclear mitochondrial sequences in great ape telomere-to-telomere genomes
inferred← citeshttps://doi.org/10.1111/1755-0998.13459openalex-snapshot
Hidden diversity of Ctenophora revealed by new mitochondrial COI primers and sequences
inferred← citeshttps://doi.org/10.1111/1755-0998.13584openalex-snapshot
ORTHOSKIM: In silico sequence capture from genomic and transcriptomic libraries for phylogenomic and barcoding applications
inferred← citeshttps://doi.org/10.1111/1755-0998.13667openalex-snapshot
Do pseudogenes pose a problem for metabarcoding marine animal communities?
inferred← citeshttps://doi.org/10.1111/cla.70061openalex-snapshot
From genomic conflict to ecological adaptation: reconstructing higher‐level phylogenetic relationships of water mites (Hydrachnidia) based on mitochondrial genomes
inferred← citeshttps://doi.org/10.1111/jzs.12380openalex-snapshot
Evolutionary implications of analyses of complete mitochondrial genomes across order Zoantharia (Cnidaria: Hexacorallia)
inferred← citeshttps://doi.org/10.1111/mec.13959openalex-snapshot
The on‐again, off‐again relationship between mitochondrial genomes and species boundaries
inferred← citeshttps://doi.org/10.1111/nph.18334openalex-snapshot
Fragaria mitogenomes evolve rapidly in structure but slowly in sequence and incur frequent multinucleotide mutations mediated by microinversions
inferred← citeshttps://doi.org/10.1111/ppl.70231openalex-snapshot
Highly variable mitochondrial chromosome content in a holoparasitic plant due to recurrent gains of foreign circular DNA
inferred← citeshttps://doi.org/10.1111/tpj.15222openalex-snapshot
Cyanophora paradoxa mitochondrial tRNAs play a double game
inferred← citeshttps://doi.org/10.1134/s0006297925602114openalex-snapshot
Gene Order in Mitochondrial DNA Affects Abundance of their Transcripts (A Case of Marine Nematodes)
inferred← citeshttps://doi.org/10.1155/2020/6540343openalex-snapshot
Exceptional Enlargement of the Mitochondrial Genome Results from Distinct Causes in Different Rain Frogs (Anura: Brevicipitidae: Breviceps)
inferred← citeshttps://doi.org/10.1155/2021/6652508openalex-snapshot
A Comparative Analyses of the Complete Mitochondrial Genomes of Fungal Endosymbionts in Sogatella furcifera, White-Backed Planthoppers
inferred← citeshttps://doi.org/10.1186/s12859-020-3532-8openalex-snapshot
Repetitive DNA profile of the amphibian mitogenome
inferred← citeshttps://doi.org/10.1186/s12862-018-1186-1openalex-snapshot
Extensive mitochondrial gene rearrangements in Ctenophora: insights from benthic Platyctenida
inferred← citeshttps://doi.org/10.1186/s12862-018-1230-1openalex-snapshot
Divergence times in demosponges (Porifera): first insights from new mitogenomes and the inclusion of fossils in a birth-death clock model
inferred← citeshttps://doi.org/10.1186/s12862-018-1246-6openalex-snapshot
The linear mitochondrial genome of the quarantine chytrid Synchytrium endobioticum; insights into the evolution and recent history of an obligate biotrophic plant pathogen
inferred← citeshttps://doi.org/10.1186/s12864-017-4237-xopenalex-snapshot
The complete mitochondrial genome of parasitic nematode Camallanus cotti: extreme discontinuity in the rate of mitogenomic architecture evolution within the Chromadorea class
inferred← citeshttps://doi.org/10.1186/s12864-022-08743-xopenalex-snapshot
Mitochondrial genome sequencing, mapping, and assembly benchmarking for Culicoides species (Diptera: Ceratopogonidae)
inferred← citeshttps://doi.org/10.1186/s12864-023-09177-9openalex-snapshot
The mitochondrial genome of Heterosentis pseudobagri (Wang & Zhang, 1987) Pichelin & Cribb, 1999 reveals novel aspects of tRNA genes evolution in Acanthocephala
inferred← citeshttps://doi.org/10.1186/s12864-024-10201-9openalex-snapshot
Mitochondrial genome plasticity of mammalian species
inferred← citeshttps://doi.org/10.1186/s12864-024-10254-wopenalex-snapshot
Evolution of myxozoan mitochondrial genomes: insights from myxobolids
inferred← citeshttps://doi.org/10.1186/s12864-024-10500-1openalex-snapshot
Comparative mitochondrial genomics in Nematoda reveal astonishing variation in compositional biases and substitution rates indicative of multi-level selection
inferred← citeshttps://doi.org/10.1186/s12864-024-10505-wopenalex-snapshot
High heteroplasmy is associated with low mitochondrial copy number and selection against non-synonymous mutations in the snail Cepaea nemoralis
inferred← citeshttps://doi.org/10.1186/s12864-026-12534-zopenalex-snapshot
The phylogeny and evolution of blow flies (Diptera: Calliphoridae) from the perspective of mitogenomics
inferred← citeshttps://doi.org/10.1186/s12864-026-12610-4openalex-snapshot
Mitogenomic organization and characteristics of deep-sea pelagic ostracods from both polar regions
inferred← citeshttps://doi.org/10.1186/s12864-026-12640-yopenalex-snapshot
Mitochondrial genomes of Terebelliformia: gene rearrangements, phylogenetic relationships, and evolutionary insights
inferred← citeshttps://doi.org/10.1186/s12867-017-0093-0openalex-snapshot
Mitochondrial RNA processing in absence of tRNA punctuations in octocorals
inferred← citeshttps://doi.org/10.1186/s12915-021-01218-7openalex-snapshot
Fragmentation in mitochondrial genomes in relation to elevated sequence divergence and extreme rearrangements
inferred← citeshttps://doi.org/10.1186/s40709-017-0060-4openalex-snapshot
Evolution and inheritance of animal mitochondrial DNA: rules and exceptions
inferred← citeshttps://doi.org/10.1186/s40851-019-0131-5openalex-snapshot
Mitochondrial genome diversity and evolution in Branchiopoda (Crustacea)
inferred← citeshttps://doi.org/10.12688/f1000research.21490.1openalex-snapshot
Recent advances in understanding mitochondrial genome diversity
inferred← citeshttps://doi.org/10.1371/journal.pbio.3002577openalex-snapshot
How do bacterial endosymbionts work with so few genes?
inferred← citeshttps://doi.org/10.1371/journal.pgen.1011266openalex-snapshot
Mitochondrial genome fragmentation is correlated with increased rates of molecular evolution
inferred← citeshttps://doi.org/10.1371/journal.pntd.0008552openalex-snapshot
First record of a tandem-repeat region within the mitochondrial genome of Clonorchis sinensis using a long-read sequencing approach
inferred← citeshttps://doi.org/10.1371/journal.pone.0177959openalex-snapshot
Deep RNA sequencing reveals the smallest known mitochondrial micro exon in animals: The placozoan cox1 single base pair exon
inferred← citeshttps://doi.org/10.1371/journal.pone.0194334openalex-snapshot
A complete logical approach to resolve the evolution and dynamics of mitochondrial genome in bilaterians
inferred← citeshttps://doi.org/10.1371/journal.pone.0273330openalex-snapshot
Intraspecies variation of the mitochondrial genome: An evaluation for phylogenetic approaches based on the conventional choices of genes and segments on mitogenome
inferred← citeshttps://doi.org/10.1371/journal.pone.0287281openalex-snapshot
Phylomitogenomics bolsters the high-level classification of Demospongiae (phylum Porifera)
inferred← citeshttps://doi.org/10.1371/journal.pone.0350115openalex-snapshot
The Copepoda mitogenome as a dynamic evolutionary landscape
inferred← citeshttps://doi.org/10.1590/1519-6984.301893openalex-snapshot
Preliminary study on genetic diversity and phylogenetic relationships of Teropong Temanggung sheep based on mitochondrial cytochrome b sequences
inferred← citeshttps://doi.org/10.17605/osf.io/rn9ftopenalex-snapshot
Data for Dynamic evolution of the MutS family in animals: multiple losses of MSH paralogues and gain of a viral MutS homologue in octocorals
inferred← citeshttps://doi.org/10.18174/476563openalex-snapshot
From metagenome to gene : Identification of the first Synchytrium endobioticum effector through comparative genomics
inferred← citeshttps://doi.org/10.18174/550785openalex-snapshot
Evolution of mutualisms in the basidiomycete genus Termitomyces
inferred← citeshttps://doi.org/10.18388/pb.2021_423openalex-snapshot
Charakterystyka kolistych DNA u Eukarya
inferred← citeshttps://doi.org/10.18699/vjgb-24-36openalex-snapshot
Lake Baikal amphipods and their genomes, great and small
inferred← citeshttps://doi.org/10.21203/rs.3.rs-11188068/v1openalex-snapshot
Extremely Divergent Repeats Made the Largest Bilaterian Mitogenome in Photosymbiotic Bivalves
inferred← citeshttps://doi.org/10.21203/rs.3.rs-3846124/v1openalex-snapshot
Draft genome from facultatively parthenogenetic Opiliones indicates frequent mitonuclear sequence transfer and novel full-length insertions
inferred← citeshttps://doi.org/10.31274/td-20240329-309openalex-snapshot
Evaluation of the evolutionary history of Clade B of Haplosclerid Sponges with an emphasis on tRNAs and tRNA synthetases
inferred← citeshttps://doi.org/10.31951/2658-3518-2018-a-2-98openalex-snapshot
Comrapative analysis of inverted sequences of noncoding region in the mitochondrial DNA of the Baikal sponges (Fam. Lubomirskiidae)
inferred← citeshttps://doi.org/10.3389/fevo.2023.1138297openalex-snapshot
Mitogenomic phylogeny of Cypraeidae (Gastropoda: Mesogastropoda)
inferred← citeshttps://doi.org/10.3389/fgene.2019.00443openalex-snapshot
Dicyemida and Orthonectida: Two Stories of Body Plan Simplification
inferred← citeshttps://doi.org/10.3389/fmars.2025.1732471openalex-snapshot
Family estates or dormitories: analyzing the kinship of Dyopedos bispinis “collective” mast populations (Crustacea: Amphipoda: Dulichiidae)
inferred← citeshttps://doi.org/10.3389/fmicb.2023.1162963openalex-snapshot
Mitochondrial genome diversity of Balamuthia mandrillaris revealed by a fatal case of granulomatous amoebic encephalitis
inferred← citeshttps://doi.org/10.3389/fpls.2023.1222186openalex-snapshot
Mitochondrial genome annotation with MFannot: a critical analysis of gene identification and gene model prediction
inferred← citeshttps://doi.org/10.3390/biology14121794openalex-snapshot
Complete Mitochondrial Genomes of Spotted Forest Musk Deer (Moschus berezovskii) from Huanglong Mountain, Shaanxi, China, and Phylogenetic Analysis of Moschidae
inferred← citeshttps://doi.org/10.3390/biology15181593openalex-snapshot
Mitochondrial Genome Comparison and Phylogenetic Analysis of the Family Carabidae (Coleoptera: Adephaga)
inferred← citeshttps://doi.org/10.3390/d16060346openalex-snapshot
The Complete Mitogenomes of Two Species of Snakehead Fish (Perciformes: Channidae): Genome Characterization and Phylogenetic Analysis
inferred← citeshttps://doi.org/10.3390/d17120813openalex-snapshot
Decoding the Mitogenome of Takydromus intermedius: Insights into the Comparative Mitogenomics and Phylogenetic Relationships of Takydromus Lizards
inferred← citeshttps://doi.org/10.3390/fishes7060317openalex-snapshot
The Complete Mitochondrial Genome of Hyotissa hyotis (Bivalvia: Gryphaeidae) Reveals a Unique Gene Order within Ostreoidea
inferred← citeshttps://doi.org/10.3390/genes10080592openalex-snapshot
Trans-Species Polymorphism in Mitochondrial Genome of Camarodont Sea Urchins
inferred← citeshttps://doi.org/10.3390/genes12122030openalex-snapshot
The Mitochondrial Genome of a Freshwater Pelagic Amphipod Macrohectopus branickii Is among the Longest in Metazoa
inferred← citeshttps://doi.org/10.3390/genes13081317openalex-snapshot
A Primer Genetic Toolkit for Exploring Mitochondrial Biology and Disease Using Zebrafish
inferred← citeshttps://doi.org/10.3390/genes14030628openalex-snapshot
Genetic Diversity in the mtDNA of Physarum polycephalum
inferred← citeshttps://doi.org/10.3390/genes15010090openalex-snapshot
Complete Mitochondrial Genome and Phylogenetic Analysis of Tarsiger indicus (Aves: Passeriformes: Muscicapidae)
inferred← citeshttps://doi.org/10.3390/genes15050557openalex-snapshot
Complete Mitochondrial Genome of Four Peristediidae Fish Species: Genome Characterization and Phylogenetic Analysis
inferred← citeshttps://doi.org/10.3390/genes15121642openalex-snapshot
Complete Mitochondrial Genomes of Pluvialis fulva and Charadrius dubius with Phylogenetic Analysis of Charadriiformes
inferred← citeshttps://doi.org/10.3390/genes16091030openalex-snapshot
Assembly of Mitochondrial Genome of Oriental Plover (Anarhynchus veredus) and Phylogenetic Relationships Within the Charadriidae
inferred← citeshttps://doi.org/10.3390/ijms20082041openalex-snapshot
Twist and Turn—Topoisomerase Functions in Mitochondrial DNA Maintenance
inferred← citeshttps://doi.org/10.3390/ijms22041811openalex-snapshot
Nanopore Sequencing Resolves Elusive Long Tandem-Repeat Regions in Mitochondrial Genomes
inferred← citeshttps://doi.org/10.3390/ijms25010067openalex-snapshot
The Complete Mitochondrial Genome and Phylogenetic Analysis of the Freshwater Shellfish Novaculina chinensis (Bivalvia: Pharidae)
inferred← citeshttps://doi.org/10.3390/ijms25010357openalex-snapshot
Characterization of the Complete Mitochondrial Genome of Agelas nakamurai from the South China Sea
inferred← citeshttps://doi.org/10.3390/ijms25042279openalex-snapshot
Comparative Mitogenome Analyses of Fifteen Ramshorn Snails and Insights into the Phylogeny of Planorbidae (Gastropoda: Hygrophila)
inferred← citeshttps://doi.org/10.3390/ijms25158218openalex-snapshot
The Mitogenomic Landscape of Hexacorallia Corals: Insight into Their Slow Evolution
inferred← citeshttps://doi.org/10.3390/insects13121101openalex-snapshot
New Mitogenome Features of Philopotamidae (Insecta: Trichoptera) with Two New Species of Gunungiella
inferred← citeshttps://doi.org/10.3390/life11030215openalex-snapshot
The Mitochondrial Genome of a Plant Fungal Pathogen Pseudocercospora fijiensis (Mycosphaerellaceae), Comparative Analysis and Diversification Times of the Sigatoka Disease Complex Using Fossil Calibrated Phylogenies
inferred← citeshttps://doi.org/10.3390/life11070663openalex-snapshot
Mitochondrial Genomic Landscape: A Portrait of the Mitochondrial Genome 40 Years after the First Complete Sequence
inferred← citeshttps://doi.org/10.3390/life12010004openalex-snapshot
Molecular Phylogenetics and Mitochondrial Evolution
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