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Endotherms, ectotherms, and mitochondrial genome-size variation

https://doi.org/10.1007/bf00175505
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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1001/jama.1951.02920260071031openalex-snapshot
Comparative Animal Physiology
inferredcites →https://doi.org/10.1007/978-1-4684-4988-4_2openalex-snapshot
The Mitochondrial Genome of Animals
inferredcites →https://doi.org/10.1007/bf00283927openalex-snapshot
Mitochondrial DNA polymorphism in Japanese
inferredcites →https://doi.org/10.1007/bf00330961openalex-snapshot
Genetics of mitochondria in Drosophila: mtDNA inheritance in heteroplasmic strains of D. mauritiana
inferredcites →https://doi.org/10.1007/bf02099951openalex-snapshot
Concerted evolution of sequence repeats inDrosophila mitochondrial DNA
inferredcites →https://doi.org/10.1007/bf02100200openalex-snapshot
Mitochondrial DNA evolution in lagomorphs: Origin of systematic heteroplasmy and organization of diversity in European rabbits
inferredcites →https://doi.org/10.1007/bf02101122openalex-snapshot
Compositional patterns in the nuclear genome of cold-blooded vertebrates
inferredcites →https://doi.org/10.1007/bf02101123openalex-snapshot
Compositional transitions in the nuclear genomes of cold-blooded vertebrates
inferredcites →https://doi.org/10.1007/bf02103135openalex-snapshot
Parallel origins of duplications and the formation of pseudogenes in mitochondrial DNA from parthenogenetic lizards (Heteronotia binoei; Gekkonidae)
inferredcites →https://doi.org/10.1007/bf02143501openalex-snapshot
The evolutionary relationships among known life forms
inferredcites →https://doi.org/10.1016/0092-8674(77)90286-0openalex-snapshot
Mouse L cell mitochondrial DNA molecules are selected randomly for replication throughout the cell cycle
inferredcites →https://doi.org/10.1016/0092-8674(82)90049-6openalex-snapshot
Replication of animal mitochondrial DNA
inferredcites →https://doi.org/10.1016/0092-8674(84)90434-3openalex-snapshot
Heterogeneous mitochondrial DNA D-loop sequences in bovine tissue
inferredcites →https://doi.org/10.1016/0168-9525(89)90111-xopenalex-snapshot
The evolutionary origins of organelles
inferredcites →https://doi.org/10.1016/s0074-7696(08)61373-xopenalex-snapshot
Animal Mitochondrial DNA: An Extreme Example of Genetic Economy
inferredcites →https://doi.org/10.1038/331717a0openalex-snapshot
Deletions of muscle mitochondrial DNA in patients with mitochondrial myopathies
inferredcites →https://doi.org/10.1038/339309a0openalex-snapshot
An autosomal dominant disorder with multiple deletions of mitochondrial DNA starting at the D-loop region
inferredcites →https://doi.org/10.1038/348337a0openalex-snapshot
Loss of photosynthetic and chlororespiratory genes from the plastid genome of a parasitic flowering plant
inferredcites →https://doi.org/10.1038/357153a0openalex-snapshot
Rates of mitochondrial DNA evolution in sharks are slow compared with mammals
inferredcites →https://doi.org/10.1038/hdy.1987.37openalex-snapshot
Mitochondrial DNA insertion polymorphism and germ line heteroplasmy in the Triturus cristatus complex
inferredcites →https://doi.org/10.1073/pnas.79.15.4686openalex-snapshot
Mitochondrial DNA polymorphism in a maternal lineage of Holstein cows.
inferredcites →https://doi.org/10.1073/pnas.80.22.6942openalex-snapshot
Mitochondrial DNA heteroplasmy in Drosophila mauritiana.
inferredcites →https://doi.org/10.1073/pnas.81.18.5633openalex-snapshot
Thymine glycol and thymidine glycol in human and rat urine: a possible assay for oxidative DNA damage.
inferredcites →https://doi.org/10.1073/pnas.83.22.8813openalex-snapshot
Extensive variation and heteroplasmy in size of mitochondrial DNA among geographic populations of Drosophila melanogaster
inferredcites →https://doi.org/10.1073/pnas.84.20.7183openalex-snapshot
Tandem duplications in animal mitochondrial DNAs: variation in incidence and gene content among lizards.
inferredcites →https://doi.org/10.1073/pnas.84.21.7595openalex-snapshot
Atypical mitochondrial DNA from the deep-sea scallop Placopecten magellanicus
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.85.21.8107openalex-snapshot
Unequal partitioning of bovine mitochondrial genotypes among siblings.
inferredcites →https://doi.org/10.1086/284325openalex-snapshot
Phylogenies and the Comparative Method
inferredcites →https://doi.org/10.1093/aesa/83.1.81openalex-snapshot
Restriction Endonuclease Cleavage Site and Length Polymorphisms in Mitochondrial DNA of Apis mellifera mellifera and A. m. carnica (Hymenoptera: Apidae)
inferredcites →https://doi.org/10.1093/auk/105.3.516openalex-snapshot
Molecular Genetic Divergence between Avian Sibling Species: King and Clapper Rails, Long-Billed and Short-Billed Dowitchers, Boat-Tailed and Great-Tailed Grackles, and Tufted and Black-Crested Titmice
inferredcites →https://doi.org/10.1093/genetics/104.4.699openalex-snapshot
LENGTH MUTATIONS IN HUMAN MITOCHONDRIAL DNA
inferredcites →https://doi.org/10.1093/genetics/105.3.681openalex-snapshot
MITOCHONDRIAL DNA EVOLUTION IN MICE
inferredcites →https://doi.org/10.1093/genetics/110.4.689openalex-snapshot
LENGTH VARIATION AND HETEROPLASMY ARE FREQUENT IN MITOCHONDRIAL DNA FROM PARTHENOGENETIC AND BISEXUAL LIZARDS (GENUS CNEMIDOPHORUS)
inferredcites →https://doi.org/10.1093/genetics/114.3.955openalex-snapshot
MITOCHONDRIAL DNA TRANSMISSION GENETICS IN CRICKETS
inferredcites →https://doi.org/10.1093/genetics/117.4.687openalex-snapshot
Drosophila Mitochondrial Genetics: Evolution of Heteroplasmy Through Germ Line Cell Divisions
inferredcites →https://doi.org/10.1093/genetics/118.3.509openalex-snapshot
Length and restriction site heteroplasmy in the mitochondrial DNA of american shad (alosa sapidissima).
inferredcites →https://doi.org/10.1093/genetics/120.3.707openalex-snapshot
Sequence amplification and gene rearrangement in parasitic nematode mitochondrial DNA.
inferredcites →https://doi.org/10.1093/genetics/121.3.551openalex-snapshot
Molecular population genetics of mtDNA size variation in crickets.
inferredcites →https://doi.org/10.1093/genetics/123.4.825openalex-snapshot
Mitochondrial DNA in the bark weevils: size, structure and heteroplasmy.
inferredcites →https://doi.org/10.1093/genetics/124.1.157openalex-snapshot
Length heteroplasmy of sturgeon mitochondrial DNA: an illegitimate elongation model.
inferredcites →https://doi.org/10.1093/genetics/124.4.845openalex-snapshot
Recent appearance and molecular characterization of mitochondrial DNA deletions within a defined nematode pedigree.
inferredcites →https://doi.org/10.1093/genetics/126.3.695openalex-snapshot
Phylogenetically informative length polymorphism and sequence variability in mitochondrial DNA of Australian songbirds (Pomatostomus).
inferredcites →https://doi.org/10.1093/genetics/128.2.393openalex-snapshot
Putative origin and function of the intergenic region between COI and COII of Apis mellifera L. mitochondrial DNA.
inferredcites →https://doi.org/10.1093/genetics/128.3.607openalex-snapshot
Length and sequence variation in evening bat D-loop mtDNA.
inferredcites →https://doi.org/10.1093/genetics/129.1.103openalex-snapshot
A comprehensive study of genic variation in natural populations of Drosophila melanogaster. IV. Mitochondrial DNA variation and the role of history vs. selection in the genetic structure of geographic populations.
inferredcites →https://doi.org/10.1093/genetics/129.1.221openalex-snapshot
Evolutionary dynamics of mitochondrial DNA duplications in parthenogenetic geckos, Heteronotia binoei.
inferredcites →https://doi.org/10.1093/genetics/129.1.247openalex-snapshot
Replacement of bovine mitochondrial DNA by a sequence variant within one generation.
inferredcites →https://doi.org/10.1093/genetics/132.1.211openalex-snapshot
Heteroplasmy of short tandem repeats in mitochondrial DNA of Atlantic cod, Gadus morhua.
inferredcites →https://doi.org/10.1093/nar/11.19.6699openalex-snapshot
Rat mitochondrial DNA polymorphism: sequence analysis of a hypervariable site for insertions/deletions
inferredcites →https://doi.org/10.1093/nar/17.20.8117openalex-snapshot
Mapping of heteroplasmic mitochondrial DNA deletions in Kearns-Sayre syndrome
inferredcites →https://doi.org/10.1093/oxfordjournals.jhered.a110230openalex-snapshot
Size polymorphism and heteropiasmy in the mitochondrial DNA of lower vertebrates
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a040421openalex-snapshot
Heteroplasmy in mice with deletion of a large coding region of mitochondrial DNA.
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a040586openalex-snapshot
Molecular characterization of a repeat element causing large-scale size variation in the mitochondrial DNA of the sea scallop Placopecten magellanicus.
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a040660openalex-snapshot
Heteroplasmy and polymorphism in the major noncoding region of mitochondrial DNA in Japanese monkeys: association with tandemly repeated sequences.
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a040711openalex-snapshot
Repeated Sequences and Large-Scale Size Variation of Mitochondrial DNA: A Common Feature among Scallops (Bivalvia: Pectinidae)
inferredcites →https://doi.org/10.1111/j.1558-5646.1992.tb01137.xopenalex-snapshot
APPARENT SELECTIVE NEUTRALITY OF MITOCHONDRIAL DNA SIZE VARIATION: A TEST IN THE DEEP-SEA SCALLOP PLACOPECTEN MAGELLANICUS
inferredcites →https://doi.org/10.1111/j.1768-322x.1985.tb00339.xopenalex-snapshot
Intra‐individual length heterogeneity of Rana esculenta mitochondrial DNA
inferredcites →https://doi.org/10.1126/science.228.4706.1446openalex-snapshot
Mitochondrial DNA Size Variation Within Individual Crickets
inferredcites →https://doi.org/10.1126/science.3018925openalex-snapshot
Tandem Duplication of D-Loop and Ribosomal RNA Sequences in Lizard Mitochondrial DNA
inferredcites →https://doi.org/10.1128/mcb.10.11.5671openalex-snapshot
Mitochondrial DNA Structure and Expression in Specialized Subtypes of Mammalian Striated Muscle
inferredcites →https://doi.org/10.1128/mmbr.46.2.208-240.1982openalex-snapshot
Structure and evolution of organelle genomes
inferredcites →https://doi.org/10.1139/z89-131openalex-snapshot
Mitochondrial DNA diversity among populations of striped bass in the southeastern United States
inferredcites →https://doi.org/10.1139/z89-187openalex-snapshot
Mitochondrial DNA patterns among endemic stickleback from the Queen Charlotte Islands: a preliminary survey
inferredcites →https://doi.org/10.1266/jjg.61.345openalex-snapshot
Mitochondrial DNA polymorphism in Japanese monkeys, Macaca fuscata.
inferredcites →https://doi.org/10.2307/1445495openalex-snapshot
Mitochondrial DNA Analysis of Chesapeake Bay White Perch, Morone americana

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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Complete mitochondrial genomes of Chionomys roberti and Chionomys nivalis (Mammalia: Rodentia) from Turkey: Insight into their phylogenetic position within Arvicolinae
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Disproportion between the Peruvian Amazonian megadiverse mammalian fauna and the available molecular information
inferred← citeshttps://doi.org/10.1002/ece3.3067openalex-snapshot
The mitochondrial genome of a sea anemone Bolocera sp. exhibits novel genetic structures potentially involved in adaptation to the deep‐sea environment
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Exploring the Mitogenomes of Acroneuriinae: The First Report of Gene Rearrangements in Plecoptera Species and Phylogenetic Analyses of Perlidae
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Orthodox and unorthodox phylogenetic relationships among tunas revealed by the nucleotide sequence analysis of the mitochondrial DNA control region
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Concerted evolution and RAPping in mitochondrial VNTRs and the molecular geography of cricket populations
inferred← citeshttps://doi.org/10.1007/978-3-642-59884-5_3openalex-snapshot
Mitochondrial DNA Inheritance in Mammals
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Cloning and characterization of the platypus mitochondrial genome
inferred← citeshttps://doi.org/10.1007/bf00170672openalex-snapshot
Molecular cloning and complete nucleotide sequence of the repeated unit and flanking gene of the scallop Pecten maximus mitochondrial DNA: Putative replication origin features
inferred← citeshttps://doi.org/10.1007/bf00173173openalex-snapshot
The sequence, organization, and evolution of the Locusta migratoria mitochondrial genome
inferred← citeshttps://doi.org/10.1007/bf00326158openalex-snapshot
Variable numbers of simple tandem repeats make birds of the order Ciconiiformes heteroplasmic in their mitochondrial genomes
inferred← citeshttps://doi.org/10.1007/bf00350683openalex-snapshot
Mitochondrial DNA heteroplasmy in European populations of the mussel Mytilus trossulus
inferred← citeshttps://doi.org/10.1007/bf01921725openalex-snapshot
Ancient DNA sequences reveal unsuspected phylogenetic relationships within New Zealand wrens (Acanthisittidae)
inferred← citeshttps://doi.org/10.1007/pl00006402openalex-snapshot
Organization and Evolution of the Mitochondrial DNA Control Region in the Avian Genus Alectoris
inferred← citeshttps://doi.org/10.1007/pl00011797openalex-snapshot
Sequence Characterization of a Unique Intergenic Spacer in Gadiformes Mitochondrial DNA
inferred← citeshttps://doi.org/10.1007/s00239-004-0214-5openalex-snapshot
Novel Repetitive Structures, Deviant Protein-Encoding Sequences andUnidentified ORFs in the Mitochondrial Genome of the BrachiopodLingula anatina
inferred← citeshttps://doi.org/10.1007/s00239-004-2619-6openalex-snapshot
Origin and Evolution of Tandem Repeats in the Mitochondrial DNA Control Region of Shrikes (Lanius spp.)
inferred← citeshttps://doi.org/10.1007/s00239-004-2621-zopenalex-snapshot
Gene Rearrangements and Evolution of tRNA Pseudogenes in the Mitochondrial Genome of the Parrotfish (Teleostei: Perciformes: Scaridae)
inferred← citeshttps://doi.org/10.1007/s00239-007-9016-xopenalex-snapshot
Complete Mitochondrial DNA Sequence of the Scallop Placopecten magellanicus: Evidence of Transposition Leading to an Uncharacteristically Large Mitochondrial Genome
inferred← citeshttps://doi.org/10.1007/s00239-013-9591-yopenalex-snapshot
Intraspecific Rearrangement of Duplicated Mitochondrial Control Regions in the Luzon Tarictic Hornbill Penelopides manillae (Aves: Bucerotidae)
inferred← citeshttps://doi.org/10.1007/s00239-014-9631-2openalex-snapshot
Control Region Length Dynamics Potentially Drives Amino Acid Evolution in Tarsier Mitochondrial Genomes
inferred← citeshttps://doi.org/10.1007/s00294-002-0328-5openalex-snapshot
Evolution of heteroplasmy at a mitochondrial tandem repeat locus in cultured rabbit cells
inferred← citeshttps://doi.org/10.1007/s00294-011-0345-3openalex-snapshot
Polymorphic minisatellites in the mitochondrial DNAs of Oryza and Brassica
inferred← citeshttps://doi.org/10.1007/s10126-001-0076-4openalex-snapshot
Length and Sequence Variability in Mitochondrial Control Region of the Milkfish, Chanos chanos
inferred← citeshttps://doi.org/10.1007/s10528-021-10129-9openalex-snapshot
Characterization and Phylogenetic Analysis of the Complete Mitochondrial Genome of Saturnia japonica
inferred← citeshttps://doi.org/10.1007/s10528-024-10991-3openalex-snapshot
The Mitochondrial Genome of Melipona fasciculata (Apidae, Meliponini): Genome Organization and Comparative Analyses, Phylogenetic Implications and Divergence Time Estimations
inferred← citeshttps://doi.org/10.1007/s10528-025-11171-7openalex-snapshot
Mitochondrial Genome and Phylogenetic Analysis of Rhinogobius virgigena
inferred← citeshttps://doi.org/10.1007/s10641-017-0648-4openalex-snapshot
Genetic variation of Japanese pink salmon populations inferred from nucleotide sequence analysis of the mitochondrial DNA control region
inferred← citeshttps://doi.org/10.1007/s10695-008-9251-0openalex-snapshot
Comparative analysis of mitochondrial control region in polyploid hybrids of red crucian carp (Carassius auratus) × blunt snout bream (Megalobrama amblycephala)
inferred← citeshttps://doi.org/10.1007/s10709-011-9576-yopenalex-snapshot
Population genetics of the cytoplasm and the units of selection on mitochondrial DNA in Drosophila melanogaster
inferred← citeshttps://doi.org/10.1007/s10709-017-9975-9openalex-snapshot
Characterization of the complete mitochondrial genome of Acanthoscelides obtectus (Coleoptera: Chrysomelidae: Bruchinae) with phylogenetic analysis
inferred← citeshttps://doi.org/10.1007/s11033-008-9379-0openalex-snapshot
The mitochondrial genome of Protohermes concolorus Yang et Yang 1988 (Insecta: Megaloptera: Corydalidae)
inferred← citeshttps://doi.org/10.1007/s11033-010-0636-7openalex-snapshot
Structure and variable numbers of tandem repeats (VNTRs) of the mitochondrial control region in mitten crab Eriocheir (Crustacean: Brachyura)
inferred← citeshttps://doi.org/10.1007/s11033-014-3438-5openalex-snapshot
A description of the complete mitochondrial genomes of Amphiporus formidabilis, Prosadenoporus spectaculum and Nipponnemertes punctatula (Nemertea: Hoplonemertea: Monostilifera)
inferred← citeshttps://doi.org/10.1007/s11692-016-9405-4openalex-snapshot
Relationships Among Powered Flight, Metabolic Rate, Body Mass, Genome Size, and the Retrotransposon Complement of Volant Birds
inferred← citeshttps://doi.org/10.1007/s11756-026-02319-wopenalex-snapshot
Phylogenetic position of Talpa levantis, T. martinorum, and T. transcaucasica based on complete mitogenomes
inferred← citeshttps://doi.org/10.1007/s11802-017-3202-2openalex-snapshot
Characterization of the complete mitochondrial genome of the hybrid Epinephelus moara♀ × Epinephelus lanceolatus♂, and phylogenetic analysis in subfamily epinephelinae
inferred← citeshttps://doi.org/10.1007/s11802-021-4707-2openalex-snapshot
Relaxation of Selective Constraint on the Ultra-Large Mitochondrial Genomes of Arcidae (Mollusca: Bivalvia)
inferred← citeshttps://doi.org/10.1007/s13258-017-0570-3openalex-snapshot
Complete mitochondrial genome of the Pleuronichthys lighti (Pleuronectiformes, Pleuronectidae) with phylogenetic consideration
inferred← citeshttps://doi.org/10.1007/s13364-025-00822-0openalex-snapshot
Comparative mitogenome sequences and phylogenetic relationships of two mongooses (Herpestes ichneumon and Urva auropunctata) from Türkiye and Iraq
inferred← citeshttps://doi.org/10.1016/0168-9525(96)30058-9openalex-snapshot
Mutant fixation via plasmid dimerization and its relation to human diseases
inferred← citeshttps://doi.org/10.1016/0169-5347(94)90176-7openalex-snapshot
Thermal habit, metabolic rate and the evolution of mitochondrial DNA
inferred← citeshttps://doi.org/10.1016/0959-437x(93)90010-mopenalex-snapshot
Evolution by DNA turnover in the control region of vertebrate mitochondrial DNA
inferred← citeshttps://doi.org/10.1016/j.aggene.2016.09.007openalex-snapshot
Comparison of full mitochondrial genomes for the rice weevil, Sitophilus oryzae and the maize weevil, Sitophilus zeamais (Coleoptera: Curculionidae)
inferred← citeshttps://doi.org/10.1016/j.dib.2019.104882openalex-snapshot
Data on heteroplasmic mutations in mitochondrial genomes of loggerhead and hawksbill sea turtles: First approach
inferred← citeshttps://doi.org/10.1016/j.ejmech.2024.117127openalex-snapshot
Synthesis and mechanistic studies of 4-aminoquinoline-Isatin molecular hybrids and Schiff's bases as promising antimicrobial agents
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Structure and evolution of the mitochondrial control region and flanking sequences in the European cave salamander Proteus anguinus
inferred← citeshttps://doi.org/10.1016/j.gene.2008.05.020openalex-snapshot
Conservation of structural elements in the mitochondrial control region of Daphnia
inferred← citeshttps://doi.org/10.1016/j.gene.2010.02.012openalex-snapshot
Intraspecific variation in the mitochondrial genome among local populations of Medaka Oryzias latipes
inferred← citeshttps://doi.org/10.1016/j.gene.2012.12.080openalex-snapshot
The complete mitochondrial genomes of three grasshoppers, Asiotmethis zacharjini, Filchnerella helanshanensis and Pseudotmethis rubimarginis (Orthoptera: Pamphagidae)
inferred← citeshttps://doi.org/10.1016/j.gene.2013.09.064openalex-snapshot
The mitochondrial genome of the Russian wheat aphid Diuraphis noxia: Large repetitive sequences between trnE and trnF in aphids
inferred← citeshttps://doi.org/10.1016/j.gene.2014.01.020openalex-snapshot
Geographic variation within a tandemly repeated mitochondrial DNA D-loop region of a North American freshwater fish, Pylodictis olivaris
inferred← citeshttps://doi.org/10.1016/j.gene.2014.06.044openalex-snapshot
The complete mitogenome of Apocheima cinerarius (Lepidoptera: Geometridae: Ennominae) and comparison with that of other lepidopteran insects
inferred← citeshttps://doi.org/10.1016/j.gene.2014.12.011openalex-snapshot
The complete mitochondrial DNA of Tegillarca granosa and comparative mitogenomic analyses of three Arcidae species
inferred← citeshttps://doi.org/10.1016/j.gene.2014.12.026openalex-snapshot
The mitochondrial genome of Dastarcus helophoroides (Coleoptera: Bothrideridae) and related phylogenetic analyses
inferred← citeshttps://doi.org/10.1016/j.gene.2016.01.027openalex-snapshot
The mitochondrial genome of Atrijuglans hetaohei Yang (Lepidoptera: Gelechioidea) and related phylogenetic analyses
inferred← citeshttps://doi.org/10.1016/j.gene.2016.06.023openalex-snapshot
Characterization of the complete mitochondrial genome of Cynoglossus gracilis and a comparative analysis with other Cynoglossinae fishes
inferred← citeshttps://doi.org/10.1016/j.gene.2018.06.066openalex-snapshot
Evolutionary progression of mitochondrial gene rearrangements and phylogenetic relationships in Strigidae (Strigiformes)
inferred← citeshttps://doi.org/10.1016/j.gene.2018.11.045openalex-snapshot
Mitogenomics of Central American weakly-electric fishes
inferred← citeshttps://doi.org/10.1016/j.gene.2022.146773openalex-snapshot
Complete mitogenomes of Turkish tree squirrels, Sciurus anomalus and S. vulgaris, (Sciuridae: Rodentia: Mammalia) and their phylogenetic status within the tribe Sciurini
inferred← citeshttps://doi.org/10.1016/j.ibmb.2019.103208openalex-snapshot
Description of soybean aphid (Aphis glycines Matsumura) mitochondrial genome and comparative mitogenomics of Aphididae (Hemiptera: Sternorrhyncha)
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2018.02.110openalex-snapshot
Characterization of the complete mitochondrial genome of Biston marginata (Lepidoptera: Geometridae) and phylogenetic analysis among lepidopteran insects
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Two new mitogenomes of Picidae (Aves, Piciformes): Sequence, structure and phylogenetic analyses
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2023.124568openalex-snapshot
Rapid evolution, rearrangements and whole mitogenome duplication in the Australian stingless bees Tetragonula (Hymenoptera: Apidae): A steppingstone towards understanding mitochondrial function and evolution
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2023.126742openalex-snapshot
Relaxed purifying selection pressure drives accelerated and dynamic gene rearrangements in thrips (Insecta: Thysanoptera) mitochondrial genomes
inferred← citeshttps://doi.org/10.1016/j.jcz.2023.12.001openalex-snapshot
The complete mitochondrial genome of Erinaceus concolor (Mammalia: Eulipotyphla) from Türkiye with phylogenetic implications
inferred← citeshttps://doi.org/10.1016/j.margen.2016.10.006openalex-snapshot
Comparative mitogenomic analysis of three species of periwinkles: Littorina fabalis, L. obtusata and L. saxatilis
inferred← citeshttps://doi.org/10.1016/j.ympev.2004.01.004openalex-snapshot
Molecular phylogenetic relationships based on mitochondrial and nuclear gene sequences for the Todies (Todus, Todidae) of the Caribbean
inferred← citeshttps://doi.org/10.1016/j.ympev.2012.04.009openalex-snapshot
Multiple independent origins of mitochondrial control region duplications in the order Psittaciformes
inferred← citeshttps://doi.org/10.1016/j.ympev.2020.106857openalex-snapshot
Mitogenomics reveals phylogenetic relationships of Arcoida (Mollusca, Bivalvia) and multiple independent expansions and contractions in mitochondrial genome size
inferred← citeshttps://doi.org/10.1016/s0044-8486(03)00168-6openalex-snapshot
Comparative analysis of the mitochondrial DNA control region in cyprinids with different ploidy level
inferred← citeshttps://doi.org/10.1016/s0305-1978(96)00042-7openalex-snapshot
Insect mitochondrial control region: A review of its structure, evolution and usefulness in evolutionary studies
inferred← citeshttps://doi.org/10.1023/a:1020288812170openalex-snapshot
DNA Polymorphism in Population Genetics
inferred← citeshttps://doi.org/10.1038/s41437-024-00712-2openalex-snapshot
Drivers of interlineage variability in mitogenomic evolutionary rates in Platyhelminthes
inferred← citeshttps://doi.org/10.1038/sj.hdy.6800484openalex-snapshot
Mitochondrial genome size variation in New World and Old World populations of Drosophila melanogaster
inferred← citeshttps://doi.org/10.1046/j.1365-294x.1996.00078.xopenalex-snapshot
Highly conserved nuclear copies of the mitochondrial control region in the desert locust Schistocerca gregaria: some implications for population studies
inferred← citeshttps://doi.org/10.1046/j.1365-294x.1998.00495.xopenalex-snapshot
Mitochondrial DNA variable number tandem repeats (VNTRs): utility and problems in molecular ecology
inferred← citeshttps://doi.org/10.1046/j.1365-294x.1999.00528.xopenalex-snapshot
Genetic variation, population structure and cryptic species within the black mudfish, Neochanna diversus, an endemic galaxiid from New Zealand
inferred← citeshttps://doi.org/10.1046/j.1471-8278.2001.00093.xopenalex-snapshot
Large mitochondrial repeats multiplied during the polymerase chain reaction
inferred← citeshttps://doi.org/10.1073/pnas.95.5.2372openalex-snapshot
Aging, mating, and the evolution of mtDNA heteroplasmy in Drosophila melanogaster
inferred← citeshttps://doi.org/10.1080/00288330.2003.9517142openalex-snapshot
Population genetic structure of the Canterbury mudfish (Neochanna burrowsius) : Biogeography and conservation implications
inferred← citeshttps://doi.org/10.1080/00305316.2017.1323038openalex-snapshot
The complete mitochondrial genomes of Xyleutes mineus and Zeuzera multistrigata (Cossidae: Zeuzerinae): genome characterisation and phylogenetic implications
inferred← citeshttps://doi.org/10.1080/00305316.2018.1483847openalex-snapshot
The complete mitochondrial genomes of three populations in Luehdorfia chinensis (Leech, 1893) (Lepidoptera: Papilionidae), with a phylogenetic analysis of Papilionidae
inferred← citeshttps://doi.org/10.1080/106351598260671openalex-snapshot
Conflicting Phylogenetic Patterns Caused by Molecular Mechanisms in Mitochondrial DNA Sequences
inferred← citeshttps://doi.org/10.1080/19768354.2015.1105866openalex-snapshot
The complete mitogenome of the wood-feeding cockroachCryptocercus kyebangensis(Blattodea: Cryptocercidae) and phylogenetic relations among cockroach families
inferred← citeshttps://doi.org/10.1080/19768354.2016.1150877openalex-snapshot
Complete mitochondrial genome sequence of the Indian pipistrellePipistrellus coromandra(Vespertilioninae)
inferred← citeshttps://doi.org/10.1080/23802359.2016.1241675openalex-snapshot
Phylogeny analysis of complete mitochondrial DNA sequences for pelagic fishes from tuna fishery
inferred← citeshttps://doi.org/10.1080/24701394.2021.1885389openalex-snapshot
Detection of high heteroplasmy in complete loggerhead and hawksbill sea turtles mitochondrial genomes using RNAseq
inferred← citeshttps://doi.org/10.1086/725805openalex-snapshot
Disentangling Positive Selection from Relaxed Selection in Animal Mitochondrial Genomes
inferred← citeshttps://doi.org/10.1093/gbe/evab193openalex-snapshot
Mitogenomes of Accipitriformes and Cathartiformes Were Subjected to Ancestral and Recent Duplications Followed by Gradual Degeneration
inferred← citeshttps://doi.org/10.1093/gbe/evt119openalex-snapshot
Evolution Along the Mutation Gradient in the Dynamic Mitochondrial Genome of Salamanders
inferred← citeshttps://doi.org/10.1093/gbe/evx205openalex-snapshot
The Evolution of Dark Matter in the Mitogenome of Seed Beetles
inferred← citeshttps://doi.org/10.1093/genetics/138.2.471openalex-snapshot
Genetic analysis of systematic mitochondrial heteroplasmy in rabbits.
inferred← citeshttps://doi.org/10.1093/genetics/142.2.507openalex-snapshot
Differences in Crossover Frequency and Distribution Among Three Sibling Species of Drosophila
inferred← citeshttps://doi.org/10.1093/genetics/142.2.525openalex-snapshot
Length Variation, Heteroplasmy and Sequence Divergence in the Mitochondrial DNA of Four Species of Sturgeon (Acipenser)
inferred← citeshttps://doi.org/10.1093/genetics/146.3.1035openalex-snapshot
Evolution of Repeated Sequence Arrays in the D-Loop Region of Bat Mitochondrial DNA
inferred← citeshttps://doi.org/10.1093/genetics/148.4.1907openalex-snapshot
Heteroplasmy, Length and Sequence Variation in the mtDNA Control Regions of Three Percid Fish Species (Perca fluviatilis, Acerina cernua, Stizostedion lucioperca)
inferred← citeshttps://doi.org/10.1093/genetics/151.1.203openalex-snapshot
Organization of the Large Mitochondrial Genome in the Isopod Armadillidium vulgare
inferred← citeshttps://doi.org/10.1093/genetics/156.4.1933openalex-snapshot
Heteroplasmy in the mtDNA Control Region of Sturgeon (Acipenser, Huso and Scaphirhynchus)
inferred← citeshttps://doi.org/10.1093/genetics/160.3.1075openalex-snapshot
History of Infection With Different Male-Killing Bacteria in the Two-Spot Ladybird BeetleAdalia bipunctataRevealed Through Mitochondrial DNA Sequence Analysis
inferred← citeshttps://doi.org/10.1093/jhered/89.1.1openalex-snapshot
Tandem repeat polymorphism and heteroplasmy in the mitochondrial control region of redfishes (Sebastes: Scorpaenidae)
inferred← citeshttps://doi.org/10.1093/jisesa/ieaa138openalex-snapshot
Characterization and Phylogenetic Analysis of the Complete Mitochondrial Genome of Laelia suffusa (Lepidoptera: Erebidae, Lymantriinae)
inferred← citeshttps://doi.org/10.1093/molbev/msg190openalex-snapshot
Patterns and Relative Rates of Nucleotide and Insertion/Deletion Evolution at Six Chloroplast Intergenic Regions in New World Species of the Lecythidaceae
inferred← citeshttps://doi.org/10.1093/molbev/msn198openalex-snapshot
A Comparative Analysis of Mitochondrial Genomes in Coleoptera (Arthropoda: Insecta) and Genome Descriptions of Six New Beetles
inferred← citeshttps://doi.org/10.1093/molbev/msx167openalex-snapshot
Adaptive Patterns of Mitogenome Evolution Are Associated with the Loss of Shell Scutes in Turtles
inferred← citeshttps://doi.org/10.1093/oxfordjournals.molbev.a004055openalex-snapshot
The Complete Sequence of the Mitochondrial Genome of the Honeybee Ectoparasite Mite Varroa destructor (Acari: Mesostigmata)
inferred← citeshttps://doi.org/10.1093/oxfordjournals.molbev.a025640openalex-snapshot
Evolution of the mammalian mitochondrial control region--comparisons of control region sequences between monotreme and therian mammals
inferred← citeshttps://doi.org/10.1093/oxfordjournals.molbev.a025726openalex-snapshot
Large, rapidly evolving intergenic spacers in the mitochondrial DNA of the salamander family Ambystomatidae (Amphibia: Caudata)
inferred← citeshttps://doi.org/10.1093/oxfordjournals.molbev.a025728openalex-snapshot
Evolutionary dynamics of tandem repeats in the mitochondrial DNA control region of the minnow Cyprinella spiloptera
inferred← citeshttps://doi.org/10.1093/oxfordjournals.molbev.a025807openalex-snapshot
Marmoset phylogenetics, conservation perspectives, and evolution of the mtDNA control region
inferred← citeshttps://doi.org/10.1093/oxfordjournals.molbev.a025818openalex-snapshot
Nonneutral evolution of tandem repeats in the mitochondrial DNA control region of lagomorphs
inferred← citeshttps://doi.org/10.1093/oxfordjournals.molbev.a026158openalex-snapshot
The novel mitochondrial gene arrangement of the cattle tick, Boophilus microplus: fivefold tandem repetition of a coding region
inferred← citeshttps://doi.org/10.1101/2022.10.05.510972openalex-snapshot
Disentangling positive vs. relaxed selection in animal mitochondrial genomes
inferred← citeshttps://doi.org/10.1101/353565openalex-snapshot
Mitochondrial genomes and phylogenetic analysis of Central American weakly-electric fishes: Apteronotus rostratus, Brachyhypopomus occidentalis and Sternopygus dariensis
inferred← citeshttps://doi.org/10.1111/1748-5967.12639openalex-snapshot
The complete mitochondrial genome of Pardosa pusiola (Araneae, Lycosidae) and its phylogenetic implications
inferred← citeshttps://doi.org/10.1111/j.1095-8312.1997.tb01634.xopenalex-snapshot
Phylogeography of the bushmaster (Lachesis muta: Viperidae): implications for neotropical biogeography, systematics, and conservation
inferred← citeshttps://doi.org/10.1111/j.1365-2583.1996.tb00047.xopenalex-snapshot
The sequence and structure of the meadow grasshopper ( Chorthippus parallelus ) mitochondrial srRNA, ND2, COl, COll ATPase8 and 9 tRNA genes
inferred← citeshttps://doi.org/10.1111/j.1365-294x.1996.tb00317.xopenalex-snapshot
Highly conserved nuclear copies of the mitochondrial control region in the desert locust Schistocerca gregaria: some implications for population studies
inferred← citeshttps://doi.org/10.1111/j.1365-294x.2011.05134.xopenalex-snapshot
Variation in repeat length and heteroplasmy of the mitochondrial DNA control region along a core–edge gradient in the eastern spadefoot toad (Pelobates syriacus)
inferred← citeshttps://doi.org/10.1111/j.1439-0426.1999.tb00199.xopenalex-snapshot
Application of mtDNA d-loop region for the study of Russian sturgeon population structure from Iranian coastline of the Caspian Sea
inferred← citeshttps://doi.org/10.1111/j.1474-919x.2003.00206.xopenalex-snapshot
Identification of Lanius species and subspecies using tandem repeats in the mitochondrial DNA control region
inferred← citeshttps://doi.org/10.1111/j.1558-5646.1997.tb02403.xopenalex-snapshot
NUCLEOTYPIC EFFECT IN HOMEOTHERMS: BODY-MASS INDEPENDENT RESTING METABOLIC RATE OF PASSERINE BIRDS IS RELATED TO GENOME SIZE
inferred← citeshttps://doi.org/10.1111/j.1558-5646.2012.01830.xopenalex-snapshot
LOW METABOLIC RATES IN SALAMANDERS ARE CORRELATED WITH WEAK SELECTIVE CONSTRAINTS ON MITOCHONDRIAL GENES
inferred← citeshttps://doi.org/10.1111/jeb.12068openalex-snapshot
You are where you live: parasitic nematode mitochondrial genome size is associated with the thermal environment generated by hosts
inferred← citeshttps://doi.org/10.1111/mec.16138openalex-snapshot
Slow crabs ‐ fast genomes: Locomotory capacity predicts skew magnitude in crustacean mitogenomes
inferred← citeshttps://doi.org/10.1134/s0032945208020057openalex-snapshot
Hypervariability of the D-loop region in mitochondrial DNA of Russian sturgeon Acipenser gueldenstaedtii (Acipenseriformes, Acipenseridae)
inferred← citeshttps://doi.org/10.1139/g00-001openalex-snapshot
Tandemly repeated sequences in mtDNA control region of whitefish,Coregonus lavaretus
inferred← citeshttps://doi.org/10.1139/g06-030openalex-snapshot
Mitochondrial genomes ofVanhornia eucnemidarum(Apocrita: Vanhorniidae) andPrimeuchroeusspp. (Aculeata: Chrysididae): evidence of rearranged mitochondrial genomes within the Apocrita (Insecta: Hymenoptera)
inferred← citeshttps://doi.org/10.1139/g06-148openalex-snapshot
Mitochondrial genomic comparisons of the subterranean termites from the Genus Reticulitermes (Insecta: Isoptera: Rhinotermitidae)
inferred← citeshttps://doi.org/10.1146/annurev.ecolsys.29.1.23openalex-snapshot
PRINCIPLES OF PHYLOGEOGRAPHY AS ILLUSTRATED BY FRESHWATER AND TERRESTRIAL TURTLES IN THE SOUTHEASTERN UNITED STATES
inferred← citeshttps://doi.org/10.1146/annurev.ecolsys.32.081501.114109openalex-snapshot
The Units of Selection on Mitochondrial DNA
inferred← citeshttps://doi.org/10.1146/annurev.ecolsys.36.091704.175513openalex-snapshot
The Population Biology of Mitochondrial DNA and Its Phylogenetic Implications
inferred← citeshttps://doi.org/10.1163/1568539042948114openalex-snapshot
Tandem Repeat Polymorphism and Heteroplasmy in the Mitochondrial DNA Control Region of Threespine Stickleback (Gasterosteus Aculeatus)
inferred← citeshttps://doi.org/10.1186/s12862-026-02520-0openalex-snapshot
Comparative mitogenomics of freshwater snails of the genus Biomphalaria (Gastropoda: Planorbidae) and new insights into mitochondrial genome evolution in Hygrophila
inferred← citeshttps://doi.org/10.1186/s12864-017-3550-8openalex-snapshot
The mitochondrial genome sequences of the round goby and the sand goby reveal patterns of recent evolution in gobiid fish
inferred← citeshttps://doi.org/10.1186/s12864-020-07360-wopenalex-snapshot
Comparative mitogenome analyses uncover mitogenome features and phylogenetic implications of the subfamily Cobitinae
inferred← citeshttps://doi.org/10.1186/s12864-022-08607-4openalex-snapshot
Inverted base composition skews and discontinuous mitochondrial genome architecture evolution in the Enoplea (Nematoda)
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/s12864-024-10657-9openalex-snapshot
The mitochondrial genome of Bottapotamon fukienense (Brachiura: Potamidae) is fragmented into two chromosomes
inferred← citeshttps://doi.org/10.1206/518.1openalex-snapshot
Mitochondrial Intergenic Spacer in Fairy Basslets (Serranidae: Anthiinae) and the Simultaneous Analysis of Nucleotide and Rearrangement Data
inferred← citeshttps://doi.org/10.1266/ggs.75.79openalex-snapshot
Sequence variation and structural conservation in the D-loop region and flanking genes of mitochondrial DNA from Japanese pond frogs.
inferred← citeshttps://doi.org/10.12794/metadc2577openalex-snapshot
Mitochondrial DNA Sequence Variation in Populations of the Nine-Banded Armadillo (Dasypus novemcinctus)
inferred← citeshttps://doi.org/10.1360/n972016-00728openalex-snapshot
The evolutionary mechanism of genome size
inferred← citeshttps://doi.org/10.1371/journal.pone.0062943openalex-snapshot
Ancestral Gene Organization in the Mitochondrial Genome of Thyridosmylus langii (McLachlan, 1870) (Neuroptera: Osmylidae) and Implications for Lacewing Evolution
inferred← citeshttps://doi.org/10.1371/journal.pone.0153666openalex-snapshot
Characterization of the Complete Mitochondrial Genome Sequence of the Globose Head Whiptail Cetonurus globiceps (Gadiformes: Macrouridae) and Its Phylogenetic Analysis
inferred← citeshttps://doi.org/10.1371/journal.pone.0196466openalex-snapshot
Comparative analyses of the complete mitochondrial genomes of Dosinia clams and their phylogenetic position within Veneridae
inferred← citeshttps://doi.org/10.1371/journal.pone.0227831openalex-snapshot
Characterization of the complete mitochondrial genome of Orthaga olivacea Warre (Lepidoptera Pyralidae) and comparison with other Lepidopteran insects
inferred← citeshttps://doi.org/10.1371/journal.pone.0288991openalex-snapshot
The complete mitochondrial genome of Echinolaelaps fukienensis provide insights into phylogeny and rearrangement in the superfamily Dermanyssoidea
inferred← citeshttps://doi.org/10.1534/genetics.106.069518openalex-snapshot
Mitochondrial Genome Haplotype Hypervariation Within the Isopod Parasitic Nematode Thaumamermis cosgrovei
inferred← citeshttps://doi.org/10.1590/s1415-47572000000200019openalex-snapshot
Mitochondrial DNA polymorphism and heteroplasmy in populations of the three species of Tropidurus of the nanuzae group (Squamata, Tropiduridae)
inferred← citeshttps://doi.org/10.1590/s1415-47572008000200030openalex-snapshot
Phylogeny of the Serrasalmidae (Characiformes) based on mitochondrial DNA sequences
inferred← citeshttps://doi.org/10.17161/dt.v0i0.5559openalex-snapshot
Part H, Brachiopoda (Revised), vol. 1, References and Index
inferred← citeshttps://doi.org/10.2108/zsj.27.662openalex-snapshot
A Comparative Analysis of Mitochondrial Genomes in Orthoptera (Arthropoda: lnsecta) and Genome Descriptions of Three Grasshopper Species
inferred← citeshttps://doi.org/10.2108/zsj.29.90openalex-snapshot
Complete Mitochondrial Genome ofLocusta Migratoria Migratoria(Orthoptera: Oedipodidae): Three tRNA-Like Sequences on the N-Strand
inferred← citeshttps://doi.org/10.3105/1881-1019-27.2.81openalex-snapshot
Mitochondrial DNA Polymorphism in Bothrops alcatraz (Serpentes, Viperidae): Evidence from RFLP Analysis
inferred← citeshttps://doi.org/10.3109/19401736.2012.716051openalex-snapshot
The complete mitochondrial genome of the Spinetail Devilray,Mobula japanica
inferred← citeshttps://doi.org/10.3109/19401736.2014.892077openalex-snapshot
An examination of the origin and evolution of additional tandem repeats in the mitochondrial DNA control region of Japanese sika deer ( Cervus Nippon )
inferred← citeshttps://doi.org/10.3109/19401736.2014.895987openalex-snapshot
Structure and evolution of the Phasianidae mitochondrial DNA control region
inferred← citeshttps://doi.org/10.3109/19401736.2014.945581openalex-snapshot
Length variation and sequence divergence in mitochondrial control region of Schizothoracine (Teleostei: Cyperinidae) species
inferred← citeshttps://doi.org/10.3109/19401736.2015.1106496openalex-snapshot
Complete mitochondrial genome sequences of thirteen globally sourced strains of fruit fly ( Drosophila melanogaster ) form a powerful model for mitochondrial research
inferred← citeshttps://doi.org/10.3390/ani13030497openalex-snapshot
New Insights into the Origin and Evolution of Mysmenid Spiders (Araneae, Mysmenidae) Based on the First Four Complete Mitochondrial Genomes
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/ijms17060841openalex-snapshot
Comparative Mitogenomic Analysis of Species Representing Six Subfamilies in the Family Tenebrionidae
inferred← citeshttps://doi.org/10.3390/ijms24054362openalex-snapshot
Amblyopinae Mitogenomes Provide Novel Insights into the Paraphyletic Origin of Their Adaptation to Mudflat Habitats
inferred← citeshttps://doi.org/10.3390/insects12090820openalex-snapshot
Comparative Mitogenomic Analysis of Two Longhorn Beetles (Coleoptera: Cerambycidae: Lamiinae) with Preliminary Investigation into Phylogenetic Relationships of Tribes of Lamiinae
inferred← citeshttps://doi.org/10.35537/10915/122099openalex-snapshot
Filogeografía de Zaedyus pichiy (Mammalia, Xenarthra) y su correlación con el paleoclima del sur de Sudamérica
inferred← citeshttps://doi.org/10.3897/zookeys.1012.59035openalex-snapshot
Complete mitochondrial genome sequence of Lepus yarkandensis Günther, 1875 (Lagomorpha, Leporidae): characterization and phylogenetic analysis
inferred← citeshttps://doi.org/10.4001/003.022.0409openalex-snapshot
Complete Mitochondrial Genome of Diuraphis noxia (Hemiptera: Aphididae) from Nine Populations, SNP Variation between Populations, and Comparison with Other Aphididae Species
inferred← citeshttps://doi.org/10.4172/2167-1206.s1-006openalex-snapshot
Mitochondrial DNA- a Tool for Phylogenetic and Biodiversity Search in Equines
inferred← citeshttps://doi.org/10.4172/2332-2543.s1-006openalex-snapshot
Mitochondrial DNA- a Tool for Phylogenetic and Biodiversity Search in Equines
inferred← citeshttps://doi.org/10.4238/2015.november.18.27openalex-snapshot
Short Communication Complete mitochondrial genome and codon usage of the Nepalese whiskered bat Myotis muricola (Vespertilionidae)
inferred← citeshttps://doi.org/10.4238/gmr16019300openalex-snapshot
Complete mitochondrial genome of the Amur hedgehog Erinaceus amurensis (Erinaceidae) and higher phylogeny of the family Erinaceidae
inferred← citeshttps://doi.org/10.6084/m9.figshare.13578739openalex-snapshot
Additional file 1 of Comparative mitogenome analyses uncover mitogenome features and phylogenetic implications of the subfamily Cobitinae
inferred← citeshttps://doi.org/10.6084/m9.figshare.13578742openalex-snapshot
Additional file 2 of Comparative mitogenome analyses uncover mitogenome features and phylogenetic implications of the subfamily Cobitinae
inferred← citeshttps://doi.org/10.6084/m9.figshare.13578745openalex-snapshot
Additional file 3 of Comparative mitogenome analyses uncover mitogenome features and phylogenetic implications of the subfamily Cobitinae
inferred← citeshttps://doi.org/10.6084/m9.figshare.13578748openalex-snapshot
Additional file 4 of Comparative mitogenome analyses uncover mitogenome features and phylogenetic implications of the subfamily Cobitinae
inferred← citeshttps://doi.org/10.6084/m9.figshare.13578751openalex-snapshot
Additional file 5 of Comparative mitogenome analyses uncover mitogenome features and phylogenetic implications of the subfamily Cobitinae
inferred← citeshttps://doi.org/10.6084/m9.figshare.13578754openalex-snapshot
Additional file 6 of Comparative mitogenome analyses uncover mitogenome features and phylogenetic implications of the subfamily Cobitinae
inferred← citeshttps://doi.org/10.6084/m9.figshare.19793277openalex-snapshot
Additional file 1 of Inverted base composition skews and discontinuous mitochondrial genome architecture evolution in the Enoplea (Nematoda)
inferred← citeshttps://doi.org/10.6084/m9.figshare.19793280openalex-snapshot
Additional file 2 of Inverted base composition skews and discontinuous mitochondrial genome architecture evolution in the Enoplea (Nematoda)
inferred← citeshttps://doi.org/10.6084/m9.figshare.19793283openalex-snapshot
Additional file 3 of Inverted base composition skews and discontinuous mitochondrial genome architecture evolution in the Enoplea (Nematoda)
inferred← citeshttps://doi.org/10.6084/m9.figshare.19793286openalex-snapshot
Additional file 4 of Inverted base composition skews and discontinuous mitochondrial genome architecture evolution in the Enoplea (Nematoda)
inferred← citeshttps://doi.org/10.7150/ijbs.12358openalex-snapshot
The Complete Mitochondrial Genome of two Tetragnatha Spiders (Araneae: Tetragnathidae): Severe Truncation of tRNAs and Novel Gene Rearrangements in Araneae
inferred← citeshttps://doi.org/10.7717/peerj.18314openalex-snapshot
Comparative mitogenomics of Cheiracanthium species (Araneae: Cheiracanthiidae) with phylogenetic implication and evolutionary insights
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