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Structural elements highly preserved during the evolution of the D-loop-containing region in vertebrate mitochondrial DNA

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What this work says

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

inferredcites →https://doi.org/10.1002/j.1460-2075.1985.tb03817.xopenalex-snapshot
Replication priming and transcription initiate from precisely the same site in mouse mitochondrial DNA.
inferredcites →https://doi.org/10.1007/bf00333271openalex-snapshot
The copy number of Bacillus plasmid pRBH1 is negatively controlled by RepB protein
inferredcites →https://doi.org/10.1007/bf02101990openalex-snapshot
A new method for calculating evolutionary substitution rates
inferredcites →https://doi.org/10.1007/bf02115653openalex-snapshot
Mammalian genes as molecular clocks?
inferredcites →https://doi.org/10.1016/0012-1606(72)90051-6openalex-snapshot
Evolution of mitochondrial DNA sequences in Xenopus
inferredcites →https://doi.org/10.1016/0014-5793(87)80041-8openalex-snapshot
Achievements and perspectives of mitochondrial research
inferredcites →https://doi.org/10.1016/0022-2836(79)90384-xopenalex-snapshot
DNA-binding site of lac repressor probed by dimethylsulfate methylation of lac operator
inferredcites →https://doi.org/10.1016/0022-2836(86)90272-xopenalex-snapshot
Structural conservation and variation in the D-loop-containing region of vertebrate mitochondrial DNA
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)90244-7openalex-snapshot
Effects of point mutations on formation and structure of the RNA primer for ColE1 DNA replication
inferredcites →https://doi.org/10.1016/0092-8674(84)90282-4openalex-snapshot
Control of cole 1 plasmid replication: Enhancement of binding of RNA I to the primer transcript by the rom protein
inferredcites →https://doi.org/10.1016/0092-8674(85)90291-0openalex-snapshot
In vitro replication of human mitochondrial DNA: Accurate initiation at the origin of light-strand synthesis
inferredcites →https://doi.org/10.1016/0378-1119(83)90145-2openalex-snapshot
Intraspecific nucleotide sequence variability surrounding the origin of replication in human mitochondrial DNA
inferredcites →https://doi.org/10.1016/0378-1119(84)90019-2openalex-snapshot
The ori sequences of the mitochondrial genome of a wild-type yeast strain: number, location, orientation and structure
inferredcites →https://doi.org/10.1016/0378-1119(86)90188-5openalex-snapshot
Paramecium mitochondrial DNA sequences and RNA transcripts for cytochrome oxidase subunit I, URF1, and three ORFs adjacent to the replication origin
inferredcites →https://doi.org/10.1016/s0021-9258(18)33188-0openalex-snapshot
In vitro transcription of human mitochondrial DNA. Identification of specific light strand transcripts from the displacement loop region.
inferredcites →https://doi.org/10.1016/s0021-9258(18)89684-3openalex-snapshot
Characterization of an RNA polymerase activity from HeLa cell mitochondria, which initiates transcription at the heavy strand rRNA promoter and the light strand promoter in human mitochondrial DNA.
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/10.1038/290457a0openalex-snapshot
Sequence and organization of the human mitochondrial genome
inferredcites →https://doi.org/10.1038/294623a0openalex-snapshot
Base pairing of RNA I with its complementary sequence in the primer precursor inhibits ColE1 replication
inferredcites →https://doi.org/10.1073/pnas.76.4.1967openalex-snapshot
Rapid evolution of animal mitochondrial DNA.
inferredcites →https://doi.org/10.1073/pnas.78.10.6096openalex-snapshot
Plasmid ColE1 incompatibility determined by interaction of RNA I with primer transcript.
inferredcites →https://doi.org/10.1073/pnas.78.10.6116openalex-snapshot
Elongation of displacement-loop strands in human and mouse mitochondrial DNA is arrested near specific template sequences.
inferredcites →https://doi.org/10.1073/pnas.78.10.6319openalex-snapshot
Extensive polymorphism in the mitochondrial DNA of apes.
inferredcites →https://doi.org/10.1073/pnas.79.4.1083openalex-snapshot
Regulatory regions of two transport operons under nitrogen control: nucleotide sequences.
inferredcites →https://doi.org/10.1093/bioinformatics/1.3.167openalex-snapshot
ACNUC – a portable retrieval system for nucleic acid sequence databases: logical and physical designs and usage
inferredcites →https://doi.org/10.1093/nar/10.13.4035openalex-snapshot
The primary structure otE. coliRNA porymerase. Nucleotide sequence of the rpoC gene and amino acid sequence of the β′-sabunit
inferredcites →https://doi.org/10.1093/nar/13.2.645openalex-snapshot
The statistical distribution of nucleic acid similarities
inferredcites →https://doi.org/10.1093/nar/9.20.5411openalex-snapshot
Sequence and properties of the human KB cell and mouse L cell D-loop regions of mitochondrial DNA
inferredcites →https://doi.org/10.1128/jvi.49.1.190-199.1984openalex-snapshot
Structural analysis of the major immediate early gene of human cytomegalovirus
inferredcites →https://doi.org/10.1146/annurev.bi.53.070184.003041openalex-snapshot
TRANSCRIPTION OF THE MAMMALIAN MITOCHONDRIAL GENOME

What points at this work

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

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Molecular evidence for clear speciation of Tachysurus adiposalis complex in Northern and Central Taiwan
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Identification of a Novel Human Mitochondrial D-Loop RNA Species Which Exhibits Upregulated Expression Following Cellular Immortalization
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A Mitochondrial Control Region and CytochromebPhylogeny of Sika Deer (Cervus nippon) and Report of Tandem Repeats in the Control Region
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Molecular Systematics of the Western Rattlesnake, Crotalus viridis (Viperidae), with Comments on the Utility of the D-Loop in Phylogenetic Studies of Snakes
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Organization and Evolution of Mitochondrial DNA in Metazoa
inferred← citeshttps://doi.org/10.1007/978-981-97-3165-7_2openalex-snapshot
Mitochondrial Genes and Their Application in Fish Diversity Studies
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Evolution and structural conservation of the control region of insect mitochondrial DNA
inferred← citeshttps://doi.org/10.1007/bf00174041openalex-snapshot
Structure and evolution of teleost mitochondrial control regions
inferred← citeshttps://doi.org/10.1007/bf00312616openalex-snapshot
The complete and symmetric transcription of the main non coding region of rat mitochondrial genome: in vivo mapping of heavy and light transcripts
inferred← citeshttps://doi.org/10.1007/bf01429220openalex-snapshot
Molecular evolution and population genetics of Greater Caribbean green turtles (Chelonia mydas) as inferred from mitochondrial DNA control region sequences
inferred← citeshttps://doi.org/10.1007/bf02100116openalex-snapshot
Rates of molecular evolution and the fraction of nucleotide positions free to vary
inferred← citeshttps://doi.org/10.1007/bf02100199openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/bf02100200openalex-snapshot
Mitochondrial DNA evolution in lagomorphs: Origin of systematic heteroplasmy and organization of diversity in European rabbits
inferred← citeshttps://doi.org/10.1007/bf02407355openalex-snapshot
Generation of VNTRs and heteroplasmy by sequence turnover in the mitochondrial control region of two elephant seal species
inferred← citeshttps://doi.org/10.1007/bf02602930openalex-snapshot
The complete nucleotide sequence of theRattus norvegicus mitochondrial genome: Cryptic signals revealed by comparative analysis between vertebrates
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/pl00006487openalex-snapshot
Nucleotide Substitution Rate of Mammalian Mitochondrial Genomes
inferred← citeshttps://doi.org/10.1007/s00239-001-0063-4openalex-snapshot
Lineage Specificity of the Evolutionary Dynamics of the mtDNA D-Loop Region in Rodents
inferred← citeshttps://doi.org/10.1007/s00239-002-2379-0openalex-snapshot
Structure and Evolution of the Mitochondrial DNA Complete Control Region in the Lizard Lacerta dugesii (Lacertidae, Sauria)
inferred← citeshttps://doi.org/10.1007/s00239-004-0033-8openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s00239-009-9246-1openalex-snapshot
Structure and Conservation of Tandem Repeats in the Mitochondrial DNA Control Region of the Least Brook Lamprey (Lampetra aepyptera)
inferred← citeshttps://doi.org/10.1007/s00239-020-09962-0openalex-snapshot
Structural Variation of the Turtle Mitochondrial Control Region
inferred← citeshttps://doi.org/10.1007/s002390010070openalex-snapshot
Dynamics and Phylogenetic Implications of MtDNA Control Region Sequences in New World Jays (Aves: Corvidae)
inferred← citeshttps://doi.org/10.1007/s00300-024-03330-0openalex-snapshot
Wolf-dog hybrids in the eastern fringe Northern European wolf population on the background of increased hunting pressure
inferred← citeshttps://doi.org/10.1007/s10126-001-0076-4openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s10126-004-4062-5openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s10336-008-0316-8openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s10530-007-9161-6openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s10592-006-9123-zopenalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s10641-011-9947-3openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s10641-021-01175-8openalex-snapshot
Genetic diversity analysis of crucian carp (Carassius auratus) based on cyt b and D-loop-containing region around Hongze Lake
inferred← citeshttps://doi.org/10.1007/s10709-020-00107-1openalex-snapshot
Complete mitochondrial genome of a blue-tailed skink Plestiodon capito (Reptilia, Squamata, Scincidae) and comparison with other Scincidae lizards
inferred← citeshttps://doi.org/10.1007/s10914-006-9008-4openalex-snapshot
Systematics and Evolution of the Dasyurid Marsupial Genus Sminthopsis: II. The Murina Species Group
inferred← citeshttps://doi.org/10.1007/s11802-014-2150-3openalex-snapshot
Structure of mitochondrial DNA control region of Pholis fangi and its phylogenetic implication
inferred← citeshttps://doi.org/10.1007/s12253-011-9378-7openalex-snapshot
Association of mtDNA D-Loop Polymorphisms with Risk of Gastric Cancer in Chinese Population
inferred← citeshttps://doi.org/10.1007/s12526-019-00995-3openalex-snapshot
Population genetic structure of Thryssa kammalensis in the Chinese Seas inferred from control region sequences
inferred← citeshttps://doi.org/10.1007/s13258-010-0023-8openalex-snapshot
Organization and variation of the mitochondrial DNA control region in five Caprinae species
inferred← citeshttps://doi.org/10.1016/0014-4827(92)90424-7openalex-snapshot
A new chick mitochondrial DNA-binding protein exhibits sequence-specific interaction near heavy-strand replication origin: Cleavage activity, stimulation of mtDNA synthesis, and enhancement in transformed fibroblasts
inferred← citeshttps://doi.org/10.1016/0022-2836(90)90225-bopenalex-snapshot
Sequence and gene organization of the chicken mitochondrial genome
inferred← citeshttps://doi.org/10.1016/0022-2836(91)80123-copenalex-snapshot
Mitochondrial D-loop sequences are integrated in the rat nuclear genome
inferred← citeshttps://doi.org/10.1016/0305-0491(96)00118-6openalex-snapshot
Sequences and comparisons of duck mitochondrial DNA control regions
inferred← citeshttps://doi.org/10.1016/0378-1119(88)90156-4openalex-snapshot
Symmetric transcription of the replication origin of rat mitochondrial DNA
inferred← citeshttps://doi.org/10.1016/0378-1119(92)90189-vopenalex-snapshot
Rainbow trout mitochondrial DNA: sequence and structural characteristics of the non-coding control region and flanking tRNA genes
inferred← citeshttps://doi.org/10.1016/0378-1119(95)00122-mopenalex-snapshot
A 67-kDa protein binding to the curved DNA in the main regulatory region of the rat mitochondrial genome
inferred← citeshttps://doi.org/10.1016/0378-1119(95)00232-uopenalex-snapshot
Unique features in the mitochondrial D-loop region of the European seabass Dicentrarchus labrax
inferred← citeshttps://doi.org/10.1016/1055-7903(92)90014-8openalex-snapshot
Evolution of the salmonid mitochondrial control region
inferred← citeshttps://doi.org/10.1016/b978-012498315-1/50005-4openalex-snapshot
Mitochondrial Control Region Sequences as Tools for Understanding Evolution
inferred← citeshttps://doi.org/10.1016/j.bbabio.2008.09.003openalex-snapshot
20 years of human mtDNA pathologic point mutations: Carefully reading the pathogenicity criteria
inferred← citeshttps://doi.org/10.1016/j.bse.2009.09.003openalex-snapshot
Genetic diversity of silver pomfret (Pampus argenteus) populations from the China Sea based on mitochondrial DNA control region sequences
inferred← citeshttps://doi.org/10.1016/j.bse.2011.05.008openalex-snapshot
Structure of mitochondrial DNA control region and molecular phylogenetic relationship among three flounders of genus Pleuronectes
inferred← citeshttps://doi.org/10.1016/j.bse.2014.07.006openalex-snapshot
Population structure of the endangered Hume's pheasant (Syrmaticus humiae) inferred from a partial sequence of the mitochondrial DNA control region
inferred← citeshttps://doi.org/10.1016/j.bse.2016.10.004openalex-snapshot
Characterization and phylogenetic analysis of the complete mitogenome of Allactaga sibirica (Rodentia: Dipodidae)
inferred← citeshttps://doi.org/10.1016/j.bse.2016.10.010openalex-snapshot
Characterization of the complete mitochondrial genome of Phodopus roborovskii (Rodentia: Cricetidae) and systematic implications for Cricetinae phylogenetics
inferred← citeshttps://doi.org/10.1016/j.ecss.2019.106488openalex-snapshot
High genetic connectivity among pink shrimp Farfantepenaeus paulensis (Pérez-Farfante, 1967) groups along the south-southeastern coast of Brazil
inferred← citeshttps://doi.org/10.1016/j.fishres.2005.11.026openalex-snapshot
Population structure of bigeye tuna (Thunnus obesus) in the South China Sea, Philippine Sea and western Pacific Ocean inferred from mitochondrial DNA
inferred← citeshttps://doi.org/10.1016/j.fishres.2007.11.006openalex-snapshot
Population structure of bigeye tuna (Thunnus obesus) in the Indian Ocean inferred from mitochondrial DNA
inferred← citeshttps://doi.org/10.1016/j.fishres.2008.07.014openalex-snapshot
Population structure of albacore (Thunnus alalunga) in the Northwestern Pacific Ocean inferred from mitochondrial DNA
inferred← citeshttps://doi.org/10.1016/j.fishres.2010.03.015openalex-snapshot
Phylogeography of yellowfin tuna (Thunnus albacares) in the Western Pacific and the Western Indian Oceans inferred from mitochondrial DNA
inferred← citeshttps://doi.org/10.1016/j.fishres.2014.10.004openalex-snapshot
Integrating genetic and otolith microchemistry data to understand population structure in the Patagonian Hoki (Macruronus magellanicus)
inferred← citeshttps://doi.org/10.1016/j.gene.2006.03.028openalex-snapshot
Finding Nemo: Molecular phylogeny and evolution of the unusual life style of anemonefish
inferred← citeshttps://doi.org/10.1016/j.gene.2016.10.003openalex-snapshot
Mitochondrial genome of Cricetulus migratorius (Rodentia: Cricetidae): Insights into the characteristics of the mitochondrial genome and the phylogenetic relationships of Cricetulus species
inferred← citeshttps://doi.org/10.1016/j.heliyon.2019.e03079openalex-snapshot
Molecular analysis of population and De Novo transcriptome sequencing of Thai medaka, Oryzias minutillus (Teleostei: Adrianichthyidae)
inferred← citeshttps://doi.org/10.1016/j.jasrep.2016.11.006openalex-snapshot
Use of next-generation molecular tools in archaeological neotropical deer sample analysis
inferred← citeshttps://doi.org/10.1016/j.livsci.2009.03.001openalex-snapshot
Mitochondrial D-loop nucleotide sequences of Egyptian river buffalo: Variation and phylogeny studies
inferred← citeshttps://doi.org/10.1016/j.mambio.2008.09.002openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.mambio.2014.04.005openalex-snapshot
Admixture of two phylogeographic lineages of the Eurasian beaver in Poland
inferred← citeshttps://doi.org/10.1016/j.mambio.2019.09.008openalex-snapshot
Prevalence of zoonotic parasites in an endangered Iberian wolf (Canis lupus signatus) population in Portugal
inferred← citeshttps://doi.org/10.1016/j.mito.2018.04.002openalex-snapshot
Mitochondrial haplotypes are not associated with mice selectively bred for high voluntary wheel running
inferred← citeshttps://doi.org/10.1016/j.rsma.2023.103085openalex-snapshot
The complete mitochondrial genome and the transfer RNA gene rearrangement of Sillago sinica (Perciformes, Sillaginidae), with reference to the evolution of related species
inferred← citeshttps://doi.org/10.1016/j.smallrumres.2022.106690openalex-snapshot
Examination of D-loop region and DBY gene as tools for identifying hybridisation in alpacas (Vicugna pacos) based on Polish populations
inferred← citeshttps://doi.org/10.1016/j.toxicon.2022.106933openalex-snapshot
Polymerase chain reaction-based snake origin tracing in commercial venom crystals by targeting the mitochondrial D-loop
inferred← citeshttps://doi.org/10.1016/j.ygeno.2019.09.016openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.ygeno.2022.110297openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.ympev.2009.12.021openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.ympev.2019.106711openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/s0378-1119(97)00404-6openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/s0378-1119(99)00270-xopenalex-snapshot
Evolutionary genomics in Metazoa: the mitochondrial DNA as a model system
inferred← citeshttps://doi.org/10.1016/s0921-8777(99)00030-0openalex-snapshot
Terminal branch haplotype analysis: a novel approach to investigate newly arisen variants of mitochondrial DNA in natural populations
inferred← citeshttps://doi.org/10.1016/s1055-7903(03)00190-8openalex-snapshot
Molecular phylogeny of the Gasterosteidae: the importance of using multiple genes
inferred← citeshttps://doi.org/10.1016/s1055-7903(03)00221-5openalex-snapshot
Analysis of mitochondrial D-loop region casts new light on domestic water buffalo (Bubalus bubalis) phylogeny
inferred← citeshttps://doi.org/10.1023/a:1008154027997openalex-snapshot
Detection and cDNA cloning of H-strand mitochondrial regulatory region RNAs in cultured human cells and human tissues
inferred← citeshttps://doi.org/10.1023/a:1011322031747openalex-snapshot
Systematics and Evolution of the Dasyurid Marsupial Genus Sminthopsis: I. The Macroura Species Group
inferred← citeshttps://doi.org/10.1038/s41598-025-89478-zopenalex-snapshot
Insight into mtDNA diversity of wild forest musk deer (Moschus berezovskii) in Shanxi Province mountains
inferred← citeshttps://doi.org/10.1046/j.1365-294x.1998.00303.xopenalex-snapshot
Conservation genetics of the endangered Pampas deer (Ozotoceros bezoarticus)
inferred← citeshttps://doi.org/10.1046/j.1365-294x.1999.00825.xopenalex-snapshot
Mitochondrial DNA phylogeography and population history of the grey wolfCanis lupus
inferred← citeshttps://doi.org/10.1080/00222930601129463openalex-snapshot
Taxonomic implications from phylogenetic relationships of subspecies ofSchizopygopsis malacanthus(Pisces: Cyprinidae) based on sequence analysis of cytochromeband mitochondrial DNA control region
inferred← citeshttps://doi.org/10.1080/00222933.2010.501911openalex-snapshot
Mitochondrial DNA genetic variation and phylogeography of the recently described vole speciesProedromys liangshanensisLiu, Sun, Zeng and Zhao, 2007 (Rodentia: Arvicolinae)
inferred← citeshttps://doi.org/10.1080/17451000.2022.2096902openalex-snapshot
Deep genetic divergence in Randall’s threadfin bream Nemipterus randalli Russell, 1986 population from northern Bay of Bengal inferred by mtDNA sequences
inferred← citeshttps://doi.org/10.1080/24701394.2026.2723762openalex-snapshot
Genetic diversity and population structure of crescent perch, Terapon jarbua (Forsskål, 1775), along the Indian coast: insights from mitochondrial D-loop analysis
inferred← citeshttps://doi.org/10.1086/344910openalex-snapshot
Unequal Transmission of Mitochondrial Haplotypes in Natural Populations of Field Mice with XY Females (GenusAkodon)
inferred← citeshttps://doi.org/10.1093/genetics/128.3.607openalex-snapshot
Length and sequence variation in evening bat D-loop mtDNA.
inferred← citeshttps://doi.org/10.1093/jhered/89.5.415openalex-snapshot
Shallow population histories in deep evolutionary lineages of marine fishes: insights from sardines and anchovies and lessons for conservation
inferred← citeshttps://doi.org/10.1093/jhered/91.3.247openalex-snapshot
Molecular phylogeny of Philippine freshwater sardines based on mitochondrial DNA analysis
inferred← citeshttps://doi.org/10.1093/jhered/esi037openalex-snapshot
Structure of the Mitochondrial Control Region of the Eurasian Otter (Lutra lutra; Carnivora, Mustelidae): Patterns of Genetic Heterogeneity and Implications for Conservation of the Species in Italy
inferred← citeshttps://doi.org/10.1093/molbev/msg061openalex-snapshot
DNA Sequence Variation in the Mitochondrial Control Region of Subterranean Mole Rats, Spalax ehrenbergi Superspecies, in Israel
inferred← citeshttps://doi.org/10.1093/molbev/msq345openalex-snapshot
Novel Protein Genes in Animal mtDNA: A New Sex Determination System in Freshwater Mussels (Bivalvia: Unionoida)?
inferred← citeshttps://doi.org/10.1093/nar/17.21.8803openalex-snapshot
Sequence-dependent DNA curvature: conformational signal present in the main regulatory region of the rat mitochondrial genome
inferred← citeshttps://doi.org/10.1093/nar/18.3.411openalex-snapshot
Organization of the mitochondrial genome of Atlantic cod, Gadusmorhua
inferred← citeshttps://doi.org/10.1093/nar/gkh634openalex-snapshot
Twinkle and POLG defects enhance age-dependent accumulation of mutations in the control region of mtDNA
inferred← citeshttps://doi.org/10.1093/nar/gkq865openalex-snapshot
Identification of species by multiplex analysis of variable-length sequences
inferred← citeshttps://doi.org/10.1093/nar/gkv299openalex-snapshot
Are mutagenic non D-loop direct repeat motifs in mitochondrial DNA under a negative selection pressure?
inferred← citeshttps://doi.org/10.1093/oxfordjournals.molbev.a003935openalex-snapshot
DNA Sequence Variation in the Mitochondrial Control Region of Red-Backed Voles (Clethrionomys)
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.a025750openalex-snapshot
Structural conservation and variation in the mitochondrial control region of fringilline finches (Fringilla spp.) and the greenfinch (Carduelis chloris)
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.a040007openalex-snapshot
Intraspecific DNA sequence variation of the mitochondrial control region of white sturgeon (Acipenser transmontanus).
inferred← citeshttps://doi.org/10.1093/oxfordjournals.molbev.a040096openalex-snapshot
Patterns of sequence variation in the mitochondrial D-loop region of shrews.
inferred← citeshttps://doi.org/10.1093/oxfordjournals.molbev.a040662openalex-snapshot
Evolution of the cetacean mitochondrial D-loop region.
inferred← citeshttps://doi.org/10.1098/rstb.1996.0074openalex-snapshot
Mitochondrial phylogeography of rock-dwelling cichlid fishes reveals evolutionary influence of historical lake level fluctuations of Lake Tanganyika, Africa
inferred← citeshttps://doi.org/10.1101/2023.12.04.569906openalex-snapshot
Wolf-dog hybrids arise: new insight into the eastern fringe of the Northern European wolf population
inferred← citeshttps://doi.org/10.1101/819557openalex-snapshot
Phylogeography of two Andean frogs: Test of vicariance versus elevational gradient models of diversification
inferred← citeshttps://doi.org/10.1111/j.1095-8312.2003.00304.xopenalex-snapshot
Subtle population genetic structure in the Hawaiian grouper, Epinephelus quernus (Serranidae) as revealed by mitochondrial DNA analyses
inferred← citeshttps://doi.org/10.1111/j.1095-8649.2007.01748.xopenalex-snapshot
Genetic structure of the killifish Aphanius fasciatus, Nardo 1827 (Teleostei, Cyprinodontidae), results of mitochondrial DNA analysis
inferred← citeshttps://doi.org/10.1111/j.1365-2052.2008.01805.xopenalex-snapshot
Genetic diversity of captive forest musk deer ( Moschus berezovskii ) inferred from the mitochondrial DNA control region
inferred← citeshttps://doi.org/10.1111/j.1365-294x.1995.tb00271.xopenalex-snapshot
Intraspecific phylogeography of the gopher tortoise, Gopherus polyphemus: RFLP analysis of amplified mtDNA segments
inferred← citeshttps://doi.org/10.1111/j.1365-294x.2005.02704.xopenalex-snapshot
Mitochondrial phylogeography of the Eurasian beaverCastor fiberL.
inferred← citeshttps://doi.org/10.1111/j.1365-294x.2008.03733.xopenalex-snapshot
Pleistocene climatic cycling and diversification of the Andean treefrog, Hypsiboas andinus
inferred← citeshttps://doi.org/10.1111/j.1439-0388.2007.00674.xopenalex-snapshot
Distribution of nuclear mitochondrial DNA in cattle nuclear genome
inferred← citeshttps://doi.org/10.1111/j.1469-7998.2009.00635.xopenalex-snapshot
Population history of the plateau pika endemic to the Qinghai‐Tibetan Plateau based on mtDNA sequence data
inferred← citeshttps://doi.org/10.1111/mec.13349openalex-snapshot
Population structure within an alpine archipelago: strong signature of past climate change in the N ew Z ealand rock wren ( X enicus gilviventris)
inferred← citeshttps://doi.org/10.1111/syen.12071openalex-snapshot
How to sequence and annotate insect mitochondrial genomes for systematic and comparative genomics research
inferred← citeshttps://doi.org/10.1126/science.276.5319.1687openalex-snapshot
Multiple and Ancient Origins of the Domestic Dog
inferred← citeshttps://doi.org/10.1134/s1022795409040115openalex-snapshot
Genetic variation of Manchurian pheasant (Phasianus colchicus pallasi Rotshild, 1903) inferred from mitochondrial DNA control region sequences
inferred← citeshttps://doi.org/10.1134/s1022795424700741openalex-snapshot
Genome Survey of Odontamblyopus sp. for Providing a New Basis for Taxonomy and Demographic History
inferred← citeshttps://doi.org/10.1134/s1062359023602240openalex-snapshot
Population Genetic Structure of the Wolf (Canis lupus L.) in Eastern Fennoscandia under Conditions of Intensive Hunting Pressure Based on mtDNA Analysis
inferred← citeshttps://doi.org/10.1139/f92-263openalex-snapshot
Population Genetic Structure of the Armorhead,Pseudopentaceros wheeleri, in the North Pacific Ocean: Application of the Polymerase Chain Reaction to Fisheries problems
inferred← citeshttps://doi.org/10.11606/t.87.2020.tde-13052022-132534openalex-snapshot
Marcadores moleculares aplicados aos estudos genéticos de peixes-de-bico do Atlântico ocidental: aspectos populacionais e técnicas forenses para manejo e conservação
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/s12864-016-3054-yopenalex-snapshot
Structure and variation of the mitochondrial genome of fishes
inferred← citeshttps://doi.org/10.1186/s12864-017-3626-5openalex-snapshot
Evolutionarily recent, insertional fission of mitochondrial cox2 into complementary genes in bilaterian Metazoa
inferred← citeshttps://doi.org/10.1201/9780203021415-13openalex-snapshot
Computational Methods for Studying the Evolution of the Mitochondrial Genome
inferred← citeshttps://doi.org/10.1201/9780203021415.ch10openalex-snapshot
Computational Methods for Studying the Evolution of the Mitochondrial Genome
inferred← citeshttps://doi.org/10.1201/b11009-6openalex-snapshot
Estimating connectivity in marine fish populations
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/10.1266/ggs.86.325openalex-snapshot
Population genetic structure of the striped silverside, Atherinomorus endrachtensis (Atherinidae, Atheriniformes, Teleostei), inhabiting marine lakes and adjacent lagoons in Palau: marine lakes are “Islands” for marine species
inferred← citeshttps://doi.org/10.13057/biodiv/d210624openalex-snapshot
The very low genetic variability on Aceh Tamiang’s (Indonesia) population of Painted Terrapin (Batagur borneoensis) inferred by cytochrome oxidase I (CO I) and D-loop (control region)
inferred← citeshttps://doi.org/10.1371/journal.pone.0019365openalex-snapshot
Evidence for a Fourteenth mtDNA-Encoded Protein in the Female-Transmitted mtDNA of Marine Mussels (Bivalvia: Mytilidae)
inferred← citeshttps://doi.org/10.1371/journal.pone.0063334openalex-snapshot
The Complete Mitochondrial Genome of Bean Goose (Anser fabalis) and Implications for Anseriformes Taxonomy
inferred← citeshttps://doi.org/10.1371/journal.pone.0123894openalex-snapshot
Mitochondrial DNA Genomes Organization and Phylogenetic Relationships Analysis of Eight Anemonefishes (Pomacentridae: Amphiprioninae)
inferred← citeshttps://doi.org/10.1371/journal.pone.0230433openalex-snapshot
What does the wolf eat? Assessing the diet of the endangered Iberian wolf (Canis lupus signatus) in northeast Portugal
inferred← citeshttps://doi.org/10.1534/genetics.103.026187openalex-snapshot
Evidence That the Large Noncoding Sequence Is the Main Control Region of Maternally and Paternally Transmitted Mitochondrial Genomes of the Marine Mussel (Mytilus spp.)
inferred← citeshttps://doi.org/10.15760/etd.5812openalex-snapshot
Analysis of mitochondrial DNA restriction fragment patterns in killer whales, Orcinus orca
inferred← citeshttps://doi.org/10.1643/h2022056openalex-snapshot
Male Dispersal Drives Gene Flow in Timber Rattlesnakes (Crotalus horridus)
inferred← citeshttps://doi.org/10.1644/1545-1542(2005)86[1059:gvapso]2.0.co;2openalex-snapshot
GENETIC VARIATION AND POPULATION STRUCTURE OF THE EURASIAN BEAVER CASTOR FIBER IN EASTERN EUROPE AND ASIA
inferred← citeshttps://doi.org/10.1644/brb-028openalex-snapshot
PHYLOGEOGRAPHY, POPULATION STRUCTURE, AND IMPLICATIONS FOR CONSERVATION OF WHITE-TAILED DEER (ODOCOILEUS VIRGINIANUS) IN VENEZUELA
inferred← citeshttps://doi.org/10.2174/1874402801407010006openalex-snapshot
Forensic Wildlife Parts and their Product Identification and Individualization Using DNA Barcoding
inferred← citeshttps://doi.org/10.2298/bah1101001ropenalex-snapshot
Characterization of two Egyptian native chicken breeds using genetic and immunological parameters
inferred← citeshttps://doi.org/10.2307/4089039openalex-snapshot
Lack of Restriction-Site Variation in Mitochondrial-DNA Control Region of Whooping Cranes (Grus americana)
inferred← citeshttps://doi.org/10.2331/fishsci.63.906openalex-snapshot
High Sequence Variability in the Mitochondrial DNA Control Region of the Japanese Flounder Paralichthys olivaceus
inferred← citeshttps://doi.org/10.24275/uami.5q47rn88vopenalex-snapshot
Análisis filogeográfico del pez blanco Chirostoma humboldtianum (Valenciennes, 1835) (Pisces: Atheriniformes: Atherinopsidae)
inferred← citeshttps://doi.org/10.25268/bimc.invemar.2008.37.1.183openalex-snapshot
CARACTERIZACIÓN GENÉTICA DE LA COLONIA REPRODUCTIVA DE LA TORTUGA MARINA GOLFINA –LEPIDOCHELYS OLIVACEA– en el PARQUE NACIONAL NATURAL GORGONA (PACÍFICO COLOMBIANO) A PARTIR DE SECUENCIAS DE ADN MITOCONDRIAL
inferred← citeshttps://doi.org/10.26686/wgtn.16997824openalex-snapshot
Characterisation of the Mitochondrial Genome and the Phylogeographic Structure of Blue Cod (Parapercis colias)
inferred← citeshttps://doi.org/10.26686/wgtn.16997824.v1openalex-snapshot
Characterisation of the Mitochondrial Genome and the Phylogeographic Structure of Blue Cod (Parapercis colias)
inferred← citeshttps://doi.org/10.2984/68.2.3openalex-snapshot
Genetic Diversity and Population Structure of Pronghorn Spiny Lobster Panulirus penicillatus in the Pacific Region1
inferred← citeshttps://doi.org/10.2991/absr.k.220406.047openalex-snapshot
CO2 Mitochondrial Gene Identification of Nisaetus cirrhatus as a Part of Indonesian Elang Brontok Genetic Conservation
inferred← citeshttps://doi.org/10.3109/19401730903180112openalex-snapshot
The structure of the Australian and South American marsupial mitochondrial control region
inferred← citeshttps://doi.org/10.3109/19401731003681103openalex-snapshot
Structure, organization and nucleotide diversity of the mitochondrial control region and cytochromebof southern water vole (Arvicola sapidus)
inferred← citeshttps://doi.org/10.3109/19401736.2012.668896openalex-snapshot
Structure of mitochondrial DNA control region ofFenneropenaeus chinensisand phylogenetic relationship among different populations
inferred← citeshttps://doi.org/10.3109/19401736.2012.710202openalex-snapshot
Genetic diversity and demographical history ofCoilia ectenes(Clupeiformes: Engraulidae) inferred from the complete control region sequences of mitochondrial DNA
inferred← citeshttps://doi.org/10.3109/19401736.2012.731401openalex-snapshot
Special structure of mitochondrial DNA control region and phylogenetic relationship among individuals of the black rockfish,Sebastes schlegelii
inferred← citeshttps://doi.org/10.3109/19401736.2013.766176openalex-snapshot
Molecular characteristics and evolution of the mitochondrial control region in three genera (Hipposideridae:HipposiderosAselliscusandCoelops) of leaf-nosed bats
inferred← citeshttps://doi.org/10.3109/19401736.2014.908355openalex-snapshot
Population genetic diversity of the northern snakehead (Channa argus) in China based on the mitochondrial DNA control region and adjacent regions sequences
inferred← citeshttps://doi.org/10.3109/24701394.2016.1149828openalex-snapshot
Genetic diversity of the captive Asian tapir population in Thailand, based on mitochondrial control region sequence data and the comparison of its nucleotide structure with Brazilian tapir
inferred← citeshttps://doi.org/10.31390/gradschool_dissertations.3963openalex-snapshot
Patterns of nucleotide substitution within and among mitochondrial gene regions in sea star (Leptasterias spp)
inferred← citeshttps://doi.org/10.31489/2026feb3/30-42openalex-snapshot
Evidence for asymmetric DNA strand inheritance in vertebrate mitochondria
inferred← citeshttps://doi.org/10.3161/15081109acc2019.21.2.004openalex-snapshot
Genetic Structure Associated with the Ecological Traits of Four Species of Phyllostomid Bats Inhabiting Selva El Ocote Biosphere Reserve, Chiapas, México
inferred← citeshttps://doi.org/10.31857/s1026347022600960openalex-snapshot
Eastern Fennoscandian Wolf (Canis lupus L.) under the Heavy Hunting Pressure: mtDNA Analysis as a Tool to Assess Hunting Impact on the Population-Genetic Structure
inferred← citeshttps://doi.org/10.3201/eid2601.191284openalex-snapshot
High Pathogenicity of Nipah Virus fromPteropus lyleiFruit Bats, Cambodia
inferred← citeshttps://doi.org/10.3354/meps07381openalex-snapshot
Lack of genetic differentiation of blue spiny lobster Panulirus inflatus along the Pacific coast of Mexico inferred from mtDNA sequences
inferred← citeshttps://doi.org/10.3389/fanim.2025.1732717openalex-snapshot
Maternal lineage diversity and genetic relationships of Sukuma chicken ecotype with other Tanzanian indigenous chickens based on mitochondrial DNA D-loop region
inferred← citeshttps://doi.org/10.3389/fmicb.2020.01807openalex-snapshot
Sequencing the Genome of Indian Flying Fox, Natural Reservoir of Nipah Virus, Using Hybrid Assembly and Conservative Secondary Scaffolding
inferred← citeshttps://doi.org/10.3390/ani13132191openalex-snapshot
mtDNA CR Evidence Indicates High Genetic Diversity of Captive Forest Musk Deer in Shaanxi Province, China
inferred← citeshttps://doi.org/10.3390/ani15152254openalex-snapshot
Genetic Diversity and Population Structure of Tufted Deer (Elaphodus cephalophus) in Chongqing, China
inferred← citeshttps://doi.org/10.3390/ani15213070openalex-snapshot
Phylogenetic Analysis of Indian Dromedary Breeds Based on the Mitochondrial D-Loop Marker
inferred← citeshttps://doi.org/10.3390/biology12040520openalex-snapshot
Conservation Genetics of the Critically Endangered Southern River Terrapin (Batagur affinis) in Malaysia: Genetic Diversity and Novel Subspecies Distribution Ranges
inferred← citeshttps://doi.org/10.3390/genes13010125openalex-snapshot
Characterisation of the Complete Mitochondrial Genome of Critically Endangered Mustela lutreola (Carnivora: Mustelidae) and Its Phylogenetic and Conservation Implications
inferred← citeshttps://doi.org/10.3390/genes13081470openalex-snapshot
Evolution of the Noncoding Features of Sea Snake Mitochondrial Genomes within Elapidae
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/10.35537/10915/2335openalex-snapshot
Desarrollo de marcadores moleculares nucleares y mitocondriales y análisis genético de poblaciones de guanaco de la Patagonia argentina
inferred← citeshttps://doi.org/10.35537/10915/34362openalex-snapshot
Estudios filogeográficos en Dasypodidae (Mammalia, Xenarthra) de Argentina: Chaetophractus villosus y Chaetophractus vellerosus como modelos de análisis
inferred← citeshttps://doi.org/10.3724/sp.j.1035.2009.00378openalex-snapshot
COMPARATIVE ANALYSIS OF THE MITOCHONDRIAL DNA CONTROL REGION IN DONGTINGKING CRUCIAN CARP AND OTHER SIX STRAINS OF CARASSIUS AURATUS
inferred← citeshttps://doi.org/10.3897/zookeys.705.11852openalex-snapshot
Complete mitochondrial genomes from two species of Chinese freshwater crabs of the genus Sinopotamon recovered using next-generation sequencing reveal a novel gene order (Brachyura, Potamidae)
inferred← citeshttps://doi.org/10.4238/2012.may.9.1openalex-snapshot
Genetic diversity of Setipinna taty (Engraulidae) populations from the China Sea based on mitochondrial DNA control region sequences
inferred← citeshttps://doi.org/10.4238/gmr16018266openalex-snapshot
Mitochondrial DNA insertions in the nuclear Capra hircus genome
inferred← citeshttps://doi.org/10.4314/ajb.v7i21.59454openalex-snapshot
Genetic variation and population structure of willowy flounder Tanakius kitaharai collected from Aomori, Ibaraki and Niigata in Northern Japan
inferred← citeshttps://doi.org/10.46754/umtjur.v2i2.146openalex-snapshot
POPULATION GENETICS OF LONGTAIL TUNA (Thunnus tonggol) (BLEEKER, 1851) FROM EAST MALAYSIA BASED ON MITOCHONDRIAL DNA D-LOOP MARKER
inferred← citeshttps://doi.org/10.53846/goediss-65openalex-snapshot
Phylogenetische Entwicklung asiatischer Wasserbüffel anhand Polymorphismen in der mitochondrialen D-loop Region
inferred← citeshttps://doi.org/10.5897/ajb11.3556openalex-snapshot
Structure of mitochondrial DNA control region of Argyrosomus amoyensis and molecular phylogenetic relationship among six species of Sciaenidae
inferred← citeshttps://doi.org/10.70675/1d48c518zc27bz4a6cz88eaz24d9d6f3e68copenalex-snapshot
Caractérisation génétique de la race de mouton Awassi du Liban en utilisant comme marqueurs des rétrovirus endogènes et l’ADN mitochondrial
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