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Organization and Evolution of the Mitochondrial DNA Control Region in the Avian Genus Alectoris

https://doi.org/10.1007/pl00006402
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What this work says

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

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A novel endoribonuclease cleaves at a priming site of mouse mitochondrial DNA replication.
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A Stochastic Model for the Evolution of Autocorrelated DNA Sequences
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A Mitochondrial CytochromeBPhylogeny of theAlectorisPartridges
inferredcites →https://doi.org/10.1007/978-1-4020-6754-9_12413openalex-snapshot
PAUP (phylogenetic analysis using parsimony)
inferredcites →https://doi.org/10.1007/bf00160154openalex-snapshot
Maximum likelihood phylogenetic estimation from DNA sequences with variable rates over sites: Approximate methods
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Rapid evolution of a heteroplasmic repetitive sequence in the mitochondrial DNA control region of carnivores
inferredcites →https://doi.org/10.1007/bf00170460openalex-snapshot
Transcribed heteroplasmic repeated sequences in the porcine mitochondrial DNA D-loop region
inferredcites →https://doi.org/10.1007/bf00175505openalex-snapshot
Endotherms, ectotherms, and mitochondrial genome-size variation
inferredcites →https://doi.org/10.1007/bf00175506openalex-snapshot
Molecular characterization and evolution of a duck mitochondrial genome
inferredcites →https://doi.org/10.1007/bf00178871openalex-snapshot
Sequence evolution in and around the mitochondrial control region in birds
inferredcites →https://doi.org/10.1007/bf00311887openalex-snapshot
Nucleotide sequence of the sheep mitochondrial DNA D-loop and its flanking tRNA genes
inferredcites →https://doi.org/10.1007/bf00313080openalex-snapshot
Gene organization of the Peking duck mitochondrial genome
inferredcites →https://doi.org/10.1007/bf00326158openalex-snapshot
Variable numbers of simple tandem repeats make birds of the order Ciconiiformes heteroplasmic in their mitochondrial genomes
inferredcites →https://doi.org/10.1007/bf02099853openalex-snapshot
Structural elements highly preserved during the evolution of the D-loop-containing region in vertebrate mitochondrial DNA
inferredcites →https://doi.org/10.1007/bf02100199openalex-snapshot
The main regulatory region of mammalian mitochondrial DNA: Structure-function model and evolutionary pattern
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/bf02101694openalex-snapshot
Dating of the human-ape splitting by a molecular clock of mitochondrial DNA
inferredcites →https://doi.org/10.1007/bf02515387openalex-snapshot
Nucleotide sequence and evolution of coding and noncoding regions of a quail mitochondrial genome
inferredcites →https://doi.org/10.1016/0014-5793(85)80122-8openalex-snapshot
Rapid isolation of animal mitochondrial DNA by alkaline extraction
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/10.1016/0022-2836(90)90225-bopenalex-snapshot
Sequence and gene organization of the chicken mitochondrial genome
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Among-site rate variation and its impact on phylogenetic analyses
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Molecular Evolution of the Mitochondrial Genome
inferredcites →https://doi.org/10.1016/b978-012498315-1/50005-4openalex-snapshot
Mitochondrial Control Region Sequences as Tools for Understanding Evolution
inferredcites →https://doi.org/10.1016/s0021-9258(18)99096-4openalex-snapshot
The transcription of DNA in chicken mitochondria initiates from one major bidirectional promoter
inferredcites →https://doi.org/10.1016/s0074-7696(08)62066-5openalex-snapshot
Animal Mitochondrial DNA: Structure and Evolution
inferredcites →https://doi.org/10.1016/s0074-7696(08)62067-7openalex-snapshot
Transcription and Replication of Animal Mitochondrial DNAs
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/10.1046/j.1365-294x.1997.00149.xopenalex-snapshot
Genetic differences between the endangered San Clemente Island loggerhead shrike Lanius ludovicianus mearnsi and two neighbouring subspecies demonstrated by mtDNA control region and cytochrome b sequence variation
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.91.26.12505openalex-snapshot
One subspecies of the red junglefowl (Gallus gallus gallus) suffices as the matriarchic ancestor of all domestic breeds.
inferredcites →https://doi.org/10.1073/pnas.92.24.11053openalex-snapshot
The genetic link between the Chinese bamboo partridge (Bambusicola thoracica) and the chicken and junglefowls of the genus Gallus.
inferredcites →https://doi.org/10.1093/genetics/137.1.243openalex-snapshot
The marsupial mitochondrial genome and the evolution of placental mammals.
inferredcites →https://doi.org/10.1093/nar/16.13.5841openalex-snapshot
Comparisons of ape and human sequences that regulate mitochondrial DNA transcription and D-loop DNA synthesis
inferredcites →https://doi.org/10.1093/nar/22.22.4673openalex-snapshot
CLUSTAL W: improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choice
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/10.1093/oxfordjournals.jhered.a111190openalex-snapshot
Signal, Noise, and Reliability in Molecular Phylogenetic Analyses
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a025568openalex-snapshot
Origin and evolution of homologous repeated sequences in the mitochondrial DNA control region of shrews
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a025578openalex-snapshot
Low diversity and biased substitution patterns in the mitochondrial DNA control region of sperm whales: implications for estimates of time since common ancestry
inferredcites →https://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
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a025664openalex-snapshot
Quartet Puzzling: A Quartet Maximum-Likelihood Method for Reconstructing Tree Topologies
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a025703openalex-snapshot
Phylogenetic analysis of slippage-like sequence variation in the V4 rRNA expansion segment in tiger beetles (Cicindelidae)
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a025725openalex-snapshot
The mitochondrial control region of Cervidae: evolutionary patterns and phylogenetic content
inferredcites →https://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)
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a025807openalex-snapshot
Marmoset phylogenetics, conservation perspectives, and evolution of the mtDNA control region
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.a040023openalex-snapshot
Estimation of the number of nucleotide substitutions in the control region of mitochondrial DNA in humans and chimpanzees.
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a040089openalex-snapshot
Mitochondrial control-region sequences in two shorebird species, the turnstone and the dunlin, and their utility in population genetic studies.
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a040096openalex-snapshot
Patterns of sequence variation in the mitochondrial D-loop region of shrews.
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a040141openalex-snapshot
Detecting substitution-rate heterogeneity among regions of a nucleotide sequence.
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a040146openalex-snapshot
Sequence evolution and phylogenetic signal in control-region and cytochrome b sequences of rainbow fishes (Melanotaeniidae).
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a040182openalex-snapshot
Tests of applicability of several substitution models for DNA sequence data.
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a040454openalex-snapshot
The neighbor-joining method: a new method for reconstructing phylogenetic trees.
inferredcites →https://doi.org/10.1111/j.1365-294x.1992.tb00162.xopenalex-snapshot
The genetic legacy of Mother Goose– phylogeographic patterns of lesser snow goose Chen caerulescens caerulescens maternal lineages
inferredcites →https://doi.org/10.1111/j.1365-294x.1995.tb00247.xopenalex-snapshot
Amplification of hypervariable simple sequence repeats (microsatellites) from excremental DNA of wild living bonobos (Pan paniscus)
inferredcites →https://doi.org/10.1111/j.1432-1033.1996.00593.xopenalex-snapshot
The Presence of Tandem Repeats and the Initiation of Replication in Rabbit Mitochondrial DNA
inferredcites →https://doi.org/10.1111/j.1558-5646.1985.tb00420.xopenalex-snapshot
CONFIDENCE LIMITS ON PHYLOGENIES: AN APPROACH USING THE BOOTSTRAP
inferredcites →https://doi.org/10.1111/j.1558-5646.1993.tb02140.xopenalex-snapshot
MITOCHONDRIAL GENE GENEALOGY AND GENE FLOW AMONG ISLAND AND MAINLAND POPULATIONS OF A SEDENTARY SONGBIRD, THE GREY‐CROWNED BABBLER (POMATOSTOMUS TEMPORALIS)
inferredcites →https://doi.org/10.1111/j.1558-5646.1996.tb04495.xopenalex-snapshot
GLOBAL MITOCHONDRIAL DNA PHYLOGEOGRAPHY OF HOLARCTIC BREEDING DUNLINS (CALIDRIS ALPINA)
inferredcites →https://doi.org/10.2307/4088204openalex-snapshot
Biochemical Analysis of Relationships of Mediterranean Alectoris Partridges
inferredcites →https://doi.org/10.2307/j.ctt1xp3v3ropenalex-snapshot
Phylogeny and Classification of the Birds

What points at this work

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

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inferred← citeshttps://doi.org/10.1002/jez.10198openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/jez.b.21282openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/bf03191253openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s00239-001-0083-0openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s00239-002-2379-0openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s00343-025-5135-8openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s10336-004-0024-yopenalex-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/s10342-022-01485-1openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s10344-012-0686-3openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s10528-005-8167-yopenalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s10528-005-9118-3openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s10528-007-9121-yopenalex-snapshot
Genetic Diversity and Systematic Evolution of Chinese Domestic Ducks Along the Yangtze-Huai River
inferred← citeshttps://doi.org/10.1007/s10528-009-9288-5openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s10592-006-9212-zopenalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s10695-008-9251-0openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s10709-017-9978-6openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s10709-017-9982-xopenalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s10709-020-00107-1openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s11033-009-9878-7openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s11802-005-0028-0openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s13258-010-0015-8openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s13258-016-0480-9openalex-snapshot
The complete mitochondrial genome sequence of the little grebe (Tachybaptus ruficollis)
inferred← citeshttps://doi.org/10.1007/s13258-017-0562-3openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/b978-0-443-15750-9.00131-2openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.bse.2017.02.001openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.gene.2009.01.001openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.gene.2011.09.020openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.gene.2015.07.022openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.gene.2018.06.066openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.genrep.2017.02.002openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.jaridenv.2005.01.011openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.ygeno.2021.08.010openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.ympev.2009.03.015openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.ympev.2009.07.002openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.ympev.2010.01.028openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.ympev.2010.03.038openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/s1055-7903(02)00021-0openalex-snapshot
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inferred← citeshttps://doi.org/10.1017/s095927090000215xopenalex-snapshot
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inferred← citeshttps://doi.org/10.1017/s0959270907000706openalex-snapshot
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inferred← citeshttps://doi.org/10.1023/b:coge.0000041024.96928.feopenalex-snapshot
Low Levels of Nucleotide Diversity in Crocodylus moreletii and Evidence of Hybridization with C. acutus
inferred← citeshttps://doi.org/10.1038/s41598-020-74210-wopenalex-snapshot
Specific cyprinid HIF isoforms contribute to cellular mitochondrial regulation
inferred← citeshttps://doi.org/10.1038/s41598-021-00567-1openalex-snapshot
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inferred← citeshttps://doi.org/10.1038/s41598-024-77604-2openalex-snapshot
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inferred← citeshttps://doi.org/10.1038/s41598-025-90985-2openalex-snapshot
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inferred← citeshttps://doi.org/10.1038/srep13227openalex-snapshot
Extreme variation in patterns of tandem repeats in mitochondrial control region of yellow-browed tits (Sylviparus modestus, Paridae)
inferred← citeshttps://doi.org/10.1046/j.1096-3642.2003.00048.xopenalex-snapshot
Suprageneric relationships of galliform birds (Aves, Galliformes): a cladistic analysis of morphological characters
inferred← citeshttps://doi.org/10.1046/j.1365-2540.1998.00413.xopenalex-snapshot
Mitochondrial DNA sequence variation and phylogeographical structure of rock partridge (Alectoris graeca) populations
inferred← citeshttps://doi.org/10.1046/j.1365-294x.2002.01467.xopenalex-snapshot
Genetic variation across the historical range of the wild turkey (Meleagris gallopavo)
inferred← citeshttps://doi.org/10.1046/j.1365-294x.2003.01899.xopenalex-snapshot
Phylogeography of the rock partridge (Alectoris graeca)
inferred← citeshttps://doi.org/10.1046/j.1420-9101.2000.00184.xopenalex-snapshot
Close relatedness between mitochondrial DNA from seven Anser goose species
inferred← citeshttps://doi.org/10.1046/j.1474-919x.2003.00135.xopenalex-snapshot
Mitochondrial DNA diversification among the subspecies of the Silver and Kalij Pheasants, Lophura nycthemera and L. leucomelanos, Phasianidae
inferred← citeshttps://doi.org/10.1051/animres:2006015openalex-snapshot
Comparative genetic analysis between red-legged partridges (Alectoris rufa) and chukar partridges (A. chukar): identification of single-nucleotide polymorphisms
inferred← citeshttps://doi.org/10.1080/10425170701563303openalex-snapshot
Sequence and organization of the complete mitochondrial genomes of spotted halibut (Verasper variegatus) and barfin flounder (Verasper moseri)
inferred← citeshttps://doi.org/10.1080/23802359.2017.1361345openalex-snapshot
Organization and variation of the Tetraonidae (Aves: Galliformes) mitochondrial DNA control region
inferred← citeshttps://doi.org/10.1080/23802359.2017.1407682openalex-snapshot
Phylogenetic association of Schizothorax plagiostomus with other schizothoracine fishes based on mitochondrial cytochrome B gene and control region
inferred← citeshttps://doi.org/10.1080/24701394.2016.1199023openalex-snapshot
Structure and variation of the Fringillidae (Aves: Passeriformes) mitochondrial DNA control region and their phylogenetic relationship
inferred← citeshttps://doi.org/10.1080/24701394.2017.1325482openalex-snapshot
Molecular phylogeny of Loliginidae inferred from mitochondrial DNA sequence variation
inferred← citeshttps://doi.org/10.1080/24701394.2020.1757664openalex-snapshot
Spatial genetic structure of black francolin ( Francolinus francolinus asiae ) in the North-Western Himalayan region based on mitochondrial control region
inferred← citeshttps://doi.org/10.1080/24750263.2017.1317041openalex-snapshot
Phylogenetic assessment of voles of the Guentheri Group (Mammalia: Microtus) in Turkish Thrace and Western Anatolia
inferred← citeshttps://doi.org/10.1081/abio-200053396openalex-snapshot
AN APPLICATION OF CONTROL REGION SEQUENCE AS A MATRILINEAGE MARKER FOR ELLIOT'S PHEASANT OF A ZOO POPULATION
inferred← citeshttps://doi.org/10.1093/auk/117.4.1003openalex-snapshot
Mitochondrial DNA Phylogeny and Speciation in the Tragopans
inferred← citeshttps://doi.org/10.1093/auk/121.3.930openalex-snapshot
Asymmetric Hybridization and Sex-Biased Gene Flow Between Eastern Spot-Billed Ducks (Anas Zonorhyncha) and Mallards (A. Platyrhynchos) in the Russian Far East
inferred← citeshttps://doi.org/10.1093/czoolo/59.4.458openalex-snapshot
Population structure and demographic history of the chukar partridge Alectoris chukar in China
inferred← citeshttps://doi.org/10.1093/jhered/esh047openalex-snapshot
Organization and Variation of the Mitochondrial Control Region in Two Vulture Species, Gypaetus barbatus and Neophron percnopterus
inferred← citeshttps://doi.org/10.1093/jhered/esn024openalex-snapshot
The Organization of the Mitochondrial Control Region in 2 Brachyuran Crustaceans: Ucides cordatus (Ocypodidae) and Cardisoma guanhumi (Gecarcinidae)
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/oxfordjournals.molbev.a003730openalex-snapshot
The Complete Sequence of the Mitochondrial Genome of Buteo buteo (Aves, Accipitridae) Indicates an Early Split in the Phylogeny of Raptors
inferred← citeshttps://doi.org/10.1093/oxfordjournals.molbev.a003917openalex-snapshot
Duplication and Concerted Evolution of the Mitochondrial Control Region in the Parrot Genus Amazona
inferred← citeshttps://doi.org/10.1093/oxfordjournals.molbev.a026280openalex-snapshot
Slow Rate of Evolution in the Mitochondrial Control Region of Gulls (Aves: Laridae)
inferred← citeshttps://doi.org/10.1111/afe.12592openalex-snapshot
Population genetic diversity in Nezara viridula by analysis of mitochondrial control region sequences
inferred← citeshttps://doi.org/10.1111/ibi.12455openalex-snapshot
Phylogeography of the Common Pheasant Phasianus colchicus
inferred← citeshttps://doi.org/10.1111/j.1095-8312.2003.00251.xopenalex-snapshot
Hybrid origin of the imperial pheasant Lophura imperialis (Delacour and Jabouille, 1924) demonstrated by morphology, hybrid experiments, and DNA analyses
inferred← citeshttps://doi.org/10.1111/j.1095-8312.2005.00536.xopenalex-snapshot
Genetic variability in the complete mitochondrial control region of the Eurasian otter (Lutra lutra) in the Iberian Peninsula
inferred← citeshttps://doi.org/10.1111/j.1365-2052.2004.01219.xopenalex-snapshot
Introgression of chukar genes into a reintroduced red‐legged partridge (Alectoris rufa) population in central Italy
inferred← citeshttps://doi.org/10.1111/j.1365-294x.2006.02935.xopenalex-snapshot
Recency, range expansion, and unsorted lineages: implications for interpreting neutral genetic variation in the sharp‐tailed grouse (Tympanuchus phasianellus)
inferred← citeshttps://doi.org/10.1111/j.1365-294x.2007.03417.xopenalex-snapshot
Detecting hybridization between wild species and their domesticated relatives
inferred← citeshttps://doi.org/10.1111/j.1365-294x.2008.03776.xopenalex-snapshot
Speciation in the highlands of Mexico: genetic and phenotypic divergence in the Mexican jay (Aphelocoma ultramarina)
inferred← citeshttps://doi.org/10.1111/j.1365-294x.2011.05111.xopenalex-snapshot
Phylogeography and genetic structure of the red‐legged partridge (Alectoris rufa): more evidence for refugia within the Iberian glacial refugium
inferred← citeshttps://doi.org/10.1111/j.1366-9516.2006.00261.xopenalex-snapshot
The role of history vs. demography in shaping genetic population structure across an ecotone: chukar partridges (Alectoris chukar) as a case study
inferred← citeshttps://doi.org/10.1111/j.1420-9101.2005.00906.xopenalex-snapshot
The Isthmus of Panama: a major physical barrier to gene flow in a highly mobile pantropical seabird
inferred← citeshttps://doi.org/10.1111/j.1420-9101.2009.01802.xopenalex-snapshot
Evolution of sexual size dimorphism in grouse and allies (Aves: Phasianidae) in relation to mating competition, fecundity demands and resource division
inferred← citeshttps://doi.org/10.1111/j.1472-4642.2006.00261.xopenalex-snapshot
The role of history vs. demography in shaping genetic population structure across an ecotone: chukar partridges (Alectoris chukar) as a case study
inferred← citeshttps://doi.org/10.1111/j.1474-919x.2001.tb04487.xopenalex-snapshot
The phylogenetic status of the Corn Bunting Miliaria calandra based on mitochondrial control‐region DNA sequences
inferred← citeshttps://doi.org/10.1111/j.1474-919x.2012.01273.xopenalex-snapshot
Taxonomic recommendations for British birds: eighth report
inferred← citeshttps://doi.org/10.1111/jzs.12039openalex-snapshot
Lack of mitochondrial genetic structure in the red-legged partridgeAlectoris rufa(Phasianidae)
inferred← citeshttps://doi.org/10.1111/lam.13538openalex-snapshot
Revisiting the Neurospora crassa mitochondrial genome
inferred← citeshttps://doi.org/10.1111/mec.12315openalex-snapshot
Phylogeography of Silver Pheasant ( L ophura nycthemera L.) across C hina: aggregate effects of refugia, introgression and riverine barriers
inferred← citeshttps://doi.org/10.1134/s0026893309010038openalex-snapshot
Polymorphism and structural features of two noncoding regions of the liver fluke Fasciola hepatica (Plathelminthes: Trematoda) mitochondrial genome
inferred← citeshttps://doi.org/10.1136/vetreccr-2020-001100openalex-snapshot
Laboratory findings on the health status of the endemic rock‐partridge ( Alectoris graeca whitakeri ) population during a two‐year conservation programme in Sicily
inferred← citeshttps://doi.org/10.1139/g00-018openalex-snapshot
A repeat complex in the mitochondrial control region of Adélie penguins from Antarctica
inferred← citeshttps://doi.org/10.1139/g04-009openalex-snapshot
Molecular architecture and rates of DNA substitutions of the mitochondrial control region of cracid birds
inferred← citeshttps://doi.org/10.1139/z02-035openalex-snapshot
Sequence variations in the mitochondrial DNA control region and their implications for the phylogeny of the Cypriniformes
inferred← citeshttps://doi.org/10.11606/t.41.2008.tde-15092008-152008openalex-snapshot
Filogenia molecular e biogeografia: jacus e jacutingas (Cracidae)
inferred← citeshttps://doi.org/10.1163/017353710x530203openalex-snapshot
The mitochondrial genome complete sequence and organization of the Pig-nosed Turtle Carettochelys insculpta (Testudines, Carettochelyidae) and its phylogeny position in Testudines
inferred← citeshttps://doi.org/10.1163/15685411-bja10110openalex-snapshot
Characterisation of the complete mitochondrial genome of the insect-parasitic nematode Heterorhabditis bacteriophora: an idiosyncratic gene order and the presence of multiple long non-coding regions
inferred← citeshttps://doi.org/10.1163/157075610x523314openalex-snapshot
Phylogeographic structure and gene flow of Himalayan snowcock (Tetraogallus himalayensis)
inferred← citeshttps://doi.org/10.1163/157075611x618183openalex-snapshot
Population genetic structure of golden pheasant Chrysolophus pictus in the Qinling Mountains, China
inferred← citeshttps://doi.org/10.1186/1471-2164-12-35openalex-snapshot
Full mitochondrial genome sequences of two endemic Philippine hornbill species (Aves: Bucerotidae) provide evidence for pervasive mitochondrial DNA recombination
inferred← citeshttps://doi.org/10.1186/s44315-025-00039-5openalex-snapshot
First report of complete mitochondrial genome of Schizothorax curvifrons using next generation sequencing platform (NGS) and phylogentic relationship with other Schizothoracinae
inferred← citeshttps://doi.org/10.13140/rg.2.1.1653.8329openalex-snapshot
Population genetics, systematics, biogeography, and evolution of the southeastern central Texas Eurycea clade Blepsimolge (Plethodontidae)
inferred← citeshttps://doi.org/10.1360/04yc0117openalex-snapshot
The complete mitochondrial genomes sequences of Asio flammeus and Asio otus and comparative analysis
inferred← citeshttps://doi.org/10.1371/journal.pone.0010639openalex-snapshot
The Origin and Genetic Variation of Domestic Chickens with Special Reference to Junglefowls Gallus g. gallus and G. varius
inferred← citeshttps://doi.org/10.1371/journal.pone.0050732openalex-snapshot
Highly Informative Ancient DNA ‘Snippets’ for New Zealand Moa
inferred← citeshttps://doi.org/10.1371/journal.pone.0051528openalex-snapshot
The Mitochondrial Genome of the Venomous Cone Snail Conus consors
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.0092033openalex-snapshot
Comparative Analysis of Mitochondrial Genomes in Distinct Nuclear Ploidy Loach Misgurnus anguillicaudatus and Its Implications for Polyploidy Evolution
inferred← citeshttps://doi.org/10.1371/journal.pone.0256573openalex-snapshot
Reduced genetic variability in a captive-bred population of the endangered Hume’s pheasant (Syrmaticus humiae, Hume 1881) revealed by microsatellite genotyping and D-loop sequencing
inferred← citeshttps://doi.org/10.14203/treubia.v47i2.3971openalex-snapshot
CHARACTERS OF MITOCHONDRIAL DNA D-LOOP HYPERVARIABLE III FRAGMENTS OF INDONESIAN RHINOCEROS HORNBILL (BUCEROS RHINOCEROS) (AVES: BUCEROTIDAE)
inferred← citeshttps://doi.org/10.1515/aoas-2017-0016openalex-snapshot
A molecular characteristic of the Anatidae mitochondrial control region – a review
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/10.1590/1806-9061-2018-0739openalex-snapshot
Genetic Diversity of Mitochondrial DNA of Chinese Black-bone Chicken
inferred← citeshttps://doi.org/10.1590/s1415-47572007000400029openalex-snapshot
Challenges and prospects of population genetic studies in terns (Charadriiformes, Aves)
inferred← citeshttps://doi.org/10.1590/s1415-4757382220140203openalex-snapshot
The complete mitochondrial genome sequence of the little egret (Egretta garzetta)
inferred← citeshttps://doi.org/10.1590/s1984-46702011000400011openalex-snapshot
Organization and variation of mitochondrial DNA control region in pleurodiran turtles
inferred← citeshttps://doi.org/10.1631/jzus.2005.b0413openalex-snapshot
A genetic diversity comparison between captive individuals and wild individuals of Elliot’s Pheasant (Syrmaticus ellioti) using mitochondrial DNA
inferred← citeshttps://doi.org/10.1642/0004-8038(2000)117[1003:mdpasi]2.0.co;2openalex-snapshot
MITOCHONDRIAL DNA PHYLOGENY AND SPECIATION IN THE TRAGOPANS
inferred← citeshttps://doi.org/10.1642/0004-8038(2004)121[0930:ahasgf]2.0.co;2openalex-snapshot
ASYMMETRIC HYBRIDIZATION AND SEX-BIASED GENE FLOW BETWEEN EASTERN SPOT-BILLED DUCKS (ANAS ZONORHYNCHA) AND MALLARDS (A. PLATYRHYNCHOS) IN THE RUSSIAN FAR EAST
inferred← citeshttps://doi.org/10.19087/jveteriner.2018.19.2.284openalex-snapshot
KAJIAN FILOGENETIK ULAR SANCA BATIK (Malayopython reticulatus) LOKALITAS JAWA BERDASAR SEKUEN GEN SITOKROM B
inferred← citeshttps://doi.org/10.2108/zsj.22.427openalex-snapshot
Molecular Phylogeny of Avian Genus Syrmaticus Based on the Mitochondrial CytochromebGene and Control Region
inferred← citeshttps://doi.org/10.2141/jpsa.0190121openalex-snapshot
Mitochondrial DNA Diversity in Commercial Lines of Laying-type Japanese Quail
inferred← citeshttps://doi.org/10.2307/4089640openalex-snapshot
Mitochondrial DNA Phylogeny and Speciation in the Tragopans
inferred← citeshttps://doi.org/10.2307/4090327openalex-snapshot
Asymmetric Hybridization and Sex-Biased Gene Flow between Eastern Spot-Billed Ducks (Anas zonorhyncha) and Mallards (A. platyrhynchos) in the Russian Far East
inferred← citeshttps://doi.org/10.24002/biota.v12i3.2804openalex-snapshot
Kajian Penanda Genetik Tarsius bancanus dan Tarsius spectrum dengan Sekuen D-Loop Parsial DNA Mitokondria
inferred← citeshttps://doi.org/10.2461/wbp.2005.1.1openalex-snapshot
Editorial
inferred← citeshttps://doi.org/10.2461/wbp.2006.2.1openalex-snapshot
Mitochondrial DNA Variability in Populations of Alectoris rufa: A Single-Stranded Conformation Polymorphism (SSCP) Approach.
inferred← citeshttps://doi.org/10.3109/19401736.2011.637109openalex-snapshot
The complete mitochondrial genome of the loggerhead turtleCaretta caretta(Testudines: Cheloniidae): Genome description and phylogenetic considerations
inferred← citeshttps://doi.org/10.3109/19401736.2012.717939openalex-snapshot
Complete mitochondrial genome of the ring-necked pheasant, Phasianus colchicus (Galliformes: Phasianidae)
inferred← citeshttps://doi.org/10.3109/19401736.2012.731407openalex-snapshot
Complete mitochondrial genome of the Red-billed Starling,Sturnus sericeus(Aves: Passeriformes): The first representative of the family Sturnidae with a single control region
inferred← citeshttps://doi.org/10.3109/19401736.2012.752481openalex-snapshot
Complete mitochondrial genome of Skylark,Alauda arvensis(Aves: Passeriformes): The first representative of the family Alaudidae with two extensive heteroplasmic control regions
inferred← citeshttps://doi.org/10.3109/19401736.2013.878911openalex-snapshot
Complete mitochondrial genome of black grouse ( Lyrurus tetrix )
inferred← citeshttps://doi.org/10.3109/19401736.2014.895987openalex-snapshot
Structure and evolution of the Phasianidae mitochondrial DNA control region
inferred← citeshttps://doi.org/10.3109/19401736.2014.974177openalex-snapshot
Structure and variation of the Anseriformes mitochondrial DNA control region
inferred← citeshttps://doi.org/10.3109/19401736.2015.1033711openalex-snapshot
Structural characteristics of the Relict Gull ( Larus relictus ) mitochondrial DNA control region and its comparison to other Laridae
inferred← citeshttps://doi.org/10.3109/19401736.2015.1110816openalex-snapshot
Extremely low genetic diversity of mtDNA control region and remarkable population differentiation of Ichthyophis bannanicus (Amphibia: Gymnophiona)
inferred← citeshttps://doi.org/10.3109/19401736.2015.1137901openalex-snapshot
Phylogeography of chukar partridge ( Alectoris chukar ) in China based on mtDNA control region
inferred← citeshttps://doi.org/10.32800/abc.2007.30.0105openalex-snapshot
Lack of genetic structure of Cypriot Alectoris chukar (Aves, Galliformes) populations as inferred from mtDNA sequencing data
inferred← citeshttps://doi.org/10.3389/fgene.2014.00448openalex-snapshot
Mito-nuclear co-evolution: the positive and negative sides of functional ancient mutations
inferred← citeshttps://doi.org/10.3389/fgene.2019.01285openalex-snapshot
Higher Order Organization of the mtDNA: Beyond Mitochondrial Transcription Factor A
inferred← citeshttps://doi.org/10.3390/biology13090709openalex-snapshot
Combining Historical and Molecular Data to Study Nearly Extinct Native Italian Grey Partridge (Perdix perdix) at the Turn of the Twentieth Century
inferred← citeshttps://doi.org/10.3390/birds6040059openalex-snapshot
Genetic Identity of the Red-legged Partridge (Alectoris rufa, Phasianidae) from the Island of Madeira
inferred← citeshttps://doi.org/10.3390/d17020079openalex-snapshot
High Diversity Unveiled by the First Genetic Survey on Wild and Captive Barbary Partridge (Alectoris barbara) from Morocco
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/genes13050726openalex-snapshot
Complete Mitochondrial Genomes of Five Racerunners (Lacertidae: Eremias) and Comparison with Other Lacertids: Insights into the Structure and Evolution of the Control Region
inferred← citeshttps://doi.org/10.3390/genes14050998openalex-snapshot
Studying Genetic Diversity and Relationships between Mountainous Meihua Chickens Using Mitochondrial DNA Control Region
inferred← citeshttps://doi.org/10.3390/genes17070739openalex-snapshot
Development and Validation of an SNP-Based OpenArray® Genotyping Panel for Discriminating Coturnix coturnix, Coturnix japonica and Their Hybrids
inferred← citeshttps://doi.org/10.3390/ijms19051292openalex-snapshot
Hemiptera Mitochondrial Control Region: New Sights into the Structural Organization, Phylogenetic Utility, and Roles of Tandem Repetitions of the Noncoding Segment
inferred← citeshttps://doi.org/10.3390/ijms26030869openalex-snapshot
Phylogenetic Relationship and Characterization of the Complete Mitochondrial Genome of the Cuckoo Species Clamator coromandus (Aves: Cuculidae)
inferred← citeshttps://doi.org/10.3390/life14070881openalex-snapshot
Selected Lark Mitochondrial Genomes Provide Insights into the Evolution of Second Control Region with Tandem Repeats in Alaudidae (Aves, Passeriformes)
inferred← citeshttps://doi.org/10.35537/10915/2369openalex-snapshot
Análisis del ADN mitocondrial en camélidos sudamericanos (Tylopoda: camelidae)
inferred← citeshttps://doi.org/10.3724/sp.j.1003.2012.09221openalex-snapshot
Genetic variation in rusty-necklaced partridge (Alectoris magna) detected by mitochondrial DNA
inferred← citeshttps://doi.org/10.3724/sp.j.1005.2012.01434openalex-snapshot
Analysis of the complete mitochondrial genome sequence of Larus brunnicephalus (Aves, Laridae)
inferred← citeshttps://doi.org/10.3724/sp.j.1141.2008.00121openalex-snapshot
Genetic Variation and Diversity of Phrynocephalus vlangalii hongyuanensis in Zoige Wetland Inferred from ND4-tRNAPleu Gene
inferred← citeshttps://doi.org/10.3724/sp.j.1141.2008.00127openalex-snapshot
Comparison of Mitochondrial Control Region Sequences Between Chelydridae and Platysternidae
inferred← citeshttps://doi.org/10.3897/compcytogen.v12i2.23743openalex-snapshot
Banding cytogenetics of the Barbary partridge Alectoris barbara and the Chukar partridge Alectoris chukar (Phasianidae): a large conservation with Domestic fowl Gallus domesticus revealed by high resolution chromosomes
inferred← citeshttps://doi.org/10.3897/zookeys.1109.81125openalex-snapshot
Comparative mitogenomics of the genus Motacilla (Aves, Passeriformes) and its phylogenetic implications
inferred← citeshttps://doi.org/10.4238/2015.august.7.5openalex-snapshot
Complete mitochondrial genome of the Chinese Hwamei Garrulax canorus (Aves: Passeriformes): the first representative of the Leiothrichidae family with a duplicated control region
inferred← citeshttps://doi.org/10.4238/gmr.15038491openalex-snapshot
Characterization and evolution of the mitochondrial DNA control region in Ranidae and their phylogenetic relationship
inferred← citeshttps://doi.org/10.4238/vol10-3gmr1205openalex-snapshot
Comparison of complete mitochondrial DNA control regions among five Asian freshwater turtle species and their phylogenetic relationships
inferred← citeshttps://doi.org/10.4238/vol9-2gmr820openalex-snapshot
Complete mitochondrial genome of Cabot’s tragopan, Tragopan caboti (Galliformes: Phasianidae)
inferred← citeshttps://doi.org/10.4238/vol9-2gmr853openalex-snapshot
Characterization of the complete mitochondrial genome of the Rock pigeon, Columba livia (Columbiformes: Columbidae)
inferred← citeshttps://doi.org/10.4308/hjb.31.3.548-558openalex-snapshot
Genetic Structure of Gallus varius Based on Middle-Lower Section of Control Region mtDNA
inferred← citeshttps://doi.org/10.5141/jefb.2007.30.4.331openalex-snapshot
Biogeography and Distribution Pattern of a Korean Wood-eating Cockroach Species, Cryptocercus kyebangensis, Based on Genetic Network Analysis and DNA Sequence Information
inferred← citeshttps://doi.org/10.5194/aab-53-609-2010openalex-snapshot
Molecular genetic diversity and origin of Chinese domestic duck breeds
inferred← citeshttps://doi.org/10.5281/zenodo.16062133openalex-snapshot
Lophura hatinhensis is an invalid taxon
inferred← citeshttps://doi.org/10.5713/ajas.2004.903openalex-snapshot
Genetic Variability of mtDNA Sequences in Chinese Native Chicken Breeds
inferred← citeshttps://doi.org/10.5846/stxb/2013/33/14openalex-snapshot
inferred← citeshttps://doi.org/10.5846/stxb201205010624openalex-snapshot
A review of the researches onAlectorispartridge
inferred← citeshttps://doi.org/10.58837/tnh.18.1.117465openalex-snapshot
Genetic Diversity of Green Peafowl (Pavo muticus) in Northern Thailand Based on Mitochondrial DNA Control Region Sequences
inferred← citeshttps://doi.org/10.58837/tnh.18.2.148166openalex-snapshot
Genetic Diversity of Captive Eastern Sarus Crane in Thailand Inferred from Mitochondrial Control Region Sequence and Microsatellite DNA markers
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