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Widespread atypical mitochondrial DNA structure in isopods (Crustacea, Peracarida) related to a constitutive heteroplasmy in terrestrial species
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1006/abio.1999.4298openalex-snapshot
A Quantitative Fluorescence-Based Microplate Assay for the Determination of Double-Stranded DNA Using SYBR Green I and a Standard Ultraviolet Transilluminator Gel Imaging System
inferredcites →https://doi.org/10.1007/bf02193629openalex-snapshot
Cloning and characterization ofDaphnia mitochondrial DNA
inferredcites →https://doi.org/10.1007/s00227-004-1353-3openalex-snapshot
Mitochondrial DNA variation and population genetic structure of the blue crab Callinectes sapidus in the eastern United States
inferredcites →https://doi.org/10.1007/s00239-007-9007-yopenalex-snapshot
Sequence and Characterization of Six Mitochondrial Subgenomes from Globodera rostochiensis: Multipartite Structure Is Conserved Among Close Nematode Relatives
inferredcites →https://doi.org/10.1007/s00239-007-9016-xopenalex-snapshot
Complete Mitochondrial DNA Sequence of the Scallop Placopecten magellanicus: Evidence of Transposition Leading to an Uncharacteristically Large Mitochondrial Genome
inferredcites →https://doi.org/10.1007/s00239-007-9037-5openalex-snapshot
Structure and Evolution of the Atypical Mitochondrial Genome of Armadillidium vulgare (Isopoda, Crustacea)
inferredcites →https://doi.org/10.1007/s00239-013-9587-7openalex-snapshot
Inverted Repeats and Genome Architecture Conversions of Terrestrial Isopods Mitochondrial DNA
inferredcites →https://doi.org/10.1007/s00294-003-0426-zopenalex-snapshot
Mitochondrial genome diversity: evolution of the molecular architecture and replication strategy
inferredcites →https://doi.org/10.1016/0003-2697(83)90418-9openalex-snapshot
A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity
inferredcites →https://doi.org/10.1016/0044-8486(94)90420-0openalex-snapshot
Mitochondrial DNA variation and markers of species identity in two penaeid shrimp species: Penaeus monodon Fabricius and P. japonicus Bate
inferredcites →https://doi.org/10.1016/j.cbd.2009.09.003openalex-snapshot
The Australian fresh water isopod (Phreatoicidea: Isopoda) allows insights into the early mitogenomic evolution of isopods
inferredcites →https://doi.org/10.1016/j.gene.2006.06.021openalex-snapshot
Mitochondrial genome of the moon jelly Aurelia aurita (Cnidaria, Scyphozoa): A linear DNA molecule encoding a putative DNA-dependent DNA polymerase
inferredcites →https://doi.org/10.1016/j.gene.2007.12.002openalex-snapshot
The mitochondrial genome of Hydra oligactis (Cnidaria, Hydrozoa) sheds new light on animal mtDNA evolution and cnidarian phylogeny
inferredcites →https://doi.org/10.1016/j.tig.2005.01.004openalex-snapshot
Transfer RNA gene recruitment in mitochondrial DNA
inferredcites →https://doi.org/10.1016/j.ympev.2006.04.008openalex-snapshot
Major rearrangements characterize the mitochondrial genome of the isopod Idotea baltica (Crustacea: Peracarida)
inferredcites →https://doi.org/10.1016/s0764-4469(00)01221-xopenalex-snapshot
Phylogenetic analysis of mitochondrial LSU rRNA in oniscids
inferredcites →https://doi.org/10.1016/s0764-4469(97)84710-5openalex-snapshot
Preliminary results on the genetic variability of mitochondrial DNA in the signal crayfish, Pacifastacus leniusculus Dana
inferredcites →https://doi.org/10.1038/hdy.2008.62openalex-snapshot
Evolution of the mitochondrial genome of Metazoa as exemplified by comparison of congeneric species
inferredcites →https://doi.org/10.1038/ng.2007.63openalex-snapshot
A reduction of mitochondrial DNA molecules during embryogenesis explains the rapid segregation of genotypes
inferredcites →https://doi.org/10.1038/ng.258openalex-snapshot
The mitochondrial DNA genetic bottleneck results from replication of a subpopulation of genomes
inferredcites →https://doi.org/10.1038/ng0208-134openalex-snapshot
Two ways to make an mtDNA bottleneck
inferredcites →https://doi.org/10.1038/sj.hdy.6885380openalex-snapshot
Mitochondrial DNA variability and Wolbachia infection in two sibling woodlice species
inferredcites →https://doi.org/10.1051/kmae:1996014openalex-snapshot
Isolation and characterization of mitochondrial DNA from the endangered white-clawed crayfish Austropotamobius pallipes pallipes, Lereboullet, 1858
inferredcites →https://doi.org/10.1073/pnas.89.18.8750openalex-snapshot
Class-level relationships in the phylum Cnidaria: evidence from mitochondrial genome structure.
inferredcites →https://doi.org/10.1093/genetics/151.1.203openalex-snapshot
Organization of the Large Mitochondrial Genome in the Isopod Armadillidium vulgare
inferredcites →https://doi.org/10.1093/molbev/msn058openalex-snapshot
Two Circular Chromosomes of Unequal Copy Number Make Up the Mitochondrial Genome of the Rotifer Brachionus plicatilis
inferredcites →https://doi.org/10.1093/molbev/mss274openalex-snapshot
Mitochondrial DNA of Clathrina clathrus (Calcarea, Calcinea): Six Linear Chromosomes, Fragmented rRNAs, tRNA Editing, and a Novel Genetic Code
inferredcites →https://doi.org/10.1093/nar/16.14.6515openalex-snapshot
Genome organization ofArtemiamitochondrial DNA
inferredcites →https://doi.org/10.1101/gr.083188.108openalex-snapshot
The single mitochondrial chromosome typical of animals has evolved into 18 minichromosomes in the human body louse, Pediculus humanus
inferredcites →https://doi.org/10.1111/j.1469-7998.1992.tb04340.xopenalex-snapshot
Mitochondrial DNA variation and phylogenetic relationships of Jasus spp. (Decapoda: Palinuridae)
inferredcites →https://doi.org/10.1126/science.1118884openalex-snapshot
Mutation Pressure and the Evolution of Organelle Genomic Architecture
inferredcites →https://doi.org/10.1126/science.283.5407.1476openalex-snapshot
Mitochondrial Evolution
inferredcites →https://doi.org/10.1146/annurev.ecolsys.32.081501.114109openalex-snapshot
The Units of Selection on Mitochondrial DNA
inferredcites →https://doi.org/10.1163/156854099503915openalex-snapshot
SOME OF THE DEEP-SEA FAUNA IS ANCIENT
inferredcites →https://doi.org/10.1163/20021975-99990204openalex-snapshot
MITOCHONDRIAL GENES AND ISOPOD PHYLOGENY (PERACARIDA: ISOPODA)
inferredcites →https://doi.org/10.1163/9789047412854_006openalex-snapshot
New Aspects in the Phylogeny of the Oniscidea Inferred from Molecular Data
inferredcites →https://doi.org/10.1186/1471-2164-7-241openalex-snapshot
The complete mitochondrial genome of the common sea slater, Ligia oceanica (Crustacea, Isopoda) bears a novel gene order and unusual control region features
inferredcites →https://doi.org/10.1186/1471-2164-9-350openalex-snapshot
A fragmented metazoan organellar genome: the two mitochondrial chromosomes of Hydra magnipapillata
inferredcites →https://doi.org/10.1371/journal.pone.0002938openalex-snapshot
A Thirty Million Year-Old Inherited Heteroplasmy
inferredcites →https://doi.org/10.1651/0278-0372(2002)022[0217:tstnat]2.0.co;2openalex-snapshot
THE SCUTOCOXIFERA TAX. NOV. AND THE INFORMATION CONTENT OF NUCLEAR SSU RDNA SEQUENCES FOR RECONSTRUCTION OF ISOPOD PHYLOGENY (PERACARIDA: ISOPODA)
inferredcites →https://doi.org/10.1651/0278-0372(2005)025[0316:br]2.0.co;2openalex-snapshot
The Biology of Terrestrial Isopods
inferredcites →https://doi.org/10.2331/fishsci.65.655openalex-snapshot
Analysis of the Population Structure of the Swimming Crab, Portunus trituberculatus in the Coastal Waters of Okayama Prefecture, by RFLPs in the Whole Region of Mitochondrial DNA
inferredcites →https://doi.org/10.3897/asp.66.e31684openalex-snapshot
Phylogeny of the terrestrial Isopoda (Oniscidea): a review
inferredcites →https://doi.org/10.3897/asp.67.e31696openalex-snapshot
The phylogenetic position of the Isopoda in the Peracarida (Crustacea: Malacostraca)
inferredcites →https://doi.org/10.5281/zenodo.16455135openalex-snapshot
A phylogenetic analysis of the Isopoda with some classificatory recommendations
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1080/00222933.2023.2258587zenodo-depositor-declared
Complete mitochondrial genome of the terrestrial isopod Cubaris murina Brandt, 1833: new family gene order and novel tRNA secondary structures
inferred← citeshttps://doi.org/10.1007/978-1-4939-3774-5_3openalex-snapshot
High-Throughput Sequencing of Complete Mitochondrial Genomes
inferred← citeshttps://doi.org/10.1007/s00239-013-9587-7openalex-snapshot
Inverted Repeats and Genome Architecture Conversions of Terrestrial Isopods Mitochondrial DNA
inferred← citeshttps://doi.org/10.1007/s10750-017-3088-4openalex-snapshot
Next-generation sequencing of Dreissena polymorpha transcriptome sheds light on its mitochondrial DNA
inferred← citeshttps://doi.org/10.1007/s13353-014-0218-9openalex-snapshot
Are “universal” DNA primers really universal?
inferred← citeshttps://doi.org/10.1016/j.cris.2022.100036openalex-snapshot
Unparalleled mitochondrial heteroplasmy and Wolbachia co-infection in the non-model bee, Amphylaeus morosus
inferred← citeshttps://doi.org/10.1016/j.gene.2024.148999openalex-snapshot
One Ring does not rule them all: Linear mtDNA in Metazoa
inferred← citeshttps://doi.org/10.1080/24701394.2020.1844677openalex-snapshot
Mitochondrial heteroplasmy and pseudogenes in the freshwater prawn, Macrobrachium amazonicum (Heller, 1862): DNA barcoding and phylogeographic implications
inferred← citeshttps://doi.org/10.1093/gbe/evae168openalex-snapshot
Mitochondrial DNA of the Demosponge Acanthella acuta: Linear Architecture and Other Unique Features
inferred← citeshttps://doi.org/10.1093/jcbiol/ruy002openalex-snapshot
Incongruence between morphological and molecular diversity in Coxicerberus fukudai (Ito, 1974) (Isopoda: Microcerberidea) from East Asia
inferred← citeshttps://doi.org/10.1093/molbev/mss274openalex-snapshot
Mitochondrial DNA of Clathrina clathrus (Calcarea, Calcinea): Six Linear Chromosomes, Fragmented rRNAs, tRNA Editing, and a Novel Genetic Code
inferred← citeshttps://doi.org/10.1093/molbev/msy184openalex-snapshot
Life History Traits Impact the Nuclear Rate of Substitution but Not the Mitochondrial Rate in Isopods
inferred← citeshttps://doi.org/10.1093/molbev/msz186openalex-snapshot
Unusual Patterns of Mitochondrial Inheritance in the Brown Alga Ectocarpus
inferred← citeshttps://doi.org/10.1098/rsos.191887openalex-snapshot
Architectural instability, inverted skews and mitochondrial phylogenomics of Isopoda: outgroup choice affects the long-branch attraction artefacts
inferred← citeshttps://doi.org/10.1098/rsos.211550openalex-snapshot
Long-read sequencing reveals atypical mitochondrial genome structure in a New Zealand marine isopod
inferred← citeshttps://doi.org/10.1099/acmi.0.000592.v3openalex-snapshot
Metagenome-assembled genomes of three Hepatoplasmataceae provide insights into isopod-mollicute symbiosis
inferred← citeshttps://doi.org/10.1101/2024.01.10.575101openalex-snapshot
Acanthella acuta Mitochondrial DNA: Linear Architecture and Other Unique Features
inferred← citeshttps://doi.org/10.1111/bij.12254openalex-snapshot
Phylogeographical analysis ofLigia oceanica(Crustacea: Isopoda) reveals two deeply divergent mitochondrial lineages
inferred← citeshttps://doi.org/10.1111/mec.14410openalex-snapshot
Metabarcoding of freshwater invertebrates to detect the effects of a pesticide spill
inferred← citeshttps://doi.org/10.1139/gen-2015-0090openalex-snapshot
Atypical mitochondrial inheritance patterns in eukaryotes
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/10.1371/journal.pone.0203089openalex-snapshot
The complete mitochondrial genome of Cymothoa indica has a highly rearranged gene order and clusters at the very base of the Isopoda clade
inferred← citeshttps://doi.org/10.1371/journal.pone.0286628openalex-snapshot
Assembly and comparative analysis of the complete mitochondrial genome of Isopyrum anemonoides (Ranunculaceae)
inferred← citeshttps://doi.org/10.1534/g3.115.018283openalex-snapshot
Multiple Conserved Heteroplasmic Sites in tRNA Genes in the Mitochondrial Genomes of Terrestrial Isopods (Oniscidea)
inferred← citeshttps://doi.org/10.1534/genetics.117.203380openalex-snapshot
Untangling Heteroplasmy, Structure, and Evolution of an Atypical Mitochondrial Genome by PacBio Sequencing
inferred← citeshttps://doi.org/10.21203/rs.3.rs-25479/v1openalex-snapshot
Phylogeny of Terrestrial Isopods Based on the Complete Mitochondrial Genomes, Subvert the Monophyly of Oniscidea
inferred← citeshttps://doi.org/10.2983/035.036.0129openalex-snapshot
Extensive Heteroplasmy and Evidence for Fragmentation in theCallinectes sapidusMitochondrial Genome
inferred← citeshttps://doi.org/10.3897/zookeys.1082.69851openalex-snapshot
Surprisingly high genetic divergence of the mitochondrial DNA barcode fragment (COI) within Central European woodlice species (Crustacea, Isopoda, Oniscidea)
inferred← citeshttps://doi.org/10.70675/404d118ez7291z44d1zb087z58dbfdf3cf84openalex-snapshot
Genetic and cellular characterisation of parthenogenesis in the brown alga Ectocarpus sp.
inferred← citeshttps://doi.org/10.70675/428a7961z0409z47adzaabbz52baacd50dc3openalex-snapshot
Origine des variations de taux d’évolution moléculaire inter-spécifiques : apport d’un modèle génomique en milieu souterrain
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