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Fragmented mitochondrial genomes in two suborders of parasitic lice of eutherian mammals (Anoplura and Rhynchophthirina, Insecta)
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1007/s00239-007-9042-8openalex-snapshot
The Mitochondrial Genome of the Screamer Louse Bothriometopus (Phthiraptera: Ischnocera): Effects of Extensive Gene Rearrangements on the Evolution of the Genome
inferredcites →https://doi.org/10.1007/s00436-005-1413-8openalex-snapshot
Multiple origins of parasitism in lice: phylogenetic analysis of SSU rDNA indicates that the Phthiraptera and Psocoptera are not monophyletic
inferredcites →https://doi.org/10.1016/0020-7519(94)90195-3openalex-snapshot
Phylogeny and classification, origins, and evolution of host associations of lice
inferredcites →https://doi.org/10.1016/j.gene.2010.11.002openalex-snapshot
Chimeric mitochondrial minichromosomes of the human body louse, Pediculus humanus: Evidence for homologous and non-homologous recombination
inferredcites →https://doi.org/10.1016/s0022-2836(05)80360-2openalex-snapshot
Basic Local Alignment Search Tool
inferredcites →https://doi.org/10.1016/s0168-9525(00)02024-2openalex-snapshot
EMBOSS: The European Molecular Biology Open Software Suite
inferredcites →https://doi.org/10.1017/s0031182000013494openalex-snapshot
The Louse of Elephants. Haematomyzus elephantis Piaget (Mallophaga: Haematomyzidae)
inferredcites →https://doi.org/10.1046/j.1463-6409.2003.00120.xopenalex-snapshot
Phylogeny of the lice (Insecta, Phthiraptera) inferred from small subunit rRNA
inferredcites →https://doi.org/10.1093/bioinformatics/btg180openalex-snapshot
MrBayes 3: Bayesian phylogenetic inference under mixed models
inferredcites →https://doi.org/10.1093/bioinformatics/btl446openalex-snapshot
RAxML-VI-HPC: maximum likelihood-based phylogenetic analyses with thousands of taxa and mixed models
inferredcites →https://doi.org/10.1093/bioinformatics/btm404openalex-snapshot
Clustal W and Clustal X version 2.0
inferredcites →https://doi.org/10.1093/bioinformatics/btm573openalex-snapshot
ARWEN: a program to detect tRNA genes in metazoan mitochondrial nucleotide sequences
inferredcites →https://doi.org/10.1093/bioinformatics/bts199openalex-snapshot
Geneious Basic: An integrated and extendable desktop software platform for the organization and analysis of sequence data
inferredcites →https://doi.org/10.1093/gbe/evs088openalex-snapshot
Evolution of Extensively Fragmented Mitochondrial Genomes in the Lice of Humans
inferredcites →https://doi.org/10.1093/gbe/evt094openalex-snapshot
Substantial Variation in the Extent of Mitochondrial Genome Fragmentation among Blood-Sucking Lice of Mammals
inferredcites →https://doi.org/10.1093/hmg/9.19.2821openalex-snapshot
Human mtDNA sublimons resemble rearranged mitochondrial genomes found in pathological states
inferredcites →https://doi.org/10.1093/icb/icm045openalex-snapshot
Key transitions in animal evolution: a mitochondrial DNA perspective
inferredcites →https://doi.org/10.1093/molbev/msg176openalex-snapshot
Rates of Gene Rearrangement and Nucleotide Substitution Are Correlated in the Mitochondrial Genomes of Insects
inferredcites →https://doi.org/10.1093/molbev/msr121openalex-snapshot
MEGA5: Molecular Evolutionary Genetics Analysis Using Maximum Likelihood, Evolutionary Distance, and Maximum Parsimony Methods
inferredcites →https://doi.org/10.1093/nar/25.5.955openalex-snapshot
tRNAscan-SE: A Program for Improved Detection of Transfer RNA Genes in Genomic Sequence
inferredcites →https://doi.org/10.1093/nar/gkh340openalex-snapshot
MUSCLE: multiple sequence alignment with high accuracy and high throughput
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a003867openalex-snapshot
Numerous Gene Rearrangements in the Mitochondrial Genome of the Wallaby Louse, Heterodoxus macropus (Phthiraptera)
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a026334openalex-snapshot
Selection of Conserved Blocks from Multiple Alignments for Their Use in Phylogenetic Analysis
inferredcites →https://doi.org/10.1098/rsbl.2011.0105openalex-snapshot
Multiple lineages of lice pass through the K–Pg boundary
inferredcites →https://doi.org/10.1098/rspb.2013.2174openalex-snapshot
Rates of genomic divergence in humans, chimpanzees and their lice
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.1365-2583.2005.00608.xopenalex-snapshot
Extraordinary number of gene rearrangements in the mitochondrial genomes of lice (Phthiraptera: Insecta)
inferredcites →https://doi.org/10.1111/j.1365-3113.1985.tb00525.xopenalex-snapshot
Phylogeny and classification of the Psocodea, with particular reference to the lice (Psocodea: Phthiraptera)
inferredcites →https://doi.org/10.1111/j.1365-3113.2005.00323.xopenalex-snapshot
Morphology of male genitalia in lice and their relatives and phylogenetic implications
inferredcites →https://doi.org/10.1186/1471-2148-10-292openalex-snapshot
Evolutionary history of mammalian sucking lice (Phthiraptera: Anoplura)
inferredcites →https://doi.org/10.1186/1471-2164-12-394openalex-snapshot
Mitochondrial genome deletions and minicircles are common in lice (Insecta: Phthiraptera)
inferredcites →https://doi.org/10.1186/1471-2164-15-44openalex-snapshot
Fragmented mitochondrial genomes of the rat lice, Polyplax asiatica and Polyplax spinulosa: intra-genus variation in fragmentation pattern and a possible link between the extent of fragmentation and the length of life cycle
inferredcites →https://doi.org/10.1186/1471-2164-15-751openalex-snapshot
Fragmented mitochondrial genomes are present in both major clades of the blood-sucking lice (suborder Anoplura): evidence from two Hoplopleura rodent lice (family Hoplopleuridae)
inferredcites →https://doi.org/10.1186/1756-3305-7-144openalex-snapshot
Variation in mitochondrial minichromosome composition between blood-sucking lice of the genus Haematopinus that infest horses and pigs
inferredcites →https://doi.org/10.1371/journal.pone.0033973openalex-snapshot
The Multipartite Mitochondrial Genome of Liposcelis bostrychophila: Insights into the Evolution of Mitochondrial Genomes in Bilateral Animals
inferredcites →https://doi.org/10.1371/journal.pone.0045925openalex-snapshot
Comparative Mitogenomic Analysis of Damsel Bugs Representing Three Tribes in the Family Nabidae (Insecta: Hemiptera)
inferredcites →https://doi.org/10.1371/journal.pone.0061685openalex-snapshot
Mitochondrial Genomes of Two Barklice, Psococerastis albimaculata and Longivalvus hyalospilus (Psocoptera: Psocomorpha): Contrasting Rates in Mitochondrial Gene Rearrangement between Major Lineages of Psocodea
inferredcites →https://doi.org/10.1371/journal.pone.0073329openalex-snapshot
Heteroplasmy in the Mitochondrial Genomes of Human Lice and Ticks Revealed by High Throughput Sequencing
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.11646/zootaxa.5214.3.1zenodo-depositor-declared
An annotated checklist of sucking lice (Phthiraptera: Anoplura) from domestic and wild mammals in Malaysia, with lists of hosts and pathogens
inferred← citeshttps://doi.org/10.1002/ece3.5542openalex-snapshot
The complete mitochondrial genomes of two vent squat lobsters, Munidopsis lauensis and M. verrilli : Novel gene arrangements and phylogenetic implications
inferred← citeshttps://doi.org/10.1007/s11230-023-10106-3openalex-snapshot
Characterization of the fragmented mitochondrial genome of domestic pig louse Haematopinus suis (Insecta: Haematopinidae) from China
inferred← citeshttps://doi.org/10.1016/j.cimid.2020.101569openalex-snapshot
Molecular detection of microorganisms in lice collected from farm animals in Northeastern Algeria
inferred← citeshttps://doi.org/10.1016/j.gene.2020.145312openalex-snapshot
Structure, gene order, and nucleotide composition of mitochondrial genomes in parasitic lice from Amblycera
inferred← citeshttps://doi.org/10.1016/j.gene.2023.147830openalex-snapshot
Complete mitochondrial genome of Stethoconus japonicus (Hemiptera: Miridae): Insights into the evolutionary traits within the family Miridae
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2018.05.021openalex-snapshot
The mitochondrial genomes of the barklice, Lepinotus reticulatus and Dorypteryx domestica (Psocodea: Trogiomorpha): Insight into phylogeny of the order Psocodea
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2019.04.034openalex-snapshot
A novel mitochondrial genome fragmentation pattern in Liposcelis brunnea, the type species of the genus Liposcelis (Psocodea: Liposcelididae)
inferred← citeshttps://doi.org/10.1016/j.ijppaw.2022.03.013openalex-snapshot
Comparative analyses of the fragmented mitochondrial genomes of wild pig louse Haematopinus apri from China and Japan
inferred← citeshttps://doi.org/10.1016/j.isci.2023.107351openalex-snapshot
The fragmented mitochondrial genomes of two Linognathus lice reveal active minichromosomal recombination and recombination hotspots
inferred← citeshttps://doi.org/10.1016/j.mito.2021.02.009openalex-snapshot
HERMES: An improved method to test mitochondrial genome molecular synapomorphies among clades
inferred← citeshttps://doi.org/10.1016/j.vprsr.2026.101424openalex-snapshot
Morphological and molecular evidence of Linognathus vituli infestation in yaks from Ganzi Tibetan Autonomous Prefecture, China
inferred← citeshttps://doi.org/10.1016/j.ygeno.2020.09.005openalex-snapshot
Fragmented mitochondrial genomes evolved in opposite directions between closely related macaque louse Pedicinus obtusus and colobus louse Pedicinus badii
inferred← citeshttps://doi.org/10.1016/j.ympev.2017.10.014openalex-snapshot
Mitochondrial phylogenomics and genome rearrangements in the barklice (Insecta: Psocodea)
inferred← citeshttps://doi.org/10.1038/s41598-017-04617-5openalex-snapshot
Novel insights into mitochondrial gene rearrangement in thrips (Insecta: Thysanoptera) from the grass thrips, Anaphothrips obscurus
inferred← citeshttps://doi.org/10.1038/s41598-018-25759-0openalex-snapshot
The bipartite mitochondrial genome of Ruizia karukerae (Rhigonematomorpha, Nematoda)
inferred← citeshttps://doi.org/10.1038/s42003-022-03625-0openalex-snapshot
Independent evolution of highly variable, fragmented mitogenomes of parasitic lice
inferred← citeshttps://doi.org/10.1038/srep30660openalex-snapshot
The mitochondrial genome of booklouse, Liposcelis sculptilis (Psocoptera: Liposcelididae) and the evolutionary timescale of Liposcelis
inferred← citeshttps://doi.org/10.1051/parasite/2020026openalex-snapshot
Development of MALDI-TOF mass spectrometry for the identification of lice isolated from farm animals
inferred← citeshttps://doi.org/10.1093/gbe/evx007openalex-snapshot
The Mitochondrial Genome of the Guanaco Louse, Microthoracius praelongiceps: Insights into the Ancestral Mitochondrial Karyotype of Sucking Lice (Anoplura, Insecta)
inferred← citeshttps://doi.org/10.1093/jme/tjaa266openalex-snapshot
Identification of Lice Stored in Alcohol Using MALDI-TOF MS
inferred← citeshttps://doi.org/10.1093/sysbio/syy062openalex-snapshot
Mitochondrial Genome Fragmentation Unites the Parasitic Lice of Eutherian Mammals
inferred← citeshttps://doi.org/10.1111/mve.12699openalex-snapshot
Mitochondrial genome sequence comparisons indicate that the elephant louse Haematomyzus elephantis ( Piaget , 1869) contains cryptic species
inferred← citeshttps://doi.org/10.1111/syen.12504openalex-snapshot
Mitochondrial genomes within bark lice (Insecta: Psocodea: Psocomorpha) reveal novel gene rearrangements containing phylogenetic signal
inferred← citeshttps://doi.org/10.1186/s12864-016-3047-xopenalex-snapshot
The mitochondrial genome of Globodera ellingtonae is composed of two circles with segregated gene content and differential copy numbers
inferred← citeshttps://doi.org/10.1186/s12864-021-07859-wopenalex-snapshot
Frequent tRNA gene translocation towards the boundaries with control regions contributes to the highly dynamic mitochondrial genome organization of the parasitic lice of mammals
inferred← citeshttps://doi.org/10.1186/s12864-022-08530-8openalex-snapshot
Fragmented mitochondrial genomes of seal lice (family Echinophthiriidae) and gorilla louse (family Pthiridae): frequent minichromosomal splits and a host switch of lice between seals
inferred← citeshttps://doi.org/10.1186/s12864-024-11005-7openalex-snapshot
Drastic variation in mitochondrial genome organization between two congeneric species of bird lice (Philopteridae: Ibidoecus)
inferred← citeshttps://doi.org/10.1186/s13071-020-04381-yopenalex-snapshot
Variation of mitochondrial minichromosome composition in Hoplopleura lice (Phthiraptera: Hoplopleuridae) from rats
inferred← citeshttps://doi.org/10.1186/s13071-021-04776-5openalex-snapshot
Highly rearranged mitochondrial genome in Falcolipeurus lice (Phthiraptera: Philopteridae) from endangered eagles
inferred← citeshttps://doi.org/10.1360/ssv-2024-0016openalex-snapshot
Evolutionary characteristics and origin of fragmented mitochondrial genomes in Psocodea
inferred← citeshttps://doi.org/10.1371/journal.pgen.1011266openalex-snapshot
Mitochondrial genome fragmentation is correlated with increased rates of molecular evolution
inferred← citeshttps://doi.org/10.1371/journal.pone.0162248openalex-snapshot
The Mitochondrial Cytochrome Oxidase Subunit I Gene Occurs on a Minichromosome with Extensive Heteroplasmy in Two Species of Chewing Lice, Geomydoecus aurei and Thomomydoecus minor
inferred← citeshttps://doi.org/10.1371/journal.pone.0254138openalex-snapshot
Mitochondrial genome of Geomydoecus aurei, a pocket-gopher louse
inferred← citeshttps://doi.org/10.1534/g3.117.300410openalex-snapshot
The Highly Divergent Mitochondrial Genomes Indicate That the Booklouse,Liposcelis bostrychophila(Psocoptera: Liposcelididae) Is a Cryptic Species
inferred← citeshttps://doi.org/10.21608/ejvs.2024.289022.2083openalex-snapshot
Prevalence and Associated Risk Factors of Lice in Sheep and Goats in Mosul City- Iraq
inferred← citeshttps://doi.org/10.3390/ani13122046openalex-snapshot
Mitochondrial Genome Fragmentation Occurred Multiple Times Independently in Bird Lice of the Families Menoponidae and Laemobothriidae
inferred← citeshttps://doi.org/10.3390/ijms17111843openalex-snapshot
The Complete Mitochondrial Genome of Aleurocanthus camelliae: Insights into Gene Arrangement and Genome Organization within the Family Aleyrodidae
inferred← citeshttps://doi.org/10.3390/ijms232113092openalex-snapshot
A Novel Mitochondrial Genome Fragmentation Pattern in the Buffalo Louse Haematopinus tuberculatus (Psocodea: Haematopinidae)
inferred← citeshttps://doi.org/10.3390/life12091442openalex-snapshot
Genomic Approaches to Uncovering the Coevolutionary History of Parasitic Lice
inferred← citeshttps://doi.org/10.6084/m9.figshare.14634146openalex-snapshot
Additional file 1 of Highly rearranged mitochondrial genome in Falcolipeurus lice (Phthiraptera: Philopteridae) from endangered eagles
inferred← citeshttps://doi.org/10.6084/m9.figshare.14634149openalex-snapshot
Additional file 2 of Highly rearranged mitochondrial genome in Falcolipeurus lice (Phthiraptera: Philopteridae) from endangered eagles
inferred← citeshttps://doi.org/10.6084/m9.figshare.15128457openalex-snapshot
Additional file 1 of Frequent tRNA gene translocation towards the boundaries with control regions contributes to the highly dynamic mitochondrial genome organization of the parasitic lice of mammals
inferred← citeshttps://doi.org/10.6084/m9.figshare.15128460openalex-snapshot
Additional file 2 of Frequent tRNA gene translocation towards the boundaries with control regions contributes to the highly dynamic mitochondrial genome organization of the parasitic lice of mammals
inferred← citeshttps://doi.org/10.6084/m9.figshare.15128463openalex-snapshot
Additional file 3 of Frequent tRNA gene translocation towards the boundaries with control regions contributes to the highly dynamic mitochondrial genome organization of the parasitic lice of mammals
inferred← citeshttps://doi.org/10.6084/m9.figshare.15128466openalex-snapshot
Additional file 4 of Frequent tRNA gene translocation towards the boundaries with control regions contributes to the highly dynamic mitochondrial genome organization of the parasitic lice of mammals
inferred← citeshttps://doi.org/10.6084/m9.figshare.19565859openalex-snapshot
Additional file 1 of Fragmented mitochondrial genomes of seal lice (family Echinophthiriidae) and gorilla louse (family Pthiridae): frequent minichromosomal splits and a host switch of lice between seals
inferred← citeshttps://doi.org/10.70675/beb3a2f3z41fez4f37zb8e2za1daf10159c7openalex-snapshot
Développement d'outils innovants pour l'identification et la classification des arthropodes
inferred← citeshttps://doi.org/10.7717/peerj.8759openalex-snapshot
Mitochondrial genomes of Columbicola feather lice are highly fragmented, indicating repeated evolution of minicircle-type genomes in parasitic lice
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