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Characterization of the first mitochondrial genome of a catenulid flatworm:Stenostomum leucops(Platyhelminthes)

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What this work says

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

inferredcites →https://doi.org/10.1002/0471142727.mb1910s89openalex-snapshot

Galaxy: A Web‐Based Genome Analysis Tool for Experimentalists

inferredcites →https://doi.org/10.1007/bf00160240openalex-snapshot

Planarian mitochondria II. The unique genetic code as deduced from cytochrome c oxidase subunit I gene sequences

inferredcites →https://doi.org/10.1007/bf00993304openalex-snapshot

Asexual reproduction and regeneration ofCatenula (Turbellaria, Archoophora)

inferredcites →https://doi.org/10.1007/bf01323123openalex-snapshot

Stem cells in microturbellarians

inferredcites →https://doi.org/10.1007/s00239-003-2559-6openalex-snapshot

Complete mtDNA of Ciona intestinalis Reveals Extensive Gene Rearrangement and the Presence of an atp8 and an Extra trnM Gene in Ascidians

inferredcites →https://doi.org/10.1007/s00239-004-0159-8openalex-snapshot

First Sequenced Mitochondrial Genome from the Phylum Acanthocephala(Leptorhynchoides thecatus) and Its Phylogenetic Position Within Metazoa

inferredcites →https://doi.org/10.1016/j.cub.2015.03.034openalex-snapshot

A Transcriptomic-Phylogenomic Analysis of the Evolutionary Relationships of Flatworms

inferredcites →https://doi.org/10.1016/j.cub.2015.06.068openalex-snapshot

Spiralian Phylogeny Informs the Evolution of Microscopic Lineages

inferredcites →https://doi.org/10.1016/j.gene.2008.03.008openalex-snapshot

The mitochondrial genome of Gyrodactylus derjavinoides (Platyhelminthes: Monogenea) — A mitogenomic approach for Gyrodactylus species and strain identification

inferredcites →https://doi.org/10.1016/j.gene.2015.08.054openalex-snapshot

Characterization of the complete mitochondrial genomes from Polycladida (Platyhelminthes) using next-generation sequencing

inferredcites →https://doi.org/10.1016/j.ijpara.2012.02.001openalex-snapshot

Mitochondrial gene order change in Schistosoma (Platyhelminthes: Digenea: Schistosomatidae)

inferredcites →https://doi.org/10.1016/j.ode.2008.09.002openalex-snapshot

Phylogeny of Catenulida and support for Platyhelminthes

inferredcites →https://doi.org/10.1016/j.ode.2008.09.003openalex-snapshot

DNA taxonomy of Swedish Catenulida (Platyhelminthes) and a phylogenetic framework for catenulid classification

inferredcites →https://doi.org/10.1016/j.parint.2007.04.001openalex-snapshot

Complete sequence of the mitochondrial genome of Taenia saginata: Comparison with T. solium and T. asiatica

inferredcites →https://doi.org/10.1016/j.parint.2011.10.007openalex-snapshot

Complete mitochondrial genomes of Diplogonoporus balaenopterae and Diplogonoporus grandis (Cestoda: Diphyllobothriidae) and clarification of their taxonomic relationships

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.tree.2006.05.009openalex-snapshot

The use of genome-level characters for phylogenetic reconstruction

inferredcites →https://doi.org/10.1016/j.ympev.2012.02.020openalex-snapshot

Adding resolution to ordinal level relationships of tapeworms (Platyhelminthes: Cestoda) with large fragments of mtDNA

inferredcites →https://doi.org/10.1016/j.ympev.2012.08.023openalex-snapshot

MITOS: Improved de novo metazoan mitochondrial genome annotation

inferredcites →https://doi.org/10.1016/j.ympev.2012.12.015openalex-snapshot

Platyzoan mitochondrial genomes

inferredcites →https://doi.org/10.1016/j.ympev.2015.02.013openalex-snapshot

Elucidating the phylogenetic position of Gnathostomulida and first mitochondrial genomes of Gnathostomulida, Gastrotricha and Polycladida (Platyhelminthes)

inferredcites →https://doi.org/10.1016/s1471-4922(02)02252-3openalex-snapshot

Mitochondrial genomes of parasitic flatworms

inferredcites →https://doi.org/10.1016/s1567-7249(02)00040-5openalex-snapshot

The complete mitochondrial DNA sequence of the cestode Echinococcus multilocularis (Cyclophyllidea: Taeniidae)

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/10.1046/j.1463-6409.2002.00090.xopenalex-snapshot

The Nemertodermatida are basal bilaterians and not members of the Platyhelminthes

inferredcites →https://doi.org/10.1073/pnas.97.21.11359openalex-snapshot

Changes in mitochondrial genetic codes as phylogenetic characters: Two examples from the flatworms

inferredcites →https://doi.org/10.1079/9780851990279.0037openalex-snapshot

Genomes and genomics of parasitic flatworms.

inferredcites →https://doi.org/10.1086/physzool.2.1.30151062openalex-snapshot

An Experimental Study of Fission and Reconstitution in Stenostomum

inferredcites →https://doi.org/10.1093/bioinformatics/btm468openalex-snapshot

CREx: inferring genomic rearrangements based on common intervals

inferredcites →https://doi.org/10.1093/bioinformatics/bts091openalex-snapshot

Unipro UGENE: a unified bioinformatics toolkit

inferredcites →https://doi.org/10.1093/genetics/131.2.397openalex-snapshot

A novel mitochondrial genome organization for the blue mussel, Mytilus edulis.

inferredcites →https://doi.org/10.1093/genetics/157.2.621openalex-snapshot

Trichinella spiralismtDNA: A Nematode Mitochondrial Genome That Encodes a Putative ATP8 and Normally Structured tRNAs and Has a Gene Arrangement Relatable to Those of Coelomate Metazoans

inferredcites →https://doi.org/10.1093/icb/icj056openalex-snapshot

Lophotrochozoan mitochondrial genomes

inferredcites →https://doi.org/10.1093/nar/gkt371openalex-snapshot

Reconstructing mitochondrial genomes directly from genomic next-generation sequencing reads—a baiting and iterative mapping approach

inferredcites →https://doi.org/10.1093/nar/gku949openalex-snapshot

SMART: recent updates, new developments and status in 2015

inferredcites →https://doi.org/10.1101/gr.4086505openalex-snapshot

Galaxy: A platform for interactive large-scale genome analysis

inferredcites →https://doi.org/10.1186/1471-2148-10-309openalex-snapshot

The phylogenetic position of Acoela as revealed by the complete mitochondrial genome of Symsagittifera roscoffensis

inferredcites →https://doi.org/10.1186/1756-3305-7-377openalex-snapshot

The mitochondrial genome of Paragyrodactylus variegatus (Platyhelminthes: Monogenea): differences in major non-coding region and gene order compared to Gyrodactylus

inferredcites →https://doi.org/10.1186/gb-2010-11-8-r86openalex-snapshot

Galaxy: a comprehensive approach for supporting accessible, reproducible, and transparent computational research in the life sciences

inferredcites →https://doi.org/10.1186/s13071-016-1586-2openalex-snapshot

The mitochondrial genome of the egg-laying flatworm Aglaiogyrodactylus forficulatus (Platyhelminthes: Monogenoidea)

inferredcites →https://doi.org/10.1371/journal.pone.0120081openalex-snapshot

Evolutionary Analysis of Mitogenomes from Parasitic and Free-Living Flatworms

inferredcites →https://doi.org/10.1534/g3.116.028175openalex-snapshot

Comparative and Transcriptome Analyses Uncover Key Aspects of Coding- and Long Noncoding RNAs in Flatworm Mitochondrial Genomes

inferredcites →https://doi.org/10.1590/0031-1049.2015.55.27openalex-snapshot

STENOSTOMUM LEUCOPS DUGÈS, 1828 (PLATYHELMINTHES, CATENULIDA): A PUTATIVE SPECIES COMPLEX WITH PHENOTYPIC PLASTICITY

inferredcites →https://doi.org/10.1645/0022-3395(2003)089[0633:tmgott]2.0.co;2openalex-snapshot

The Mitochondrial Genome of the Tapeworm Taenia solium: A Finding of the Abbreviated Stop Codon U

inferredcites →https://doi.org/10.2225/vol12-issue2-fulltext-4openalex-snapshot

Isolation of high quality DNA: a protocol combining “rennet” and glass milk

inferredcites →https://doi.org/10.2225/vol12-issue2-fulltext-9openalex-snapshot

Aerobic removal of stigmasterol contained in kraft mill effluents

inferredcites →https://doi.org/10.7554/elife.05503openalex-snapshot

Nuclear genomic signals of the ‘microturbellarian’ roots of platyhelminth evolutionary innovation

What points at this work

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

inferred← citeshttps://doi.org/10.3897/zse.100.114016zenodo-depositor-declared

Integrative description of a new species of Dugesia (Platyhelminthes, Tricladida, Dugesiidae) from southern China, with its complete mitogenome and a biogeographic evaluation

inferred← citeshttps://doi.org/10.1016/j.angen.2023.200161openalex-snapshot

Does Atp8 Exist in the Mitochondrial Genome of Proseriata (Metazoa: Platyhelminthes)?

inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2020.06.025openalex-snapshot

The first mitochondrial genomes of endosymbiotic rhabdocoels illustrate evolutionary relaxation of atp8 and genome plasticity in flatworms

inferred← citeshttps://doi.org/10.1016/j.mito.2021.02.003openalex-snapshot

Mitochondrial gene order of the freshwater bryozoan Cristatella mucedo retains ancestral lophotrochozoan features

inferred← citeshttps://doi.org/10.1016/j.watbs.2022.100033openalex-snapshot

Evolutionary rates of mitochondrial sequences and gene orders in Spirurina (Nematoda) are episodic but synchronised

inferred← citeshttps://doi.org/10.1038/s41437-023-00650-5openalex-snapshot

Mitochondrially mediated RNA interference, a retrograde signaling system affecting nuclear gene expression

inferred← citeshttps://doi.org/10.1038/s41437-024-00712-2openalex-snapshot

Drivers of interlineage variability in mitogenomic evolutionary rates in Platyhelminthes

inferred← citeshttps://doi.org/10.1038/s41467-026-70576-zopenalex-snapshot

Patterns and determinants of mitogenomic evolution in Bilateria

inferred← citeshttps://doi.org/10.1038/s41598-019-55659-wopenalex-snapshot

The Catenulida flatworm can express genes from its microbiome or from the DNA it ingests

inferred← citeshttps://doi.org/10.1038/s42003-023-04471-4openalex-snapshot

The metazoan landscape of mitochondrial DNA gene order and content is shaped by selection and affects mitochondrial transcription

inferred← citeshttps://doi.org/10.1093/zoolinnean/zlag003openalex-snapshot

Molecular phylogeny of Catenulida (Platyhelminthes) with special focus on their diversity in Poland

inferred← citeshttps://doi.org/10.1101/283788openalex-snapshot

The first next-generation sequencing approach to the mitochondrial phylogeny of African monogenean parasites (Platyhelminthes: Gyrodactylidae and Dactylogyridae)

inferred← citeshttps://doi.org/10.1111/1749-4877.12605openalex-snapshot

Integrative taxonomy unveils a new species of Dugesia (Platyhelminthes, Tricladida, Dugesiidae) from the southern portion of the Taihang Mountains in northern China, with the description of its complete mitogenome and an exploratory analysis of mitochondrial gene order as a taxonomic character

inferred← citeshttps://doi.org/10.1111/mec.70015openalex-snapshot

Signatures of Endosymbiosis in Mitochondrial Genomes of Rhabdocoel Flatworms

inferred← citeshttps://doi.org/10.1186/s12864-017-3807-2openalex-snapshot

Atp8 is in the ground pattern of flatworm mitochondrial genomes

inferred← citeshttps://doi.org/10.1186/s12864-018-4893-5openalex-snapshot

The first next-generation sequencing approach to the mitochondrial phylogeny of African monogenean parasites (Platyhelminthes: Gyrodactylidae and Dactylogyridae)

inferred← citeshttps://doi.org/10.3390/ani13182857openalex-snapshot

Two-Fold ND5 Genes, Three-Fold Control Regions, lncRNA, and the “Missing” ATP8 Found in the Mitogenomes of Polypedates megacephalus (Rhacophridae: Polypedates)

inferred← citeshttps://doi.org/10.3390/life11070663openalex-snapshot

Mitochondrial Genomic Landscape: A Portrait of the Mitochondrial Genome 40 Years after the First Complete Sequence

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