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Complete Mitochondrial DNA Sequence of the Scallop Placopecten magellanicus: Evidence of Transposition Leading to an Uncharacteristically Large Mitochondrial Genome
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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/bf00175505openalex-snapshot
Endotherms, ectotherms, and mitochondrial genome-size variation
inferredcites →https://doi.org/10.1007/bf00310901openalex-snapshot
Dispersed discrete length polymorphism of mitochondrial DNA in the scallop Placopecten magellanicus (Gmelin)
inferredcites →https://doi.org/10.1007/bf00435506openalex-snapshot
Conserved tRNA gene cluster in starfish mitochondrial DNA
inferredcites →https://doi.org/10.1007/bf01731581openalex-snapshot
A simple method for estimating evolutionary rates of base substitutions through comparative studies of nucleotide sequences
inferredcites →https://doi.org/10.1007/s00239-004-0214-5openalex-snapshot
Novel Repetitive Structures, Deviant Protein-Encoding Sequences andUnidentified ORFs in the Mitochondrial Genome of the BrachiopodLingula anatina
inferredcites →https://doi.org/10.1016/0022-2836(82)90515-0openalex-snapshot
A simple method for displaying the hydropathic character of a protein
inferredcites →https://doi.org/10.1016/0092-8674(80)90350-5openalex-snapshot
The tRNA genes punctuate the reading of genetic information in human mitochondrial DNA
inferredcites →https://doi.org/10.1016/b978-0-444-82235-2.50029-1openalex-snapshot
Mitochondrial Genomes of Anthozoa (Cnidaria)
inferredcites →https://doi.org/10.1016/s0022-2836(05)80360-2openalex-snapshot
Basic Local Alignment Search Tool
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/10.1016/s0074-7696(08)62066-5openalex-snapshot
Animal Mitochondrial DNA: Structure and Evolution
inferredcites →https://doi.org/10.1016/s0959-437x(98)80035-xopenalex-snapshot
Big trees from little genomes: mitochondrial gene order as a phylogenetic tool
inferredcites →https://doi.org/10.1038/294626a0openalex-snapshot
Two conserved sequence blocks within eukaryotic tRNA genes are major promoter elements
inferredcites →https://doi.org/10.1038/317819a0openalex-snapshot
Repeat sequence families derived from mammalian tRNA genes
inferredcites →https://doi.org/10.1038/35001059openalex-snapshot
Ancestral chloroplast genome in Mesostigma viride reveals an early branch of green plant evolution
inferredcites →https://doi.org/10.1038/387247a0openalex-snapshot
Animal mitochondrial DNA recombination
inferredcites →https://doi.org/10.1073/pnas.84.21.7595openalex-snapshot
Atypical mitochondrial DNA from the deep-sea scallop Placopecten magellanicus
inferredcites →https://doi.org/10.1074/jbc.271.44.27536openalex-snapshot
Mammalian Mitochondria Possess Homologous DNA Recombination Activity
inferredcites →https://doi.org/10.1074/jbc.m510136200openalex-snapshot
C to U Editing Stimulates A to I Editing in the Anticodon Loop of a Cytoplasmic Threonyl tRNA in Trypanosoma brucei
inferredcites →https://doi.org/10.1093/bioinformatics/16.3.296openalex-snapshot
RRTree: Relative-Rate Tests between groups of sequences on a phylogenetic tree
inferredcites →https://doi.org/10.1093/genetics/123.4.825openalex-snapshot
Mitochondrial DNA in the bark weevils: size, structure and heteroplasmy.
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/molbev/msg058openalex-snapshot
Evidence for Recombination of mtDNA in the Marine Mussel Mytilus trossulus from the Baltic
inferredcites →https://doi.org/10.1093/molbev/msg218openalex-snapshot
Complete mtDNA Sequence of the North American Freshwater Mussel, Lampsilis ornata (Unionidae): An Examination of the Evolution and Phylogenetic Utility of Mitochondrial Genome Organization in Bivalvia (Mollusca)
inferredcites →https://doi.org/10.1093/molbev/msh090openalex-snapshot
Complete Sequences of the Highly Rearranged Molluscan Mitochondrial Genomes of the Scaphopod Graptacme eborea and the Bivalve Mytilus edulis
inferredcites →https://doi.org/10.1093/molbev/msh227openalex-snapshot
Long-Term Conservation of Six Duplicated Structural Genes in Cephalopod Mitochondrial Genomes
inferredcites →https://doi.org/10.1093/molbev/msh244openalex-snapshot
A Broad Survey of Recombination in Animal Mitochondria
inferredcites →https://doi.org/10.1093/molbev/msi079openalex-snapshot
The Complete Maternal and Paternal Mitochondrial Genomes of the Mediterranean Mussel Mytilus galloprovincialis: Implications for the Doubly Uniparental Inheritance Mode of mtDNA
inferredcites →https://doi.org/10.1093/molbev/msi084openalex-snapshot
Widespread Recombination in Published Animal mtDNA Sequences1
inferredcites →https://doi.org/10.1093/nar/21.7.1523openalex-snapshot
Editing of a tRNA anticodon in marsupial mitochondria changes its codon recognition
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/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/27.2.573openalex-snapshot
Tandem repeats finder: a program to analyze DNA sequences
inferredcites →https://doi.org/10.1093/nar/29.22.4633openalex-snapshot
REPuter: the manifold applications of repeat analysis on a genomic scale
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a003755openalex-snapshot
Recombination in Animal Mitochondrial DNA: Evidence from Published Sequences
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a003904openalex-snapshot
Direct Evidence for Homologous Recombination in Mussel (Mytilus galloprovincialis) Mitochondrial DNA
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a003917openalex-snapshot
Duplication and Concerted Evolution of the Mitochondrial Control Region in the Parrot Genus Amazona
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a004049openalex-snapshot
Heteroplasmy and Evidence for Recombination in the Mitochondrial Control Region of the Flatfish Platichthys flesus
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a040442openalex-snapshot
Slipped-strand mispairing: a major mechanism for DNA sequence evolution.
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a040586openalex-snapshot
Molecular characterization of a repeat element causing large-scale size variation in the mitochondrial DNA of the sea scallop Placopecten magellanicus.
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a040711openalex-snapshot
Repeated Sequences and Large-Scale Size Variation of Mitochondrial DNA: A Common Feature among Scallops (Bivalvia: Pectinidae)
inferredcites →https://doi.org/10.1105/tpc.11.9.1717openalex-snapshot
The Complete Mitochondrial DNA Sequences of Nephroselmis olivacea and Pedinomonas minor: Two Radically Different Evolutionary Patterns within Green Algae
inferredcites →https://doi.org/10.1645/ge-284ropenalex-snapshot
THE MITOCHONDRIAL GENOME OF BIOMPHALARIA GLABRATA (GASTROPODA: BASOMMATOPHORA), INTERMEDIATE HOST OF SCHISTOSOMA MANSONI*
inferredcites →https://doi.org/10.5860/choice.37-5647openalex-snapshot
Phylogeography: the history and formation of species
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.3897/zookeys.1232.139844zenodo-depositor-declared
Complete mitochondrial genomes of Sinonovacula rivularis and Novaculina chinensis and their phylogenetic relationships within family Pharidae
inferred← citeshttps://doi.org/10.1002/jez.b.20251openalex-snapshot
Role‐reversal of gender‐associated mitochondrial DNA affects mitochondrial function in Mytilus edulis (Bivalvia: Mytilidae)
inferred← citeshttps://doi.org/10.1007/s00239-009-9308-4openalex-snapshot
The Mitochondrial Genomes of Two Scallops, Argopecten irradians and Chlamys farreri (Mollusca: Bivalvia): The Most Highly Rearranged Gene Order in the Family Pectinidae
inferred← citeshttps://doi.org/10.1007/s11033-010-9974-8openalex-snapshot
Complete mitochondrial DNA sequence and phylogenetic analysis of Zhikong scallop Chlamys farreri (Bivalvia: Pectinidae)
inferred← citeshttps://doi.org/10.1007/s11033-011-0825-zopenalex-snapshot
Complete mitochondrial DNA sequence of Crassostrea nippona: comparative and phylogenomic studies on seven commercial Crassostrea species
inferred← citeshttps://doi.org/10.1007/s11033-011-0861-8openalex-snapshot
The complete mitochondrial genome of the grand jackknife clam, Solen grandis (Bivalvia: Solenidae): a novel gene order and unusual non-coding region
inferred← citeshttps://doi.org/10.1007/s11033-025-10335-3openalex-snapshot
A novel mitochondrial gene rearrangement delineate Magallana gryphoides species from other Magallana crassostreine oysters
inferred← citeshttps://doi.org/10.1007/s11802-021-4707-2openalex-snapshot
Relaxation of Selective Constraint on the Ultra-Large Mitochondrial Genomes of Arcidae (Mollusca: Bivalvia)
inferred← citeshttps://doi.org/10.1007/s12562-013-0662-1openalex-snapshot
Complete mitochondrial genome sequence of Japanese cockle Fulvia mutica (Cardiidae)
inferred← citeshttps://doi.org/10.1007/s12562-014-0819-6openalex-snapshot
The variable 5′ end of the 16S rRNA gene as a novel barcoding tool for scallops (Bivalvia, Pectinidae)
inferred← citeshttps://doi.org/10.1007/s13258-017-0548-1openalex-snapshot
Complete mitochondrial genome sequence of Cucullaea labiata (Arcoida: Cucullaeidae) and phylogenetic implications
inferred← citeshttps://doi.org/10.1016/b978-0-444-62710-0.00009-2openalex-snapshot
Scallop Genetics and Genomics
inferred← citeshttps://doi.org/10.1016/j.bse.2015.06.015openalex-snapshot
The mitochondrial genomes of Pecten albicans and Pecten maximus (Bivalvia: Pectinidae) reveal a novel gene arrangement with low genetic differentiation
inferred← citeshttps://doi.org/10.1016/j.cbd.2012.12.003openalex-snapshot
Complete mitochondrial DNA sequence of the ark shell Scapharca broughtonii: An ultra-large metazoan mitochondrial genome
inferred← citeshttps://doi.org/10.1016/j.cbd.2015.08.001openalex-snapshot
Complete mitochondrial genome of Anadara vellicata (Bivalvia: Arcidae): A unique gene order and large atypical non-coding region
inferred← citeshttps://doi.org/10.1016/j.cbd.2020.100739openalex-snapshot
Comparative mitogenomic analysis of the superfamily Tellinoidea (Mollusca: Bivalvia): Insights into the evolution of the gene rearrangements
inferred← citeshttps://doi.org/10.1016/j.gene.2011.12.002openalex-snapshot
Comparative studies of the complete mitochondrial genomes of four Paphia clams and reconsideration of subgenus Neotapes (Bivalvia: Veneridae)
inferred← citeshttps://doi.org/10.1016/j.gene.2012.07.032openalex-snapshot
New features of Asian Crassostrea oyster mitochondrial genomes: A novel alloacceptor tRNA gene recruitment and two novel ORFs
inferred← citeshttps://doi.org/10.1016/j.gene.2012.08.037openalex-snapshot
A unique tRNA gene family and a novel, highly expressed ORF in the mitochondrial genome of the silver-lip pearl oyster, Pinctada maxima (Bivalvia: Pteriidae)
inferred← citeshttps://doi.org/10.1016/j.gene.2014.12.011openalex-snapshot
The complete mitochondrial DNA of Tegillarca granosa and comparative mitogenomic analyses of three Arcidae species
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2018.06.008openalex-snapshot
Mitochondrial genome of Argopecten irradians reveals higher-level phylogenetic relationships in Anisomyaria
inferred← citeshttps://doi.org/10.1016/j.margen.2010.01.001openalex-snapshot
Characterization of a mitochondrial ORF from the gender-associated mtDNAs of Mytilus spp. (Bivalvia: Mytilidae): Identification of the “missing” ATPase 8 gene
inferred← citeshttps://doi.org/10.1016/j.tig.2007.05.011openalex-snapshot
The unusual system of doubly uniparental inheritance of mtDNA: isn’t one enough?
inferred← citeshttps://doi.org/10.1016/j.ygeno.2023.110747openalex-snapshot
Chromosome-level genome assembly of sea scallop Placopecten magellanicus provides insights into the genetic characteristics and adaptive evolution of large scallops
inferred← citeshttps://doi.org/10.1016/j.ympev.2010.05.029openalex-snapshot
Comparison of seven Crassostrea mitogenomes and phylogenetic analyses
inferred← citeshttps://doi.org/10.1016/j.ympev.2012.11.017openalex-snapshot
Mitogenomics does not resolve deep molluscan relationships (yet?)
inferred← citeshttps://doi.org/10.1016/j.ympev.2013.07.016openalex-snapshot
Mitogenomics at the base of Metazoa
inferred← citeshttps://doi.org/10.1016/j.ympev.2017.03.004openalex-snapshot
Curious bivalves: Systematic utility and unusual properties of anomalodesmatan mitochondrial genomes
inferred← citeshttps://doi.org/10.1016/j.ympev.2019.106710openalex-snapshot
Hidden cases of tRNA gene duplication and remolding in mitochondrial genomes of amphipods
inferred← citeshttps://doi.org/10.1016/j.ympev.2020.106857openalex-snapshot
Mitogenomics reveals phylogenetic relationships of Arcoida (Mollusca, Bivalvia) and multiple independent expansions and contractions in mitochondrial genome size
inferred← citeshttps://doi.org/10.1038/srep33794openalex-snapshot
Complete mitochondrial genomes of Trisidos kiyoni and Potiarca pilula: Varied mitochondrial genome size and highly rearranged gene order in Arcidae
inferred← citeshttps://doi.org/10.1080/19401730902964425openalex-snapshot
The complete mitochondrial genome of the clamMeretrix petechialis(Mollusca: Bivalvia: Veneridae)
inferred← citeshttps://doi.org/10.1093/gbe/evac089openalex-snapshot
Contrasting Modes of Mitochondrial Genome Evolution in Sister Taxa of Wood-Eating Marine Bivalves (Teredinidae and Xylophagaidae)
inferred← citeshttps://doi.org/10.1093/jhered/esn012openalex-snapshot
An Induced Mass Spawn of the Hermaphroditic Lion-Paw Scallop, Nodipecten subnodosus: Genetic Assignment of Maternal and Paternal Parentage
inferred← citeshttps://doi.org/10.1093/mollus/eyab018openalex-snapshot
Insight into the adaptive evolution of mitochondrial genomes in intertidal chitons
inferred← citeshttps://doi.org/10.1093/mollus/eyad003openalex-snapshot
The mitochondrial genome ofIsognomon nucleusand mitogenomics of pteriomorphia (Bivalvia: Autobranchia)
inferred← citeshttps://doi.org/10.1093/mollus/eyz009openalex-snapshot
The complete mitochondrial genomes of three species of Macridiscus Dall, 1902 (Bivalvia: Veneroidea: Veneridae) and their phylogenetic implications
inferred← citeshttps://doi.org/10.1098/rstb.2020.0159openalex-snapshot
Molluscan mitochondrial genomes break the rules
inferred← citeshttps://doi.org/10.1101/gr.091132.109openalex-snapshot
‘Why genomes in pieces?’ revisited: Sucking lice do their own thing in mtDNA circle game
inferred← citeshttps://doi.org/10.1139/g10-096openalex-snapshot
The mitogenome of Paphia euglypta (Bivalvia: Veneridae) and comparative mitogenomic analyses of three venerids
inferred← citeshttps://doi.org/10.1139/g2012-008openalex-snapshot
Widespread atypical mitochondrial DNA structure in isopods (Crustacea, Peracarida) related to a constitutive heteroplasmy in terrestrial species
inferred← citeshttps://doi.org/10.1186/1471-2148-10-394openalex-snapshot
Unusual conservation of mitochondrial gene order in Crassostreaoysters: evidence for recent speciation in Asia
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The mitochondrial and plastid genomes of Volvox carteri: bloated molecules rich in repetitive DNA
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inferred← citeshttps://doi.org/10.1186/1756-0500-4-400openalex-snapshot
Complete mitochondrial DNA sequence of the European flat oyster Ostrea edulis confirms Ostreidae classification
inferred← citeshttps://doi.org/10.1186/s12862-016-0829-3openalex-snapshot
Monoplacophoran mitochondrial genomes: convergent gene arrangements and little phylogenetic signal
inferred← citeshttps://doi.org/10.1186/s12862-022-01976-0openalex-snapshot
Complex mitogenomic rearrangements within the Pectinidae (Mollusca: Bivalvia).
inferred← citeshttps://doi.org/10.1186/s12864-022-09040-3openalex-snapshot
A comparative analysis of mitochondrial ORFs provides new insights on expansion of mitochondrial genome size in Arcidae
inferred← citeshttps://doi.org/10.1186/s12864-024-10505-wopenalex-snapshot
High heteroplasmy is associated with low mitochondrial copy number and selection against non-synonymous mutations in the snail Cepaea nemoralis
inferred← citeshttps://doi.org/10.1371/journal.pone.0082857openalex-snapshot
The Mitochondrial Genome of Arctica islandica; Phylogeny and Variation
inferred← citeshttps://doi.org/10.1371/journal.pone.0168263openalex-snapshot
Monogonont Rotifer, Brachionus calyciflorus, Possesses Exceptionally Large, Fragmented Mitogenome
inferred← citeshttps://doi.org/10.1371/journal.pone.0184464openalex-snapshot
First complete female mitochondrial genome in four bivalve species genus Donax and their phylogenetic relationships within the Veneroida order
inferred← citeshttps://doi.org/10.21203/rs.3.rs-11188068/v1openalex-snapshot
Extremely Divergent Repeats Made the Largest Bilaterian Mitogenome in Photosymbiotic Bivalves
inferred← citeshttps://doi.org/10.29822/jfst.201103.0004openalex-snapshot
Mitochondrial Cytochrome b Gene Sequences of Five Common Stingrays in Taiwan
inferred← citeshttps://doi.org/10.3109/19401736.2013.772152openalex-snapshot
The complete mitochondrial genome of the clamMactra veneriformis(Bivalvia: Mactridae): Has a unique non-coding region, missingatp8and typicaltRNASer
inferred← citeshttps://doi.org/10.3389/fmolb.2021.626042openalex-snapshot
Long-Lived Species of Bivalves Exhibit Low MT-DNA Substitution Rates
inferred← citeshttps://doi.org/10.3390/genes12122030openalex-snapshot
The Mitochondrial Genome of a Freshwater Pelagic Amphipod Macrohectopus branickii Is among the Longest in Metazoa
inferred← citeshttps://doi.org/10.3390/genes14040910openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/ijms25168755openalex-snapshot
The Mitochondrial Genome of Ylistrum japonicum (Bivalvia, Pectinidae) and Its Phylogenetic Analysis
inferred← citeshttps://doi.org/10.6084/m9.figshare.26036423openalex-snapshot
Additional file 1 of High heteroplasmy is associated with low mitochondrial copy number and selection against non-synonymous mutations in the snail Cepaea nemoralis
inferred← citeshttps://doi.org/10.6084/m9.figshare.26036537openalex-snapshot
Additional file 2 of High heteroplasmy is associated with low mitochondrial copy number and selection against non-synonymous mutations in the snail Cepaea nemoralis
inferred← citeshttps://doi.org/10.6084/m9.figshare.26551057openalex-snapshot
Additional file 1 of A comparative analysis of mitochondrial ORFs provides new insights on expansion of mitochondrial genome size in Arcidae
inferred← citeshttps://doi.org/10.6084/m9.figshare.26551060openalex-snapshot
Additional file 2 of A comparative analysis of mitochondrial ORFs provides new insights on expansion of mitochondrial genome size in Arcidae
inferred← citeshttps://doi.org/10.6084/m9.figshare.26551120openalex-snapshot
Additional file 3 of A comparative analysis of mitochondrial ORFs provides new insights on expansion of mitochondrial genome size in Arcidae
inferred← citeshttps://doi.org/10.6084/m9.figshare.26551126openalex-snapshot
Additional file 4 of A comparative analysis of mitochondrial ORFs provides new insights on expansion of mitochondrial genome size in Arcidae
inferred← citeshttps://doi.org/10.6084/m9.figshare.26551129openalex-snapshot
Additional file 5 of A comparative analysis of mitochondrial ORFs provides new insights on expansion of mitochondrial genome size in Arcidae
inferred← citeshttps://doi.org/10.6084/m9.figshare.26551132openalex-snapshot
Additional file 6 of A comparative analysis of mitochondrial ORFs provides new insights on expansion of mitochondrial genome size in Arcidae
inferred← citeshttps://doi.org/10.6084/m9.figshare.26551135openalex-snapshot
Additional file 7 of A comparative analysis of mitochondrial ORFs provides new insights on expansion of mitochondrial genome size in Arcidae
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