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Mitochondrial DNA polymorphism and feminizing sex factors dynamics in a natural population of Armadillidium vulgare (Crustacea, Isopoda)
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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/bf02214332openalex-snapshot
Evolutionary consequences of cytoplasmic sex ratio distorters
inferredcites →https://doi.org/10.1016/0022-2011(89)90118-3openalex-snapshot
Wolbachia-like organisms and cytoplasmic incompatibility in Drosophila simulans
inferredcites →https://doi.org/10.1016/0022-2011(89)90137-7openalex-snapshot
Ultrastructural evidence of Wolbachia rickettsiales in Drosophila simulans and their relationships with unidirectional cross-incompatibility
inferredcites →https://doi.org/10.1016/0169-5347(88)90105-xopenalex-snapshot
Selfish genetic elements
inferredcites →https://doi.org/10.1038/hdy.1987.95openalex-snapshot
Paternal transmission of an extrachromosomal factor in a wasp: evolutionary implications
inferredcites →https://doi.org/10.1038/hdy.1992.138openalex-snapshot
Evolution of sex-determining mechanisms in a wild population of Armadillidium vulgare Latr. (Crustacea, Isopoda): competition between two feminizing parasitic sex factors
inferredcites →https://doi.org/10.1046/j.1420-9101.1991.4040603.xopenalex-snapshot
Experimental study of temperature effects on the sex ratio of broods in Terrestrial Crustacea Armadillidium vulgare Latr. Possible implications in natural populations
inferredcites →https://doi.org/10.1046/j.1420-9101.1993.6040511.xopenalex-snapshot
Transfer of a parasitic sex factor to the nuclear genome of the host: A hypothesis on the evolution of sex‐determining mechanisms in the terrestrial Isopod Armadillidium vulgare Latr.
inferredcites →https://doi.org/10.1086/285172openalex-snapshot
The Paternal-Sex-Ratio Chromosome of Nasonia
inferredcites →https://doi.org/10.1086/417973openalex-snapshot
Wild Pigs of the United States: Their History, Morphology, and Current Status.John J. Mayer , I. Lehr Brisbin, Jr.
inferredcites →https://doi.org/10.1093/genetics/125.3.551openalex-snapshot
Is there selection on RFLP differences in mitochondrial DNA?
inferredcites →https://doi.org/10.1093/genetics/129.2.399openalex-snapshot
Geographic distribution and inheritance of three cytoplasmic incompatibility types in Drosophila simulans.
inferredcites →https://doi.org/10.1093/genetics/132.1.205openalex-snapshot
Frequencies of mitochondrial DNA haplotypes in laboratory cage populations of the mosquito, Aedes albopictus.
inferredcites →https://doi.org/10.1093/genetics/132.3.713openalex-snapshot
Dynamics of cytoplasmic incompatibility and mtDNA variation in natural Drosophila simulans populations.
inferredcites →https://doi.org/10.1098/rspb.1992.0135openalex-snapshot
Wolbachiaendosymbionts responsible for various alterations of sexuality in arthropods
inferredcites →https://doi.org/10.1111/j.1469-185x.1987.tb01637.xopenalex-snapshot
SEX DETERMINATION IN CRUSTACEA
inferredcites →https://doi.org/10.1111/j.1469-185x.1993.tb00733.xopenalex-snapshot
THE INCIDENCES. MECHANISMS AND EVOLUTION OF CYTOPLASMIC SEX RATIO DISTORTERS IN ANIMALS
inferredcites →https://doi.org/10.1111/j.1558-5646.1986.tb00505.xopenalex-snapshot
RACE FORMATION, SPECIATION, AND INTROGRESSION WITHINDROSOPHILA SIMULANS, D. MAURITIANA, ANDD. SECHELLIAINFERRED FROM MITOCHONDRIAL DNA ANALYSIS
inferredcites →https://doi.org/10.1111/j.1558-5646.1990.tb05241.xopenalex-snapshot
MITOCHONDRIAL DNA POLYMORPHISM AND CYTOPLASMIC INCOMPATIBILITY IN NATURAL POPULATIONS OFDROSOPHILA SIMULANS
inferredcites →https://doi.org/10.1126/science.3358129openalex-snapshot
A "Selfish" B Chromosome That Enhances Its Transmission by Eliminating the Paternal Genome
inferredcites →https://doi.org/10.1186/1297-9686-16-1-57openalex-snapshot
Nouvelles données sur le déterminisme génétique et épigénétique de la monogénie chez le crustacé isopode terrestre Armadillidium vulgare Latr
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/10.1002/ece3.434openalex-snapshot
Deep sympatric mt DNA divergence in the autumnal moth (Epirrita autumnata)
inferred← citeshttps://doi.org/10.1007/bf00054417openalex-snapshot
What generates the diversity of Wolbachia—arthropod interactions?
inferred← citeshttps://doi.org/10.1007/s00239-007-9037-5openalex-snapshot
Structure and Evolution of the Atypical Mitochondrial Genome of Armadillidium vulgare (Isopoda, Crustacea)
inferred← citeshttps://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
inferred← citeshttps://doi.org/10.1016/j.actatropica.2025.107561openalex-snapshot
Effects of Wolbachia on mitochondrial DNA variation in Aedes albopictus (Diptera: Culicidae)
inferred← citeshttps://doi.org/10.1016/s2095-3119(18)62019-2openalex-snapshot
No evidence for an effect of Wolbachia on mtDNA variation and evolution in natural populations of Sesamia inferens (Lepidoptera: Noctuidae)
inferred← citeshttps://doi.org/10.1038/sj.hdy.6885380openalex-snapshot
Mitochondrial DNA variability and Wolbachia infection in two sibling woodlice species
inferred← citeshttps://doi.org/10.1080/24701394.2016.1197216openalex-snapshot
Effects of Wolbachia on mitochondrial DNA variation in populations of Athetis lepigone (Lepidoptera: Noctuidae) in China
inferred← citeshttps://doi.org/10.1093/genetics/151.1.203openalex-snapshot
Organization of the Large Mitochondrial Genome in the Isopod Armadillidium vulgare
inferred← citeshttps://doi.org/10.1093/genetics/152.4.1669openalex-snapshot
Mitochondrial DNA Polymorphism, Sex Ratio Distorters and Population Genetics in the Isopod Armadillidium vulgare
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/oxfordjournals.molbev.a004228openalex-snapshot
The Rate of Recombination in Wolbachia Bacteria
inferred← citeshttps://doi.org/10.1098/rsbl.2022.0457openalex-snapshot
Heterogeneous distribution of sex ratio distorters in natural populations of the isopod Armadillidium vulgare
inferred← citeshttps://doi.org/10.1098/rspb.2005.3056openalex-snapshot
Problems with mitochondrial DNA as a marker in population, phylogeographic and phylogenetic studies: the effects of inherited symbionts
inferred← citeshttps://doi.org/10.1111/j.1365-2621.1996.tb14712.xopenalex-snapshot
PCR‐RFLP Analysis of Mitochondrial DNA for Identification of Snail Meat Species
inferred← citeshttps://doi.org/10.1111/j.1420-9101.2011.02413.xopenalex-snapshot
Effects of parasitic sex‐ratio distorters on host genetic structure in the Armadillidium vulgare–Wolbachia association
inferred← citeshttps://doi.org/10.1163/156854096x01041openalex-snapshot
Skewed Sex-Ratio, Monogeny, and Maternal Sex Determination in Two Geographical Populations of Asellus Aquaticus (L., 1758) (Isopoda)
inferred← citeshttps://doi.org/10.1163/193724098x00377openalex-snapshot
GENETIC AND MORPHOLOGICAL SYSTEMATIC STUDIES ON THE CRAYFISH AUSTROPOTAMOBIUS PALLIPES (DECAPODA: ASTACIDAE)
inferred← citeshttps://doi.org/10.1371/journal.pone.0003286openalex-snapshot
Wolbachia Mediate Variation of Host Immunocompetence
inferred← citeshttps://doi.org/10.1371/journal.pone.0076639openalex-snapshot
Isolation and Characterization of Microsatellite Loci for the Isopod Crustacean Armadillidium vulgare and Transferability in Terrestrial Isopods
inferred← citeshttps://doi.org/10.1371/journal.pone.0082633openalex-snapshot
Multi-Infections of Feminizing Wolbachia Strains in Natural Populations of the Terrestrial Isopod Armadillidium Vulgare
inferred← citeshttps://doi.org/10.70675/5929f5a3zf2a0z41afzb1bdza8345feddd0bopenalex-snapshot
Prévalences et impact de Wolbachia sur la diversité génétique chez les isopodes terrestres, Armadillidium vulgare et Porcellionides pruinosus
inferred← citeshttps://doi.org/10.70675/907af94cze6c1z4c6bza835z94679c54a0f7openalex-snapshot
Diversity and dynamics of Wolbachia-host associations in arthropods from the Society archipelago, French Polynesia
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