On the public citation graph
Transfer of paternal mitochondrial DNA during fertilization of honeybee (Apis mellifera L.) eggs
0 signed · 135 inferred · view as graph
Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.
Is this your work? Sign in with ORCID and put your name on the
claims that are yours.
Reference health. See whether every reference in this work resolves to a
known work and none has been retracted — and get a dated CiteStamped
badge you can embed.
What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1007/978-3-540-47184-4_2openalex-snapshot
Spermatogenesis in Drosophila
inferredcites →https://doi.org/10.1007/bf00260866openalex-snapshot
The generation of transplasmic Drosophila simulans by cytoplasmic injection Effects of segregation and selection on the perpetuation of mitochondrial DNA heteroplasmy
inferredcites →https://doi.org/10.1007/bf00362088openalex-snapshot
Rapid disappearance of one parental mitochondrial genotype after isogamous mating in the myxomycete Physarum polycephalum
inferredcites →https://doi.org/10.1007/bf01539968openalex-snapshot
A mitochondrial plasmid that promotes mitochondrial fusion inPhysarum polycephalum
inferredcites →https://doi.org/10.1007/bf01941730openalex-snapshot
Polymorphisms in mitochondrial DNA of european and Africanized honeybees (Apis mellifera)
inferredcites →https://doi.org/10.1007/bf01942522openalex-snapshot
A mitochondrial DNA polymorphism in honeybees (Apis mellifera L.)
inferredcites →https://doi.org/10.1016/0012-1606(63)90015-0openalex-snapshot
Fertilization in Drosophila
inferredcites →https://doi.org/10.1016/0012-1606(72)90052-8openalex-snapshot
Maternal and cytoplasmic inheritance of mitochondrial DNA in Xenopus
inferredcites →https://doi.org/10.1016/0012-1606(76)90253-0openalex-snapshot
Number of mitochondria and some properties of mitochondrial DNA in the mouse egg
inferredcites →https://doi.org/10.1016/0014-5793(88)80957-8openalex-snapshot
Developmental genetics of higher organisms
inferredcites →https://doi.org/10.1016/0020-7322(80)90035-5openalex-snapshot
Monospermic fertilization in Chrysopa carnea (neuroptera; chrysopidae) : Behaviour of the fertilizing spermatozoa prior to syngamy
inferredcites →https://doi.org/10.1016/0307-4412(83)90068-7openalex-snapshot
Molecular Cloning. A Laboratory Manual
inferredcites →https://doi.org/10.1016/s0022-2836(75)80083-0openalex-snapshot
Detection of specific sequences among DNA fragments separated by gel electrophoresis
inferredcites →https://doi.org/10.1016/s0022-5320(68)90067-1openalex-snapshot
Structure and fate of the paternal mitochondrion during early embryogenesis of Paracentrotus lividus
inferredcites →https://doi.org/10.1017/s0016672300018899openalex-snapshot
Models of mitochondrial DNA transmission genetics and evolution in higher eucaryotes
inferredcites →https://doi.org/10.1017/s0016672300020292openalex-snapshot
A mathematical model of extranuclear genes and the genetic variability maintained in a finite population
inferredcites →https://doi.org/10.1017/s0016672300027245openalex-snapshot
Dubious maternal inheritance of mitochondrial DNA inD. simulansand evolution ofD. mauritiana
inferredcites →https://doi.org/10.1017/s0016672300030287openalex-snapshot
Further observation of paternal transmission ofDrosophilamitochondrial DNA by PCR selective amplification method
inferredcites →https://doi.org/10.1038/339211a0openalex-snapshot
Evidence from mitochondrial DNA that African honey bees spread as continuous maternal lineages
inferredcites →https://doi.org/10.1038/339213a0openalex-snapshot
Neotropical Africanized honey bees have African mitochondrial DNA
inferredcites →https://doi.org/10.1038/349782a0openalex-snapshot
Gene flow between African- and European-derived honey bee populations in Argentina
inferredcites →https://doi.org/10.1038/352255a0openalex-snapshot
Paternal inheritance of mitochondrial DNA in mice
inferredcites →https://doi.org/10.1038/359412a0openalex-snapshot
Direct evidence for extensive paternal mitochondrial DNA inheritance in the marine mussel Mytilus
inferredcites →https://doi.org/10.1051/apido:19920207openalex-snapshot
Mitochondrial DNA length variation in the cytochrome oxidase region of honey bee (Apis mellifera L)
inferredcites →https://doi.org/10.1073/pnas.56.1.269openalex-snapshot
Evidence for the mitochondrial origin of frog egg cytoplasmic DNA.
inferredcites →https://doi.org/10.1073/pnas.80.7.1969openalex-snapshot
Critical experimental test of the possibility of "paternal leakage" of mitochondrial DNA.
inferredcites →https://doi.org/10.1073/pnas.86.23.9347openalex-snapshot
Chloroplast and mitochondrial DNA are paternally inherited in Sequoia sempervirens D. Don Endl
inferredcites →https://doi.org/10.1093/aibsbulletin/3.1.15-fopenalex-snapshot
Lillie's Development of the Chick
inferredcites →https://doi.org/10.1093/genetics/109.2.441openalex-snapshot
EXTRANUCLEAR DIFFERENTIATION AND GENE FLOW IN THE FINITE ISLAND MODEL
inferredcites →https://doi.org/10.1093/genetics/126.3.657openalex-snapshot
Incomplete maternal transmission of mitochondrial DNA in Drosophila.
inferredcites →https://doi.org/10.1093/genetics/128.2.393openalex-snapshot
Putative origin and function of the intergenic region between COI and COII of Apis mellifera L. mitochondrial DNA.
inferredcites →https://doi.org/10.1093/genetics/132.1.221openalex-snapshot
Mitochondrial DNA length variation and heteroplasmy in populations of white sturgeon (Acipenser transmontanus).
inferredcites →https://doi.org/10.1093/genetics/50.6.1439openalex-snapshot
DIPLOID TISSUE DERIVED FROM ACCESSORY SPERM IN THE HONEY BEE
inferredcites →https://doi.org/10.1093/nar/15.5.2388openalex-snapshot
Nucleotide sequence of the large ribosomal RNA of honeybee mitochondria
inferredcites →https://doi.org/10.1093/oxfordjournals.jhered.a106712openalex-snapshot
DIPLOID MALE TISSUE AS NEW EVIDENCE ON SEX DETERMINATION IN HONEY BEES
inferredcites →https://doi.org/10.1093/oxfordjournals.jhered.a107247openalex-snapshot
GYNANDROMORPH PRODUCTION BY EGG CHILLING: Cytological Mechanisms in Honey Bees
inferredcites →https://doi.org/10.1093/oxfordjournals.jhered.a110103openalex-snapshot
Maternal inheritance of mitochondrial DNA during backcrossing of two species of mice
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a040553openalex-snapshot
The CO-I and CO-II region of honeybee mitochondrial DNA: evidence for variation in insect mitochondrial evolutionary rates.
inferredcites →https://doi.org/10.1101/087969145.12.333openalex-snapshot
Mitochondrial Transmission Genetics: Replication, Recombination, and Segregation of Mitochondrial DNA and Its Inheritance in Crosses
inferredcites →https://doi.org/10.1111/j.1095-8312.1985.tb02048.xopenalex-snapshot
Mitochondrial DNA and two perspectives on evolutionary genetics
inferredcites →https://doi.org/10.1126/science.115.2998.637openalex-snapshot
Androgenesis with Zygogenesis in Gynandromorphic Honeybees ( Apis mellifera L.)
inferredcites →https://doi.org/10.1126/science.1672472openalex-snapshot
Heteroplasmy Suggests Limited Biparental Inheritance of Mytilus Mitochondrial DNA
inferredcites →https://doi.org/10.1146/annurev.ge.12.120178.002351openalex-snapshot
TRANSMISSION GENETICS OF MITOCHONDRIA AND CHLOROPLASTS
inferredcites →https://doi.org/10.5860/choice.26-2699openalex-snapshot
Africanized honey bees and bee mites
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.4168.1.1zenodo-depositor-declared
Worldwide revision of the genus Fraseroscyphus Boero and Bouillon, 1993 (Cnidaria: Hydrozoa): an integrative approach to establish new generic diagnoses
inferred← citeshttps://doi.org/10.1002/9780470015902.a0006165.pub2openalex-snapshot
Mitochondrial DNA : Fate of the Paternal Mitochondrial Genome
inferred← citeshttps://doi.org/10.1002/9780470015902.a0006165.pub3openalex-snapshot
Mitochondrial DNA : Fate of the Paternal Mitochondrial Genome
inferred← citeshttps://doi.org/10.1002/jez.b.21031openalex-snapshot
Giant spermatozoon coiled in small egg: Fertilization mechanisms and their implications for evolutionary studies on ostracoda (crustacea)
inferred← citeshttps://doi.org/10.1007/978-1-4939-2208-6_25openalex-snapshot
Genetics as a Tool for Biodiversity Conservation: Examples from Central America
inferred← citeshttps://doi.org/10.1007/978-3-540-69111-2_3openalex-snapshot
Imprinting and Paternal Genome Elimination in Insects
inferred← citeshttps://doi.org/10.1007/bf02879339openalex-snapshot
Paternal inheritance of mitochondrial DNA in the sheep (Ovine aries)
inferred← citeshttps://doi.org/10.1007/pl00006417openalex-snapshot
Sociality and the Rate of rDNA Sequence Evolution in Wasps (Vespidae) and Honeybees (Apis)
inferred← citeshttps://doi.org/10.1007/s00114-004-0571-3openalex-snapshot
The evolutionary processes of mitochondrial and chloroplast genomes differ from those of nuclear genomes
inferred← citeshttps://doi.org/10.1007/s00239-008-9157-6openalex-snapshot
Recombination in Mitochondrial DNA of European Mussels Mytilus
inferred← citeshttps://doi.org/10.1007/s00441-012-1444-2openalex-snapshot
Transmission, inheritance and replication of mitochondrial DNA in mammals: implications for reproductive processes and infertility
inferred← citeshttps://doi.org/10.1007/s10528-006-9030-5openalex-snapshot
Mitochondrial DNA Diversity and Genetic Differentiation of the Honeybee (Apis cerana) in Thailand
inferred← citeshttps://doi.org/10.1007/s10709-012-9650-0openalex-snapshot
Paternal leakage of mitochondrial DNA in experimental crosses of populations of the potato cyst nematode Globodera pallida
inferred← citeshttps://doi.org/10.1007/s10709-012-9651-zopenalex-snapshot
Evidence of animal mtDNA recombination between divergent populations of the potato cyst nematode Globodera pallida
inferred← citeshttps://doi.org/10.1007/s11427-024-2736-7openalex-snapshot
Sequencing and characterizing human mitochondrial genomes in the biobank-based genomic research paradigm
inferred← citeshttps://doi.org/10.1007/s13131-020-1689-7openalex-snapshot
The complete mitochondrial genome of the hybrid grouper Epinephelus moara (♀)×Epinephelus tukula (♂), and phylogenetic analysis in subfamily Epinephelinae
inferred← citeshttps://doi.org/10.1007/s13592-021-00863-9openalex-snapshot
A qPCR assay for sensitive and rapid detection of African A-lineage honey bees (Apis mellifera)
inferred← citeshttps://doi.org/10.1016/j.bbamcr.2020.118916openalex-snapshot
Mechanisms for sperm mitochondrial removal in embryos
inferred← citeshttps://doi.org/10.1016/j.fgb.2014.10.014openalex-snapshot
Discordant phylogenies suggest repeated host shifts in the Fusarium–Euwallacea ambrosia beetle mutualism
inferred← citeshttps://doi.org/10.1016/j.foodcont.2020.107634openalex-snapshot
EPIC markers of the genus Apis as diagnostic tools for detection of honey fraud
inferred← citeshttps://doi.org/10.1016/j.gene.2016.01.031openalex-snapshot
Mitochondrial genome characterization of Tecia solanivora (Lepidoptera: Gelechiidae) and its phylogenetic relationship with other lepidopteran insects
inferred← citeshttps://doi.org/10.1016/j.ijpara.2025.104767openalex-snapshot
Long-term presence of emerging pathogens in island honey bee colonies
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2017.01.113openalex-snapshot
Weight of evidence evaluation of a network of adverse outcome pathways linking activation of the nicotinic acetylcholine receptor in honey bees to colony death
inferred← citeshttps://doi.org/10.1016/j.sjbs.2021.07.062openalex-snapshot
Genetic diversity and phylogenetic relationship among the western and the Asian honey bees based on two mitochondrial gene segments (COI and ND5)
inferred← citeshttps://doi.org/10.1016/j.ympev.2006.02.023openalex-snapshot
Molecular phylogeny of silkmoths reveals the origin of domesticated silkmoth, Bombyx mori from Chinese Bombyx mandarina and paternal inheritance of Antheraea proylei mitochondrial DNA
inferred← citeshttps://doi.org/10.1016/s0065-2806(08)60064-8openalex-snapshot
Molecular Biology of the Honeybee
inferred← citeshttps://doi.org/10.1016/s0169-5347(03)00125-3openalex-snapshot
Animal mitochondrial DNA recombination revisited
inferred← citeshttps://doi.org/10.1016/s1472-6483(10)60495-6openalex-snapshot
Degradation of paternal mitochondria after fertilization: implications for heteroplasmy, assisted reproductive technologies and mtDNA inheritance
inferred← citeshttps://doi.org/10.1017/cbo9780511975943.005openalex-snapshot
Nucleo-cytoplasmic conflict and the evolution of gamete dimorphism
inferred← citeshttps://doi.org/10.1038/hdy.2008.74openalex-snapshot
Lost in the zygote: the dilution of paternal mtDNA upon fertilization
inferred← citeshttps://doi.org/10.1038/s41598-018-38001-8openalex-snapshot
Paternal leakage and mtDNA heteroplasmy in Rhipicephalus spp. ticks
inferred← citeshttps://doi.org/10.1038/sj.hdy.6800516openalex-snapshot
Further evidence for paternal inheritance of mitochondrial DNA in the sheep (Ovis aries)
inferred← citeshttps://doi.org/10.1042/bcj20230415openalex-snapshot
Evolution and maintenance of mtDNA gene content across eukaryotes
inferred← citeshttps://doi.org/10.1073/pnas.1821192116openalex-snapshot
Paternal comeback in mitochondrial DNA inheritance
inferred← citeshttps://doi.org/10.1073/pnas.91.16.7463openalex-snapshot
An unusual type of mitochondrial DNA inheritance in the blue mussel Mytilus.
inferred← citeshttps://doi.org/10.1073/pnas.92.25.11331openalex-snapshot
Uniparental inheritance of mitochondrial and chloroplast genes: mechanisms and evolution.
inferred← citeshttps://doi.org/10.1080/00218839.2005.11101178openalex-snapshot
Non-lethal DNA sampling of wing tips discriminates subspecies ofApis melliferaoccurring in Greece
inferred← citeshttps://doi.org/10.1080/00218839.2006.11101347openalex-snapshot
Diagnostic molecular markers discriminating Africanized honey bees from Greek and Cypriot honey bees (Apis mellifera, Hymenoptera: Apidae)
inferred← citeshttps://doi.org/10.1080/23802359.2019.1682477openalex-snapshot
Mitochondrial heteroplasmy in an avian hybrid form (Passer italiae: Aves, Passeriformes)
inferred← citeshttps://doi.org/10.1080/24701394.2018.1431228openalex-snapshot
Extensive mitochondrial heteroplasmy in the neotropical ants of the Ectatomma ruidum complex (Formicidae: Ectatomminae)
inferred← citeshttps://doi.org/10.1093/humrep/deaa308openalex-snapshot
Germline transmission of donor, maternal and paternal mtDNA in primates
inferred← citeshttps://doi.org/10.1093/humupd/dml011openalex-snapshot
Transmission of mitochondrial DNA following assisted reproduction and nuclear transfer
inferred← citeshttps://doi.org/10.1093/jhered/esaa037openalex-snapshot
Disentangling Complex Inheritance Patterns of Plant Organellar Genomes: An Example From Carrot
inferred← citeshttps://doi.org/10.1093/molbev/msm068openalex-snapshot
Analysis of Nuclear Copies of Mitochondrial Sequences in Honeybee (Apis mellifera) Genome
inferred← citeshttps://doi.org/10.1093/oxfordjournals.molbev.a003934openalex-snapshot
Mitochondrial Pseudogenes Are Pervasive and Often Insidious in the Snapping Shrimp Genus Alpheus
inferred← citeshttps://doi.org/10.1098/rsbl.2023.0385openalex-snapshot
Evidence for hybridization-driven heteroplasmy maintained across generations in a ricefish endemic to a Wallacean ancient lake
inferred← citeshttps://doi.org/10.1111/j.1365-294x.2008.03982.xopenalex-snapshot
Revealing the hidden complexities of mtDNA inheritance
inferred← citeshttps://doi.org/10.1111/j.1365-294x.2011.05422.xopenalex-snapshot
Numts help to reconstruct the demographic history of the ocellated lizard (Lacerta lepida) in a secondary contact zone
inferred← citeshttps://doi.org/10.1111/j.1469-8137.2005.01492.xopenalex-snapshot
Inheritance and recombination of mitochondrial genomes in plants, fungi and animals
inferred← citeshttps://doi.org/10.1111/j.1755-0998.2009.02724.xopenalex-snapshot
Tissue segregation of mitochondrial haplotypes in heteroplasmic Hawaiian bees: implications for DNA barcoding
inferred← citeshttps://doi.org/10.1111/mec.12256openalex-snapshot
Extensive paternal mt DNA leakage in natural populations of D rosophila melanogaster
inferred← citeshttps://doi.org/10.1139/gen-2015-0090openalex-snapshot
Atypical mitochondrial inheritance patterns in eukaryotes
inferred← citeshttps://doi.org/10.1155/2019/5823219openalex-snapshot
Genetic Diversity ofApisspp. in Thailand Inferred from 28S rRNA Nuclear and Cytochrome b Mitochondrial Gene Sequences
inferred← citeshttps://doi.org/10.1186/1471-2148-10-174openalex-snapshot
Mitochondrial heteroplasmy and DNA barcoding in Hawaiian Hylaeus (Nesoprosopis) bees (Hymenoptera: Colletidae)
inferred← citeshttps://doi.org/10.1201/9781420028843-10openalex-snapshot
Using Mitochondrial DNA in Population Surveys
inferred← citeshttps://doi.org/10.1201/9781420028843.ch1openalex-snapshot
Introduction to Mitochondria
inferred← citeshttps://doi.org/10.1201/9781420028843.ch5openalex-snapshot
Using Mitochondrial DNA in Population Surveys
inferred← citeshttps://doi.org/10.13102/sociobiology.v65i3.2876openalex-snapshot
Genetic Variation in Iranian Honey bees, Apis mellifera meda Skorikow, 1829, (Hymenoptera: Apidae) Inferred from PCR-RFLP Analysis of two mtDNA Gene Segments (COI and 16S rDNA)
inferred← citeshttps://doi.org/10.1371/journal.pgen.1005040openalex-snapshot
Extreme-Depth Re-sequencing of Mitochondrial DNA Finds No Evidence of Paternal Transmission in Humans
inferred← citeshttps://doi.org/10.1371/journal.pone.0000892openalex-snapshot
Evidence for Paternal Leakage in Hybrid Periodical Cicadas (Hemiptera: Magicicada spp.)
inferred← citeshttps://doi.org/10.14293/s2199-1006.1.sor-.pp4s0ep.v1openalex-snapshot
Bio-inertia resonates life into evolution
inferred← citeshttps://doi.org/10.14293/s2199-1006.1.sor-.ppkgyra.v1openalex-snapshot
Bio-inertia resonates life into evolution
inferred← citeshttps://doi.org/10.1534/genetics.107.085274openalex-snapshot
Delimiting the Frequency of Paternal Leakage of Mitochondrial DNA in Chinook Salmon
inferred← citeshttps://doi.org/10.1603/0013-8746(2000)093[0001:ipcrbm]2.0.co;2openalex-snapshot
Improved Polymerase Chain Reaction-Based Mitochondrial Genotype Assay for Identification of the Africanized Honey Bee (Hymenoptera: Apidae)
inferred← citeshttps://doi.org/10.1603/ec09241openalex-snapshot
Interspecific Hybridization as a Source of Novel Genetic Markers for the Sterile Insect Technique in Bactrocera tryoni (Diptera: Tephritidae)
inferred← citeshttps://doi.org/10.1603/en13318openalex-snapshot
Haplotype-Habitat Associations ofCoptotermes gestroi(Termitoidae: Rhinotermitidae) From Mitochondrial Dna Genes
inferred← citeshttps://doi.org/10.21275/art20203017openalex-snapshot
Bio-inertia Resonates Life into Evolution
inferred← citeshttps://doi.org/10.2174/1566524014666141203100940openalex-snapshot
Complex Evolutionary Patterns Revealed by Mitochondrial Genomes of the Domestic Horse
inferred← citeshttps://doi.org/10.2298/avb0706465kopenalex-snapshot
Analysis of mitochondrial DNA in honey bees (Apis mellifera) from Serbia
inferred← citeshttps://doi.org/10.2478/aoas-2018-0049openalex-snapshot
Paternal Leakage of Mitochondrial DNA in the Raccoon Dog ( Nyctereutes Procyonoides Gray 1834)
inferred← citeshttps://doi.org/10.2478/jas-2020-0018openalex-snapshot
HRM Analysis of Spermathecal Contents to Determine the Origin of Drones that Inseminated Honey Bee Queens
inferred← citeshttps://doi.org/10.26190/unsworks/15370openalex-snapshot
Paternal transmission of mitochondrial DNA in interspecific crosses of Drosophila simulans
inferred← citeshttps://doi.org/10.26686/wgtn.17011544openalex-snapshot
Evolution of New Zealand's Marine Caddisflies: A Phylogenetic and Phylogeographic Assessment of the Chathamiidae (Insecta: Trichoptera)
inferred← citeshttps://doi.org/10.26686/wgtn.17011544.v1openalex-snapshot
Evolution of New Zealand's Marine Caddisflies: A Phylogenetic and Phylogeographic Assessment of the Chathamiidae (Insecta: Trichoptera)
inferred← citeshttps://doi.org/10.30843/nzpp.2006.59.4478openalex-snapshot
Methods to distinguish between the Microctonus aethiopoides strains that parasitise Sitona lepidus and Sitona discoideus
inferred← citeshttps://doi.org/10.3109/19401736.2015.1022730openalex-snapshot
Extent and divergence of heteroplasmy of the DNA barcoding region in Anapodisma miramae (Orthoptera: Acrididae)
inferred← citeshttps://doi.org/10.31396/biodiv.jour.2020.11.1.7.14openalex-snapshot
Genetic diversity of the Honeybee Apis mellifera Linnaeus, 1758 (Hymenoptera Apidae) from Jijel (Northeast Algeria)
inferred← citeshttps://doi.org/10.3389/fevo.2022.850600openalex-snapshot
The Movement of Western Honey Bees (Apis mellifera L.) Among U.S. States and Territories: History, Benefits, Risks, and Mitigation Strategies
inferred← citeshttps://doi.org/10.3390/biology13080604openalex-snapshot
Paternal Mitochondrial DNA Leakage in Natural Populations of Large-Scale Loach, Paramisgurnus dabryanus
inferred← citeshttps://doi.org/10.3390/biology14050475openalex-snapshot
Evolutionary Origin and Genetic Diversity of the Pannonian Ecotype of Apis mellifera carnica Colonies in Hungary Based on Mitochondrial DNA and Microsatellite Markers
inferred← citeshttps://doi.org/10.3390/insects12121066openalex-snapshot
A New Mitochondrial Genome of Sogatella furcifera (Horváth) (Hemiptera: Delphacidae) and Mitogenome-Wide Investigation on Polymorphisms
inferred← citeshttps://doi.org/10.3390/insects13050403openalex-snapshot
The Carniolan Honeybee from Slovenia—A Complete and Annotated Mitochondrial Genome with Comparisons to Closely Related Apis mellifera Subspecies
inferred← citeshttps://doi.org/10.3896/ibra.1.50.1.05openalex-snapshot
Phylogenetic relationships of Greek Apis mellifera subspecies based on sequencing of mtDNA segments (COI and ND5)
inferred← citeshttps://doi.org/10.3897/jhr.94.84617openalex-snapshot
A metabarcoding framework for wild bee assessment in Luxembourg
inferred← citeshttps://doi.org/10.4172/2153-0602.1000166openalex-snapshot
An Insightful Molecular Analysis Reveals Foreign Honeybees Among Algerian Honeybee Populations (Apis mellifera L.)
inferred← citeshttps://doi.org/10.4308/hjb.31.4.768-780openalex-snapshot
Apis cerana Fabricius, 1793 in Sumatra: Haplotype Variations of Mitochondrial DNA and the Molecular Relationship with the Asian Honey Bees (Hymenoptera: Apidae)
inferred← citeshttps://doi.org/10.5772/intechopen.73306openalex-snapshot
Methods for Genotyping of the Honey Bee (Apis mellifera L.: Hymenoptera: Apidae) in Bulgaria
inferred← citeshttps://doi.org/10.70675/1d48c518zc27bz4a6cz88eaz24d9d6f3e68copenalex-snapshot
Caractérisation génétique de la race de mouton Awassi du Liban en utilisant comme marqueurs des rétrovirus endogènes et l’ADN mitochondrial
Editorial review for independent work. ICSAC — the Institute for Complexity
Science and Advanced Computing — runs a structured editorial panel for researchers
publishing outside journals, and publishes on CiteStamp rails. Submission is free
and goes through ORCID: icsacinstitute.org/submit.