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Parasite-insecticide interactions: a case study of Nosema ceranae and fipronil synergy on honeybee
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/9781118032985openalex-snapshot
The Statistical Analysis of Failure Time Data
inferredcites →https://doi.org/10.1006/pest.1993.1035openalex-snapshot
Action of Phenylpyrazole Insecticides at the GABA-Gated Chloride Channel
inferredcites →https://doi.org/10.1007/s00128-010-0069-yopenalex-snapshot
Exposure to Pesticides at Sublethal Level and Their Distribution Within a Honey Bee (Apis mellifera) Colony
inferredcites →https://doi.org/10.1016/j.actatropica.2005.01.010openalex-snapshot
Microsporidiosis: An emerging and opportunistic infection in humans and animals
inferredcites →https://doi.org/10.1016/j.aquatox.2009.09.017openalex-snapshot
Interactive effects of infectious diseases and pollution in aquatic molluscs
inferredcites →https://doi.org/10.1016/j.biocontrol.2009.06.008openalex-snapshot
Synergies between biological and neonicotinoid insecticides for the curative control of the white grubs Amphimallon majale and Popillia japonica
inferredcites →https://doi.org/10.1016/j.ecolecon.2008.06.014openalex-snapshot
Economic valuation of the vulnerability of world agriculture confronted with pollinator decline
inferredcites →https://doi.org/10.1016/j.envpol.2011.09.021openalex-snapshot
Microsporidia parasites disrupt the responses to cadmium exposure in a gammarid
inferredcites →https://doi.org/10.1016/j.jinsphys.2008.07.016openalex-snapshot
The ontogeny of immunity: Development of innate immune strength in the honey bee (Apis mellifera)
inferredcites →https://doi.org/10.1016/j.jinsphys.2010.05.016openalex-snapshot
Parasitic infection leads to decline in hemolymph sugar levels in honeybee foragers
inferredcites →https://doi.org/10.1016/j.jinsphys.2011.04.020openalex-snapshot
The ontogeny of immunity in the honey bee, Apis mellifera L. following an immune challenge
inferredcites →https://doi.org/10.1016/j.jip.2006.02.005openalex-snapshot
Nosema ceranae, a new microsporidian parasite in honeybees in Europe
inferredcites →https://doi.org/10.1016/j.jip.2007.02.014openalex-snapshot
Widespread dispersal of the microsporidian Nosema ceranae, an emergent pathogen of the western honey bee, Apis mellifera
inferredcites →https://doi.org/10.1016/j.jip.2008.12.001openalex-snapshot
Energetic stress in the honeybee Apis mellifera from Nosema ceranae infection
inferredcites →https://doi.org/10.1016/j.jip.2009.06.011openalex-snapshot
A historical review of managed honey bee populations in Europe and the United States and the factors that may affect them
inferredcites →https://doi.org/10.1016/j.jip.2011.08.006openalex-snapshot
Evidence for emerging parasites and pathogens influencing outbreaks of stress-related diseases like chalkbrood
inferredcites →https://doi.org/10.1016/j.neuro.2011.04.006openalex-snapshot
Fipronil is a powerful uncoupler of oxidative phosphorylation that triggers apoptosis in human neuronal cell line SHSY5Y
inferredcites →https://doi.org/10.1016/j.resmic.2011.03.004openalex-snapshot
Extreme reduction and compaction of microsporidian genomes
inferredcites →https://doi.org/10.1016/j.scitotenv.2009.10.067openalex-snapshot
Interactions between effects of environmental chemicals and natural stressors: A review
inferredcites →https://doi.org/10.1016/j.scitotenv.2009.11.045openalex-snapshot
Eco-SpaCE: An object-oriented, spatially explicit model to assess the risk of multiple environmental stressors on terrestrial vertebrate populations
inferredcites →https://doi.org/10.1016/j.tiv.2009.01.017openalex-snapshot
Phenylpyrazole insecticides induce cytotoxicity by altering mechanisms involved in cellular energy supply in the human epithelial cell model Caco-2
inferredcites →https://doi.org/10.1016/j.tree.2010.01.007openalex-snapshot
Global pollinator declines: trends, impacts and drivers
inferredcites →https://doi.org/10.1016/s1049-9644(02)00008-7openalex-snapshot
Comparison of neonicotinoid insecticides as synergists for entomopathogenic nematodes
inferredcites →https://doi.org/10.1016/s1286-4579(01)01395-8openalex-snapshot
Microsporidiosis: human diseases and diagnosis
inferredcites →https://doi.org/10.1016/s1369-5274(02)00356-9openalex-snapshot
Functional and evolutionary analysis of a eukaryotic parasitic genome
inferredcites →https://doi.org/10.1021/es0481934openalex-snapshot
Impact of Environmental Stressors on the Dynamics of Disease Transmission
inferredcites →https://doi.org/10.1038/35039671openalex-snapshot
Insecticides and mosquito-borne disease
inferredcites →https://doi.org/10.1051/apido/2010018openalex-snapshot
Pesticides and honey bee toxicity – USA
inferredcites →https://doi.org/10.1051/apido/2010019openalex-snapshot
Nosema ceranaein Europe: an emergent type C nosemosis
inferredcites →https://doi.org/10.1051/apido:19660106openalex-snapshot
NOTE TECHNIQUE NOUVEAU MODÈLE DE CAGETTES EXPÉRIMENTALES POUR LE MAINTIEN D'ABEILLES EN CAPTIVITÉ
inferredcites →https://doi.org/10.1051/apido:19990503openalex-snapshot
Comparison of the responses of two races of honeybees to infection with Nosema apis Zander
inferredcites →https://doi.org/10.1051/apido:2007038openalex-snapshot
Acaricide residues in honey and wax after treatment of honey bee colonies with Apivar®or Asuntol®50
inferredcites →https://doi.org/10.1051/parasite/2008153434openalex-snapshot
Environmental Parasitology. Interactions between parasites and pollutants in the aquatic environment
inferredcites →https://doi.org/10.1073/pnas.0908530106openalex-snapshot
Fungal infection counters insecticide resistance in African malaria mosquitoes
inferredcites →https://doi.org/10.1080/00401706.1982.10487769openalex-snapshot
The Statistical Analysis of Failure Time Data
inferredcites →https://doi.org/10.1111/j.0014-3820.2004.tb01680.xopenalex-snapshot
PARASITISM INCREASES AND DECREASES THE COSTS OF INSECTICIDE RESISTANCE IN MOSQUITOES
inferredcites →https://doi.org/10.1111/j.1365-2427.2007.01912.xopenalex-snapshot
Long‐term dynamics and community structure of freshwater gastropods exposed to parasitism and other environmental stressors
inferredcites →https://doi.org/10.1111/j.1461-0248.2006.00966.xopenalex-snapshot
Assessing the ecology in ecotoxicology: a review and synthesis in freshwater systems
inferredcites →https://doi.org/10.1111/j.1462-2920.2009.02123.xopenalex-snapshot
Interactions between Nosema microspores and a neonicotinoid weaken honeybees ( Apis mellifera )
inferredcites →https://doi.org/10.1111/j.1558-5646.2011.01331.xopenalex-snapshot
COLLATERAL DAMAGE: RAPID EXPOSURE-INDUCED EVOLUTION OF PESTICIDE RESISTANCE LEADS TO INCREASED SUSCEPTIBILITY TO PARASITES
inferredcites →https://doi.org/10.1111/j.1600-0706.2008.17028.xopenalex-snapshot
Pesticide exposure strongly enhances parasite virulence in an invertebrate host model
inferredcites →https://doi.org/10.1126/science.1146498openalex-snapshot
A Metagenomic Survey of Microbes in Honey Bee Colony Collapse Disorder
inferredcites →https://doi.org/10.1371/journal.pbio.0050168openalex-snapshot
What's Killing American Honey Bees?
inferredcites →https://doi.org/10.1371/journal.pone.0009754openalex-snapshot
High Levels of Miticides and Agrochemicals in North American Apiaries: Implications for Honey Bee Health
inferredcites →https://doi.org/10.1371/journal.pone.0012081openalex-snapshot
Synergy in Efficacy of Fungal Entomopathogens and Permethrin against West African Insecticide-Resistant Anopheles gambiae Mosquitoes
inferredcites →https://doi.org/10.1371/journal.pone.0021550openalex-snapshot
Exposure to Sublethal Doses of Fipronil and Thiacloprid Highly Increases Mortality of Honeybees Previously Infected by Nosema ceranae
inferredcites →https://doi.org/10.1371/journal.pone.0023591openalex-snapshot
Lethal and Pre-Lethal Effects of a Fungal Biopesticide Contribute to Substantial and Rapid Control of Malaria Vectors
inferredcites →https://doi.org/10.1371/journal.ppat.1001000openalex-snapshot
Insecticide Control of Vector-Borne Diseases: When Is Insecticide Resistance a Problem?
inferredcites →https://doi.org/10.1603/0022-0493-93.1.71openalex-snapshot
Biological Control Agents for White Grubs (Coleoptera: Scarabaeidae) in Anticipation of the Establishment of the Japanese Beetle in California
inferredcites →https://doi.org/10.1603/ec09429openalex-snapshot
Weighing Risk Factors Associated With Bee Colony Collapse Disorder by Classification and Regression Tree Analysis
inferredcites →https://doi.org/10.3390/ijerph8103844openalex-snapshot
Detection of Pesticides in Active and Depopulated Beehives in Uruguay
inferredcites →https://doi.org/10.4161/viru.2.1.14606openalex-snapshot
Shrink it or lose it: balancing loss of function with shrinking genomes in the microsporidia
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1016/j.ijppaw.2022.06.001zenodo-depositor-declared
Do pesticide and pathogen interactions drive wild bee declines?
inferred← citeshttps://doi.org/10.1002/etc.2655openalex-snapshot
Fipronil and imidacloprid reduce honeybee mitochondrial activity
inferred← citeshttps://doi.org/10.1002/etc.2889openalex-snapshot
Fipronil promotes motor and behavioral changes in honey bees ( Apis mellifera ) and affects the development of colonies exposed to sublethal doses
inferred← citeshttps://doi.org/10.1007/978-3-030-93306-7_7openalex-snapshot
Nosema apis and N. ceranae Infection in Honey bees: A Model for Host-Pathogen Interactions in Insects
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Bee Diversity and Current Status of Beekeeping in Japan
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Development of a loop-mediated isothermal amplification (LAMP) and a direct LAMP for the specific detection of Nosema ceranae, a parasite of honey bees
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Detrimental effects of amitraz exposure in honey bees (Apis mellifera) infected with Nosema ceranae
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inferred← citeshttps://doi.org/10.1007/s10646-018-1925-5openalex-snapshot
Sublethal effects of clothianidin and Nosema spp. on the longevity and foraging activity of free flying honey bees
inferred← citeshttps://doi.org/10.1007/s10646-021-02416-3openalex-snapshot
Toxicity assessment of chronic exposure to common insecticides and bee medications on colony development and drones sperm parameters
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The “parasite detoxification hypothesis”: lead exposure potentially changes the ecological interaction from parasitism to mutualism
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Effects of neonicotinoids and fipronil on non-target invertebrates
inferred← citeshttps://doi.org/10.1007/s11356-017-9240-xopenalex-snapshot
The environmental risks of neonicotinoid pesticides: a review of the evidence post 2013
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Environmental pollution effect on honey bees and their derived products: a comprehensive analysis
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Beneficial Bacteria and Plant Extracts Promote Honey Bee Health and Reduce Nosema ceranae Infection
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The effects of Nosema ceranae (Microspora: Nosematidae) isolated from wild Apis cerana japonica (Hymenoptera: Apidae) on Apis mellifera
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Pesticide exposure of honeybees (Apis mellifera) pollinating melon crops
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Honeybee health in Africa—a review
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Modulation of pesticide response in honeybees
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Predictive systems models can help elucidate bee declines driven by multiple combined stressors
inferred← citeshttps://doi.org/10.1007/s13592-017-0535-1openalex-snapshot
Nosema ceranae disease of the honey bee (Apis mellifera)
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Honey bees are more vulnerable to amitraz under organophosphate insecticide exposure
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An Overview of Complex Threats to Bee Populations: Pesticides, Contaminants, and the Urgency for Research
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Can infection with Trypanosoma cruzi modify the toxicological response of Triatoma infestans susceptible and resistant to deltamethrin?
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Indirect effects of agricultural pesticide use on parasite prevalence in wild pollinators
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Antimicrosporidian activity of sulphated polysaccharides from algae and their potential to control honeybee nosemosis
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Hazard of a neonicotinoid insecticide on the homing flight of the honeybee depends on climatic conditions and Varroa infestation
inferred← citeshttps://doi.org/10.1016/j.chroma.2018.06.062openalex-snapshot
Matrix solid-phase dispersion associated to gas chromatography for the assessment in honey bee of a group of pesticides of concern in the apicultural field
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Interactions between pesticides and pathogen susceptibility in honey bees
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Effects of the gut parasite Nosema ceranae on honey bee physiology and behavior
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Neonicotinoids, bee disorders and the sustainability of pollinator services
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Natural habitat partially mitigates negative pesticide effects on tropical pollinator communities
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Combined exposure to mitochondrial-targeting fungicide formulations and Nosema ceranae affects survival and midgut transcriptomic responses in the honeybee Apis mellifera
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Divergent forms of endoplasmic reticulum stress trigger a robust unfolded protein response in honey bees
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The neonicotinoids thiacloprid, imidacloprid, and clothianidin affect the immunocompetence of honey bees (Apis mellifera L.)
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Sperm viability and gene expression in honey bee queens (Apis mellifera) following exposure to the neonicotinoid insecticide imidacloprid and the organophosphate acaricide coumaphos
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Emerging dangers: Deadly effects of an emergent parasite in a new pollinator host
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Thiacloprid–Nosema ceranae interactions in honey bees: Host survivorship but not parasite reproduction is dependent on pesticide dose
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Differential proteomic analysis of midguts from Nosema ceranae-infected honeybees reveals manipulation of key host functions
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The influence of Nosema (Microspora: Nosematidae) infection on honey bee (Hymenoptera: Apidae) defense against Varroa destructor (Mesostigmata: Varroidae)
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Amitraz and its metabolite modulate honey bee cardiac function and tolerance to viral infection
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Impact of the microsporidian Nosema ceranae on the gut epithelium renewal of the honeybee, Apis mellifera
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Honeybee gut microbiota dysbiosis in pesticide/parasite co-exposures is mainly induced by Nosema ceranae
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A combined LC-MS and NMR approach to reveal metabolic changes in the hemolymph of honeybees infected by the gut parasite Nosema ceranae
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Natural extracts as potential control agents for Nosema ceranae infection in honeybees, Apis mellifera
inferred← citeshttps://doi.org/10.1016/j.meegid.2012.12.031openalex-snapshot
Immunity and the emergence of virulent pathogens
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Comparative susceptibility of three Western honeybee taxa to the microsporidian parasite Nosema ceranae
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Metabolisation of thiamethoxam (a neonicotinoid pesticide) and interaction with the Chronic bee paralysis virus in honeybees
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A Pediococcus strain to rescue honeybees by decreasing Nosema ceranae- and pesticide-induced adverse effects
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Method for detection of mtDNA damages for evaluating of pesticides toxicity for bumblebees (Bombus terrestris L.)
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Interactive effects of dinotefuran and Nosema ceranae on the survival status and gut microbial community of honey bees
inferred← citeshttps://doi.org/10.1016/j.pt.2017.04.006openalex-snapshot
Malaria Vector Control Still Matters despite Insecticide Resistance
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Enhancement of chronic bee paralysis virus levels in honeybees acute exposed to imidacloprid: A Chinese case study
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Bees as environmental and toxicological bioindicators in the light of pesticide non-targeted exposure
inferred← citeshttps://doi.org/10.1016/j.tree.2013.05.008openalex-snapshot
Combined effects of global change pressures on animal-mediated pollination
inferred← citeshttps://doi.org/10.1017/s0031182024001446openalex-snapshot
Nosemosis negatively affects honeybee survival: experimental and meta-analytic evidence
inferred← citeshttps://doi.org/10.1038/s41598-017-04734-1openalex-snapshot
Immunosuppression in Honeybee Queens by the Neonicotinoids Thiacloprid and Clothianidin
inferred← citeshttps://doi.org/10.1038/s41598-017-08380-5openalex-snapshot
Nosema ceranae, Fipronil and their combination compromise honey bee reproduction via changes in male physiology
inferred← citeshttps://doi.org/10.1038/s41598-017-09448-yopenalex-snapshot
ATP-sensitive inwardly rectifying potassium channel regulation of viral infections in honey bees
inferred← citeshttps://doi.org/10.1038/s41598-017-13171-zopenalex-snapshot
The neonicotinoid insecticide Clothianidin adversely affects immune signaling in a human cell line
inferred← citeshttps://doi.org/10.1038/s41598-017-15358-wopenalex-snapshot
Protein nutrition governs within-host race of honey bee pathogens
inferred← citeshttps://doi.org/10.1038/s41598-019-40347-6openalex-snapshot
Intensity of Nosema ceranae infection is associated with specific honey bee gut bacteria and weakly associated with gut microbiome structure
inferred← citeshttps://doi.org/10.1038/s41598-019-56224-1openalex-snapshot
Consequences of a short time exposure to a sublethal dose of Flupyradifurone (Sivanto) pesticide early in life on survival and immunity in the honeybee (Apis mellifera)
inferred← citeshttps://doi.org/10.1038/s41598-020-61371-xopenalex-snapshot
From antagonism to synergism: Extreme differences in stressor interactions in one species
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Virtual 2-D map of the fungal proteome
inferred← citeshttps://doi.org/10.1038/s41598-021-86293-0openalex-snapshot
Exposure to low doses of pesticides induces an immune response and the production of nitric oxide in honeybees
inferred← citeshttps://doi.org/10.1038/s41598-022-18534-9openalex-snapshot
Effect of amide protoporphyrin derivatives on immune response in Apis mellifera
inferred← citeshttps://doi.org/10.1038/s41598-023-40847-6openalex-snapshot
Quantifying synergistic interactions: a meta-analysis of joint effects of chemical and parasitic stressors
inferred← citeshttps://doi.org/10.1038/s41598-024-67796-yopenalex-snapshot
Exploring the interactions between Nosema ceranae infection and the honey bee gut microbiome
inferred← citeshttps://doi.org/10.1038/s41598-025-00564-8openalex-snapshot
Neonicotinoids and Varroa mites force a bee colony to forget the extending of longevity during overwintering
inferred← citeshttps://doi.org/10.1038/srep05566openalex-snapshot
Delayed and time-cumulative toxicity of imidacloprid in bees, ants and termites
inferred← citeshttps://doi.org/10.1038/srep09727openalex-snapshot
A modelling methodology to assess the effect of insect pest control on agro-ecosystems
inferred← citeshttps://doi.org/10.1038/srep22042openalex-snapshot
Parasite infection accelerates age polyethism in young honey bees
inferred← citeshttps://doi.org/10.1038/srep31904openalex-snapshot
Drone exposure to the systemic insecticide Fipronil indirectly impairs queen reproductive potential
inferred← citeshttps://doi.org/10.1038/srep40853openalex-snapshot
Sublethal pesticide doses negatively affect survival and the cellular responses in American foulbrood-infected honeybee larvae
inferred← citeshttps://doi.org/10.1073/pnas.1314923110openalex-snapshot
Neonicotinoid clothianidin adversely affects insect immunity and promotes replication of a viral pathogen in honey bees
inferred← citeshttps://doi.org/10.1079/9781786393548.0001openalex-snapshot
Pesticides and Crop Pollination by Bees
inferred← citeshttps://doi.org/10.1080/0005772x.2015.1118962openalex-snapshot
Neonicotinoids and the prevalence of parasites and disease in bees
inferred← citeshttps://doi.org/10.1080/00218839.2016.1189231openalex-snapshot
Long term effects of a food supplement HiveAlive™ on honey bee colony strength and Nosema ceranae spore counts
inferred← citeshttps://doi.org/10.1080/00218839.2017.1304878openalex-snapshot
Spring mortality in honey bees in northeastern Italy: detection of pesticides and viruses in dead honey bees and other matrices
inferred← citeshttps://doi.org/10.1080/00218839.2017.1332541openalex-snapshot
Larval exposure to thiamethoxam and American foulbrood: effects on mortality and cognition in the honey bee Apis mellifera
inferred← citeshttps://doi.org/10.1080/00218839.2019.1634463openalex-snapshot
Immune gene expression in developing honey bees ( Apis mellifera L.) simultaneously exposed to imidacloprid and Varroa destructor in laboratory conditions
inferred← citeshttps://doi.org/10.1080/00218839.2020.1866233openalex-snapshot
The neonicotinoid imidacloprid alone alters the cognitive behavior in Apis mellifera L. and the combined exposure of imidacloprid and Varroa destructor mites synergistically contributes to trial attrition
inferred← citeshttps://doi.org/10.1080/00218839.2021.1880760openalex-snapshot
Interactions between sublethal doses of thiamethoxam and Nosema ceranae in the honey bee, Apis mellifera
inferred← citeshttps://doi.org/10.1080/00218839.2024.2380936openalex-snapshot
Effects of landscape variation on thermoregulation and performance in Apis mellifera honey bee colonies: insights from mtDNA haplotypes
inferred← citeshttps://doi.org/10.1080/00218839.2024.2406108openalex-snapshot
The influence of sub-lethal neonicotinoid doses and ambient temperature on individual Apis mellifera scutellata flight efficiency
inferred← citeshttps://doi.org/10.1080/00218839.2026.2666446openalex-snapshot
Pest control or pollinator peril? Evaluating entomopathogenic nematodes risks to Apis mellifera honey bees
inferred← citeshttps://doi.org/10.1080/0194262x.2014.912573openalex-snapshot
Reviews of Science for Science Librarians: An Update on Honeybee Colony Collapse Disorder
inferred← citeshttps://doi.org/10.1093/ee/nvag023openalex-snapshot
What’s in a pollen provision? Using larval provisions to quantify pesticide exposure in Megachile rotundata (Hymenoptera: Megachilidae)
inferred← citeshttps://doi.org/10.1093/jee/tov251openalex-snapshot
Effects of Oral Exposure to Fungicides on Honey Bee Nutrition and Virus Levels
inferred← citeshttps://doi.org/10.1093/jee/toy026openalex-snapshot
Seasonal Effects and the Impact of In-Hive Pesticide Treatments on Parasite, Pathogens, and Health of Honey Bees
inferred← citeshttps://doi.org/10.1096/fasebj.28.1_supplement.880.1openalex-snapshot
Understanding how honey bee flight and senescence are connected through oxidative stress (880.1)
inferred← citeshttps://doi.org/10.1098/rsos.160444openalex-snapshot
Age structure is critical to the population dynamics and survival of honeybee colonies
inferred← citeshttps://doi.org/10.1098/rspb.2016.0246openalex-snapshot
Chronic neonicotinoid pesticide exposure and parasite stress differentially affects learning in honeybees and bumblebees
inferred← citeshttps://doi.org/10.1101/2020.02.27.967455openalex-snapshot
Artificial diets modulate infection rates by Nosema ceranae in bumblebees
inferred← citeshttps://doi.org/10.1101/2023.08.11.553037openalex-snapshot
Honey bee Apis mellifera L. Responses to Oxidative Stress Induced by Pharmacological and Pesticide Compounds
inferred← citeshttps://doi.org/10.1101/2023.10.26.564284openalex-snapshot
Neonicotinoids and Varroa mites force the extending of longevity in a bee colony during overwintering to forget
inferred← citeshttps://doi.org/10.1111/1365-2435.12292openalex-snapshot
Chronic impairment of bumblebee natural foraging behaviour induced by sublethal pesticide exposure
inferred← citeshttps://doi.org/10.1111/1365-2664.12205openalex-snapshot
Impact of chronic exposure to a pyrethroid pesticide on bumblebees and interactions with a trypanosome parasite
inferred← citeshttps://doi.org/10.1111/1365-2664.13811openalex-snapshot
Parasites and pesticides act antagonistically on honey bee health
inferred← citeshttps://doi.org/10.1111/1462-2920.12825openalex-snapshot
Effects, but no interactions, of ubiquitous pesticide and parasite stressors on honey bee ( A pis mellifera ) lifespan and behaviour in a colony environment
inferred← citeshttps://doi.org/10.1111/1462-2920.14103openalex-snapshot
Nosema ceranae in Apis mellifera : a 12 years postdetection perspective
inferred← citeshttps://doi.org/10.1111/1749-4877.12752openalex-snapshot
Biotic and abiotic stresses on honeybee health
inferred← citeshttps://doi.org/10.1111/1751-7915.12772openalex-snapshot
Disruption of oxidative balance in the gut of the western honeybee Apis mellifera exposed to the intracellular parasite Nosema ceranae and to the insecticide fipronil
inferred← citeshttps://doi.org/10.1111/1758-2229.12024openalex-snapshot
N osema ceranae (Microsporidia), a controversial 21st century honey bee pathogen
inferred← citeshttps://doi.org/10.1111/1758-2229.12434openalex-snapshot
Flight performance of actively foraging honey bees is reduced by a common pathogen
inferred← citeshttps://doi.org/10.1111/brv.12206openalex-snapshot
Interactive effects of pesticide exposure and pathogen infection on bee health – a critical analysis
inferred← citeshttps://doi.org/10.1111/gcb.16928openalex-snapshot
Bees exposed to climate change are more sensitive to pesticides
inferred← citeshttps://doi.org/10.1126/science.1255957openalex-snapshot
Bee declines driven by combined stress from parasites, pesticides, and lack of flowers
inferred← citeshttps://doi.org/10.1128/aem.00545-18openalex-snapshot
Imidacloprid Decreases Honey Bee Survival Rates but Does Not Affect the Gut Microbiome
inferred← citeshttps://doi.org/10.11606/t.17.2016.tde-26082016-110015openalex-snapshot
Estudo do melhoramento genético no sistema produtivo de pólen apícola e suas implicações na saúde das abelhas Apis mellifera L.
inferred← citeshttps://doi.org/10.1186/1471-2164-14-451openalex-snapshot
Genome sequencing and comparative genomics of honey bee microsporidia, Nosema apis reveal novel insights into host-parasite interactions
inferred← citeshttps://doi.org/10.1186/s12864-018-5007-0openalex-snapshot
Transcriptional response of honey bee (Apis mellifera) to differential nutritional status and Nosema infection
inferred← citeshttps://doi.org/10.1264/jsme2.me18169openalex-snapshot
The Honeybee Gut Microbiota Is Altered after Chronic Exposure to Different Families of Insecticides and Infection by Nosema ceranae
inferred← citeshttps://doi.org/10.1371/journal.pntd.0004133openalex-snapshot
Nodular Worm Infections in Wild Non-human Primates and Humans Living in the Sebitoli Area (Kibale National Park, Uganda): Do High Spatial Proximity Favor Zoonotic Transmission?
inferred← citeshttps://doi.org/10.1371/journal.pone.0067007openalex-snapshot
Widespread Occurrence of Chemical Residues in Beehive Matrices from Apiaries Located in Different Landscapes of Western France
inferred← citeshttps://doi.org/10.1371/journal.pone.0085261openalex-snapshot
Sex-Specific Differences in Pathogen Susceptibility in Honey Bees (Apis mellifera)
inferred← citeshttps://doi.org/10.1371/journal.pone.0091573openalex-snapshot
Chronic Exposure of Imidacloprid and Clothianidin Reduce Queen Survival, Foraging, and Nectar Storing in Colonies of Bombus impatiens
inferred← citeshttps://doi.org/10.1371/journal.pone.0091686openalex-snapshot
Transcriptome Analyses of the Honeybee Response to Nosema ceranae and Insecticides
inferred← citeshttps://doi.org/10.1371/journal.pone.0099465openalex-snapshot
Infra-Population and -Community Dynamics of the Parasites Nosema apis and Nosema ceranae, and Consequences for Honey Bee (Apis mellifera) Hosts
inferred← citeshttps://doi.org/10.1371/journal.pone.0125790openalex-snapshot
Neonicotinoid-Coated Zea mays Seeds Indirectly Affect Honeybee Performance and Pathogen Susceptibility in Field Trials
inferred← citeshttps://doi.org/10.1371/journal.pone.0126330openalex-snapshot
Nosema ceranae Can Infect Honey Bee Larvae and Reduces Subsequent Adult Longevity
inferred← citeshttps://doi.org/10.1371/journal.pone.0143596openalex-snapshot
Metformin Radiosensitizes p53-Deficient Colorectal Cancer Cells through Induction of G2/M Arrest and Inhibition of DNA Repair Proteins
inferred← citeshttps://doi.org/10.1371/journal.pone.0191256openalex-snapshot
Increased survival of honeybees in the laboratory after simultaneous exposure to low doses of pesticides and bacteria
inferred← citeshttps://doi.org/10.1371/journal.pone.0215466openalex-snapshot
Glyphosate, but not its metabolite AMPA, alters the honeybee gut microbiota
inferred← citeshttps://doi.org/10.1371/journal.pone.0220029openalex-snapshot
An assessment of acute insecticide toxicity loading (AITL) of chemical pesticides used on agricultural land in the United States
inferred← citeshttps://doi.org/10.1371/journal.pone.0220703openalex-snapshot
Influence of chronic exposure to thiamethoxam and chronic bee paralysis virus on winter honey bees
inferred← citeshttps://doi.org/10.1371/journal.pone.0277455openalex-snapshot
Validation of quantitative real-time PCR reference genes and spatial expression profiles of detoxication-related genes under pesticide induction in honey bee, Apis mellifera
inferred← citeshttps://doi.org/10.1371/journal.ppat.1003185openalex-snapshot
Nosema ceranae Escapes Fumagillin Control in Honey Bees
inferred← citeshttps://doi.org/10.15389/agrobiology.2023.2.345engopenalex-snapshot
EFFECT OF ACARICIDE TREATMENT ON BODY WEIGHT AND REPRODUCTIVE CHARACTERISTICS OF DRONES OF THE PRIOKSKY BREED TYPE OF CENTRAL RUSSIAN HONEYBEES (Apis mellifera Linnaeus, 1758)
inferred← citeshttps://doi.org/10.15389/agrobiology.2023.2.345rusopenalex-snapshot
МАССА ТЕЛА И КАЧЕСТВО СПЕРМЫ У ТРУТНЕЙ МЕДОНОСНЫХ ПЧЕЛ (Apis mellifera Linnaeus, 1758) ПОРОДНОГО ТИПА ПРИОКСКИЙ СРЕДНЕРУССКОЙ ПОРОДЫ ПОД ВЛИЯНИЕМ АКАРИЦИДОВ
inferred← citeshttps://doi.org/10.1603/ec13068openalex-snapshot
Lufenuron Suppresses the Resistance of Formosan Subterranean Termites (Isoptera: Rhinotermitidae) to Entomopathogenic Bacteria
inferred← citeshttps://doi.org/10.20914/2310-1202-2020-4-54-59openalex-snapshot
Toxicity of new fungicides for eukaryotic microorganisms isolated from the gut of the food-important vegetable pollinator Bombus terrestris L.
inferred← citeshttps://doi.org/10.2139/ssrn.6914468openalex-snapshot
Mitochondrial-targeting fungicide formulations exacerbate the effects of Nosema ceranae infection in the honeybee Apis mellifera
inferred← citeshttps://doi.org/10.2478/acve-2019-0001openalex-snapshot
Looking for the causes of and solutions to the issue of honey bee colony losses
inferred← citeshttps://doi.org/10.2478/v10289-012-0029-3openalex-snapshot
Residues of Neonicotinoid Insecticides in Bee Collected Plant Materials from Oilseed Rape Crops and their Effect on Bee Colonies
inferred← citeshttps://doi.org/10.2903/j.efsa.2013.3158openalex-snapshot
Conclusion on the peer review of the pesticide risk assessment for bees for the active substance fipronil
inferred← citeshttps://doi.org/10.2903/j.efsa.2015.4125openalex-snapshot
Statement on the suitability of the BEEHAVE model for its potential use in a regulatory context and for the risk assessment of multiple stressors in honeybees at the landscape level
inferred← citeshttps://doi.org/10.2903/sp.efsa.2016.en-1069openalex-snapshot
A mechanistic model to assess risks to honeybee colonies from exposure to pesticides under different scenarios of combined stressors and factors
inferred← citeshttps://doi.org/10.31390/gradschool_dissertations.598openalex-snapshot
Research in Biological Control of the Formosan Subterranean Termite
inferred← citeshttps://doi.org/10.3166/bspe-2018-0042openalex-snapshot
Les substrats sucrés contaminés par les intrants agricoles favorisent la prolifération du moustique Aedes albopictus (Diptera : Culicidae)
inferred← citeshttps://doi.org/10.3389/fevo.2021.755226openalex-snapshot
Genetic Variation in Antimicrobial Activity of Honey Bee (Apis mellifera) Seminal Fluid
inferred← citeshttps://doi.org/10.3389/finsc.2026.1871985openalex-snapshot
Tropilaelaps mercedesae: an emerging global threat to apiculture – a comprehensive review
inferred← citeshttps://doi.org/10.3389/fphys.2023.1198070openalex-snapshot
Overlapping exposure effects of pathogen and dimethoate on honeybee (Apis mellifera Linnaeus) metabolic rate and longevity
inferred← citeshttps://doi.org/10.3389/frbee.2023.1219991openalex-snapshot
Altered synaptic organization in the mushroom bodies of honey bees exposed as foragers to the pesticide fipronil
inferred← citeshttps://doi.org/10.3389/frbee.2023.1275862openalex-snapshot
Honey bee Apis mellifera L. responses to oxidative stress induced by pharmacological and pesticidal compounds
inferred← citeshttps://doi.org/10.3390/ani13223543openalex-snapshot
Effects of Plant-Based Supplement on Oxidative Stress of Honey Bees (Apis mellifera) Infected with Nosema ceranae
inferred← citeshttps://doi.org/10.3390/antiox15081016openalex-snapshot
Disruption of Antioxidant Defense Systems in Honey Bees and Wild Bees Under Environmental Xenobiotic Pressure
inferred← citeshttps://doi.org/10.3390/d11120237openalex-snapshot
Biotic and Abiotic Factors Associated with Colonies Mortalities of Managed Honey Bee (Apis mellifera)
inferred← citeshttps://doi.org/10.3390/d12010024openalex-snapshot
Monitoring the Field-Realistic Exposure of Honeybee Colonies to Neonicotinoids by An Integrative Approach: A Case Study in Romania
inferred← citeshttps://doi.org/10.3390/ijms252211923openalex-snapshot
Molecular Impact of Sublethal Spinetoram Exposure on Honeybee (Apis mellifera) Larval and Adult Transcriptomes
inferred← citeshttps://doi.org/10.3390/ijms26146850openalex-snapshot
Synergistic Effects of Amitraz and Dinotefuran on Honey Bee Health: Impacts on Survival, Gene Expression, and Hypopharyngeal Gland Morphology
inferred← citeshttps://doi.org/10.3390/insects10080245openalex-snapshot
Genome-Wide Identification of Long Non-Coding RNAs and Their Regulatory Networks Involved in Apis mellifera ligustica Response to Nosema ceranae Infection
inferred← citeshttps://doi.org/10.3390/insects11030153openalex-snapshot
Government Policy Ecosystem for Entrepreneurship Development in MSEs Sector
inferred← citeshttps://doi.org/10.3390/insects13090844openalex-snapshot
Epidemiology of the Microsporidium Nosema ceranae in Four Mediterranean Countries
inferred← citeshttps://doi.org/10.3390/insects17060559openalex-snapshot
Genetic and Molecular Mechanisms of Detoxification and Immunity in Honeybees (Apis mellifera)
inferred← citeshttps://doi.org/10.3390/insects3041271openalex-snapshot
General Stress Responses in the Honey Bee
inferred← citeshttps://doi.org/10.3390/insects8010020openalex-snapshot
Cold Ambient Temperature Promotes Nosema spp. Intensity in Honey Bees (Apis mellifera)
inferred← citeshttps://doi.org/10.3390/insects8010031openalex-snapshot
Bee++: An Object-Oriented, Agent-Based Simulator for Honey Bee Colonies
inferred← citeshttps://doi.org/10.3390/insects9020065openalex-snapshot
Honey Bee Survival and Pathogen Prevalence: From the Perspective of Landscape and Exposure to Pesticides
inferred← citeshttps://doi.org/10.3390/life16050743openalex-snapshot
Cumulative Soil Metal Contamination Reshapes Oxidative and Neuroenzymatic Stress Responses in Ants Across an Industrial Pollution Gradient
inferred← citeshttps://doi.org/10.3390/metabo13020185openalex-snapshot
A GABA Receptor Modulator and Semiochemical Compounds Evidenced Using Volatolomics as Candidate Markers of Chronic Exposure to Fipronil in Apis mellifera
inferred← citeshttps://doi.org/10.3390/microorganisms9010158openalex-snapshot
Artificial Diets Modulate Infection Rates by Nosema ceranae in Bumblebees
inferred← citeshttps://doi.org/10.3390/microorganisms9030505openalex-snapshot
RNA Interference-Mediated Knockdown of Genes Encoding Spore Wall Proteins Confers Protection against Nosema ceranae Infection in the European Honey Bee, Apis mellifera
inferred← citeshttps://doi.org/10.3390/molecules25081954openalex-snapshot
Cyclic Synthetic Peroxides Inhibit Growth of Entomopathogenic Fungus Ascosphaera apis without Toxic Effect on Bumblebees
inferred← citeshttps://doi.org/10.3390/pathogens14010094openalex-snapshot
The Role of Pathogens in Bumblebee Decline: A Review
inferred← citeshttps://doi.org/10.3390/v12050566openalex-snapshot
Pesticide–Virus Interactions in Honey Bees: Challenges and Opportunities for Understanding Drivers of Bee Declines
inferred← citeshttps://doi.org/10.3390/v7052654openalex-snapshot
Dynamics of Apis mellifera Filamentous Virus (AmFV) Infections in Honey Bees and Relationships with Other Parasites
inferred← citeshttps://doi.org/10.3390/vetsci7040166openalex-snapshot
Factors Associated with Honey Bee Colony Losses: A Mini-Review
inferred← citeshttps://doi.org/10.3390/vetsci7040199openalex-snapshot
Effects of Synthetic Acaricides and Nosema ceranae (Microsporidia: Nosematidae) on Molecules Associated with Chemical Communication and Recognition in Honey Bees
inferred← citeshttps://doi.org/10.3390/vetsci9030130openalex-snapshot
The Role of Nosema ceranae (Microsporidia: Nosematidae) in Honey Bee Colony Losses and Current Insights on Treatment
inferred← citeshttps://doi.org/10.3390/vetsci9050199openalex-snapshot
Bee Stressors from an Immunological Perspective and Strategies to Improve Bee Health
inferred← citeshttps://doi.org/10.35690/978-2-7592-2203-2openalex-snapshot
Faune sauvage, biodiversité et santé, quels défis ?
inferred← citeshttps://doi.org/10.3896/ibra.1.52.4.14openalex-snapshot
Standard methods for toxicology research inApis mellifera
inferred← citeshttps://doi.org/10.4025/actascianimsci.v45i1.58412openalex-snapshot
Toxicological evaluation of different pesticides in Tetragonisca angustula Latreille (Hymenoptera, Apidae)
inferred← citeshttps://doi.org/10.4067/s0301-732x2015000200002openalex-snapshot
Distribution, epidemiological characteristics and control methods of the pathogen Nosema ceranae Fries in honey bees Apis mellifera L. (Hymenoptera, Apidae)
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