On the public citation graph

Yeasts Associated with Culex pipiens and Culex theileri Mosquito Larvae and the Effect of Selected Yeast Strains on the Ontogeny of Culex pipiens

https://doi.org/10.1007/s00248-015-0709-1
0 signed · 143 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.
Claim with ORCID
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 See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.
See reference health

What this work says

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

inferredcites →https://doi.org/10.1007/978-0-387-78225-6_4openalex-snapshot
Bacteria of the Genus Asaia: A Potential Paratransgenic Weapon Against Malaria
inferredcites →https://doi.org/10.1007/978-1-61779-539-8_38openalex-snapshot
Murine Model of Concurrent Oral and Vaginal Candida albicans Colonisation
inferredcites →https://doi.org/10.1007/s00248-010-9704-8openalex-snapshot
Mosquito-Bacteria Symbiosis: The Case of Anopheles gambiae and Asaia
inferredcites →https://doi.org/10.1007/s10482-010-9532-3openalex-snapshot
Different mosquito species host Wickerhamomyces anomalus (Pichia anomala): perspectives on vector-borne diseases symbiotic control
inferredcites →https://doi.org/10.1007/s10750-007-9037-xopenalex-snapshot
Global diversity of mosquitoes (Insecta: Diptera: Culicidae) in freshwater
inferredcites →https://doi.org/10.1007/s11046-010-9328-zopenalex-snapshot
Pathogenesis of Pulmonary Cryptococcus gattii Infection: A Rat Model
inferredcites →https://doi.org/10.1016/0031-9422(80)85004-7openalex-snapshot
Deviations from michaelis-menten behaviour of plant glutamate dehydrogenase with ammonium as variable substrate
inferredcites →https://doi.org/10.1016/0968-0004(90)90252-7openalex-snapshot
PCR protocols — A guide to methods and applications
inferredcites →https://doi.org/10.1016/b978-0-12-372180-8.50042-1openalex-snapshot
AMPLIFICATION AND DIRECT SEQUENCING OF FUNGAL RIBOSOMAL RNA GENES FOR PHYLOGENETICS
inferredcites →https://doi.org/10.1016/b978-0-444-52149-1.00001-xopenalex-snapshot
Definition, Classification and Nomenclature of the Yeasts
inferredcites →https://doi.org/10.1016/b978-044481312-1/50014-9openalex-snapshot
Methods for the isolation, maintenance and identification of yeasts
inferredcites →https://doi.org/10.1016/j.actatropica.2008.06.008openalex-snapshot
Transstadial and horizontal transfer of bacteria within a colony of Anopheles gambiae (Diptera: Culicidae) and oviposition response to bacteria-containing water
inferredcites →https://doi.org/10.1016/j.actatropica.2010.04.011openalex-snapshot
Culture-dependent and culture-independent characterization of microorganisms associated with Aedes aegypti (Diptera: Culicidae) (L.) and dynamics of bacterial colonization in the midgut
inferredcites →https://doi.org/10.1016/j.biocontrol.2004.06.006openalex-snapshot
Reconsideration of the role of yeasts associated with Chrysoperla green lacewings
inferredcites →https://doi.org/10.1016/j.cell.2009.11.042openalex-snapshot
A Wolbachia Symbiont in Aedes aegypti Limits Infection with Dengue, Chikungunya, and Plasmodium
inferredcites →https://doi.org/10.1016/j.mib.2012.03.004openalex-snapshot
Mosquito/microbiota interactions: from complex relationships to biotechnological perspectives
inferredcites →https://doi.org/10.1016/j.micres.2006.09.002openalex-snapshot
A marine killer yeast against the pathogenic yeast strain in crab (Portunus trituberculatus) and an optimization of the toxin production
inferredcites →https://doi.org/10.1016/j.tim.2011.07.010openalex-snapshot
Cryptococcus gattii: a resurgent fungal pathogen
inferredcites →https://doi.org/10.1016/s0044-8486(02)00271-5openalex-snapshot
Infection and mortality by the yeast Metschnikowia bicuspidata var. bicuspidata in chinook salmon fed live adult brine shrimp (Artemia franciscana)
inferredcites →https://doi.org/10.1016/s1567-1356(03)00173-9openalex-snapshot
Yeast communities associated with stingless bees
inferredcites →https://doi.org/10.1038/163688a0openalex-snapshot
Measurement of Diversity
inferredcites →https://doi.org/10.1038/466432aopenalex-snapshot
Ecology: A world without mosquitoes
inferredcites →https://doi.org/10.1038/ismej.2007.95openalex-snapshot
Thorsellia anophelis is the dominant bacterium in a Kenyan population of adult Anopheles gambiae mosquitoes
inferredcites →https://doi.org/10.1038/nature04220openalex-snapshot
Same-sex mating and the origin of the Vancouver Island Cryptococcus gattii outbreak
inferredcites →https://doi.org/10.1046/j.1365-2311.2003.00476.xopenalex-snapshot
Biological warfare in the garden pond: tadpoles suppress the growth of mosquito larvae
inferredcites →https://doi.org/10.1073/pnas.0702813104openalex-snapshot
Multitrophic interaction facilitates parasite–host relationship between an invasive beetle and the honey bee
inferredcites →https://doi.org/10.1080/00218839.2008.11101459openalex-snapshot
Detection and characterization of Kodamaea ohmeri associated with small hive beetle Aethina tumida infesting honey bee hives
inferredcites →https://doi.org/10.1093/jac/dks060openalex-snapshot
A murine model of Cryptococcus gattii meningoencephalitis
inferredcites →https://doi.org/10.1093/jmedent/35.3.222openalex-snapshot
Midgut Bacteria in Anopheles gambiae and An. funestus (Diptera: Culicidae) from Kenya and Mali
inferredcites →https://doi.org/10.1099/00207713-50-3-1351openalex-snapshot
Biodiversity and systematics of basidiomycetous yeasts as determined by large-subunit rDNA D1/D2 domain sequence analysis.
inferredcites →https://doi.org/10.1111/1462-2920.12381openalex-snapshot
Exploring A nopheles gut bacteria for P lasmodium blocking activity
inferredcites →https://doi.org/10.1111/j.1365-2656.2006.01048.xopenalex-snapshot
Evaluating the performance of species richness estimators: sensitivity to sample grain size
inferredcites →https://doi.org/10.1111/j.1365-2672.2010.04770.xopenalex-snapshot
Effects of small increases in copper levels on culturable basidiomycetous yeasts in low-nutrient soils
inferredcites →https://doi.org/10.1111/j.1439-0418.2011.01613.xopenalex-snapshot
Mosquito symbioses: from basic research to the paratransgenic control of mosquito-borne diseases
inferredcites →https://doi.org/10.1111/j.1462-2920.2010.02395.xopenalex-snapshot
The yeast Wickerhamomyces anomalus ( Pichia anomala ) inhabits the midgut and reproductive system of the Asian malaria vector Anopheles stephensi
inferredcites →https://doi.org/10.1111/mec.12771openalex-snapshot
Mosquitoes rely on their gut microbiota for development
inferredcites →https://doi.org/10.1126/science.1201618openalex-snapshot
Natural Microbe-Mediated Refractoriness to Plasmodium Infection in Anopheles gambiae
inferredcites →https://doi.org/10.1128/aem.00361-09openalex-snapshot
Negative Fitness Consequences and Transmission Dynamics of a Heritable Fungal Symbiont of a Parasitic Wasp
inferredcites →https://doi.org/10.1128/aem.01741-12openalex-snapshot
Yeast Communities of Diverse Drosophila Species: Comparison of Two Symbiont Groups in the Same Hosts
inferredcites →https://doi.org/10.1128/ec.00020-08openalex-snapshot
Evidence of Recombination in Mixed-Mating-Type and α-Only Populations of Cryptococcus gattii Sourced from Single Eucalyptus Tree Hollows
inferredcites →https://doi.org/10.1128/ec.05005-11openalex-snapshot
Live Imaging of Disseminated Candidiasis in Zebrafish Reveals Role of Phagocyte Oxidase in Limiting Filamentous Growth
inferredcites →https://doi.org/10.1146/annurev.en.40.010195.002303openalex-snapshot
Mosquito Sugar Feeding and Reproductive Energetics
inferredcites →https://doi.org/10.1159/000321157openalex-snapshot
Organ-Specific Innate Immune Responses in a Mouse Model of Invasive Candidiasis
inferredcites →https://doi.org/10.1186/1471-2180-12-s1-s2openalex-snapshot
Delayed larval development in Anopheles mosquitoes deprived of Asaiabacterial symbionts
inferredcites →https://doi.org/10.1371/journal.pntd.0000989openalex-snapshot
Towards a Semen Proteome of the Dengue Vector Mosquito: Protein Identification and Potential Functions
inferredcites →https://doi.org/10.1371/journal.pntd.0001381openalex-snapshot
Epidemiological Tracking and Population Assignment of the Non-Clonal Bacterium, Burkholderia pseudomallei
inferredcites →https://doi.org/10.1371/journal.pone.0016076openalex-snapshot
Cryptococcus gattii Virulence Composite: Candidate Genes Revealed by Microarray Analysis of High and Less Virulent Vancouver Island Outbreak Strains
inferredcites →https://doi.org/10.1371/journal.pone.0095988openalex-snapshot
A Wickerhamomyces anomalus Killer Strain in the Malaria Vector Anopheles stephensi
inferredcites →https://doi.org/10.1371/journal.ppat.1000098openalex-snapshot
The Aedes aegypti Toll Pathway Controls Dengue Virus Infection
inferredcites →https://doi.org/10.1371/journal.ppat.1000423openalex-snapshot
Implication of the Mosquito Midgut Microbiota in the Defense against Malaria Parasites
inferredcites →https://doi.org/10.1371/journal.ppat.1000850openalex-snapshot
Emergence and Pathogenicity of Highly Virulent Cryptococcus gattii Genotypes in the Northwest United States
inferredcites →https://doi.org/10.1371/journal.ppat.1002459openalex-snapshot
Legionella pneumophila Secretes a Mitochondrial Carrier Protein during Infection
inferredcites →https://doi.org/10.1371/journal.ppat.1002742openalex-snapshot
Midgut Microbiota of the Malaria Mosquito Vector Anopheles gambiae and Interactions with Plasmodium falciparum Infection
inferredcites →https://doi.org/10.1371/journal.ppat.1003634openalex-snapshot
NADPH Oxidase-Driven Phagocyte Recruitment Controls Candida albicans Filamentous Growth and Prevents Mortality
inferredcites →https://doi.org/10.1590/s0074-02762007000800005openalex-snapshot
First isolation of microorganisms from the gut diverticulum of Aedes aegypti (Diptera: Culicidae): new perspectives for an insect-bacteria association
inferredcites →https://doi.org/10.1603/0022-2585-38.1.29openalex-snapshot
Meconial Peritrophic Membranes and the Fate of Midgut Bacteria During Mosquito (Diptera: Culicidae) Metamorphosis
inferredcites →https://doi.org/10.1603/0022-2585-40.3.371openalex-snapshot
Bacteria in Midguts of Field-Collected Anopheles albimanus Block Plasmodium vivax Sporogonic Development
inferredcites →https://doi.org/10.3201/eid1601.090369openalex-snapshot
Projecting Global Occurrence ofCryptococcus gattii
inferredcites →https://doi.org/10.3390/pathogens3030549openalex-snapshot
Host Pathogen Relations: Exploring Animal Models for Fungal Pathogens
inferredcites →https://doi.org/10.3791/4051openalex-snapshot
Non-invasive Imaging of Disseminated Candidiasis in Zebrafish Larvae
inferredcites →https://doi.org/10.3827/ibra.1.47.3.07openalex-snapshot
Detection and characterization of kodamaea ohmeri associated with small hive beetle Aethina tumida infesting honey bee hives.
inferredcites →https://doi.org/10.4081/mr.2012.e24openalex-snapshot
Yeasts and yeast-like fungal contaminants of water used for domestic purposes in Jos, Nigeria
inferredcites →https://doi.org/10.4269/ajtmh.1996.54.214openalex-snapshot
Bacterial Population Dynamics in Three Anopheline Species: The Impact on Plasmodium Sporogonic Development
inferredcites →https://doi.org/10.5281/zenodo.15145663openalex-snapshot
Table 1 in A new Gammarus species from Xinjiang Uygur Autonomous Region (China) with a key to Xinjiang freshwater gammarids (Crustacea, Amphipoda, Gammaridae)
inferredcites →https://doi.org/10.5772/24108openalex-snapshot
Biodiversity of Yeasts in the Gastrointestinal Ecosystem with Emphasis on Its Importance for the Host

What points at this work

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

inferred← citeshttps://doi.org/10.2139/ssrn.4195220openalex-extracted
Fungi Associated with Anopheles Darlingi Root, 1926, Larval Breeding Sites in the Brazilian Amazon
inferred← citeshttps://doi.org/10.1002/ece3.3676openalex-snapshot
Mosquito vector‐associated microbiota: Metabarcoding bacteria and eukaryotic symbionts across habitat types in Thailand endemic for dengue and other arthropod‐borne diseases
inferred← citeshttps://doi.org/10.1007/978-3-030-29654-4_4openalex-snapshot
Suspension and Filter Feeding in Aquatic Insects
inferred← citeshttps://doi.org/10.1007/978-981-97-4163-2_12openalex-snapshot
Mosquito-Borne Veterinary Diseases
inferred← citeshttps://doi.org/10.1007/s10886-025-01685-0openalex-snapshot
Flower- and Water-Dwelling Yeasts Influence Nectar-Seeking and Oviposition Behavior in the Asian Tiger Mosquito with Distinct Volatile Organic Compound Profiles
inferred← citeshttps://doi.org/10.1007/s13199-018-0577-9openalex-snapshot
The digestive tract of Phylloicus (Trichoptera: Calamoceratidae) harbours different yeast taxa in Cerrado streams, Brazil
inferred← citeshttps://doi.org/10.1007/s42690-022-00761-2openalex-snapshot
Gut bacterium induced pesticide resistance in insects with special emphasis to mosquitoes
inferred← citeshttps://doi.org/10.1016/bs.aiip.2016.04.006openalex-snapshot
Influences of the Mosquito Microbiota on Vector Competence
inferred← citeshttps://doi.org/10.1016/bs.aiip.2020.03.004openalex-snapshot
Functions and mechanisms of symbionts of insect disease vectors
inferred← citeshttps://doi.org/10.1016/j.actatropica.2020.105732openalex-snapshot
Larvicidal activity, route of interaction and ultrastructural changes in Aedes aegypti exposed to entomopathogenic fungi
inferred← citeshttps://doi.org/10.1016/j.actatropica.2023.106938openalex-snapshot
RNAi-mediated mortality of Culex quinquefasciatus using two delivery methods of potential field application
inferred← citeshttps://doi.org/10.1016/j.cois.2018.05.008openalex-snapshot
Composition and functional roles of the gut microbiota in mosquitoes
inferred← citeshttps://doi.org/10.1016/j.funeco.2019.02.004openalex-snapshot
Aedes albopictus mosquitoes host a locally structured mycobiota with evidence of reduced fungal diversity in invasive populations
inferred← citeshttps://doi.org/10.1016/j.ibmb.2019.103182openalex-snapshot
Mosquito-fungus interactions and antifungal immunity
inferred← citeshttps://doi.org/10.1016/j.jip.2020.107505openalex-snapshot
Antifungal immune responses in mosquitoes (Diptera: Culicidae): A review
inferred← citeshttps://doi.org/10.1016/j.pt.2019.12.001openalex-snapshot
Mosquito Microbiota and Implications for Disease Control
inferred← citeshttps://doi.org/10.1038/s41579-023-00901-6openalex-snapshot
Microbiota in disease-transmitting vectors
inferred← citeshttps://doi.org/10.1038/s41598-026-39702-1openalex-snapshot
Ecotoxicological and behavioural responses of aquatic model organisms to the MosChito raft bioinsecticide delivery system
inferred← citeshttps://doi.org/10.1051/jbio/2019003openalex-snapshot
Le microbiote de moustique et son influence sur la transmission vectorielle
inferred← citeshttps://doi.org/10.1073/pnas.2101080118openalex-snapshot
Riboflavin instability is a key factor underlying the requirement of a gut microbiota for mosquito development
inferred← citeshttps://doi.org/10.1073/pnas.2536902123openalex-snapshot
Scent and adhesion drive insect dispersal of environmental yeast
inferred← citeshttps://doi.org/10.1101/2023.08.11.552965openalex-snapshot
Interkingdom interactions shape the fungal microbiome of mosquitoes
inferred← citeshttps://doi.org/10.1111/1462-2920.14915openalex-snapshot
Who is eating fructose within the Aedes albopictus gut microbiota?
inferred← citeshttps://doi.org/10.1111/1744-7917.13259openalex-snapshot
Survival effects of antibiotic exposure during the larval and adult stages in the West Nile virus vector Culex pipiens
inferred← citeshttps://doi.org/10.1111/1758-2229.12569openalex-snapshot
Mosquitoes can harbour yeasts of clinical significance and contribute to their environmental dissemination
inferred← citeshttps://doi.org/10.1128/msphere.00646-21openalex-snapshot
Host-Environment Interplay Shapes Fungal Diversity in Mosquitoes
inferred← citeshttps://doi.org/10.1134/s2079086425601644openalex-snapshot
Microbiota of Mosquitoes at Different Stages of Development, Its Diversity, Interaction, and Influence on Host Physiology
inferred← citeshttps://doi.org/10.1186/s12936-021-03754-7openalex-snapshot
Microbiota identified from preserved Anopheles
inferred← citeshttps://doi.org/10.1186/s13071-019-3587-4openalex-snapshot
Killer yeasts exert anti-plasmodial activities against the malaria parasite Plasmodium berghei in the vector mosquito Anopheles stephensi and in mice
inferred← citeshttps://doi.org/10.1186/s13071-022-05367-8openalex-snapshot
Contemporary exploitation of natural products for arthropod-borne pathogen transmission-blocking interventions
inferred← citeshttps://doi.org/10.1186/s13071-024-06281-xopenalex-snapshot
Isolation, characterization and functional analysis of a bacteriophage targeting Culex pipiens pallens resistance-associated Aeromonas hydrophila
inferred← citeshttps://doi.org/10.1186/s13104-026-07832-4openalex-snapshot
Culturable microbiota of reared mosquito fauna in Osogbo, Nigeria and their potential biological roles: a molecular insight
inferred← citeshttps://doi.org/10.1186/s40168-018-0435-2openalex-snapshot
The mosquito holobiont: fresh insight into mosquito-microbiota interactions
inferred← citeshttps://doi.org/10.1186/s40168-021-01073-2openalex-snapshot
The microbiome and mosquito vectorial capacity: rich potential for discovery and translation
inferred← citeshttps://doi.org/10.1186/s40168-022-01325-9openalex-snapshot
Mosquito sex and mycobiota contribute to fructose metabolism in the Asian tiger mosquito Aedes albopictus
inferred← citeshttps://doi.org/10.1186/s40168-025-02099-6openalex-snapshot
Environmental yeasts differentially impact the development and oviposition behavior of the Asian tiger mosquito Aedes albopictus
inferred← citeshttps://doi.org/10.1186/s42523-024-00298-4openalex-snapshot
Interkingdom interactions shape the fungal microbiome of mosquitoes
inferred← citeshttps://doi.org/10.12688/wellcomeopenres.25128.1openalex-snapshot
Fungal microbiota diversity in Aedes, Anopheles and Culex and their potential use as biological tools to control vector-borne diseases, a systematic review.
inferred← citeshttps://doi.org/10.1371/journal.pone.0151403openalex-snapshot
Digestion of Yeasts and Beta-1,3-Glucanases in Mosquito Larvae: Physiological and Biochemical Considerations
inferred← citeshttps://doi.org/10.1371/journal.pone.0312624openalex-snapshot
Fungi from Anopheles darlingi Root, 1926, larval breeding sites in the Brazilian Amazon
inferred← citeshttps://doi.org/10.1590/0074-02760160373openalex-snapshot
Microbial control of arthropod-borne disease
inferred← citeshttps://doi.org/10.21203/rs.3.rs-3307938/v1openalex-snapshot
Interkingdom interactions shape the fungal microbiome of mosquitoes
inferred← citeshttps://doi.org/10.21203/rs.3.rs-8958698/v1openalex-snapshot
Yeasts Associated with Mosquito Larval Habitats Produce Volatile Cues That Attract Gravid Females and Show Potential as Safe Tools for Behavioural Control
inferred← citeshttps://doi.org/10.3114/sim.2024.108.01openalex-snapshot
What are the 100 most cited fungal genera?
inferred← citeshttps://doi.org/10.3389/fcimb.2020.596750openalex-snapshot
Comparative Analysis of the Gut Microbiota of Adult Mosquitoes From Eight Locations in Hainan, China
inferred← citeshttps://doi.org/10.3389/fevo.2022.911085openalex-snapshot
Patterns of Fungal Community Assembly Across Two Culex Mosquito Species
inferred← citeshttps://doi.org/10.3389/ffunb.2022.918052openalex-snapshot
Culex quinquefasciatus Holobiont: A Fungal Metagenomic Approach
inferred← citeshttps://doi.org/10.3389/fimmu.2025.1648091openalex-snapshot
Fungal communities in Florida salt marsh mosquito midguts vary between species and over time but have low structure
inferred← citeshttps://doi.org/10.3389/fmicb.2020.01629openalex-snapshot
Saccharomyces cerevisiae – Insects Association: Impacts, Biogeography, and Extent
inferred← citeshttps://doi.org/10.3389/fmicb.2020.621605openalex-snapshot
Wickerhamomyces anomalus in Mosquitoes: A Promising Yeast-Based Tool for the “Symbiotic Control” of Mosquito-Borne Diseases
inferred← citeshttps://doi.org/10.3389/fmicb.2021.650743openalex-snapshot
Diet–Microbiota Interactions Alter Mosquito Development
inferred← citeshttps://doi.org/10.3389/fmicb.2022.891573openalex-snapshot
Malaria-Transmitting Vectors Microbiota: Overview and Interactions With Anopheles Mosquito Biology
inferred← citeshttps://doi.org/10.3389/fmicb.2023.1157299openalex-snapshot
Tripartite interactions comprising yeast-endobacteria systems in the gut of vector mosquitoes
inferred← citeshttps://doi.org/10.3390/applmicrobiol6090104openalex-snapshot
Diversity of Microbiomes of Culex pipiens f. pipiens and f. molestus from Geographically Distant Collection Sites
inferred← citeshttps://doi.org/10.3390/insects12070645openalex-snapshot
The Possible Role of Microorganisms in Mosquito Mass Rearing
inferred← citeshttps://doi.org/10.3390/microorganisms11061525openalex-snapshot
Application of Novel Short Tandem Repeat Typing for Wickerhamomyces anomalus Reveals Simultaneous Outbreaks within a Single Hospital
inferred← citeshttps://doi.org/10.3390/microorganisms9081552openalex-snapshot
Diversity and Functions of Yeast Communities Associated with Insects
inferred← citeshttps://doi.org/10.3390/microorganisms9081589openalex-snapshot
Microorganisms Associated with Mosquito Oviposition Sites: Implications for Habitat Selection and Insect Life Histories
inferred← citeshttps://doi.org/10.3390/pathogens9070564openalex-snapshot
Mosquito Mycobiota: An Overview of Non-Entomopathogenic Fungal Interactions
inferred← citeshttps://doi.org/10.3390/toxins13100676openalex-snapshot
Formulation and Safety Tests of a Wickerhamomyces anomalus–Based Product: Potential Use of Killer Toxins of a Mosquito Symbiotic Yeast to Limit Malaria Transmission
inferred← citeshttps://doi.org/10.6084/m9.figshare.14650581openalex-snapshot
Additional file 11 of Microbiota identified from preserved Anopheles
inferred← citeshttps://doi.org/10.6084/m9.figshare.14650584openalex-snapshot
Additional file 12 of Microbiota identified from preserved Anopheles
inferred← citeshttps://doi.org/10.6084/m9.figshare.14650587openalex-snapshot
Additional file 13 of Microbiota identified from preserved Anopheles
inferred← citeshttps://doi.org/10.6084/m9.figshare.14650590openalex-snapshot
Additional file 14 of Microbiota identified from preserved Anopheles
inferred← citeshttps://doi.org/10.6084/m9.figshare.14650602openalex-snapshot
Additional file 4 of Microbiota identified from preserved Anopheles
inferred← citeshttps://doi.org/10.6084/m9.figshare.14650605openalex-snapshot
Additional file 5 of Microbiota identified from preserved Anopheles
inferred← citeshttps://doi.org/10.6084/m9.figshare.14650614openalex-snapshot
Additional file 8 of Microbiota identified from preserved Anopheles
inferred← citeshttps://doi.org/10.6084/m9.figshare.20625097openalex-snapshot
Additional file 1 of Contemporary exploitation of natural products for arthropod-borne pathogen transmission-blocking interventions
inferred← citeshttps://doi.org/10.6084/m9.figshare.26690264openalex-snapshot
Additional file 1 of Interkingdom interactions shape the fungal microbiome of mosquitoes
inferred← citeshttps://doi.org/10.6084/m9.figshare.26690267openalex-snapshot
Additional file 2 of Interkingdom interactions shape the fungal microbiome of mosquitoes
inferred← citeshttps://doi.org/10.6084/m9.figshare.26690270openalex-snapshot
Additional file 3 of Interkingdom interactions shape the fungal microbiome of mosquitoes
inferred← citeshttps://doi.org/10.6084/m9.figshare.26690273openalex-snapshot
Additional file 4 of Interkingdom interactions shape the fungal microbiome of mosquitoes
inferred← citeshttps://doi.org/10.6084/m9.figshare.26690276openalex-snapshot
Additional file 5 of Interkingdom interactions shape the fungal microbiome of mosquitoes
inferred← citeshttps://doi.org/10.6084/m9.figshare.26690279openalex-snapshot
Additional file 6 of Interkingdom interactions shape the fungal microbiome of mosquitoes
inferred← citeshttps://doi.org/10.6084/m9.figshare.26690282openalex-snapshot
Additional file 7 of Interkingdom interactions shape the fungal microbiome of mosquitoes
inferred← citeshttps://doi.org/10.6084/m9.figshare.26690285openalex-snapshot
Additional file 8 of Interkingdom interactions shape the fungal microbiome of mosquitoes
inferred← citeshttps://doi.org/10.6084/m9.figshare.26690288openalex-snapshot
Additional file 9 of Interkingdom interactions shape the fungal microbiome of mosquitoes
inferred← citeshttps://doi.org/10.6084/m9.figshare.26720601openalex-snapshot
Additional file 1 of Isolation, characterization and functional analysis of a bacteriophage targeting Culex pipiens pallens resistance-associated Aeromonas hydrophila
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.