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Vibrio cholerae Infection of Drosophila melanogaster Mimics the Human Disease Cholera

https://doi.org/10.1371/journal.ppat.0010008

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What this work says

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

inferreduses_data →https://doi.org/10.5281/zenodo.10723540zenodo-depositor-declared

inferredcites →https://doi.org/10.1002/(sici)1097-4695(199609)31:1<88::aid-neu8>3.0.co;2-bopenalex-snapshot

The Drosophila brain revisited by enhancer detection

inferredcites →https://doi.org/10.1002/jss.400080410openalex-snapshot

Mechanism of action of choleragen

inferredcites →https://doi.org/10.1007/978-1-4757-9688-9_7openalex-snapshot

The Epidemiology of Cholera

inferredcites →https://doi.org/10.1007/s00248-003-2007-6openalex-snapshot

Chironomid Egg Masses as a Natural Reservoir of Vibrio cholerae Non-O1 and Non-O139 in Freshwater Habitats

inferredcites →https://doi.org/10.1016/j.femsim.2004.11.003openalex-snapshot

Invertebrates as animal models forStaphylococcus aureuspathogenesis: a window into host–pathogen interaction

inferredcites →https://doi.org/10.1016/j.tibs.2003.10.002openalex-snapshot

The intracellular voyage of cholera toxin: going retro

inferredcites →https://doi.org/10.1016/s0001-706x(00)00162-5openalex-snapshot

Vector potential of houseflies (Musca domestica) in the transmission of Vibrio cholerae in India

inferredcites →https://doi.org/10.1016/s0021-9258(17)40578-3openalex-snapshot

Mechanism of action of choleragen. Evidence for ADP-ribosyltransferase activity with arginine as an acceptor.

inferredcites →https://doi.org/10.1016/s0021-9258(18)33691-3openalex-snapshot

Mechanism of action of cholera toxin on intact cells. Generation of A1 peptide and activation of adenylate cyclase.

inferredcites →https://doi.org/10.1016/s0092-8674(01)00289-6openalex-snapshot

Protein Disulfide Isomerase Acts as a Redox-Dependent Chaperone to Unfold Cholera Toxin

inferredcites →https://doi.org/10.1016/s0140-6736(03)15328-7openalex-snapshot

Cholera

inferredcites →https://doi.org/10.1016/s0959-4388(00)00147-1openalex-snapshot

Behavioral functions of the insect mushroom bodies

inferredcites →https://doi.org/10.1016/s1074-7613(00)80208-3openalex-snapshot

The Rel Protein DIF Mediates the Antifungal but Not the Antibacterial Host Defense in Drosophila

inferredcites →https://doi.org/10.1038/35083691openalex-snapshot

Chironomid egg masses and Vibrio cholerae

inferredcites →https://doi.org/10.1038/35083694openalex-snapshot

Photosynthesis in a marine diatom

inferredcites →https://doi.org/10.1038/ng1314openalex-snapshot

A complementary transposon tool kit for Drosophila melanogaster using P and piggyBac

inferredcites →https://doi.org/10.1038/sj.embor.embor730openalex-snapshot

A single gene that promotes interaction of a phytopathogenic bacterium with its insect vector, Drosophila melanogaster

inferredcites →https://doi.org/10.1046/j.1365-2958.2002.03023.xopenalex-snapshot

Vibrio cholerae CytR is a repressor of biofilm development

inferredcites →https://doi.org/10.1046/j.1462-5822.2003.00329.xopenalex-snapshot

Exploration of host-pathogen interactions using Listeria monocytogenes and Drosophila melanogaster

inferredcites →https://doi.org/10.1073/pnas.0409181102openalex-snapshot

The Toll pathway is important for an antiviral response in Drosophila

inferredcites →https://doi.org/10.1073/pnas.0409588102openalex-snapshot

Profiling early infection responses: Pseudomonas aeruginosa eludes host defenses by suppressing antimicrobial peptide gene expression

inferredcites →https://doi.org/10.1073/pnas.91.24.11388openalex-snapshot

The Vibrio cholerae O139 serogroup antigen includes an O-antigen capsule and lipopolysaccharide virulence determinants.

inferredcites →https://doi.org/10.1083/jcb.131.4.951openalex-snapshot

Targeting of cholera toxin and Escherichia coli heat labile toxin in polarized epithelia: role of COOH-terminal KDEL.

inferredcites →https://doi.org/10.1084/jem.130.1.185openalex-snapshot

PATHOGENESIS OF EXPERIMENTAL CHOLERA

inferredcites →https://doi.org/10.1086/428587openalex-snapshot

Toll‐DeficientDrosophilaFlies as a Fast, High‐Throughput Model for the Study of Antifungal Drug Efficacy against Invasive Aspergillosis andAspergillusVirulence

inferredcites →https://doi.org/10.1091/mbc.e03-06-0354openalex-snapshot

Gangliosides That Associate with Lipid Rafts Mediate Transport of Cholera and Related Toxins from the Plasma Membrane to Endoplasmic Reticulm

inferredcites →https://doi.org/10.1093/genetics/158.3.1189openalex-snapshot

Genetic Analysis of the Drosophila Gsα Gene

inferredcites →https://doi.org/10.1093/infdis/114.3.203openalex-snapshot

Pathogenesis of Experimental Cholera in Infant Rabbits: I. Observations on the Intraintestinal Infection and Experimental Cholera Produced with Cell-Free Products

inferredcites →https://doi.org/10.1093/infdis/170.2.278openalex-snapshot

Emergence of a New Cholera Pandemic: Molecular Analysis of Virulence Determinants in Vibrio cholerae 0139 and Development of a Live Vaccine Prototype

inferredcites →https://doi.org/10.1101/lm.7.1.18openalex-snapshot

Tissue-Specific Expression of a Type I Adenylyl Cyclase Rescues the rutabaga Mutant Memory Defect: In Search of the Engram

inferredcites →https://doi.org/10.1111/j.1574-695x.1995.tb00182.xopenalex-snapshot

Attachment of non-culturable toxigenicVibrio cholerae01 and non-01 andAeromonasspp. to the aquatic arthropodGerris spinolaeand plants in the River Ganga, Varanasi

inferredcites →https://doi.org/10.1126/science.288.5475.2376openalex-snapshot

Malaria Parasite Development in a Drosophila Model

inferredcites →https://doi.org/10.1128/aem.45.1.275-283.1983openalex-snapshot

Ecological relationships between Vibrio cholerae and planktonic crustacean copepods

inferredcites →https://doi.org/10.1128/aem.46.1.32-36.1983openalex-snapshot

Flies as a source of enteric pathogens in a rural village in Thailand

inferredcites →https://doi.org/10.1128/aem.52.3.586-588.1986openalex-snapshot

Colonization of the gut of the blue crab (Callinectes sapidus) by Vibrio cholerae

inferredcites →https://doi.org/10.1128/aem.56.6.1977-1980.1990openalex-snapshot

Attachment of Vibrio cholerae serogroup O1 to zooplankton and phytoplankton of Bangladesh waters

inferredcites →https://doi.org/10.1128/aem.62.7.2508-2512.1996openalex-snapshot

A simple filtration method to remove plankton-associated Vibrio cholerae in raw water supplies in developing countries

inferredcites →https://doi.org/10.1128/aem.67.7.3220-3225.2001openalex-snapshot

The Mannose-Sensitive Hemagglutinin of Vibrio cholerae Promotes Adherence to Zooplankton

inferredcites →https://doi.org/10.1128/aem.69.7.4200-4204.2003openalex-snapshot

Vibrio cholerae Hemagglutinin/Protease Degrades Chironomid Egg Masses

inferredcites →https://doi.org/10.1128/iai.15.3.704-712.1977openalex-snapshot

Intestinal fluid accumulation induced by oral challenge with Vibrio cholerae or cholera toxin in infant mice

inferredcites →https://doi.org/10.1128/iai.67.10.5215-5222.1999openalex-snapshot

Purification and Characterization of Novel Toxin Produced byVibrio choleraeO1

inferredcites →https://doi.org/10.1128/iai.67.8.3733-3739.1999openalex-snapshot

Vibrio cholerae Intestinal Population Dynamics in the Suckling Mouse Model of Infection

inferredcites →https://doi.org/10.1128/mmbr.47.4.510-550.1983openalex-snapshot

New knowledge on pathogenesis of bacterial enteric infections as applied to vaccine development

inferredcites →https://doi.org/10.1152/ajpgi.1990.258.1.g96openalex-snapshot

Interaction of cholera toxin with cloned human goblet cells in monolayer culture

inferredcites →https://doi.org/10.1172/jci119012openalex-snapshot

The antifungal antibiotic, clotrimazole, inhibits Cl- secretion by polarized monolayers of human colonic epithelial cells.

inferredcites →https://doi.org/10.1172/jci119866openalex-snapshot

The antifungal antibiotic, clotrimazole, inhibits chloride secretion by human intestinal T84 cells via blockade of distinct basolateral K+ conductances. Demonstration of efficacy in intact rabbit colon and in an in vivo mouse model of cholera.

inferredcites →https://doi.org/10.1371/journal.pbio.0020418openalex-snapshot

Secreted Bacterial Effectors and Host-Produced Eiger/TNF Drive Death in a Salmonella-Infected Fruit Fly

inferredcites →https://doi.org/10.1534/genetics.104.026427openalex-snapshot

The BDGP Gene Disruption Project

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inferred← citeshttps://doi.org/10.1002/9780471729259.mc06a06s38openalex-snapshot

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inferred← citeshttps://doi.org/10.1007/978-1-4939-8685-9_8openalex-snapshot

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inferred← citeshttps://doi.org/10.1007/978-3-031-22997-8_2openalex-snapshot

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inferred← citeshttps://doi.org/10.1007/978-3-211-99079-7_15openalex-snapshot

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inferred← citeshttps://doi.org/10.1016/b978-0-323-85704-8.00015-3openalex-snapshot

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inferred← citeshttps://doi.org/10.1016/bs.aiip.2019.10.001openalex-snapshot

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inferred← citeshttps://doi.org/10.1016/j.celrep.2019.12.094openalex-snapshot

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inferred← citeshttps://doi.org/10.1016/j.celrep.2022.110572openalex-snapshot

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inferred← citeshttps://doi.org/10.1016/j.celrep.2022.111368openalex-snapshot

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inferred← citeshttps://doi.org/10.1016/j.celrep.2024.113750openalex-snapshot

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inferred← citeshttps://doi.org/10.1016/j.celrep.2025.116293openalex-snapshot

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inferred← citeshttps://doi.org/10.1016/j.chom.2013.08.001openalex-snapshot

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inferred← citeshttps://doi.org/10.1016/j.chom.2013.08.009openalex-snapshot

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inferred← citeshttps://doi.org/10.1016/j.chom.2014.10.006openalex-snapshot

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inferred← citeshttps://doi.org/10.1016/j.chom.2018.01.011openalex-snapshot

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inferred← citeshttps://doi.org/10.1016/j.coi.2012.11.008openalex-snapshot

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inferred← citeshttps://doi.org/10.1016/j.cois.2018.05.014openalex-snapshot

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inferred← citeshttps://doi.org/10.1016/j.copbio.2008.04.002openalex-snapshot

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inferred← citeshttps://doi.org/10.1016/j.fsi.2013.09.019openalex-snapshot

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inferred← citeshttps://doi.org/10.1016/j.gene.2023.147815openalex-snapshot

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inferred← citeshttps://doi.org/10.1016/j.ibmb.2011.05.007openalex-snapshot

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inferred← citeshttps://doi.org/10.1016/j.isci.2020.100865openalex-snapshot

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inferred← citeshttps://doi.org/10.1016/j.jphotochem.2021.113610openalex-snapshot

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inferred← citeshttps://doi.org/10.1016/j.mib.2006.12.001openalex-snapshot

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inferred← citeshttps://doi.org/10.1016/j.mib.2009.12.005openalex-snapshot

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inferred← citeshttps://doi.org/10.1016/j.mib.2021.09.007openalex-snapshot

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inferred← citeshttps://doi.org/10.1016/j.micinf.2022.104946openalex-snapshot

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inferred← citeshttps://doi.org/10.1016/j.micpath.2022.105485openalex-snapshot

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inferred← citeshttps://doi.org/10.1038/ismej.2011.19openalex-snapshot

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inferred← citeshttps://doi.org/10.1038/nprot.2009.124openalex-snapshot

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inferred← citeshttps://doi.org/10.1038/nrmicro1870openalex-snapshot

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inferred← citeshttps://doi.org/10.1038/s41467-019-13353-5openalex-snapshot

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inferred← citeshttps://doi.org/10.1038/s41467-026-70629-3openalex-snapshot

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inferred← citeshttps://doi.org/10.1038/s41522-022-00331-xopenalex-snapshot

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inferred← citeshttps://doi.org/10.1038/s41596-025-01311-zopenalex-snapshot

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inferred← citeshttps://doi.org/10.1038/s41598-017-13631-6openalex-snapshot

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inferred← citeshttps://doi.org/10.1042/bcj20200124openalex-snapshot

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inferred← citeshttps://doi.org/10.1073/pnas.0510748103openalex-snapshot

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inferred← citeshttps://doi.org/10.1073/pnas.0600477103openalex-snapshot

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inferred← citeshttps://doi.org/10.1073/pnas.1001294107openalex-snapshot

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inferred← citeshttps://doi.org/10.1073/pnas.1111530108openalex-snapshot

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inferred← citeshttps://doi.org/10.1080/19490976.2021.1937015openalex-snapshot

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inferred← citeshttps://doi.org/10.1080/19490976.2022.2163839openalex-snapshot

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inferred← citeshttps://doi.org/10.1093/database/bau105openalex-snapshot

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inferred← citeshttps://doi.org/10.1093/infdis/jiw435openalex-snapshot

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inferred← citeshttps://doi.org/10.1101/2020.09.03.282350openalex-snapshot

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inferred← citeshttps://doi.org/10.1101/2020.10.02.323444openalex-snapshot

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inferred← citeshttps://doi.org/10.1101/2023.06.29.547108openalex-snapshot

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inferred← citeshttps://doi.org/10.1101/2025.04.21.649765openalex-snapshot

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inferred← citeshttps://doi.org/10.1101/746305openalex-snapshot

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inferred← citeshttps://doi.org/10.1111/1462-2920.14976openalex-snapshot

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inferred← citeshttps://doi.org/10.1111/cmi.12292openalex-snapshot

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inferred← citeshttps://doi.org/10.1111/j.1462-2920.2008.01714.xopenalex-snapshot

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inferred← citeshttps://doi.org/10.1111/j.1462-5822.2007.01042.xopenalex-snapshot

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inferred← citeshttps://doi.org/10.1111/j.1462-5822.2008.01267.xopenalex-snapshot

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inferred← citeshttps://doi.org/10.1111/j.1758-2229.2009.00101.xopenalex-snapshot

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inferred← citeshttps://doi.org/10.1111/mve.12183openalex-snapshot

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inferred← citeshttps://doi.org/10.1128/aem.00371-20openalex-snapshot

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inferred← citeshttps://doi.org/10.1128/aem.00783-17openalex-snapshot

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inferred← citeshttps://doi.org/10.1128/aem.01113-18openalex-snapshot

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inferred← citeshttps://doi.org/10.1128/aem.03580-13openalex-snapshot

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inferred← citeshttps://doi.org/10.1128/jb.00380-18openalex-snapshot

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inferred← citeshttps://doi.org/10.1128/mbio.00276-21openalex-snapshot

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inferred← citeshttps://doi.org/10.1128/mbio.00337-13openalex-snapshot

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inferred← citeshttps://doi.org/10.1128/mbio.03432-22openalex-snapshot

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inferred← citeshttps://doi.org/10.1128/spectrum.02652-22openalex-snapshot

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inferred← citeshttps://doi.org/10.1166/jbn.2024.3923openalex-snapshot

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inferred← citeshttps://doi.org/10.1186/1476-072x-7-62openalex-snapshot

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inferred← citeshttps://doi.org/10.1186/gb-2009-10-4-r45openalex-snapshot

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inferred← citeshttps://doi.org/10.1242/bio.015016openalex-snapshot

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inferred← citeshttps://doi.org/10.1242/dmm.000406openalex-snapshot

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inferred← citeshttps://doi.org/10.13140/rg.2.2.33862.50243openalex-snapshot

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inferred← citeshttps://doi.org/10.1371/journal.pgen.1002272openalex-snapshot

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inferred← citeshttps://doi.org/10.1371/journal.pgen.1005156openalex-snapshot

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inferred← citeshttps://doi.org/10.1371/journal.pgen.1011982openalex-snapshot

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inferred← citeshttps://doi.org/10.1371/journal.pntd.0004330openalex-snapshot

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inferred← citeshttps://doi.org/10.1371/journal.pone.0007167openalex-snapshot

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inferred← citeshttps://doi.org/10.1371/journal.pone.0047442openalex-snapshot

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inferred← citeshttps://doi.org/10.1371/journal.pone.0087800openalex-snapshot

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inferred← citeshttps://doi.org/10.1371/journal.pone.0123066openalex-snapshot

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inferred← citeshttps://doi.org/10.1371/journal.pone.0153259openalex-snapshot

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inferred← citeshttps://doi.org/10.1371/journal.pone.0177825openalex-snapshot

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inferred← citeshttps://doi.org/10.1371/journal.ppat.1000184openalex-snapshot

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inferred← citeshttps://doi.org/10.1371/journal.ppat.1000518openalex-snapshot

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inferred← citeshttps://doi.org/10.1371/journal.ppat.1006428openalex-snapshot

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inferred← citeshttps://doi.org/10.1371/journal.ppat.1010825openalex-snapshot

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inferred← citeshttps://doi.org/10.15226/sojmid/9/1/001110openalex-snapshot

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inferred← citeshttps://doi.org/10.15226/sojmid/9/1/001111openalex-snapshot

Myc Mediates Toxin Response in Female Drosophila melanogaster.

inferred← citeshttps://doi.org/10.17912/micropub.biology.000938openalex-snapshot

Drosophila melanogaster larvae are tolerant to oral infection with the bacterial pathogen Photorhabdus luminescens

inferred← citeshttps://doi.org/10.3389/fcimb.2020.587948openalex-snapshot

From Welfare to Warfare: The Arbitration of Host-Microbiota Interplay by the Type VI Secretion System

inferred← citeshttps://doi.org/10.3389/fimmu.2019.03128openalex-snapshot

Host-Microbe-Pathogen Interactions: A Review of Vibrio cholerae Pathogenesis in Drosophila

inferred← citeshttps://doi.org/10.3389/fmicb.2022.947767openalex-snapshot

Effects of intestinal microbiota on physiological metabolism and pathogenicity of Vibrio

inferred← citeshttps://doi.org/10.3389/fmicb.2023.1178538openalex-snapshot

Advances in cholera research: from molecular biology to public health initiatives

inferred← citeshttps://doi.org/10.3390/ijms22052724openalex-snapshot

Drosophila as a Model for Infectious Diseases

inferred← citeshttps://doi.org/10.3390/ijms232012486openalex-snapshot

Insights into Carbapenem Resistance in Vibrio Species: Current Status and Future Perspectives

inferred← citeshttps://doi.org/10.3402/jom.v4i0.10368openalex-snapshot

The Drosophila melanogaster host model

inferred← citeshttps://doi.org/10.4049/jimmunol.1103301openalex-snapshot

The Drosophila Protein Mustard Tailors the Innate Immune Response Activated by the Immune Deficiency Pathway

inferred← citeshttps://doi.org/10.4161/fly.5.3.17028openalex-snapshot

Drosophila immunity research on the move

inferred← citeshttps://doi.org/10.4161/viru.27524openalex-snapshot

Human pathogenic bacteria, fungi, and viruses inDrosophila

inferred← citeshttps://doi.org/10.5772/intechopen.90073openalex-snapshot

Drosophila melanogaster: A Robust Tool to Study Candidate Drug against Epidemic and Pandemic Diseases

inferred← citeshttps://doi.org/10.7939/r3-0bhx-5r30openalex-snapshot

Characterization of the crosstalk between immunity and metabolism in Drosophila melanogaster model

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