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Drosophila melanogaster as a model host to study arbovirus–vector interaction
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1007/s00705-010-0728-7openalex-snapshot
Dengue-2-virus-interacting polypeptides involved in mosquito cell infection
inferredcites →https://doi.org/10.1007/s00705-012-1596-0openalex-snapshot
Surface proteins of C6/36 cells involved in dengue virus 4 binding and entry
inferredcites →https://doi.org/10.1007/s12038-014-9436-xopenalex-snapshot
Identification of chikungunya virus interacting proteins in mammalian cells
inferredcites →https://doi.org/10.1016/j.dci.2010.01.006openalex-snapshot
The Toll immune signaling pathway control conserved anti-dengue defenses across diverse Ae. aegypti strains and against multiple dengue virus serotypes
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.ibmb.2005.07.006openalex-snapshot
Sindbis virus induces transport processes and alters expression of innate immunity pathway genes in the midgut of the disease vector, Aedes aegypti
inferredcites →https://doi.org/10.1016/j.virol.2005.05.026openalex-snapshot
Characterization of plasma membrane-associated proteins from Aedes albopictus mosquito (C6/36) cells that mediate West Nile virus binding and infection
inferredcites →https://doi.org/10.1016/j.virol.2008.04.021openalex-snapshot
West Nile virus infection of Drosophila melanogaster induces a protective RNAi response
inferredcites →https://doi.org/10.1016/j.virol.2010.07.015openalex-snapshot
Identification and characterization of prohibitin as a receptor protein mediating DENV-2 entry into insect cells
inferredcites →https://doi.org/10.1016/j.virol.2011.11.016openalex-snapshot
Drosophila as a genetic model for studying pathogenic human viruses
inferredcites →https://doi.org/10.1016/j.virol.2013.11.008openalex-snapshot
Cellular DDX3 regulates Japanese encephalitis virus replication by interacting with viral un-translated regions
inferredcites →https://doi.org/10.1038/nature04104openalex-snapshot
A protein interaction network of the malaria parasite Plasmodium falciparum
inferredcites →https://doi.org/10.1038/nature07967openalex-snapshot
Discovery of insect and human dengue virus host factors
inferredcites →https://doi.org/10.1038/nrg1503openalex-snapshot
Drosophila, the golden bug, emerges as a tool for human genetics
inferredcites →https://doi.org/10.1038/nrg3462openalex-snapshot
Argonaute proteins: functional insights and emerging roles
inferredcites →https://doi.org/10.1038/nsmb.1735openalex-snapshot
Loqs and R2D2 act sequentially in the siRNA pathway in Drosophila
inferredcites →https://doi.org/10.1038/s41586-018-0692-zopenalex-snapshot
Improved reference genome of Aedes aegypti informs arbovirus vector control
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.0905006106openalex-snapshot
An evolutionary conserved function of the JAK-STAT pathway in anti-dengue defense
inferredcites →https://doi.org/10.1073/pnas.0911353107openalex-snapshot
Virus discovery by deep sequencing and assembly of virus-derived small silencing RNAs
inferredcites →https://doi.org/10.1074/mcp.m111.008128openalex-snapshot
Extracellular Matrix Composition and Remodeling in Human Abdominal Aortic Aneurysms: A Proteomics Approach
inferredcites →https://doi.org/10.1080/19336934.2015.1072662openalex-snapshot
Expression of dengue virus NS3 protein inDrosophilaalters its susceptibility to infection
inferredcites →https://doi.org/10.1099/mic.0.27116-0openalex-snapshot
Drosophila melanogaster as a model host for Staphylococcus aureus infection
inferredcites →https://doi.org/10.1099/vir.0.053850-0openalex-snapshot
Knockdown of piRNA pathway proteins results in enhanced Semliki Forest virus production in mosquito cells
inferredcites →https://doi.org/10.1111/imb.12008openalex-snapshot
Transgene‐mediated suppression of the RNA interference pathway in A edes aegypti interferes with gene silencing and enhances S indbis virus and dengue virus type 2 replication
inferredcites →https://doi.org/10.1111/imb.12070openalex-snapshot
MicroRNA levels are modulated in A edes aegypti after exposure to D engue‐2
inferredcites →https://doi.org/10.1124/pr.110.003293openalex-snapshot
Human Disease Models in Drosophila melanogaster and the Role of the Fly in Therapeutic Drug Discovery
inferredcites →https://doi.org/10.1126/science.288.5475.2376openalex-snapshot
Malaria Parasite Development in a Drosophila Model
inferredcites →https://doi.org/10.1128/iai.71.6.3540-3550.2003openalex-snapshot
Drosophila melanogaster Is a Genetically Tractable Model Host for Mycobacterium marinum
inferredcites →https://doi.org/10.1128/jcm.30.3.545-551.1992openalex-snapshot
Rapid detection and typing of dengue viruses from clinical samples by using reverse transcriptase-polymerase chain reaction
inferredcites →https://doi.org/10.1128/jvi.00131-12openalex-snapshot
Drosophila melanogaster as a Model Organism for Bluetongue Virus Replication and Tropism
inferredcites →https://doi.org/10.1128/jvi.01522-13openalex-snapshot
The Toll and Imd Pathways Are Not Required for Wolbachia-Mediated Dengue Virus Interference
inferredcites →https://doi.org/10.1128/jvi.02052-10openalex-snapshot
Antiviral RNA Interference Responses Induced by Semliki Forest Virus Infection of Mosquito Cells: Characterization, Origin, and Frequency-Dependent Functions of Virus-Derived Small Interfering RNAs
inferredcites →https://doi.org/10.1146/annurev.neuro.26.041002.131425openalex-snapshot
H UMAN N EURODEGENERATIVE D ISEASE M ODELING U SING D ROSOPHILA
inferredcites →https://doi.org/10.1159/000097394openalex-snapshot
Entry into and Production of the Japanese Encephalitis Virus from C6/36 Cells
inferredcites →https://doi.org/10.1186/1471-2180-10-127openalex-snapshot
RNA interference modulates replication of dengue virus in Drosophila melanogaster cells
inferredcites →https://doi.org/10.1186/1471-2180-10-130openalex-snapshot
The RNA interference pathway affects midgut infection- and escape barriers for Sindbis virus in Aedes aegypti
inferredcites →https://doi.org/10.1186/1471-2180-11-45openalex-snapshot
Small RNA profiling of Dengue virus-mosquito interactions implicates the PIWI RNA pathway in anti-viral defense
inferredcites →https://doi.org/10.1186/1471-2180-8-47openalex-snapshot
Aedes aegyptiuses RNA interference in defense against Sindbis virus infection
inferredcites →https://doi.org/10.1186/1743-422x-4-83openalex-snapshot
Does Japanese encephalitis virus share the same cellular receptor with other mosquito-borne flaviviruses on the C6/36 mosquito cells?
inferredcites →https://doi.org/10.1242/dev.099408openalex-snapshot
Src64B phosphorylates Dumbfounded and regulates slit diaphragm dynamics: Drosophila as a model to study nephropathies
inferredcites →https://doi.org/10.1371/journal.pbio.1001571openalex-snapshot
Dual Host-Virus Arms Races Shape an Essential Housekeeping Protein
inferredcites →https://doi.org/10.1371/journal.pntd.0000848openalex-snapshot
Comparison of Dengue Virus Type 2-Specific Small RNAs from RNA Interference-Competent and –Incompetent Mosquito Cells
inferredcites →https://doi.org/10.1371/journal.pntd.0001385openalex-snapshot
Global Cross-Talk of Genes of the Mosquito Aedes aegypti in Response to Dengue Virus Infection
inferredcites →https://doi.org/10.1371/journal.pntd.0001565openalex-snapshot
Anopheles gambiae Antiviral Immune Response to Systemic O'nyong-nyong Infection
inferredcites →https://doi.org/10.1371/journal.pone.0006838openalex-snapshot
The Transcriptional Response of Drosophila melanogaster to Infection with the Sigma Virus (Rhabdoviridae)
inferredcites →https://doi.org/10.1371/journal.pone.0030861openalex-snapshot
Arbovirus-Derived piRNAs Exhibit a Ping-Pong Signature in Mosquito Cells
inferredcites →https://doi.org/10.1371/journal.pone.0040401openalex-snapshot
Serratia odorifera a Midgut Inhabitant of Aedes aegypti Mosquito Enhances Its Susceptibility to Dengue-2 Virus
inferredcites →https://doi.org/10.1371/journal.pone.0050512openalex-snapshot
Complex Modulation of the Aedes aegypti Transcriptome in Response to Dengue Virus Infection
inferredcites →https://doi.org/10.1371/journal.ppat.0010008openalex-snapshot
Vibrio cholerae Infection of Drosophila melanogaster Mimics the Human Disease Cholera
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.1000299openalex-snapshot
Dengue Virus Type 2 Infections of Aedes aegypti Are Modulated by the Mosquito's RNA Interference Pathway
inferredcites →https://doi.org/10.1371/journal.ppat.1002189openalex-snapshot
Alterations in the Aedes aegypti Transcriptome during Infection with West Nile, Dengue and Yellow Fever Viruses
inferredcites →https://doi.org/10.1371/journal.ppat.1002470openalex-snapshot
Production of Virus-Derived Ping-Pong-Dependent piRNA-like Small RNAs in the Mosquito Soma
inferredcites →https://doi.org/10.1371/journal.ppat.1002548openalex-snapshot
The Relative Importance of Innate Immune Priming in Wolbachia-Mediated Dengue Interference
inferredcites →https://doi.org/10.1371/journal.ppat.1003579openalex-snapshot
Functional Specialization of the Small Interfering RNA Pathway in Response to Virus Infection
inferredcites →https://doi.org/10.1534/g3.113.007021openalex-snapshot
FlyPrimerBank: An Online Database for Drosophila melanogaster Gene Expression Analysis and Knockdown Evaluation of RNAi Reagents
inferredcites →https://doi.org/10.1534/genetics.113.157602openalex-snapshot
Genetic Complexity in aDrosophilaModel of Diabetes-Associated Misfolded Human Proinsulin
inferredcites →https://doi.org/10.2217/fmb.11.11openalex-snapshot
Mosquito RNAi Is The Major Innate Immune Pathway Controlling Arbovirus Infection And Transmission
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Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.3389/fphys.2021.642237openalex-snapshot
Comprehensive Quantitative Proteome Analysis of Aedes aegypti Identifies Proteins and Pathways Involved in Wolbachia pipientis and Zika Virus Interference Phenomenon
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