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The Drosophila IMD pathway in the activation of the humoral immune response
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Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/bies.950190806openalex-snapshot
Dueling orphans–interacting nuclear receptors coordinate Drosophila metamorphosis
inferredcites →https://doi.org/10.1002/j.1460-2075.1991.tb07932.xopenalex-snapshot
The andropin gene and its product, a male‐specific antibacterial peptide in Drosophila melanogaster.
inferredcites →https://doi.org/10.1006/dbio.2000.0123openalex-snapshot
Postembryonic Hematopoiesis in Drosophila
inferredcites →https://doi.org/10.1006/niox.2000.0294openalex-snapshot
Nitric Oxide Involvement in Drosophila Immunity
inferredcites →https://doi.org/10.1016/0014-5793(93)81414-uopenalex-snapshot
The humoral antibacterial response of Drosophila
inferredcites →https://doi.org/10.1016/0965-1748(95)00076-3openalex-snapshot
Ecdysone and insect immunity: The maturation of the inducibility of the diptericin gene in Drosophila larvae
inferredcites →https://doi.org/10.1016/j.cell.2009.05.037openalex-snapshot
Phosphorylation-Driven Assembly of the RIP1-RIP3 Complex Regulates Programmed Necrosis and Virus-Induced Inflammation
inferredcites →https://doi.org/10.1016/j.cell.2012.06.019openalex-snapshot
The RIP1/RIP3 Necrosome Forms a Functional Amyloid Signaling Complex Required for Programmed Necrosis
inferredcites →https://doi.org/10.1016/j.chom.2008.04.002openalex-snapshot
The Drosophila Peptidoglycan Recognition Protein PGRP-LF Blocks PGRP-LC and IMD/JNK Pathway Activation
inferredcites →https://doi.org/10.1016/j.chom.2008.07.004openalex-snapshot
PIMS Modulates Immune Tolerance by Negatively Regulating Drosophila Innate Immune Signaling
inferredcites →https://doi.org/10.1016/j.chom.2009.09.007openalex-snapshot
The Drosophila Ubiquitin-Specific Protease dUSP36/Scny Targets IMD to Prevent Constitutive Immune Signaling
inferredcites →https://doi.org/10.1016/j.chom.2012.06.001openalex-snapshot
Infection-Induced Host Translational Blockage Inhibits Immune Responses and Epithelial Renewal in the Drosophila Gut
inferredcites →https://doi.org/10.1016/j.dci.2007.01.004openalex-snapshot
Iap2 is required for a sustained response in the Drosophila Imd pathway
inferredcites →https://doi.org/10.1016/j.dci.2008.07.021openalex-snapshot
Dnr1-dependent regulation of the Drosophila immune deficiency signaling pathway
inferredcites →https://doi.org/10.1016/j.dci.2008.12.002openalex-snapshot
The N-terminal half of the Drosophila Rel/NF-κB factor Relish, REL-68, constitutively activates transcription of specific Relish target genes
inferredcites →https://doi.org/10.1016/j.dci.2012.10.007openalex-snapshot
Transcription factor zfh1 downregulates Drosophila Imd pathway
inferredcites →https://doi.org/10.1016/j.devcel.2007.07.012openalex-snapshot
Tumor Suppressor CYLD Regulates JNK-Induced Cell Death in Drosophila
inferredcites →https://doi.org/10.1016/j.ibmb.2005.02.017openalex-snapshot
Insect renal tubules constitute a cell-autonomous immune system that protects the organism against bacterial infection
inferredcites →https://doi.org/10.1016/j.ibmb.2007.08.003openalex-snapshot
Peptidoglycan recognition protein LF: A negative regulator of Drosophila immunity
inferredcites →https://doi.org/10.1016/j.immuni.2006.02.012openalex-snapshot
The Drosophila Amidase PGRP-LB Modulates the Immune Response to Bacterial Infection
inferredcites →https://doi.org/10.1016/j.immuni.2011.08.015openalex-snapshot
Pathogen-Derived Effectors Trigger Protective Immunity via Activation of the Rac2 Enzyme and the IMD or Rip Kinase Signaling Pathway
inferredcites →https://doi.org/10.1016/j.jsbmb.2010.03.058openalex-snapshot
The role of the glucocorticoid receptor in inflammation and immunity
inferredcites →https://doi.org/10.1016/j.micinf.2005.03.014openalex-snapshot
Functional analysis of immune response genes in Drosophila identifies JNK pathway as a regulator of antimicrobial peptide gene expression in S2 cells
inferredcites →https://doi.org/10.1016/j.molcel.2004.08.008openalex-snapshot
TAB2 and TAB3 Activate the NF-κB Pathway through Binding to Polyubiquitin Chains
inferredcites →https://doi.org/10.1016/j.molcel.2008.05.014openalex-snapshot
cIAP1 and cIAP2 Facilitate Cancer Cell Survival by Functioning as E3 Ligases that Promote RIP1 Ubiquitination
inferredcites →https://doi.org/10.1016/j.molcel.2009.10.002openalex-snapshot
A Ubiquitin Replacement Strategy in Human Cells Reveals Distinct Mechanisms of IKK Activation by TNFα and IL-1β
inferredcites →https://doi.org/10.1016/j.molcel.2009.12.036openalex-snapshot
Caspase-Mediated Cleavage, IAP Binding, and Ubiquitination: Linking Three Mechanisms Crucial for Drosophila NF-κB Signaling
inferredcites →https://doi.org/10.1016/j.molimm.2003.10.011openalex-snapshot
Peptidoglycan recognition proteins (PGRPs)
inferredcites →https://doi.org/10.1016/s0092-8674(00)80172-5openalex-snapshot
The Dorsoventral Regulatory Gene Cassette spätzle/Toll/cactus Controls the Potent Antifungal Response in Drosophila Adults
inferredcites →https://doi.org/10.1016/s0960-9822(02)00873-4openalex-snapshot
Inducible Expression of Double-Stranded RNA Reveals a Role for dFADD in the Regulation of the Antibacterial Response in Drosophila Adults
inferredcites →https://doi.org/10.1016/s0960-9822(02)01214-9openalex-snapshot
A Ubiquitin-Proteasome Pathway Represses the Drosophila Immune Deficiency Signaling Cascade
inferredcites →https://doi.org/10.1016/s0965-1748(97)00072-6openalex-snapshot
Treatment of l(2)mbn Drosophila tumorous blood cells with the steroid hormone ecdysone amplifies the inducibility of antimicrobial peptide gene expression
inferredcites →https://doi.org/10.1016/s1074-7613(00)00072-8openalex-snapshot
Tissue-Specific Inducible Expression of Antimicrobial Peptide Genes in Drosophila Surface Epithelia
inferredcites →https://doi.org/10.1016/s1074-7613(02)00454-5openalex-snapshot
The Drosophila Immune Defense against Gram-Negative Infection Requires the Death Protein dFADD
inferredcites →https://doi.org/10.1016/s1074-7613(04)00104-9openalex-snapshot
Monomeric and Polymeric Gram-Negative Peptidoglycan but Not Purified LPS Stimulate the Drosophila IMD Pathway
inferredcites →https://doi.org/10.1016/s1097-2765(00)80392-5openalex-snapshot
Relish, a Central Factor in the Control of Humoral but Not Cellular Immunity in Drosophila
inferredcites →https://doi.org/10.1016/s1534-5807(01)00059-4openalex-snapshot
Drosophila Immune Deficiency (IMD) Is a Death Domain Protein that Activates Antibacterial Defense and Can Promote Apoptosis
inferredcites →https://doi.org/10.1038/237232a0openalex-snapshot
Inducible Antibacterial Defence System in Drosophila
inferredcites →https://doi.org/10.1038/35050012openalex-snapshot
Structural basis of IAP recognition by Smac/DIABLO
inferredcites →https://doi.org/10.1038/35085597openalex-snapshot
TAK1 is a ubiquitin-dependent kinase of MKK and IKK
inferredcites →https://doi.org/10.1038/79801openalex-snapshot
Role of Drosophila IKKγ in a Toll-independent antibacterial immune response
inferredcites →https://doi.org/10.1038/cr.2010.170openalex-snapshot
Expanding role of ubiquitination in NF-κB signaling
inferredcites →https://doi.org/10.1038/emboj.2012.121openalex-snapshot
Ubiquitylation of the initiator caspase DREDD is required for innate immune signalling
inferredcites →https://doi.org/10.1038/emboj.2013.100openalex-snapshot
Ecdysone triggered PGRP‐LC expression controls Drosophila innate immunity
inferredcites →https://doi.org/10.1038/embor.2011.19openalex-snapshot
The Drosophila peptidoglycan‐recognition protein LF interacts with peptidoglycan‐recognition protein LC to downregulate the Imd pathway
inferredcites →https://doi.org/10.1038/nature01802openalex-snapshot
The tumour suppressor CYLD negatively regulates NF-κB signalling by deubiquitination
inferredcites →https://doi.org/10.1038/nature01803openalex-snapshot
CYLD is a deubiquitinating enzyme that negatively regulates NF-κB activation by TNFR family members
inferredcites →https://doi.org/10.1038/nature734openalex-snapshot
The Drosophila immune response against Gram-negative bacteria is mediated by a peptidoglycan recognition protein
inferredcites →https://doi.org/10.1038/nature735openalex-snapshot
Functional genomic analysis of phagocytosis and identification of a Drosophila receptor for E. coli
inferredcites →https://doi.org/10.1038/ncb799openalex-snapshot
The DIAP1 RING finger mediates ubiquitination of Dronc and is indispensable for regulating apoptosis
inferredcites →https://doi.org/10.1038/ni.1634openalex-snapshot
Autophagic control of listeria through intracellular innate immune recognition in drosophila
inferredcites →https://doi.org/10.1038/ni1356openalex-snapshot
PGRP-LC and PGRP-LE have essential yet distinct functions in the drosophila immune response to monomeric DAP-type peptidoglycan
inferredcites →https://doi.org/10.1038/ni1543openalex-snapshot
Akirins are highly conserved nuclear proteins required for NF-κB-dependent gene expression in drosophila and mice
inferredcites →https://doi.org/10.1038/ni922openalex-snapshot
The Drosophila immune system detects bacteria through specific peptidoglycan recognition
inferredcites →https://doi.org/10.1038/nrg1581openalex-snapshot
Nuclear receptors — a perspective from Drosophila
inferredcites →https://doi.org/10.1038/nri1184openalex-snapshot
Signalling pathways of the TNF superfamily: a double-edged sword
inferredcites →https://doi.org/10.1038/nrm1471openalex-snapshot
The SCF ubiquitin ligase: insights into a molecular machine
inferredcites →https://doi.org/10.1038/nsmb.1731openalex-snapshot
Two-sided ubiquitin binding explains specificity of the TAB2 NZF domain
inferredcites →https://doi.org/10.1038/sj.cdd.4401237openalex-snapshot
Molecular evidence for the nuclear localization of FADD
inferredcites →https://doi.org/10.1038/sj.cdd.4401868openalex-snapshot
Systematic in vivo RNAi analysis of putative components of the Drosophila cell death machinery
inferredcites →https://doi.org/10.1038/sj.emboj.7600466openalex-snapshot
Peptidoglycan recognition protein (PGRP)‐LE and PGRP‐LC act synergistically in Drosophila immunity
inferredcites →https://doi.org/10.1038/sj.emboj.7600807openalex-snapshot
Inhibitor of apoptosis 2 and TAK1‐binding protein are components of the Drosophila Imd pathway
inferredcites →https://doi.org/10.1038/sj.emboj.7601182openalex-snapshot
Cooperative control of Drosophila immune responses by the JNK and NF‐κB signaling pathways
inferredcites →https://doi.org/10.1038/sj.embor.7400530openalex-snapshot
An RNA interference screen ide.jpgies Inhibitor of Apoptosis Protein 2 as a regulator of innate immune signalling in Drosophila
inferredcites →https://doi.org/10.1038/sj.embor.7400537openalex-snapshot
The RING‐finger scaffold protein Plenty of SH3s targets TAK1 to control immunity signalling in Drosophila
inferredcites →https://doi.org/10.1042/bst0370937openalex-snapshot
The emerging complexity of protein ubiquitination
inferredcites →https://doi.org/10.1073/pnas.0404952102openalex-snapshot
Drosophila peptidoglycan recognition protein LC (PGRP-LC) acts as a signal-transducing innate immune receptor
inferredcites →https://doi.org/10.1073/pnas.0407559102openalex-snapshot
Ligand-induced dimerization of Drosophila peptidoglycan recognition proteins in vitro
inferredcites →https://doi.org/10.1073/pnas.0431215100openalex-snapshot
Fas-associated death domain protein interacts with methyl-CpG binding domain protein 4: A potential link between genome surveillance and apoptosis
inferredcites →https://doi.org/10.1073/pnas.0502240102openalex-snapshot
Drosophila host defense after oral infection by an entomopathogenic Pseudomonas species
inferredcites →https://doi.org/10.1073/pnas.0504547102openalex-snapshot
Structure of the ectodomain of Drosophila peptidoglycan-recognition protein LCa suggests a molecular mechanism for pattern recognition
inferredcites →https://doi.org/10.1073/pnas.0603238103openalex-snapshot
Caspar, a suppressor of antibacterial immunity in Drosophila
inferredcites →https://doi.org/10.1073/pnas.0711122105openalex-snapshot
Both cIAP1 and cIAP2 regulate TNFα-mediated NF-κB activation
inferredcites →https://doi.org/10.1073/pnas.0812022106openalex-snapshot
Two roles for the Drosophila IKK complex in the activation of Relish and the induction of antimicrobial peptide genes
inferredcites →https://doi.org/10.1073/pnas.1035902100openalex-snapshot
Caspase-mediated processing of the Drosophila NF-κB factor Relish
inferredcites →https://doi.org/10.1073/pnas.1306220110openalex-snapshot
Dnr1 mutations cause neurodegeneration in Drosophila by activating the innate immune response in the brain
inferredcites →https://doi.org/10.1073/pnas.212301199openalex-snapshot
Overexpression of a pattern-recognition receptor, peptidoglycan-recognition protein-LE, activates imd/relish-mediated antibacterial defense and the prophenoloxidase cascade in Drosophila larvae
inferredcites →https://doi.org/10.1073/pnas.221458698openalex-snapshot
Genome-wide analysis of the Drosophila immune response by using oligonucleotide microarrays
inferredcites →https://doi.org/10.1073/pnas.84.15.5449openalex-snapshot
Magainins, a class of antimicrobial peptides from Xenopus skin: isolation, characterization of two active forms, and partial cDNA sequence of a precursor.
inferredcites →https://doi.org/10.1073/pnas.92.21.9465openalex-snapshot
A recessive mutation, immune deficiency (imd), defines two distinct control pathways in the Drosophila host defense.
inferredcites →https://doi.org/10.1073/pnas.92.25.11894openalex-snapshot
A Fas-associated protein factor, FAF1, potentiates Fas-mediated apoptosis.
inferredcites →https://doi.org/10.1073/pnas.93.19.10343openalex-snapshot
Origins of immunity: Relish, a compound Rel-like gene in the antibacterial defense of Drosophila.
inferredcites →https://doi.org/10.1073/pnas.94.26.14614openalex-snapshot
Drosophila host defense: Differential induction of antimicrobial peptide genes after infection by various classes of microorganisms
inferredcites →https://doi.org/10.1073/pnas.95.19.11342openalex-snapshot
Differential display of peptides induced during the immune response of Drosophila : A matrix-assisted laser desorption ionization time-of-flight mass spectrometry study
inferredcites →https://doi.org/10.1073/pnas.97.25.13772openalex-snapshot
A family of peptidoglycan recognition proteins in the fruit fly Drosophila melanogaster
inferredcites →https://doi.org/10.1074/jbc.c000341200openalex-snapshot
dFADD, a Novel Death Domain-containing Adapter Protein for theDrosophila Caspase DREDD
inferredcites →https://doi.org/10.1074/jbc.c300184200openalex-snapshot
Functional Diversity of the Drosophila PGRP-LC Gene Cluster in the Response to Lipopolysaccharide and Peptidoglycan
inferredcites →https://doi.org/10.1074/jbc.c700106200openalex-snapshot
FAF1 Suppresses IκB Kinase (IKK) Activation by Disrupting the IKK Complex Assembly
inferredcites →https://doi.org/10.1074/jbc.m208900200openalex-snapshot
A Scavenger Function for a DrosophilaPeptidoglycan Recognition Protein
inferredcites →https://doi.org/10.1074/jbc.m302200200openalex-snapshot
Fas-associated Factor 1, FAF1, Is a Member of Fas Death-inducing Signaling Complex
inferredcites →https://doi.org/10.1074/jbc.m304565200openalex-snapshot
Fas-associated Factor-1 Inhibits Nuclear Factor-κB (NF-κB) Activity by Interfering with Nuclear Translocation of the RelA (p65) Subunit of NF-κB
inferredcites →https://doi.org/10.1074/jbc.m304802200openalex-snapshot
Immune Activation of NF-κB and JNK Requires Drosophila TAK1
inferredcites →https://doi.org/10.1074/jbc.m506655200openalex-snapshot
The Role of Ubiquitination in Drosophila Innate Immunity
inferredcites →https://doi.org/10.1074/jbc.m513030200openalex-snapshot
Structural Basis for Preferential Recognition of Diaminopimelic Acid-type Peptidoglycan by a Subset of Peptidoglycan Recognition Proteins
inferredcites →https://doi.org/10.1074/jbc.m608051200openalex-snapshot
The Drosophila Inhibitor of Apoptosis (IAP) DIAP2 Is Dispensable for Cell Survival, Required for the Innate Immune Response to Gram-negative Bacterial Infection, and Can Be Negatively Regulated by the Reaper/Hid/Grim Family of IAP-binding Apoptosis Inducers
inferredcites →https://doi.org/10.1091/mbc.e12-11-0841openalex-snapshot
akirinis required for diakinesis bivalent structure and synaptonemal complex disassembly at meiotic prophase I
inferredcites →https://doi.org/10.1093/embo-reports/kvd072openalex-snapshot
Activation of the Drosophila NF‐κB factor Relish by rapid endoproteolytic cleavage
inferredcites →https://doi.org/10.1093/embo-reports/kvd073openalex-snapshot
The Drosophila caspase Dredd is required to resist Gram‐negative bacterial infection
inferredcites →https://doi.org/10.1093/emboj/17.5.1217openalex-snapshot
A drosomycin–GFP reporter transgene reveals a local immune response in Drosophila that is not dependent on the Toll pathway
inferredcites →https://doi.org/10.1093/emboj/21.11.2568openalex-snapshot
The Toll and Imd pathways are the major regulators of the immune response in Drosophila
inferredcites →https://doi.org/10.1093/jb/mvr083openalex-snapshot
Intracellular recognition of pathogens and autophagy as an innate immune host defence
inferredcites →https://doi.org/10.1101/gad.1018503openalex-snapshot
Nitric oxide contributes to induction of innate immune responses to gram-negative bacteria in Drosophila
inferredcites →https://doi.org/10.1101/gad.203301openalex-snapshot
Mutations in the Drosophila dTAK1 gene reveal a conserved function for MAPKKKs in the control of rel/NF-κB-dependent innate immune responses
inferredcites →https://doi.org/10.1101/gad.2080411openalex-snapshot
Nitric oxide directly regulates gene expression during Drosophila development: need some gas to drive into metamorphosis?: Figure 1.
inferredcites →https://doi.org/10.1101/gad.817800openalex-snapshot
A Drosophila IκB kinase complex required for Relish cleavage and antibacterial immunity
inferredcites →https://doi.org/10.1101/gad.856901openalex-snapshot
The antibacterial arm of the Drosophila innate immune response requires an IκB kinase
inferredcites →https://doi.org/10.1111/j.1432-1033.1980.tb05991.xopenalex-snapshot
Insect Immunity. Purification and Properties of Three Inducible Bactericidal Proteins from Hemolymph of Immunized Pupae of Hyalophora cecropia
inferredcites →https://doi.org/10.1111/j.1462-5822.2005.00504.xopenalex-snapshot
Bacterial recognition and signalling by the Drosophila IMD pathway
inferredcites →https://doi.org/10.1111/j.1474-9728.2005.00147.xopenalex-snapshot
Aging of the innate immune response in Drosophila melanogaster
inferredcites →https://doi.org/10.1126/science.1070216openalex-snapshot
Requirement for a Peptidoglycan Recognition Protein (PGRP) in Relish Activation and Antibacterial Immune Responses in Drosophila
inferredcites →https://doi.org/10.1126/science.1123056openalex-snapshot
Structure of Tracheal Cytotoxin in Complex with a Heterodimeric Pattern-Recognition Receptor
inferredcites →https://doi.org/10.1126/science.1149357openalex-snapshot
Innate Immune Homeostasis by the Homeobox Gene Caudal and Commensal-Gut Mutualism in Drosophila
inferredcites →https://doi.org/10.1126/science.276.5309.114openalex-snapshot
Coordination of Drosophila Metamorphosis by Two Ecdysone-Induced Nuclear Receptors
inferredcites →https://doi.org/10.1128/mcb.00223-10openalex-snapshot
The POU Transcription Factor Drifter/Ventral veinless Regulates Expression of Drosophila Immune Defense Genes
inferredcites →https://doi.org/10.1128/mcb.00548-06openalex-snapshot
The Drosophila Inhibitor of Apoptosis Protein DIAP2 Functions in Innate Immunity and Is Essential To Resist Gram-Negative Bacterial Infection
inferredcites →https://doi.org/10.1159/000086648openalex-snapshot
Antimicrobial Peptides in Drosophila: Structures,Activities and Gene Regulation
inferredcites →https://doi.org/10.1172/jci112120openalex-snapshot
Defensins. Natural peptide antibiotics of human neutrophils.
inferredcites →https://doi.org/10.1177/09680519050110060201openalex-snapshot
Peptidoglycan recognition by the Drosophila Imd pathway
inferredcites →https://doi.org/10.1242/dev.02859openalex-snapshot
ADrosophilaortholog of the human cylindromatosis tumor suppressor gene regulates triglyceride content and antibacterial defense
inferredcites →https://doi.org/10.1242/jcs.03417openalex-snapshot
Interactions of DNR1 with the apoptotic machinery ofDrosophilamelanogaster
inferredcites →https://doi.org/10.1242/jeb.014878openalex-snapshot
Hormonal regulation of the humoral innate immune response inDrosophila melanogaster
inferredcites →https://doi.org/10.1371/journal.pbio.0020203openalex-snapshot
Functional Dissection of an Innate Immune Response by a Genome-Wide RNAi Screen
inferredcites →https://doi.org/10.1371/journal.pbio.0050238openalex-snapshot
Down-Regulation of NF-κB Target Genes by the AP-1 and STAT Complex during the Innate Immune Response in Drosophila
inferredcites →https://doi.org/10.1371/journal.pgen.1002547openalex-snapshot
Akirin Links Twist-Regulated Transcription with the Brahma Chromatin Remodeling Complex during Embryogenesis
inferredcites →https://doi.org/10.1371/journal.pone.0007436openalex-snapshot
The Imd Pathway Is Involved in Antiviral Immune Responses in Drosophila
inferredcites →https://doi.org/10.1371/journal.ppat.0020014openalex-snapshot
Downregulation of the Drosophila Immune Response by Peptidoglycan-Recognition Proteins SC1 and SC2
inferredcites →https://doi.org/10.1371/journal.ppat.1000120openalex-snapshot
Rudra Interrupts Receptor Signaling Complexes to Negatively Regulate the IMD Pathway
inferredcites →https://doi.org/10.1371/journal.ppat.1000582openalex-snapshot
A Novel System for the Launch of Alphavirus RNA Synthesis Reveals a Role for the Imd Pathway in Arthropod Antiviral Response
inferredcites →https://doi.org/10.1371/journal.ppat.1002319openalex-snapshot
Toll-8/Tollo Negatively Regulates Antimicrobial Response in the Drosophila Respiratory Epithelium
inferredcites →https://doi.org/10.4049/jimmunol.1201022openalex-snapshot
Tissue- and Ligand-Specific Sensing of Gram-Negative Infection in Drosophila by PGRP-LC Isoforms and PGRP-LE
inferredcites →https://doi.org/10.4049/jimmunol.173.12.7339openalex-snapshot
Peptidoglycan Molecular Requirements Allowing Detection by the Drosophila Immune Deficiency Pathway
inferredcites →https://doi.org/10.4049/jimmunol.180.8.5413openalex-snapshot
Pirk Is a Negative Regulator of the Drosophila Imd Pathway
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.4620748openalex-extracted
Molecular Characterization of FADD Gene in T. Molitor and its Requirement for Survivability Against E. Coli Infection
inferred← citeshttps://doi.org/10.2139/ssrn.4655826openalex-extracted
Molecular Characterization of Fadd Gene in T. Molitor and its Requirement for Survivability Against E. Coli Infection
inferred← citeshttps://doi.org/10.1002/aah.10216openalex-snapshot
Characterization of a novel immune deficiency gene of Macrobrachium rosenbergii reveals antibacterial and antiviral defenses
inferred← citeshttps://doi.org/10.1002/arch.21464openalex-snapshot
Overexpression of antimicrobial peptides contributes to aging through cytotoxic effects in Drosophila tissues
inferred← citeshttps://doi.org/10.1002/arch.21629openalex-snapshot
Immune signaling pathways in the endoparasitoid, Pteromalus puparum
inferred← citeshttps://doi.org/10.1002/arch.70148openalex-snapshot
The Origin of Hyperspread Cells, a Group of Circulating Hemocytes in Mythimna separata
inferred← citeshttps://doi.org/10.1002/evl3.261openalex-snapshot
Transcriptomic evidence for a trade-off between germline proliferation and immunity inDrosophila
inferred← citeshttps://doi.org/10.1002/evl3.89openalex-snapshot
Evolution of longevity improves immunity inDrosophila
inferred← citeshttps://doi.org/10.1002/ps.5945openalex-snapshot
A C‐type lectin with dual‐CRD from Tribolium castaneum is induced in response to bacterial challenge
inferred← citeshttps://doi.org/10.1002/tox.23726openalex-snapshot
Eucalyptol antagonized the apoptosis and immune dysfunction of grass carp hepatocytes induced by tetrabromobisphenol A by regulating ROS / ASK1 / JNK pathway
inferred← citeshttps://doi.org/10.1002/wdev.378openalex-snapshot
The Drosophila gut: A gatekeeper and coordinator of organism fitness and physiology
inferred← citeshttps://doi.org/10.1007/978-3-030-60204-8_11openalex-snapshot
The Drosophila melanogaster as Genetic Model System to Dissect the Mechanisms of Disease that Lead to Neurodegeneration in Adrenoleukodystrophy
inferred← citeshttps://doi.org/10.1007/978-3-030-64548-9_14openalex-snapshot
The Immune System of Triatomines
inferred← citeshttps://doi.org/10.1007/978-3-031-70591-5_15openalex-snapshot
Genomics of Triatominae, the Chagas Disease Vectors
inferred← citeshttps://doi.org/10.1007/978-3-031-94928-9_19openalex-snapshot
Unraveling Insect Immunity: A Cross-Order Comparative Genomic Analysis of Key Immune Proteins
inferred← citeshttps://doi.org/10.1007/978-4-431-56068-5_10openalex-snapshot
The Drosophila Toll Pathway: A Model of Innate Immune Signalling Activated by Endogenous Ligands
inferred← citeshttps://doi.org/10.1007/978-94-024-0884-3_7openalex-snapshot
Defense and Immune Systems
inferred← citeshttps://doi.org/10.1007/s00018-016-2203-4openalex-snapshot
Necroptosis-independent signaling by the RIP kinases in inflammation
inferred← citeshttps://doi.org/10.1007/s00018-017-2453-9openalex-snapshot
Innate and intrinsic antiviral immunity in Drosophila
inferred← citeshttps://doi.org/10.1007/s00018-021-03784-zopenalex-snapshot
Insect antimicrobial peptides: potential weapons to counteract the antibiotic resistance
inferred← citeshttps://doi.org/10.1007/s00203-025-04617-4openalex-snapshot
The symbiotic Wolbachia in Anopheles and its role in reducing the transmission of Plasmodium: updates and prospects
inferred← citeshttps://doi.org/10.1007/s00203-026-04903-9openalex-snapshot
Insect immunity unveiled: exploring the molecular and cellular defenses against microbial threats
inferred← citeshttps://doi.org/10.1007/s00251-019-01119-8openalex-snapshot
Transcript analysis reveals the involvement of NF-κB transcription factors for the activation of TGF-β signaling in nematode-infected Drosophila
inferred← citeshttps://doi.org/10.1007/s00436-023-08043-7openalex-snapshot
Interactions between Leishmania parasite and sandfly: a review
inferred← citeshttps://doi.org/10.1007/s10340-026-02072-8openalex-snapshot
RNAi-mediated immune suppression enhances Serratia marcescens pathogenicity against the oriental fruit fly, Bactrocera dorsalis
inferred← citeshttps://doi.org/10.1007/s10989-025-10731-0openalex-snapshot
Abundance of Antimicrobial Peptides in Mesenchymal Stem Cells and Tissues: Variations Among Species
inferred← citeshttps://doi.org/10.1007/s13592-026-01270-8openalex-snapshot
Developmental and behavioral modulation of humoral immunity in the stingless bee Frieseomelitta varia
inferred← citeshttps://doi.org/10.1016/b978-0-12-803252-7.00009-6openalex-snapshot
How Insects Combat Infections
inferred← citeshttps://doi.org/10.1016/b978-0-12-805350-8.00004-0openalex-snapshot
Modulation of Mosquito Immune Defenses as a Control Strategy
inferred← citeshttps://doi.org/10.1016/b978-0-12-818731-9.00010-0openalex-snapshot
Kissing Bugs (Triatominae)
inferred← citeshttps://doi.org/10.1016/b978-0-323-95424-2.00020-0openalex-snapshot
Structures and functions of insulin-like peptides in insects
inferred← citeshttps://doi.org/10.1016/bs.aiip.2017.02.003openalex-snapshot
Insect Antimicrobial Defences
inferred← citeshttps://doi.org/10.1016/bs.aiip.2025.02.001openalex-snapshot
The immune and non-immune defenses of aphids
inferred← citeshttps://doi.org/10.1016/bs.apcsb.2025.08.003openalex-snapshot
The multifaceted role of antimicrobial peptides in neurodegeneration: Insights from Drosophila and beyond
inferred← citeshttps://doi.org/10.1016/bs.ctdb.2016.07.002openalex-snapshot
Drosophila as a Model for Human Diseases—Focus on Innate Immunity in Barrier Epithelia
inferred← citeshttps://doi.org/10.1016/j.actatropica.2026.108263openalex-snapshot
Immune signaling pathways in Rhipicephalus microplus: A stage-specific response to Theileria equi infection
inferred← citeshttps://doi.org/10.1016/j.aquaculture.2023.739252openalex-snapshot
Investigating host-gut microbial relationship in Penaeus monodon upon exposure to Vibrio harveyi
inferred← citeshttps://doi.org/10.1016/j.bbagen.2016.05.033openalex-snapshot
A novel mosquito ubiquitin targets viral envelope protein for degradation and reduces virion production during dengue virus infection
inferred← citeshttps://doi.org/10.1016/j.bbrc.2015.09.138openalex-snapshot
Ex vivo genome-wide RNAi screening of the Drosophila Toll signaling pathway elicited by a larva-derived tissue extract
inferred← citeshttps://doi.org/10.1016/j.bbrc.2017.11.004openalex-snapshot
Unexpected role of the IMD pathway in Drosophila gut defense against Staphylococcus aureus
inferred← citeshttps://doi.org/10.1016/j.biocontrol.2023.105204openalex-snapshot
Drosophila suzukii displays a sex-dependent immune response to Microbacterium thalassium and Providencia sp. infection
inferred← citeshttps://doi.org/10.1016/j.bpj.2026.01.013openalex-snapshot
Heterogeneous NF-κB activation and enhancer features shape transcription in Drosophila immunity
inferred← citeshttps://doi.org/10.1016/j.cbd.2021.100803openalex-snapshot
Analysis of the Glyphodes pyloalis larvae immune transcriptome in response to parasitization by its endoparasitoid, Aulacococentrum confusum
inferred← citeshttps://doi.org/10.1016/j.cbpc.2024.110004openalex-snapshot
Acute lipopolysaccharide (LPS)-induced cell membrane hyperpolarization is independent of voltage gated and calcium activated potassium channels
inferred← citeshttps://doi.org/10.1016/j.cell.2015.12.029openalex-snapshot
Toll Receptor-Mediated Hippo Signaling Controls Innate Immunity in Drosophila
inferred← citeshttps://doi.org/10.1016/j.cellsig.2021.110003openalex-snapshot
Regulators and signalling in insect antimicrobial innate immunity: Functional molecules and cellular pathways
inferred← citeshttps://doi.org/10.1016/j.celrep.2022.111143openalex-snapshot
A dRASSF-STRIPAK-Imd-JAK/STAT axis controls antiviral immune response in Drosophila
inferred← citeshttps://doi.org/10.1016/j.celrep.2022.111368openalex-snapshot
Vibrio cholerae high cell density quorum sensing activates the host intestinal innate immune response
inferred← citeshttps://doi.org/10.1016/j.celrep.2022.111795openalex-snapshot
A Toll-dependent Bre1/Rad6-cact feedback loop in controlling host innate immune response
inferred← citeshttps://doi.org/10.1016/j.celrep.2024.113750openalex-snapshot
Vibrio cholerae arrests intestinal epithelial proliferation through T6SS-dependent activation of the bone morphogenetic protein pathway
inferred← citeshttps://doi.org/10.1016/j.celrep.2024.115082openalex-snapshot
A nonsecretory antimicrobial peptide mediates inflammatory organ damage in Drosophila renal tubules
inferred← citeshttps://doi.org/10.1016/j.celrep.2025.115811openalex-snapshot
Endosymbiont control through non-canonical immune signaling and gut metabolic remodeling
inferred← citeshttps://doi.org/10.1016/j.celrep.2025.116225openalex-snapshot
Mask protein keeps NF-κB precursor inactive by inducing a closed conformation and isolating it in biomolecular condensates
inferred← citeshttps://doi.org/10.1016/j.chom.2014.12.012openalex-snapshot
Bacterial Uracil Modulates Drosophila DUOX-Dependent Gut Immunity via Hedgehog-Induced Signaling Endosomes
inferred← citeshttps://doi.org/10.1016/j.chom.2018.05.022openalex-snapshot
Inflammation-Induced, STING-Dependent Autophagy Restricts Zika Virus Infection in the Drosophila Brain
inferred← citeshttps://doi.org/10.1016/j.cmet.2018.05.026openalex-snapshot
The Drosophila Immune Deficiency Pathway Modulates Enteroendocrine Function and Host Metabolism
inferred← citeshttps://doi.org/10.1016/j.cris.2020.100006openalex-snapshot
Rhodnius prolixus uses the peptidoglycan recognition receptor rpPGRP-LC/LA to detect Gram-negative bacteria and activate the IMD pathway
inferred← citeshttps://doi.org/10.1016/j.cris.2026.100133openalex-snapshot
Chemical modulation of IMD signaling in the cat flea (Ctenocephalides felis) reveals reduced antimicrobial activity in vitro without corresponding effects on bacterial infection in vivo
inferred← citeshttps://doi.org/10.1016/j.cub.2019.07.012openalex-snapshot
The Taiman Transcriptional Coactivator Engages Toll Signals to Promote Apoptosis and Intertissue Invasion in Drosophila
inferred← citeshttps://doi.org/10.1016/j.dci.2015.12.006openalex-snapshot
Insect immunology and hematopoiesis
inferred← citeshttps://doi.org/10.1016/j.dci.2015.12.018openalex-snapshot
Exploring the immune signalling pathway-related genes of the cattle tick Rhipicephalus microplus: From molecular characterization to transcriptional profile upon microbial challenge
inferred← citeshttps://doi.org/10.1016/j.dci.2015.12.019openalex-snapshot
Cellular immune defenses of Drosophila melanogaster
inferred← citeshttps://doi.org/10.1016/j.dci.2016.01.001openalex-snapshot
Bacteria sensing mechanisms in Drosophila gut: Local and systemic consequences
inferred← citeshttps://doi.org/10.1016/j.dci.2016.11.011openalex-snapshot
c-Jun N-terminal kinase (JNK) is involved in immune defense against bacterial infection in Crassostrea hongkongensis
inferred← citeshttps://doi.org/10.1016/j.dci.2017.11.008openalex-snapshot
Beyond immunity: The Imd pathway as a coordinator of host defense, organismal physiology and behavior
inferred← citeshttps://doi.org/10.1016/j.dci.2018.02.014openalex-snapshot
Identification and functional analysis of inhibitor of NF-κB kinase (IKK) from Scylla paramamosain: The first evidence of three IKKs in crab species and their expression profiles under biotic and abiotic stresses
inferred← citeshttps://doi.org/10.1016/j.dci.2019.04.007openalex-snapshot
The innate immune system of kissing bugs, vectors of chagas disease
inferred← citeshttps://doi.org/10.1016/j.dci.2019.103529openalex-snapshot
A novel ML domain-containing protein (SpMD2) functions as a potential LPS receptor involved in anti-Vibrio immune response
inferred← citeshttps://doi.org/10.1016/j.dci.2020.103966openalex-snapshot
Innate immune responses against viral pathogens in Macrobrachium
inferred← citeshttps://doi.org/10.1016/j.dci.2021.104010openalex-snapshot
Genetic determinants of antiviral immunity in dipteran insects – Compiling the experimental evidence
inferred← citeshttps://doi.org/10.1016/j.dci.2022.104406openalex-snapshot
Relish regulates innate immunity via mediating ATG5 activity in Antheraea pernyi
inferred← citeshttps://doi.org/10.1016/j.dci.2022.104513openalex-snapshot
The IMD pathway in Hemipteran: A comparative analysis and discussion
inferred← citeshttps://doi.org/10.1016/j.dci.2023.104756openalex-snapshot
Duox and Jak/Stat signalling influence disease tolerance in Drosophila during Pseudomonas entomophila infection
inferred← citeshttps://doi.org/10.1016/j.dci.2023.104761openalex-snapshot
IKKβ regulates antimicrobial innate immune responses in the yellow mealworm, Tenebrio molitor
inferred← citeshttps://doi.org/10.1016/j.dci.2025.105418openalex-snapshot
A Comprehensive review of humoral immune defense in the silkworm, Bombyx mori: Mechanistic insights and responses to microbial pathogens
inferred← citeshttps://doi.org/10.1016/j.ejphar.2026.178968openalex-snapshot
Carboplatin alleviates astrocytic TDP-43 neurotoxicity by inhibiting NF-κB activation
inferred← citeshttps://doi.org/10.1016/j.enceco.2026.09.008openalex-snapshot
Poly(methyl methacrylate) micro- and nanoplastics induce early mitochondrial dysfunction and cellular perturbations in Drosophila melanogaster
inferred← citeshttps://doi.org/10.1016/j.envadv.2026.100766openalex-snapshot
Axenic condition modulates triclosan-induced immune dysfunction in Drosophila melanogaster larvae
inferred← citeshttps://doi.org/10.1016/j.fbio.2026.109480openalex-snapshot
Propolis reduces oxidative stress, modulates Imd-dependent immune responses, and improves survival in a Drosophila melanogaster autoinflammatory model
inferred← citeshttps://doi.org/10.1016/j.fsi.2013.12.019openalex-snapshot
TLR and IMD signaling pathways from Caligus rogercresseyi (Crustacea: Copepoda): In silico gene expression and SNPs discovery
inferred← citeshttps://doi.org/10.1016/j.fsi.2015.06.024openalex-snapshot
Identification and functional characterization of the TAB2 gene from Litopenaeus vannamei
inferred← citeshttps://doi.org/10.1016/j.fsi.2015.12.014openalex-snapshot
Identification and characterization of MKK7 as an upstream activator of JNK in Litopenaeus vannamei
inferred← citeshttps://doi.org/10.1016/j.fsi.2016.03.149openalex-snapshot
Identification and characterization of transforming growth factor β-activated kinase 1 from Litopenaeus vannamei involved in anti-bacterial host defense
inferred← citeshttps://doi.org/10.1016/j.fsi.2017.12.023openalex-snapshot
Identification and analysis of an MKK4 homologue in response to the nucleus grafting operation and antigens in the pearl oyster, Pinctada fucata
inferred← citeshttps://doi.org/10.1016/j.fsi.2018.09.005openalex-snapshot
Characterization of an immune deficiency (IMD) homolog from the oriental river prawn, Macrobrachium nipponense
inferred← citeshttps://doi.org/10.1016/j.fsi.2018.10.043openalex-snapshot
WSSV–host interaction: Host response and immune evasion
inferred← citeshttps://doi.org/10.1016/j.fsi.2020.02.003openalex-snapshot
Two relish isoforms produced by alternative splicing participate in the regulation of antimicrobial peptides expression in Procambarus clarkii intestine
inferred← citeshttps://doi.org/10.1016/j.fsi.2022.06.069openalex-snapshot
Redclaw crayfish (Cherax quadricarinatus) responds to Vibrio parahaemolyticus infection by activating toll and immune deficiency signaling pathways and transcription of associated immune response genes
inferred← citeshttps://doi.org/10.1016/j.fsi.2023.108852openalex-snapshot
Insight into crustacean cathepsins: Structure-evolutionary relationships and functional roles in physiological processes
inferred← citeshttps://doi.org/10.1016/j.fsi.2023.108984openalex-snapshot
Cellular responses in crustaceans under white spot syndrome virus infection
inferred← citeshttps://doi.org/10.1016/j.fsi.2023.109076openalex-snapshot
mARC dependent NO synthesis activates CanA-Relish-AMPs signal pathway in Eriocheir sinensis during nitrite stress
inferred← citeshttps://doi.org/10.1016/j.fsi.2024.109804openalex-snapshot
Characterization of c-Jun N-terminal kinase (JNK) gene reveals involvement of immune defense against Vibrio splendidus infection in Apostichopus japonicus
inferred← citeshttps://doi.org/10.1016/j.fsi.2025.110868openalex-snapshot
Crayfish IMD responds rapidly to WSSV infection and the activated IMD–Relish–AMPs pathway inhibits viral replication
inferred← citeshttps://doi.org/10.1016/j.fsi.2026.111672openalex-snapshot
Role of scavenger receptors in innate immunity in crustaceans
inferred← citeshttps://doi.org/10.1016/j.gene.2016.12.010openalex-snapshot
Identification and functional analysis of pointed homologs in Bombyx mori
inferred← citeshttps://doi.org/10.1016/j.gene.2018.06.052openalex-snapshot
Wounding-induced upregulation of the Bone Morphogenic Protein signaling pathway in Drosophila promotes survival against parasitic nematode infection
inferred← citeshttps://doi.org/10.1016/j.hazadv.2026.101656openalex-snapshot
Chronic nanoplastic exposure progressively disrupts immune-related traits across generations in Drosophila melanogaster
inferred← citeshttps://doi.org/10.1016/j.heliyon.2022.e10382openalex-snapshot
Microbiota aggravates the pathogenesis of Drosophila acutely exposed to vehicle exhaust
inferred← citeshttps://doi.org/10.1016/j.heliyon.2023.e16139openalex-snapshot
Drosophila melanogaster Imd signaling interacts with insulin signaling and alters feeding rate upon parasitic nematode infection
inferred← citeshttps://doi.org/10.1016/j.hlife.2024.10.001openalex-snapshot
Drosophila Cul3 contributes to Diap2-mediated innate immune signaling for antimicrobial defense
inferred← citeshttps://doi.org/10.1016/j.ibmb.2013.10.008openalex-snapshot
Involvement of the Anopheles gambiae Nimrod gene family in mosquito immune responses
inferred← citeshttps://doi.org/10.1016/j.ibmb.2015.03.006openalex-snapshot
The immune signaling pathways of Manduca sexta
inferred← citeshttps://doi.org/10.1016/j.ibmb.2019.103225openalex-snapshot
A tandem death effector domain-containing protein inhibits the IMD signaling pathway via forming amyloid-like aggregates with the caspase-8 homolog DREDD
inferred← citeshttps://doi.org/10.1016/j.ibmb.2025.104422openalex-snapshot
Drosophila proteasome subunit Rpn8 controls IMD pathway activation via PGRP-SC2 degradation
inferred← citeshttps://doi.org/10.1016/j.ibmb.2026.104541openalex-snapshot
Drosophila PcG-repressive deubiquitinase complex mediates antibacterial immune defense via transcriptional regulation of Calcineurin A1
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2022.08.162openalex-snapshot
Four peptidoglycan recognition proteins are indispensable for antibacterial immunity in the cigarette beetle Lasioderma serricorne (Fabricius)
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2023.125840openalex-snapshot
Partner of neuropeptide bursicon homodimer pburs mediates a novel antimicrobial peptide Ten3LP via Dif/Dorsal2 in Tribolium castaneum
inferred← citeshttps://doi.org/10.1016/j.imbio.2016.07.011openalex-snapshot
TGF-β signaling regulates resistance to parasitic nematode infection in Drosophila melanogaster
inferred← citeshttps://doi.org/10.1016/j.immuni.2016.10.029openalex-snapshot
PGRP-SD, an Extracellular Pattern-Recognition Receptor, Enhances Peptidoglycan-Mediated Activation of the Drosophila Imd Pathway
inferred← citeshttps://doi.org/10.1016/j.immuni.2016.11.002openalex-snapshot
ReaDAPting the Role of PGRP-SD in Bacterial Sensing and Immune Activation
inferred← citeshttps://doi.org/10.1016/j.immuni.2017.09.011openalex-snapshot
Peptidoglycan-Sensing Receptors Trigger the Formation of Functional Amyloids of the Adaptor Protein Imd to Initiate Drosophila NF-κB Signaling
inferred← citeshttps://doi.org/10.1016/j.immuni.2018.04.010openalex-snapshot
Cell-Specific Imd-NF-κB Responses Enable Simultaneous Antibacterial Immunity and Intestinal Epithelial Cell Shedding upon Bacterial Infection
inferred← citeshttps://doi.org/10.1016/j.immuni.2018.07.013openalex-snapshot
The Kinase IKKβ Regulates a STING- and NF-κB-Dependent Antiviral Response Pathway in Drosophila
inferred← citeshttps://doi.org/10.1016/j.immuni.2018.09.017openalex-snapshot
Microbiota-Derived Lactate Activates Production of Reactive Oxygen Species by the Intestinal NADPH Oxidase Nox and Shortens Drosophila Lifespan
inferred← citeshttps://doi.org/10.1016/j.immuni.2021.05.017openalex-snapshot
Microbiota-derived acetate activates intestinal innate immunity via the Tip60 histone acetyltransferase complex
inferred← citeshttps://doi.org/10.1016/j.imu.2021.100811openalex-snapshot
Structural modulation of dual oxidase (Duox) in Drosophila melanogaster by phyto-elicitors: A free energy study with molecular dynamics approach
inferred← citeshttps://doi.org/10.1016/j.isci.2020.101152openalex-snapshot
Drosophila Aversive Behavior toward Erwinia carotovora carotovora Is Mediated by Bitter Neurons and Leukokinin
inferred← citeshttps://doi.org/10.1016/j.isci.2021.102150openalex-snapshot
Theaflavin-regulated Imd condensates control Drosophila intestinal homeostasis and aging
inferred← citeshttps://doi.org/10.1016/j.isci.2023.107335openalex-snapshot
Role of Rab5 early endosomes in regulating Drosophila gut antibacterial response
inferred← citeshttps://doi.org/10.1016/j.it.2018.09.003openalex-snapshot
Vector Immunity and Evolutionary Ecology: The Harmonious Dissonance
inferred← citeshttps://doi.org/10.1016/j.jgg.2021.02.010openalex-snapshot
Genomes of 12 fig wasps provide insights into the adaptation of pollinators to fig syconia
inferred← citeshttps://doi.org/10.1016/j.jip.2015.09.003openalex-snapshot
Peptidoglycan recognition protein genes and their roles in the innate immune pathways of the red flour beetle, Tribolium castaneum
inferred← citeshttps://doi.org/10.1016/j.jip.2015.10.008openalex-snapshot
Prophenoloxidase genes and antimicrobial host defense of the model beetle, Tribolium castaneum
inferred← citeshttps://doi.org/10.1016/j.jip.2016.11.009openalex-snapshot
Chitin synthase 1 gene is crucial to antifungal host defense of the model beetle, Tribolium castaneum
inferred← citeshttps://doi.org/10.1016/j.jip.2018.04.006openalex-snapshot
The IMD pathway regulates lysozyme-like proteins (LLPs) in the silkmoth Antheraea mylitta
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.jip.2023.108049openalex-snapshot
Differential induction of NF-κB pathways by non-pathogenic and pathogenic bacteria in Helicoverpa armigera is critical for an efficient immune response and survival
inferred← citeshttps://doi.org/10.1016/j.jip.2024.108166openalex-snapshot
Differential inducibility of transmembrane peptidoglycan recognition proteins (PGRPs) by bacterial challenges in the earthworm, Eisenia andrei
inferred← citeshttps://doi.org/10.1016/j.jip.2025.108315openalex-snapshot
The Enhanced activation of innate immunity in Drosophila S2 cells by Micrococcus luteus VKM Ac-2230 is mediated by Relish
inferred← citeshttps://doi.org/10.1016/j.jneuroim.2020.577302openalex-snapshot
An interplay between immune response and neurodegenerative disease progression: An assessment using Drosophila as a model
inferred← citeshttps://doi.org/10.1016/j.micinf.2023.105149openalex-snapshot
Intake of caffeine containing sugar diet remodels gut microbiota and perturbs Drosophila melanogaster immunity and lifespan
inferred← citeshttps://doi.org/10.1016/j.micpath.2019.103664openalex-snapshot
The peptidoglycan recognition protein PGRP-LE regulates the Drosophila immune response against the pathogen Photorhabdus
inferred← citeshttps://doi.org/10.1016/j.molcel.2018.01.029openalex-snapshot
The Circulating Protease Persephone Is an Immune Sensor for Microbial Proteolytic Activities Upstream of the Drosophila Toll Pathway
inferred← citeshttps://doi.org/10.1016/j.molimm.2017.10.002openalex-snapshot
The archaic roles of the lamprey NF-κB (lj-NF-κB) in innate immune responses
inferred← citeshttps://doi.org/10.1016/j.molimm.2021.07.011openalex-snapshot
A novel JNK induces innate immune response by activating the expression of antimicrobial peptides in Chinese mitten crab Eriocheir sinensis
inferred← citeshttps://doi.org/10.1016/j.pestbp.2022.105120openalex-snapshot
Termicin silencing enhances the toxicity of Serratia marcescens Bizio (SM1) to Odontotermes formosanus (Shiraki)
inferred← citeshttps://doi.org/10.1016/j.pestbp.2024.105951openalex-snapshot
Pathogenic fungi synergistically cooperate with Serratia marcescens to increase cockroach mortality
inferred← citeshttps://doi.org/10.1016/j.pt.2021.06.001openalex-snapshot
Nematode infection and antinematode immunity in Drosophila
inferred← citeshttps://doi.org/10.1016/j.tcb.2016.06.004openalex-snapshot
An evolutionary perspective on the necroptotic pathway
inferred← citeshttps://doi.org/10.1016/j.tim.2018.04.007openalex-snapshot
Refining the Natural Product Repertoire in Entomopathogenic Bacteria
inferred← citeshttps://doi.org/10.1016/j.vetpar.2026.110867openalex-snapshot
Comparative in silico analysis of Apis mellifera immune responses to Varroa destructor and Tropilaelaps mercedesae: Common and mite-specific molecular signatures
inferred← citeshttps://doi.org/10.1016/j.ydbio.2020.10.006openalex-snapshot
There and back again: The mechanisms of differentiation and transdifferentiation in Drosophila blood cells
inferred← citeshttps://doi.org/10.1021/acs.est.6c07239openalex-snapshot
Benzotriazole Ultraviolet Stabilizer UV-PS Exposure Induces Immune Hyperactivation and Metabolic Reprogramming in Drosophila in a Microbiota-Dependent Manner
inferred← citeshttps://doi.org/10.1021/acs.jafc.4c09514openalex-snapshot
Chemical Proteomics Reveals That Camptothecin Weakens Insect Immunity against Bacteria by Suppressing Antimicrobial Peptide Expression
inferred← citeshttps://doi.org/10.1021/acs.jafc.6b05769openalex-snapshot
Possible Insecticidal Mechanisms Mediated by Immune-Response-Related Cry-Binding Proteins in the Midgut Juice of Plutella xylostella and Spodoptera exigua
inferred← citeshttps://doi.org/10.1021/acs.jafc.6c04482openalex-snapshot
BmMBF2–11 Couples FADD-Mediated IMD Signaling to Gut Microbial Homeostasis in the Silkworm
inferred← citeshttps://doi.org/10.1021/acsomega.4c00134openalex-snapshot
Evaluating the Impact of Vitamin D 3 on NF-κB and JAK/STAT Signaling Pathways in Drosophila melanogaster
inferred← citeshttps://doi.org/10.1038/ncomms14401openalex-snapshot
Infection-derived lipids elicit an immune deficiency circuit in arthropods
inferred← citeshttps://doi.org/10.1038/ni.3536openalex-snapshot
The regulatory isoform rPGRP-LC induces immune resolution via endosomal degradation of receptors
inferred← citeshttps://doi.org/10.1038/s41467-017-01287-9openalex-snapshot
Kenny mediates selective autophagic degradation of the IKK complex to control innate immune responses
inferred← citeshttps://doi.org/10.1038/s41467-023-44542-yopenalex-snapshot
Innate immune and proinflammatory signals activate the Hippo pathway via a Tak1-STRIPAK-Tao axis
inferred← citeshttps://doi.org/10.1038/s41467-026-70629-3openalex-snapshot
A conserved, immune-regulated peritrophin promotes Vibrio cholerae colonization of the arthropod intestine
inferred← citeshttps://doi.org/10.1038/s41557-022-00923-2openalex-snapshot
Global analysis of biosynthetic gene clusters reveals conserved and unique natural products in entomopathogenic nematode-symbiotic bacteria
inferred← citeshttps://doi.org/10.1038/s41598-017-15940-2openalex-snapshot
Drosophila muscles regulate the immune response against wasp infection via carbohydrate metabolism
inferred← citeshttps://doi.org/10.1038/s41598-018-30527-1openalex-snapshot
Sexual dimorphism in Drosophila melanogaster survival of Beauveria bassiana infection depends on core immune signaling
inferred← citeshttps://doi.org/10.1038/s41598-019-48977-6openalex-snapshot
Innate immune responses to paraquat exposure in a Drosophila model of Parkinson’s disease
inferred← citeshttps://doi.org/10.1038/s41598-019-53497-4openalex-snapshot
TmDorX2 positively regulates antimicrobial peptides in Tenebrio molitor gut, fat body, and hemocytes in response to bacterial and fungal infection
inferred← citeshttps://doi.org/10.1038/s41598-020-70455-7openalex-snapshot
Gut bacteria-derived peptidoglycan induces a metabolic syndrome-like phenotype via NF-κB-dependent insulin/PI3K signaling reduction in Drosophila renal system
inferred← citeshttps://doi.org/10.1038/s41598-020-80620-7openalex-snapshot
Thiamethoxam exposure deregulates short ORF gene expression in the honey bee and compromises immune response to bacteria
inferred← citeshttps://doi.org/10.1038/s41598-021-93364-9openalex-snapshot
Transcriptomic analysis of the black tiger shrimp (Penaeus monodon) reveals insights into immune development in their early life stages
inferred← citeshttps://doi.org/10.1038/s41598-023-45978-4openalex-snapshot
Effects of TmTak1 silencing on AMP production as an Imd pathway component in Tenebrio molitor
inferred← citeshttps://doi.org/10.1038/s41598-025-02641-4openalex-snapshot
Functionality of highly diverged Imd like genes identified in stinkbugs and bedbugs
inferred← citeshttps://doi.org/10.1038/s41598-025-30434-2openalex-snapshot
Transcriptomic analysis reveals members and expression characteristics of innate immunity genes in Chinese scorpion Mesobuthus martensii
inferred← citeshttps://doi.org/10.1038/s44319-024-00067-zopenalex-snapshot
Drosophila eIF3f1 mediates host immune defense by targeting dTak1
inferred← citeshttps://doi.org/10.1039/c7np00054eopenalex-snapshot
Chemical language and warfare of bacterial natural products in bacteria–nematode–insect interactions
inferred← citeshttps://doi.org/10.1073/pnas.1516122113openalex-snapshot
Cytokine Diedel and a viral homologue suppress the IMD pathway in Drosophila
inferred← citeshttps://doi.org/10.1073/pnas.2208673120openalex-snapshot
Croquemort elicits activation of the immune deficiency pathway in ticks
inferred← citeshttps://doi.org/10.1074/jbc.m113.544841openalex-snapshot
The Caspase-8 Homolog Dredd Cleaves Imd and Relish but Is Not Inhibited by p35
inferred← citeshttps://doi.org/10.1074/jbc.m115.664193openalex-snapshot
The Role of the Phylogenetically Conserved Cochaperone Protein Droj2/DNAJA3 in NF-κB Signaling
inferred← citeshttps://doi.org/10.1079/978178924881.0003openalex-snapshot
Entomopathogenic Nematodes as a Model for Probing the Insect Immune System
inferred← citeshttps://doi.org/10.1079/9781789248814.0003openalex-snapshot
Entomopathogenic Nematodes as a Model for Probing the Insect Immune System
inferred← citeshttps://doi.org/10.1079/9781800620322.0003openalex-snapshot
Insect Innate Immunity against Entomopathogenic Nematodes
inferred← citeshttps://doi.org/10.1080/19336934.2016.1182269openalex-snapshot
Tissue communication in a systemic immune response ofDrosophila
inferred← citeshttps://doi.org/10.1080/19336934.2016.1202387openalex-snapshot
WntD and Diedel: Two immunomodulatory cytokines inDrosophilaimmunity
inferred← citeshttps://doi.org/10.1080/19336934.2020.1808402openalex-snapshot
SUMO conjugation regulates immune signalling
inferred← citeshttps://doi.org/10.1080/19336934.2022.2149204openalex-snapshot
The role of micro RNAs (miRNAs) in the regulation of Drosophila melanogaster’s innate immunity
inferred← citeshttps://doi.org/10.1080/19336934.2025.2586357openalex-snapshot
Innate immunity pathways activate cell proliferation after penetrating traumatic brain injury in adult Drosophila
inferred← citeshttps://doi.org/10.1080/21505594.2018.1526531openalex-snapshot
Innate humoral immune defences in mammals and insects: The same, with differences ?
inferred← citeshttps://doi.org/10.1080/21505594.2020.1731137openalex-snapshot
Immune priming: the secret weapon of the insect world
inferred← citeshttps://doi.org/10.1080/24750263.2023.2276353openalex-snapshot
Changes in histamine, HSF1, Cysteinyl leukotriene, TLR1 and TLR2 in Galleria mellonella hemolymph after Conidiobolus coronatus infection
inferred← citeshttps://doi.org/10.1086/741105openalex-snapshot
Shielded by the Dead: How Killed Bacteria Shape the Dynamics and Evolution of Innate Immunity
inferred← citeshttps://doi.org/10.1091/mbc.e18-07-0434openalex-snapshot
Dysfunctional peroxisomes compromise gut structure and host defense by increased cell death and Tor-dependent autophagy
inferred← citeshttps://doi.org/10.1093/aesa/saab047openalex-snapshot
The Innate Immune Response of Eusocial Hymenopterans to Viral Pathogen Challenge
inferred← citeshttps://doi.org/10.1093/aesa/saw083openalex-snapshot
Flourishing in Filth: House Fly–Microbe Interactions Across Life History
inferred← citeshttps://doi.org/10.1093/braincomms/fcaf144openalex-snapshot
Loss of the NF-κB negative regulator Pirk in Drosophila links brain and gut immunity to neurodegeneration
inferred← citeshttps://doi.org/10.1093/g3journal/jkac163openalex-snapshot
Enteric bacterial infection in Drosophila induces whole-body alterations in metabolic gene expression independently of the immune deficiency signaling pathway
inferred← citeshttps://doi.org/10.1093/molbev/msaf104openalex-snapshot
How the Structure of Signaling Regulation Evolves: Insights From an Evolutionary Model
inferred← citeshttps://doi.org/10.1098/rspb.2021.0786openalex-snapshot
Host–pathogen immune feedbacks can explain widely divergent outcomes from similar infections
inferred← citeshttps://doi.org/10.1098/rspb.2022.1642openalex-snapshot
Ageing leads to reduced specificity of antimicrobial peptide responses in Drosophila melanogaster
inferred← citeshttps://doi.org/10.1099/jmm.0.001064openalex-snapshot
From cell culture to cynomolgus macaque: infection models show lineage-specific virulence potential of Coxiella burnetii
inferred← citeshttps://doi.org/10.1101/2020.04.30.070292openalex-snapshot
Downregulation of Perilipin1 by IMD leads to LD reconfiguration and adaptation to bacterial infection in Drosophila
inferred← citeshttps://doi.org/10.1101/2021.04.06.438672openalex-snapshot
The Drosophila TNF Eiger contributes to Myc super-competition independent of JNK activity
inferred← citeshttps://doi.org/10.1101/2021.08.31.458430openalex-snapshot
The unfolded protein response triggers the immune deficiency pathway in ticks
inferred← citeshttps://doi.org/10.1101/2021.09.23.461574openalex-snapshot
Negative immune regulation contributes to disease tolerance in Drosophila
inferred← citeshttps://doi.org/10.1101/2021.09.23.461578openalex-snapshot
Duox and Jak/Stat signalling influence disease tolerance in Drosophila during Pseudomonas entomophila infection
inferred← citeshttps://doi.org/10.1101/2021.11.19.469298openalex-snapshot
Loss of self-tolerance leads to altered gene expression and IMD pathway activation in Drosophila melanogaster
inferred← citeshttps://doi.org/10.1101/2022.02.09.479763openalex-snapshot
CD36 homologs determine microbial resistance to the Lyme disease spirochete
inferred← citeshttps://doi.org/10.1101/2022.05.11.491537openalex-snapshot
Enteric bacterial infection in Drosophila induces whole-body alterations in metabolic gene expression independently of the Immune Deficiency (Imd) signalling pathway
inferred← citeshttps://doi.org/10.1101/2022.06.25.497570openalex-snapshot
Ageing leads to nonspecific antimicrobial peptide responses in Drosophila melanogaster
inferred← citeshttps://doi.org/10.1101/2023.06.29.547108openalex-snapshot
Vibrio cholerae Arrests Intestinal Epithelial Proliferation through T6SS-dependent Activation of the Bone Morphogenetic Protein Pathway
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