On the public citation graph

Immune Regulation of Intestinal Stem Cell Proliferation and Differentiation in Drosophila

https://doi.org/10.1101/721662
0 signed · 117 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 See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.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/10.1016/0016-5085(94)90526-6openalex-snapshot
Microflora modulates endocrine cells in the gastrointestinal mucosa of the rat
inferredcites →https://doi.org/10.1016/bs.ai.2014.11.003openalex-snapshot
Epithelial Cell Contributions to Intestinal Immunity
inferredcites →https://doi.org/10.1016/j.cell.2009.05.014openalex-snapshot
Cytokine/Jak/Stat Signaling Mediates Regeneration and Homeostasis in the Drosophila Midgut
inferredcites →https://doi.org/10.1016/j.cell.2013.12.018openalex-snapshot
PGRP-SC2 Promotes Gut Immune Homeostasis to Limit Commensal Dysbiosis and Extend Lifespan
inferredcites →https://doi.org/10.1016/j.cell.2018.10.008openalex-snapshot
T Helper Cell Cytokines Modulate Intestinal Stem Cell Renewal and Differentiation
inferredcites →https://doi.org/10.1016/j.celrep.2013.04.001openalex-snapshot
Morphological and Molecular Characterization of Adult Midgut Compartmentalization in Drosophila
inferredcites →https://doi.org/10.1016/j.celrep.2014.05.024openalex-snapshot
Slit/Robo Signaling Regulates Cell Fate Decisions in the Intestinal Stem Cell Lineage of Drosophila
inferredcites →https://doi.org/10.1016/j.celrep.2015.06.009openalex-snapshot
Regional Cell-Specific Transcriptome Mapping Reveals Regulatory Complexity in the Adult Drosophila Midgut
inferredcites →https://doi.org/10.1016/j.celrep.2015.08.004openalex-snapshot
Distinct Shifts in Microbiota Composition during Drosophila Aging Impair Intestinal Function and Drive Mortality
inferredcites →https://doi.org/10.1016/j.celrep.2017.07.078openalex-snapshot
Constitutive Immune Activity Promotes Tumorigenesis in Drosophila Intestinal Progenitor Cells
inferredcites →https://doi.org/10.1016/j.celrep.2017.08.059openalex-snapshot
Piwi Is Required to Limit Exhaustion of Aging Somatic Stem Cells
inferredcites →https://doi.org/10.1016/j.celrep.2019.11.048openalex-snapshot
The Cellular Diversity and Transcription Factor Code of Drosophila Enteroendocrine Cells
inferredcites →https://doi.org/10.1016/j.celrep.2019.12.094openalex-snapshot
Vibrio cholerae-Symbiont Interactions Inhibit Intestinal Repair in Drosophila
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.2009.01.003openalex-snapshot
Drosophila Intestinal Response to Bacterial Infection: Activation of Host Defense and Stem Cell Proliferation
inferredcites →https://doi.org/10.1016/j.chom.2012.06.002openalex-snapshot
Peptidoglycan Sensing by the Receptor PGRP-LE in the Drosophila Gut Induces Immune Responses to Infectious Bacteria and Tolerance to Microbiota
inferredcites →https://doi.org/10.1016/j.chom.2014.05.003openalex-snapshot
The Cytosolic Bacterial Peptidoglycan Sensor Nod2 Affords Stem Cell Protection and Links Microbes to Gut Epithelial Regeneration
inferredcites →https://doi.org/10.1016/j.chom.2014.10.006openalex-snapshot
The Acetate Switch of an Intestinal Pathogen Disrupts Host Insulin Signaling and Lipid Metabolism
inferredcites →https://doi.org/10.1016/j.chom.2016.08.003openalex-snapshot
Signal Integration by the IκB Protein Pickle Shapes Drosophila Innate Host Defense
inferredcites →https://doi.org/10.1016/j.chom.2019.07.001openalex-snapshot
Sugar Alcohols of Polyol Pathway Serve as Alarmins to Mediate Local-Systemic Innate Immune Communication in Drosophila
inferredcites →https://doi.org/10.1016/j.cmet.2007.06.006openalex-snapshot
Increased Internal and External Bacterial Load during Drosophila Aging without Life-Span Trade-Off
inferredcites →https://doi.org/10.1016/j.cmet.2018.05.026openalex-snapshot
The Drosophila Immune Deficiency Pathway Modulates Enteroendocrine Function and Host Metabolism
inferredcites →https://doi.org/10.1016/j.dci.2016.01.001openalex-snapshot
Bacteria sensing mechanisms in Drosophila gut: Local and systemic consequences
inferredcites →https://doi.org/10.1016/j.dci.2016.02.020openalex-snapshot
The zebrafish as a model to study intestinal inflammation
inferredcites →https://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
inferredcites →https://doi.org/10.1016/j.devcel.2018.08.013openalex-snapshot
Dietary Lipids Modulate Notch Signaling and Influence Adult Intestinal Development and Metabolism in Drosophila
inferredcites →https://doi.org/10.1016/j.devcel.2019.04.009openalex-snapshot
NF-κB Shapes Metabolic Adaptation by Attenuating Foxo-Mediated Lipolysis in Drosophila
inferredcites →https://doi.org/10.1016/j.gde.2012.04.002openalex-snapshot
Intestinal stem cell function in Drosophila and mice
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.2011.09.018openalex-snapshot
Negative Regulation by Amidase PGRPs Shapes the Drosophila Antibacterial Response and Protects the Fly from Innocuous Infection
inferredcites →https://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
inferredcites →https://doi.org/10.1016/j.immuni.2018.07.016openalex-snapshot
A Map of Toll-like Receptor Expression in the Intestinal Epithelium Reveals Distinct Spatial, Cell Type-Specific, and Temporal Patterns
inferredcites →https://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
inferredcites →https://doi.org/10.1016/j.immuni.2019.06.003openalex-snapshot
T Cell Recruitment to the Intestinal Stem Cell Compartment Drives Immune-Mediated Intestinal Damage after Allogeneic Transplantation
inferredcites →https://doi.org/10.1016/j.immuni.2019.08.020openalex-snapshot
Nephrocytes Remove Microbiota-Derived Peptidoglycan from Systemic Circulation to Maintain Immune Homeostasis
inferredcites →https://doi.org/10.1016/j.it.2018.12.008openalex-snapshot
The Intestinal Epithelium: Central Coordinator of Mucosal Immunity
inferredcites →https://doi.org/10.1016/j.mod.2004.10.009openalex-snapshot
Intestinal growth and differentiation in zebrafish
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.stem.2009.01.009openalex-snapshot
Intestinal Stem Cells in Mammals and Drosophila
inferredcites →https://doi.org/10.1016/j.ydbio.2011.03.018openalex-snapshot
EGFR, Wingless and JAK/STAT signaling cooperatively maintain Drosophila intestinal stem cells
inferredcites →https://doi.org/10.1038/35079107openalex-snapshot
Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease
inferredcites →https://doi.org/10.1038/35079114openalex-snapshot
A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease
inferredcites →https://doi.org/10.1038/ismej.2017.28openalex-snapshot
The role of adaptive immunity as an ecological filter on the gut microbiota in zebrafish
inferredcites →https://doi.org/10.1038/labinvest.2010.100openalex-snapshot
Toll-like receptor 4 differentially regulates epidermal growth factor-related growth factors in response to intestinal mucosal injury
inferredcites →https://doi.org/10.1038/mi.2015.112openalex-snapshot
Intestinal FoxO signaling is required to survive oral infection in Drosophila
inferredcites →https://doi.org/10.1038/nature04333openalex-snapshot
The adult Drosophila posterior midgut is maintained by pluripotent stem cells
inferredcites →https://doi.org/10.1038/nature04371openalex-snapshot
Evidence that stem cells reside in the adult Drosophila midgut epithelium
inferredcites →https://doi.org/10.1038/ncb1500openalex-snapshot
Maintenance of colonic homeostasis by distinctive apical TLR9 signalling in intestinal epithelial cells
inferredcites →https://doi.org/10.1038/ncomms5560openalex-snapshot
Automated monitoring and quantitative analysis of feeding behaviour 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/nrm3721openalex-snapshot
Adult intestinal stem cells: critical drivers of epithelial homeostasis and regeneration
inferredcites →https://doi.org/10.1038/nrmicro3074openalex-snapshot
Gut homeostasis in a microbial world: insights from Drosophila melanogaster
inferredcites →https://doi.org/10.1038/onc.2012.581openalex-snapshot
Constitutive TLR4 signalling in intestinal epithelium reduces tumor load by increasing apoptosis in APCMin/+ mice
inferredcites →https://doi.org/10.1038/s41467-019-08982-9openalex-snapshot
Loss of a proteostatic checkpoint in intestinal stem cells contributes to age-related epithelial dysfunction
inferredcites →https://doi.org/10.1053/j.gastro.2006.06.017openalex-snapshot
Cox-2 Is Regulated by Toll-Like Receptor-4 (TLR4) Signaling: Role in Proliferation and Apoptosis in the Intestine
inferredcites →https://doi.org/10.1053/j.gastro.2011.06.003openalex-snapshot
Notch: Architect, Landscaper, and Guardian of the Intestine
inferredcites →https://doi.org/10.1073/pnas.1000072107openalex-snapshot
Epithelial cell proliferation in the developing zebrafish intestine is regulated by the Wnt pathway and microbial signaling via Myd88
inferredcites →https://doi.org/10.1073/pnas.1012759107openalex-snapshot
Hippo signaling regulates Drosophila intestine stem cell proliferation through multiple pathways
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.1902788117openalex-snapshot
Innate immune receptor NOD2 mediates LGR5 + intestinal stem cell protection against ROS cytotoxicity via mitophagy stimulation
inferredcites →https://doi.org/10.1073/pnas.1916820117openalex-snapshot
A Cell Atlas of the Adult Drosophila Midgut
inferredcites →https://doi.org/10.1074/jbc.m111.220285openalex-snapshot
The Protein Dredd Is an Essential Component of the c-Jun N-terminal Kinase Pathway in the Drosophila Immune Response
inferredcites →https://doi.org/10.1074/jbc.m112.375881openalex-snapshot
Toll-like Receptor 4 Is Expressed on Intestinal Stem Cells and Regulates Their Proliferation and Apoptosis via the p53 Up-regulated Modulator of Apoptosis
inferredcites →https://doi.org/10.1074/jbc.m113.544841openalex-snapshot
The Caspase-8 Homolog Dredd Cleaves Imd and Relish but Is Not Inhibited by p35
inferredcites →https://doi.org/10.1084/jem.20120504openalex-snapshot
Familial transmission rather than defective innate immunity shapes the distinct intestinal microbiota of TLR-deficient mice
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/10.1098/rsob.180120openalex-snapshot
Tales from the crypt: intestinal niche signals in tissue renewal, plasticity and cancer
inferredcites →https://doi.org/10.1101/gad.1827009openalex-snapshot
Invasive and indigenous microbiota impact intestinal stem cell activity through multiple pathways in Drosophila
inferredcites →https://doi.org/10.1111/febs.15910openalex-snapshot
Microbial recognition regulates intestinal epithelial growth in homeostasis and disease
inferredcites →https://doi.org/10.1111/j.1462-5822.2008.01267.xopenalex-snapshot
Genetic analysis ofDrosophila melanogastersusceptibility to intestinalVibrio choleraeinfection
inferredcites →https://doi.org/10.1111/j.1474-9726.2006.00251.xopenalex-snapshot
Trade‐offs between longevity and pathogen resistance in Drosophila melanogaster are mediated by NFκB signaling
inferredcites →https://doi.org/10.1126/science.1136606openalex-snapshot
Multipotent Drosophila Intestinal Stem Cells Specify Daughter Cell Fates by Differential Notch Signaling
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.aab0988openalex-snapshot
Bidirectional Notch signaling regulates Drosophila intestinal stem cell multipotency
inferredcites →https://doi.org/10.1126/sciimmunol.aay8556openalex-snapshot
T cell–derived interferon-γ programs stem cell death in immune-mediated intestinal damage
inferredcites →https://doi.org/10.1126/stke.2202004pl6openalex-snapshot
Spatiotemporal Gene Expression Targeting with the TARGET and Gene-Switch Systems in Drosophila
inferredcites →https://doi.org/10.1128/mbio.00337-13openalex-snapshot
Mutations in the IMD Pathway and Mustard Counter Vibrio cholerae Suppression of Intestinal Stem Cell Division in Drosophila
inferredcites →https://doi.org/10.1128/mbio.00860-13openalex-snapshot
Frequent Replenishment Sustains the Beneficial Microbiome of Drosophila melanogaster
inferredcites →https://doi.org/10.1128/mbio.01117-13openalex-snapshot
Dual Role for Inflammasome Sensors NLRP1 and NLRP3 in Murine Resistance to Toxoplasma gondii
inferredcites →https://doi.org/10.1128/mbio.01117-14openalex-snapshot
Microbiota-Induced Changes in Drosophila melanogaster Host Gene Expression and Gut Morphology
inferredcites →https://doi.org/10.1128/mbio.01680-17openalex-snapshot
Lipopolysaccharide from Crypt-Specific Core Microbiota Modulates the Colonic Epithelial Proliferation-to-Differentiation Balance
inferredcites →https://doi.org/10.1128/mcb.00259-17openalex-snapshot
A Complex Relationship between Immunity and Metabolism in Drosophila Diet-Induced Insulin Resistance
inferredcites →https://doi.org/10.1128/mcb.24.1.172-185.2004openalex-snapshot
The Homeobox Gene Caudal Regulates Constitutive Local Expression of Antimicrobial Peptide Genes in Drosophila Epithelia
inferredcites →https://doi.org/10.1128/msystems.00162-16openalex-snapshot
Balance Trees Reveal Microbial Niche Differentiation
inferredcites →https://doi.org/10.1159/000475771openalex-snapshot
Oligopeptide Transporters of the SLC15 Family Are Dispensable for Peptidoglycan Sensing and Transport in Drosophila
inferredcites →https://doi.org/10.1172/jci62236openalex-snapshot
NOD2-mediated dysbiosis predisposes mice to transmissible colitis and colorectal cancer
inferredcites →https://doi.org/10.1186/1741-7007-8-152openalex-snapshot
DrosophilaEGFR pathway coordinates stem cell proliferation and gut remodeling following infection
inferredcites →https://doi.org/10.1203/00006450-200104000-00023openalex-snapshot
Evidence for an Innate Immune Response in the Immature Human Intestine: Toll-Like Receptors on Fetal Enterocytes
inferredcites →https://doi.org/10.1242/dev.039404openalex-snapshot
Transcriptional control of stem cell maintenance in the Drosophila intestine
inferredcites →https://doi.org/10.1242/dev.065292openalex-snapshot
Distinct levels of Notch activity for commitment and terminal differentiation of stem cells in the adult fly intestine
inferredcites →https://doi.org/10.1242/dev.113357openalex-snapshot
Enteroendocrine cells are generated from stem cells through a distinct progenitor in the adult Drosophila posterior midgut
inferredcites →https://doi.org/10.1242/dev.114959openalex-snapshot
Generation of enteroendocrine cell diversity in midgut stem cell lineages
inferredcites →https://doi.org/10.1242/dev.155317openalex-snapshot
Microbiota promote secretory cell determination in the intestinal epithelium by modulating host Notch signaling
inferredcites →https://doi.org/10.1242/dmm.017400openalex-snapshot
How informative is the mouse for human gut microbiota research?
inferredcites →https://doi.org/10.1371/journal.pbio.2002054openalex-snapshot
Genomic dissection of conserved transcriptional regulation in intestinal epithelial cells
inferredcites →https://doi.org/10.1371/journal.pgen.1004117openalex-snapshot
Loss of Trabid, a New Negative Regulator of the Drosophila Immune-Deficiency Pathway at the Level of TAK1, Reduces Life Span
inferredcites →https://doi.org/10.1371/journal.pgen.1007931openalex-snapshot
Intestinal NF-κB and STAT signalling is important for uptake and clearance in a Drosophila-Herpetomonas interaction model
inferredcites →https://doi.org/10.1371/journal.pone.0094729openalex-snapshot
Drosophila Microbiota Modulates Host Metabolic Gene Expression via IMD/NF-κB Signaling
inferredcites →https://doi.org/10.1371/journal.ppat.0030173openalex-snapshot
A Model of Bacterial Intestinal Infections in Drosophila melanogaster
inferredcites →https://doi.org/10.1371/journal.ppat.1000694openalex-snapshot
Long-Range Activation of Systemic Immunity through Peptidoglycan Diffusion in Drosophila
inferredcites →https://doi.org/10.1371/journal.ppat.1006277openalex-snapshot
Drosophila as a model for homeostatic, antibacterial, and antiviral mechanisms in the gut
inferredcites →https://doi.org/10.15252/embr.201540188openalex-snapshot
Stem cell and progenitor fate in the mammalian intestine: Notch and lateral inhibition in homeostasis and disease
inferredcites →https://doi.org/10.1534/genetics.107.081968openalex-snapshot
Spatial and Temporal Control of Gene Expression in Drosophila Using the Inducible GeneSwitch GAL4 System. I. Screen for Larval Nervous System Drivers
inferredcites →https://doi.org/10.1534/genetics.116.190215openalex-snapshot
Interaction Between Familial Transmission and a Constitutively Active Immune System Shapes Gut Microbiota in Drosophila melanogaster
inferredcites →https://doi.org/10.1534/genetics.118.300224openalex-snapshot
Anatomy and Physiology of the Digestive Tract of Drosophila melanogaster
inferredcites →https://doi.org/10.1538/expanim.45.155openalex-snapshot
Histochemical, Lectin-Histochemical and Morphometrical Characteristics of Intestinal Goblet Cells of Germfree and Conventional Mice.
inferredcites →https://doi.org/10.3791/55024openalex-snapshot
The CApillary FEeder Assay Measures Food Intake in Drosophila melanogaster
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.1303309openalex-snapshot
The Drosophila Imd Signaling Pathway
inferredcites →https://doi.org/10.4049/jimmunol.1600185openalex-snapshot
The Cytosolic Microbial Receptor Nod2 Regulates Small Intestinal Crypt Damage and Epithelial Regeneration following T Cell–Induced Enteropathy
inferredcites →https://doi.org/10.4049/jimmunol.1801632openalex-snapshot
The Immune Deficiency Pathway Regulates Metabolic Homeostasis in Drosophila
inferredcites →https://doi.org/10.4161/gmic.19896openalex-snapshot
Gut-associated microbes of Drosophila melanogaster

What points at this work

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

inferred← citeshttps://doi.org/10.1002/wdev.396openalex-snapshot
Single‐cell RNA sequencing in Drosophila: Technologies and applications
inferred← citeshttps://doi.org/10.1101/746305openalex-snapshot
Complex symbiont-pathogen interactions inhibit intestinal repair
inferred← citeshttps://doi.org/10.1111/febs.15910openalex-snapshot
Microbial recognition regulates intestinal epithelial growth in homeostasis and disease
inferred← citeshttps://doi.org/10.3389/fimmu.2019.03128openalex-snapshot
Host-Microbe-Pathogen Interactions: A Review of Vibrio cholerae Pathogenesis in Drosophila
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.