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Accumulation of differentiating intestinal stem cell progenies drives tumorigenesis

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What this work says

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

inferredcites →https://doi.org/10.1002/9780470151808.sc02f02s27openalex-snapshot
RNA Expression Profiling from FACS‐Isolated Cells of the Drosophila Intestine
inferredcites →https://doi.org/10.1002/dvg.20661openalex-snapshot
Characterization of midgut stem cell‐ and enteroblast‐specific Gal4 lines in drosophila
inferredcites →https://doi.org/10.1006/dbio.2000.9923openalex-snapshot
Dissecting the Mechanisms of Suppressor of Hairless Function
inferredcites →https://doi.org/10.1016/j.cell.2008.01.038openalex-snapshot
Stem Cells and Niches: Mechanisms That Promote Stem Cell Maintenance throughout Life
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.2011.02.013openalex-snapshot
Hallmarks of Cancer: The Next Generation
inferredcites →https://doi.org/10.1016/j.cell.2011.05.033openalex-snapshot
Strategies for Homeostatic Stem Cell Self-Renewal in Adult Tissues
inferredcites →https://doi.org/10.1016/j.cell.2011.08.048openalex-snapshot
Altered Modes of Stem Cell Division Drive Adaptive Intestinal Growth
inferredcites →https://doi.org/10.1016/j.cell.2014.02.057openalex-snapshot
Transit-Amplifying Cells Orchestrate Stem Cell Activity and Tissue Regeneration
inferredcites →https://doi.org/10.1016/j.cell.2015.05.033openalex-snapshot
Apc Restoration Promotes Cellular Differentiation and Reestablishes Crypt Homeostasis in Colorectal Cancer
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.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.cmet.2014.01.012openalex-snapshot
Supercompetitor Status of Drosophila Myc Cells Requires p53 as a Fitness Sensor to Reprogram Metabolism and Promote Viability
inferredcites →https://doi.org/10.1016/j.cub.2006.04.042openalex-snapshot
Loss of Cell Polarity Drives Tumor Growth and Invasion through JNK Activation in Drosophila
inferredcites →https://doi.org/10.1016/j.devcel.2004.07.022openalex-snapshot
Invasive Cell Behavior during Drosophila Imaginal Disc Eversion Is Mediated by the JNK Signaling Cascade
inferredcites →https://doi.org/10.1016/j.devcel.2007.12.002openalex-snapshot
Keap1/Nrf2 Signaling Regulates Oxidative Stress Tolerance and Lifespan in Drosophila
inferredcites →https://doi.org/10.1016/j.devcel.2009.11.004openalex-snapshot
Spatial Restriction of FGF Signaling by a Matrix Metalloprotease Controls Branching Morphogenesis
inferredcites →https://doi.org/10.1016/j.devcel.2010.05.014openalex-snapshot
Oncogenic Ras Diverts a Host TNF Tumor Suppressor Activity into Tumor Promoter
inferredcites →https://doi.org/10.1016/j.devcel.2014.09.012openalex-snapshot
The Conserved Misshapen-Warts-Yorkie Pathway Acts in Enteroblasts to Regulate Intestinal Stem Cells in Drosophila
inferredcites →https://doi.org/10.1016/j.devcel.2015.02.012openalex-snapshot
Systemic Organ Wasting Induced by Localized Expression of the Secreted Insulin/IGF Antagonist ImpL2
inferredcites →https://doi.org/10.1016/j.devcel.2015.03.001openalex-snapshot
Malignant Drosophila Tumors Interrupt Insulin Signaling to Induce Cachexia-like Wasting
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.modgep.2006.08.003openalex-snapshot
GFP reporters detect the activation of the Drosophila JAK/STAT pathway in vivo
inferredcites →https://doi.org/10.1016/j.stem.2008.07.024openalex-snapshot
JNK Activity in Somatic Stem Cells Causes Loss of Tissue Homeostasis in the Aging Drosophila Gut
inferredcites →https://doi.org/10.1016/j.stem.2010.11.026openalex-snapshot
EGFR/Ras/MAPK Signaling Mediates Adult Midgut Epithelial Homeostasis and Regeneration in Drosophila
inferredcites →https://doi.org/10.1016/j.stem.2011.10.004openalex-snapshot
Maintaining Tissue Homeostasis: Dynamic Control of Somatic Stem Cell Activity
inferredcites →https://doi.org/10.1016/j.stem.2012.06.017openalex-snapshot
The Par Complex and Integrins Direct Asymmetric Cell Division in Adult Intestinal Stem Cells
inferredcites →https://doi.org/10.1016/j.stem.2012.12.007openalex-snapshot
The Sox Family of Transcription Factors: Versatile Regulators of Stem and Progenitor Cell Fate
inferredcites →https://doi.org/10.1016/j.tcb.2012.11.002openalex-snapshot
Competitive cell interactions in cancer: a cellular tug of war
inferredcites →https://doi.org/10.1016/j.ydbio.2009.10.045openalex-snapshot
JAK/STAT signaling coordinates stem cell proliferation and multilineage differentiation in the Drosophila intestinal stem cell lineage
inferredcites →https://doi.org/10.1016/j.ydbio.2012.10.023openalex-snapshot
The UPD3 cytokine couples environmental challenge and intestinal stem cell division through modulation of JAK/STAT signaling in the stem cell microenvironment
inferredcites →https://doi.org/10.1016/j.ydbio.2013.03.020openalex-snapshot
APC loss-induced intestinal tumorigenesis in Drosophila: Roles of Ras in Wnt signaling activation and tumor progression
inferredcites →https://doi.org/10.1016/s0166-2236(00)01791-4openalex-snapshot
Mosaic analysis with a repressible cell marker (MARCM) for Drosophila neural development
inferredcites →https://doi.org/10.1038/emboj.2012.248openalex-snapshot
Inducible progenitor‐derived Wingless regulates adult midgut regeneration in Drosophila
inferredcites →https://doi.org/10.1038/embor.2012.44openalex-snapshot
Immune response to bacteria induces dissemination of Ras‐activated Drosophila hindgut cells
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/nature07329openalex-snapshot
Paracrine Wingless signalling controls self-renewal of Drosophila intestinal stem cells
inferredcites →https://doi.org/10.1038/nbt.2978openalex-snapshot
Modulating the stem cell niche for tissue regeneration
inferredcites →https://doi.org/10.1038/ncb3214openalex-snapshot
Niche appropriation by Drosophila intestinal stem cell tumours
inferredcites →https://doi.org/10.1038/nmeth.1923openalex-snapshot
Fast gapped-read alignment with Bowtie 2
inferredcites →https://doi.org/10.1038/nrc2252openalex-snapshot
Is cell competition relevant to cancer?
inferredcites →https://doi.org/10.1038/nrd4002openalex-snapshot
Modulation of oxidative stress as an anticancer strategy
inferredcites →https://doi.org/10.1038/nrm3272openalex-snapshot
A family business: stem cell progeny join the niche to regulate homeostasis
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/onc.2014.163openalex-snapshot
Src kinase function controls progenitor cell pools during regeneration and tumor onset in the Drosophila intestine
inferredcites →https://doi.org/10.1038/sj.emboj.7601401openalex-snapshot
JNK‐ and Fos‐regulated Mmp1 expression cooperates with Ras to induce invasive tumors in Drosophila
inferredcites →https://doi.org/10.1073/pnas.0911797106openalex-snapshot
Synergy between bacterial infection and genetic predisposition in intestinal dysplasia
inferredcites →https://doi.org/10.1083/jcb.201409025openalex-snapshot
Injury-stimulated Hedgehog signaling promotes regenerative proliferation of Drosophila intestinal stem cells
inferredcites →https://doi.org/10.1093/emboj/cdg548openalex-snapshot
scribble mutants cooperate with oncogenic Ras or Notch to cause neoplastic overgrowth in Drosophila
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/10.1101/gr.772403openalex-snapshot
PANTHER: A Library of Protein Families and Subfamilies Indexed by Function
inferredcites →https://doi.org/10.1126/science.1088474openalex-snapshot
A Genetic Screen in Drosophila for Metastatic Behavior
inferredcites →https://doi.org/10.1126/science.1117311openalex-snapshot
A Direct Role for Dual Oxidase in Drosophila Gut Immunity
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/stke.2202004pl6openalex-snapshot
Spatiotemporal Gene Expression Targeting with the TARGET and Gene-Switch Systems in Drosophila
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/10.1186/gb-2010-11-10-r106openalex-snapshot
Differential expression analysis for sequence count data
inferredcites →https://doi.org/10.1186/s12915-015-0126-4openalex-snapshot
Dawn- and dusk-phased circadian transcription rhythms coordinate anabolic and catabolic functions in Neurospora
inferredcites →https://doi.org/10.1242/dev.035196openalex-snapshot
Adenomatous polyposis coli regulates Drosophila intestinal stem cell proliferation
inferredcites →https://doi.org/10.1242/dev.078261openalex-snapshot
Non-autonomous crosstalk between the Jak/Stat and Egfr pathways mediates Apc1-driven intestinal stem cell hyperplasia in the Drosophila adult midgut
inferredcites →https://doi.org/10.1242/jcs.113100openalex-snapshot
Autocrine and paracrine unpaired signaling regulate intestinal stem cell maintenance and division
inferredcites →https://doi.org/10.1371/journal.pgen.1004659openalex-snapshot
The Drosophila MAPK p38c Regulates Oxidative Stress and Lipid Homeostasis in the Intestine
inferredcites →https://doi.org/10.1371/journal.pgen.1005595openalex-snapshot
ROS-Induced JNK and p38 Signaling Is Required for Unpaired Cytokine Activation during Drosophila Regeneration
inferredcites →https://doi.org/10.1371/journal.pone.0088413openalex-snapshot
Conserved Mechanisms of Tumorigenesis in the Drosophila Adult Midgut
inferredcites →https://doi.org/10.15252/embj.201489072openalex-snapshot
Escargot maintains stemness and suppresses differentiation in Drosophila intestinal stem cells
inferredcites →https://doi.org/10.15252/embj.201591517openalex-snapshot
Robust intestinal homeostasis relies on cellular plasticity in enteroblasts mediated by miR‐8–Escargot switch
inferredcites →https://doi.org/10.1534/genetics.113.156737openalex-snapshot
Highly Improved Gene Targeting by Germline-Specific Cas9 Expression in Drosophila
inferredcites →https://doi.org/10.7554/elife.05338openalex-snapshot
A library of MiMICs allows tagging of genes and reversible, spatial and temporal knockdown of proteins in Drosophila

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.3329888openalex-extracted
Tumor Establishment Requires Tumor Autonomous and Non-Autonomous Decoupling of EGF Signaling from Apoptosis
inferred← citeshttps://doi.org/10.1002/jcb.30545openalex-snapshot
InR and Pi3K maintain intestinal homeostasis through STAT/EGFR and Notch signaling in enteroblasts
inferred← citeshttps://doi.org/10.1007/5584_2021_686openalex-snapshot
Epithelial Stem Cells: Making, Shaping and Breaking the Niche
inferred← citeshttps://doi.org/10.1007/978-1-4939-8697-2_9openalex-snapshot
Markers and Methods to Study Adult Midgut Stem Cells
inferred← citeshttps://doi.org/10.1007/978-3-031-97035-1_6openalex-snapshot
Drosophila Intestine as a Model to Study Tumors
inferred← citeshttps://doi.org/10.1007/s00018-016-2235-9openalex-snapshot
Intestinal stem cell response to injury: lessons from Drosophila
inferred← citeshttps://doi.org/10.1007/s00343-018-7138-1openalex-snapshot
Involvement of clustered oyster Wnt genes in gut formation
inferred← citeshttps://doi.org/10.1016/bs.mcb.2022.02.013openalex-snapshot
Identification of progenitor cells and their progenies in adult Drosophila midgut
inferred← citeshttps://doi.org/10.1016/j.cdev.2023.203862openalex-snapshot
Intestinal stem cells and their niches in homeostasis and disease
inferred← citeshttps://doi.org/10.1016/j.ceb.2017.06.005openalex-snapshot
Tissue homeostasis and aging: new insight from the fly intestine
inferred← citeshttps://doi.org/10.1016/j.celrep.2019.11.048openalex-snapshot
The Cellular Diversity and Transcription Factor Code of Drosophila Enteroendocrine Cells
inferred← citeshttps://doi.org/10.1016/j.celrep.2020.01.041openalex-snapshot
A Switch in Tissue Stem Cell Identity Causes Neuroendocrine Tumors in Drosophila Gut
inferred← citeshttps://doi.org/10.1016/j.celrep.2020.107683openalex-snapshot
The Drosophila Ortholog of Mammalian Transcription Factor Sox9 Regulates Intestinal Homeostasis and Regeneration at an Appropriate Level
inferred← citeshttps://doi.org/10.1016/j.celrep.2022.110572openalex-snapshot
Microbes affect gut epithelial cell composition through immune-dependent regulation of intestinal stem cell differentiation
inferred← citeshttps://doi.org/10.1016/j.celrep.2023.113245openalex-snapshot
The roles of the native cell differentiation program aberrantly recapitulated in Drosophila intestinal tumors
inferred← citeshttps://doi.org/10.1016/j.celrep.2023.113485openalex-snapshot
Molecular underpinnings and environmental drivers of loss of heterozygosity in Drosophila intestinal stem cells
inferred← citeshttps://doi.org/10.1016/j.celrep.2025.115398openalex-snapshot
A bHLH interaction code controls bipotential differentiation and self-renewal in the Drosophila gut
inferred← citeshttps://doi.org/10.1016/j.cub.2020.01.082openalex-snapshot
Disruption of EGF Feedback by Intestinal Tumors and Neighboring Cells in Drosophila
inferred← citeshttps://doi.org/10.1016/j.devcel.2018.04.014openalex-snapshot
Ingestion of Food Particles Regulates the Mechanosensing Misshapen-Yorkie Pathway in Drosophila Intestinal Growth
inferred← citeshttps://doi.org/10.1016/j.devcel.2020.03.002openalex-snapshot
Peroxisome Elevation Induces Stem Cell Differentiation and Intestinal Epithelial Repair
inferred← citeshttps://doi.org/10.1016/j.devcel.2020.03.023openalex-snapshot
The Peroxisome: A New Player in Intestinal Epithelial Repair
inferred← citeshttps://doi.org/10.1016/j.devcel.2021.06.007openalex-snapshot
Microenvironmental innate immune signaling and cell mechanical responses promote tumor growth
inferred← citeshttps://doi.org/10.1016/j.devcel.2024.06.020openalex-snapshot
Very long-chain fatty acids control peroxisome dynamics via a feedback loop in intestinal stem cells during gut regeneration
inferred← citeshttps://doi.org/10.1016/j.devcel.2025.12.003openalex-snapshot
Impaired VLCFA-peroxisome-mediated intestinal epithelial repair causes gastrointestinal sequelae of long COVID
inferred← citeshttps://doi.org/10.1016/j.gde.2016.06.009openalex-snapshot
Maintenance of the adult Drosophila intestine: all roads lead to homeostasis
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.isci.2020.100954openalex-snapshot
IRBIT Directs Differentiation of Intestinal Stem Cell Progeny to Maintain Tissue Homeostasis
inferred← citeshttps://doi.org/10.1016/j.isci.2023.106901openalex-snapshot
The septate junction component bark beetle is required for Drosophila intestinal barrier function and homeostasis
inferred← citeshttps://doi.org/10.1016/j.isci.2025.111967openalex-snapshot
Aberrant enterocyte progenitor clustering as an early life biomarker of Drosophila aging
inferred← citeshttps://doi.org/10.1016/j.jgg.2025.04.017openalex-snapshot
Oncogenic Ras, Yki and Notch signals converge to confer clone competitiveness through Upd2
inferred← citeshttps://doi.org/10.1016/j.stemcr.2018.03.014openalex-snapshot
The POU/Oct Transcription Factor Nubbin Controls the Balance of Intestinal Stem Cell Maintenance and Differentiation by Isoform-Specific Regulation
inferred← citeshttps://doi.org/10.1016/j.stemcr.2020.01.003openalex-snapshot
Sox100B Regulates Progenitor-Specific Gene Expression and Cell Differentiation in the Adult Drosophila Intestine
inferred← citeshttps://doi.org/10.1016/j.xpro.2024.102946openalex-snapshot
Protocol to analyze Drosophila intestinal tumor cellular heterogeneity using immunofluorescence imaging and nuclear size quantification
inferred← citeshttps://doi.org/10.1038/s41467-020-15617-xopenalex-snapshot
Circadian regulation of mitochondrial uncoupling and lifespan
inferred← citeshttps://doi.org/10.1038/s41467-024-45942-4openalex-snapshot
The emergence of circadian timekeeping in the intestine
inferred← citeshttps://doi.org/10.1038/s41467-024-46956-8openalex-snapshot
Cell-fate conversion of intestinal cells in adult Drosophila midgut by depleting a single transcription factor
inferred← citeshttps://doi.org/10.1038/s41467-024-53675-7openalex-snapshot
Nutrient-sensing alteration leads to age-associated distortion of intestinal stem cell differentiating direction
inferred← citeshttps://doi.org/10.1038/s41467-024-55664-2openalex-snapshot
Steroid hormone-induced wingless ligands tune female intestinal size in Drosophila
inferred← citeshttps://doi.org/10.1038/s41467-025-62043-yopenalex-snapshot
Age mosaic of gut epithelial cells prevents aging
inferred← citeshttps://doi.org/10.1038/s41556-021-00674-1openalex-snapshot
Remodelling of oxygen-transporting tracheoles drives intestinal regeneration and tumorigenesis in Drosophila
inferred← citeshttps://doi.org/10.1038/s41556-023-01116-wopenalex-snapshot
Basal stem cell progeny establish their apical surface in a junctional niche during turnover of an adult barrier epithelium
inferred← citeshttps://doi.org/10.1038/s41598-021-81261-0openalex-snapshot
Non-apoptotic enteroblast-specific role of the initiator caspase Dronc for development and homeostasis of the Drosophila intestine
inferred← citeshttps://doi.org/10.1038/s44319-026-00693-9openalex-snapshot
Toll signaling controls stem cell proliferation in intestinal regeneration and tumorigenesis
inferred← citeshttps://doi.org/10.1073/pnas.1719169115openalex-snapshot
Drosophila intestinal stem and progenitor cells are major sources and regulators of homeostatic niche signals
inferred← citeshttps://doi.org/10.1073/pnas.1913976117openalex-snapshot
JNK-dependent intestinal barrier failure disrupts host–microbe homeostasis during tumorigenesis
inferred← citeshttps://doi.org/10.1091/mbc.e19-10-0560openalex-snapshot
Mitochondria regulate intestinal stem cell proliferation and epithelial homeostasis through FOXO
inferred← citeshttps://doi.org/10.1093/g3journal/jkad084openalex-snapshot
Regulation of intestinal stem cell activity by a mitotic cell cycle regulator Polo in Drosophila
inferred← citeshttps://doi.org/10.1101/2019.12.19.882530openalex-snapshot
α-Phenylalanyl tRNA synthetase competes with Notch signaling through its N-terminal domain
inferred← citeshttps://doi.org/10.1101/2022.06.01.494390openalex-snapshot
The native cell differentiation program aberrantly recapitulated in yki 3S / A -induced intestinal hyperplasia drives invasiveness and cachexia-like wasting phenotypes
inferred← citeshttps://doi.org/10.1101/2022.07.21.500951openalex-snapshot
Molecular Underpinnings and Environmental Drivers of Spontaneous Loss of Heterozygosity in Drosophila Intestinal Stem Cells
inferred← citeshttps://doi.org/10.1101/2024.03.10.584282openalex-snapshot
Regenerative clustering of Enteroblasts in the Drosophila midgut revealed by a morphometric analysis
inferred← citeshttps://doi.org/10.1101/541912openalex-snapshot
Tumor establishment requires tumor autonomous and non-autonomous deregulation of homeostatic feedback control
inferred← citeshttps://doi.org/10.1101/685347openalex-snapshot
A bHLH interaction code controls bipotential differentiation and self-renewal in the Drosophila gut
inferred← citeshttps://doi.org/10.1126/sciadv.ads4229openalex-snapshot
Sex-dimorphic tumor growth is regulated by tumor microenvironmental and systemic signals
inferred← citeshttps://doi.org/10.1172/jci.insight.150894openalex-snapshot
Zinc finger protein 277 is an intestinal transit-amplifying cell marker and colon cancer oncogene
inferred← citeshttps://doi.org/10.1186/s12864-025-12451-7openalex-snapshot
Genome-wide identification and expression analysis of Wnt gene family in the forest musk deer (Moschus berezovskii) under musk secretion stage
inferred← citeshttps://doi.org/10.1186/s12964-017-0184-zopenalex-snapshot
Tissue-resident stem cell activity: a view from the adult Drosophila gastrointestinal tract
inferred← citeshttps://doi.org/10.1242/bio.059523openalex-snapshot
Drosophila hemocytes recognize lymph gland tumors of mxc mutants and activate the innate immune pathway in a reactive oxygen species-dependent manner
inferred← citeshttps://doi.org/10.1242/dev.153114openalex-snapshot
Inter-organ regulation of Drosophila intestinal stem cell proliferation by a hybrid organ boundary zone
inferred← citeshttps://doi.org/10.1242/dev.167643openalex-snapshot
JAK/STAT signaling in stem cells and regeneration: fromDrosophilato vertebrates
inferred← citeshttps://doi.org/10.1242/dev.189472openalex-snapshot
Evidence of two types of balance between stem cell mitosis and enterocyte nucleus growth in the Drosophila midgut
inferred← citeshttps://doi.org/10.1242/dev.204794openalex-snapshot
Toll signalling controls intestinal regeneration in Drosophila
inferred← citeshttps://doi.org/10.1242/dmm.052214openalex-snapshot
Autophagy inhibition in intestinal stem cells favors enteroendocrine cell differentiation through Stat92E activity
inferred← citeshttps://doi.org/10.12688/wellcomeopenres.23515.1openalex-snapshot
Drosophila AHR limits tumor growth and stem cell proliferation in the intestine
inferred← citeshttps://doi.org/10.12688/wellcomeopenres.23515.2openalex-snapshot
Drosophila AHR limits tumor growth and stem cell proliferation in the intestine
inferred← citeshttps://doi.org/10.12688/wellcomeopenres.23515.3openalex-snapshot
Drosophila AHR limits tumor growth and stem cell proliferation in the intestine
inferred← citeshttps://doi.org/10.1289/ehp6471openalex-snapshot
Effects of Inorganic Arsenic on Human Prostate Stem-Progenitor Cell Transformation, Autophagic Flux Blockade, and NRF2 Pathway Activation
inferred← citeshttps://doi.org/10.1371/journal.pbio.3003121openalex-snapshot
Werner syndrome exonuclease promotes gut regeneration and causes age-associated gut hyperplasia in Drosophila
inferred← citeshttps://doi.org/10.1371/journal.pgen.1006854openalex-snapshot
A genetic framework controlling the differentiation of intestinal stem cells during regeneration in Drosophila
inferred← citeshttps://doi.org/10.1371/journal.pgen.1008553openalex-snapshot
zfh2 controls progenitor cell activation and differentiation in the adult Drosophila intestinal absorptive lineage
inferred← citeshttps://doi.org/10.1371/journal.pgen.1009649openalex-snapshot
Aging-related upregulation of the homeobox gene caudal represses intestinal stem cell differentiation in Drosophila
inferred← citeshttps://doi.org/10.1371/journal.pgen.1010185openalex-snapshot
α-Phenylalanyl tRNA synthetase competes with Notch signaling through its N-terminal domain
inferred← citeshttps://doi.org/10.1371/journal.pgen.1011105openalex-snapshot
Glucocerebrosidase deficiency leads to neuropathology via cellular immune activation
inferred← citeshttps://doi.org/10.15252/embj.2018101346openalex-snapshot
Notch and EGFR regulate apoptosis in progenitor cells to ensure gut homeostasis in Drosophila
inferred← citeshttps://doi.org/10.15252/embj.2019104319openalex-snapshot
Loss of aryl hydrocarbon receptor potentiates FoxM1 signaling to enhance self‐renewal of colonic stem and progenitor cells
inferred← citeshttps://doi.org/10.15252/embr.201948892openalex-snapshot
Non‐apoptotic caspase activation preserves Drosophila intestinal progenitor cells in quiescence
inferred← citeshttps://doi.org/10.1534/g3.119.400633openalex-snapshot
Regulation of Drosophila Intestinal Stem Cell Proliferation by Enterocyte Mitochondrial Pyruvate Metabolism
inferred← citeshttps://doi.org/10.1534/genetics.118.300224openalex-snapshot
Anatomy and Physiology of the Digestive Tract of Drosophila melanogaster
inferred← citeshttps://doi.org/10.3389/fcell.2022.886773openalex-snapshot
Epithelial Cell Polarity During Drosophila Midgut Development
inferred← citeshttps://doi.org/10.3390/cells13221856openalex-snapshot
Regulation of the Intestinal Stem Cell Pool and Proliferation in Drosophila
inferred← citeshttps://doi.org/10.5772/intechopen.72318openalex-snapshot
The Hypoxia-Inducible Factor-1α in Angiogenesis and Cancer: Insights from the Drosophila Model
inferred← citeshttps://doi.org/10.64898/2026.05.29.728682openalex-snapshot
The Transcription Factor Sob Maintains Intestinal Stem Cell Homeostasis to Delay Ageing
inferred← citeshttps://doi.org/10.64898/2026.07.15.738595openalex-snapshot
Homeostatic control of stem cell activity during intestinal regeneration
inferred← citeshttps://doi.org/10.7554/elife.14330openalex-snapshot
A feedback amplification loop between stem cells and their progeny promotes tissue regeneration and tumorigenesis
inferred← citeshttps://doi.org/10.7554/elife.19662openalex-snapshot
Actin is an evolutionarily-conserved damage-associated molecular pattern that signals tissue injury in Drosophila melanogaster
inferred← citeshttps://doi.org/10.7554/elife.76366openalex-snapshot
De novo apical domain formation inside the Drosophila adult midgut epithelium
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