On the public citation graph

A genetic framework controlling the differentiation of intestinal stem cells during regeneration in Drosophila

https://doi.org/10.1371/journal.pgen.1006854

0 signed · 138 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 See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.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/10.1002/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/10.1007/s00018-008-8281-1openalex-snapshot

The cell-cell adhesion molecule E-cadherin

inferredcites →https://doi.org/10.1016/0092-8674(92)90426-dopenalex-snapshot

Connectin: A homophilic cell adhesion molecule expressed on a subset of muscles and the motoneurons that innervate them in Drosophila

inferredcites →https://doi.org/10.1016/j.bbagen.2012.08.009openalex-snapshot

Sending the right signal: Notch and stem cells

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.2011.08.048openalex-snapshot

Altered Modes of Stem Cell Division Drive Adaptive Intestinal Growth

inferredcites →https://doi.org/10.1016/j.cell.2014.10.028openalex-snapshot

Age-Associated Loss of Lamin-B Leads to Systemic Inflammation and Gut Hyperplasia

inferredcites →https://doi.org/10.1016/j.celrep.2013.02.022openalex-snapshot

Homeostatic Epithelial Renewal in the Gut Is Required for Dampening a Fatal Systemic Wound Response in Drosophila

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.2015.09.061openalex-snapshot

A Sox Transcription Factor Is a Critical Regulator of Adult Stem Cell Proliferation in the Drosophila Intestine

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.devcel.2017.02.009openalex-snapshot

Cell-Cell Contact Area Affects Notch Signaling and Notch-Dependent Patterning

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.gde.2016.06.009openalex-snapshot

Maintenance of the adult Drosophila intestine: all roads lead to homeostasis

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.2008.10.016openalex-snapshot

Tissue Damage-Induced Intestinal Stem Cell Division in Drosophila

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.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.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.2014.12.017openalex-snapshot

Dpp/Gbb signaling is required for normal intestinal regeneration during infection

inferredcites →https://doi.org/10.1016/j.ydbio.2015.12.017openalex-snapshot

GATAe regulates intestinal stem cell maintenance and differentiation in Drosophila adult midgut

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/10.1016/s0896-6273(00)80327-xopenalex-snapshot

Connectin Mediates Adhesion in Drosophila

inferredcites →https://doi.org/10.1038/emboj.2012.106openalex-snapshot

Drosophila midgut homeostasis involves neutral competition between symmetrically dividing intestinal stem 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/nature16170openalex-snapshot

Signal integration by Ca2+ regulates intestinal stem-cell activity

inferredcites →https://doi.org/10.1038/nature16953openalex-snapshot

The sexual identity of adult intestinal stem cells controls organ size and plasticity

inferredcites →https://doi.org/10.1038/ncb3214openalex-snapshot

Niche appropriation by Drosophila intestinal stem cell tumours

inferredcites →https://doi.org/10.1038/ncomms10219openalex-snapshot

Accumulation of differentiating intestinal stem cell progenies drives tumorigenesis

inferredcites →https://doi.org/10.1038/ng.225openalex-snapshot

MYO5B mutations cause microvillus inclusion disease and disrupt epithelial cell polarity

inferredcites →https://doi.org/10.1038/nrm.2016.94openalex-snapshot

Notch signalling in context

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.2008.343openalex-snapshot

Cadherins and cancer: how does cadherin dysfunction promote tumor progression?

inferredcites →https://doi.org/10.1073/pnas.1109348108openalex-snapshot

Nonautonomous regulation of Drosophila midgut stem cell proliferation by the insulin-signaling pathway

inferredcites →https://doi.org/10.1083/jcb.201302049openalex-snapshot

Injury-induced BMP signaling negatively regulates Drosophila midgut homeostasis

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/gad.287404openalex-snapshot

Loss of Apc in vivo immediately perturbs Wnt signaling, differentiation, and migration

inferredcites →https://doi.org/10.1111/j.1365-2443.2008.01239.xopenalex-snapshot

E‐cadherin prolongs the moment for interaction between intestinal stem cell and its progenitor cell to ensure Notch signaling in adult Drosophila midgut

inferredcites →https://doi.org/10.1111/j.1474-9726.2008.00380.xopenalex-snapshot

Age‐related changes in Drosophila midgut are associated with PVF2, a PDGF/VEGF‐like growth factor

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/10.1146/annurev.physiol.010908.163145openalex-snapshot

Stem Cells, Self-Renewal, and Differentiation in the Intestinal Epithelium

inferredcites →https://doi.org/10.1242/dev.080614openalex-snapshot

Stem cells living with a Notch

inferredcites →https://doi.org/10.1242/dev.104240openalex-snapshot

Sara endosomes and the asymmetric division of intestinal stem cells

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.137950openalex-snapshot

Diversity of fate outcomes in cell pairs under lateral inhibition

inferredcites →https://doi.org/10.1371/journal.pgen.1006089openalex-snapshot

Remote Control of Intestinal Stem Cell Activity by Haemocytes in Drosophila

inferredcites →https://doi.org/10.15252/embj.201489050openalex-snapshot

Regulation of Drosophila intestinal stem cell maintenance and differentiation by the transcription factor Escargot

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/10.7554/elife.00886openalex-snapshot

Physiological and stem cell compartmentalization within the Drosophila midgut

inferredcites →https://doi.org/10.7554/elife.01857openalex-snapshot

Intestinal epithelium-derived BMP controls stem cell self-renewal in Drosophila adult midgut

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

inferredcites →https://doi.org/10.7554/elife.06930openalex-snapshot

Endocrine remodelling of the adult intestine sustains reproduction in Drosophila

inferredcites →https://doi.org/10.7554/elife.10956openalex-snapshot

Sex difference in pathology of the ageing gut mediates the greater response of female lifespan to dietary restriction

inferredcites →https://doi.org/10.7554/elife.12068openalex-snapshot

A genome-wide resource for the analysis of protein localisation in Drosophila

inferredcites →https://doi.org/10.7554/elife.14330openalex-snapshot

A feedback amplification loop between stem cells and their progeny promotes tissue regeneration and tumorigenesis

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.3295385openalex-extracted

Heparan Sulfate Maintains Tissue Homeostasis in Drosophila Adult Midgut

inferred← citeshttps://doi.org/10.2139/ssrn.3300045openalex-extracted

Heparan Sulfate Maintains Tissue Homeostasis in Drosophila Adult Midgut

inferred← citeshttps://doi.org/10.1002/bies.201700128openalex-snapshot

Cell Polarity and Notch Signaling: Linked by the E3 Ubiquitin Ligase Neuralized?

inferred← citeshttps://doi.org/10.1002/cbin.11289openalex-snapshot

Heparan sulfate maintains adult midgut homeostasis in Drosophila

inferred← citeshttps://doi.org/10.1016/b978-0-12-820071-1.00017-7openalex-snapshot

Gut stem cells: Interplay with immune system, microbiota, and aging

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.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.2025.115505openalex-snapshot

Mitochondrial fission regulates midgut muscle assembly and tick feeding capacity

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.chom.2019.08.006openalex-snapshot

Recruitment of Adult Precursor Cells Underlies Limited Repair of the Infected Larval Midgut in Drosophila

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.2021.06.007openalex-snapshot

Microenvironmental innate immune signaling and cell mechanical responses promote tumor growth

inferred← citeshttps://doi.org/10.1016/j.devcel.2023.08.022openalex-snapshot

Nutrient-driven dedifferentiation of enteroendocrine cells promotes adaptive intestinal growth in Drosophila

inferred← citeshttps://doi.org/10.1016/j.ibmb.2019.103306openalex-snapshot

GATAe transcription factor is involved in Bacillus thuringiensis Cry1Ac toxin receptor gene expression inducing toxin susceptibility

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.2025.111967openalex-snapshot

Aberrant enterocyte progenitor clustering as an early life biomarker of Drosophila aging

inferred← citeshttps://doi.org/10.1016/j.it.2020.01.002openalex-snapshot

Taking Insect Immunity to the Single-Cell Level

inferred← citeshttps://doi.org/10.1016/j.jinsphys.2021.104309openalex-snapshot

Anchor maintains gut homeostasis by restricting the JNK and Notch pathways in Drosophila

inferred← citeshttps://doi.org/10.1016/j.pestbp.2023.105516openalex-snapshot

Helicoverpa armigera GATAe transcriptional factor regulates the expression of Bacillus thuringiensis Cry1Ac receptor gene ABCC2 by its interplay with additional transcription factors

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.stemcr.2022.03.010openalex-snapshot

Auxilin regulates intestinal stem cell proliferation through EGFR

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/10.1016/j.ydbio.2023.10.008openalex-snapshot

Experimental validation and characterization of putative targets of Escargot and STAT, two master regulators of the intestinal stem cells in Drosophila melanogaster

inferred← citeshttps://doi.org/10.1038/s41419-025-07954-wopenalex-snapshot

Auxilin in enterocytes controls intestinal homeostasis through inter-cell communication

inferred← citeshttps://doi.org/10.1038/s41467-023-44553-9openalex-snapshot

Drosophila activins adapt gut size to food intake and promote regenerative growth

inferred← citeshttps://doi.org/10.1038/s41467-024-46119-9openalex-snapshot

Polycomb-mediated silencing of miR-8 is required for maintenance of intestinal stemness in Drosophila melanogaster

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/s41467-024-55255-1openalex-snapshot

A feedback loop between Paxillin and Yorkie sustains Drosophila intestinal homeostasis and regeneration

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/s41598-024-80994-yopenalex-snapshot

Remote disruption of intestinal homeostasis by Mycobacterium abscessus is detrimental to Drosophila survival

inferred← citeshttps://doi.org/10.1080/19336934.2022.2066952openalex-snapshot

Cellular mechanisms underlying adult tissue plasticity in Drosophila

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/10.1101/2023.05.08.539820openalex-snapshot

Nutrient-driven dedifferentiation of enteroendocrine cells promotes adaptive intestinal growth

inferred← citeshttps://doi.org/10.1101/2023.07.04.547653openalex-snapshot

Highly regenerative species-specific genes improve age-associated features in the adult Drosophila midgut

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/10.1101/2024.12.29.630675openalex-snapshot

Organ injury accelerates stem cell differentiation by modulating a fate-transducing lateral inhibition circuit

inferred← citeshttps://doi.org/10.1101/2025.04.04.647274openalex-snapshot

Loofah, a newly characterized adhesion protein, suppresses cell death in long-lived Drosophila hindgut enterocytes

inferred← citeshttps://doi.org/10.1101/707380openalex-snapshot

Non-apoptotic caspase-dependent regulation of enteroblast quiescence in Drosophila

inferred← citeshttps://doi.org/10.1126/sciadv.ady7272openalex-snapshot

Drosophila and mouse intestinal stem cells are spatiotemporally specified by Notch suppression and Wnt activation

inferred← citeshttps://doi.org/10.1186/s12915-024-01956-4openalex-snapshot

Highly regenerative species-specific genes improve age-associated features in the adult Drosophila midgut

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.047126openalex-snapshot

Heparan sulfate negatively regulates intestinal stem cell proliferation in Drosophila adult midgut

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.173781openalex-snapshot

Model systems for regeneration: Drosophila

inferred← citeshttps://doi.org/10.1242/dev.178087openalex-snapshot

Novel roles for GATAe in growth, maintenance and proliferation of cell populations in the Drosophila renal tubule

inferred← citeshttps://doi.org/10.1242/dev.204789openalex-snapshot

Kuzbanian expression levels dictate Notch signaling outcomes via interplay between cis- and trans- Delta

inferred← citeshttps://doi.org/10.1242/dev.204835openalex-snapshot

Loofah suppresses cell death in long-lived Drosophila hindgut enterocytes

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/10.1242/jeb.242262openalex-snapshot

Thermal stress induces tissue damage and a broad shift in regenerative signaling pathways in the honey bee digestive tract

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/10.1387/ijdb.180056cropenalex-snapshot

Reservoirs for repair? Damage-responsive stem cells and adult tissue regeneration in Drosophila

inferred← citeshttps://doi.org/10.15252/embr.201948892openalex-snapshot

Non‐apoptotic caspase activation preserves Drosophila intestinal progenitor cells in quiescence

inferred← citeshttps://doi.org/10.15252/embr.202050047openalex-snapshot

Ageing, metabolism and the intestine

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/10.3389/fcell.2022.886773openalex-snapshot

Epithelial Cell Polarity During Drosophila Midgut Development

inferred← citeshttps://doi.org/10.3389/fcell.2025.1508714openalex-snapshot

The Batten disease gene Cln3 is required for the activation of intestinal stem cell during regeneration via JAK/STAT signaling in Drosophila

inferred← citeshttps://doi.org/10.3389/fimmu.2025.1744692openalex-snapshot

The paradigm shift: re-evaluating preclinical animal models for colorectal cancer in the precision medicine era

inferred← citeshttps://doi.org/10.3390/cancers17132163openalex-snapshot

Exploring Experimental Models of Colorectal Cancer: A Critical Appraisal from 2D Cell Systems to Organoids, Humanized Mouse Avatars, Organ-on-Chip, CRISPR Engineering, and AI-Driven Platforms—Challenges and Opportunities for Translational Precision Oncology

inferred← citeshttps://doi.org/10.3390/genes9030138openalex-snapshot

Wnt Signalling in Intestinal Stem Cells: Lessons from Mice and Flies

inferred← citeshttps://doi.org/10.3390/ijms21176362openalex-snapshot

Tissue Adaptation to Environmental Cues by Symmetric and Asymmetric Division Modes of Intestinal Stem Cells

inferred← citeshttps://doi.org/10.3390/jdb6010002openalex-snapshot

The Biology of SUMO-Targeted Ubiquitin Ligases in Drosophila Development, Immunity, and Cancer

inferred← citeshttps://doi.org/10.64898/2026.02.12.705584openalex-snapshot

Evidence that injury can cause Drosophila gut differentiated, polyploid enterocytes to be recruited as stem cells via paligenosis

inferred← citeshttps://doi.org/10.64898/2026.07.15.738595openalex-snapshot

Homeostatic control of stem cell activity during intestinal regeneration

inferred← citeshttps://doi.org/10.64898/2026.08.13.744616openalex-snapshot

Higher-Order Mechanical Neighbourhood Sensing Governs Cell Fate in Complex Tissues

inferred← citeshttps://doi.org/10.70675/28d7e4efzd3bfz4e34zb4c4z2c4a0a12f300openalex-snapshot

Contributions to the study of host-pathogen interactions between Drosophila melanogaster and Seatia marcescens

inferred← citeshttps://doi.org/10.70675/7780fc44z241cz4a6fz95bez2efbc90bd685openalex-snapshot

Effet des bioinsecticides à base de Bacillus thuringiensis sur la physiologie intestinale de la Drosophile

inferred← citeshttps://doi.org/10.70675/bc56be9ez511ez4984z976cz95d9aa85e1d9openalex-snapshot

Identification des facteurs de susceptibilité de l'hôte à l'infection par Mycobacterium abscessus en utilisant Drosophila melanogaster comme modèle

inferred← citeshttps://doi.org/10.7554/elife.36248openalex-snapshot

Long-term live imaging of the Drosophila adult midgut reveals real-time dynamics of division, differentiation and loss

inferred← citeshttps://doi.org/10.7554/elife.72836openalex-snapshot

Vinculin recruitment to α-catenin halts the differentiation and maturation of enterocyte progenitors to maintain homeostasis of the Drosophila intestine

inferred← citeshttps://doi.org/10.7554/elife.76366openalex-snapshot

De novo apical domain formation inside the Drosophila adult midgut epithelium

inferred← citeshttps://doi.org/10.7554/elife.80179openalex-snapshot

Bacillus thuringiensis toxins divert progenitor cells toward enteroendocrine fate by decreasing cell adhesion with intestinal stem cells 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.