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

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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/dvg.20661openalex-snapshot

Characterization of midgut stem cell‐ and enteroblast‐specific Gal4 lines in drosophila

inferredcites →https://doi.org/10.1002/jcp.24872openalex-snapshot

The Role of Notch Receptors in Transcriptional Regulation

inferredcites →https://doi.org/10.1007/978-3-319-89512-3_8openalex-snapshot

Integration of Drosophila and Human Genetics to Understand Notch Signaling Related Diseases

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.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.devcel.2004.08.019openalex-snapshot

Apoptotic Cells Can Induce Compensatory Cell Proliferation through the JNK and the Wingless Signaling Pathways

inferredcites →https://doi.org/10.1016/j.devcel.2004.09.016openalex-snapshot

The Apical Caspase dronc Governs Programmed and Unprogrammed Cell Death in Drosophila

inferredcites →https://doi.org/10.1016/j.devcel.2018.01.020openalex-snapshot

Activation of the Notch Signaling Pathway In Vivo Elicits Changes in CSL Nuclear Dynamics

inferredcites →https://doi.org/10.1016/j.devcel.2018.04.020openalex-snapshot

Plasma Membrane Localization of Apoptotic Caspases for Non-apoptotic Functions

inferredcites →https://doi.org/10.1016/j.semcdb.2017.10.034openalex-snapshot

Non-apoptotic Caspase regulation of stem cell properties

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.stemcr.2017.04.002openalex-snapshot

Intestinal Stem Cell Pool Regulation in Drosophila

inferredcites →https://doi.org/10.1016/j.str.2016.11.002openalex-snapshot

A Near-Atomic Structure of the Dark Apoptosome Provides Insight into Assembly and Activation

inferredcites →https://doi.org/10.1016/j.yexcr.2011.07.020openalex-snapshot

Intestinal stem cells in the adult Drosophila midgut

inferredcites →https://doi.org/10.1016/j.ymeth.2014.03.029openalex-snapshot

Tools and methods for studying Notch signaling in Drosophila melanogaster

inferredcites →https://doi.org/10.1016/s0960-9822(01)00657-1openalex-snapshot

sickle, a Novel Drosophila Death Gene in the reaper/hid/grim Region, Encodes an IAP-Inhibitory Protein

inferredcites →https://doi.org/10.1016/s0960-9822(01)00658-3openalex-snapshot

The Damage-Responsive Drosophila Gene sickle Encodes a Novel IAP Binding Protein Similar to but Distinct from reaper, grim, and hid

inferredcites →https://doi.org/10.1016/s0960-9822(01)00664-9openalex-snapshot

Drosophila sickle Is a Novel grim-reaper Cell Death Activator

inferredcites →https://doi.org/10.1038/12984openalex-snapshot

Dark is a Drosophila homologue of Apaf-1/CED-4 and functions in an evolutionarily conserved death pathway

inferredcites →https://doi.org/10.1038/cdd.2008.50openalex-snapshot

Regulation of apoptosis in Drosophila

inferredcites →https://doi.org/10.1038/cdd.2017.111openalex-snapshot

CDPs: caspase-dependent non-lethal cellular processes

inferredcites →https://doi.org/10.1038/cdd.2017.37openalex-snapshot

Evolution of caspase-mediated cell death and differentiation: twins separated at birth

inferredcites →https://doi.org/10.1038/jid.2015.119openalex-snapshot

Regulation and Function of the Caspase-1 in an Inflammatory Microenvironment

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/nmeth.2019openalex-snapshot

Fiji: an open-source platform for biological-image analysis

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.cdd.4401920openalex-snapshot

The effector caspases drICE and dcp-1 have partially overlapping functions in the apoptotic pathway in Drosophila

inferredcites →https://doi.org/10.1073/pnas.1719169115openalex-snapshot

Drosophila intestinal stem and progenitor cells are major sources and regulators of homeostatic niche signals

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/10.1080/15216549600201061openalex-snapshot

Paraquat induced DNA damage by reactive oxygen species

inferredcites →https://doi.org/10.1093/emboj/19.4.589openalex-snapshot

Induction of apoptosis by Drosophila reaper, hid and grim through inhibition of IAP function

inferredcites →https://doi.org/10.1101/cshperspect.a008672openalex-snapshot

Cellular Mechanisms Controlling Caspase Activation and Function

inferredcites →https://doi.org/10.1101/cshperspect.a008730openalex-snapshot

Inhibitor of Apoptosis (IAP) Proteins-Modulators of Cell Death and Inflammation

inferredcites →https://doi.org/10.1101/gad.7.10.1949openalex-snapshot

Antineurogenic phenotypes induced by truncated Notch proteins indicate a role in signal transduction and may point to a novel function for Notch in nuclei.

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.aab0988openalex-snapshot

Bidirectional Notch signaling regulates Drosophila intestinal stem cell multipotency

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/10.1146/annurev-biochem-061809-121639openalex-snapshot

Caspase Substrates and Cellular Remodeling

inferredcites →https://doi.org/10.1146/annurev-ento-112408-085450openalex-snapshot

Regulation of Midgut Growth, Development, and Metamorphosis

inferredcites →https://doi.org/10.1146/annurev.neuro.051508.135600openalex-snapshot

The Glial Nature of Embryonic and Adult Neural Stem Cells

inferredcites →https://doi.org/10.1155/2018/5473180openalex-snapshot

Learning on the Fly: The Interplay between Caspases and Cancer

inferredcites →https://doi.org/10.1186/s12859-017-1934-zopenalex-snapshot

ImageJ2: ImageJ for the next generation of scientific image data

inferredcites →https://doi.org/10.1242/dev.01790openalex-snapshot

The CARD-carrying caspase Dronc is essential for most, but not all,developmental cell death in Drosophila

inferredcites →https://doi.org/10.1242/dev.058347openalex-snapshot

Dronc caspase exerts a non-apoptotic function to restrain phospho-Numb-induced ectopic neuroblast formation in Drosophila

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

Stem cells living with a Notch

inferredcites →https://doi.org/10.1242/dev.100933openalex-snapshot

Accelerated homologous recombination and subsequent genome modification in Drosophila

inferredcites →https://doi.org/10.1242/dev.149807openalex-snapshot

A fluorescent toolkit for spatiotemporal tracking of apoptotic cells in living Drosophila tissues

inferredcites →https://doi.org/10.1242/dev.170811openalex-snapshot

Novel initiator caspase reporters uncover previously unknown features of caspase-activating cells

inferredcites →https://doi.org/10.1242/dmm.006908openalex-snapshot

Modeling tumor invasion and metastasis inDrosophila

inferredcites →https://doi.org/10.1242/dmm.024232openalex-snapshot

Gastrointestinal stem cells in health and disease: from flies to humans

inferredcites →https://doi.org/10.1242/jcs.01376openalex-snapshot

Mechanism of Dronc activation in Drosophila cells

inferredcites →https://doi.org/10.1242/jcs.125294openalex-snapshot

TSC1/2 regulates intestinal stem cell maintenance and lineage differentiation via Rheb-TORC1-S6K but independent of nutrition status or Notch regulation

inferredcites →https://doi.org/10.1371/journal.pgen.1003045openalex-snapshot

Notch-Mediated Suppression of TSC2 Expression Regulates Cell Differentiation in the Drosophila Intestinal Stem Cell Lineage

inferredcites →https://doi.org/10.1371/journal.pgen.1006438openalex-snapshot

An inhibitory mono-ubiquitylation of the Drosophila initiator caspase Dronc functions in both apoptotic and non-apoptotic pathways

inferredcites →https://doi.org/10.1371/journal.pgen.1006854openalex-snapshot

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

inferredcites →https://doi.org/10.1371/journal.pgen.1007054openalex-snapshot

A systems level approach to temporal expression dynamics in Drosophila reveals clusters of long term memory genes

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/10.15252/embj.2018101346openalex-snapshot

Notch and EGFR regulate apoptosis in progenitor cells to ensure gut homeostasis in Drosophila

inferredcites →https://doi.org/10.1534/g3.113.007021openalex-snapshot

FlyPrimerBank: An Online Database for Drosophila melanogaster Gene Expression Analysis and Knockdown Evaluation of RNAi Reagents

inferredcites →https://doi.org/10.1534/genetics.118.300224openalex-snapshot

Anatomy and Physiology of the Digestive Tract of Drosophila melanogaster

inferredcites →https://doi.org/10.22034/apjcp.2018.19.5.1277openalex-snapshot

Expression Level of Caspase Genes in Colorectal Cancer

inferredcites →https://doi.org/10.7554/elife.00999openalex-snapshot

Brahma is essential for Drosophila intestinal stem cell proliferation and regulated by Hippo signaling

What points at this work

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

inferred← citeshttps://doi.org/10.1016/j.celrep.2022.110718openalex-snapshot

Non-apoptotic activation of Drosophila caspase-2/9 modulates JNK signaling, the tumor microenvironment, and growth of wound-like tumors

inferred← citeshttps://doi.org/10.1101/722330openalex-snapshot

Non-apoptotic caspase activation sustains ovarian somatic stem cell functions by modulating Hedgehog-signalling and autophagy

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