On the public citation graph

Steroid regulation of programmed cell death during Drosophila development

https://doi.org/10.1038/sj.cdd.4400753
0 signed · 191 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 See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.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/(sici)1097-4695(199903)38:4<455::aid-neu2>3.0.co;2-fopenalex-snapshot
Genetic and hormonal regulation of the death of peptidergic neurons in theDrosophila central nervous system
inferredcites →https://doi.org/10.1002/bies.950170806openalex-snapshot
The making of a fly leg: A model for epithelial morphogenesis
inferredcites →https://doi.org/10.1002/j.1460-2075.1994.tb06657.xopenalex-snapshot
The Broad‐Complex directly controls a tissue‐specific response to the steroid hormone ecdysone at the onset of Drosophila metamorphosis.
inferredcites →https://doi.org/10.1002/j.1460-2075.1995.tb00314.xopenalex-snapshot
Molecular analysis of a steroid‐induced regulatory hierarchy: the Drosophila E74A protein directly regulates L71–6 transcription.
inferredcites →https://doi.org/10.1002/j.1460-2075.1995.tb07021.xopenalex-snapshot
Glucocorticoid‐induced apoptosis of human leukemic cells is caused by the repressive function of the glucocorticoid receptor.
inferredcites →https://doi.org/10.1002/jmor.1050590207openalex-snapshot
The metamorphosis of Drosophila melanogaster, including an accurately timed account of the principal morphological changes
inferredcites →https://doi.org/10.1002/pros.2990050510openalex-snapshot
Antagonistic effect of androgen on prostatic cell death
inferredcites →https://doi.org/10.1002/tera.1420070306openalex-snapshot
The morphology of various types of cell death in prenatal tissues
inferredcites →https://doi.org/10.1006/dbio.1996.0343openalex-snapshot
TheDrosophila Broad-ComplexEarly Gene Directly Regulates Late Gene Transcription during the Ecdysone-Induced Puffing Cascade
inferredcites →https://doi.org/10.1006/dbio.1997.8696openalex-snapshot
Genes That Induce Apoptosis: Transcriptional Regulation in Identified, Doomed Neurons of theDrosophilaCNS
inferredcites →https://doi.org/10.1006/dbio.1998.9000openalex-snapshot
Dredd,a Novel Effector of the Apoptosis ActivatorsReaper, Grim,andHidinDrosophila
inferredcites →https://doi.org/10.1006/jmbi.1996.0032openalex-snapshot
Molecular Characterization of the 71E Late Puff in Reveals a Family of Novel Genes
inferredcites →https://doi.org/10.1007/bf00048064openalex-snapshot
Active cell death in hormone-dependent tissues
inferredcites →https://doi.org/10.1007/bf00174615openalex-snapshot
Developmental cell death: morphological diversity and multiple mechanisms
inferredcites →https://doi.org/10.1007/bf00188753openalex-snapshot
Mutations in a steroid hormone-regulated gene disrupt the metamorphosis of internal tissues in Drosophila: salivary glands, muscle, and gut
inferredcites →https://doi.org/10.1007/bf00220285openalex-snapshot
Substrate-histochemical investigations and ultrahistochemical demonstrations of acid phosphatase in larval and prepupal salivary glands of Drosophila melanogaster
inferredcites →https://doi.org/10.1007/bf00327339openalex-snapshot
Die Puffs der Speicheldr�senchromosomen von Drosophila melanogaster
inferredcites →https://doi.org/10.1007/bf00336950openalex-snapshot
Patterns of puffing activity in the salivary gland chromosomes of Drosophila
inferredcites →https://doi.org/10.1007/bf00396591openalex-snapshot
Die Puffs der Speicheldrüsenchromosomen von Drosophila Melanogastee
inferredcites →https://doi.org/10.1016/0012-1606(82)90240-8openalex-snapshot
Ecdysteroid titers during pupal and adult development in Drosophila melanogaster
inferredcites →https://doi.org/10.1016/0012-1606(84)90179-9openalex-snapshot
Steroid regulation of RNAs transcribed from the Drosophila 68C polytene chromosome puff
inferredcites →https://doi.org/10.1016/0022-1910(64)90034-4openalex-snapshot
Programmed cell death—II. Endocrine potentiation of the breakdown of the intersegmental muscles of silkmoths
inferredcites →https://doi.org/10.1016/0022-1910(65)90099-5openalex-snapshot
Programmed cell death—I. Cytology of degeneration in the intersegmental muscles of the Pernyi silkmoth
inferredcites →https://doi.org/10.1016/0092-8674(90)90205-sopenalex-snapshot
Puffs, genes, and hormones revisited
inferredcites →https://doi.org/10.1016/0092-8674(90)90217-3openalex-snapshot
The Drosophila 74EF early puff contains E74, a complex ecdysone-inducible gene that encodes two ets-related proteins
inferredcites →https://doi.org/10.1016/0092-8674(90)90287-oopenalex-snapshot
Molecular interactions within the ecdysone regulatory hierarchy: DNA binding properties of the Drosophila ecdysone-inducible E74A protein
inferredcites →https://doi.org/10.1016/0092-8674(91)90572-gopenalex-snapshot
The drosophila EcR gene encodes an ecdysone receptor, a new member of the steroid receptor superfamily
inferredcites →https://doi.org/10.1016/0092-8674(92)90266-fopenalex-snapshot
Drosophila ultraspiracle modulates ecdysone receptor function via heterodimer formation
inferredcites →https://doi.org/10.1016/0092-8674(94)90546-0openalex-snapshot
A molecular mechanism for the stage specificity of the Drosophila prepupal genetic response to ecdysone
inferredcites →https://doi.org/10.1016/0092-8674(95)90150-7openalex-snapshot
Drosophila homologs of baculovirus inhibitor of apoptosis proteins function to block cell death
inferredcites →https://doi.org/10.1016/0168-9525(92)90079-jopenalex-snapshot
Hormones, puffs and flies: the molecular control of metamorphosis by ecdysone
inferredcites →https://doi.org/10.1016/0303-7207(81)90013-7openalex-snapshot
The radioimmune assay of ecdysteroid titres in drosophila melanogaster
inferredcites →https://doi.org/10.1016/0965-1748(93)90087-9openalex-snapshot
The reaction with polytene chromosomes of antibodies raised against Drosophila E75A protein
inferredcites →https://doi.org/10.1016/s0022-2836(86)80002-xopenalex-snapshot
An ecdysterone-responsive puff site in Drosophila contains a cluster of seven differentially regulated genes
inferredcites →https://doi.org/10.1016/s0092-8674(00)80466-3openalex-snapshot
Drosophila Ecdysone Receptor Mutations Reveal Functional Differences among Receptor Isoforms
inferredcites →https://doi.org/10.1016/s0092-8674(00)80564-4openalex-snapshot
Cell Death in Development
inferredcites →https://doi.org/10.1016/s0092-8674(00)81873-5openalex-snapshot
Programmed Cell Death in Animal Development
inferredcites →https://doi.org/10.1016/s0092-8674(00)81974-1openalex-snapshot
The Drosophila Caspase Inhibitor DIAP1 Is Essential for Cell Survival and Is Negatively Regulated by HID
inferredcites →https://doi.org/10.1016/s0168-9525(97)01126-8openalex-snapshot
Facing death in the fly: genetic analysis of apoptosis in Drosophila
inferredcites →https://doi.org/10.1016/s0960-9822(00)00474-7openalex-snapshot
The Drosophila Bcl-2 family member dBorg-1 functions in the apoptotic response to UV-irradiation
inferredcites →https://doi.org/10.1016/s0962-8924(99)01646-3openalex-snapshot
An emerging blueprint for apoptosis in Drosophila
inferredcites →https://doi.org/10.1016/s1097-2765(00)00042-3openalex-snapshot
E93 Directs Steroid-Triggered Programmed Cell Death in Drosophila
inferredcites →https://doi.org/10.1016/s1097-2765(00)80305-6openalex-snapshot
The Drosophila βFTZ-F1 Orphan Nuclear Receptor Provides Competence for Stage-Specific Responses to the Steroid Hormone Ecdysone
inferredcites →https://doi.org/10.1016/s1097-2765(00)80385-8openalex-snapshot
HAC-1, a Drosophila Homolog of APAF-1 and CED-4, Functions in Developmental and Radiation-Induced Apoptosis
inferredcites →https://doi.org/10.1016/s1097-2765(00)80386-xopenalex-snapshot
Control of the Cell Death Pathway by Dapaf-1, a Drosophila Apaf-1/CED-4-Related Caspase Activator
inferredcites →https://doi.org/10.1016/s1097-2765(00)80439-6openalex-snapshot
A Steroid-Triggered Transcriptional Hierarchy Controls Salivary Gland Cell Death during Drosophila Metamorphosis
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/10.1038/284555a0openalex-snapshot
Glucocorticoid-induced thymocyte apoptosis is associated with endogenous endonuclease activation
inferredcites →https://doi.org/10.1038/347298a0openalex-snapshot
Relationship between the product of the Drosophila ultraspiracle locus and the vertebrate retinoid X receptor
inferredcites →https://doi.org/10.1038/362471a0openalex-snapshot
Heterodimerization of the Drosophila ecdysone receptor with retinoid X receptor and ultraspiracle
inferredcites →https://doi.org/10.1038/sj.cdd.4400216openalex-snapshot
Rearrangement of the tubulin and actin cytoskeleton during programmed cell death in Drosophila salivary glands
inferredcites →https://doi.org/10.1073/pnas.90.3.980openalex-snapshot
Do all programmed cell deaths occur via apoptosis?
inferredcites →https://doi.org/10.1073/pnas.94.20.10717openalex-snapshot
CLARP, a death effector domain-containing protein interacts with caspase-8 and regulates apoptosis
inferredcites →https://doi.org/10.1073/pnas.96.8.4307openalex-snapshot
DRONC, an ecdysone-inducible Drosophila caspase
inferredcites →https://doi.org/10.1073/pnas.97.2.662openalex-snapshot
Drob-1, a Drosophila member of the Bcl-2/CED-9 family that promotes cell death
inferredcites →https://doi.org/10.1074/jbc.274.43.30778openalex-snapshot
DECAY, a Novel Drosophila Caspase Related to Mammalian Caspase-3 and Caspase-7
inferredcites →https://doi.org/10.1080/01483918708066815openalex-snapshot
A Developmental Analysis of Ecdysteroids During the Metamorphosis ofDrosophila Melanogaster
inferredcites →https://doi.org/10.1083/jcb.101.1.189openalex-snapshot
The pupal cuticle of Drosophila: biphasic synthesis of pupal cuticle proteins in vivo and in vitro in response to 20-hydroxyecdysone.
inferredcites →https://doi.org/10.1083/jcb.148.4.703openalex-snapshot
Debcl, a Proapoptotic Bcl-2 Homologue, Is a Component of the Drosophila melanogaster Cell Death Machinery
inferredcites →https://doi.org/10.1093/emboj/16.10.2805openalex-snapshot
Identification of a Drosophila melanogaster ICE/CED‐3‐related protease, drICE
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/10.1093/genetics/129.2.385openalex-snapshot
The Drosophila Broad-Complex encodes a family of related proteins containing zinc fingers.
inferredcites →https://doi.org/10.1093/genetics/130.3.555openalex-snapshot
Developmental arrest and ecdysteroid deficiency resulting from mutations at the dre4 locus of Drosophila.
inferredcites →https://doi.org/10.1093/genetics/141.3.1025openalex-snapshot
The ecdysone-inducible Broad-complex and E74 early genes interact to regulate target gene transcription and Drosophila metamorphosis.
inferredcites →https://doi.org/10.1093/genetics/154.2.669openalex-snapshot
Diverse Domains of THREAD/DIAP1 Are Required to Inhibit Apoptosis Induced by REAPER and HID in Drosophila
inferredcites →https://doi.org/10.1093/nar/18.14.4143openalex-snapshot
A steroid/thyroid hormone receptor superfamily member inDrosophila melanogasterthat shares extensive sequence similarity with a mammalian homologue
inferredcites →https://doi.org/10.1101/gad.10.14.1773openalex-snapshot
grim, a novel cell death gene in Drosophila.
inferredcites →https://doi.org/10.1101/gad.4.2.204openalex-snapshot
The E75 ecdysone-inducible gene responsible for the 75B early puff in Drosophila encodes two new members of the steroid receptor superfamily.
inferredcites →https://doi.org/10.1101/gad.4.7.1128openalex-snapshot
Proteins that bind to Drosophila chorion cis-regulatory elements: a new C2H2 zinc finger protein and a C2C2 steroid receptor-like component.
inferredcites →https://doi.org/10.1101/gad.9.14.1694openalex-snapshot
The head involution defective gene of Drosophila melanogaster functions in programmed cell death.
inferredcites →https://doi.org/10.1101/sqb.1974.038.01.070openalex-snapshot
Temporal Control of Puffing Activity in Polytene Chromosomes
inferredcites →https://doi.org/10.1111/j.1601-5223.1989.tb00418.xopenalex-snapshot
Steroid regulation of glue protein genes in Drosophila melanogaster
inferredcites →https://doi.org/10.1126/science.146.3645.794openalex-snapshot
Actinomycin and Puromycin: Effects on Sequential Gene Activation by Ecdysone
inferredcites →https://doi.org/10.1126/science.275.5299.536openalex-snapshot
DCP-1, a Drosophila Cell Death Protease Essential for Development
inferredcites →https://doi.org/10.1126/science.7878464openalex-snapshot
Apoptosis in the Pathogenesis and Treatment of Disease
inferredcites →https://doi.org/10.1126/science.8171319openalex-snapshot
Genetic Control of Programmed Cell Death in Drosophila
inferredcites →https://doi.org/10.1128/mcb.12.2.589openalex-snapshot
Transcriptional Transactivation Functions Localized to the Glucocorticoid Receptor N Terminus Are Necessary for Steroid Induction of Lymphocyte Apoptosis
inferredcites →https://doi.org/10.1210/en.133.5.2204openalex-snapshot
Estrogens inhibit and androgens enhance ovarian granulosa cell apoptosis
inferredcites →https://doi.org/10.1210/endo-118-1-38openalex-snapshot
Rapidin VivoEffects of Glucocorticoids on the Integrity of Rat Lymphocyte Genomic Deoxyribonucleic Acid*
inferredcites →https://doi.org/10.1210/mend-5-10-1381openalex-snapshot
Isolation and Characterization of Transcripts Induced by Androgen Withdrawal and Apoptotic Cell Death in the Rat Ventral Prostate
inferredcites →https://doi.org/10.1242/dev.119.4.1251openalex-snapshot
Programmed cell death in the Drosophila CNS is ecdysone-regulated and coupled with a specific ecdysone receptor isoform
inferredcites →https://doi.org/10.1242/dev.120.1.219openalex-snapshot
Ecdysone receptor expression in the CNS correlates with stage-specific responses to ecdysteroids during Drosophila and Manduca development
inferredcites →https://doi.org/10.1242/dev.121.5.1455openalex-snapshot
The Drosophila E74 gene is required for metamorphosis and plays a role in the polytene chromosome puffing response to ecdysone
inferredcites →https://doi.org/10.1242/dev.124.22.4673openalex-snapshot
Steroid regulated programmed cell death during Drosophila metamorphosis
inferredcites →https://doi.org/10.1242/dev.125.23.4709openalex-snapshot
The RXR homolog Ultraspiracle is an essential component of the Drosophila ecdysone receptor
inferredcites →https://doi.org/10.4049/jimmunol.132.1.38openalex-snapshot
Glucocorticoid activation of a calcium-dependent endonuclease in thymocyte nuclei leads to cell death.
inferredcites →https://doi.org/10.4049/jimmunol.163.3.1327openalex-snapshot
Thymus-Derived Glucocorticoids Set the Thresholds for Thymocyte Selection by Inhibiting TCR-Mediated Thymocyte Activation

What points at this work

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

inferred← citeshttps://doi.org/10.3906/zoo-1905-21zenodo-depositor-declared
Vertebrate insulin alters the expression profile of steroid hormone ecdysone receptor complex components and autophagy-related genes in the pupal fat body of the silkworm, Bombyxmori
inferred← citeshttps://doi.org/10.1002/arch.10011openalex-snapshot
Pathology of the adult central nervous system induced by genetic inhibition of programmed cell death in Drosophila pupae
inferred← citeshttps://doi.org/10.1002/dvg.20527openalex-snapshot
Precise temporal regulation of roughest is required for correct salivary gland autophagic cell death in Drosophila
inferred← citeshttps://doi.org/10.1002/dvg.22025openalex-snapshot
Fhos encodes a Drosophila Formin‐Like Protein participating in autophagic programmed cell death
inferred← citeshttps://doi.org/10.1002/glia.21098openalex-snapshot
Keeping the CNS clear: Glial phagocytic functions in Drosophila
inferred← citeshttps://doi.org/10.1002/ps.4198openalex-snapshot
Apoptotic activity and gene responses in Drosophila melanogaster S2 cells, induced by azadirachtin A
inferred← citeshttps://doi.org/10.1006/dbio.2002.0784openalex-snapshot
Steroid Regulation of Midgut Cell Death during Drosophila Development
inferred← citeshttps://doi.org/10.1006/dbio.2002.0838openalex-snapshot
Genetic Mechanism for the Stage- and Tissue-Specific Regulation of Steroid Triggered Programmed Cell Death in Drosophila
inferred← citeshttps://doi.org/10.1007/978-0-387-40049-5_26openalex-snapshot
Cell Death and Transcription
inferred← citeshttps://doi.org/10.1007/978-1-4939-3581-9_11openalex-snapshot
Detection of Cell Death in Drosophila Tissues
inferred← citeshttps://doi.org/10.1007/978-1-59745-199-4_17openalex-snapshot
The Biology of Caspases
inferred← citeshttps://doi.org/10.1007/s00344-025-11633-7openalex-snapshot
Trans-kingdom Regulation of Programmed Cell Death in Plants
inferred← citeshttps://doi.org/10.1016/b0-44-451924-6/00027-2openalex-snapshot
Programmed Cell Death in Insect Neuromuscular Systems during Metamorphosis
inferred← citeshttps://doi.org/10.1016/b978-0-12-385979-2.00001-0openalex-snapshot
Developmental Checkpoints and Feedback Circuits Time Insect Maturation
inferred← citeshttps://doi.org/10.1016/b978-0-12-391500-9.00005-xopenalex-snapshot
Recent Progress in Juvenile Hormone Analogs (JHA) Research
inferred← citeshttps://doi.org/10.1016/b978-0-12-396968-2.00002-6openalex-snapshot
Nutrient Signaling and Developmental Timing of Maturation
inferred← citeshttps://doi.org/10.1016/b978-0-323-95424-2.00057-1openalex-snapshot
Hormonal control of insect metamorphosis
inferred← citeshttps://doi.org/10.1016/bs.ircmb.2019.08.003openalex-snapshot
Molecular mechanisms of selective autophagy in Drosophila
inferred← citeshttps://doi.org/10.1016/j.acthis.2008.02.001openalex-snapshot
Morphological changes and patterns of ecdysone receptor B1 immunolocalization in the anterior silk gland undergoing programmed cell death in the silkworm, Bombyx mori
inferred← citeshttps://doi.org/10.1016/j.bbamcr.2013.06.014openalex-snapshot
Developmentally programmed cell death in Drosophila
inferred← citeshttps://doi.org/10.1016/j.bbrc.2024.150024openalex-snapshot
Illuminating intercellular autophagy: A comprehensive review of cell non-autonomous autophagy
inferred← citeshttps://doi.org/10.1016/j.cub.2009.08.042openalex-snapshot
Autophagy, Not Apoptosis, Is Essential for Midgut Cell Death in Drosophila
inferred← citeshttps://doi.org/10.1016/j.dci.2005.08.003openalex-snapshot
Contribution of circulating hemocytes to the regeneration of heavy ion beams (12C5+) irradiated hematopoietic organs in the silkworm, Bombyx mori, through the way of phagocytosis of injured cells after invasion
inferred← citeshttps://doi.org/10.1016/j.devcel.2018.09.015openalex-snapshot
The Proton-Coupled Monocarboxylate Transporter Hermes Is Necessary for Autophagy during Cell Death
inferred← citeshttps://doi.org/10.1016/j.ibmb.2017.01.010openalex-snapshot
Cathepsin L participates in the remodeling of the midgut through dissociation of midgut cells and activation of apoptosis via caspase-1
inferred← citeshttps://doi.org/10.1016/j.ibmb.2026.104587openalex-snapshot
Ecdysone-inducible SP transcription factor SPTF3L controls wing development by regulating cell proliferation and metabolic homeostasis in Locusta migratoria
inferred← citeshttps://doi.org/10.1016/j.jinsphys.2006.09.009openalex-snapshot
Stage- and cell-specific expression of ecdysone receptors and ecdysone-induced transcription factors during midgut remodeling in the yellow fever mosquito, Aedes aegypti
inferred← citeshttps://doi.org/10.1016/j.jinsphys.2012.06.004openalex-snapshot
Programmed cell death of larval tissues induced by juvenile hormone in the bamboo borer, Omphisa fuscidentalis
inferred← citeshttps://doi.org/10.1016/j.mod.2005.04.003openalex-snapshot
The Drosophila caspase DRONC is required for metamorphosis and cell death in response to irradiation and developmental signals
inferred← citeshttps://doi.org/10.1016/j.mod.2006.05.005openalex-snapshot
Mechanisms of midgut remodeling: Juvenile hormone analog methoprene blocks midgut metamorphosis by modulating ecdysone action
inferred← citeshttps://doi.org/10.1016/j.mod.2006.09.002openalex-snapshot
Developmental and hormonal regulation of midgut remodeling in a lepidopteran insect, Heliothis virescens
inferred← citeshttps://doi.org/10.1016/j.pestbp.2020.104703openalex-snapshot
Effects of selected insecticidal substances on mRNA transcriptome in larvae of Apis mellifera
inferred← citeshttps://doi.org/10.1016/j.ydbio.2005.03.019openalex-snapshot
Phenotypic analysis of EcR-A mutants suggests that EcR isoforms have unique functions during Drosophila development
inferred← citeshttps://doi.org/10.1016/j.ydbio.2016.08.028openalex-snapshot
PINK1 is required for timely cell-type specific mitochondrial clearance during Drosophila midgut metamorphosis
inferred← citeshttps://doi.org/10.1016/s0022-1759(02)00068-6openalex-snapshot
Death to flies: Drosophila as a model system to study programmed cell death
inferred← citeshttps://doi.org/10.1016/s0076-6879(08)01602-9openalex-snapshot
Chapter 2 Methods and Protocols for Studying Cell Death in Drosophila
inferred← citeshttps://doi.org/10.1017/cbo9780511663543.003openalex-snapshot
Developmental apoptosis in health and disease
inferred← citeshttps://doi.org/10.1038/cdd.2015.108openalex-snapshot
Ligand-independent requirements of steroid receptors EcR and USP for cell survival
inferred← citeshttps://doi.org/10.1038/ncb795openalex-snapshot
Regulation of Drosophila IAP1 degradation and apoptosis by reaper and ubcD1
inferred← citeshttps://doi.org/10.1038/ng1792openalex-snapshot
Genome-wide profiling of PRC1 and PRC2 Polycomb chromatin binding in Drosophila melanogaster
inferred← citeshttps://doi.org/10.1038/nrm931openalex-snapshot
How death shapes life during development
inferred← citeshttps://doi.org/10.1038/s41418-018-0154-zopenalex-snapshot
Dpp regulates autophagy-dependent midgut removal and signals to block ecdysone production
inferred← citeshttps://doi.org/10.1038/s41419-019-1368-9openalex-snapshot
Crosstalk between Dpp and Tor signaling coordinates autophagy-dependent midgut degradation
inferred← citeshttps://doi.org/10.1038/sj.cdd.4400763openalex-snapshot
Cell death in the fly comes of age
inferred← citeshttps://doi.org/10.1038/sj.cdd.4400864openalex-snapshot
STRICA, a novel Drosophila melanogaster caspase with an unusual serine/threonine-rich prodomain, interacts with DIAP1 and DIAP2
inferred← citeshttps://doi.org/10.1038/sj.cdd.4401312openalex-snapshot
Distinct promoter regions regulate spatial and temporal expression of the Drosophila caspase dronc
inferred← citeshttps://doi.org/10.1038/sj.cdd.4402098openalex-snapshot
Proteomic analysis of steroid-triggered autophagic programmed cell death during Drosophila development
inferred← citeshttps://doi.org/10.1038/sj.cr.7290048openalex-snapshot
Genetic regulation of programmed cell death in Drosophila
inferred← citeshttps://doi.org/10.1038/sj.onc.1205839openalex-snapshot
reaper and bax initiate two different apoptotic pathways affecting mitochondria and antagonized by bcl-2 in Drosophila
inferred← citeshttps://doi.org/10.1042/bse0390011openalex-snapshot
Apoptosis and development
inferred← citeshttps://doi.org/10.1046/j.1432-1033.2002.03293.xopenalex-snapshot
Activation of transcription through the ligand‐binding pocket of the orphan nuclear receptor ultraspiracle
inferred← citeshttps://doi.org/10.1057/palgrave.ivs.9500061openalex-snapshot
Dynamic Query Tools for Time Series Data Sets: Timebox Widgets for Interactive Exploration
inferred← citeshttps://doi.org/10.1073/pnas.0702733104openalex-snapshot
Local initiation of caspase activation in Drosophila salivary gland programmed cell death in vivo
inferred← citeshttps://doi.org/10.1073/pnas.1410488111openalex-snapshot
Sexual transfer of the steroid hormone 20E induces the postmating switch in Anopheles gambiae
inferred← citeshttps://doi.org/10.1073/pnas.2118871119openalex-snapshot
Juvenile hormone-induced histone deacetylase 3 suppresses apoptosis to maintain larval midgut in the yellow fever mosquito
inferred← citeshttps://doi.org/10.1074/jbc.m114.581876openalex-snapshot
Juvenile Hormone Prevents 20-Hydroxyecdysone-induced Metamorphosis by Regulating the Phosphorylation of a Newly Identified Broad Protein
inferred← citeshttps://doi.org/10.1074/jbc.m115.643783openalex-snapshot
The Steroid Hormone 20-Hydroxyecdysone Up-regulates Ste-20 Family Serine/Threonine Kinase Hippo to Induce Programmed Cell Death
inferred← citeshttps://doi.org/10.1074/jbc.m303763200openalex-snapshot
Inhibition of Apoptosis by Z-VAD-fmk in SMN-depleted S2 Cells
inferred← citeshttps://doi.org/10.1074/jbc.m400972200openalex-snapshot
An Arginine-Histone Methyltransferase, CARMER, Coordinates Ecdysone-mediated Apoptosis in Drosophila Cells
inferred← citeshttps://doi.org/10.1074/jbc.m413971200openalex-snapshot
Ecdysone-mediated Up-regulation of the Effector Caspase DRICE Is Required for Hormone-dependent Apoptosis in Drosophila Cells
inferred← citeshttps://doi.org/10.1083/jcb.200111107openalex-snapshot
The role of cytochrome c in caspase activation in Drosophila melanogaster cells
inferred← citeshttps://doi.org/10.1083/jcb.200201034openalex-snapshot
Ecdysone-induced expression of the caspase DRONC during hormone-dependent programmed cell death in Drosophila is regulated by Broad-Complex
inferred← citeshttps://doi.org/10.1083/jcb.200311057openalex-snapshot
Ecdysone receptor directly binds the promoter of the Drosophila caspase dronc, regulating its expression in specific tissues
inferred← citeshttps://doi.org/10.1093/emboj/cdg355openalex-snapshot
Buffy, a Drosophila Bcl‐2 protein, has anti‐apoptotic and cell cycle inhibitory functions
inferred← citeshttps://doi.org/10.1101/cshperspect.a008664openalex-snapshot
Apoptotic and Nonapoptotic Caspase Functions in Animal Development
inferred← citeshttps://doi.org/10.1101/cshperspect.a019117openalex-snapshot
The Systemic Control of Growth
inferred← citeshttps://doi.org/10.1101/pdb.top070433openalex-snapshot
Studying Apoptosis in Drosophila
inferred← citeshttps://doi.org/10.1111/imb.12758openalex-snapshot
MiR ‐3017b contributes to metamorphosis by targeting sarco/endoplasmic reticulum Ca 2+ ATPase in Tribolium castaneum
inferred← citeshttps://doi.org/10.1111/j.1365-2583.2007.00758.xopenalex-snapshot
Aedes Dronc: a novel ecdysone‐inducible caspase in the yellow fever mosquito, Aedes aegypti
inferred← citeshttps://doi.org/10.1111/j.1365-2583.2012.01158.xopenalex-snapshot
Hsp70 and small Hsps are the major heat shock protein members involved in midgut metamorphosis in the common cutworm, Spodoptera litura
inferred← citeshttps://doi.org/10.1111/j.1440-169x.2012.01340.xopenalex-snapshot
Spatio‐temporal pattern of programmed cell death in the developing Drosophila optic lobe
inferred← citeshttps://doi.org/10.1111/j.1582-4934.2005.tb00360.xopenalex-snapshot
Pathways of apoptosis and importance in developement
inferred← citeshttps://doi.org/10.1126/science.1080539openalex-snapshot
Steroid Control of Longevity in Drosophila melanogaster
inferred← citeshttps://doi.org/10.1128/mcb.01391-13openalex-snapshot
Ecdysone-Induced Receptor Tyrosine Phosphatase PTP52F Regulates Drosophila Midgut Histolysis by Enhancement of Autophagy and Apoptosis
inferred← citeshttps://doi.org/10.1186/1471-213x-11-66openalex-snapshot
Identification of common and cell type specific LXXLL motif EcR cofactors using a bioinformatics refined candidate RNAi screen in Drosophila melanogastercell lines
inferred← citeshttps://doi.org/10.1186/1747-1028-4-3openalex-snapshot
Impact of steroid hormone signals on Drosophila cell cycle during development
inferred← citeshttps://doi.org/10.1186/gb-2003-5-1-r1openalex-snapshot
MicroRNA targets in Drosophila
inferred← citeshttps://doi.org/10.1242/bio.20148417openalex-snapshot
The Drosophila TIPE family member Sigmar interacts with the Ste20-like kinase Misshapen and modulates JNK signaling, cytoskeletal remodeling and autophagy
inferred← citeshttps://doi.org/10.1242/dev.00933openalex-snapshot
Caspases function in autophagic programmed cell death inDrosophila
inferred← citeshttps://doi.org/10.1242/dev.021766openalex-snapshot
The Ecdysone-inducible zinc-finger transcription factor Crol regulates Wg transcription and cell cycle progression inDrosophila
inferred← citeshttps://doi.org/10.1242/dev.083030openalex-snapshot
Broad relays hormone signals to regulate stem cell differentiation in Drosophila midgut during metamorphosis
inferred← citeshttps://doi.org/10.1242/dev.129.6.1467openalex-snapshot
reaperis required for neuroblast apoptosis duringDrosophiladevelopment
inferred← citeshttps://doi.org/10.1242/jeb.00855openalex-snapshot
Overexpression of broad : a new insight into its role in the Drosophila prothoracic gland cells
inferred← citeshttps://doi.org/10.13028/m20s36openalex-snapshot
A Novel Autophagy Regulatory Mechanism that Functions During Programmed Cell Death: A Dissertation
inferred← citeshttps://doi.org/10.1371/journal.pgen.1000379openalex-snapshot
Steroid Hormone Control of Cell Death and Cell Survival: Molecular Insights Using RNAi
inferred← citeshttps://doi.org/10.1371/journal.pgen.1004581openalex-snapshot
Low Levels of p53 Protein and Chromatin Silencing of p53 Target Genes Repress Apoptosis in Drosophila Endocycling Cells
inferred← citeshttps://doi.org/10.1371/journal.pone.0000412openalex-snapshot
The Extrachromosomal EAST Protein of Drosophila Can Associate with Polytene Chromosomes and Regulate Gene Expression
inferred← citeshttps://doi.org/10.1371/journal.pone.0025502openalex-snapshot
Programmed Autophagy in the Fat Body of Aedes aegypti Is Required to Maintain Egg Maturation Cycles
inferred← citeshttps://doi.org/10.1371/journal.pone.0039378openalex-snapshot
Inhibition of CLIC4 Enhances Autophagy and Triggers Mitochondrial and ER Stress-Induced Apoptosis in Human Glioma U251 Cells under Starvation
inferred← citeshttps://doi.org/10.1371/journal.pone.0045019openalex-snapshot
A Critical Role of the Nuclear Receptor HR3 in Regulation of Gonadotrophic Cycles of the Mosquito Aedes aegypti
inferred← citeshttps://doi.org/10.1371/journal.pone.0098088openalex-snapshot
Dimorphic Ovary Differentiation in Honeybee (Apis mellifera) Larvae Involves Caste-Specific Expression of Homologs of Ark and Buffy Cell Death Genes
inferred← citeshttps://doi.org/10.1371/journal.pone.0143078openalex-snapshot
The Deubiquitinating Enzyme UBPY Is Required for Lysosomal Biogenesis and Productive Autophagy in Drosophila
inferred← citeshttps://doi.org/10.1387/ijdb.190190mtopenalex-snapshot
Transcriptome profiling identifies multistep regulation through E93, Forkhead and Ecdysone Oxidase in survival of Malpighian tubules during metamorphosis in Drosophila
inferred← citeshttps://doi.org/10.14411/eje.2009.041openalex-snapshot
Apoptosis of neuronal cells in the brains of postembryonic silkworms Bombyx mori (Lepidoptera: Bombycidae)
inferred← citeshttps://doi.org/10.14411/eje.2017.029openalex-snapshot
Juvenile hormone analogue, fenoxycarb, modulates ecdysone-triggered transcriptional hierarchy during programmed cell death of midgut in silkworm, Bombyx mori (Lepidoptera: Bombycidae)
inferred← citeshttps://doi.org/10.3389/fceld.2024.1478258openalex-snapshot
Exploring advanced Drosophila cell death techniques and cancer-related studies
inferred← citeshttps://doi.org/10.3389/fcell.2026.1859086openalex-snapshot
Developmentally-regulated post-apocrine cell death of Drosophila salivary glands utilizes ER stress-linked apoptosis
inferred← citeshttps://doi.org/10.3390/cells13040347openalex-snapshot
Understanding Developmental Cell Death Using Drosophila as a Model System
inferred← citeshttps://doi.org/10.3390/ijms140510229openalex-snapshot
Molecular Cloning and Characterization of the First Caspase in the Striped Stem Borer, Chilo suppressalis
inferred← citeshttps://doi.org/10.3390/ijms252111467openalex-snapshot
Biological Characteristics of the Cytochrome P 450 Family and the Mechanism of Terpinolene Metabolism in Hyalomma asiaticum (Acari: Ixodidae)
inferred← citeshttps://doi.org/10.3390/jdb6040026openalex-snapshot
I Spy in the Developing Fly a Multitude of Ways to Die
inferred← citeshttps://doi.org/10.5772/27927openalex-snapshot
Steroid Hormones in Drosophila: How Ecdysone Coordinates Developmental Signalling with Cell Growth and Division
inferred← citeshttps://doi.org/10.64898/2025.12.29.696923openalex-snapshot
Hepatocyte-like cells die via steroid hormone and nuclear receptor E75-mediated apoptosis
inferred← citeshttps://doi.org/10.7290/pur31pmfxopenalex-snapshot
Neurogenetic Studies on the Role of DIAP1 in Neuronal Programmed Cell Death 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.