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Wengen, a Member of the Drosophila Tumor Necrosis Factor Receptor Superfamily, Is Required for Eiger Signaling

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What this work says

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

inferredcites →https://doi.org/10.1016/s0092-8674(00)00129-xopenalex-snapshot
Transducing the Hedgehog Signal
inferredcites →https://doi.org/10.1016/s0092-8674(01)00237-9openalex-snapshot
The TNF and TNF Receptor Superfamilies
inferredcites →https://doi.org/10.1016/s0968-0004(01)01995-8openalex-snapshot
The molecular architecture of the TNF superfamily
inferredcites →https://doi.org/10.1016/s0968-0004(97)01164-xopenalex-snapshot
Modularity in the TNF-receptor family
inferredcites →https://doi.org/10.1016/s1097-2765(00)80334-2openalex-snapshot
The Structural Basis for the Recognition of Diverse Receptor Sequences by TRAF2
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/10.1093/emboj/cdf306openalex-snapshot
Eiger, a TNF superfamily ligand that triggers the Drosophila JNK pathway
inferredcites →https://doi.org/10.1093/genetics/107.4.657openalex-snapshot
FORMATION OF CHROMOSOME REARRANGEMENTS BY P FACTORS IN DROSOPHILA
inferredcites →https://doi.org/10.1126/science.290.5491.523openalex-snapshot
Two-Amino Acid Molecular Switch in an Epithelial Morphogen That Regulates Binding to Two Distinct Receptors
inferredcites →https://doi.org/10.1242/dev.27.2.353openalex-snapshot
Cell lines derived from late embryonic stages of Drosophila melanogaster
inferredcites →https://doi.org/10.1242/jcs.111.6.667openalex-snapshot
Caenorhabditis elegans anti-apoptotic gene ced-9 prevents ced-3-induced cell death in Drosophila cells

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.4695723openalex-extracted
Characterization, Functional Analysis, and Expression of TNFR16 from Pinctada Fucata Martensii in Response to Exogenous Stimuli and RNA Interference
inferred← citeshttps://doi.org/10.1002/1873-3468.14716openalex-snapshot
Drosophila TNF / TNFRs : At the crossroad between metabolism, immunity, and tissue homeostasis
inferred← citeshttps://doi.org/10.1002/cbin.11521openalex-snapshot
Deltex cooperates with TRAF6 to promote apoptosis and cell migration through Eiger‐independent JNK activation in Drosophila
inferred← citeshttps://doi.org/10.1002/dvdy.20283openalex-snapshot
Dissecting JNK signaling, one KKKinase at a time
inferred← citeshttps://doi.org/10.1002/dvdy.22186openalex-snapshot
POSH misexpression induces caspase‐dependent cell death in Drosophila
inferred← citeshttps://doi.org/10.1002/dvg.20306openalex-snapshot
Noncanonical cell death pathways act during Drosophila oogenesis
inferred← citeshttps://doi.org/10.1007/3-540-26511-2_7openalex-snapshot
Signaling and Reverse Signaling in the Tumor Necrosis Factor/TNF Receptor System
inferred← citeshttps://doi.org/10.1007/4735_2007_0251openalex-snapshot
Stress-activated Protein Kinase Signaling in Drosophila
inferred← citeshttps://doi.org/10.1007/978-1-4020-6397-8_3openalex-snapshot
Insects as Models for Studying the Virulence of Fungal Pathogens of Humans
inferred← citeshttps://doi.org/10.1007/978-1-4419-6612-4_5openalex-snapshot
Eiger and Wengen: The Drosophila Orthologs of TNF/TNFR
inferred← citeshttps://doi.org/10.1007/978-3-030-23629-8_4openalex-snapshot
Two Sides of the Same Coin – Compensatory Proliferation in Regeneration and Cancer
inferred← citeshttps://doi.org/10.1007/978-3-030-42246-2_9openalex-snapshot
Drosophila Cancer Modeling Using the Eye Imaginal Discs
inferred← citeshttps://doi.org/10.1007/978-3-319-39406-0_4openalex-snapshot
Apoptotic Caspases in Promoting Cancer: Implications from Their Roles in Development and Tissue Homeostasis
inferred← citeshttps://doi.org/10.1007/978-3-642-18670-7_6openalex-snapshot
Functional Convergence of Invertebrate and Vertebrate Cytokine-Like Molecules Based on a Similar Lectin-Like Activity
inferred← citeshttps://doi.org/10.1007/978-981-13-9913-8_2openalex-snapshot
Evolution of Neuroglia
inferred← citeshttps://doi.org/10.1007/s00018-024-05560-1openalex-snapshot
Glial-derived TNF/Eiger signaling promotes somatosensory neurite sculpting
inferred← citeshttps://doi.org/10.1007/s10495-009-0361-7openalex-snapshot
Correcting developmental errors by apoptosis: lessons from Drosophila JNK signaling
inferred← citeshttps://doi.org/10.1007/s10495-009-0442-7openalex-snapshot
Apoptosis in pre-Bilaterians: Hydra as a model
inferred← citeshttps://doi.org/10.1007/s10495-009-0443-6openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s10495-015-1104-6openalex-snapshot
Lipid rafts and raft-mediated supramolecular entities in the regulation of CD95 death receptor apoptotic signaling
inferred← citeshttps://doi.org/10.1007/s11033-010-0578-0openalex-snapshot
cDNA cloning and characterization of a new member of the tumor necrosis factor receptor family gene from scallop, Chlamys farreri
inferred← citeshttps://doi.org/10.1007/s12013-012-9336-3openalex-snapshot
Differential DNA Methylation Status Between Human Preadipocytes and Mature Adipocytes
inferred← citeshttps://doi.org/10.1016/b978-0-12-391498-9.00001-2openalex-snapshot
Mechanisms of Systemic Wound Response in Drosophila
inferred← citeshttps://doi.org/10.1016/bs.aivir.2020.06.001openalex-snapshot
Immunopathology and immune homeostasis during viral infection in insects
inferred← citeshttps://doi.org/10.1016/j.aqrep.2024.102115openalex-snapshot
Characterization, functional analysis, and expression of TNFR16 from Pinctada fucata martensii in response to exogenous stimuli and RNA interference
inferred← citeshttps://doi.org/10.1016/j.bbamcr.2003.09.007openalex-snapshot
Role of Bcl-2 family members in invertebrates
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.cellsig.2018.05.003openalex-snapshot
Deltex interacts with Eiger and consequently influences the cell death in Drosophila melanogaster
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/10.1016/j.chom.2008.07.004openalex-snapshot
PIMS Modulates Immune Tolerance by Negatively Regulating Drosophila Innate Immune Signaling
inferred← citeshttps://doi.org/10.1016/j.cmet.2016.03.003openalex-snapshot
The Drosophila TNF Eiger Is an Adipokine that Acts on Insulin-Producing Cells to Mediate Nutrient Response
inferred← citeshttps://doi.org/10.1016/j.cub.2006.04.042openalex-snapshot
Loss of Cell Polarity Drives Tumor Growth and Invasion through JNK Activation in Drosophila
inferred← citeshttps://doi.org/10.1016/j.cub.2009.03.062openalex-snapshot
Cytokine Signaling Mediates UV-Induced Nociceptive Sensitization in Drosophila Larvae
inferred← citeshttps://doi.org/10.1016/j.cub.2011.08.020openalex-snapshot
Hedgehog Signaling Regulates Nociceptive Sensitization
inferred← citeshttps://doi.org/10.1016/j.cub.2015.12.064openalex-snapshot
Extracellular Reactive Oxygen Species Drive Apoptosis-Induced Proliferation via Drosophila Macrophages
inferred← citeshttps://doi.org/10.1016/j.dci.2011.02.013openalex-snapshot
A TRAF and TNF receptor-associated protein (TTRAP) in mollusk with endonuclease activity
inferred← citeshttps://doi.org/10.1016/j.dci.2011.03.031openalex-snapshot
Origin and evolution of TNF and TNF receptor superfamilies
inferred← citeshttps://doi.org/10.1016/j.dci.2011.06.002openalex-snapshot
Molecular cloning, characterization and expression analysis of the tumor necrosis factor (TNF) superfamily gene, TNF receptor superfamily gene and lipopolysaccharide-induced TNF-α factor (LITAF) gene from Litopenaeus vannamei
inferred← citeshttps://doi.org/10.1016/j.devcel.2007.07.012openalex-snapshot
Tumor Suppressor CYLD Regulates JNK-Induced Cell Death in Drosophila
inferred← citeshttps://doi.org/10.1016/j.devcel.2009.01.002openalex-snapshot
Intrinsic Tumor Suppression and Epithelial Maintenance by Endocytic Activation of Eiger/TNF Signaling in Drosophila
inferred← citeshttps://doi.org/10.1016/j.devcel.2009.04.015openalex-snapshot
Regenerative Growth in Drosophila Imaginal Discs Is Regulated by Wingless and Myc
inferred← citeshttps://doi.org/10.1016/j.devcel.2018.04.002openalex-snapshot
Drosophila TNF Modulates Tissue Tension in the Embryo to Facilitate Macrophage Invasive Migration
inferred← citeshttps://doi.org/10.1016/j.devcel.2018.05.012openalex-snapshot
A Drosophila Tumor Suppressor Gene Prevents Tonic TNF Signaling through Receptor N-Glycosylation
inferred← citeshttps://doi.org/10.1016/j.fsi.2009.06.019openalex-snapshot
A novel Fas ligand in mollusk abalone: Molecular characterization, immune responses and biological activity of the recombinant protein
inferred← citeshttps://doi.org/10.1016/j.fsi.2009.07.009openalex-snapshot
First molluscan TNFR homologue in Zhikong scallop: Molecular characterization and expression analysis
inferred← citeshttps://doi.org/10.1016/j.fsi.2013.07.034openalex-snapshot
Identification of a LPS-induced TNF-α factor (LITAF) from mollusk Solen grandis and its expression pattern towards PAMPs stimulation
inferred← citeshttps://doi.org/10.1016/j.fsi.2015.06.035openalex-snapshot
Cloning and characterization of a novel caspase-8-like gene in Crassostrea gigas
inferred← citeshttps://doi.org/10.1016/j.fsi.2016.03.010openalex-snapshot
Genome-wide identification, characterization and expression analyses of two TNFRs in Yesso scallop (Patinopecten yessoensis) provide insight into the disparity of responses to bacterial infections and heat stress in bivalves
inferred← citeshttps://doi.org/10.1016/j.fsi.2016.09.041openalex-snapshot
Cloning, characterization and comparative analysis of four death receptorTNFRs from the oyster Crassostrea hongkongensis
inferred← citeshttps://doi.org/10.1016/j.fsi.2019.08.008openalex-snapshot
The first cloned echinoderm tumor necrosis factor receptor from Holothuria leucospilota: Molecular characterization and functional analysis
inferred← citeshttps://doi.org/10.1016/j.fsi.2020.01.010openalex-snapshot
Molecular cloning, characterization, and expression of two TNFRs from the pearl oyster Pinctada fucata martensii
inferred← citeshttps://doi.org/10.1016/j.fsi.2025.111092openalex-snapshot
A TNF receptor involved in regulating haemocyte apoptosis by triggering apoptotic factors in the oyster Crassostrea gigas
inferred← citeshttps://doi.org/10.1016/j.imlet.2015.12.005openalex-snapshot
Cytokines in Drosophila immunity
inferred← citeshttps://doi.org/10.1016/j.isci.2020.101823openalex-snapshot
A Two-Clone Approach to Study Signaling Interactions among Neuronal Cells in a Pre-clinical Alzheimer's Disease Model
inferred← citeshttps://doi.org/10.1016/j.isci.2023.106440openalex-snapshot
FSBP suppresses tumor cell migration by inhibiting the JNK pathway
inferred← citeshttps://doi.org/10.1016/j.margen.2015.03.003openalex-snapshot
Evolutionary evidence of tumor necrosis factor super family members in the Japanese pufferfish (Takifugu rubripes): Comprehensive genomic identification and expression analysis
inferred← citeshttps://doi.org/10.1016/j.micinf.2009.03.004openalex-snapshot
Bacterial detection by Drosophila peptidoglycan recognition proteins
inferred← citeshttps://doi.org/10.1016/j.molimm.2003.10.008openalex-snapshot
Antimicrobial defences in Drosophila: the story so far
inferred← citeshttps://doi.org/10.1016/j.molimm.2006.04.011openalex-snapshot
Bbt-TNFR1 and Bbt-TNFR2, two tumor necrosis factor receptors from Chinese amphioxus involve in host defense
inferred← citeshttps://doi.org/10.1016/j.molimm.2015.03.015openalex-snapshot
Functional roles and gene regulation of tumor necrosis factor receptor 1 in freshwater striped murrel
inferred← citeshttps://doi.org/10.1016/j.neuron.2011.09.031openalex-snapshot
Glial-Derived Prodegenerative Signaling in the Drosophila Neuromuscular System
inferred← citeshttps://doi.org/10.1016/j.semcdb.2022.04.002openalex-snapshot
Regulating metabolism to shape immune function: Lessons from Drosophila
inferred← citeshttps://doi.org/10.1016/j.semcdb.2025.103602openalex-snapshot
Death fuels growth: Emerging players bridging apoptosis and cell proliferation in Drosophila and beyond
inferred← citeshttps://doi.org/10.1016/j.smim.2014.05.003openalex-snapshot
The Drosophila TNF ortholog Eiger: Emerging physiological roles and evolution of the TNF system
inferred← citeshttps://doi.org/10.1016/j.tcb.2012.11.002openalex-snapshot
Competitive cell interactions in cancer: a cellular tug of war
inferred← citeshttps://doi.org/10.1016/j.ydbio.2004.07.017openalex-snapshot
Eggs over easy: cell death in the Drosophila ovary
inferred← citeshttps://doi.org/10.1016/j.ydbio.2007.02.011openalex-snapshot
The Edar subfamily in feather placode formation
inferred← citeshttps://doi.org/10.1016/j.ydbio.2013.05.013openalex-snapshot
dUev1a modulates TNF-JNK mediated tumor progression and cell death in Drosophila
inferred← citeshttps://doi.org/10.1016/j.ygeno.2006.06.011openalex-snapshot
Analysis of ESTs from Lutzomyia longipalpis sand flies and their contribution toward understanding the insect–parasite relationship
inferred← citeshttps://doi.org/10.1016/s0074-7696(06)52002-9openalex-snapshot
Intracellular Signals and Events Activated by Cytokines of the Tumor Necrosis Factor Superfamily: From Simple Paradigms to Complex Mechanisms
inferred← citeshttps://doi.org/10.1016/s0083-6729(05)73001-6openalex-snapshot
Hormonal Control of Insect Ecdysis: Endocrine Cascades for Coordinating Behavior with Physiology
inferred← citeshttps://doi.org/10.1016/s0083-6729(05)73007-7openalex-snapshot
Insect Neuropeptide and Peptide Hormone Receptors: Current Knowledge and Future Directions
inferred← citeshttps://doi.org/10.1016/s0092-8674(04)00166-7openalex-snapshot
Tumor Necrosis Factor
inferred← citeshttps://doi.org/10.1016/s1359-6101(03)00023-6openalex-snapshot
The TNF family members BAFF and APRIL: the growing complexity
inferred← citeshttps://doi.org/10.1016/s1471-4906(03)00166-2openalex-snapshot
A co-evolution perspective of the TNFSF and TNFRSF families in the immune system
inferred← citeshttps://doi.org/10.1017/s0031182002002755openalex-snapshot
Activation of host constitutive immune defence by an intestinal trypanosome parasite of bumble bees
inferred← citeshttps://doi.org/10.1038/cdd.2013.154openalex-snapshot
Bendless modulates JNK-mediated cell death and migration in Drosophila
inferred← citeshttps://doi.org/10.1038/cddis.2016.80openalex-snapshot
Eiger-induced cell death relies on Rac1-dependent endocytosis
inferred← citeshttps://doi.org/10.1038/cr.2010.66openalex-snapshot
The molecular cell death machinery in the simple cnidarian Hydra includes an expanded caspase family and pro- and anti-apoptotic Bcl-2 proteins
inferred← citeshttps://doi.org/10.1038/cr.2011.135openalex-snapshot
NOPO modulates Egr-induced JNK-independent cell death in Drosophila
inferred← citeshttps://doi.org/10.1038/nature14298openalex-snapshot
The Drosophila TNF receptor Grindelwald couples loss of cell polarity and neoplastic growth
inferred← citeshttps://doi.org/10.1038/s41388-021-01831-4openalex-snapshot
Yorkie-Cactus (IκBα)-JNK axis promotes tumor growth and progression in Drosophila
inferred← citeshttps://doi.org/10.1038/s41419-019-1350-6openalex-snapshot
MKK3 modulates JNK-dependent cell migration and invasion
inferred← citeshttps://doi.org/10.1038/s41419-019-1862-0openalex-snapshot
Characterization of TNF-induced cell death in Drosophila reveals caspase- and JNK-dependent necrosis and its role in tumor suppression
inferred← citeshttps://doi.org/10.1038/s41420-018-0074-1openalex-snapshot
Pontin/Tip49 negatively regulates JNK-mediated cell death in Drosophila
inferred← citeshttps://doi.org/10.1038/s41467-021-22080-9openalex-snapshot
Drosophila TNFRs Grindelwald and Wengen bind Eiger with different affinities and promote distinct cellular functions
inferred← citeshttps://doi.org/10.1038/s41467-023-41549-3openalex-snapshot
The TNFR Wengen regulates the FGF pathway by an unconventional mechanism
inferred← citeshttps://doi.org/10.1038/s41467-024-49786-wopenalex-snapshot
Inter-cell type interactions that control JNK signaling in the Drosophila intestine
inferred← citeshttps://doi.org/10.1038/s41467-025-65996-2openalex-snapshot
Apoptosis-resistant cells drive compensatory proliferation via cell-autonomous and non-autonomous functions of the initiator caspase Dronc
inferred← citeshttps://doi.org/10.1038/s41586-023-06627-yopenalex-snapshot
Cholinergic neurons trigger epithelial Ca2+ currents to heal the gut
inferred← citeshttps://doi.org/10.1038/s41598-017-05482-yopenalex-snapshot
GLYAT regulates JNK-mediated cell death in Drosophila
inferred← citeshttps://doi.org/10.1038/s41598-020-68313-7openalex-snapshot
Upregulated TNF/Eiger signaling mediates stem cell recovery and tissue homeostasis during nutrient resupply in Drosophila testis
inferred← citeshttps://doi.org/10.1038/s41598-022-23780-yopenalex-snapshot
Identification of a TNF-TNFR-like system in malaria vectors (Anopheles stephensi) likely to influence Plasmodium resistance
inferred← citeshttps://doi.org/10.1038/s44318-024-00155-9openalex-snapshot
Reactive oxygen species activate the Drosophila TNF receptor Wengen for damage-induced regeneration
inferred← citeshttps://doi.org/10.1038/s44318-024-00170-wopenalex-snapshot
Wengen’s hidden powers: ROS triggers a TNFR-dependent tissue regenerative pathway in Drosophila
inferred← citeshttps://doi.org/10.1038/sj.cdd.4401107openalex-snapshot
Death of HT29 adenocarcinoma cells induced by TNF family receptor activation is caspase-independent and displays features of both apoptosis and necrosis
inferred← citeshttps://doi.org/10.1038/sj.cdd.4402015openalex-snapshot
Delineation of the cell-extrinsic apoptosis pathway in the zebrafish
inferred← citeshttps://doi.org/10.1038/sj.emboj.7601461openalex-snapshot
Drosophila homologs of mammalian TNF/TNFR‐related molecules regulate segregation of Miranda/Prospero in neuroblasts
inferred← citeshttps://doi.org/10.1038/sj.onc.1206715openalex-snapshot
Eiger and its receptor, Wengen, comprise a TNF-like system in Drosophila
inferred← citeshttps://doi.org/10.1038/sj.onc.1207522openalex-snapshot
Caspase activation – stepping on the gas or releasing the brakes? Lessons from humans and flies
inferred← citeshttps://doi.org/10.1073/pnas.1103242108openalex-snapshot
Conserved metabolic energy production pathways govern Eiger/TNF-induced nonapoptotic cell death
inferred← citeshttps://doi.org/10.1073/pnas.1701791114openalex-snapshot
Feedback amplification loop drives malignant growth in epithelial tissues
inferred← citeshttps://doi.org/10.1074/jbc.m407363200openalex-snapshot
Induction of Apoptosis by X-linked Ectodermal Dysplasia Receptor via a Caspase 8-dependent Mechanism
inferred← citeshttps://doi.org/10.1074/jbc.m601553200openalex-snapshot
Interactions of Tumor Necrosis Factor (TNF) and TNF Receptor Family Members in the Mouse and Human
inferred← citeshttps://doi.org/10.1091/mbc.e23-12-0511openalex-snapshot
ILP4 and InR regulate paclitaxel-induced hypersensitivity differently in Drosophila larvae
inferred← citeshttps://doi.org/10.1093/gbe/evad025openalex-snapshot
Population Structure, Demographic History, and Adaptation of Giant Honeybees in China Revealed by Population Genomic Data
inferred← citeshttps://doi.org/10.1093/genetics/iyae107openalex-snapshot
The Drosophila tumor necrosis factor Eiger promotes Myc supercompetition independent of canonical Jun N-terminal kinase signaling
inferred← citeshttps://doi.org/10.1093/genetics/iyaf147openalex-snapshot
Activation of a Src-JNK pathway in unscheduled endocycling cells of the Drosophila wing disc induces a chronic wounding response
inferred← citeshttps://doi.org/10.1093/hmg/ddt296openalex-snapshot
RNA binding mediates neurotoxicity in the transgenic Drosophila model of TDP-43 proteinopathy
inferred← citeshttps://doi.org/10.1093/hmg/ddy046openalex-snapshot
Self-assembly of FUS through its low-complexity domain contributes to neurodegeneration
inferred← citeshttps://doi.org/10.1098/rsob.140171openalex-snapshot
Toll pathway modulates TNF-induced JNK-dependent cell death inDrosophila
inferred← citeshttps://doi.org/10.1101/2021.04.06.438672openalex-snapshot
The Drosophila TNF Eiger contributes to Myc super-competition independent of JNK activity
inferred← citeshttps://doi.org/10.1101/2021.12.26.474206openalex-snapshot
PITA, a pre-bilaterian p75NTR, is the evolutionary ancestor of TNF receptors
inferred← citeshttps://doi.org/10.1101/2023.01.26.525651openalex-snapshot
Wengen, a Tumour Necrosis Factor Receptor, regulates the Fibroblast Growth Factor pathway by an unconventional mechanism
inferred← citeshttps://doi.org/10.1101/2023.08.14.553227openalex-snapshot
Epithelial Ca 2+ waves triggered by enteric neurons heal the gut
inferred← citeshttps://doi.org/10.1101/2023.11.13.566843openalex-snapshot
ROS-mediated TNFR Wengen activation in response to apoptosis
inferred← citeshttps://doi.org/10.1101/2024.07.27.603686openalex-snapshot
TNF-TNFR Signaling Modality Conserved Across Invertebrate
inferred← citeshttps://doi.org/10.1111/febs.12206openalex-snapshot
Structure of the extracellular domains of human and X enopus F n14: implications in the evolution of TWEAK and F n14 interactions
inferred← citeshttps://doi.org/10.1111/febs.17028openalex-snapshot
Ubiquitin signalling in Drosophila innate immune responses
inferred← citeshttps://doi.org/10.1111/j.0105-2896.2004.0130.xopenalex-snapshot
The immune response of Drosophila melanogaster
inferred← citeshttps://doi.org/10.1111/j.1365-2443.2011.01579.xopenalex-snapshot
Beyond apoptosis: caspase regulatory mechanisms and functions in vivo
inferred← citeshttps://doi.org/10.1111/j.1440-169x.2009.01108.xopenalex-snapshot
Expression of the apoptosis inducer genehead involution defectivein primordial germ cells of theDrosophilaembryo requireseiger,p53, andlokifunction
inferred← citeshttps://doi.org/10.1111/j.1462-5822.2008.01267.xopenalex-snapshot
Genetic analysis ofDrosophila melanogastersusceptibility to intestinalVibrio choleraeinfection
inferred← citeshttps://doi.org/10.1111/raq.12976openalex-snapshot
Cell Death in Crustacean Immune Defense
inferred← citeshttps://doi.org/10.1126/sciadv.add4977openalex-snapshot
The Drosophila tumor necrosis factor receptor, Wengen, couples energy expenditure with gut immunity
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/10.1126/scisignal.2000906openalex-snapshot
Characterization of the Extrinsic Apoptotic Pathway in the Basal Chordate Amphioxus
inferred← citeshttps://doi.org/10.1128/mcb.24.3.1219-1231.2004openalex-snapshot
Drosophila melanogaster MNK/Chk2 and p53 Regulate Multiple DNA Repair and Apoptotic Pathways following DNA Damage
inferred← citeshttps://doi.org/10.1146/annurev.immunol.21.120601.141152openalex-snapshot
BAFF and APRIL: A Tutorial on B Cell Survival
inferred← citeshttps://doi.org/10.1155/2016/2456062openalex-snapshot
Neurotrophin, p75, and Trk Signaling Module in the Developing Nervous System of the Marine AnnelidPlatynereis dumerilii
inferred← citeshttps://doi.org/10.1159/000094082openalex-snapshot
Evolution of the Neurotrophin Signaling System in Invertebrates
inferred← citeshttps://doi.org/10.1186/1471-213x-9-53openalex-snapshot
Ras promotes cell survival by antagonizing both JNK and Hid signals in the Drosophilaeye
inferred← citeshttps://doi.org/10.1186/1471-2148-9-243openalex-snapshot
The genome sequence of the protostome Daphnia pulex encodes respective orthologues of a neurotrophin, a Trk and a p75NTR: Evolution of neurotrophin signaling components and related proteins in the bilateria
inferred← citeshttps://doi.org/10.1186/1471-2180-10-290openalex-snapshot
Response to Dengue virus infections altered by cytokine-like substances from mosquito cell cultures
inferred← citeshttps://doi.org/10.1186/s13008-023-00097-4openalex-snapshot
Slik maintains tissue homeostasis by preventing JNK-mediated apoptosis
inferred← citeshttps://doi.org/10.1186/s13024-015-0014-yopenalex-snapshot
Calcium-responsive transactivator (CREST) protein shares a set of structural and functional traits with other proteins associated with amyotrophic lateral sclerosis
inferred← citeshttps://doi.org/10.1210/en.2007-1591openalex-snapshot
Tumor Necrosis Factor-α Attenuates Thyroid Hormone-Induced Apoptosis in Vascular Endothelial Cell Line XLgoo Established from Xenopus Tadpole Tails
inferred← citeshttps://doi.org/10.1242/dev.00293openalex-snapshot
Discovery of genes with highly restricted expression patterns in theDrosophilawing disc using DNA oligonucleotide microarrays
inferred← citeshttps://doi.org/10.1371/journal.pbio.0000035openalex-snapshot
The Drosophila Sterile-20 Kinase Slik Controls Cell Proliferation and Apoptosis during Imaginal Disc Development
inferred← citeshttps://doi.org/10.1371/journal.pgen.1007724openalex-snapshot
Astrocyte expression of the Drosophila TNF-alpha homologue, Eiger, regulates sleep in flies
inferred← citeshttps://doi.org/10.1371/journal.pgen.1008062openalex-snapshot
Reproduction disrupts stem cell homeostasis in testes of aged male Drosophila via an induced microenvironment
inferred← citeshttps://doi.org/10.1371/journal.pone.0034310openalex-snapshot
The HIV-1 Vpu Protein Induces Apoptosis in Drosophila via Activation of JNK Signaling
inferred← citeshttps://doi.org/10.1371/journal.pone.0060091openalex-snapshot
Wengen, the Sole Tumour Necrosis Factor Receptor in Drosophila, Collaborates with Moesin to Control Photoreceptor Axon Targeting during Development
inferred← citeshttps://doi.org/10.1371/journal.pone.0136356openalex-snapshot
Tumor Suppressor WWOX Contributes to the Elimination of Tumorigenic Cells in Drosophila melanogaster
inferred← citeshttps://doi.org/10.1379/csc-137r.1openalex-snapshot
A genomewide analysis of genes for the heat shock protein 70 chaperone system in the ascidian Ciona intestinalis
inferred← citeshttps://doi.org/10.1385/1-59259-812-9:191openalex-snapshot
Detection of Apoptosis in Drosophila
inferred← citeshttps://doi.org/10.14393/ufu.di.2014.373openalex-snapshot
Desenvolvimento de um modelo de doenças inflamatórias sistêmicas em Drosophila melanogaster
inferred← citeshttps://doi.org/10.15252/embj.2020104415openalex-snapshot
ADAM17‐triggered TNF signalling protects the ageing Drosophila retina from lipid droplet‐mediated degeneration
inferred← citeshttps://doi.org/10.15252/embr.202255903openalex-snapshot
PcEiger links the Imd/Relish pathway to ROS production in the intestine of the red swamp crayfish
inferred← citeshttps://doi.org/10.1534/genetics.105.045534openalex-snapshot
A Genetic Screen Targeting the Tumor Necrosis Factor/Eiger Signaling Pathway: Identification of Drosophila TAB2 as a Functionally Conserved Component
inferred← citeshttps://doi.org/10.1679/aohc.65.291openalex-snapshot
Molecular Genetic Control of Caspases and JNK-mediated Neural Cell Death.
inferred← citeshttps://doi.org/10.2174/138161206777947489openalex-snapshot
Biological Activity of Cytokines: An Evolutionary Perspective
inferred← citeshttps://doi.org/10.2741/3517openalex-snapshot
Mitochondria, Bcl-2 family proteins and apoptosomes: of worms, flies and men
inferred← citeshttps://doi.org/10.3109/07853890.2011.573806openalex-snapshot
MAGED1:Molecular insights and clinical implications
inferred← citeshttps://doi.org/10.3109/08880018.2015.1071903openalex-snapshot
Prognostic Biomarkers for Hodgkin Lymphoma
inferred← citeshttps://doi.org/10.3389/fcell.2020.00042openalex-snapshot
Two-Faced: Roles of JNK Signalling During Tumourigenesis in the Drosophila Model
inferred← citeshttps://doi.org/10.3389/fcell.2020.00117openalex-snapshot
A Positive Feedback Loop of Hippo- and c-Jun-Amino-Terminal Kinase Signaling Pathways Regulates Amyloid-Beta-Mediated Neurodegeneration
inferred← citeshttps://doi.org/10.3389/fgene.2019.00051openalex-snapshot
Drosophila melanogaster: A Model Organism to Study Cancer
inferred← citeshttps://doi.org/10.3389/fimmu.2022.905370openalex-snapshot
Drosophila Innate Immunity Involves Multiple Signaling Pathways and Coordinated Communication Between Different Tissues
inferred← citeshttps://doi.org/10.3389/fimmu.2023.1150628openalex-snapshot
Comparative transcriptomic analysis of gill reveals genes belonging to mTORC1 signaling pathway associated with the resistance trait of shrimp to VPAHPND
inferred← citeshttps://doi.org/10.3390/biomedicines11020263openalex-snapshot
Gene Set Enrichment Analysis and Genetic Experiment Reveal Changes in Cell Signaling Pathways Induced by α-Synuclein Overexpression
inferred← citeshttps://doi.org/10.3390/biomedicines7040082openalex-snapshot
Cyst Reduction in a Polycystic Kidney Disease Drosophila Model Using Smac Mimics
inferred← citeshttps://doi.org/10.3390/ijms21134580openalex-snapshot
Rounding up the Usual Suspects: Assessing Yorkie, AP-1, and Stat Coactivation in Tumorigenesis
inferred← citeshttps://doi.org/10.3390/ijms22083918openalex-snapshot
Modeling Neoplastic Growth in Renal Cell Carcinoma and Polycystic Kidney Disease
inferred← citeshttps://doi.org/10.3390/ijms22115519openalex-snapshot
The Emerging Roles of JNK Signaling in Drosophila Stem Cell Homeostasis
inferred← citeshttps://doi.org/10.3390/ijms22158317openalex-snapshot
Drosophila Larval Models of Invasive Tumorigenesis for In Vivo Studies on Tumour/Peripheral Host Tissue Interactions during Cancer Cachexia
inferred← citeshttps://doi.org/10.3390/ijms22168873openalex-snapshot
RasV12; scrib−/− Tumors: A Cooperative Oncogenesis Model Fueled by Tumor/Host Interactions
inferred← citeshttps://doi.org/10.3390/ijms22168927openalex-snapshot
The Duality of Caspases in Cancer, as Told through the Fly
inferred← citeshttps://doi.org/10.3390/ijms231911244openalex-snapshot
Drosophila as a Model Organism to Study Basic Mechanisms of Longevity
inferred← citeshttps://doi.org/10.3390/molecules25225477openalex-snapshot
Cyst Reduction by Melatonin in a Novel Drosophila Model of Polycystic Kidney Disease
inferred← citeshttps://doi.org/10.3402/jom.v4i0.10368openalex-snapshot
The Drosophila melanogaster host model
inferred← citeshttps://doi.org/10.4049/jimmunol.1901059openalex-snapshot
Molecular Drivers of Lymphocyte Organization in Vertebrate Mucosal Surfaces: Revisiting the TNF Superfamily Hypothesis
inferred← citeshttps://doi.org/10.4103/1673-5374.354516openalex-snapshot
Signaling interactions among neurons impact cell fitness and death in Alzheimer’s disease
inferred← citeshttps://doi.org/10.4161/cc.10.23.18243openalex-snapshot
Drosophila endocytic neoplastic tumor suppressor genes regulate Sav/Wts/Hpo signaling and the c-Jun N-terminal kinase pathway
inferred← citeshttps://doi.org/10.5282/edoc.2522openalex-snapshot
Charakterisierung des Zytokins BAFF als wichtiger Regulator der B-Zellfunktion beim Haushuhn
inferred← citeshttps://doi.org/10.6084/m9.figshare.24248085openalex-snapshot
Additional file 1 of Slik maintains tissue homeostasis by preventing JNK-mediated apoptosis
inferred← citeshttps://doi.org/10.70675/219b82abz0e78z4a44za2dbz305abfd286d2openalex-snapshot
Rôle de MIF (Macrophage Migration Inhibitory Factor) dans l'immunité innée et la réponse anti-schistosome chez Biomphalaria glabrata
inferred← citeshttps://doi.org/10.7554/elife.01004openalex-snapshot
Apoptotic cells can induce non-autonomous apoptosis through the TNF pathway
inferred← citeshttps://doi.org/10.7554/elife.10735openalex-snapshot
Tachykinin acts upstream of autocrine Hedgehog signaling during nociceptive sensitization in Drosophila
inferred← citeshttps://doi.org/10.7554/elife.61276openalex-snapshot
Single-cell transcriptomics of the Drosophila wing disc reveals instructive epithelium-to-myoblast interactions
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