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Metabolic adjustment of Drosophila hemocyte number and sessility by an adipokine
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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/j.1460-2075.1995.tb07285.xopenalex-snapshot
Activation of a Drosophila Janus kinase (JAK) causes hematopoietic neoplasia and developmental defects.
inferredcites →https://doi.org/10.1006/dbio.1996.0318openalex-snapshot
Cell Contact-Dependent Signaling
inferredcites →https://doi.org/10.1006/dbio.2000.0123openalex-snapshot
Postembryonic Hematopoiesis in Drosophila
inferredcites →https://doi.org/10.1007/bf00848799openalex-snapshot
A mutant affecting the crystal cells inDrosophila melanogaster
inferredcites →https://doi.org/10.1016/j.cell.2008.02.052openalex-snapshot
Six-Microns-Under Acts Upstream of Draper in the Glial Phagocytosis of Apoptotic Neurons
inferredcites →https://doi.org/10.1016/j.cell.2011.06.040openalex-snapshot
Anaplastic Lymphoma Kinase Spares Organ Growth during Nutrient Restriction in Drosophila
inferredcites →https://doi.org/10.1016/j.cub.2006.08.052openalex-snapshot
Akt and foxo Dysregulation Contribute to Infection-Induced Wasting in Drosophila
inferredcites →https://doi.org/10.1016/j.cub.2007.02.041openalex-snapshot
Nimrod, a Putative Phagocytosis Receptor with EGF Repeats in Drosophila Plasmatocytes
inferredcites →https://doi.org/10.1016/j.cub.2011.06.033openalex-snapshot
Coordinating Growth and Maturation — Insights from Drosophila
inferredcites →https://doi.org/10.1016/j.dci.2013.06.005openalex-snapshot
The cell-mediated immunity of Drosophila melanogaster: Hemocyte lineages, immune compartments, microanatomy and regulation
inferredcites →https://doi.org/10.1016/j.devcel.2009.10.009openalex-snapshot
A Drosophila Insulin-like Peptide Promotes Growth during Nonfeeding States
inferredcites →https://doi.org/10.1016/j.devcel.2010.05.007openalex-snapshot
The Steroid Hormone Ecdysone Controls Systemic Growth by Repressing dMyc Function in Drosophila Fat Cells
inferredcites →https://doi.org/10.1016/j.devcel.2015.02.012openalex-snapshot
Systemic Organ Wasting Induced by Localized Expression of the Secreted Insulin/IGF Antagonist ImpL2
inferredcites →https://doi.org/10.1016/j.devcel.2015.03.001openalex-snapshot
Malignant Drosophila Tumors Interrupt Insulin Signaling to Induce Cachexia-like Wasting
inferredcites →https://doi.org/10.1016/j.immuni.2011.09.018openalex-snapshot
Negative Regulation by Amidase PGRPs Shapes the Drosophila Antibacterial Response and Protects the Fly from Innocuous Infection
inferredcites →https://doi.org/10.1016/j.immuni.2014.12.023openalex-snapshot
Macrophage-Derived upd3 Cytokine Causes Impaired Glucose Homeostasis and Reduced Lifespan in Drosophila Fed a Lipid-Rich Diet
inferredcites →https://doi.org/10.1016/j.jim.2008.11.019openalex-snapshot
A novel method to determine the engulfment of apoptotic cells by macrophages using pHrodo succinimidyl ester
inferredcites →https://doi.org/10.1016/j.molimm.2010.04.017openalex-snapshot
Cell lineage tracing reveals the plasticity of the hemocyte lineages and of the hematopoietic compartments in Drosophila melanogaster
inferredcites →https://doi.org/10.1016/s0092-8674(03)00713-xopenalex-snapshot
A Nutrient Sensor Mechanism Controls Drosophila Growth
inferredcites →https://doi.org/10.1016/s0896-6273(03)00289-7openalex-snapshot
Unwrapping Glial Biology
inferredcites →https://doi.org/10.1016/s1079-9796(03)00028-7openalex-snapshot
Transcriptional regulation of hematopoiesis in Drosophila
inferredcites →https://doi.org/10.1017/s0031182002001750openalex-snapshot
Costs of resistance in insect-parasite and insect-parasitoid interactions
inferredcites →https://doi.org/10.1038/38483openalex-snapshot
Trade-off between parasitoid resistance and larval competitive ability in Drosophila melanogaster
inferredcites →https://doi.org/10.1038/nature09715openalex-snapshot
The developmental transcriptome of Drosophila melanogaster
inferredcites →https://doi.org/10.1038/ncb2453openalex-snapshot
Direct sensing of systemic and nutritional signals by haematopoietic progenitors in Drosophila
inferredcites →https://doi.org/10.1038/ncomms15990openalex-snapshot
Regulation of Drosophila hematopoietic sites by Activin-β from active sensory neurons
inferredcites →https://doi.org/10.1038/nrm2202openalex-snapshot
Drosophila melanogaster embryonic haemocytes: masters of multitasking
inferredcites →https://doi.org/10.1038/sj.cdd.4400714openalex-snapshot
Bcl-2 and Bax mammalian regulators of apoptosis are functional in Drosophila
inferredcites →https://doi.org/10.1038/sj.onc.1208156openalex-snapshot
Increased expression of Drosophila tetraspanin, Tsp68C, suppresses the abnormal proliferation of ytr-deficient and Ras/Raf-activated hemocytes
inferredcites →https://doi.org/10.1073/pnas.0709951105openalex-snapshot
Circulating blood cells function as a surveillance system for damaged tissue in Drosophila larvae
inferredcites →https://doi.org/10.1073/pnas.0903971106openalex-snapshot
Elimination of plasmatocytes by targeted apoptosis reveals their role in multiple aspects of the Drosophila immune response
inferredcites →https://doi.org/10.1073/pnas.1001744107openalex-snapshot
Loss of lipid synthesis as an evolutionary consequence of a parasitic lifestyle
inferredcites →https://doi.org/10.1074/jbc.m110.102392openalex-snapshot
Two-color Photoactivatable Probe for Selective Tracking of Proteins and Cells
inferredcites →https://doi.org/10.1074/jbc.m408597200openalex-snapshot
Draper-mediated and Phosphatidylserine-independent Phagocytosis of Apoptotic Cells by Drosophila Hemocytes/Macrophages
inferredcites →https://doi.org/10.1080/01635581.2016.1115100openalex-snapshot
Variation of resting energy expenditure after the first chemotherapy cycle in acute leukemia patients
inferredcites →https://doi.org/10.1086/587658openalex-snapshot
The Interaction between Nutrition and Infection
inferredcites →https://doi.org/10.1093/acprof:oso/9780199229482.001.0001openalex-snapshot
Evolutionary Parasitology
inferredcites →https://doi.org/10.1093/embo-reports/kvf242openalex-snapshot
PVF2, a PDGF/VEGF‐like growth factor, induces hemocyte proliferation in Drosophila larvae
inferredcites →https://doi.org/10.1093/molbev/msn180openalex-snapshot
Evolution of Genes and Repeats in the Nimrod Superfamily
inferredcites →https://doi.org/10.1101/cshperspect.a019117openalex-snapshot
The Systemic Control of Growth
inferredcites →https://doi.org/10.1101/gr.213694.116openalex-snapshot
The developmental proteome of Drosophila melanogaster
inferredcites →https://doi.org/10.1111/febs.14857openalex-snapshot
Two Nimrod receptors, NimC1 and Eater, synergistically contribute to bacterial phagocytosis in Drosophila melanogaster
inferredcites →https://doi.org/10.1111/j.1365-2435.2010.01800.xopenalex-snapshot
Trade‐off between growth and immune function: a meta‐analysis of selection experiments
inferredcites →https://doi.org/10.1111/j.1462-5822.2007.00930.xopenalex-snapshot
Drosophila haematopoiesis
inferredcites →https://doi.org/10.1126/science.1119432openalex-snapshot
Antagonistic Actions of Ecdysone and Insulins Determine Final Size in Drosophila
inferredcites →https://doi.org/10.1126/science.290.5494.1166openalex-snapshot
Survival for Immunity: The Price of Immune System Activation for Bumblebee Workers
inferredcites →https://doi.org/10.1128/mbio.01006-16openalex-snapshot
The Role of Lipid Competition for Endosymbiont-Mediated Protection against Parasitoid Wasps in Drosophila
inferredcites →https://doi.org/10.1146/annurev-ento-011613-162056openalex-snapshot
The Development and Functions of Oenocytes
inferredcites →https://doi.org/10.1159/000210264openalex-snapshot
Genetic Ablation of Drosophila Phagocytes Reveals Their Contribution to Both Development and Resistance to Bacterial Infection
inferredcites →https://doi.org/10.1186/1471-2121-11-7openalex-snapshot
Nutritional control of gene expression in Drosophila larvae via TOR, Myc and a novel cis-regulatory element
inferredcites →https://doi.org/10.1186/s12915-015-0193-6openalex-snapshot
Drosophila innate immunity: regional and functional specialization of prophenoloxidases
inferredcites →https://doi.org/10.1242/bio.201410595openalex-snapshot
The Nimrod transmembrane receptor Eater is required for hemocyte attachment to the sessile compartment in Drosophila melanogaster
inferredcites →https://doi.org/10.1242/dev.00702openalex-snapshot
The two origins of hemocytes in Drosophila
inferredcites →https://doi.org/10.1242/dev.01837openalex-snapshot
TheDrosophilalymph gland as a developmental model of hematopoiesis
inferredcites →https://doi.org/10.1242/dev.067322openalex-snapshot
The peripheral nervous system supports blood cell homing and survival in the Drosophila larva
inferredcites →https://doi.org/10.1242/dev.074203openalex-snapshot
Multifaceted roles of PTEN and TSC orchestrate growth and differentiation of Drosophila blood progenitors
inferredcites →https://doi.org/10.1242/dev.080259openalex-snapshot
Dual role for Insulin/TOR signaling in the control of hematopoietic progenitor maintenance in Drosophila
inferredcites →https://doi.org/10.1242/dev.121798openalex-snapshot
Bag of Marbles controls the size and organization of the Drosophila hematopoietic niche through interactions with the Insulin-like growth factor pathway and Retinoblastoma-family protein
inferredcites →https://doi.org/10.1242/dev.122.2.409openalex-snapshot
Two distinct roles for Ras in a developmentally regulated cell migration
inferredcites →https://doi.org/10.1371/journal.pone.0008549openalex-snapshot
Gene Expression in a Drosophila Model of Mitochondrial Disease
inferredcites →https://doi.org/10.1371/journal.pone.0014051openalex-snapshot
Lineage Tracing of Lamellocytes Demonstrates Drosophila Macrophage Plasticity
inferredcites →https://doi.org/10.1371/journal.pone.0041759openalex-snapshot
Fetal Liver Blood Flow Distribution: Role in Human Developmental Strategy to Prioritize Fat Deposition versus Brain Development
inferredcites →https://doi.org/10.1371/journal.ppat.1004067openalex-snapshot
Prophenoloxidase Activation Is Required for Survival to Microbial Infections in Drosophila
inferredcites →https://doi.org/10.1371/journal.ppat.1004507openalex-snapshot
The Toll-Dorsal Pathway Is Required for Resistance to Viral Oral Infection in Drosophila
inferredcites →https://doi.org/10.1371/journal.ppat.1005746openalex-snapshot
Transdifferentiation and Proliferation in Two Distinct Hemocyte Lineages in Drosophila melanogaster Larvae after Wasp Infection
inferredcites →https://doi.org/10.1534/genetics.118.300223openalex-snapshot
Drosophila as a Genetic Model for Hematopoiesis
inferredcites →https://doi.org/10.3389/fgene.2012.00267openalex-snapshot
Immune response from a resource allocation perspective
inferredcites →https://doi.org/10.3791/52733openalex-snapshot
Assaying Blood Cell Populations of the Drosophila melanogaster Larva
inferredcites →https://doi.org/10.4049/jimmunol.0901032openalex-snapshot
Identification of Lipoteichoic Acid as a Ligand for Draper in the Phagocytosis of Staphylococcus aureus by Drosophila Hemocytes
inferredcites →https://doi.org/10.4161/fly.22267openalex-snapshot
Of blood cells and the nervous system
inferredcites →https://doi.org/10.7554/elife.06166openalex-snapshot
Drosophila sessile hemocyte clusters are true hematopoietic tissues that regulate larval blood cell differentiation
inferredcites →https://doi.org/10.7554/elife.12068openalex-snapshot
A genome-wide resource for the analysis of protein localisation in Drosophila
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1016/j.cbpc.2021.109188openalex-snapshot
Dietary cadmium (Cd) reduces hemocyte level by induction of apoptosis in Drosophila melanogaster
inferred← citeshttps://doi.org/10.15252/embj.2020104486openalex-snapshot
Temporal specificity and heterogeneity of Drosophila immune cells
inferred← citeshttps://doi.org/10.3389/fimmu.2020.00063openalex-snapshot
Subpopulation of Macrophage-Like Plasmatocytes Attenuates Systemic Growth via JAK/STAT in the Drosophila Fat Body
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