On the public citation graph

Extracellular DNA traps in a ctenophore demonstrate conserved immune cell behaviors in a non-bilaterian

https://doi.org/10.1101/2020.06.09.141010

0 signed · 79 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 See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.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/10.1006/fsim.1998.0205openalex-snapshot

The inter-relationships of bivalve haemocytes

inferredcites →https://doi.org/10.1007/978-1-0716-2172-1_18openalex-snapshot

Isolation and Maintenance of In Vitro Cell Cultures from the Ctenophore Mnemiopsis leidyi

inferredcites →https://doi.org/10.1007/s00251-010-0428-1openalex-snapshot

Domain architecture evolution of pattern-recognition receptors

inferredcites →https://doi.org/10.1007/s00412-016-0614-5openalex-snapshot

Nuclear morphologies: their diversity and functional relevance

inferredcites →https://doi.org/10.1007/s00441-018-2787-0openalex-snapshot

Earthworm coelomocyte extracellular traps: structural and functional similarities with neutrophil NETs

inferredcites →https://doi.org/10.1016/0014-4827(91)90477-copenalex-snapshot

Ionophore-induced apoptosis: Role of DNA fragmentation and calcium fluxes

inferredcites →https://doi.org/10.1016/j.alit.2020.02.002openalex-snapshot

The roles of IL-5 and anti-IL-5 treatment in eosinophilic diseases: Asthma, eosinophilic granulomatosis with polyangiitis, and eosinophilic chronic rhinosinusitis

inferredcites →https://doi.org/10.1016/j.alit.2020.10.002openalex-snapshot

How to detect eosinophil ETosis (EETosis) and extracellular traps

inferredcites →https://doi.org/10.1016/j.cell.2006.02.015openalex-snapshot

Pathogen Recognition and Innate Immunity

inferredcites →https://doi.org/10.1016/j.cub.2019.08.059openalex-snapshot

CTENO64 Is Required for Coordinated Paddling of Ciliary Comb Plate in Ctenophores

inferredcites →https://doi.org/10.1016/j.dci.2018.01.012openalex-snapshot

DNA extracellular traps are part of the immune repertoire of Periplaneta americana

inferredcites →https://doi.org/10.1016/j.dci.2019.103585openalex-snapshot

Extracellular traps (ETosis) can be activated through NADPH-dependent and -independent mechanisms in bivalve mollusks

inferredcites →https://doi.org/10.1016/j.dci.2021.104094openalex-snapshot

Mitochondria are essential for antibacterial extracellular trap formation mediated by zymosan in hemocytes of Ruditapes philippinarum

inferredcites →https://doi.org/10.1016/j.devcel.2018.01.019openalex-snapshot

Neutrophil Extracellular Traps: The Biology of Chromatin Externalization

inferredcites →https://doi.org/10.1016/j.fsi.2015.02.040openalex-snapshot

The new insights into the oyster antimicrobial defense: Cellular, molecular and genetic view

inferredcites →https://doi.org/10.1016/j.fsi.2023.108616openalex-snapshot

Nigericin treatment activates endoplasmic reticulum apoptosis pathway in goldfish kidney leukocytes

inferredcites →https://doi.org/10.1016/j.mib.2006.12.005openalex-snapshot

Neutrophil extracellular traps: casting the NET over pathogenesis

inferredcites →https://doi.org/10.1016/s0301-0082(03)00090-xopenalex-snapshot

Regulation and critical role of potassium homeostasis in apoptosis

inferredcites →https://doi.org/10.1038/cdd.2011.1openalex-snapshot

Dying for a cause: NETosis, mechanisms behind an antimicrobial cell death modality

inferredcites →https://doi.org/10.1038/nature06614openalex-snapshot

Broad phylogenomic sampling improves resolution of the animal tree of life

inferredcites →https://doi.org/10.1038/nature09201openalex-snapshot

The Amphimedon queenslandica genome and the evolution of animal complexity

inferredcites →https://doi.org/10.1038/nature13400openalex-snapshot

The ctenophore genome and the evolutionary origins of neural systems

inferredcites →https://doi.org/10.1038/ncomms10917openalex-snapshot

αv Integrins combine with LC3 and atg5 to regulate Toll-like receptor signalling in B cells

inferredcites →https://doi.org/10.1038/ncomms10938openalex-snapshot

Social amoebae trap and kill bacteria by casting DNA nets

inferredcites →https://doi.org/10.1038/ncomms11615openalex-snapshot

Negative magnetoresistance without well-defined chirality in the Weyl semimetal TaP

inferredcites →https://doi.org/10.1038/ncomms5357openalex-snapshot

Plasmofluidic single-molecule surface-enhanced Raman scattering from dynamic assembly of plasmonic nanoparticles

inferredcites →https://doi.org/10.1038/ncomms5627openalex-snapshot

Invertebrate extracellular phagocyte traps show that chromatin is an ancient defence weapon

inferredcites →https://doi.org/10.1038/ni.f.220openalex-snapshot

Calcium signaling in immune cells

inferredcites →https://doi.org/10.1038/nm.1855openalex-snapshot

Catapult-like release of mitochondrial DNA by eosinophils contributes to antibacterial defense

inferredcites →https://doi.org/10.1038/nm.4027openalex-snapshot

Neutrophil extracellular traps enriched in oxidized mitochondrial DNA are interferogenic and contribute to lupus-like disease

inferredcites →https://doi.org/10.1038/nri.2017.105openalex-snapshot

Neutrophil extracellular traps in immunity and disease

inferredcites →https://doi.org/10.1038/s41467-021-22074-7openalex-snapshot

Evidence for sponges as sister to all other animals from partitioned phylogenomics with mixture models and recoding

inferredcites →https://doi.org/10.1038/s41559-017-0331-3openalex-snapshot

Ctenophore relationships and their placement as the sister group to all other animals

inferredcites →https://doi.org/10.1038/s41586-023-05936-6openalex-snapshot

Ancient gene linkages support ctenophores as sister to other animals

inferredcites →https://doi.org/10.1038/s41598-019-53202-5openalex-snapshot

Machine Learning to Quantitate Neutrophil NETosis

inferredcites →https://doi.org/10.1038/srep41749openalex-snapshot

Transcriptional firing helps to drive NETosis

inferredcites →https://doi.org/10.1073/pnas.1320678111openalex-snapshot

Structure of the Toll-Spätzle complex, a molecular hub in Drosophila development and innate immunity

inferredcites →https://doi.org/10.1073/pnas.1414055112openalex-snapshot

SK3 channel and mitochondrial ROS mediate NADPH oxidase-independent NETosis induced by calcium influx

inferredcites →https://doi.org/10.1073/pnas.1617722114openalex-snapshot

Toll-like receptor pathway evolution in deuterostomes

inferredcites →https://doi.org/10.1074/jbc.m114.576546openalex-snapshot

Antimicrobial Histones and DNA Traps in Invertebrate Immunity

inferredcites →https://doi.org/10.1083/jcb.200606027openalex-snapshot

Novel cell death program leads to neutrophil extracellular traps

inferredcites →https://doi.org/10.1083/jcb.201203170openalex-snapshot

Neutrophil extracellular traps: Is immunity the second function of chromatin?

inferredcites →https://doi.org/10.1084/jem.20200652openalex-snapshot

Targeting potential drivers of COVID-19: Neutrophil extracellular traps

inferredcites →https://doi.org/10.1093/eurheartj/ehv419openalex-snapshot

Histopathological evaluation of thrombus in patients presenting with stent thrombosis. A multicenter European study: a report of the prevention of late stent thrombosis by an interdisciplinary global European effort consortium

inferredcites →https://doi.org/10.1093/icb/icz116openalex-snapshot

Still Enigmatic: Innate Immunity in the Ctenophore Mnemiopsis leidyi

inferredcites →https://doi.org/10.1093/molbev/msab170openalex-snapshot

Rooting the Animal Tree of Life

inferredcites →https://doi.org/10.1093/molbev/msad133openalex-snapshot

Bivalves Present the Largest and Most Diversified Repertoire of Toll-Like Receptors in the Animal Kingdom, Suggesting Broad-Spectrum Pathogen Recognition in Marine Waters

inferredcites →https://doi.org/10.1093/molbev/msn077openalex-snapshot

Unicellular Ca2+ Signaling 'Toolkit' at the Origin of Metazoa

inferredcites →https://doi.org/10.1098/rsbl.2013.0864openalex-snapshot

Specific immune priming in the invasive ctenophore Mnemiopsis leidyi

inferredcites →https://doi.org/10.1104/pp.109.142067openalex-snapshot

Extracellular DNA Is Required for Root Tip Resistance to Fungal Infection

inferredcites →https://doi.org/10.1111/j.1365-2567.2009.03071.xopenalex-snapshot

A central role for monocytes in Toll‐like receptor‐mediated activation of the vasculature

inferredcites →https://doi.org/10.1126/science.1092385openalex-snapshot

Neutrophil Extracellular Traps Kill Bacteria

inferredcites →https://doi.org/10.1126/science.1139158openalex-snapshot

Sea Anemone Genome Reveals Ancestral Eumetazoan Gene Repertoire and Genomic Organization

inferredcites →https://doi.org/10.1126/science.1242592openalex-snapshot

The Genome of the Ctenophore Mnemiopsis leidyi and Its Implications for Cell Type Evolution

inferredcites →https://doi.org/10.1126/scisignal.aax7942openalex-snapshot

The cytosolic DNA sensor cGAS recognizes neutrophil extracellular traps

inferredcites →https://doi.org/10.1128/iai.00766-20openalex-snapshot

Beyond Homeostasis: Potassium and Pathogenesis during Bacterial Infections

inferredcites →https://doi.org/10.1146/annurev.immunol.20.091301.131133openalex-snapshot

MAP Kinases in the Immune Response

inferredcites →https://doi.org/10.1155/2016/4604713openalex-snapshot

How Neutrophil Extracellular Traps Become Visible

inferredcites →https://doi.org/10.1179/1351000213y.0000000044openalex-snapshot

Redox regulation of the immune response

inferredcites →https://doi.org/10.1186/1471-2407-14-36openalex-snapshot

PMA synergistically enhances apicularen A-induced cytotoxicity by disrupting microtubule networks in HeLa cells

inferredcites →https://doi.org/10.1186/s12862-017-0940-0openalex-snapshot

Evolutionary origin and function of NOX4-art, an arthropod specific NADPH oxidase

inferredcites →https://doi.org/10.1186/s13071-016-1961-zopenalex-snapshot

Gastropod-derived haemocyte extracellular traps entrap metastrongyloid larval stages of Angiostrongylus vasorum, Aelurostrongylus abstrusus and Troglostrongylus brevior

inferredcites →https://doi.org/10.1186/s13227-019-0138-1openalex-snapshot

Genomic analysis of the tryptome reveals molecular mechanisms of gland cell evolution

inferredcites →https://doi.org/10.1189/jlb.4ri1014-521ropenalex-snapshot

Extracellular traps and macrophages: new roles for the versatile phagocyte

inferredcites →https://doi.org/10.1242/dev.199771openalex-snapshot

Krüppel-like factor gene function in the ctenophore Mnemiopsis leidyi assessed by CRISPR/Cas9-mediated genome editing

inferredcites →https://doi.org/10.1242/jeb.026971openalex-snapshot

Expression of a poriferan potassium channel: insights into the evolution of ion channels in metazoans

inferredcites →https://doi.org/10.1242/jeb.152371openalex-snapshot

Establishing and maintaining primary cell cultures derived from the ctenophore Mnemiopsis leidyi

inferredcites →https://doi.org/10.1371/journal.pbio.2005970openalex-snapshot

CellProfiler 3.0: Next-generation image processing for biology

inferredcites →https://doi.org/10.1371/journal.pone.0159031openalex-snapshot

Conservative Mechanisms of Extracellular Trap Formation by Annelida Eisenia andrei: Serine Protease Activity Requirement

inferredcites →https://doi.org/10.3389/fimmu.2014.00459openalex-snapshot

Evolution of Innate Immunity: Clues from Invertebrates via Fish to Mammals

inferredcites →https://doi.org/10.3389/fimmu.2017.00290openalex-snapshot

Neutrophil Extracellular Traps of Cynoglossus semilaevis: Production Characteristics and Antibacterial Effect

inferredcites →https://doi.org/10.3389/fimmu.2021.621311openalex-snapshot

Multiple Origins of Extracellular DNA Traps

inferredcites →https://doi.org/10.3390/biology9080234openalex-snapshot

Conservation of Cell Communication Systems in Invertebrate Host–Defence Mechanisms: Possible Role in Immunity and Disease

inferredcites →https://doi.org/10.3390/cells10081853openalex-snapshot

Evolution of Cellular Immunity Effector Cells; Perspective on Cytotoxic and Phagocytic Cellular Lineages

inferredcites →https://doi.org/10.4049/jimmunol.1700905openalex-snapshot

A High-Throughput Real-Time Imaging Technique To Quantify NETosis and Distinguish Mechanisms of Cell Death in Human Neutrophils

inferredcites →https://doi.org/10.7554/elife.24437openalex-snapshot

Diverse stimuli engage different neutrophil extracellular trap pathways

inferredcites →https://doi.org/10.7554/elife.81050openalex-snapshot

Evolutionary gain and loss of a plant pattern-recognition receptor for HAMP recognition

inferredcites →https://doi.org/10.7717/peerj.2590openalex-snapshot

Functional characterisation of phagocytes in the Pacific oyster Crassostrea gigas

What points at this work

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

inferred← citeshttps://doi.org/10.1007/978-1-0716-2172-1_18openalex-snapshot

Isolation and Maintenance of In Vitro Cell Cultures from the Ctenophore Mnemiopsis leidyi

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.