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Gradual specialization of phagocytic ameboid cells may have impaired regenerative capacities in metazoan lineages
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Outgoing claims: the papers this work cites, builds on, or argues with.
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The promise of perfect adult tissue repair and regeneration in mammals: Learning from regenerative amphibians and fish
inferredcites →https://doi.org/10.1002/dvdy.21335openalex-snapshot
Caenorhabditis elegans germ line: A model for stem cell biology
inferredcites →https://doi.org/10.1002/dvdy.386openalex-snapshot
Hydrogen peroxide is necessary during tail regeneration in juvenile axolotl
inferredcites →https://doi.org/10.1002/jemt.1187openalex-snapshot
Microscopic overview of crinoid regeneration
inferredcites →https://doi.org/10.1002/jez.1401950107openalex-snapshot
Mitosis in the intact and regenerating planarian Dugesia mediterranea n.sp. II. Mitotic studies during regeneration, and a possible mechanism of blastema formation
inferredcites →https://doi.org/10.1002/jez.1402380212openalex-snapshot
Immunocompetence in Hydra: Epithelial cells recognize self‐nonself and react against it
inferredcites →https://doi.org/10.1002/path.4133openalex-snapshot
Macrophage plasticity and polarization in tissue repair and remodelling
inferredcites →https://doi.org/10.1002/wdev.312openalex-snapshot
The zebrafish: A fintastic model for hematopoietic development and disease
inferredcites →https://doi.org/10.1006/bbrc.1995.1477openalex-snapshot
Signals from the IL-1 Receptor Homolog, Toll, Can Activate an Immune Response in a Drosophila Hemocyte Cell Line
inferredcites →https://doi.org/10.1006/dbio.1993.1028openalex-snapshot
Minimum Tissue Size Required for Hydra Regeneration
inferredcites →https://doi.org/10.1006/jipa.1995.1022openalex-snapshot
Wound Repair in the Amphioxus (Branchiostoma platae), an Animal Deprived of Inflammatory Phagocytes
inferredcites →https://doi.org/10.1007/978-3-319-92486-1_14openalex-snapshot
Regeneration in Stellate Echinoderms: Crinoidea, Asteroidea and Ophiuroidea
inferredcites →https://doi.org/10.1007/bf00027602openalex-snapshot
Phagocytic response of planarian reticular cells to heat-killed bacteria
inferredcites →https://doi.org/10.1007/bf00036385openalex-snapshot
Structure and function of the reticular cell in the planarian Dugesia dorotocephala
inferredcites →https://doi.org/10.1007/bf00539786openalex-snapshot
Ultrastructural changes in the gastrodermal phagocytic cells of the planarian Dugesia gonocephala s.l. during food digestion (Plathelminthes)
inferredcites →https://doi.org/10.1007/bf02055779openalex-snapshot
The fine structure of the planarianPolycelis tenuis Iijima
inferredcites →https://doi.org/10.1007/bf02161491openalex-snapshot
Experimental studies of the regeneration of Planaria maculata
inferredcites →https://doi.org/10.1007/s001140050444openalex-snapshot
Origin of Metazoa: Sponges as Living Fossils
inferredcites →https://doi.org/10.1007/s00239-002-2424-zopenalex-snapshot
Phylogeny of Choanozoa, Apusozoa, and Other Protozoa and Early Eukaryote Megaevolution
inferredcites →https://doi.org/10.1007/s004350050037openalex-snapshot
Detection of distinct endocytotic and phagocytotic activities in epithelial cells (pinacocytes) of freshwater sponges (Porifera, Spongillidae)
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/10.1007/s00441-019-03096-6openalex-snapshot
Phagocytosis in cellular defense and nutrition: a food-centered approach to the evolution of macrophages
inferredcites →https://doi.org/10.1007/s00441-020-03337-zopenalex-snapshot
Coelomocyte replenishment in adult Asterias rubens: the possible ways
inferredcites →https://doi.org/10.1007/s10142-010-0199-7openalex-snapshot
Identification and expression of liver-specific genes after LPS challenge in amphioxus: the hepatic cecum as liver-like organ and “pre-hepatic” acute phase response
inferredcites →https://doi.org/10.1007/s11427-011-4237-zopenalex-snapshot
Characterization of the immune defense related tissues, cells, and genes in amphioxus
inferredcites →https://doi.org/10.1007/s12562-020-01476-4openalex-snapshot
Fish cytokines: current research and applications
inferredcites →https://doi.org/10.1007/s42995-020-00080-wopenalex-snapshot
Hepatic cecum: a key integrator of immunity in amphioxus
inferredcites →https://doi.org/10.1016/0169-4758(92)90126-mopenalex-snapshot
Nematode surface coats: Actively evading immunity
inferredcites →https://doi.org/10.1016/0300-9629(93)90237-xopenalex-snapshot
The myelo-erythroid nature of the chloragogenous-like tissues of the annelids
inferredcites →https://doi.org/10.1016/b978-0-12-374279-7.12007-7openalex-snapshot
The Immune System of Echinoderms
inferredcites →https://doi.org/10.1016/b978-0-12-801975-7.00002-5openalex-snapshot
Origin and Functions of Tunicate Hemocytes
inferredcites →https://doi.org/10.1016/j.ajpath.2013.06.034openalex-snapshot
Phenotypic Transitions of Macrophages Orchestrate Tissue Repair
inferredcites →https://doi.org/10.1016/j.ajpath.2015.06.001openalex-snapshot
Monocyte and Macrophage Plasticity in Tissue Repair and Regeneration
inferredcites →https://doi.org/10.1016/j.bbrc.2018.09.126openalex-snapshot
Inflammatory production of reactive oxygen species by Drosophila hemocytes activates cellular immune defenses
inferredcites →https://doi.org/10.1016/j.burns.2018.05.018openalex-snapshot
Optimal skin regeneration after full thickness thermal burn injury in the spiny mouse, Acomys cahirinus
inferredcites →https://doi.org/10.1016/j.coi.2007.08.003openalex-snapshot
Evolution and development of immunological structures in the lamprey
inferredcites →https://doi.org/10.1016/j.coi.2019.12.006openalex-snapshot
Evolutionary perspective on the hematopoietic system through a colonial chordate: allogeneic immunity and hematopoiesis
inferredcites →https://doi.org/10.1016/j.cub.2010.09.014openalex-snapshot
Multicellular development in a choanoflagellate
inferredcites →https://doi.org/10.1016/j.cub.2013.01.058openalex-snapshot
Calcium Flashes Orchestrate the Wound Inflammatory Response through DUOX Activation and Hydrogen Peroxide Release
inferredcites →https://doi.org/10.1016/j.cub.2015.07.037openalex-snapshot
Toll-like Receptor Signaling Promotes Development and Function of Sensory Neurons Required for a C. elegans Pathogen-Avoidance Behavior
inferredcites →https://doi.org/10.1016/j.cub.2015.12.064openalex-snapshot
Extracellular Reactive Oxygen Species Drive Apoptosis-Induced Proliferation via Drosophila Macrophages
inferredcites →https://doi.org/10.1016/j.cub.2020.07.035openalex-snapshot
Cell Sorting in Hydra vulgaris Arises from Differing Capacities for Epithelialization between Cell Types
inferredcites →https://doi.org/10.1016/j.dci.2004.04.001openalex-snapshot
Macrophage migration inhibitory factor (MIF) in chinese amphioxus as a molecular marker of immune evolution during the transition of invertebrate/vertebrate
inferredcites →https://doi.org/10.1016/j.dci.2010.03.009openalex-snapshot
The primitive immune system of amphioxus provides insights into the ancestral structure of the vertebrate immune system
inferredcites →https://doi.org/10.1016/j.dci.2011.03.018openalex-snapshot
Lipopolysaccharide enhances bactericidal activity in Dictyostelium discoideum cells
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.dci.2013.08.009openalex-snapshot
Molecular cloning and expression of TLR in the Eisenia andrei earthworm
inferredcites →https://doi.org/10.1016/j.dci.2014.03.005openalex-snapshot
Structural and functional characterization of a TGFβ molecule from amphioxus reveals an ancient origin of both immune-enhancing and -inhibitory functions
inferredcites →https://doi.org/10.1016/j.dci.2016.02.015openalex-snapshot
Inflammation and immunity in organ regeneration
inferredcites →https://doi.org/10.1016/j.dci.2020.103840openalex-snapshot
Epigenetic control of myeloid cells behavior by Histone Deacetylase activity (HDAC) during tissue and organ regeneration in Xenopus laevis
inferredcites →https://doi.org/10.1016/j.devcel.2009.07.014openalex-snapshot
Apoptotic Cells Provide an Unexpected Source of Wnt3 Signaling to Drive Hydra Head Regeneration
inferredcites →https://doi.org/10.1016/j.devcel.2017.09.016openalex-snapshot
The Origin of Animal Multicellularity and Cell Differentiation
inferredcites →https://doi.org/10.1016/j.diff.2014.02.002openalex-snapshot
Scar-free wound healing and regeneration in amphibians: Immunological influences on regenerative success
inferredcites →https://doi.org/10.1016/j.ejphar.2020.173090openalex-snapshot
Macrophage M1/M2 polarization
inferredcites →https://doi.org/10.1016/j.exphem.2014.06.001openalex-snapshot
Developmental hematopoiesis: Ontogeny, genetic programming and conservation
inferredcites →https://doi.org/10.1016/j.expneurol.2013.09.004openalex-snapshot
Cyclic AMP promotes axon regeneration, lesion repair and neuronal survival in lampreys after spinal cord injury
inferredcites →https://doi.org/10.1016/j.fsi.2018.03.013openalex-snapshot
Regeneration of coelomocytes after evisceration in the sea cucumber, Apostichopus japonicus
inferredcites →https://doi.org/10.1016/j.hazl.2021.100031openalex-snapshot
Expanded polystyrene microplastic is more cytotoxic to seastar coelomocytes than its nonexpanded counterpart: A comparative analysis
inferredcites →https://doi.org/10.1016/j.imbio.2013.09.001openalex-snapshot
Macrophages: Supportive cells for tissue repair and regeneration
inferredcites →https://doi.org/10.1016/j.isci.2021.103281openalex-snapshot
Bacterial lipopolysaccharides can initiate regeneration of the Xenopus tadpole tail
inferredcites →https://doi.org/10.1016/j.it.2004.03.004openalex-snapshot
Coagulation in arthropods: defence, wound closure and healing
inferredcites →https://doi.org/10.1016/j.jdermsci.2009.09.005openalex-snapshot
Scarless healing of oral mucosa is characterized by faster resolution of inflammation and control of myofibroblast action compared to skin wounds in the red Duroc pig model
inferredcites →https://doi.org/10.1016/j.matbio.2014.02.002openalex-snapshot
The predicted secretomes of Monosiga brevicollis and Capsaspora owczarzaki, close unicellular relatives of metazoans, reveal new insights into the evolution of the metazoan extracellular matrix
inferredcites →https://doi.org/10.1016/j.mod.2012.11.005openalex-snapshot
Innate immune cells are dispensable for regenerative growth of imaginal discs
inferredcites →https://doi.org/10.1016/j.molimm.2009.03.022openalex-snapshot
An amphioxus TLR with dynamic embryonic expression pattern responses to pathogens and activates NF-κB pathway via MyD88
inferredcites →https://doi.org/10.1016/j.molmed.2011.07.009openalex-snapshot
Metchnikoff's policemen: macrophages in development, homeostasis and regeneration
inferredcites →https://doi.org/10.1016/j.neuron.2011.07.009openalex-snapshot
Axon Regeneration Pathways Identified by Systematic Genetic Screening in C. elegans
inferredcites →https://doi.org/10.1016/j.pharmthera.2021.107879openalex-snapshot
Resolution of inflammation: An organizing principle in biology and medicine
inferredcites →https://doi.org/10.1016/j.regen.2020.100029openalex-snapshot
Single cell sequencing analysis of lizard phagocytic cell populations and their role in tail regeneration
inferredcites →https://doi.org/10.1016/j.semcdb.2006.05.006openalex-snapshot
The stem cell concept in sponges (Porifera): Metazoan traits
inferredcites →https://doi.org/10.1016/j.smim.2016.03.013openalex-snapshot
Early hematopoiesis and macrophage development
inferredcites →https://doi.org/10.1016/j.stemcr.2014.06.001openalex-snapshot
Neoblast Specialization in Regeneration of the Planarian Schmidtea mediterranea
inferredcites →https://doi.org/10.1016/j.tree.2009.08.005openalex-snapshot
Evolution of animal regeneration: re-emergence of a field
inferredcites →https://doi.org/10.1016/j.ydbio.2010.05.500openalex-snapshot
Piwi positive cells that line the vasculature epithelium, underlie whole body regeneration in a basal chordate
inferredcites →https://doi.org/10.1016/j.ydbio.2012.11.006openalex-snapshot
Phagocyte dynamics in a highly regenerative urochordate: Insights into development and host defense
inferredcites →https://doi.org/10.1016/j.ydbio.2012.11.015openalex-snapshot
The evolutionary origins of chordate hematopoiesis and vertebrate endothelia
inferredcites →https://doi.org/10.1016/j.ydbio.2013.06.019openalex-snapshot
An ancient role for Gata-1/2/3 and Scl transcription factor homologs in the development of immunocytes
inferredcites →https://doi.org/10.1016/j.ydbio.2014.12.015openalex-snapshot
A diffusible signal derived from hematopoietic cells supports the survival and proliferation of regenerative cells during zebrafish fin fold regeneration
inferredcites →https://doi.org/10.1016/j.ydbio.2015.03.008openalex-snapshot
Xenopus: An in vivo model for imaging the inflammatory response following injury and bacterial infection
inferredcites →https://doi.org/10.1016/j.ymeth.2014.02.038openalex-snapshot
Drosophila hematopoiesis: Markers and methods for molecular genetic analysis
inferredcites →https://doi.org/10.1016/j.zool.2014.07.002openalex-snapshot
Phagocytic efficiency and cytotoxic responses of Indian freshwater sponge (Eunapius carteri) cells isolated by density gradient centrifugation and flow cytometry: a morphofunctional analysis
inferredcites →https://doi.org/10.1016/j.zool.2019.125737openalex-snapshot
Microscopic observations on amputated and scarring lizard digits show an intense inflammatory reaction
inferredcites →https://doi.org/10.1016/s0070-2153(03)53004-6openalex-snapshot
3 Ontogeny of hematopoiesis: Examining the emergence of hematopoietic cells in the vertebrate embryo
inferredcites →https://doi.org/10.1016/s0960-9822(01)00241-xopenalex-snapshot
A reverse genetic analysis of components of the Toll signaling pathway in Caenorhabditis elegans
inferredcites →https://doi.org/10.1017/s1462399411001943openalex-snapshot
Inflammation and wound healing: the role of the macrophage
inferredcites →https://doi.org/10.1034/j.1600-0854.2002.30103.xopenalex-snapshot
Deciphering Endocytosis in Caenorhabditis elegans
inferredcites →https://doi.org/10.1038/cddis.2017.374openalex-snapshot
TNF signaling and macrophages govern fin regeneration in zebrafish larvae
inferredcites →https://doi.org/10.1038/ncomms10938openalex-snapshot
Social amoebae trap and kill bacteria by casting DNA nets
inferredcites →https://doi.org/10.1038/s41467-018-06614-2openalex-snapshot
Early redox activities modulate Xenopus tail regeneration
inferredcites →https://doi.org/10.1038/s41467-018-07604-0openalex-snapshot
Transcriptomic landscape of the blastema niche in regenerating adult axolotl limbs at single-cell resolution
inferredcites →https://doi.org/10.1038/s41559-017-0285-5openalex-snapshot
Gut-like ectodermal tissue in a sea anemone challenges germ layer homology
inferredcites →https://doi.org/10.1038/s41577-018-0003-9openalex-snapshot
A cold-blooded view of adaptive immunity
inferredcites →https://doi.org/10.1038/s41586-018-0783-xopenalex-snapshot
Complex mammalian-like haematopoietic system found in a colonial chordate
inferredcites →https://doi.org/10.1038/s41598-020-79588-1openalex-snapshot
Reactive oxygen species rescue regeneration after silencing the MAPK–ERK signaling pathway in Schmidtea mediterranea
inferredcites →https://doi.org/10.1073/pnas.1100045109openalex-snapshot
Vertebrate-like regeneration in the invertebrate chordate amphioxus
inferredcites →https://doi.org/10.1073/pnas.1213110109openalex-snapshot
MyD88-deficient Hydra reveal an ancient function of TLR signaling in sensing bacterial colonizers
inferredcites →https://doi.org/10.1073/pnas.1300290110openalex-snapshot
Macrophages are required for adult salamander limb regeneration
inferredcites →https://doi.org/10.1074/jbc.m112.349126openalex-snapshot
Live Imaging Reveals Differing Roles of Macrophages and Neutrophils during Zebrafish Tail Fin Regeneration
inferredcites →https://doi.org/10.1083/jcb.7.4.717openalex-snapshot
The Fine Structure of Some Blood Vessels of the Earthworm, Eisenia foetida
inferredcites →https://doi.org/10.1084/jem.20070075openalex-snapshot
Inflammatory monocytes recruited after skeletal muscle injury switch into antiinflammatory macrophages to support myogenesis
inferredcites →https://doi.org/10.1089/wound.2014.0549openalex-snapshot
Analysis of the Molecular Mechanisms of Reepithelialization in Drosophila Embryos
inferredcites →https://doi.org/10.1093/genetics/159.1.133openalex-snapshot
Genetic Analysis of Endocytosis in Caenorhabditis elegans: Coelomocyte Uptake Defective Mutants
inferredcites →https://doi.org/10.1093/icb/23.1.145openalex-snapshot
Inflammatory Responses in Annelids
inferredcites →https://doi.org/10.1093/molbev/msl208openalex-snapshot
Toll-Like Receptors Are Part of the Innate Immune Defense System of Sponges (Demospongiae: Porifera)
inferredcites →https://doi.org/10.1096/fj.11-201442openalex-snapshot
Macrophage proresolving mediator maresin 1 stimulates tissue regeneration and controls pain
inferredcites →https://doi.org/10.1096/fj.201801966rrropenalex-snapshot
Macrophage migration inhibitory factor derived from spinal cord is involved in activation of macrophages following gecko tail amputation
inferredcites →https://doi.org/10.1111/1365-2435.12867openalex-snapshot
Immunocompetence in a long‐lived ectothermic vertebrate is temperature dependent but shows no decline in older adults
inferredcites →https://doi.org/10.1111/j.1440-169x.2009.01159.xopenalex-snapshot
Regeneration in crinoids
inferredcites →https://doi.org/10.1111/j.1469-7998.1980.tb01446.xopenalex-snapshot
Phylogenetic development of melano–macrophage centres in fish
inferredcites →https://doi.org/10.1111/j.1525-142x.2010.00413.xopenalex-snapshot
Piwi expression in archeocytes and choanocytes in demosponges: insights into the stem cell system in demosponges
inferredcites →https://doi.org/10.1111/wrr.12385openalex-snapshot
Cellular events during scar‐free skin regeneration in the spiny mouse, Acomys
inferredcites →https://doi.org/10.1126/science.1092385openalex-snapshot
Neutrophil Extracellular Traps Kill Bacteria
inferredcites →https://doi.org/10.1126/science.1143991openalex-snapshot
Immune-like Phagocyte Activity in the Social Amoeba
inferredcites →https://doi.org/10.1134/s1062360418080015openalex-snapshot
Lampreys, “Living Fossils,” in Research on Early Development and Regeneration in Vertebrates
inferredcites →https://doi.org/10.1134/s106307402002011xopenalex-snapshot
The Immunocytochemical Identification of PIWI-Positive Cells during the Recovery of a Coelomocyte Population after Evisceration in the Holothurian Eupentacta fraudatrix (Djakonov et Baranova, 1958) (Holothuroidea: Dendrochirota)
inferredcites →https://doi.org/10.1146/annurev-genet-110711-155550openalex-snapshot
Neural Regeneration in Caenorhabditis elegans
inferredcites →https://doi.org/10.1146/annurev.immunol.17.1.593openalex-snapshot
MECHANISMS OF PHAGOCYTOSIS IN MACROPHAGES
inferredcites →https://doi.org/10.1155/2018/7359267openalex-snapshot
Drosophila as a Model System to Study Cell Signaling in Organ Regeneration
inferredcites →https://doi.org/10.1159/000013853openalex-snapshot
Functional Recovery in the Avian Ear after Hair Cell Regeneration
inferredcites →https://doi.org/10.1172/jci200522675openalex-snapshot
Selective depletion of macrophages reveals distinct, opposing roles during liver injury and repair
inferredcites →https://doi.org/10.1172/jci72181openalex-snapshot
Macrophages are required for neonatal heart regeneration
inferredcites →https://doi.org/10.1182/blood-2008-04-150268openalex-snapshot
spib is required for primitive myeloid development in Xenopus
inferredcites →https://doi.org/10.1182/blood-2013-09-526970openalex-snapshot
Mapping hematopoiesis in a fully regenerative vertebrate: the axolotl
inferredcites →https://doi.org/10.1182/blood.v98.3.643openalex-snapshot
Myelopoiesis in the zebrafish, Danio rerio
inferredcites →https://doi.org/10.1186/1745-6150-4-9openalex-snapshot
The origins of phagocytosis and eukaryogenesis
inferredcites →https://doi.org/10.1186/s12967-019-1998-9openalex-snapshot
The epigenome as a putative target for skin repair: the HDAC inhibitor Trichostatin A modulates myeloid progenitor plasticity and behavior and improves wound healing
inferredcites →https://doi.org/10.1186/s13227-019-0144-3openalex-snapshot
Putative stem cells in the hemolymph and in the intestinal submucosa of the solitary ascidian Styela plicata
inferredcites →https://doi.org/10.1189/jlb.0802406openalex-snapshot
Accelerated wound closure in neutrophil-depleted mice
inferredcites →https://doi.org/10.1242/dev.00702openalex-snapshot
The two origins of hemocytes in Drosophila
inferredcites →https://doi.org/10.1242/dev.033985openalex-snapshot
Suppression of the immune response potentiates tadpole tail regeneration during the refractory period
inferredcites →https://doi.org/10.1242/dev.098459openalex-snapshot
Macrophages modulate adult zebrafish tail fin regeneration
inferredcites →https://doi.org/10.1242/dev.120.7.1829openalex-snapshot
Embryonic origin of hemocytes and their relationship to cell death in Drosophila
inferredcites →https://doi.org/10.1242/dev.125.13.2479openalex-snapshot
MyoD and the specification of muscle and non-muscle fates during postembryonic development of the C. elegans mesoderm
inferredcites →https://doi.org/10.1242/dev.167700openalex-snapshot
Model systems for regeneration: salamanders
inferredcites →https://doi.org/10.1242/dev.185496openalex-snapshot
The myeloid lineage is required for the emergence of a regeneration-permissive environment following Xenopus tail amputation
inferredcites →https://doi.org/10.1242/dev.199916openalex-snapshot
Toll signalling promotes blastema cell proliferation during cricket leg regeneration via insect macrophages
inferredcites →https://doi.org/10.1242/jcs.49.1.311openalex-snapshot
Mechanisms of nutritive endocytosis i. phagocytic versatility and cellular recognition in Chlorohydra digestive cells, a scanning electron microscope study
inferredcites →https://doi.org/10.1242/jeb.207894openalex-snapshot
Insights into the evolution of metazoan regenerative mechanisms: TGF superfamily member roles in tissue regeneration of the marine sponge Chondrosia reniformis Nardo, 1847
inferredcites →https://doi.org/10.1371/journal.pbio.3000226openalex-snapshot
The architecture of cell differentiation in choanoflagellates and sponge choanocytes
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.0022820openalex-snapshot
The Regenerative Capacity of the Zebrafish Caudal Fin Is Not Affected by Repeated Amputations
inferredcites →https://doi.org/10.1371/journal.pone.0023992openalex-snapshot
Corals Use Similar Immune Cells and Wound-Healing Processes as Those of Higher Organisms
inferredcites →https://doi.org/10.1371/journal.pone.0051574openalex-snapshot
Depletion of Resident Macrophages Does Not Alter Sensory Regeneration in the Avian Cochlea
inferredcites →https://doi.org/10.1371/journal.pone.0080477openalex-snapshot
Changes in the Inflammatory Response to Injury and Its Resolution during the Loss of Regenerative Capacity in Developing Xenopus Limbs
inferredcites →https://doi.org/10.1371/journal.pone.0086255openalex-snapshot
Evolutionary Conservation of Divergent Pro-Inflammatory and Homeostatic Responses in Lamprey Phagocytes
inferredcites →https://doi.org/10.1371/journal.pone.0095577openalex-snapshot
Prey Capture and Phagocytosis in the Choanoflagellate Salpingoeca rosetta
inferredcites →https://doi.org/10.1371/journal.pone.0102568openalex-snapshot
Control of Drosophila Blood Cell Activation via Toll Signaling in the Fat Body
inferredcites →https://doi.org/10.1371/journal.pone.0132984openalex-snapshot
Epigenetic Control of Macrophage Shape Transition towards an Atypical Elongated Phenotype by Histone Deacetylase Activity
inferredcites →https://doi.org/10.1387/ijdb.072408jsopenalex-snapshot
Hair cell regeneration in the avian auditory epithelium
inferredcites →https://doi.org/10.1387/ijdb.180016nfopenalex-snapshot
The cellular and molecular bases of the sponge stem cell systems underlying reproduction, homeostasis and regeneration
inferredcites →https://doi.org/10.2307/1539415openalex-snapshot
NUTRIENT TRANSPORT IN STARFISH. I. PROPERTIES OF THE COELOMIC FLUID
inferredcites →https://doi.org/10.2460/ajvr.79.12.1298openalex-snapshot
Influence of injection protocol and measurement technique on computed tomographic assessment of glomerular filtration rate in healthy Beagles
inferredcites →https://doi.org/10.2744/ccb-1202.1openalex-snapshot
Immune Response of Green Sea Turtles with and without Fibropapillomatosis: Evaluating Oxidative Burst and Phagocytosis via Flow Cytometry
inferredcites →https://doi.org/10.3389/fimmu.2017.00674openalex-snapshot
Immunity in Protochordates: The Tunicate Perspective
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What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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