On the public citation graph
Acute Inflammation Initiates the Regenerative Response in the Adult Zebrafish Brain
0 signed · 540 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.
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known work and none has been retracted — and get a dated CiteStamped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.
What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/bies.20615openalex-snapshot
Adult neurogenesis in non‐mammalian vertebrates
inferredcites →https://doi.org/10.1002/cm.20133openalex-snapshot
Imaging macrophage chemotaxis in vivo: Studies of microtubule function in zebrafish wound inflammation
inferredcites →https://doi.org/10.1002/dneu.20918openalex-snapshot
Adult neurogenesis and brain regeneration in zebrafish
inferredcites →https://doi.org/10.1002/glia.22269openalex-snapshot
Stab wound injury of the zebrafish telencephalon: A model for comparative analysis of reactive gliosis
inferredcites →https://doi.org/10.1016/j.brainres.2005.06.046openalex-snapshot
Pranlukast, a cysteinyl leukotriene receptor-1 antagonist, protects against chronic ischemic brain injury and inhibits the glial scar formation in mice
inferredcites →https://doi.org/10.1016/j.devcel.2012.10.014openalex-snapshot
Regenerative Neurogenesis from Neural Progenitor Cells Requires Injury-Induced Expression of Gata3
inferredcites →https://doi.org/10.1016/j.expneurol.2007.05.014openalex-snapshot
CNS injury, glial scars, and inflammation: Inhibitory extracellular matrices and regeneration failure
inferredcites →https://doi.org/10.1016/j.febslet.2011.05.030openalex-snapshot
Innate immune responses in central nervous system inflammation
inferredcites →https://doi.org/10.1016/j.nurt.2010.07.002openalex-snapshot
Role of Microglia in Neurotrauma
inferredcites →https://doi.org/10.1016/j.ydbio.2006.03.023openalex-snapshot
Conserved and acquired features of adult neurogenesis in the zebrafish telencephalon
inferredcites →https://doi.org/10.1016/j.ydbio.2006.03.040openalex-snapshot
Neural stem cells and neurogenesis in the adult zebrafish brain: Origin, proliferation dynamics, migration and cell fate
inferredcites →https://doi.org/10.1073/pnas.2234031100openalex-snapshot
Inflammation is detrimental for neurogenesis in adult brain
inferredcites →https://doi.org/10.1093/jnen/61.7.623openalex-snapshot
The Neuropathological and Behavioral Consequences of Intraspinal Microglial/Macrophage Activation
inferredcites →https://doi.org/10.1098/rstb.2006.2015openalex-snapshot
Proliferation, neurogenesis and regeneration in the non-mammalian vertebrate brain
inferredcites →https://doi.org/10.1126/science.1088417openalex-snapshot
Inflammatory Blockade Restores Adult Hippocampal Neurogenesis
inferredcites →https://doi.org/10.1126/science.1110647openalex-snapshot
Resting Microglial Cells Are Highly Dynamic Surveillants of Brain Parenchyma in Vivo
inferredcites →https://doi.org/10.1161/01.str.0000190020.30282.ccopenalex-snapshot
Neurogenesis in Rats After Focal Cerebral Ischemia is Enhanced by Indomethacin
inferredcites →https://doi.org/10.1172/jci58644openalex-snapshot
Innate immunity in the central nervous system
inferredcites →https://doi.org/10.1186/1749-8104-7-27openalex-snapshot
The chemokine receptor cxcr5 regulates the regenerative neurogenesis response in the adult zebrafish brain
inferredcites →https://doi.org/10.1242/dev.058156openalex-snapshot
Clonal analysis by distinct viral vectors identifies bona fide neural stem cells in the adult zebrafish telencephalon and characterizes their division properties and fate
inferredcites →https://doi.org/10.1242/dev.072587openalex-snapshot
Regeneration of the adult zebrafish brain from neurogenic radial glia-type progenitors
inferredcites →https://doi.org/10.1242/dmm.007336openalex-snapshot
Neuronal regeneration in a zebrafish model of adult brain injury
inferredcites →https://doi.org/10.1371/journal.pone.0027395openalex-snapshot
Cerebroventricular Microinjection (CVMI) into Adult Zebrafish Brain Is an Efficient Misexpression Method for Forebrain Ventricular Cells
inferredcites →https://doi.org/10.1523/jneurosci.2723-06.2006openalex-snapshot
Tumor Necrosis Factor Receptor 1 Is a Negative Regulator of Progenitor Proliferation in Adult Hippocampal Neurogenesis
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.4753794openalex-extracted
HDAC Activity Inhibition Alters Histone H4 Acetylation Dynamics Coupled to HDAC Expression and Lipid Mediator 12(S)HETE Biogenesis in Xenopus laevis Tail Regeneration
inferred← citeshttps://doi.org/10.1002/9780470015902.a0022101.pub2openalex-snapshot
Regeneration of Organs and Appendages in Zebrafish: A Window into Underlying Control Mechanisms
inferred← citeshttps://doi.org/10.1002/9781118628003.ch19openalex-snapshot
Retinoid Signaling in the Central Nervous System
inferred← citeshttps://doi.org/10.1002/advs.201700278openalex-snapshot
Netrin‐1 Promotes Inflammation Resolution to Achieve Endothelialization of Small‐Diameter Tissue Engineering Blood Vessels by Improving Endothelial Progenitor Cells Function In Situ
inferred← citeshttps://doi.org/10.1002/ame2.12363openalex-snapshot
Neurotrophins and neural stem cells in posttraumatic brain injury repair
inferred← citeshttps://doi.org/10.1002/bdrc.21039openalex-snapshot
Recent advances in heart regeneration
inferred← citeshttps://doi.org/10.1002/cne.23733openalex-snapshot
Comprehensive expression map of transcription regulators in the adult zebrafish telencephalon reveals distinct neurogenic niches
inferred← citeshttps://doi.org/10.1002/cne.24489openalex-snapshot
Involvement of sonic hedgehog and notch signaling in regenerative neurogenesis in adult zebrafish optic tectum after stab injury
inferred← citeshttps://doi.org/10.1002/cne.24669openalex-snapshot
Expression of adiponectin receptors in the brain of adult zebrafish and mouse: Links with neurogenic niches and brain repair
inferred← citeshttps://doi.org/10.1002/cne.25421openalex-snapshot
Distribution of microglia/immune cells in the brain of adult zebrafish in homeostatic and regenerative conditions: Focus on oxidative stress during brain repair
inferred← citeshttps://doi.org/10.1002/cne.25542openalex-snapshot
Insulin signaling promotes neurogenesis in the brain of adult zebrafish
inferred← citeshttps://doi.org/10.1002/cph4.70088openalex-snapshot
Red Blood Cell Glycation Triggers In Vivo Cerebral Erythrophagocytosis in Adult Zebrafish in a Model Mimicking Hemorrhagic Stroke
inferred← citeshttps://doi.org/10.1002/dneu.22497openalex-snapshot
Upregulation of matrix metalloproteinase triggers transdifferentiation of retinal pigmented epithelial cells inXenopus laevis: A Link between inflammatory response and regeneration
inferred← citeshttps://doi.org/10.1002/dneu.22665openalex-snapshot
A Comparative Perspective on Brain Regeneration in Amphibians and Teleost Fish
inferred← citeshttps://doi.org/10.1002/dvdy.24167openalex-snapshot
Sensory hair cell regeneration in the zebrafish lateral line
inferred← citeshttps://doi.org/10.1002/dvdy.24342openalex-snapshot
MicroRNA dysregulation in response to RARβ2 inhibition reveals a negative feedback loop between MicroRNAs 1, 133a, and RARβ2 during tail and spinal cord regeneration in the adult newt
inferred← citeshttps://doi.org/10.1002/dvdy.24466openalex-snapshot
Concomitant differentiation of a population of mouse embryonic stem cells into neuron‐like cells and schwann cell–like cells in a slow‐flow microfluidic device
inferred← citeshttps://doi.org/10.1002/dvdy.251openalex-snapshot
Immunity in salamander regeneration: Where are we standing and where are we headed?
inferred← citeshttps://doi.org/10.1002/dvdy.70181openalex-snapshot
A proteomic investigation of forebrain regeneration in the leopard gecko ( Eublepharis macularius )
inferred← citeshttps://doi.org/10.1002/dvg.22406openalex-snapshot
Spinal cord regeneration: Lessons for mammals from non‐mammalian vertebrates
inferred← citeshttps://doi.org/10.1002/emmm.201303687openalex-snapshot
Prostaglandin E2 promotes post‐infarction cardiomyocyte replenishment by endogenous stem cells
inferred← citeshttps://doi.org/10.1002/glia.22703openalex-snapshot
Reactive microglia and macrophage facilitate the formation of Müller glia‐derived retinal progenitors
inferred← citeshttps://doi.org/10.1002/glia.22726openalex-snapshot
Excitotoxic brain injury in adult zebrafish stimulates neurogenesis and long‐distance neuronal integration
inferred← citeshttps://doi.org/10.1002/glia.22780openalex-snapshot
Immune cell dynamics in the CNS: Learning from the zebrafish
inferred← citeshttps://doi.org/10.1002/glia.22856openalex-snapshot
Radial glia and neural progenitors in the adult zebrafish central nervous system
inferred← citeshttps://doi.org/10.1002/glia.23601openalex-snapshot
Retinal microglia signaling affects Müller cell behavior in the zebrafish following laser injury induction
inferred← citeshttps://doi.org/10.1002/glia.23707openalex-snapshot
Inflammation‐induced mammalian target of rapamycin signaling is essential for retina regeneration
inferred← citeshttps://doi.org/10.1002/glia.23792openalex-snapshot
Inflammation and matrix metalloproteinase 9 (Mmp‐9) regulate photoreceptor regeneration in adult zebrafish
inferred← citeshttps://doi.org/10.1002/glia.23849openalex-snapshot
Radial glia in the zebrafish brain: Functional, structural, and physiological comparison with the mammalian glia
inferred← citeshttps://doi.org/10.1002/glia.23972openalex-snapshot
Müller glia–myeloid cell crosstalk accelerates optic nerve regeneration in the adult zebrafish
inferred← citeshttps://doi.org/10.1002/glia.24444openalex-snapshot
Microglial depletion after brain injury prolongs inflammation and impairs brain repair, adult neurogenesis and pro‐regenerative signaling
inferred← citeshttps://doi.org/10.1002/glia.70158openalex-snapshot
A Dynamic Change of Microglial States Occurs During the Transition From Photoreceptor Degeneration to Regeneration in Zebrafish pde6c Mutants
inferred← citeshttps://doi.org/10.1002/glia.70234openalex-snapshot
Molecular Control of Neural Stem Cell Quiescence in the Adult Zebrafish Telencephalon: Established Mechanisms and an Integrative Hypothesis
inferred← citeshttps://doi.org/10.1002/jbio.202000067openalex-snapshot
Long‐term and in vivo assessment of Aβ protein‐induced brain atrophy in a zebrafish model by optical coherence tomography
inferred← citeshttps://doi.org/10.1002/jbm.a.35203openalex-snapshot
Scaffold structure and fabrication method affect proinflammatory milieu in three‐dimensional‐cultured chondrocytes
inferred← citeshttps://doi.org/10.1002/jbmr.3231openalex-snapshot
Immune Suppressive and Bone Inhibitory Effects of Prednisolone in Growing and Regenerating Zebrafish Tissues
inferred← citeshttps://doi.org/10.1002/jnr.23480openalex-snapshot
Current states of endogenous stem cells in adult spinal cord
inferred← citeshttps://doi.org/10.1002/jnr.70112openalex-snapshot
Non‐Mammalian Models in Ischemic Stroke Research: Advances, Applications, and Translational Potential
inferred← citeshttps://doi.org/10.1002/jor.22853openalex-snapshot
Tendon regeneration and scar formation: The concept of scarless healing
inferred← citeshttps://doi.org/10.1002/reg2.39openalex-snapshot
Skeletal callus formation is a nerve‐independent regenerative response to limb amputation in mice and Xenopus
inferred← citeshttps://doi.org/10.1002/reg2.83openalex-snapshot
Zebrafish heart regeneration: 15 years of discoveries
inferred← citeshttps://doi.org/10.1002/sctm.17-0213openalex-snapshot
Concise Review: Translating Regenerative Biology into Clinically Relevant Therapies: Are We on the Right Path?
inferred← citeshttps://doi.org/10.1002/smll.202205890openalex-snapshot
See the Unseen: Red‐Emissive Carbon Dots for Visualizing the Nucleolar Structures in Two Model Animals and In Vivo Drug Toxicity
inferred← citeshttps://doi.org/10.1002/stem.1883openalex-snapshot
The Helix-Loop-Helix Protein Id1 Controls Stem Cell Proliferation During Regenerative Neurogenesis in the Adult Zebrafish Telencephalon
inferred← citeshttps://doi.org/10.1002/stem.3182openalex-snapshot
Bone morphogenetic protein signaling regulates Id1-mediated neural stem cell quiescence in the adult zebrafish brain via a phylogenetically conserved enhancer module
inferred← citeshttps://doi.org/10.1002/term.2560openalex-snapshot
A co‐culture system with three different primary human cell populations reveals that biomaterials and MSC modulate macrophage‐driven fibroblast recruitment
inferred← citeshttps://doi.org/10.1002/wdev.321openalex-snapshot
Wound‐induced cell proliferation during animal regeneration
inferred← citeshttps://doi.org/10.1007/978-1-4939-0787-8_3openalex-snapshot
The Regenerative Potential of the Vertebrate Retina: Lessons from the Zebrafish
inferred← citeshttps://doi.org/10.1007/978-1-4939-1908-6_1openalex-snapshot
Adult Neurogenesis and Regeneration: Focus on Nonmammalian Vertebrates
inferred← citeshttps://doi.org/10.1007/978-1-4939-9068-9_4openalex-snapshot
Fluorescence-Activated Cell Sorting-Based Isolation and Characterization of Neural Stem Cells from the Adult Zebrafish Telencephalon
inferred← citeshttps://doi.org/10.1007/978-3-031-23104-9_8openalex-snapshot
A Comparative View of Cerebellar Morphology and Diversity in Fishes
inferred← citeshttps://doi.org/10.1007/978-3-319-08798-6_2openalex-snapshot
Insights into Heart Development and Regeneration
inferred← citeshttps://doi.org/10.1007/978-3-319-16733-6_3openalex-snapshot
The MRL Mouse: A Model of Regeneration and Cancer
inferred← citeshttps://doi.org/10.1007/978-3-319-27583-3_8openalex-snapshot
Development and Regeneration of the Vertebrate Brain
inferred← citeshttps://doi.org/10.1007/978-3-319-27583-3_9openalex-snapshot
Role of Innate Immune Signaling in Nuclear Reprogramming
inferred← citeshttps://doi.org/10.1007/978-981-16-5217-2_16openalex-snapshot
Growing Importance of Zebrafish in Translational Neuroscience
inferred← citeshttps://doi.org/10.1007/978-981-19-7376-5_5openalex-snapshot
Animal Inflammation-Based Models of Neuropsychiatric Disorders
inferred← citeshttps://doi.org/10.1007/s00018-023-05021-1openalex-snapshot
Molecular basis of retinal remodeling in a zebrafish model of retinitis pigmentosa
inferred← citeshttps://doi.org/10.1007/s00018-024-05538-zopenalex-snapshot
Genetic modeling of degenerative diseases and mechanisms of neuronal regeneration in the zebrafish cerebellum
inferred← citeshttps://doi.org/10.1007/s00244-022-00969-wopenalex-snapshot
Impact of Copper Nanoparticles and Copper Ions on Transcripts Involved in Neural Repair Mechanisms in Rainbow Trout Olfactory Mucosa
inferred← citeshttps://doi.org/10.1007/s00359-022-01591-wopenalex-snapshot
Proteomic characterization of spontaneously regrowing spinal cord following injury in the teleost fish Apteronotus leptorhynchus, a regeneration-competent vertebrate
inferred← citeshttps://doi.org/10.1007/s00427-012-0425-5openalex-snapshot
Comparative aspects of adult neural stem cell activity in vertebrates
inferred← citeshttps://doi.org/10.1007/s00441-014-2048-9openalex-snapshot
How to make neurons—thoughts on the molecular logic of neurogenesis in the central nervous system
inferred← citeshttps://doi.org/10.1007/s00441-020-03334-2openalex-snapshot
Diving into the streams and waves of constitutive and regenerative olfactory neurogenesis: insights from zebrafish
inferred← citeshttps://doi.org/10.1007/s00441-021-03477-wopenalex-snapshot
New insights into glial scar formation after spinal cord injury
inferred← citeshttps://doi.org/10.1007/s11055-022-01254-yopenalex-snapshot
Traumatic Brain Injury Models in Zebrafish (Danio rerio)
inferred← citeshttps://doi.org/10.1007/s11062-021-09904-6openalex-snapshot
Constitutive Neurogenesis in the Brain of Different Vertebrate Groups
inferred← citeshttps://doi.org/10.1007/s11427-015-4838-zopenalex-snapshot
Using zebrafish as the model organism to understand organ regeneration
inferred← citeshttps://doi.org/10.1007/s11910-016-0642-9openalex-snapshot
Mapping the Connectome Following Traumatic Brain Injury
inferred← citeshttps://doi.org/10.1007/s12015-014-9553-9openalex-snapshot
Stem Cells in Canine Spinal Cord Injury – Promise for Regenerative Therapy in a Large Animal Model of Human Disease
inferred← citeshttps://doi.org/10.1007/s12035-013-8533-4openalex-snapshot
HMGB1 Contributes to Regeneration After Spinal Cord Injury in Adult Zebrafish
inferred← citeshttps://doi.org/10.1007/s12035-022-02857-9openalex-snapshot
Context-dependent effects of inflammation on retina regeneration
inferred← citeshttps://doi.org/10.1007/s12035-023-03210-4openalex-snapshot
High-fat diet feeding triggers a regenerative response in the adult zebrafish brain
inferred← citeshttps://doi.org/10.1007/s12268-014-0419-0openalex-snapshot
Der Zebrabärbling als Modell für die Regeneration von Nervengewebe
inferred← citeshttps://doi.org/10.1007/s12640-013-9388-1openalex-snapshot
The Role of Glutamate and the Immune System in Organophosphate-induced CNS Damage
inferred← citeshttps://doi.org/10.1007/s12640-020-00298-7openalex-snapshot
Adult Endogenous Dopaminergic Neuroregeneration Against Parkinson’s Disease: Ideal Animal Models?
inferred← citeshttps://doi.org/10.1007/s40139-015-0063-5openalex-snapshot
Dedifferentiation, Transdifferentiation, and Proliferation: Mechanisms Underlying Cardiac Muscle Regeneration in Zebrafish
inferred← citeshttps://doi.org/10.1007/s40139-018-0158-xopenalex-snapshot
Mechanisms of Pathology-Induced Neural Stem Cell Plasticity and Neural Regeneration in Adult Zebrafish Brain
inferred← citeshttps://doi.org/10.1016/b978-0-12-801479-0.00005-xopenalex-snapshot
Aromatase and Estrogens
inferred← citeshttps://doi.org/10.1016/b978-0-12-801732-6.00001-xopenalex-snapshot
Advances and Challenges for Neural Regeneration Research
inferred← citeshttps://doi.org/10.1016/b978-0-12-809479-2.00008-1openalex-snapshot
Big Regeneration Mechanisms via Systems Biology and Big Database Mining Methods
inferred← citeshttps://doi.org/10.1016/b978-0-12-814405-3.00026-6openalex-snapshot
Neurogenesis in zebrafish
inferred← citeshttps://doi.org/10.1016/b978-0-323-85841-0.00016-xopenalex-snapshot
Neuroimmunology: Translational lessons from zebrafish models
inferred← citeshttps://doi.org/10.1016/b978-0-323-90801-6.00029-xopenalex-snapshot
Adult neurogenesis and regeneration in the teleost central nervous system
inferred← citeshttps://doi.org/10.1016/b978-0-443-15580-2.00003-5openalex-snapshot
Multimodal translational imaging of central nervous system structure and function and its integrative value in neuroregeneration strategies
inferred← citeshttps://doi.org/10.1016/bs.fp.2026.08.008openalex-snapshot
Neuroimmune physiology in teleost fish
inferred← citeshttps://doi.org/10.1016/bs.ircmb.2016.04.002openalex-snapshot
Endogenous Mechanisms of Cardiac Regeneration
inferred← citeshttps://doi.org/10.1016/j.actbio.2019.07.037openalex-snapshot
Regulation of the inflammatory response by vascular grafts modified with Aspirin-Triggered Resolvin D1 promotes blood vessel regeneration
inferred← citeshttps://doi.org/10.1016/j.addr.2017.09.010openalex-snapshot
Transflammation: Innate immune signaling in nuclear reprogramming
inferred← citeshttps://doi.org/10.1016/j.bbadis.2024.167442openalex-snapshot
Systemic inhibition of mitochondrial fatty acid β-oxidation impedes zebrafish ventricle regeneration
inferred← citeshttps://doi.org/10.1016/j.bbamcr.2016.01.011openalex-snapshot
The neonate versus adult mammalian immune system in cardiac repair and regeneration
inferred← citeshttps://doi.org/10.1016/j.bbi.2017.05.013openalex-snapshot
Exogenous FGF2 reverses depressive-like behaviors and restores the suppressed FGF2-ERK1/2 signaling and the impaired hippocampal neurogenesis induced by neuroinflammation
inferred← citeshttps://doi.org/10.1016/j.bbi.2024.06.022openalex-snapshot
Neutrophil immune profile guides spinal cord regeneration in zebrafish
inferred← citeshttps://doi.org/10.1016/j.biocel.2014.07.010openalex-snapshot
Delineating the roles of neutrophils and macrophages in zebrafish regeneration models
inferred← citeshttps://doi.org/10.1016/j.biomaterials.2016.10.006openalex-snapshot
Convective exosome-tracing microfluidics for analysis of cell-non-autonomous neurogenesis
inferred← citeshttps://doi.org/10.1016/j.biomaterials.2017.02.026openalex-snapshot
Chitosan degradation products facilitate peripheral nerve regeneration by improving macrophage-constructed microenvironments
inferred← citeshttps://doi.org/10.1016/j.brainres.2015.09.004openalex-snapshot
Structural and functional evolution of 2′,3′-cyclic nucleotide 3′-phosphodiesterase
inferred← citeshttps://doi.org/10.1016/j.brainresbull.2019.12.014openalex-snapshot
Cerebral ischemia-reperfusion aggravated cerebral infarction injury and possible differential genes identified by RNA-Seq in rats
inferred← citeshttps://doi.org/10.1016/j.brainresbull.2025.111225openalex-snapshot
Neurological function is restored post-ischemic stroke in zebrafish, with aging exerting a deleterious effect on its pathology
inferred← citeshttps://doi.org/10.1016/j.cbpc.2025.110385openalex-snapshot
Lipopolysaccharides increase the resorption levels and affect zebrafish scales de novo bone formation
inferred← citeshttps://doi.org/10.1016/j.cell.2020.02.013openalex-snapshot
Repopulating Microglia Promote Brain Repair in an IL-6-Dependent Manner
inferred← citeshttps://doi.org/10.1016/j.celrep.2016.09.075openalex-snapshot
IL4/STAT6 Signaling Activates Neural Stem Cell Proliferation and Neurogenesis upon Amyloid-β42 Aggregation in Adult Zebrafish Brain
inferred← citeshttps://doi.org/10.1016/j.celrep.2016.09.088openalex-snapshot
A Nuclear Role for miR-9 and Argonaute Proteins in Balancing Quiescent and Activated Neural Stem Cell States
inferred← citeshttps://doi.org/10.1016/j.celrep.2018.11.055openalex-snapshot
The Aryl Hydrocarbon Receptor Pathway Defines the Time Frame for Restorative Neurogenesis
inferred← citeshttps://doi.org/10.1016/j.celrep.2019.03.090openalex-snapshot
Single-Cell Transcriptomics Analyses of Neural Stem Cell Heterogeneity and Contextual Plasticity in a Zebrafish Brain Model of Amyloid Toxicity
inferred← citeshttps://doi.org/10.1016/j.celrep.2025.116469openalex-snapshot
Biphasic inflammation control by fibroblasts enables spinal cord regeneration in zebrafish
inferred← citeshttps://doi.org/10.1016/j.chom.2021.03.003openalex-snapshot
Bacteria Induce Skin Regeneration Via Il-1β Signaling
inferred← citeshttps://doi.org/10.1016/j.conb.2016.11.008openalex-snapshot
Adult NSC diversity and plasticity: the role of the niche
inferred← citeshttps://doi.org/10.1016/j.conb.2025.102976openalex-snapshot
Timing neural development and regeneration
inferred← citeshttps://doi.org/10.1016/j.cophys.2020.01.009openalex-snapshot
Dynamic cell interactions allow spinal cord regeneration in zebrafish
inferred← citeshttps://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
inferred← citeshttps://doi.org/10.1016/j.dci.2020.103922openalex-snapshot
Expression analysis of Hsp90α and cytokines in zebrafish caudal fin regeneration
inferred← citeshttps://doi.org/10.1016/j.devcel.2012.11.009openalex-snapshot
A Universal Program for Tissue Regeneration?
inferred← citeshttps://doi.org/10.1016/j.devcel.2015.01.001openalex-snapshot
Neuronal Regeneration from Ependymo-Radial Glial Cells: Cook, Little Pot, Cook!
inferred← citeshttps://doi.org/10.1016/j.devcel.2016.01.018openalex-snapshot
Mechanisms of Cardiac Regeneration
inferred← citeshttps://doi.org/10.1016/j.devcel.2017.11.010openalex-snapshot
Zebrafish Regulatory T Cells Mediate Organ-Specific Regenerative Programs
inferred← citeshttps://doi.org/10.1016/j.devcel.2018.06.005openalex-snapshot
3D Culture Method for Alzheimer's Disease Modeling Reveals Interleukin-4 Rescues Aβ42-Induced Loss of Human Neural Stem Cell Plasticity
inferred← citeshttps://doi.org/10.1016/j.devcel.2021.04.031openalex-snapshot
A unique macrophage subpopulation signals directly to progenitor cells to promote regenerative neurogenesis in the zebrafish spinal cord
inferred← citeshttps://doi.org/10.1016/j.devcel.2021.07.021openalex-snapshot
RNA-induced inflammation and migration of precursor neurons initiates neuronal circuit regeneration in zebrafish
inferred← citeshttps://doi.org/10.1016/j.devcel.2022.03.001openalex-snapshot
Single-cell transcriptome analysis reveals three sequential phases of gene expression during zebrafish sensory hair cell regeneration
inferred← citeshttps://doi.org/10.1016/j.devcel.2024.07.005openalex-snapshot
Restoration of cone-circuit functionality in the regenerating adult zebrafish retina
inferred← citeshttps://doi.org/10.1016/j.drudis.2020.09.036openalex-snapshot
Zebrafish as a model for inflammation and drug discovery
inferred← citeshttps://doi.org/10.1016/j.ejphar.2024.176969openalex-snapshot
Nanomedicine: A great boon for cardiac regenerative medicine
inferred← citeshttps://doi.org/10.1016/j.envpol.2018.02.047openalex-snapshot
Brain morphometric profiles and their seasonal modulation in fish (Liza aurata) inhabiting a mercury contaminated estuary
inferred← citeshttps://doi.org/10.1016/j.exer.2013.07.012openalex-snapshot
Regulation of Müller glial dependent neuronal regeneration in the damaged adult zebrafish retina
inferred← citeshttps://doi.org/10.1016/j.exer.2018.09.015openalex-snapshot
Photo-regulation of rod precursor cell proliferation
inferred← citeshttps://doi.org/10.1016/j.expneurol.2013.12.023openalex-snapshot
Non-mammalian model systems for studying neuro-immune interactions after spinal cord injury
inferred← citeshttps://doi.org/10.1016/j.expneurol.2017.09.009openalex-snapshot
The role of jab1, a putative downstream effector of the neurotrophic cytokine macrophage migration inhibitory factor (MIF) in zebrafish inner ear hair cell development
inferred← citeshttps://doi.org/10.1016/j.expneurol.2017.10.009openalex-snapshot
Chemokines and cytokines on the neuroimmunoaxis: Inner ear neurotrophic cytokines in development and disease. Prospects for repair?
inferred← citeshttps://doi.org/10.1016/j.expneurol.2018.01.017openalex-snapshot
Interactions between the Immune and Nervous systems in Nervous System Development, Diseases and Repair Processes
inferred← citeshttps://doi.org/10.1016/j.expneurol.2018.04.008openalex-snapshot
Glia maturation factor beta is required for reactive gliosis after traumatic brain injury in zebrafish
inferred← citeshttps://doi.org/10.1016/j.expneurol.2023.114543openalex-snapshot
Stem cells in central nervous system diseases: Promising therapeutic strategies
inferred← citeshttps://doi.org/10.1016/j.fsi.2013.08.006openalex-snapshot
Molecular characterization, expression analysis, and biological effects of interleukin-8 in grass carp Ctenopharyngodon idellus
inferred← citeshttps://doi.org/10.1016/j.fsi.2019.03.058openalex-snapshot
Excessive inflammation impairs heart regeneration in zebrafish breakdance mutant after cryoinjury
inferred← citeshttps://doi.org/10.1016/j.fsi.2020.03.044openalex-snapshot
Anti-inflammatory and immune properties of the peltatoside, isolated from the leaves of Annona crassiflora Mart., in a new experimental model zebrafish
inferred← citeshttps://doi.org/10.1016/j.gde.2016.05.006openalex-snapshot
Old questions, new models: unraveling complex organ regeneration with new experimental approaches
inferred← citeshttps://doi.org/10.1016/j.gde.2018.05.011openalex-snapshot
Understanding direct neuronal reprogramming — from pioneer factors to 3D chromatin
inferred← citeshttps://doi.org/10.1016/j.gene.2022.147026openalex-snapshot
Caloric restriction reinforces the stem cell pool in the aged brain without affecting overall proliferation status
inferred← citeshttps://doi.org/10.1016/j.immuni.2013.10.011openalex-snapshot
Plasticity of Leukocytic Exudates in Resolving Acute Inflammation Is Regulated by MicroRNA and Proresolving Mediators
inferred← citeshttps://doi.org/10.1016/j.immuni.2016.03.008openalex-snapshot
Macrophages Mediate the Repair of Brain Vascular Rupture through Direct Physical Adhesion and Mechanical Traction
inferred← citeshttps://doi.org/10.1016/j.insi.2025.100146openalex-snapshot
Interactome and expression profile of class II transactivator (CIITA) in lipopolysaccharides mediated neuroinflammation: A combined network analysis and zebrafish model study
inferred← citeshttps://doi.org/10.1016/j.intimp.2015.05.026openalex-snapshot
Ozone promotes regeneration by regulating the inflammatory response in zebrafish
inferred← citeshttps://doi.org/10.1016/j.isci.2018.08.008openalex-snapshot
Histone Deacetylase-Mediated Müller Glia Reprogramming through Her4.1-Lin28a Axis Is Essential for Retina Regeneration in Zebrafish
inferred← citeshttps://doi.org/10.1016/j.jare.2024.01.006openalex-snapshot
Current perspectives on microglia-neuron communication in the central nervous system: Direct and indirect modes of interaction
inferred← citeshttps://doi.org/10.1016/j.jcmgh.2022.05.003openalex-snapshot
Robust Colonic Epithelial Regeneration and Amelioration of Colitis via FZD-Specific Activation of Wnt Signaling
inferred← citeshttps://doi.org/10.1016/j.jneumeth.2013.11.022openalex-snapshot
Characterization of a novel primary culture system of adult zebrafish brainstem cells
inferred← citeshttps://doi.org/10.1016/j.jneumeth.2018.10.014openalex-snapshot
Reversible deafferentation of the zebrafish olfactory bulb with wax plug insertion
inferred← citeshttps://doi.org/10.1016/j.jns.2016.10.052openalex-snapshot
Hippocampal adult neurogenesis: Does the immune system matter?
inferred← citeshttps://doi.org/10.1016/j.jot.2018.01.002openalex-snapshot
Skeletal muscle regeneration is modulated by inflammation
inferred← citeshttps://doi.org/10.1016/j.jphotobiol.2019.04.003openalex-snapshot
Photobiomodulation associated to cellular therapy improve wound healing of experimental full thickness burn wounds in rats
inferred← citeshttps://doi.org/10.1016/j.mtbio.2024.101151openalex-snapshot
Contribution of Tregs to the promotion of constructive remodeling after decellularized extracellular matrix material implantation
inferred← citeshttps://doi.org/10.1016/j.nbd.2015.08.013openalex-snapshot
Inflammation without neuronal death triggers striatal neurogenesis comparable to stroke
inferred← citeshttps://doi.org/10.1016/j.neubiorev.2015.06.021openalex-snapshot
New neurons for injured brains? The emergence of new genetic model organisms to study brain regeneration
inferred← citeshttps://doi.org/10.1016/j.neuint.2023.105584openalex-snapshot
Time-dependent dual effect of microglia in ischemic stroke
inferred← citeshttps://doi.org/10.1016/j.neulet.2021.135978openalex-snapshot
Histone acetyltransferase EP300 regulates the proliferation and differentiation of neural stem cells during adult neurogenesis and regenerative neurogenesis in the zebrafish optic tectum
inferred← citeshttps://doi.org/10.1016/j.neurobiolaging.2017.08.013openalex-snapshot
Successful optic nerve regeneration in the senescent zebrafish despite age-related decline of cell intrinsic and extrinsic response processes
inferred← citeshttps://doi.org/10.1016/j.neuron.2020.12.008openalex-snapshot
Behaviorally consequential astrocytic regulation of neural circuits
inferred← citeshttps://doi.org/10.1016/j.neuron.2022.09.023openalex-snapshot
CNS remyelination and inflammation: From basic mechanisms to therapeutic opportunities
inferred← citeshttps://doi.org/10.1016/j.neuroscience.2014.06.071openalex-snapshot
Estradiol treatment decreases cell proliferation in the neurogenic zones of adult female zebrafish (Danio rerio) brain
inferred← citeshttps://doi.org/10.1016/j.neuroscience.2017.02.032openalex-snapshot
Cellular responses to recurrent pentylenetetrazole-induced seizures in the adult zebrafish brain
inferred← citeshttps://doi.org/10.1016/j.physbeh.2016.04.034openalex-snapshot
Hippocampal neurogenesis dysfunction linked to depressive-like behaviors in a neuroinflammation induced model of depression
inferred← citeshttps://doi.org/10.1016/j.pneurobio.2016.04.004openalex-snapshot
Help-me signaling: Non-cell autonomous mechanisms of neuroprotection and neurorecovery
inferred← citeshttps://doi.org/10.1016/j.pneurobio.2016.05.001openalex-snapshot
Functions and mechanisms of microglia/macrophages in neuroinflammation and neurogenesis after stroke
inferred← citeshttps://doi.org/10.1016/j.pneurobio.2018.04.002openalex-snapshot
The spinal ependymal zone as a source of endogenous repair cells across vertebrates
inferred← citeshttps://doi.org/10.1016/j.pneurobio.2018.04.006openalex-snapshot
Homeostatic and regenerative neurogenesis in salamanders
inferred← citeshttps://doi.org/10.1016/j.pneurobio.2018.06.004openalex-snapshot
The role of neuro-epithelial-like and radial-glial stem and progenitor cells in development, plasticity, and repair
inferred← citeshttps://doi.org/10.1016/j.preteyeres.2013.12.007openalex-snapshot
Müller glia: Stem cells for generation and regeneration of retinal neurons in teleost fish
inferred← citeshttps://doi.org/10.1016/j.preteyeres.2017.06.002openalex-snapshot
On phagocytes and macular degeneration
inferred← citeshttps://doi.org/10.1016/j.prostaglandins.2014.08.003openalex-snapshot
Lysophospholipid acyltransferases and eicosanoid biosynthesis in zebrafish myeloid cells
inferred← citeshttps://doi.org/10.1016/j.psyneuen.2018.03.014openalex-snapshot
Psychoneuroimmunology and immunopsychiatry of zebrafish
inferred← citeshttps://doi.org/10.1016/j.redox.2024.103057openalex-snapshot
A natural small molecule aspidosperma-type alkaloid, hecubine, as a new TREM2 activator for alleviating lipopolysaccharide-induced neuroinflammation in vitro and in vivo
inferred← citeshttps://doi.org/10.1016/j.regen.2019.100023openalex-snapshot
The role of the immune system during regeneration of the central nervous system
inferred← citeshttps://doi.org/10.1016/j.regen.2019.100024openalex-snapshot
The molecular interplay between progenitors and immune cells in tissue regeneration and homeostasis
inferred← citeshttps://doi.org/10.1016/j.scr.2014.06.003openalex-snapshot
A neonatal blueprint for cardiac regeneration
inferred← citeshttps://doi.org/10.1016/j.semcdb.2016.08.010openalex-snapshot
It takes nerve to fight back: The significance of neural innervation of the bone marrow and spleen for immune function
inferred← citeshttps://doi.org/10.1016/j.semcdb.2018.04.002openalex-snapshot
Role of the immune system in regeneration and its dynamic interplay with adult stem cells
inferred← citeshttps://doi.org/10.1016/j.semcdb.2019.07.002openalex-snapshot
Convergence of human cellular models and genetics to study neural stem cell signaling to enhance central nervous system regeneration and repair
inferred← citeshttps://doi.org/10.1016/j.smim.2014.04.007openalex-snapshot
Inflammation and wound repair
inferred← citeshttps://doi.org/10.1016/j.smim.2014.09.001openalex-snapshot
Evolution of immune pathways in regeneration and repair: Recent concepts and translational perspectives
inferred← citeshttps://doi.org/10.1016/j.stem.2014.06.009openalex-snapshot
Immune Modulation of Stem Cells and Regeneration
inferred← citeshttps://doi.org/10.1016/j.stem.2020.10.016openalex-snapshot
Adult Neural Stem Cells Are Alerted by Systemic Inflammation through TNF-α Receptor Signaling
inferred← citeshttps://doi.org/10.1016/j.stemcr.2026.102966openalex-snapshot
Optimized chemogenetic ablation and regeneration of enteric nervous system neurons in zebrafish
inferred← citeshttps://doi.org/10.1016/j.tcb.2013.08.004openalex-snapshot
Neuroinflammation and central nervous system regeneration in vertebrates
inferred← citeshttps://doi.org/10.1016/j.tibtech.2014.09.009openalex-snapshot
High-throughput screening for integrative biomaterials design: exploring advances and new trends
inferred← citeshttps://doi.org/10.1016/j.tig.2013.07.003openalex-snapshot
The zebrafish as a model for complex tissue regeneration
inferred← citeshttps://doi.org/10.1016/j.tig.2015.03.012openalex-snapshot
Signaling networks organizing regenerative growth of the zebrafish fin
inferred← citeshttps://doi.org/10.1016/j.tig.2016.06.006openalex-snapshot
Nothobranchius furzeri: A Model for Aging Research and More
inferred← citeshttps://doi.org/10.1016/j.ydbio.2014.08.001openalex-snapshot
Axolotls with an under- or oversupply of neural crest can regulate the sizes of their dorsal root ganglia to normal levels
inferred← citeshttps://doi.org/10.1016/j.ydbio.2015.03.025openalex-snapshot
Wnt/ß-catenin signaling is required for radial glial neurogenesis following spinal cord injury
inferred← citeshttps://doi.org/10.1016/j.yfrne.2019.100788openalex-snapshot
Neurosteroids as regulators of neuroinflammation
inferred← citeshttps://doi.org/10.1016/j.yjmcc.2021.07.003openalex-snapshot
Can polarization of macrophage metabolism enhance cardiac regeneration?
inferred← citeshttps://doi.org/10.1016/s0140-6736(13)60257-3openalex-snapshot
Targeting innate immunity in type 1 diabetes: strike one
inferred← citeshttps://doi.org/10.1021/acs.est.2c01531openalex-snapshot
Bisphenol F Impaired Zebrafish Cognitive Ability through Inducing Neural Cell Heterogeneous Responses
inferred← citeshttps://doi.org/10.1038/cr.2015.58openalex-snapshot
Combination of inflammation-related cytokines promotes long-term muscle stem cell expansion
inferred← citeshttps://doi.org/10.1038/jcbfm.2014.130openalex-snapshot
Neurogenesis and Inflammation after Ischemic Stroke: What is Known and Where We Go from Here
showing the first 200 of 514 · page through all 514
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.