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Regenerative Capacity and the Developing Immune System
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1007/978-1-4899-0185-9_18openalex-snapshot
Fetal Wound Healing and the Development of Antiscarring Therapies for Adult Wound Healing
inferredcites →https://doi.org/10.1007/978-1-4939-1865-2openalex-snapshot
Tissue and Organ Regeneration in Adults
inferredcites →https://doi.org/10.1016/b978-0-12-381422-7.10006-9openalex-snapshot
Scarless Wound Healing
inferredcites →https://doi.org/10.1016/b978-012283245-1/50020-8openalex-snapshot
Metamorphosis: An Immunologically Unique Period in the Life of the Frog
inferredcites →https://doi.org/10.1016/b978-012455851-9/50077-8openalex-snapshot
DCs in wound healing
inferredcites →https://doi.org/10.1126/science.276.5309.75openalex-snapshot
Wound Healing--Aiming for Perfect Skin Regeneration
inferredcites →https://doi.org/10.1146/annurev.immunol.10.1.51openalex-snapshot
Peripheral T Cell Tolerance
inferredcites →https://doi.org/10.1201/b14004-13openalex-snapshot
Characteristics of Fetal Wound Repair
inferredcites →https://doi.org/10.2307/1439568openalex-snapshot
Normal Table of Xenopus Laevis (Daudin)
inferredcites →https://doi.org/10.3109/9780203909652-10openalex-snapshot
The Role of Hyaluronan–Receptor Interactions in Wound Repair
inferredcites →https://doi.org/10.3109/9780203909652-11openalex-snapshot
Hyaluronan: Aiming for Perfect Skin Regeneration
inferredcites →https://doi.org/10.3109/9780203909652-14openalex-snapshot
The Role of Transforming Growth Factors–Beta in Cutaneous Scarring
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.15407/zoo2024.05.429zenodo-depositor-declared
Pathological Changes in the Liver Parenchyma of Reptiles as a Factor Influencing the Processes of Hematopoiesis (on the Example of Lacertidae: Eremias arguta)
inferred← citeshttps://doi.org/10.1002/9780470015902.a0001104.pub2openalex-snapshot
Regeneration: Growth Factors in Limb Regeneration
inferred← citeshttps://doi.org/10.1002/9781118025338.ch8openalex-snapshot
Vernix Caseosa and Innate Immunity
inferred← citeshttps://doi.org/10.1002/ar.22443openalex-snapshot
The Developing Xenopus Limb as a Model for Studies on the Balance between Inflammation and Regeneration
inferred← citeshttps://doi.org/10.1002/bdrc.20137openalex-snapshot
Mammalian regeneration and regenerative medicine
inferred← citeshttps://doi.org/10.1002/dvdy.20897openalex-snapshot
Global analysis of gene expression in Xenopus hindlimbs during stage‐dependent complete and incomplete regeneration
inferred← citeshttps://doi.org/10.1002/dvdy.21998openalex-snapshot
Gene expression profiles of lens regeneration and development in Xenopus laevis
inferred← citeshttps://doi.org/10.1002/dvdy.22553openalex-snapshot
Looking proximally and distally: 100 years of limb regeneration and beyond
inferred← citeshttps://doi.org/10.1002/dvdy.24375openalex-snapshot
Müller glial cell‐dependent regeneration of the neural retina: An overview across vertebrate model systems
inferred← citeshttps://doi.org/10.1002/dvdy.341openalex-snapshot
Regeneration in anamniotes was replaced by regengrow and scarring in amniotes after land colonization and the evolution of terrestrial biological cycles
inferred← citeshttps://doi.org/10.1002/dvdy.379openalex-snapshot
Tgf‐β superfamily and limb regeneration: Tgf‐β to start and Bmp to end
inferred← citeshttps://doi.org/10.1002/ggn2.10042openalex-snapshot
Genetic, epigenetic, and post‐transcriptional basis of divergent tissue regenerative capacities among vertebrates
inferred← citeshttps://doi.org/10.1002/jbm.a.31850openalex-snapshot
Activation of human leukocytes on tantalum trabecular metal in comparison to commonly used orthopedic metal implant materials
inferred← citeshttps://doi.org/10.1002/jez.b.22974openalex-snapshot
Evolutionary bedfellows: Reconstructing the ancestral state of autotomy and regeneration
inferred← citeshttps://doi.org/10.1002/path.4644openalex-snapshot
Regeneration versus scarring in vertebrate appendages and heart
inferred← citeshttps://doi.org/10.1002/reg2.24openalex-snapshot
Angiogenesis is inhibitory for mammalian digit regeneration
inferred← citeshttps://doi.org/10.1002/reg2.32openalex-snapshot
The axolotl limb blastema: cellular and molecular mechanisms driving blastema formation and limb regeneration in tetrapods
inferred← citeshttps://doi.org/10.1002/reg2.77openalex-snapshot
Macrophages and fibroblasts during inflammation and tissue repair in models of organ regeneration
inferred← citeshttps://doi.org/10.1002/stem.140openalex-snapshot
Toward the Identification of a “Renopoietic System”?
inferred← citeshttps://doi.org/10.1002/wdev.307openalex-snapshot
Dermal fibroblast in cutaneous development and healing
inferred← citeshttps://doi.org/10.1007/978-1-4939-2495-0_17openalex-snapshot
Methods for Axolotl Blood Collection, Intravenous Injection, and Efficient Leukocyte Isolation from Peripheral Blood and the Regenerating Limb
inferred← citeshttps://doi.org/10.1007/978-3-030-45784-6_4openalex-snapshot
Exaptation for the Good and the Bad: Regeneration and Cancer
inferred← citeshttps://doi.org/10.1007/978-3-319-27583-3_7openalex-snapshot
Organ and Appendage Regeneration in the Axolotl
inferred← citeshttps://doi.org/10.1007/978-3-642-11865-4_1openalex-snapshot
The Emperor’s New Body: Seeking for a Blueprint of Limb Regeneration in Humans
inferred← citeshttps://doi.org/10.1007/978-3-662-56179-9_10openalex-snapshot
Dedifferentiation and Organ Regeneration
inferred← citeshttps://doi.org/10.1007/s00395-025-01104-1openalex-snapshot
Critical analysis of descriptive microRNA data in the translational research on cardioprotection and cardiac repair: lost in the complexity of bioinformatics
inferred← citeshttps://doi.org/10.1007/s00441-011-1136-3openalex-snapshot
Tail regenerative capacity and iNOS immunolocalization in Xenopus laevis tadpoles
inferred← citeshttps://doi.org/10.1007/s00441-020-03174-0openalex-snapshot
Recombinant HvRNASET2 protein induces marked connective tissue remodelling in the invertebrate model Hirudo verbana
inferred← citeshttps://doi.org/10.1007/s00441-020-03201-0openalex-snapshot
Extracellular matrix gene expression during arm regeneration in Amphiura filiformis
inferred← citeshttps://doi.org/10.1007/s10753-016-0488-yopenalex-snapshot
MicroRNA-155: a Novel Armamentarium Against Inflammatory Diseases
inferred← citeshttps://doi.org/10.1007/s11427-020-1915-yopenalex-snapshot
Biodiversity-based development and evolution: the emerging research systems in model and non-model organisms
inferred← citeshttps://doi.org/10.1007/s12265-012-9383-6openalex-snapshot
Myocardial Regenerative Properties of Macrophage Populations and Stem Cells
inferred← citeshttps://doi.org/10.1007/s13770-024-00667-9openalex-snapshot
Collagen-Heparin-FGF2-VEGF Scaffolds Induce a Regenerative Gene Expression Profile in a Fetal Sheep Wound Model
inferred← citeshttps://doi.org/10.1007/s40139-018-0161-2openalex-snapshot
Tissue Repair and Epimorphic Regeneration: an Overview
inferred← citeshttps://doi.org/10.1007/s40778-017-0086-4openalex-snapshot
Of Salamanders and Spiny Mice: Common Features of Regeneration and Stem Cells
inferred← citeshttps://doi.org/10.1007/s40883-020-00157-zopenalex-snapshot
Diversity of Electrospinning Approach for Vascular Implants: Multilayered Tubular Scaffolds
inferred← citeshttps://doi.org/10.1016/b978-0-12-381422-7.10003-3openalex-snapshot
Mechanisms of Blastema Formation in Regenerating Amphibian Limbs
inferred← citeshttps://doi.org/10.1016/b978-0-12-384860-4.00002-2openalex-snapshot
Repair of Skin by Fibrosis
inferred← citeshttps://doi.org/10.1016/b978-0-12-384860-4.00008-3openalex-snapshot
Regeneration of Appendages
inferred← citeshttps://doi.org/10.1016/b978-0-12-385942-6.00015-9openalex-snapshot
Developmental Mechanisms of Regeneration
inferred← citeshttps://doi.org/10.1016/b978-0-12-801238-3.99510-2openalex-snapshot
Limb Regeneration in Amphibians
inferred← citeshttps://doi.org/10.1016/b978-0-12-814879-2.00008-xopenalex-snapshot
Regenerative Potential Across Species: An Eco-Evo-Devo Perspective
inferred← citeshttps://doi.org/10.1016/b978-0-12-816388-7.00006-1openalex-snapshot
Immune Response and Tissue Damage
inferred← citeshttps://doi.org/10.1016/b978-0-12-821440-4.00003-7openalex-snapshot
Electrospun tissue regeneration biomaterials for immunomodulation
inferred← citeshttps://doi.org/10.1016/b978-012369371-6/50031-9openalex-snapshot
Regeneration of Appendages
inferred← citeshttps://doi.org/10.1016/b978-012369410-2.50008-5openalex-snapshot
Developmental Mechanisms of Regeneration
inferred← citeshttps://doi.org/10.1016/bs.ctdb.2021.12.017openalex-snapshot
A remarkable rodent: Regeneration and reproduction in spiny mice (Acomys)
inferred← citeshttps://doi.org/10.1016/j.bbamcr.2019.118623openalex-snapshot
Cardiac regeneration as an environmental adaptation
inferred← citeshttps://doi.org/10.1016/j.bbrc.2014.09.077openalex-snapshot
Acute downregulation of miR-155 at wound sites leads to a reduced fibrosis through attenuating inflammatory response
inferred← citeshttps://doi.org/10.1016/j.coi.2019.10.001openalex-snapshot
New function of zebrafish regulatory T cells in organ regeneration
inferred← citeshttps://doi.org/10.1016/j.coi.2020.10.012openalex-snapshot
Metabolic regulation of innate immune cell phenotypes during wound repair and regeneration
inferred← citeshttps://doi.org/10.1016/j.dci.2006.07.001openalex-snapshot
Cells of cutaneous immunity in Xenopus: Studies during larval development and limb regeneration
inferred← citeshttps://doi.org/10.1016/j.dci.2016.02.015openalex-snapshot
Inflammation and immunity in organ regeneration
inferred← citeshttps://doi.org/10.1016/j.dci.2017.03.023openalex-snapshot
Zebrafish FOXP3 is required for the maintenance of immune tolerance
inferred← citeshttps://doi.org/10.1016/j.dci.2024.105297openalex-snapshot
Molecular dynamics and spatial response of proliferation and apoptosis in wound healing and early intestinal regeneration of sea cucumber Apostichopus japonicus
inferred← citeshttps://doi.org/10.1016/j.devcel.2012.11.017openalex-snapshot
Imparting Regenerative Capacity to Limbs by Progenitor Cell Transplantation
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.diff.2014.02.002openalex-snapshot
Scar-free wound healing and regeneration in amphibians: Immunological influences on regenerative success
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.gde.2020.05.019openalex-snapshot
Regeneration in the spiny mouse, Acomys, a new mammalian model
inferred← citeshttps://doi.org/10.1016/j.immuni.2019.01.008openalex-snapshot
A Macrophage-Pericyte Axis Directs Tissue Restoration via Amphiregulin-Induced Transforming Growth Factor Beta Activation
inferred← citeshttps://doi.org/10.1016/j.matbio.2006.07.008openalex-snapshot
Matrix metalloproteinase 9 (MMP-9) is upregulated during scarless wound healing in athymic nude mice
inferred← citeshttps://doi.org/10.1016/j.matpr.2020.11.250openalex-snapshot
Whole body vibration: Effects on human body and role of biomaterials in repairing fracture joints and tissues
inferred← citeshttps://doi.org/10.1016/j.micpath.2014.10.005openalex-snapshot
Relationship between growth factors and its implication in the pathogenesis of leprosy
inferred← citeshttps://doi.org/10.1016/j.mod.2010.04.004openalex-snapshot
Tissue factor expression in newt iris coincides with thrombin activation and lens regeneration
inferred← citeshttps://doi.org/10.1016/j.molimm.2013.01.016openalex-snapshot
Carp head kidney leukocytes display different patterns of oxygen radical production after stimulation with PAMPs and DAMPs
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.2014.04.036openalex-snapshot
The role of the immune system in central nervous system plasticity after acute injury
inferred← citeshttps://doi.org/10.1016/j.porgcoat.2023.108118openalex-snapshot
New insights into biomaterials for wound dressings and care: Challenges and trends
inferred← citeshttps://doi.org/10.1016/j.preteyeres.2010.07.002openalex-snapshot
Molecular and cellular aspects of amphibian lens regeneration
inferred← citeshttps://doi.org/10.1016/j.preteyeres.2021.100969openalex-snapshot
The retinal pigment epithelium: Development, injury responses, and regenerative potential in mammalian and non-mammalian systems
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.regen.2020.100029openalex-snapshot
Single cell sequencing analysis of lizard phagocytic cell populations and their role in tail regeneration
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2018.10.275openalex-snapshot
Effects of 17α‑ethinylestradiol on caudal fin regeneration in zebrafish larvae
inferred← citeshttps://doi.org/10.1016/j.semcdb.2009.04.009openalex-snapshot
Interrelation of immunity and tissue repair or regeneration
inferred← citeshttps://doi.org/10.1016/j.smim.2013.04.002openalex-snapshot
Complement-triggered pathways orchestrate regenerative responses throughout phylogenesis
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.ydbio.2017.08.007openalex-snapshot
The blastema and epimorphic regeneration in mammals
inferred← citeshttps://doi.org/10.1016/j.ydbio.2023.12.008openalex-snapshot
Regenerative loss in the animal kingdom as viewed from the mouse digit tip and heart
inferred← citeshttps://doi.org/10.1016/j.yjmcc.2023.02.002openalex-snapshot
Unlocking cardiomyocyte renewal potential for myocardial regeneration therapy
inferred← citeshttps://doi.org/10.1038/nrn2398openalex-snapshot
Can the immune system be harnessed to repair the CNS?
inferred← citeshttps://doi.org/10.1038/s41467-019-14263-2openalex-snapshot
Macrophages directly contribute collagen to scar formation during zebrafish heart regeneration and mouse heart repair
inferred← citeshttps://doi.org/10.1038/s41536-017-0019-yopenalex-snapshot
Bioelectric regulation of innate immune system function in regenerating and intact Xenopus laevis
inferred← citeshttps://doi.org/10.1038/s41540-017-0042-zopenalex-snapshot
Regeneration in distantly related species: common strategies and pathways
inferred← citeshttps://doi.org/10.1038/s41598-017-16895-0openalex-snapshot
Immune tuning scaffold for the local induction of a pro-regenerative environment
inferred← citeshttps://doi.org/10.1038/s41598-019-56829-6openalex-snapshot
Integrative Analysis of Axolotl Gene Expression Data from Regenerative and Wound Healing Limb Tissues
inferred← citeshttps://doi.org/10.1038/s41598-020-77052-8openalex-snapshot
Anatomical and histological analyses reveal that tail repair is coupled with regrowth in wild-caught, juvenile American alligators (Alligator mississippiensis)
inferred← citeshttps://doi.org/10.1038/s41598-023-41572-wopenalex-snapshot
A system for bioelectronic delivery of treatment directed toward wound healing
inferred← citeshttps://doi.org/10.1038/s41598-026-45001-6openalex-snapshot
Resistance to tumorigenesis in the african spiny mouse (Acomys) correlates with upregulation of multiple tumor suppressor genes
inferred← citeshttps://doi.org/10.1038/s42003-024-05901-7openalex-snapshot
The ctenophore Mnemiopsis leidyi deploys a rapid injury response dating back to the last common animal ancestor
inferred← citeshttps://doi.org/10.1073/pnas.1300290110openalex-snapshot
Macrophages are required for adult salamander limb regeneration
inferred← citeshttps://doi.org/10.1080/03602532.2021.2025387openalex-snapshot
Cell-Biomaterial constructs for wound healing and skin regeneration
inferred← citeshttps://doi.org/10.1089/wound.2012.0371openalex-snapshot
Axolotl as a Model to Study Scarless Wound Healing in Vertebrates: Role of the Transforming Growth Factor Beta Signaling Pathway
inferred← citeshttps://doi.org/10.1093/biosci/biw079openalex-snapshot
What Determines the Regenerative Capacity in Animals?
inferred← citeshttps://doi.org/10.1093/icb/icz023openalex-snapshot
Regeneration-Competent and -Incompetent Murids Differ in Neutrophil Quantity and Function
inferred← citeshttps://doi.org/10.1093/intimm/dxy054openalex-snapshot
Macrophages in inflammation, repair and regeneration
inferred← citeshttps://doi.org/10.1095/biolreprod.111.090993openalex-snapshot
Extracellular Matrix Dynamics in Scar-Free Endometrial Repair: Perspectives from Mouse In Vivo and Human In Vitro Studies
inferred← citeshttps://doi.org/10.1097/sla.0b013e318207f39copenalex-snapshot
AmbLOXe—An Epidermal Lipoxygenase of the Mexican Axolotl in the Context of Amphibian Regeneration and Its Impact on Human Wound Closure In Vitro
inferred← citeshttps://doi.org/10.1098/rsif.2005.0062openalex-snapshot
Similarities and differences between induced organ regeneration in adults and early foetal regeneration
inferred← citeshttps://doi.org/10.1100/tsw.2006.323openalex-snapshot
Limb Regeneration in Amphibians: Immunological Considerations
inferred← citeshttps://doi.org/10.1100/tsw.2011.113openalex-snapshot
From Hydra Regeneration to Human Brain Structural Plasticity: A Long Trip through Narrowing Roads
inferred← citeshttps://doi.org/10.1101/2021.05.12.443424openalex-snapshot
Reprogramming adult tendon healing using regenerative neonatal regulatory T cells
inferred← citeshttps://doi.org/10.1101/2024.10.24.620065openalex-snapshot
Resistance to Carcinogenesis in the African Spiny Mouse ( Acomys ) correlates with upregulation of tumor suppressor genes
inferred← citeshttps://doi.org/10.1101/367474openalex-snapshot
A macrophage-pericyte axis directs tissue restoration via Amphiregulin-induced TGFβ activation
inferred← citeshttps://doi.org/10.1101/693911openalex-snapshot
Comparison of Gene Expression During Early Phases of Limb Regeneration Between Regeneration-permissive Neotenic and Regeneration-deficient Metamorphic Axolotl
inferred← citeshttps://doi.org/10.1101/cshperspect.a008078openalex-snapshot
Wnt Signaling and Injury Repair
inferred← citeshttps://doi.org/10.1101/gad.267724.115openalex-snapshot
A cellular, molecular, and pharmacological basis for appendage regeneration in mice
inferred← citeshttps://doi.org/10.1111/brv.13102openalex-snapshot
Loss of the ability to regenerate body appendages in vertebrates: from side effects of evolutionary innovations to gene loss
inferred← citeshttps://doi.org/10.1111/cei.13661openalex-snapshot
Decoding the proregenerative competence of regulatory T cells through complex tissue regeneration in zebrafish
inferred← citeshttps://doi.org/10.1111/dgd.12911openalex-snapshot
Macrophages enhance regeneration of lateral line neuromast derived from interneuromast cells through TGF ‐β in zebrafish
inferred← citeshttps://doi.org/10.1111/exd.12609openalex-snapshot
Improved cutaneous wound healing after intraperitoneal injection of alpha‐melanocyte‐stimulating hormone
inferred← citeshttps://doi.org/10.1111/exd.13847openalex-snapshot
Insights into the regeneration of skin from Acomys, the spiny mouse
inferred← citeshttps://doi.org/10.1111/j.1365-2613.2010.00737.xopenalex-snapshot
Characteristic pattern of skeletal muscle remodelling in different mouse strains
inferred← citeshttps://doi.org/10.1111/j.1440-169x.2009.01138.xopenalex-snapshot
Stem cell system in tissue regeneration in fish
inferred← citeshttps://doi.org/10.1111/j.1469-7580.2006.00626.xopenalex-snapshot
Regeneration, tissue injury and the immune response
inferred← citeshttps://doi.org/10.1111/j.1469-7580.2011.01452.xopenalex-snapshot
Denervation affects regenerative responses in MRL/MpJ and repair in C57BL/6 ear wounds
inferred← citeshttps://doi.org/10.1111/j.1524-475x.2010.00646.xopenalex-snapshot
Combination of stromal cell‐derived factor‐1 and collagen–glycosaminoglycan scaffold delays contraction and accelerates reepithelialization of dermal wounds in wild‐type mice
inferred← citeshttps://doi.org/10.1111/j.1524-475x.2011.00700.xopenalex-snapshot
Indirect effects of oral tolerance improve wound healing in skin
inferred← citeshttps://doi.org/10.1111/j.1743-6109.2006.00154.xopenalex-snapshot
Timing the commitment to a wound‐healing response of denervated limb stumps in the adult newt, Notophthalmus viridescens
inferred← citeshttps://doi.org/10.1111/wrr.12385openalex-snapshot
Cellular events during scar‐free skin regeneration in the spiny mouse, Acomys
inferred← citeshttps://doi.org/10.1111/wrr.13000openalex-snapshot
To regenerate or not to regenerate: Vertebrate model organisms of regeneration‐competency and ‐incompetency
inferred← citeshttps://doi.org/10.1113/jp284426openalex-snapshot
Homeostasis and evolution in relation to regeneration and repair
inferred← citeshttps://doi.org/10.1134/s1062359007040048openalex-snapshot
Immunostimulation exacerbates the biological effects of chemical carcinogens
inferred← citeshttps://doi.org/10.1134/s1062360416020041openalex-snapshot
High regenerative ability of tailed amphibians (Urodela) as a result of the expression of juvenile traits by mature animals
inferred← citeshttps://doi.org/10.1146/annurev.cellbio.24.110707.175336openalex-snapshot
Comparative Aspects of Animal Regeneration
inferred← citeshttps://doi.org/10.1152/physrev.00032.2010openalex-snapshot
Brain Regeneration in Physiology and Pathology: The Immune Signature Driving Therapeutic Plasticity of Neural Stem Cells
inferred← citeshttps://doi.org/10.1159/000504294openalex-snapshot
Advancements to the Axolotl Model for Regeneration and Aging
inferred← citeshttps://doi.org/10.11606/d.25.2016.tde-04082016-221543openalex-snapshot
Reparação óssea com o uso do beta fosfato tricálcico (B-tcp)® na calota craniana de ratos submetidos ao alcoolismo experimental: análises histomorfológica e histomorfométrica
inferred← citeshttps://doi.org/10.11606/d.87.2009.tde-15032010-164402openalex-snapshot
Bordetella pertussis: participação da arginase, TGF-b e TLR4 no controle da síntese de óxido nítrico em macrófagos derivados de medula óssea murina.
inferred← citeshttps://doi.org/10.11606/t.87.2016.tde-25082016-151946openalex-snapshot
Interação de Escherichia coli enteropatogênica (EPEC) atípica com fagócito profissional.
inferred← citeshttps://doi.org/10.1177/15347346221090758openalex-snapshot
Denervation Affected Skin Wound Healing in a Modified Rat Model
inferred← citeshttps://doi.org/10.1186/1471-213x-14-32openalex-snapshot
Proteomic analysis of fibroblastema formation in regenerating hind limbs of Xenopus laevis froglets and comparison to axolotl
inferred← citeshttps://doi.org/10.1186/1741-7007-7-83openalex-snapshot
Proteomic analysis of blastema formation in regenerating axolotl limbs
inferred← citeshttps://doi.org/10.1186/s12864-015-2075-2openalex-snapshot
Transcriptome profiling reveals distinctive traits of retinol metabolism and neonatal parallels in the MRL/MpJ mouse
inferred← citeshttps://doi.org/10.1186/s13227-019-0124-7openalex-snapshot
Common themes in tetrapod appendage regeneration: a cellular perspective
inferred← citeshttps://doi.org/10.1186/s13287-024-03740-1openalex-snapshot
Macrophages modulate fibrosis during newt lens regeneration
inferred← citeshttps://doi.org/10.1186/s13619-020-00068-yopenalex-snapshot
Vertebrate cardiac regeneration: evolutionary and developmental perspectives
inferred← citeshttps://doi.org/10.1186/s40824-020-0185-7openalex-snapshot
Biomaterials in orthopaedics: the past and future with immune modulation
inferred← citeshttps://doi.org/10.1242/dev.033985openalex-snapshot
Suppression of the immune response potentiates tadpole tail regeneration during the refractory period
inferred← citeshttps://doi.org/10.1242/dev.167718openalex-snapshot
Model systems for regeneration: the spiny mouse, Acomys cahirinus
inferred← citeshttps://doi.org/10.1242/dev.199906openalex-snapshot
Immune cells in cardiac repair and regeneration
inferred← citeshttps://doi.org/10.1371/journal.pone.0032875openalex-snapshot
Skin Regeneration in Adult Axolotls: A Blueprint for Scar-Free Healing in Vertebrates
inferred← citeshttps://doi.org/10.1371/journal.pone.0066613openalex-snapshot
Treatment of Glucocorticoids Inhibited Early Immune Responses and Impaired Cardiac Repair in Adult Zebrafish
inferred← citeshttps://doi.org/10.1387/ijdb.082719mkopenalex-snapshot
Proteomics analysis of regenerating amphibian limbs: changes during the onset of regeneration
inferred← citeshttps://doi.org/10.1387/ijdb.200227dqopenalex-snapshot
A roadmap for intestinal regeneration
inferred← citeshttps://doi.org/10.14440/jbm.2015.43openalex-snapshot
Generation of axolotl hematopoietic chimeras
inferred← citeshttps://doi.org/10.1515/biol-2019-0047openalex-snapshot
Adaptive immunity and skin wound healing in amphibian adults
inferred← citeshttps://doi.org/10.15252/embr.201643795openalex-snapshot
Animal regeneration: ancestral character or evolutionary novelty?
inferred← citeshttps://doi.org/10.15406/jccr.2019.12.00445openalex-snapshot
Inflammatio us a procoagulant state for appearing thrombus in patient with secondary dilated cardiomyopathy
inferred← citeshttps://doi.org/10.17760/d20248796openalex-snapshot
Exploring the neural control of axolotl limb regeneration
inferred← citeshttps://doi.org/10.21516/2072-0076-2024-17-4-116-120openalex-snapshot
Wound healing in glaucoma surgery. Part 1. Wound healing morphology
inferred← citeshttps://doi.org/10.2174/1389450116666150506112817openalex-snapshot
Redox-Related Mechanisms to Rebalance Cancer-Deregulated Cell Growth
inferred← citeshttps://doi.org/10.22038/ijbms.2021.53841.12104openalex-snapshot
Novel function of Nanos2 in expression of innate immunity genes and its probable roles in maintenance of pluripotency state.
inferred← citeshttps://doi.org/10.22074/cellj.2018.4710openalex-snapshot
Isolation, Characterization and Osteogenic Potential of Mouse Digit Tip Blastema Cells in Comparison with Bone Marrow-Derived Mesenchymal Stem Cells In Vitro.
inferred← citeshttps://doi.org/10.33233/rbfe.v12i3.3333openalex-snapshot
Treinamento de força: inflamação e reparo
inferred← citeshttps://doi.org/10.3389/fcell.2020.587320openalex-snapshot
Beyond Adult Stem Cells: Dedifferentiation as a Unifying Mechanism Underlying Regeneration in Invertebrate Deuterostomes
inferred← citeshttps://doi.org/10.3389/fcell.2021.641987openalex-snapshot
Timing Does Matter: Nerve-Mediated HDAC1 Paces the Temporal Expression of Morphogenic Genes During Axolotl Limb Regeneration
inferred← citeshttps://doi.org/10.3389/fcell.2021.750587openalex-snapshot
Identification of the Adult Hematopoietic Liver as the Primary Reservoir for the Recruitment of Pro-regenerative Macrophages Required for Salamander Limb Regeneration
inferred← citeshttps://doi.org/10.3389/fcvm.2021.744615openalex-snapshot
The Roles of Macrophages in Heart Regeneration and Repair After Injury
inferred← citeshttps://doi.org/10.3389/fevo.2022.783818openalex-snapshot
Comparative Study in Zebrafish and Medaka Unravels the Mechanisms of Tissue Regeneration
inferred← citeshttps://doi.org/10.3389/fimmu.2021.688106openalex-snapshot
Stem Cells and Innate Immunity in Aquatic Invertebrates: Bridging Two Seemingly Disparate Disciplines for New Discoveries in Biology
inferred← citeshttps://doi.org/10.3389/fmed.2022.916145openalex-snapshot
Main Pathological Changes of Benign Ureteral Strictures
inferred← citeshttps://doi.org/10.3389/fphar.2021.700050openalex-snapshot
Therapeutic Effect of Combining Anisodamine With Neostigmine on Local Scar Formation Following Roux-en-Y Choledochojejunostomy in a Novel Rat Model
inferred← citeshttps://doi.org/10.3389/fragi.2021.655315openalex-snapshot
From Autonomy to Integration, From Integration to Dynamically Balanced Integrated Co-existence: Non-aging as the Third Stage of Development
inferred← citeshttps://doi.org/10.3390/biomedicines9121892openalex-snapshot
Skin Wound Healing of the Adult Newt, Cynops pyrrhogaster: A Unique Re-Epithelialization and Scarless Model
inferred← citeshttps://doi.org/10.3390/cells10081853openalex-snapshot
Evolution of Cellular Immunity Effector Cells; Perspective on Cytotoxic and Phagocytic Cellular Lineages
inferred← citeshttps://doi.org/10.3390/ijms20153722openalex-snapshot
A Low Molecular Weight Hyaluronic Acid Derivative Accelerates Excisional Wound Healing by Modulating Pro-Inflammation, Promoting Epithelialization and Neovascularization, and Remodeling Collagen
inferred← citeshttps://doi.org/10.3390/ijms22052363openalex-snapshot
Injury-Induced Innate Immune Response During Segment Regeneration of the Earthworm, Eisenia andrei
inferred← citeshttps://doi.org/10.3390/ijms22115474openalex-snapshot
Mechanical and Immunological Regulation in Wound Healing and Skin Reconstruction
inferred← citeshttps://doi.org/10.3390/ijms22147336openalex-snapshot
Tissue Regeneration: The Dark Side of Opioids
inferred← citeshttps://doi.org/10.3390/ijms26178255openalex-snapshot
Stem Cells in Regenerative Medicine: A Journey from Adult Stem Cells to Induced Pluripotent Cells
inferred← citeshttps://doi.org/10.3390/jcdd10090357openalex-snapshot
Comparative Analysis of Heart Regeneration: Searching for the Key to Heal the Heart—Part II: Molecular Mechanisms of Cardiac Regeneration
inferred← citeshttps://doi.org/10.3390/jdb9010002openalex-snapshot
Study of Natural Longlife Juvenility and Tissue Regeneration in Caudate Amphibians and Potential Application of Resulting Data in Biomedicine
inferred← citeshttps://doi.org/10.3390/life13101981openalex-snapshot
Cellular and Molecular Triggers of Retinal Regeneration in Amphibians
inferred← citeshttps://doi.org/10.64898/2026.05.17.725704openalex-snapshot
Sustained immune activation suppresses planarian regeneration
inferred← citeshttps://doi.org/10.70675/d0da7bd7z184az4d75z9eabz05e11ff44036openalex-snapshot
Élucidation des bases cellulaires et moléculaires de la formation du blastème lors de la régénération épimorphique chez les vertébrés
inferred← citeshttps://doi.org/10.70675/ffef6377z3968z4ab7zb677z254b4877f6a0openalex-snapshot
Bases cellulaires et moléculaires de la régénération chez la méduse Clytia hemisphaerica
inferred← citeshttps://doi.org/10.7912/c2/947openalex-snapshot
Condition-specific differential subnetwork analysis for biological systems
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