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Inflammation and immunity in organ regeneration
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Expression ofMsx genes in regenerating and developing limbs of axolotl
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Expression of Mmp9 and related matrix metalloproteinase genes during axolotl limb regeneration
inferredcites →https://doi.org/10.1002/(sici)1521-4141(199909)29:09<2897::aid-immu2897>3.0.co;2-2openalex-snapshot
Axolotl MHC architecture and polymorphism
inferredcites →https://doi.org/10.1002/1097-0177(2000)9999:9999<::aid-dvdy1085>3.0.co;2-8openalex-snapshot
Expression patterns ofFgf-8 during development and limb regeneration of the axolotl
inferredcites →https://doi.org/10.1002/9780470514368.ch10openalex-snapshot
Mechanisms Mediating the Effects of Cytokines on Neuroendocrine Functions in the Rat
inferredcites →https://doi.org/10.1002/ar.1092140414openalex-snapshot
Changes in the extracellular matrix and glycosaminoglycan synthesis during the initiation of regeneration in adult newt forelimbs
inferredcites →https://doi.org/10.1002/ar.22443openalex-snapshot
The Developing Xenopus Limb as a Model for Studies on the Balance between Inflammation and Regeneration
inferredcites →https://doi.org/10.1002/ar.22660openalex-snapshot
Comparative Anatomy of Mouse and Human Nail Units
inferredcites →https://doi.org/10.1002/bies.201300144openalex-snapshot
The promise of perfect adult tissue repair and regeneration in mammals: Learning from regenerative amphibians and fish
inferredcites →https://doi.org/10.1002/dvdy.10049openalex-snapshot
Expression of fibroblast growth factors 4, 8, and 10 in limbs, flanks, and blastemas of Ambystoma
inferredcites →https://doi.org/10.1002/dvdy.10229openalex-snapshot
Identification of genes induced in regenerating Xenopus tadpole tails by using the differential display method
inferredcites →https://doi.org/10.1002/dvdy.10239openalex-snapshot
Regeneration or scarring: An immunologic perspective
inferredcites →https://doi.org/10.1002/dvdy.10250openalex-snapshot
Identification of genes expressed during Xenopus laevis limb regeneration by using subtractive hybridization
inferredcites →https://doi.org/10.1002/dvdy.20508openalex-snapshot
Strategies to reduce variation in Xenopus regeneration studies
inferredcites →https://doi.org/10.1002/dvdy.20897openalex-snapshot
Global analysis of gene expression in Xenopus hindlimbs during stage‐dependent complete and incomplete regeneration
inferredcites →https://doi.org/10.1002/dvdy.21891openalex-snapshot
Comparative and developmental study of the immune system in Xenopus
inferredcites →https://doi.org/10.1002/dvdy.22011openalex-snapshot
Effects of activation of hedgehog signaling on patterning, growth, and differentiation in Xenopus froglet limb regeneration
inferredcites →https://doi.org/10.1002/dvdy.22503openalex-snapshot
Matrix metalloproteinase expression during blastema formation in regeneration‐competent versus regeneration‐deficient amphibian limbs
inferredcites →https://doi.org/10.1002/dvdy.22553openalex-snapshot
Looking proximally and distally: 100 years of limb regeneration and beyond
inferredcites →https://doi.org/10.1002/dvdy.22554openalex-snapshot
Dedifferentiation and the role of sall4 in reprogramming and patterning during amphibian limb regeneration
inferredcites →https://doi.org/10.1002/dvdy.22608openalex-snapshot
“Soft” tissue patterning: Muscles and tendons of the limb take their form
inferredcites →https://doi.org/10.1002/dvdy.24265openalex-snapshot
Injuries to appendage extremities and digit tips: A clinical and cellular update
inferredcites →https://doi.org/10.1002/jez.1401180307openalex-snapshot
Beryllium inhibition of regeneration. III. Histological effects of beryllium on the amputated fore limbs of Amblystoma larvae
inferredcites →https://doi.org/10.1002/jez.1401360207openalex-snapshot
The effects of microquantities of beryllium ion on the regenerating forelimb of the adult newt, Triturus
inferredcites →https://doi.org/10.1002/jez.1401770110openalex-snapshot
The stress response in the abundance of circulating leucocytes in the killifish, Fundulus heteroclitus I. The cold‐shock sequence and the effects of hypophysectomy
inferredcites →https://doi.org/10.1002/jez.1401950111openalex-snapshot
Effects on adult newt limb regeneration of partial and complete skin flaps over the amputation surface
inferredcites →https://doi.org/10.1002/jez.1402010112openalex-snapshot
Accumulation of glucocorticoids in regenerating areas of limbs of the newt, Notophthalmus viridescens
inferredcites →https://doi.org/10.1002/jez.b.21371openalex-snapshot
Skin wound healing in axolotls: a scarless process
inferredcites →https://doi.org/10.1002/jmor.1051100105openalex-snapshot
Limb regeneration in larvae and metamorphosing individuals of the South African clawed toad
inferredcites →https://doi.org/10.1002/jmor.1051380406openalex-snapshot
Suppression of the allograft response by implants of mature lymphoid tissues in larval Xenopus laevis
inferredcites →https://doi.org/10.1002/jmor.20155openalex-snapshot
Skin wound healing in different aged Xenopus laevis
inferredcites →https://doi.org/10.1002/lt.22480openalex-snapshot
Identification of a novel biomarker gene set with sensitivity and specificity for distinguishing between allograft rejection and tolerance#*
inferredcites →https://doi.org/10.1002/reg2.40openalex-snapshot
Positional information in axolotl and mouse limb extracellular matrix is mediated via heparan sulfate and fibroblast growth factor during limb regeneration in the axolotl (Ambystoma mexicanum)
inferredcites →https://doi.org/10.1002/reg2.8openalex-snapshot
Experimentally induced metamorphosis in axolotls reduces regenerative rate and fidelity
inferredcites →https://doi.org/10.1006/dbio.1994.1348openalex-snapshot
Developmental Regulation of a Matrix Metalloproteinase during Regeneration of Axolotl Appendages
inferredcites →https://doi.org/10.1006/dbio.1999.9587openalex-snapshot
Mesenchyme with fgf-10 Expression Is Responsible for Regenerative Capacity in Xenopus Limb Buds
inferredcites →https://doi.org/10.1006/dbio.2001.0180openalex-snapshot
FGF-10 Stimulates Limb Regeneration Ability in Xenopus laevis
inferredcites →https://doi.org/10.1006/gcen.1995.1031openalex-snapshot
Effect of Induced Metamorphosis on the Immune System of the Axolotl, Ambystoma mexicanum
inferredcites →https://doi.org/10.1007/82_2012_305openalex-snapshot
Wound Healing in Mammals and Amphibians: Toward Limb Regeneration in Mammals
inferredcites →https://doi.org/10.1007/b99966openalex-snapshot
Regenerative Capacity and the Developing Immune System
inferredcites →https://doi.org/10.1007/s12026-014-8517-0openalex-snapshot
Effects of stress on immune function: the good, the bad, and the beautiful
inferredcites →https://doi.org/10.1016/0012-1606(70)90005-9openalex-snapshot
Immunological maturation and lymphoreticular cancer transformation in larvalXenopus laevis, the South African clawed toad
inferredcites →https://doi.org/10.1016/0012-1606(75)90022-6openalex-snapshot
Hyaluronidase activity and glycosaminoglycan synthesis in the amputated newt limb: Comparison of denervated, nonregenerating limbs with regenerates
inferredcites →https://doi.org/10.1016/0012-1606(92)90154-9openalex-snapshot
Molecular aspects of regeneration in developing vertebrate limbs
inferredcites →https://doi.org/10.1016/0016-6480(84)90061-3openalex-snapshot
Variations in aldosterone and corticosterone plasma levels during metamorphosis in Xenopus laevis tadpoles
inferredcites →https://doi.org/10.1016/b978-0-12-381422-7.10006-9openalex-snapshot
Scarless Wound Healing
inferredcites →https://doi.org/10.1016/b978-0-12-800100-4.00005-2openalex-snapshot
The CD200–CD200R1 Inhibitory Signaling Pathway
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.2013.01.005openalex-snapshot
Expression analysis of XPhyH-like during development and tail regeneration in Xenopus tadpoles: Possible role of XPhyH-like expressing immune cells in impaired tail regenerative ability
inferredcites →https://doi.org/10.1016/j.biocel.2014.07.010openalex-snapshot
Delineating the roles of neutrophils and macrophages in zebrafish regeneration models
inferredcites →https://doi.org/10.1016/j.biocel.2014.07.022openalex-snapshot
MSCs and hyaluronan: Sticking together for new therapeutic potential?
inferredcites →https://doi.org/10.1016/j.biocel.2014.10.011openalex-snapshot
Extracellular matrix considerations for scar-free repair and regeneration: Insights from regenerative diversity among vertebrates
inferredcites →https://doi.org/10.1016/j.cell.2012.09.034openalex-snapshot
Activation of Innate Immunity Is Required for Efficient Nuclear Reprogramming
inferredcites →https://doi.org/10.1016/j.cell.2013.10.054openalex-snapshot
A Special Population of Regulatory T Cells Potentiates Muscle Repair
inferredcites →https://doi.org/10.1016/j.cell.2015.08.021openalex-snapshot
A Distinct Function of Regulatory T Cells in Tissue Protection
inferredcites →https://doi.org/10.1016/j.cellimm.2015.01.002openalex-snapshot
Immunomodulatory characteristics of mesenchymal stem cells and their role in the treatment of Multiple Sclerosis
inferredcites →https://doi.org/10.1016/j.clindermatol.2011.11.003openalex-snapshot
Psychological stress and immunoprotection versus immunopathology in the skin
inferredcites →https://doi.org/10.1016/j.coi.2013.07.012openalex-snapshot
T cell recognition of beryllium
inferredcites →https://doi.org/10.1016/j.dci.2006.07.001openalex-snapshot
Cells of cutaneous immunity in Xenopus: Studies during larval development and limb regeneration
inferredcites →https://doi.org/10.1016/j.devcel.2012.11.017openalex-snapshot
Imparting Regenerative Capacity to Limbs by Progenitor Cell Transplantation
inferredcites →https://doi.org/10.1016/j.devcel.2015.07.015openalex-snapshot
Adaptive Immune Regulation of Mammary Postnatal Organogenesis
inferredcites →https://doi.org/10.1016/j.devcel.2015.09.005openalex-snapshot
The Role of Cell Plasticity in Tissue Repair: Adaptive Cellular Reprogramming
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.gde.2012.09.006openalex-snapshot
Regeneration and reprogramming
inferredcites →https://doi.org/10.1016/j.gde.2014.11.002openalex-snapshot
Innate immunity and epigenetic plasticity in cellular reprogramming
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.jdermsci.2015.04.011openalex-snapshot
Exploring the biology of the nail: An intriguing but less-investigated skin appendage
inferredcites →https://doi.org/10.1016/j.jri.2015.05.005openalex-snapshot
The CD200 tolerance-signaling molecule and its receptor, CD200R1, are expressed in human placental villus trophoblast and in peri-implant decidua by 5 weeks’ gestation
inferredcites →https://doi.org/10.1016/j.mce.2013.05.007openalex-snapshot
Extra-adrenal glucocorticoid synthesis: Immune regulation and aspects on local organ homeostasis
inferredcites →https://doi.org/10.1016/j.mod.2004.03.015openalex-snapshot
Large-scale analysis of the genes involved in fin regeneration and blastema formation in the medaka, Oryzias latipes
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Immune cells in the healing skin wound: Influential players at each stage of repair
inferredcites →https://doi.org/10.1016/j.semcdb.2009.04.009openalex-snapshot
Interrelation of immunity and tissue repair or regeneration
inferredcites →https://doi.org/10.1016/j.semcdb.2012.09.013openalex-snapshot
Regeneration: The ultimate example of wound healing
inferredcites →https://doi.org/10.1016/j.smim.2013.04.002openalex-snapshot
Complement-triggered pathways orchestrate regenerative responses throughout phylogenesis
inferredcites →https://doi.org/10.1016/j.smim.2015.05.003openalex-snapshot
New insights into the resolution of inflammation
inferredcites →https://doi.org/10.1016/j.stem.2013.11.007openalex-snapshot
Fundamental Differences in Dedifferentiation and Stem Cell Recruitment during Skeletal Muscle Regeneration in Two Salamander Species
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Signaling networks organizing regenerative growth of the zebrafish fin
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.vph.2015.02.007openalex-snapshot
The innate immune system, toll-like receptors and dermal wound healing: A review
inferredcites →https://doi.org/10.1016/j.ydbio.2004.12.003openalex-snapshot
Normal newt limb regeneration requires matrix metalloproteinase function
inferredcites →https://doi.org/10.1016/j.ydbio.2007.12.025openalex-snapshot
Development and regeneration of the neonatal digit tip in mice
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.ydbio.2015.08.013openalex-snapshot
Epigenetic modification maintains intrinsic limb-cell identity in Xenopus limb bud regeneration
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The effects of stress on wound healing in male tree lizards (Urosaurus ornatus)
inferredcites →https://doi.org/10.1016/j.ygcen.2012.11.010openalex-snapshot
Neuroendocrine–immune interaction: Regulation of inflammation via G-protein coupled receptors
inferredcites →https://doi.org/10.1016/j.ygcen.2015.04.013openalex-snapshot
Treatment with corticosterone delays cutaneous wound healing in male and female salamanders
inferredcites →https://doi.org/10.1016/s0002-9610(03)00296-4openalex-snapshot
Understanding the role of immune regulation in wound healing
inferredcites →https://doi.org/10.1016/s0074-7696(08)60426-xopenalex-snapshot
Aspects of Amphibian Metamorphosis: Hormonal Control
inferredcites →https://doi.org/10.1016/s0165-6147(98)01229-2openalex-snapshot
Induction of cytokine receptors by glucocorticoids: functional and pathological significance
inferredcites →https://doi.org/10.1016/s0168-9525(00)89129-5openalex-snapshot
Normal table of Xenopus laevis (Daudin)
inferredcites →https://doi.org/10.1016/s0960-9822(03)00396-8openalex-snapshot
Wound Healing in the PU.1 Null Mouse—Tissue Repair Is Not Dependent on Inflammatory Cells
inferredcites →https://doi.org/10.1016/s1054-3589(08)60819-4openalex-snapshot
Catecholamines, Catecholamine Receptors, Cell Adhesion Molecules, and Acute Stressor-Related Changes in Cellular Immunity
inferredcites →https://doi.org/10.1016/s1534-5807(03)00233-8openalex-snapshot
Molecular Pathways Needed for Regeneration of Spinal Cord and Muscle in a Vertebrate
inferredcites →https://doi.org/10.1038/71002openalex-snapshot
Thymosin β 4 sulfoxide is an anti-inflammatory agent generated by monocytes in the presence of glucocorticoids
inferredcites →https://doi.org/10.1038/jid.2011.223openalex-snapshot
Prx-1 Expression in Xenopus laevis Scarless Skin-Wound Healing and Its Resemblance to Epimorphic Regeneration
inferredcites →https://doi.org/10.1038/jid.2014.265openalex-snapshot
Paradoxical Benefits of Psychological Stress in Inflammatory Dermatoses Models Are Glucocorticoid Mediated
inferredcites →https://doi.org/10.1038/jid.2014.363openalex-snapshot
Stressing the Steroids in Skin: Paradox or Fine-Tuning?
inferredcites →https://doi.org/10.1038/ki.2009.259openalex-snapshot
Foxp3+ regulatory T cells participate in repair of ischemic acute kidney injury
inferredcites →https://doi.org/10.1038/nature08119openalex-snapshot
A tissue-scale gradient of hydrogen peroxide mediates rapid wound detection in zebrafish
inferredcites →https://doi.org/10.1038/nature08152openalex-snapshot
Cells keep a memory of their tissue origin during axolotl limb regeneration
inferredcites →https://doi.org/10.1038/nature12214openalex-snapshot
Wnt activation in nail epithelium couples nail growth to digit regeneration
inferredcites →https://doi.org/10.1038/nature15397openalex-snapshot
Deep-time evolution of regeneration and preaxial polarity in tetrapod limb development
inferredcites →https://doi.org/10.1038/ncb2659openalex-snapshot
Amputation-induced reactive oxygen species are required for successful Xenopus tadpole tail regeneration
inferredcites →https://doi.org/10.1038/ncomms3081openalex-snapshot
Thymosin β4-sulfoxide attenuates inflammatory cell infiltration and promotes cardiac wound healing
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Preparing the ground for tissue regeneration: from mechanism to therapy
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Bridging the regeneration gap: genetic insights from diverse animal models
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Advances in understanding tissue regenerative capacity and mechanisms in animals
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WNT signalling in the immune system: WNT is spreading its wings
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The Inflammation–Fibrosis Link? A Jekyll and Hyde Role for Blood Cells during Wound Repair
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Chronic beryllium disease: immune‐mediated destruction with implications for organ‐specific autoimmunity
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Expression of helix–loop–helix type negative regulators of differentiation during limb regeneration in urodeles and anurans
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Wound contraction and scar synthesis during development of the amphibian Rana catesbeiana
inferredcites →https://doi.org/10.1073/pnas.1300290110openalex-snapshot
Macrophages are required for adult salamander limb regeneration
inferredcites →https://doi.org/10.1074/jbc.273.21.13230openalex-snapshot
Characterization of Recombinant Human Fibroblast Growth Factor (FGF)-10 Reveals Functional Similarities with Keratinocyte Growth Factor (FGF-7)
inferredcites →https://doi.org/10.1074/jbc.m110.188268openalex-snapshot
Cortisol Synthesis in Epidermis Is Induced by IL-1 and Tissue Injury
inferredcites →https://doi.org/10.1074/jbc.m307304200openalex-snapshot
Distinctive Expression Patterns of Heparan Sulfate O-Sulfotransferases and Regional Differences in Heparan Sulfate Structure in Chick Limb Buds
inferredcites →https://doi.org/10.1074/jbc.m706640200openalex-snapshot
Unraveling Tissue Regeneration Pathways Using Chemical Genetics
inferredcites →https://doi.org/10.1084/jem.20121871openalex-snapshot
Loss of epidermal Evi/Wls results in a phenotype resembling psoriasiform dermatitis
inferredcites →https://doi.org/10.1086/398873openalex-snapshot
The Influence of the Nerve in Regeneration of the Amphibian Extremity
inferredcites →https://doi.org/10.1089/ten.tea.2013.0673openalex-snapshot
Systemic Infusion of Mesenchymal Stem Cells Improves Cell-Based Bone Regeneration via Upregulation of Regulatory T Cells
inferredcites →https://doi.org/10.1093/ajcp/aqaa163openalex-snapshot
Robbins and Cotran Pathologic Basis of Disease
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Specific inhibition of FGF-2 signaling with 2-O-sulfated octasaccharides of heparan sulfate
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Amphibian Transplantation Reactions: A Review
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Evidence for the Local Evolution of Mechanisms Underlying Limb Regeneration in Salamanders
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Restoration of intrahepatic regulatory T cells through MMP-9/13-dependent activation of TGF- is critical for immune homeostasis following acute liver injury
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Global analysis of gene expression in Xenopus limbs during stage‐dependent complete and incomplete regeneration
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Effects of Cortisone and Vitamin A on Wound Healing
inferredcites →https://doi.org/10.1097/00007890-197208000-00001openalex-snapshot
RESPONSE TO SKIN ALLOGRAFTS IN XENOPUS LAEVIS FOLLOWING THYMECTOMY AT EARLY STAGES OF LYMPHOID ORGAN MATURATION
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PROLONGED SURVIVAL OF MAJOR HISTOCOMPATIBILITY COMPLEX-DISPARATE SKIN ALLOGRAFTS TRANSPLANTED TO THE METAMORPHOSING FROG, XENOPUS LAEVIS
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Secondary Ion Mass Spectroscopy Demonstrates Retention of Beryllium in Chronic Beryllium Disease Granulomas
inferredcites →https://doi.org/10.1097/01.pap.0000155072.86944.7dopenalex-snapshot
Robbins and Cotran Pathologic Basis of Disease
inferredcites →https://doi.org/10.1098/rspb.2014.1550openalex-snapshot
Early evolution of limb regeneration in tetrapods: evidence from a 300-million-year-old amphibian
inferredcites →https://doi.org/10.1098/rstb.2004.1463openalex-snapshot
Cellular and molecular mechanisms of regeneration in Xenopus
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Immunology of the Human Nail Apparatus: The Nail Matrix Is a Site of Relative Immune Privilege
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Without nerves, immunology remains incomplete –in vivo veritas
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Hyaluronate accumulation and nerve-dependent growth during regeneration of larval Ambystoma limbs
inferredcites →https://doi.org/10.1111/j.1440-169x.2007.00919.xopenalex-snapshot
Unifying principles of regeneration I: Epimorphosis versus morphallaxis
inferredcites →https://doi.org/10.1111/j.1440-169x.2008.01072.xopenalex-snapshot
Regulation of dermal fibroblast dedifferentiation and redifferentiation during wound healing and limb regeneration in the Axolotl
inferredcites →https://doi.org/10.1111/j.1440-169x.2009.01148.xopenalex-snapshot
Functional analysis of chick heparan sulfate 6‐O‐sulfotransferases in limb bud development
inferredcites →https://doi.org/10.1111/j.1600-065x.1998.tb01268.xopenalex-snapshot
Structure of MHC class I and class II cDNAs and possible immunodeficiency linked to class II expression in the Mexican axolotl
inferredcites →https://doi.org/10.1111/j.1743-6109.2006.00121.xopenalex-snapshot
Scarless skin repair in immunodeficient mice
inferredcites →https://doi.org/10.1111/j.1749-6632.1974.tb20520.xopenalex-snapshot
NEUROTROPHIC CONTROL OF LIMB REGENERATION IN THE NEWT*
inferredcites →https://doi.org/10.1111/j.1749-6632.2010.05479.xopenalex-snapshot
Animal studies with thymosin β4, a multifunctional tissue repair and regeneration peptide
inferredcites →https://doi.org/10.1126/science.1147710openalex-snapshot
Molecular Basis for the Nerve Dependence of Limb Regeneration in an Adult Vertebrate
inferredcites →https://doi.org/10.1126/science.276.5309.75openalex-snapshot
Wound Healing--Aiming for Perfect Skin Regeneration
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Wound repair and regeneration: Mechanisms, signaling, and translation
inferredcites →https://doi.org/10.1126/scitranslmed.3010076openalex-snapshot
Effectiveness of exome and genome sequencing guided by acuity of illness for diagnosis of neurodevelopmental disorders
inferredcites →https://doi.org/10.1146/annurev.cellbio.24.110707.175336openalex-snapshot
Comparative Aspects of Animal Regeneration
inferredcites →https://doi.org/10.1146/annurev.immunol.20.082401.104914openalex-snapshot
Neuroendocrine Regulation of Immunity
inferredcites →https://doi.org/10.1146/annurev.immunol.5.1.621openalex-snapshot
Lymphocyte Hormone Receptors
inferredcites →https://doi.org/10.1155/1997/38464openalex-snapshot
Involvement of Thyroid Hormones in the Expression of MHC class I Antigens During Ontogeny in Xenopus
inferredcites →https://doi.org/10.1182/blood.v46.2.235.235openalex-snapshot
The effect of Hydrocortisone on the kinetics of normal human lymphocytes
inferredcites →https://doi.org/10.1186/1471-213x-8-66openalex-snapshot
Identification of genes associated with regenerative success of Xenopus laevishindlimbs
inferredcites →https://doi.org/10.1186/1741-7007-8-5openalex-snapshot
Regeneration and reprogramming compared
inferredcites →https://doi.org/10.1186/1741-7015-10-3openalex-snapshot
Reversal of type 1 diabetes via islet β cell regeneration following immune modulation by cord blood-derived multipotent stem cells
inferredcites →https://doi.org/10.1186/gb-2004-6-1-r5openalex-snapshot
Wound healing and inflammation genes revealed by array analysis of 'macrophageless' PU.1 null mice
inferredcites →https://doi.org/10.1186/s12861-014-0049-2openalex-snapshot
Denervation impairs regeneration of amputated zebrafish fins
inferredcites →https://doi.org/10.1210/endo-64-2-292openalex-snapshot
LIMB REGENERATION TN THE SALAMANDER, TRITURUS VIRIDESCENT, AFTER LARGE INITIAL AND DURING PROLONGED SMALLER INJECTIONS OF CORTISONE ACETATE1
inferredcites →https://doi.org/10.1242/bio.20121594openalex-snapshot
Gene expression patterns specific to the regenerating limb of the Mexican axolotl
inferredcites →https://doi.org/10.1242/dev.023176openalex-snapshot
Wnt and FGF signals interact to coordinate growth with cell fate specification during limb development
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.105.3.585openalex-snapshot
Organization of connective tissue patterns by dermal fibroblasts in the regenerating axolotl limb
inferredcites →https://doi.org/10.1242/dev.127.11.2269openalex-snapshot
Postnatal mammary gland development requires macrophages and eosinophils
inferredcites →https://doi.org/10.1289/ehp.0800455openalex-snapshot
A Reconsideration of Acute Beryllium Disease
inferredcites →https://doi.org/10.1371/journal.pone.0001227openalex-snapshot
Transforming Growth Factor: β Signaling Is Essential for Limb Regeneration in Axolotls
inferredcites →https://doi.org/10.1371/journal.pone.0032875openalex-snapshot
Skin Regeneration in Adult Axolotls: A Blueprint for Scar-Free Healing in Vertebrates
inferredcites →https://doi.org/10.1371/journal.pone.0052375openalex-snapshot
Multi-Tissue Microarray Analysis Identifies a Molecular Signature of Regeneration
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.0111655openalex-snapshot
Unique Gene Expression Profile of the Proliferating Xenopus Tadpole Tail Blastema Cells Deciphered by RNA-Sequencing Analysis
inferredcites →https://doi.org/10.1371/journal.pone.0128094openalex-snapshot
FOXP3+ T Cells Recruited to Sites of Sterile Skeletal Muscle Injury Regulate the Fate of Satellite Cells and Guide Effective Tissue Regeneration
inferredcites →https://doi.org/10.1385/ir:23:2-3:273openalex-snapshot
Neuroendocrine-Immune System Interactions in Amphibians: Implications for Understanding Global Amphibian Declines
inferredcites →https://doi.org/10.1387/ijdb.082719mkopenalex-snapshot
Proteomics analysis of regenerating amphibian limbs: changes during the onset of regeneration
inferredcites →https://doi.org/10.1387/ijdb.12455626openalex-snapshot
Vertebrate limb regeneration and the origin of limb stem cells
inferredcites →https://doi.org/10.1387/ijdb.8877452openalex-snapshot
The cellular basis of limb regeneration in urodeles
inferredcites →https://doi.org/10.15252/embj.201490147openalex-snapshot
The wound inflammatory response exacerbates growth of pre‐neoplastic cells and progression to cancer
inferredcites →https://doi.org/10.15252/embr.201439702openalex-snapshot
Effects of inflammation on stem cells: together they strive?
inferredcites →https://doi.org/10.2307/1439568openalex-snapshot
Normal Table of Xenopus Laevis (Daudin)
inferredcites →https://doi.org/10.3389/fimmu.2015.00019openalex-snapshot
Turning 21: Induction of miR-21 as a Key Switch in the Inflammatory Response
inferredcites →https://doi.org/10.3390/cells2010001openalex-snapshot
The “Stars and Stripes” Metaphor for Animal Regeneration-Elucidating Two Fundamental Strategies along a Continuum
inferredcites →https://doi.org/10.4049/jimmunol.1400625openalex-snapshot
Skin Wound Healing Is Accelerated and Scarless in the Absence of Commensal Microbiota
inferredcites →https://doi.org/10.4049/jimmunol.161.12.6819openalex-snapshot
Expression of the Third Component of Complement, C3, in Regenerating Limb Blastema Cells of Urodeles
inferredcites →https://doi.org/10.4161/derm.3.1.14617openalex-snapshot
Neuroendocrinology of the skin
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/ar.24029openalex-snapshot
Review: The Regenerating Tail Blastema of Lizards as a Model to Study Organ Regeneration and Tumor Growth Regulation in Amniotes
inferred← citeshttps://doi.org/10.1002/bies.202200080openalex-snapshot
The buried gems of disease tolerance in animals: Evolutionary and interspecies comparative approaches
inferred← citeshttps://doi.org/10.1002/dvdy.178openalex-snapshot
Wound healing across the animal kingdom: Crosstalk between the immune system and the extracellular matrix
inferred← citeshttps://doi.org/10.1002/dvdy.269openalex-snapshot
Bringing tendon biology to heel: Leveraging mechanisms of tendon development, healing, and regeneration to advance therapeutic strategies
inferred← citeshttps://doi.org/10.1002/dvdy.340openalex-snapshot
Distinct toll‐like receptor signaling in the salamander response to tissue damage
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.543openalex-snapshot
Gradual specialization of phagocytic ameboid cells may have impaired regenerative capacities in metazoan lineages
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/jez.b.22754openalex-snapshot
Review: Biological and Molecular Differences between Tail Regeneration and Limb Scarring in Lizard: An Inspiring Model Addressing Limb Regeneration in Amniotes
inferred← citeshttps://doi.org/10.1002/jez.b.22771openalex-snapshot
Hyaluronic acid in the tail and limb of amphibians and lizards recreates permissive embryonic conditions for regeneration due to its hygroscopic and immunosuppressive properties
inferred← citeshttps://doi.org/10.1002/jez.b.22835openalex-snapshot
Perspective: Appendage regeneration in amphibians and some reptiles derived from specific evolutionary histories
inferred← citeshttps://doi.org/10.1002/jmor.20631openalex-snapshot
Re‐epithelialization of large wound in paedomorphic and metamorphic axolotls
inferred← citeshttps://doi.org/10.1002/jmor.20762openalex-snapshot
Ultrastructural immunolocalization of hyaluronate in regenerating tail of lizards and amphibians supports an immune‐suppressive role to favor regeneration
inferred← citeshttps://doi.org/10.1002/jmor.21251openalex-snapshot
Appendage regeneration in anamniotes utilizes genes active during larval‐metamorphic stages that have been lost or altered in amniotes: The case for studying lizard tail regeneration
inferred← citeshttps://doi.org/10.1002/jmor.21297openalex-snapshot
Tail regeneration in a cephalochordate, the Bahamas lancelet, Asymmetron lucayanum
inferred← citeshttps://doi.org/10.1002/reg2.69openalex-snapshot
The cellular and molecular mechanisms of tissue repair and regeneration as revealed by studies in Xenopus
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/reg2.92openalex-snapshot
Mechanisms of urodele limb regeneration
inferred← citeshttps://doi.org/10.1007/978-1-0716-2172-1_1openalex-snapshot
The Hazards of Regeneration: From Morgan’s Legacy to Evo-Devo
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/10.1007/978-3-031-93677-7_18openalex-snapshot
Tissue Regeneration: Cellular and Molecular Mechanisms
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/s00709-017-1107-yopenalex-snapshot
Downregulation of lizard immuno-genes in the regenerating tail and myogenes in the scarring limb suggests that tail regeneration occurs in an immuno-privileged organ
inferred← citeshttps://doi.org/10.1016/b978-0-12-801238-3.99510-2openalex-snapshot
Limb Regeneration in Amphibians
inferred← citeshttps://doi.org/10.1016/b978-0-12-809880-6.00003-5openalex-snapshot
Mechanisms of Blastema Formation and Growth in Regenerating Urodele Limbs
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/j.aanat.2016.12.001openalex-snapshot
Microscopic observations show invasion of inflammatory cells in the limb blastema and epidermis in pre-metamorphic frog tadpoles which destroy the Apical Epidermal CAP and impede regeneration
inferred← citeshttps://doi.org/10.1016/j.aanat.2017.12.008openalex-snapshot
Review: Limb regeneration in humans: Dream or reality?
inferred← citeshttps://doi.org/10.1016/j.aanat.2018.12.005openalex-snapshot
Organ regeneration evolved in fish and amphibians in relation to metamorphosis: Speculations on a post-embryonic developmental process lost in amniotes after the water to land transition
inferred← citeshttps://doi.org/10.1016/j.aanat.2020.151549openalex-snapshot
Autoradiography and inmmunolabeling suggests that lizard blastema contains arginase-positive M2-like macrophages that may support tail regeneration
inferred← citeshttps://doi.org/10.1016/j.aanat.2022.151940openalex-snapshot
Immunohistochemistry indicates that persistent inflammation determines failure of tail, limb and finger regeneration in the Lizard Podarcis muralis
inferred← citeshttps://doi.org/10.1016/j.actbio.2018.09.056openalex-snapshot
The inflammasome in host response to biomaterials: Bridging inflammation and tissue regeneration
inferred← citeshttps://doi.org/10.1016/j.ajpath.2021.01.008openalex-snapshot
Early Inflammation in Muscular Dystrophy Differs between Limb and Respiratory Muscles and Increases with Dystrophic Severity
inferred← citeshttps://doi.org/10.1016/j.apmt.2022.101547openalex-snapshot
Study on bioactive PEGDA/ECM hybrid bi-layered hydrogel scaffolds fabricated by electro-writing for cartilage regeneration
inferred← citeshttps://doi.org/10.1016/j.apmt.2022.101560openalex-snapshot
Smart/stimuli-responsive hydrogels: State-of-the-art platforms for bone tissue engineering
inferred← citeshttps://doi.org/10.1016/j.aquatox.2022.106156openalex-snapshot
Inhibitory effects of estrogenic endocrine disrupting chemicals on fin regeneration in zebrafish are dependent on estrogen receptors
inferred← citeshttps://doi.org/10.1016/j.biomaterials.2021.121205openalex-snapshot
Healing through the lens of immunothrombosis: Biology-inspired, evolution-tailored, and human-engineered biomimetic therapies
inferred← citeshttps://doi.org/10.1016/j.biopha.2021.111516openalex-snapshot
Macro- and microtranscriptomic evidence of the monocyte recruitment to regenerating liver after partial hepatectomy in mouse model
inferred← citeshttps://doi.org/10.1016/j.cbpc.2025.110358openalex-snapshot
Developmental toxicity of functionalized polystyrene microplastics and their inhibitory effects on fin regeneration in zebrafish
inferred← citeshttps://doi.org/10.1016/j.ccell.2017.02.005openalex-snapshot
Nerve Dependence: From Regeneration to Cancer
inferred← citeshttps://doi.org/10.1016/j.cdev.2024.203901openalex-snapshot
Reactive nitrogen species-mediated cell proliferation during tail regeneration and retinoic acid as a putative modulator of tissue regeneration in the geckos
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.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.devcel.2023.12.017openalex-snapshot
Tissue-resident macrophages specifically express Lactotransferrin and Vegfc during ear pinna regeneration in spiny mice
inferred← citeshttps://doi.org/10.1016/j.ecoenv.2022.113872openalex-snapshot
Ferroptosis is partially responsible for dexamethasone-induced T cell ablation, but not osteoporosis in larval zebrafish
inferred← citeshttps://doi.org/10.1016/j.envpol.2020.114664openalex-snapshot
Inhibitory effects of polystyrene microplastics on caudal fin regeneration in zebrafish larvae
inferred← citeshttps://doi.org/10.1016/j.fsi.2018.06.029openalex-snapshot
Tissue regeneration promotion effects of phenanthroimidazole derivatives through pro-inflammatory pathway activation
inferred← citeshttps://doi.org/10.1016/j.fsi.2020.02.071openalex-snapshot
Isoliquiritin promote angiogenesis by recruiting macrophages to improve the healing of zebrafish wounds
inferred← citeshttps://doi.org/10.1016/j.fsi.2020.08.026openalex-snapshot
Phylogeny of Slc15 family and response to Aeromonas hydrophila infection following Lactococcus lactis dietary supplementation in Cyprinus carpio
inferred← citeshttps://doi.org/10.1016/j.fsi.2026.111365openalex-snapshot
Post traumatic response of coelomocytes in the common sea star Echinaster sepositus
inferred← citeshttps://doi.org/10.1016/j.gene.2018.03.015openalex-snapshot
Transcriptomic analysis of Portunus trituberculatus reveals a critical role for WNT4 and WNT signalling in limb regeneration
inferred← citeshttps://doi.org/10.1016/j.indcrop.2026.122941openalex-snapshot
Pro-regenerative potential of Artemisia annua L. essential oil: Toward a plant-derived ingredient for wound healing applications
inferred← citeshttps://doi.org/10.1016/j.intimp.2021.107696openalex-snapshot
Intra-nasal administration of sperm head turns neutrophil into reparative mode after PGE1- and/or Ang II receptor-mediated phagocytosis followed by expression of sperm head’s coding RNA
inferred← citeshttps://doi.org/10.1016/j.molmed.2018.08.004openalex-snapshot
Autotherapies: Enhancing Endogenous Healing and Regeneration
inferred← citeshttps://doi.org/10.1016/j.msec.2021.112172openalex-snapshot
Addition of lactoferrin and substance P in a chitin/PLGA-CaSO4 hydrogel for regeneration of calvarial bone defects
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.scitotenv.2018.10.275openalex-snapshot
Effects of 17α‑ethinylestradiol on caudal fin regeneration in zebrafish larvae
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2021.147288openalex-snapshot
Development and validation of an activated immune model with zebrafish eleutheroembryo based on caudal fin acupuncture
inferred← citeshttps://doi.org/10.1016/j.semcdb.2016.04.012openalex-snapshot
Macrophages and regeneration: Lessons from the heart
inferred← citeshttps://doi.org/10.1016/j.semcdb.2016.08.008openalex-snapshot
Chasing the recipe for a pro-regenerative immune system
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.2020.06.008openalex-snapshot
Bone marrow contribution to the heart from development to adulthood
inferred← citeshttps://doi.org/10.1016/j.stem.2018.11.019openalex-snapshot
Cellular Plasticity in Intestinal Homeostasis and Disease
inferred← citeshttps://doi.org/10.1016/j.ydbio.2017.09.025openalex-snapshot
Learning from regeneration research organisms: The circuitous road to scar free wound healing
inferred← citeshttps://doi.org/10.1016/j.ydbio.2023.06.013openalex-snapshot
Regeneration among animals: An evolutionary hypothesis related to aquatic versus terrestrial environment
inferred← citeshttps://doi.org/10.1016/j.yexcr.2020.112149openalex-snapshot
Identification of immune and non-immune cells in regenerating axolotl limbs by single-cell sequencing
inferred← citeshttps://doi.org/10.1016/j.ygcen.2019.113220openalex-snapshot
Endocrine regulation of regeneration: Linking global signals to local processes
inferred← citeshttps://doi.org/10.1016/j.zool.2018.09.002openalex-snapshot
Immunolocalization of serpins in the regenerating tail of lizard suggests a role for epidermal and neural barrier formation
inferred← citeshttps://doi.org/10.1016/j.zool.2019.125737openalex-snapshot
Microscopic observations on amputated and scarring lizard digits show an intense inflammatory reaction
inferred← citeshttps://doi.org/10.1016/j.zool.2020.125745openalex-snapshot
Presence of immune cells in the regenerating caudal spinal cord of frog tadpoles indicates active immune-surveillance before metamorphosis
inferred← citeshttps://doi.org/10.1016/j.zool.2026.126327openalex-snapshot
Histologic and immunohistochemical changes in amputated and scarring lizard limb of Scincella tsinlingensis
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/s41536-021-00151-1openalex-snapshot
Driving regeneration, instead of healing, in adult mammals: the decisive role of resident macrophages through efferocytosis
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/s41580-025-00917-1openalex-snapshot
Signal control during tissue regeneration in adult animals
inferred← citeshttps://doi.org/10.1038/s41598-019-51092-1openalex-snapshot
Concentrates of two subsets of extracellular vesicles from cow’s milk modulate symptoms and inflammation in experimental colitis
inferred← citeshttps://doi.org/10.1038/s42003-024-06527-5openalex-snapshot
Moderate beta-cell ablation triggers synergic compensatory mechanisms even in the absence of overt metabolic disruption
inferred← citeshttps://doi.org/10.1073/pnas.2519994122openalex-snapshot
Neural crest cell recruitment and reprogramming as central drivers of embryonic limb regeneration
inferred← citeshttps://doi.org/10.1073/pnas.2536457123openalex-snapshot
Hypoxia-mediated epicardial signaling coordinates coronary angiogenesis and myocardial expansion during zebrafish ventricle maturation
inferred← citeshttps://doi.org/10.1089/omi.2020.0024openalex-snapshot
Preclinical Molecular Signatures of Spinal Cord Functional Restoration: Optimizing the Metamorphic Axolotl ( Ambystoma mexicanum ) Model in Regenerative Medicine
inferred← citeshttps://doi.org/10.1093/humupd/dmy035openalex-snapshot
The role of mesenchymal–epithelial transition in endometrial function
inferred← citeshttps://doi.org/10.1093/icb/icz023openalex-snapshot
Regeneration-Competent and -Incompetent Murids Differ in Neutrophil Quantity and Function
inferred← citeshttps://doi.org/10.1098/rstb.2022.0119openalex-snapshot
Contrasting effects of transdermal and implant corticosterone treatments in the American bullfrog wound healing
inferred← citeshttps://doi.org/10.1101/2020.02.05.936294openalex-snapshot
Epigenetic immune-modulation by Histone Deacetylase Activity (HDAC) of tissue and organ regeneration in Xenopus laevis
inferred← citeshttps://doi.org/10.1101/2021.07.30.454490openalex-snapshot
Roscovitine exacerbates Mycobacterium abscessus infection by reducing NADPH oxidase-dependent neutrophil trafficking
inferred← citeshttps://doi.org/10.1101/2022.09.05.506659openalex-snapshot
Self-assembly of cellular neighborhoods converts stochastic signaling into sustained olfactory neurogenesis
inferred← citeshttps://doi.org/10.1101/723783openalex-snapshot
Mammalian musculoskeletal regeneration is associated with reduced inflammatory cytokines and an influx of T cells
inferred← citeshttps://doi.org/10.1101/pdb.top100966openalex-snapshot
Xenopus , a Model to Study Wound Healing and Regeneration: Experimental Approaches
inferred← citeshttps://doi.org/10.1111/azo.12321openalex-snapshot
Immunogold labelling reveals intense distribution of hyaluronate in the regenerating fin blastema of the goldfish
inferred← citeshttps://doi.org/10.1111/azo.12371openalex-snapshot
Epidermal changes during tail regeneration in the Bahamas lancelet, Asymmetron lucayanum (Cephalochordata)
inferred← citeshttps://doi.org/10.1111/azo.12380openalex-snapshot
Immunoreactivity for Dab2 and Foxp3 suggests that immune‐suppressive cells are present in the regenerating tail blastema of lizard
inferred← citeshttps://doi.org/10.1111/azo.12413openalex-snapshot
Microscopy suggests that glutathione S‐transferase is stored in large granules of myeloid cells in bone marrow and sparse granulocytes of the regenerating tail of lizard
inferred← citeshttps://doi.org/10.1111/azo.12457openalex-snapshot
Immunolocalization of CD3 , CD5 and MHCII in amputated tail and limb of the lizard Podarcis muralis marks a scarring healing program
inferred← citeshttps://doi.org/10.1111/azo.12487openalex-snapshot
Regeneration and regengrow in multicellular animals derive from the presence of processes of organ metamorphosis and continuous growth in their life cycles
inferred← citeshttps://doi.org/10.1111/azo.12498openalex-snapshot
Speculations on the loss of regeneration derived from developmental modifications during land adaptation in some evolutionary lineages of animals
inferred← citeshttps://doi.org/10.1111/bph.15156openalex-snapshot
Pro‐resolving mediator protectin D1 promotes epimorphic regeneration by controlling immune cell function in vertebrates
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/10.1126/sciadv.abf7207openalex-snapshot
Mesenchymal stromal exosome–functionalized scaffolds induce innate and adaptive immunomodulatory responses toward tissue repair
inferred← citeshttps://doi.org/10.1155/2022/8343763openalex-snapshot
New Paradigm in Cell Therapy Using Sperm Head to Restore Brain Function and Structure in Animal Model of Alzheimer’s Disease: Support for Boosting Constructive Inflammation vs. Anti-Inflammatory Approach
inferred← citeshttps://doi.org/10.1159/000518036openalex-snapshot
Axolotls’ and Mices’ Oral-Maxillofacial Trephining Wounds Heal Differently
inferred← citeshttps://doi.org/10.1165/rcmb.2021-0406ocopenalex-snapshot
Roscovitine Worsens Mycobacterium abscessus Infection by Reducing DUOX2-mediated Neutrophil Response
inferred← citeshttps://doi.org/10.1177/09592989251324288openalex-snapshot
Biomechanical properties of regenerated digital flexor tendon in immature newt following complete transection
inferred← citeshttps://doi.org/10.1186/s12929-018-0445-1openalex-snapshot
MARCKS and MARCKS-like proteins in development and regeneration
inferred← citeshttps://doi.org/10.1186/s13578-017-0199-6openalex-snapshot
Heart regeneration in adult Xenopus tropicalis after apical resection
inferred← citeshttps://doi.org/10.1186/s13619-020-00073-1openalex-snapshot
The engine initiating tissue regeneration: does a common mechanism exist during evolution?
inferred← citeshttps://doi.org/10.1210/en.2019-00321openalex-snapshot
Endocrine Regulation of Epimorphic Regeneration
inferred← citeshttps://doi.org/10.1242/dev.185496openalex-snapshot
The myeloid lineage is required for the emergence of a regeneration-permissive environment following Xenopus tail amputation
inferred← citeshttps://doi.org/10.1242/dev.191957openalex-snapshot
Transposon control as a checkpoint for tissue regeneration
inferred← citeshttps://doi.org/10.1371/journal.pgen.1009628openalex-snapshot
mTOR activity is essential for retinal pigment epithelium regeneration in zebrafish
inferred← citeshttps://doi.org/10.1371/journal.pone.0232981openalex-snapshot
Active Notch signaling is required for arm regeneration in a brittle star
inferred← citeshttps://doi.org/10.22141/2224-0551.13.4.2018.137018openalex-snapshot
Взаємозв’язок сироваткового вмісту цитокінів і нейропептидів у дітей з рекурентним бронхітом і синдромом вертебробазилярної артеріальної системи
inferred← citeshttps://doi.org/10.22363/2313-0245-2023-27-4-449-458openalex-snapshot
Migration, proliferation and cell death of regenerating liver macrophages in an experimental model
inferred← citeshttps://doi.org/10.24272/j.issn.2095-8137.2018.050openalex-snapshot
蜥蜴重复断尾或烧灼减弱尾部再生与芽基内免疫细胞的增加
inferred← citeshttps://doi.org/10.3389/fcell.2020.604030openalex-snapshot
The Olfactory Organ Is Populated by Neutrophils and Macrophages During Early Development
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/fevo.2021.621686openalex-snapshot
Evolution of Regeneration in Animals: A Tangled Story
inferred← citeshttps://doi.org/10.3389/fimmu.2018.02058openalex-snapshot
Amphibian (Xenopus laevis) Interleukin-8 (CXCL8): A Perspective on the Evolutionary Divergence of Granulocyte Chemotaxis
inferred← citeshttps://doi.org/10.3389/fimmu.2020.01695openalex-snapshot
Complex Tissue Regeneration in Mammals Is Associated With Reduced Inflammatory Cytokines and an Influx of T Cells
inferred← citeshttps://doi.org/10.3389/fimmu.2020.01733openalex-snapshot
Deletion of cftr Leads to an Excessive Neutrophilic Response and Defective Tissue Repair in a Zebrafish Model of Sterile Inflammation
inferred← citeshttps://doi.org/10.3389/fimmu.2026.1910184openalex-snapshot
Immunoguided cutaneous regeneration: a theoretical framework linking extracellular matrix, immunity, and skin allografts
inferred← citeshttps://doi.org/10.3389/fphys.2021.632506openalex-snapshot
HvRNASET2 Regulate Connective Tissue and Collagen I Remodeling During Wound Healing Process
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/biomedicines13071552openalex-snapshot
Epigenetic Modifications in the Retinal Pigment Epithelium of the Eye During RPE-Related Regeneration or Retinal Diseases in Vertebrates
inferred← citeshttps://doi.org/10.3390/biomedicines9091129openalex-snapshot
MARCO+ Macrophage Dynamics in Regenerating Liver after 70% Liver Resection in Mice
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/cells11182851openalex-snapshot
Biomaterials and Extracellular Vesicle Delivery: Current Status, Applications and Challenges
inferred← citeshttps://doi.org/10.3390/genes15111448openalex-snapshot
Exposure to High Concentrations of Tetrabromobisphenol A Slows the Process of Tissue Regeneration and Induces an Imbalance of Metabolic Homeostasis in the Regenerated Intestines of Apostichopus japonicus
inferred← citeshttps://doi.org/10.3390/ijerph18094424openalex-snapshot
The Effectiveness of Massage Therapy for Improving Sequelae in Post-Stroke Survivors. A Systematic Review and Meta-Analysis
inferred← citeshttps://doi.org/10.3390/ijms18051054openalex-snapshot
First Insights into Human Fingertip Regeneration by Echo-Doppler Imaging and Wound Microenvironment Assessment
inferred← citeshttps://doi.org/10.3390/ijms20030636openalex-snapshot
Biomaterials: Foreign Bodies or Tuners for the Immune Response?
inferred← citeshttps://doi.org/10.3390/jdb13010002openalex-snapshot
Regeneration, Regengrow and Tissue Repair in Animals: Evolution Indicates That No Regeneration Occurs in Terrestrial Environments but Only Recovery Healing
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/jfmk2030023openalex-snapshot
Proliferating Cells in Knee Epiphyses of Lizards Allow for Somatic Growth and Regeneration after Damage
inferred← citeshttps://doi.org/10.3390/life13101981openalex-snapshot
Cellular and Molecular Triggers of Retinal Regeneration in Amphibians
inferred← citeshttps://doi.org/10.4103/1673-5374.324850openalex-snapshot
Growth associated protein 43 and neurofilament immunolabeling in the transected lumbar spinal cord of lizard indicates limited axonal regeneration
inferred← citeshttps://doi.org/10.46889/jrmbr.2026.7207openalex-snapshot
Hypothesis and Reflections on the Bases of Regeneration-Incompetence: Healing Through a Fibrotic Scarring Process
inferred← citeshttps://doi.org/10.64898/2026.04.08.717325openalex-snapshot
Injury-induced Cxcl11 and neutrophil signaling drive zebrafish kidney regeneration by generating a nephrogenic niche of Fgf and Wnt expression
inferred← citeshttps://doi.org/10.64898/2026.07.25.740716openalex-snapshot
Actively cycling cells in uninjured connective tissue are not a prerequisite for appendage regeneration
inferred← citeshttps://doi.org/10.70675/672b0e2ezef3bz4593za5a2ze1aec6c30175openalex-snapshot
Les opioïdes : un verrou à la régénération chez le mammifère adulte ? Dialogue avec le système immunitaire et l'innervation sensorielle
inferred← citeshttps://doi.org/10.70675/fe270cfcz6d95z4dfaz86a6z01efaf8a5ef7openalex-snapshot
Dynamics of macrophage polarization in zebrafish during the tissue injury and infection
inferred← citeshttps://doi.org/10.7150/ijbs.21916openalex-snapshot
Altered Neuroendocrine Immune Responses, a Two-Sword Weapon against Traumatic Inflammation
inferred← citeshttps://doi.org/10.7554/elife.24623openalex-snapshot
Macrophages are necessary for epimorphic regeneration in African spiny mice
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