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Suppression of the immune response potentiates tadpole tail regeneration during the refractory period
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/dvdy.10229openalex-snapshot
Identification of genes induced in regenerating Xenopus tadpole tails by using the differential display method
inferredcites →https://doi.org/10.1002/eji.1830270708openalex-snapshot
An amphibian CD3 homologue of the mammalian CD3 γ and δ genes
inferredcites →https://doi.org/10.1002/j.1460-2075.1996.tb00949.xopenalex-snapshot
Targeted disruption of the PU.1 gene results in multiple hematopoietic abnormalities.
inferredcites →https://doi.org/10.1002/jez.1401340209openalex-snapshot
The effect of apical cap removal on limb regeneration in Amblystoma larvae
inferredcites →https://doi.org/10.1007/b99966openalex-snapshot
Regenerative Capacity and the Developing Immune System
inferredcites →https://doi.org/10.1007/s00018-003-2186-9openalex-snapshot
Cathelicidins - a family of multifunctional antimicrobial peptides
inferredcites →https://doi.org/10.1007/s00251-002-0474-4openalex-snapshot
Structure and diversity of T-lymphocyte antigen receptors alpha and gamma in Xenopus
inferredcites →https://doi.org/10.1007/s00251-006-0114-5openalex-snapshot
Polymorphism, natural selection, and structural modeling of class Ia MHC in the African clawed frog (Xenopus laevis)
inferredcites →https://doi.org/10.1007/s002510050627openalex-snapshot
Molecular cloning of the gene for interleukin-1? from Xenopus laevis and analysis of expression in vivo and in vitro
inferredcites →https://doi.org/10.1016/0952-7915(93)90135-fopenalex-snapshot
Cyclosporin A and FK506: molecular mechanisms of immunosuppression and probes for transplantation biology
inferredcites →https://doi.org/10.1016/j.bbrc.2004.07.186openalex-snapshot
Celastrol inhibits pro-inflammatory cytokine secretion in Crohn’s disease biopsies
inferredcites →https://doi.org/10.1016/j.bcp.2006.08.014openalex-snapshot
Inhibition of NF-κB activation through targeting IκB kinase by celastrol, a quinone methide triterpenoid
inferredcites →https://doi.org/10.1016/j.bmcl.2005.09.035openalex-snapshot
Design and preparation of 2-benzamido-pyrimidines as inhibitors of IKK
inferredcites →https://doi.org/10.1016/j.cyto.2008.07.469openalex-snapshot
Regulatory T cells in health and disease
inferredcites →https://doi.org/10.1016/j.ydbio.2005.11.017openalex-snapshot
Lymphangiogenesis promotes lens destruction and subsequent lens regeneration in the newt eyeball, and both processes can be accelerated by transplantation of dendritic cells
inferredcites →https://doi.org/10.1016/s0145-305x(02)00034-4openalex-snapshot
Xenopus class II A genes: studies of genetics, polymorphism, and expression
inferredcites →https://doi.org/10.1016/s0965-1748(98)00087-3openalex-snapshot
Cloning of cDNA for regenectin, a humoral C-type lectin of Periplaneta americana, and expression of the regenectin gene during leg regeneration
inferredcites →https://doi.org/10.1016/s1074-7613(00)80354-4openalex-snapshot
Bipotential Primitive-Definitive Hematopoietic Progenitors in the Vertebrate Embryo
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/10.1073/pnas.012025199openalex-snapshot
Large-scale analysis of the human and mouse transcriptomes
inferredcites →https://doi.org/10.1074/jbc.m709279200openalex-snapshot
The Extracellular Adenosine Deaminase Growth Factor, ADGF/CECR1, Plays a Role in Xenopus Embryogenesis via the Adenosine/P1 Receptor
inferredcites →https://doi.org/10.1101/gad.1475106openalex-snapshot
Wnt/β-catenin signaling regulates vertebrate limb regeneration
inferredcites →https://doi.org/10.1126/science.1079490openalex-snapshot
Control of Regulatory T Cell Development by the Transcription Factor Foxp3
inferredcites →https://doi.org/10.1126/science.1117637openalex-snapshot
fgf20 Is Essential for Initiating Zebrafish Fin Regeneration
inferredcites →https://doi.org/10.1126/science.276.5309.81openalex-snapshot
Amphibian Limb Regeneration: Rebuilding a Complex Structure
inferredcites →https://doi.org/10.1242/dev.001115openalex-snapshot
Controlling morpholino experiments: don't stop making antisense
inferredcites →https://doi.org/10.1242/dev.02812openalex-snapshot
H+ pump-dependent changes in membrane voltage are an early mechanism necessary and sufficient to induce Xenopus tail regeneration
inferredcites →https://doi.org/10.1242/jcs.00718openalex-snapshot
RIN3: a novel Rab5 GEF interacting with amphiphysin II involved in the early endocytic pathway
inferredcites →https://doi.org/10.4049/jimmunol.153.12.5682openalex-snapshot
Monoclonal antibodies detect different distribution patterns of IL-8 receptor A and IL-8 receptor B on human peripheral blood leukocytes.
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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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.a0001101.pub2openalex-snapshot
Regeneration of the Vertebrate Tail
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
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Transducing Bioelectric Signals into Epigenetic Pathways During Tadpole Tail Regeneration
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Dedifferentiation and the role of sall4 in reprogramming and patterning during amphibian limb regeneration
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.543openalex-snapshot
Gradual specialization of phagocytic ameboid cells may have impaired regenerative capacities in metazoan lineages
inferred← citeshttps://doi.org/10.1002/dvg.23003openalex-snapshot
Seeing the future: using Xenopus to understand eye regeneration
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/glia.23165openalex-snapshot
Müller glial cell reactivation in Xenopus models of retinal degeneration
inferred← citeshttps://doi.org/10.1002/jmor.20542openalex-snapshot
The spleen and skin wound healing in Xenopus adults
inferred← citeshttps://doi.org/10.1002/med.21865openalex-snapshot
Cell transplantation and secretome based approaches in spinal cord injury regenerative medicine
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/10.1007/15695_2018_132openalex-snapshot
Extracellular Matrix and Other Factors that Impact on Cutaneous Scarring
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Now that We Got There, What Next?
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Biomaterials for Tissue Engineered Cartilage Product for Orthopedic (Osteoarthritis) Reconstruction
inferred← citeshttps://doi.org/10.1007/978-3-319-44996-8_3openalex-snapshot
Dependency on Non-myogenic Cells for Regeneration of Skeletal Muscle
inferred← citeshttps://doi.org/10.1007/978-3-319-51436-9_4openalex-snapshot
Use of Xenopus Frogs to Study Renal Development/Repair
inferred← citeshttps://doi.org/10.1007/978-3-662-56179-9_10openalex-snapshot
Dedifferentiation and Organ Regeneration
inferred← citeshttps://doi.org/10.1007/s00018-022-04261-xopenalex-snapshot
Mitochondrial function in spinal cord injury and regeneration
inferred← citeshttps://doi.org/10.1007/s00203-019-01768-zopenalex-snapshot
Dominant mutants of the calcineurin catalytic subunit (CNA-1) showed developmental defects, increased sensitivity to stress conditions, and CNA-1 interacts with CaM and CRZ-1 in Neurospora crassa
inferred← citeshttps://doi.org/10.1007/s00251-025-01372-0openalex-snapshot
Primary regulatory T cell activator FOXP3 is present across Amphibia
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/s10126-020-09951-wopenalex-snapshot
The Rapid Regenerative Response of a Model Sea Anemone Species Exaiptasia pallida Is Characterised by Tissue Plasticity and Highly Coordinated Cell Communication
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/10.1016/b978-0-12-803252-7.00020-5openalex-snapshot
Immunity and Wound Healing
inferred← citeshttps://doi.org/10.1016/b978-0-12-818084-6.00018-0openalex-snapshot
Animal models of central nervous system disorders
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.bbamcr.2019.118623openalex-snapshot
Cardiac regeneration as an environmental adaptation
inferred← citeshttps://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
inferred← citeshttps://doi.org/10.1016/j.bbrc.2016.03.039openalex-snapshot
Phyhd1, an XPhyH-like homologue, is induced in mouse T cells upon T cell stimulation
inferred← citeshttps://doi.org/10.1016/j.celrep.2023.112547openalex-snapshot
Chemical-induced epigenome resetting for regeneration program activation in human cells
inferred← citeshttps://doi.org/10.1016/j.dci.2011.01.014openalex-snapshot
The genus Xenopus as a multispecies model for evolutionary and comparative immunobiology of the 21st century
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.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.2022.104594openalex-snapshot
Amphibians as a model to study the role of immune cell heterogeneity in host and mycobacterial interactions
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.2014.01.019openalex-snapshot
Calcineurin Regulates Coordinated Outgrowth of Zebrafish Regenerating Fins
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.isci.2021.103281openalex-snapshot
Bacterial lipopolysaccharides can initiate regeneration of the Xenopus tadpole tail
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.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.2019.100023openalex-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.regen.2019.100025openalex-snapshot
Transcriptional analysis of scar-free wound healing during early stages of tail regeneration in the green anole lizard, Anolis carolinensis
inferred← citeshttps://doi.org/10.1016/j.semcdb.2012.09.013openalex-snapshot
Regeneration: The ultimate example of wound healing
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.smim.2014.06.004openalex-snapshot
Injury-induced immune responses in Hydra
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.tree.2009.08.005openalex-snapshot
Evolution of animal regeneration: re-emergence of a field
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.2021.01.005openalex-snapshot
Nutrient availability contributes to a graded refractory period for regeneration in Xenopus tropicalis
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.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/10.1038/npjregenmed.2016.12openalex-snapshot
Evolution, comparative biology and ontogeny of vertebrate heart regeneration
inferred← citeshttps://doi.org/10.1038/nrn2707openalex-snapshot
Considering the evolution of regeneration in the central nervous system
inferred← citeshttps://doi.org/10.1038/s41467-017-00594-5openalex-snapshot
interleukin-11 induces and maintains progenitors of different cell lineages during Xenopus tadpole tail regeneration
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/s41467-024-53608-4openalex-snapshot
Reintroduction of resistant frogs facilitates landscape-scale recovery in the presence of a lethal fungal disease
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/s41536-020-0087-2openalex-snapshot
An in vivo brain–bacteria interface: the developing brain as a key regulator of innate immunity
inferred← citeshttps://doi.org/10.1038/s41580-024-00719-xopenalex-snapshot
Mechanical state transitions in the regulation of tissue form and function
inferred← citeshttps://doi.org/10.1038/s41586-022-04593-5openalex-snapshot
Chemical reprogramming of human somatic cells to pluripotent stem cells
inferred← citeshttps://doi.org/10.1038/s41598-020-79436-2openalex-snapshot
Transcriptomic analysis of early stages of intestinal regeneration in Holothuria glaberrima
inferred← citeshttps://doi.org/10.1042/bst20140061openalex-snapshot
Tadpole tail regeneration in Xenopus
inferred← citeshttps://doi.org/10.1073/pnas.0907931107openalex-snapshot
Latent regeneration abilities persist following recent evolutionary loss in asexual annelids
inferred← citeshttps://doi.org/10.1073/pnas.1300290110openalex-snapshot
Macrophages are required for adult salamander limb regeneration
inferred← citeshttps://doi.org/10.1073/pnas.2009539118openalex-snapshot
Calcineurin controls proximodistal blastema polarity in zebrafish fin regeneration
inferred← citeshttps://doi.org/10.1080/15476278.2016.1163463openalex-snapshot
The role of stem cells in limb regeneration
inferred← citeshttps://doi.org/10.1093/icb/icae058openalex-snapshot
What Can Frogs Teach Us about Resilience? Adaptive Renewal in Amphibian and Academic Ecosystems
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/10.1101/180612openalex-snapshot
Insights into regeneration from the genome, transcriptome and metagenome analysis of Eisenia fetida
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/dgd.12326openalex-snapshot
Acute phase response in amputated tail stumps and neural tissue‐preferential expression in tail bud embryos of the Xenopus neuronal pentraxin I gene
inferred← citeshttps://doi.org/10.1111/dgd.12795openalex-snapshot
Cellular responses in the FGF10 ‐mediated improvement of hindlimb regenerative capacity in Xenopus laevis revealed by single‐cell transcriptomics
inferred← citeshttps://doi.org/10.1111/gtc.12349openalex-snapshot
In vivo tracking of histone H3 lysine 9 acetylation in Xenopus laevis during tail regeneration
inferred← citeshttps://doi.org/10.1111/mec.70348openalex-snapshot
Genomic Correlates of Disease Recovery in Natural Populations of the Sierra Nevada Yellow‐Legged Frog ( Rana sierrae )
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/scitranslmed.3009337openalex-snapshot
Wound repair and regeneration: Mechanisms, signaling, and translation
inferred← citeshttps://doi.org/10.1134/s1062360418050028openalex-snapshot
Patterns of Mitosis and Activation of the Map-Kinase Cascade during Tadpole Tail Regeneration in the Refractory Period of Xenopus laevis Development
inferred← citeshttps://doi.org/10.1177/20417314231203824openalex-snapshot
Adipose tissue derived stem cell secretome induces motor and histological gains after complete spinal cord injury in Xenopus laevis and mice
inferred← citeshttps://doi.org/10.1186/s13064-021-00152-2openalex-snapshot
Cellular response to spinal cord injury in regenerative and non-regenerative stages in Xenopus laevis
inferred← citeshttps://doi.org/10.1186/s13578-021-00582-9openalex-snapshot
Evolutionary divergence in tail regeneration between Xenopus laevis and Xenopus tropicalis
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.180844openalex-snapshot
Model systems for regeneration: Xenopus
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/10.1261/rna.058859.116openalex-snapshot
XenopusPiwi proteins interact with a broad proportion of the oocyte transcriptome
inferred← citeshttps://doi.org/10.1371/journal.pone.0024953openalex-snapshot
Long-Distance Signals Are Required for Morphogenesis of the Regenerating Xenopus Tadpole Tail, as Shown by Femtosecond-Laser Ablation
inferred← citeshttps://doi.org/10.1371/journal.pone.0026382openalex-snapshot
HDAC Activity Is Required during Xenopus Tail Regeneration
inferred← citeshttps://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
inferred← citeshttps://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
inferred← citeshttps://doi.org/10.1371/journal.pone.0150988openalex-snapshot
Missed, Not Missing: Phylogenomic Evidence for the Existence of Avian FoxP3
inferred← citeshttps://doi.org/10.1371/journal.pone.0204234openalex-snapshot
Large scale changes in the transcriptome of Eisenia fetida during regeneration
inferred← citeshttps://doi.org/10.1371/journal.pone.0220416openalex-snapshot
Comparative transcriptomic analysis and structure prediction of novel Newt proteins
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.201439702openalex-snapshot
Effects of inflammation on stem cells: together they strive?
inferred← citeshttps://doi.org/10.2139/ssrn.7506123openalex-snapshot
The dynamin-related GTPase Drp1 is required for tail regeneration in Xenopus laevis
inferred← citeshttps://doi.org/10.3389/fcell.2017.00070openalex-snapshot
Paying the Toll in Nuclear Reprogramming
inferred← citeshttps://doi.org/10.3389/fcell.2021.655048openalex-snapshot
From Cell Death to Regeneration: Rebuilding After Injury
inferred← citeshttps://doi.org/10.3389/fcell.2021.738940openalex-snapshot
The Secreted Protein Disulfide Isomerase Ag1 Lost by Ancestors of Poorly Regenerating Vertebrates Is Required for Xenopus laevis Tail Regeneration
inferred← citeshttps://doi.org/10.3389/fevo.2015.00067openalex-snapshot
Reconsidering regeneration in metazoans: an evo-devo approach
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.2015.00111openalex-snapshot
Microbiota and Mucosal Immunity in Amphibians
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/10.3390/genes12071072openalex-snapshot
The Tentacular Spectacular: Evolution of Regeneration in Sea Anemones
inferred← citeshttps://doi.org/10.3390/ijms252111597openalex-snapshot
Tail Tales: What We Have Learned About Regeneration from Xenopus Laevis Tadpoles
inferred← citeshttps://doi.org/10.5204/thesis.eprints.204192openalex-snapshot
Understanding the role of innate immune and novel genes in the evolution and regeneration of sea anemones
inferred← citeshttps://doi.org/10.6084/m9.figshare.14385133openalex-snapshot
Additional file 1 of Evolutionary divergence in tail regeneration between Xenopus laevis and Xenopus tropicalis
inferred← citeshttps://doi.org/10.70675/ffef6377z3968z4ab7zb677z254b4877f6a0openalex-snapshot
Bases cellulaires et moléculaires de la régénération chez la méduse Clytia hemisphaerica
inferred← citeshttps://doi.org/10.7554/elife.61804openalex-snapshot
Non-canonical Hedgehog signaling regulates spinal cord and muscle regeneration in Xenopus laevis larvae
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