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Identification of a regeneration-organizing cell in the Xenopus tail
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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.20472openalex-snapshot
Macroarray‐based analysis of tail regeneration in Xenopus laevis larvae
inferredcites →https://doi.org/10.1002/dvdy.21100openalex-snapshot
Conditional targeted cell ablation in zebrafish: A new tool for regeneration studies
inferredcites →https://doi.org/10.1002/reg2.69openalex-snapshot
The cellular and molecular mechanisms of tissue repair and regeneration as revealed by studies in Xenopus
inferredcites →https://doi.org/10.1016/0925-4773(95)00492-0openalex-snapshot
‘Regeneration’ of wing bud stumps of chick embryos and reactivation of Msx-1 and Shh expression in response to FGF-4 and ridge signals
inferredcites →https://doi.org/10.1016/j.cell.2016.05.038openalex-snapshot
The Molecular and Cellular Choreography of Appendage Regeneration
inferredcites →https://doi.org/10.1016/j.cub.2018.02.040openalex-snapshot
Comprehensive Identification and Spatial Mapping of Habenular Neuronal Types Using Single-Cell RNA-Seq
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.mod.2006.07.001openalex-snapshot
Temporal requirement for bone morphogenetic proteins in regeneration of the tail and limb of Xenopus tadpoles
inferredcites →https://doi.org/10.1016/j.mod.2008.10.002openalex-snapshot
Xenopus Wnt-5a induces an ectopic larval tail at injured site, suggesting a crucial role for noncanonical Wnt signal in tail regeneration
inferredcites →https://doi.org/10.1016/j.ydbio.2007.12.031openalex-snapshot
TGF-β signaling is required for multiple processes during Xenopus tail regeneration
inferredcites →https://doi.org/10.1016/j.ydbio.2008.01.032openalex-snapshot
Requirement for Wnt and FGF signaling in Xenopus tadpole tail regeneration
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/10.1038/75556openalex-snapshot
Gene Ontology: tool for the unification of biology
inferredcites →https://doi.org/10.1038/cddis.2017.490openalex-snapshot
Neuron and microglia/macrophage-derived FGF10 activate neuronal FGFR2/PI3K/Akt signaling and inhibit microglia/macrophages TLR4/NF-κB-dependent neuroinflammation to improve functional recovery after spinal cord injury
inferredcites →https://doi.org/10.1038/nature17644openalex-snapshot
Modulation of tissue repair by regeneration enhancer elements
inferredcites →https://doi.org/10.1038/nature19840openalex-snapshot
Genome evolution in the allotetraploid frog Xenopus laevis
inferredcites →https://doi.org/10.1038/nbt.4096openalex-snapshot
Integrating single-cell transcriptomic data across different conditions, technologies, and species
inferredcites →https://doi.org/10.1038/nbt.4314openalex-snapshot
Dimensionality reduction for visualizing single-cell data using UMAP
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/ncomms8866openalex-snapshot
A draft network of ligand–receptor-mediated multicellular signalling in human
inferredcites →https://doi.org/10.1038/nmeth.4295openalex-snapshot
Testing for differential abundance in mass cytometry data
inferredcites →https://doi.org/10.1038/nmeth.4463openalex-snapshot
SCENIC: single-cell regulatory network inference and clustering
inferredcites →https://doi.org/10.1038/nprot.2006.208openalex-snapshot
High-throughput transgenesis in Xenopus using I-SceI meganuclease
inferredcites →https://doi.org/10.1038/nrg.2016.167openalex-snapshot
Limb development: a paradigm of gene regulation
inferredcites →https://doi.org/10.1038/s41467-018-06614-2openalex-snapshot
Early redox activities modulate Xenopus tail regeneration
inferredcites →https://doi.org/10.1073/pnas.1007725107openalex-snapshot
Wnt/β-catenin signaling is involved in the induction and maintenance of primitive hematopoiesis in the vertebrate embryo
inferredcites →https://doi.org/10.1093/bioinformatics/btp616openalex-snapshot
edgeR : a Bioconductor package for differential expression analysis of digital gene expression data
inferredcites →https://doi.org/10.1101/gad.1540507openalex-snapshot
Advances in signaling in vertebrate regeneration as a prelude to regenerative medicine
inferredcites →https://doi.org/10.1101/pdb.prot100974openalex-snapshot
Rod-Specific Ablation Using the Nitroreductase/Metronidazole System to Investigate Regeneration in Xenopus
inferredcites →https://doi.org/10.1111/j.1440-169x.2007.00981.xopenalex-snapshot
Spinal cord is required for proper regeneration of the tail in Xenopus tadpoles
inferredcites →https://doi.org/10.1126/science.aad0501openalex-snapshot
Dissecting the multicellular ecosystem of metastatic melanoma by single-cell RNA-seq
inferredcites →https://doi.org/10.1146/annurev-genet-120116-024554openalex-snapshot
Regeneration Genetics
inferredcites →https://doi.org/10.1186/1471-213x-11-70openalex-snapshot
Genome-wide analysis of gene expression during Xenopus tropicalis tadpole tail regeneration
inferredcites →https://doi.org/10.1186/s13059-016-0888-1openalex-snapshot
Classification of low quality cells from single-cell RNA-seq data
inferredcites →https://doi.org/10.1242/dev.01155openalex-snapshot
Cell lineage tracing duringXenopustail regeneration
inferredcites →https://doi.org/10.1242/dev.01331openalex-snapshot
Sp8 and Sp9 , two closely related buttonhead -like transcription factors, regulate Fgf8 expression and limb outgrowth in vertebrate embryos
inferredcites →https://doi.org/10.1242/dev.042424openalex-snapshot
BMP signaling induces digit regeneration in neonatal mice
inferredcites →https://doi.org/10.1242/dev.066498openalex-snapshot
pTransgenesis: a cross-species, modular transgenesis resource
inferredcites →https://doi.org/10.1242/dev.142034openalex-snapshot
Early bioelectric activities mediate redox-modulated regeneration
inferredcites →https://doi.org/10.12688/f1000research.9501.1openalex-snapshot
A step-by-step workflow for low-level analysis of single-cell RNA-seq data
inferredcites →https://doi.org/10.12688/f1000research.9501.2openalex-snapshot
A step-by-step workflow for low-level analysis of single-cell RNA-seq data with Bioconductor
inferredcites →https://doi.org/10.21105/joss.00861openalex-snapshot
UMAP: Uniform Manifold Approximation and Projection
inferredcites →https://doi.org/10.48550/arxiv.1802.03426openalex-snapshot
UMAP: Uniform Manifold Approximation and Projection for Dimension Reduction
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.2139/ssrn.4753794openalex-extracted
HDAC Activity Inhibition Alters Histone H4 Acetylation Dynamics Coupled to HDAC Expression and Lipid Mediator 12(S)HETE Biogenesis in Xenopus laevis Tail Regeneration
inferred← citeshttps://doi.org/10.1002/bdr2.1768openalex-snapshot
Cellular and developmental basis of orofacial clefts
inferred← citeshttps://doi.org/10.1002/dvdy.268openalex-snapshot
Tissue disaggregation and isolation of specific cell types from transgenic Xenopus appendages for transcriptional analysis by FACS
inferred← citeshttps://doi.org/10.1002/dvdy.70088openalex-snapshot
Commensal skin bacteria interact with the innate immune system to promote tail regeneration in Xenopus laevis tadpoles
inferred← citeshttps://doi.org/10.1002/dvg.23383openalex-snapshot
A cell type annotation Jamboree—Revival of а communal science forum
inferred← citeshttps://doi.org/10.1002/dvg.23405openalex-snapshot
Xenopus leads the way: Frogs as a pioneering model to understand the human brain
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/10.1007/978-3-319-08831-0_66openalex-snapshot
Basics of Self-Regeneration
inferred← citeshttps://doi.org/10.1007/978-3-319-37076-7_66-1openalex-snapshot
Basics of Self-Regeneration
inferred← citeshttps://doi.org/10.1007/s00018-019-03311-1openalex-snapshot
The vertebrate tail: a gene playground for evolution
inferred← citeshttps://doi.org/10.1007/s00018-021-03760-7openalex-snapshot
Animal regeneration in the era of transcriptomics
inferred← citeshttps://doi.org/10.1007/s00418-026-02538-xopenalex-snapshot
Dexamethasone suppresses the sox3 gene during tail regeneration in the electric black ghost knifefish, Apteronotus albifrons (Linnaeus 1766)
inferred← citeshttps://doi.org/10.1016/j.cdev.2024.203988openalex-snapshot
The evolutionary origin and mechanism of chordate tail regeneration. An ancient tale?
inferred← citeshttps://doi.org/10.1016/j.ceb.2022.102101openalex-snapshot
Mining cell–cell signaling in single-cell transcriptomics atlases
inferred← citeshttps://doi.org/10.1016/j.cell.2025.06.009openalex-snapshot
A clinical road map for single-cell omics
inferred← citeshttps://doi.org/10.1016/j.celrep.2025.116567openalex-snapshot
Cadherins modulate the self-organizing potential of pseudo-embryos
inferred← citeshttps://doi.org/10.1016/j.csbj.2023.12.021openalex-snapshot
scQA: A dual-perspective cell type identification model for single cell transcriptome data
inferred← citeshttps://doi.org/10.1016/j.cub.2019.06.026openalex-snapshot
Development: How Tadpoles ROC Tail Regeneration
inferred← citeshttps://doi.org/10.1016/j.cub.2022.06.040openalex-snapshot
Ets21C sustains a pro-regenerative transcriptional program in blastema cells of Drosophila imaginal discs
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.envpol.2020.115809openalex-snapshot
Xenopus in revealing developmental toxicity and modeling human diseases
inferred← citeshttps://doi.org/10.1016/j.gde.2024.102231openalex-snapshot
Single-cell genomic profiling to study regeneration
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.kint.2022.07.027openalex-snapshot
A comparative study of cellular diversity between the Xenopus pronephric and mouse metanephric nephron
inferred← citeshttps://doi.org/10.1016/j.semcdb.2024.12.005openalex-snapshot
Zebrafish tailfin as an in vivo model for capturing tissue-scale cell dynamics
inferred← citeshttps://doi.org/10.1016/j.stemcr.2022.08.011openalex-snapshot
Single-cell mapping of regenerative and fibrotic healing responses after musculoskeletal injury
inferred← citeshttps://doi.org/10.1016/j.xjidi.2026.100540openalex-snapshot
De Novo Regeneration of Rete Ridges during Cetacean skin 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.2022.08.007openalex-snapshot
Cellular and molecular profiles of larval and adult Xenopus corneal epithelia resolved at the single-cell level
inferred← citeshttps://doi.org/10.1016/j.ydbio.2025.01.015openalex-snapshot
Shh signaling directs dorsal ventral patterning in the regenerating X. tropicalis spinal cord
inferred← citeshttps://doi.org/10.1016/j.yexcr.2020.112316openalex-snapshot
Elucidating the framework for specification and determination of the embryonic retina
inferred← citeshttps://doi.org/10.1038/s41413-021-00184-8openalex-snapshot
On the horizon: Hedgehog signaling to heal broken bones
inferred← citeshttps://doi.org/10.1038/s41467-021-25960-2openalex-snapshot
Confronting false discoveries in single-cell differential expression
inferred← citeshttps://doi.org/10.1038/s41467-022-30412-6openalex-snapshot
The planarian wound epidermis gene equinox is required for blastema formation in regeneration
inferred← citeshttps://doi.org/10.1038/s41467-022-31949-2openalex-snapshot
Cell landscape of larval and adult Xenopus laevis at single-cell resolution
inferred← citeshttps://doi.org/10.1038/s41467-023-35937-yopenalex-snapshot
Wnt/β-catenin signalling is required for pole-specific chromatin remodeling during planarian regeneration
inferred← citeshttps://doi.org/10.1038/s41467-026-68538-6openalex-snapshot
Ependymoglial cells are critical for cortex regeneration in axolotls
inferred← citeshttps://doi.org/10.1038/s41467-026-75273-5openalex-snapshot
Spinal cord regeneration deploys cell-type specific developmental and non-developmental strategies to restore neuron diversity
inferred← citeshttps://doi.org/10.1038/s41467-026-76555-8openalex-snapshot
A flexible repertoire of wound closure strategies precedes whole-body regeneration
inferred← citeshttps://doi.org/10.1038/s41536-021-00134-2openalex-snapshot
Regenerative medicine meets mathematical modelling: developing symbiotic relationships
inferred← citeshttps://doi.org/10.1038/s41536-021-00179-3openalex-snapshot
Analysis of the early response to spinal cord injury identified a key role for mTORC1 signaling in the activation of neural stem progenitor cells
inferred← citeshttps://doi.org/10.1038/s41536-022-00225-8openalex-snapshot
A murine model of large-scale bone regeneration reveals a selective requirement for Sonic Hedgehog
inferred← citeshttps://doi.org/10.1038/s41567-023-02103-6openalex-snapshot
Mechanical waves identify the amputation position during wound healing in the amputated zebrafish tailfin
inferred← citeshttps://doi.org/10.1038/s41576-020-0239-7openalex-snapshot
Gene regulatory programmes of tissue regeneration
inferred← citeshttps://doi.org/10.1038/s41587-020-0605-1openalex-snapshot
Cell type prioritization in single-cell data
inferred← citeshttps://doi.org/10.1038/s41588-024-01996-0openalex-snapshot
Analysis of multi-condition single-cell data with latent embedding multivariate regression
inferred← citeshttps://doi.org/10.1038/s41598-022-05954-wopenalex-snapshot
Xenopus laevis il11ra.L is an experimentally proven interleukin-11 receptor component that is required for tadpole tail regeneration
inferred← citeshttps://doi.org/10.1038/s41598-022-26434-1openalex-snapshot
Correspondence analysis for dimension reduction, batch integration, and visualization of single-cell RNA-seq data
inferred← citeshttps://doi.org/10.1038/s41598-024-54522-xopenalex-snapshot
Multi-omics resources for the Australian southern stuttering frog (Mixophyes australis) reveal assorted antimicrobial peptides
inferred← citeshttps://doi.org/10.1038/s44222-023-00132-7openalex-snapshot
Single-cell transcriptomics in tissue engineering and regenerative medicine
inferred← citeshttps://doi.org/10.1073/pnas.2200342119openalex-snapshot
Voltage-gated sodium channel scn8a is required for innervation and regeneration of amputated adult zebrafish fins
inferred← citeshttps://doi.org/10.1073/pnas.2414865121openalex-snapshot
CTCF-dependent insulation of Hoxb13 and the heterochronic control of tail length
inferred← citeshttps://doi.org/10.1073/pnas.2504410122openalex-snapshot
Putative muscle stem cells promote Xenopus tail regeneration by modifying macrophage function via c1qtnf3
inferred← citeshttps://doi.org/10.1093/icb/icaf006openalex-snapshot
Investigating the evolution and features of regeneration using cnidarians
inferred← citeshttps://doi.org/10.1097/shk.0000000000002274openalex-snapshot
SINGLE-CELL TRANSCRIPTOME ANALYSIS IN HEALTH AND DISEASE
inferred← citeshttps://doi.org/10.1098/rsob.210126openalex-snapshot
Appendage regeneration is context dependent at the cellular level
inferred← citeshttps://doi.org/10.1098/rspb.2019.2939openalex-snapshot
Salamander-like tail regeneration in the West African lungfish
inferred← citeshttps://doi.org/10.1101/2020.08.06.240036openalex-snapshot
Single-cell analyses of the corneal epithelium: Unique cell types and gene expression profiles
inferred← citeshttps://doi.org/10.1101/2021.06.29.450229openalex-snapshot
Distinct epicardial gene regulatory programmes drive development and regeneration of the zebrafish heart
inferred← citeshttps://doi.org/10.1101/2021.07.08.451678openalex-snapshot
Critical genetic program for Drosophila imaginal disc regeneration revealed by single-cell analysis
inferred← citeshttps://doi.org/10.1101/2022.05.17.492329openalex-snapshot
Integrative analysis of Hydra head regeneration reveals actions of conserved signaling pathways and transposable elements
inferred← citeshttps://doi.org/10.1101/2022.05.20.492823openalex-snapshot
The rise of sparser single-cell RNAseq datasets; consequences and opportunities
inferred← citeshttps://doi.org/10.1101/2022.06.10.495631openalex-snapshot
Skeletal muscle lineage is dispensable for appendage regeneration in axolotl
inferred← citeshttps://doi.org/10.1101/2023.03.25.534232openalex-snapshot
Clustering scRNA-seq data via qualitative and quantitative analysis
inferred← citeshttps://doi.org/10.1101/2023.03.30.534908openalex-snapshot
Characterization of regeneration initiating cells during Xenopus laevis tail regeneration
inferred← citeshttps://doi.org/10.1101/2023.11.22.568291openalex-snapshot
Cadherins modulate the self-organizing potential of gastruloids
inferred← citeshttps://doi.org/10.1101/2024.07.19.604337openalex-snapshot
Axis reset is rate limiting for onset of whole-body regenerative abilities during planarian development
inferred← citeshttps://doi.org/10.1101/2025.02.03.636261openalex-snapshot
A dynamic repertoire of wound closure strategies precedes whole-body regeneration
inferred← citeshttps://doi.org/10.1101/2025.09.20.677431openalex-snapshot
Piezo1–Yap1 signalling translates tissue mechanics into regenerative cell states
inferred← citeshttps://doi.org/10.1101/2025.10.09.680955openalex-snapshot
Innovations in spinal cord cell type heterogeneity across vertebrate evolution
inferred← citeshttps://doi.org/10.1101/cshperspect.a040931openalex-snapshot
The Diverse Manifestations of Regeneration and Why We Need to Study Them
inferred← citeshttps://doi.org/10.1101/pdb.top100966openalex-snapshot
Xenopus , a Model to Study Wound Healing and Regeneration: Experimental Approaches
inferred← citeshttps://doi.org/10.1101/pdb.top106625openalex-snapshot
Experimental Platform Using the Amphibian Xenopus laevis for Research in Fundamental and Medical Immunology
inferred← citeshttps://doi.org/10.1109/bigdata50022.2020.9378126openalex-snapshot
Approximate kNN Classification for Biomedical Data
inferred← citeshttps://doi.org/10.1109/cec60901.2024.10612207openalex-snapshot
Hyperdimensional Computing Approaches in Single Cell RNA Sequencing Classification
inferred← citeshttps://doi.org/10.1109/lra.2023.3333690openalex-snapshot
A Robotic Surgery Platform for Automated Tissue Micromanipulation in Zebrafish Embryos
inferred← citeshttps://doi.org/10.1111/dgd.12635openalex-snapshot
Cell type‐specific transcriptome analysis unveils secreted signaling molecule genes expressed in apical epithelial cap during appendage regeneration
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/dgd.12797openalex-snapshot
Effective enrichment of stem cells in regenerating Xenopus laevis tadpole tails using the side population method
inferred← citeshttps://doi.org/10.1111/ede.12332openalex-snapshot
von Willebrand factor D and EGF domains is an evolutionarily conserved and required feature of blastemas capable of multitissue appendage regeneration
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/10.1111/wrr.13003openalex-snapshot
Manipulating the microbiome alters regenerative outcomes in Xenopus laevis tadpoles via lipopolysaccharide signalling
inferred← citeshttps://doi.org/10.1111/wrr.13057openalex-snapshot
Chromatin accessibility analysis reveals distinct functions for HDAC and EZH2 activities in early appendage regeneration
inferred← citeshttps://doi.org/10.1126/sciadv.add5745openalex-snapshot
A single-cell, time-resolved profiling of Xenopus mucociliary epithelium reveals nonhierarchical model of development
inferred← citeshttps://doi.org/10.1126/sciadv.ady7682openalex-snapshot
Specialized signaling centers direct cell fate and spatial organization in a mesodermal organoid model
inferred← citeshttps://doi.org/10.1126/sciadv.aeb8034openalex-snapshot
Deciphering the ancestral mechanisms of neural regeneration through single-cell analyses of jellyfish rhopalium repair
inferred← citeshttps://doi.org/10.1152/ajpcell.00403.2022openalex-snapshot
Regeneration enhancers: a field in development
inferred← citeshttps://doi.org/10.1186/s12864-023-09205-8openalex-snapshot
Unravelling the limb regeneration mechanisms of Polypedates maculatus, a sub-tropical frog, by transcriptomics
inferred← citeshttps://doi.org/10.1186/s12864-024-11175-4openalex-snapshot
Thyroid hormone receptor- and stage-dependent transcriptome changes affect the initial period of Xenopus tropicalis tail regeneration
inferred← citeshttps://doi.org/10.1186/s13059-023-02949-2openalex-snapshot
Modeling group heteroscedasticity in single-cell RNA-seq pseudo-bulk data
inferred← citeshttps://doi.org/10.1186/s13059-024-03396-3openalex-snapshot
Characterization of regeneration initiating cells during Xenopus laevis tail regeneration
inferred← citeshttps://doi.org/10.1186/s13059-025-03542-5openalex-snapshot
Chromosome-level genome assembly and single-cell analysis unveil molecular mechanisms of arm regeneration in the ophiuroid Ophiura sarsii vadicola
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/s13578-023-00989-6openalex-snapshot
Thyroid hormone receptor knockout prevents the loss of Xenopus tail regeneration capacity at metamorphic climax
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.180844openalex-snapshot
Model systems for regeneration: Xenopus
inferred← citeshttps://doi.org/10.1242/dev.181016openalex-snapshot
Can laboratory model systems instruct human limb 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.199158openalex-snapshot
Secreted inhibitors drive the loss of regeneration competence in Xenopus limbs
inferred← citeshttps://doi.org/10.1242/dev.202541openalex-snapshot
Mechanisms of regeneration: to what extent do they recapitulate development?
inferred← citeshttps://doi.org/10.1242/dev.204632openalex-snapshot
A threshold level of JNK activates damage-responsive enhancers via JAK/STAT to promote tissue regeneration
inferred← citeshttps://doi.org/10.1242/dmm.050754openalex-snapshot
Modelling human genetic disorders in Xenopus tropicalis
inferred← citeshttps://doi.org/10.1371/journal.pbio.3003583openalex-snapshot
Foxi1 regulates multipotent mucociliary progenitors and ionocyte specification through transcriptional and epigenetic mechanisms
inferred← citeshttps://doi.org/10.15252/embr.202050932openalex-snapshot
Foxm1 regulates neural progenitor fate during spinal cord regeneration
inferred← citeshttps://doi.org/10.21037/sci-2019-044openalex-snapshot
Xvent-2 expression in regenerating Xenopus tails
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/10.26881/tutg.2025.1.04openalex-snapshot
Star Trek: The Next Regeneration – czyli o tym, jak żaby nie są w tych tematach zielone
inferred← citeshttps://doi.org/10.30802/aalas-cm-20-000069openalex-snapshot
Axial Skeletal Malformations in Genetically Modified Xenopus laevis and Xenopus tropicalis
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.2021.738940openalex-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/fcell.2021.743421openalex-snapshot
Characterization of the Zebrafish Cell Landscape at Single-Cell Resolution
inferred← citeshttps://doi.org/10.3389/fcell.2024.1487644openalex-snapshot
An improved method for whole-mount in situ hybridization in regenerating tails of Xenopus laevis tadpoles
inferred← citeshttps://doi.org/10.3389/fgene.2022.1036641openalex-snapshot
Muscles are barely required for the patterning and cell dynamics in axolotl limb regeneration
inferred← citeshttps://doi.org/10.3389/fphys.2021.771040openalex-snapshot
Tissues and Cell Types of Appendage Regeneration: A Detailed Look at the Wound Epidermis and Its Specialized Forms
inferred← citeshttps://doi.org/10.3390/biology12060890openalex-snapshot
Xenopus laevis (Daudin, 1802) as a Model Organism for Bioscience: A Historic Review and Perspective
inferred← citeshttps://doi.org/10.3390/fishes4040051openalex-snapshot
No Correlation between Endo- and Exoskeletal Regenerative Capacities in Teleost Species
inferred← citeshttps://doi.org/10.3390/ijms23031464openalex-snapshot
MAPK/ERK Pathway as a Central Regulator in Vertebrate Organ Regeneration
inferred← citeshttps://doi.org/10.3390/ijms241813938openalex-snapshot
The Promising Role of a Zebrafish Model Employed in Neural Regeneration Following a Spinal Cord Injury
inferred← citeshttps://doi.org/10.3390/ijms252111597openalex-snapshot
Tail Tales: What We Have Learned About Regeneration from Xenopus Laevis Tadpoles
inferred← citeshttps://doi.org/10.3390/info11110502openalex-snapshot
Ensemble Classification through Random Projections for Single-Cell RNA-Seq Data
inferred← citeshttps://doi.org/10.3390/jdb10040044openalex-snapshot
Quantitative Experimental Embryology: A Modern Classical Approach
inferred← citeshttps://doi.org/10.3390/jdb8040031openalex-snapshot
Transcriptional Trajectories in Mouse Limb Buds Reveal the Transition from Anterior-Posterior to Proximal-Distal Patterning at Early Limb Bud Stage
inferred← citeshttps://doi.org/10.3390/life11070716openalex-snapshot
Single-Cell Transcriptome Profiling Simulation Reveals the Impact of Sequencing Parameters and Algorithms on Clustering
inferred← citeshttps://doi.org/10.3390/life14050594openalex-snapshot
Tail and Spinal Cord Regeneration in Urodelean Amphibians
inferred← citeshttps://doi.org/10.4062/biomolther.2024.096openalex-snapshot
An Amphibians-Derived Protein Provides Novel Biotherapeutics for Various Wounds Treatment
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/10.6084/m9.figshare.26570968openalex-snapshot
Additional file 1 of Thyroid hormone receptor knockout prevents the loss of Xenopus tail regeneration capacity at metamorphic climax
inferred← citeshttps://doi.org/10.64898/2026.07.27.740807openalex-snapshot
Single-cell foundation modeling with species-native protein tokens links regenerative competence across frog and mouse
inferred← citeshttps://doi.org/10.64898/2026.09.01.748728openalex-snapshot
VLCFA-mediated inter-cell layer communication controls cellular pluripotency in Arabidopsis callus
inferred← citeshttps://doi.org/10.64898/2026.09.20.752982openalex-snapshot
A blastema in sea star larvae integrates wound signaling to drive regeneration-specific and developmental gene expression patterns
inferred← citeshttps://doi.org/10.70675/16c4a6f1z6fa5z4443za73azacfdf9be258aopenalex-snapshot
Exploring cell diversity and fidelity in crustacean limb regeneration using single-nucleus RNA sequencing
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/10.7554/elife.106410.3openalex-snapshot
Single-cell transcriptomics of X-ray irradiated Drosophila wing discs reveals heterogeneity related to cell-cycle status and cell location
inferred← citeshttps://doi.org/10.7554/elife.45976openalex-snapshot
Distinct inflammatory and wound healing responses to complex caudal fin injuries of larval zebrafish
inferred← citeshttps://doi.org/10.7554/elife.52648openalex-snapshot
Chromatin accessibility dynamics and single cell RNA-Seq reveal new regulators of regeneration in neural progenitors
inferred← citeshttps://doi.org/10.7554/elife.61804openalex-snapshot
Non-canonical Hedgehog signaling regulates spinal cord and muscle regeneration in Xenopus laevis larvae
inferred← citeshttps://doi.org/10.7554/elife.98277openalex-snapshot
Marcks and Marcks-like 1 proteins promote spinal cord development and regeneration in Xenopus
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