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β-Catenin Defines Head Versus Tail Identity During Planarian Regeneration and Homeostasis
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1006/dbio.1995.0009openalex-snapshot
β-Catenin Has Wnt-like Activity and Mimics the Nieuwkoop Signaling Center inXenopusDorsal–Ventral Patterning
inferredcites →https://doi.org/10.1016/0925-4773(96)00546-1openalex-snapshot
β-catenin translocation into nuclei demarcates the dorsalizing centers in frog and fish embryos
inferredcites →https://doi.org/10.1016/j.cell.2006.12.037openalex-snapshot
Microtubule Plus-End-Tracking Proteins Target Gap Junctions Directly from the Cell Interior to Adherens Junctions
inferredcites →https://doi.org/10.1016/j.cub.2005.12.037openalex-snapshot
Animal Cognition: How Archer Fish Learn to Down Rapidly Moving Targets
inferredcites →https://doi.org/10.1016/j.cub.2006.04.019openalex-snapshot
Transcription under the Control of Nuclear Arm/β-Catenin
inferredcites →https://doi.org/10.1016/j.devcel.2007.05.002openalex-snapshot
β-Catenin Asymmetries after All Animal/Vegetal- Oriented Cell Divisions in Platynereis dumerilii Embryos Mediate Binary Cell-Fate Specification
inferredcites →https://doi.org/10.1016/j.ydbio.2005.09.002openalex-snapshot
Characterization of innexin gene expression and functional roles of gap-junctional communication in planarian regeneration
inferredcites →https://doi.org/10.1016/j.ydbio.2007.03.014openalex-snapshot
Wnt/β-catenin signaling has an essential role in the initiation of limb regeneration
inferredcites →https://doi.org/10.1016/j.ydbio.2007.04.010openalex-snapshot
Wnt signaling is required for antero-posterior patterning of the planarian brain
inferredcites →https://doi.org/10.1016/s0092-8674(00)80531-0openalex-snapshot
Wnt Signaling and an APC-Related Gene Specify Endoderm in Early C. elegans Embryos
inferredcites →https://doi.org/10.1016/s0092-8674(00)80784-9openalex-snapshot
WRM-1 Activates the LIT-1 Protein Kinase to Transduce Anterior/Posterior Polarity Signals in C. elegans
inferredcites →https://doi.org/10.1038/nature02113openalex-snapshot
An ancient role for nuclear β-catenin in the evolution of axial polarity and germ layer segregation
inferredcites →https://doi.org/10.1074/jbc.r600015200openalex-snapshot
Wnt Signaling: Multiple Pathways, Multiple Receptors, and Multiple Transcription Factors
inferredcites →https://doi.org/10.1083/jcb.134.5.1283openalex-snapshot
An in vivo structure-function study of armadillo, the beta-catenin homologue, reveals both separate and overlapping regions of the protein required for cell adhesion and for wingless signaling.
inferredcites →https://doi.org/10.1083/jcb.136.5.1123openalex-snapshot
Establishment of the Dorso-ventral Axis in Xenopus Embryos Is Presaged by Early Asymmetries in β-Catenin That Are Modulated by the Wnt Signaling Pathway
inferredcites →https://doi.org/10.1101/gad.1424006openalex-snapshot
Wnt signaling: is the party in the nucleus?
inferredcites →https://doi.org/10.1101/gad.317604openalex-snapshot
Essential role of BCL9-2 in the switch between β-catenin's adhesive and transcriptional functions
inferredcites →https://doi.org/10.1126/stke.3612006pe48openalex-snapshot
The Emergence of Pattern in Embryogenesis: Regulation of β-Catenin Localization During Early Sea Urchin Development
inferredcites →https://doi.org/10.1146/annurev.cellbio.20.010403.095114openalex-snapshot
FUNDAMENTALS OF PLANARIAN REGENERATION
inferredcites →https://doi.org/10.1146/annurev.cellbio.20.010403.113126openalex-snapshot
THE WNT SIGNALING PATHWAY IN DEVELOPMENT AND DISEASE
inferredcites →https://doi.org/10.1242/dev.001123openalex-snapshot
Distinct Wnt signaling pathways have opposing roles in appendage regeneration
inferredcites →https://doi.org/10.1242/dev.02068openalex-snapshot
The developmental biology of Dishevelled: an enigmatic protein governing cell fate and cell polarity
inferredcites →https://doi.org/10.1242/dev.126.2.345openalex-snapshot
Nuclear β-catenin is required to specify vegetal cell fates in the sea urchin embryo
inferredcites →https://doi.org/10.2108/jsz.17.375openalex-snapshot
Organization and Regeneration Ability of Spontaneous Supernumerary Eyes in Planarians —Eye Regeneration Field and Pathway Selection by Optic Nerves—
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.3275291openalex-extracted
Emergence of Bilateral Symmetry from Chiral Components in the Planarian Epidermis
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Regeneration in Invertebrates: Model Systems
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Lumbriculus variegatusand the Need for Speed: A Model System for Rapid Escape, Regeneration and Asexual Reproduction
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Restoring Tissue Homeostasis
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Beta‐catenin and axis formation in planarians
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HydraRegeneration: Closing the Loop with Mechanical Processes in Morphogenesis
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Rücken‐WNT für die Primärachse der Tiere
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Gene nomenclature guidelines for the planarian Schmidtea mediterranea
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Stretching the limits: Stem cells in regeneration science
inferred← citeshttps://doi.org/10.1002/dvdy.21849openalex-snapshot
Formaldehyde‐based whole‐mount in situ hybridization method for planarians
inferred← citeshttps://doi.org/10.1002/dvdy.21928openalex-snapshot
Flow cytometry methods for the study of cell‐cycle parameters of planarian stem cells
inferred← citeshttps://doi.org/10.1002/dvdy.22774openalex-snapshot
Induction of canonical Wnt signaling by alsterpaullone is sufficient for oral tissue fate during regeneration and embryogenesis in Nematostella vectensis
inferred← citeshttps://doi.org/10.1002/dvdy.23775openalex-snapshot
A Lissencephaly‐1 homologue is essential for mitotic progression in the planarian Schmidtea mediterranea
inferred← citeshttps://doi.org/10.1002/dvdy.23950openalex-snapshot
RNA interference by feeding in vitro–synthesized double‐stranded RNA to planarians: Methodology and dynamics
inferred← citeshttps://doi.org/10.1002/dvdy.400openalex-snapshot
Defined diets for freshwater planarians
inferred← citeshttps://doi.org/10.1002/dvdy.712openalex-snapshot
Muscular remodeling and anteroposterior patterning during tapeworm segmentation
inferred← citeshttps://doi.org/10.1002/jcb.29905openalex-snapshot
TBX2/3 is required for regeneration of dorsal‐ventral and medial‐lateral polarity in planarians
inferred← citeshttps://doi.org/10.1002/jez.b.23046openalex-snapshot
Porcupine/Wntless‐dependent trafficking of the conserved WntA ligand in butterflies
inferred← citeshttps://doi.org/10.1002/mrd.22203openalex-snapshot
Triangle Consortium for Reproductive Biology 22nd Annual Meeting
inferred← citeshttps://doi.org/10.1002/pmic.201200397openalex-snapshot
Understanding regeneration through proteomics
inferred← citeshttps://doi.org/10.1002/reg2.54openalex-snapshot
Physiological controls of large‐scale patterning in planarian regeneration: a molecular and computational perspective on growth and form
inferred← citeshttps://doi.org/10.1002/reg2.56openalex-snapshot
Go ahead, grow a head! A planarian's guide to anterior regeneration
inferred← citeshttps://doi.org/10.1002/reg2.79openalex-snapshot
Planarian regeneration in space: Persistent anatomical, behavioral, and bacteriological changes induced by space travel
inferred← citeshttps://doi.org/10.1002/reg2.90openalex-snapshot
Bipolarity in planarians is not induced by space travel
inferred← citeshttps://doi.org/10.1002/wdev.266openalex-snapshot
Nervous system development and regeneration in freshwater planarians
inferred← citeshttps://doi.org/10.1002/wdev.82openalex-snapshot
The history and enduring contributions of planarians to the study of animal regeneration
inferred← citeshttps://doi.org/10.1007/978-1-4939-6424-6_23openalex-snapshot
Analyzing pERK Activation During Planarian Regeneration
inferred← citeshttps://doi.org/10.1007/978-1-4939-7802-1_17openalex-snapshot
Systemic RNA Interference in Planarians by Feeding of dsRNA Containing Bacteria
inferred← citeshttps://doi.org/10.1007/978-1-4939-7802-1_2openalex-snapshot
Stem Cells, Patterning and Regeneration in Planarians: Self-Organization at the Organismal Scale
inferred← citeshttps://doi.org/10.1007/978-1-4939-7802-1_3openalex-snapshot
The Ecology of Freshwater Planarians
inferred← citeshttps://doi.org/10.1007/978-1-4939-7802-1_4openalex-snapshot
Planarians and the History of Animal Regeneration: Paradigm Shifts and Key Concepts in Biology
inferred← citeshttps://doi.org/10.1007/978-1-61779-246-5_16openalex-snapshot
Zebrafish as a Model to Study Stem Cells in Development, Disease, and Cancer
inferred← citeshttps://doi.org/10.1007/978-3-319-33921-4_24openalex-snapshot
Computing a Worm: Reverse-Engineering Planarian Regeneration
inferred← citeshttps://doi.org/10.1007/978-3-662-56179-9_10openalex-snapshot
Dedifferentiation and Organ Regeneration
inferred← citeshttps://doi.org/10.1007/978-3-7091-1868-9_3openalex-snapshot
Hexapoda: Comparative Aspects of Later Embryogenesis and Metamorphosis
inferred← citeshttps://doi.org/10.1007/978-3-7091-1871-9_4openalex-snapshot
Regeneration and Growth as Modes of Adult Development: The Platyhelminthes as a Case Study
inferred← citeshttps://doi.org/10.1007/978-4-431-54634-4_6openalex-snapshot
Determination of Stem Cell Fate in Planarian Regeneration
inferred← citeshttps://doi.org/10.1007/978-4-431-56469-0_4openalex-snapshot
Functional Specification of a Primitive Bilaterian Brain in Planarians
inferred← citeshttps://doi.org/10.1007/978-4-431-56609-0_33openalex-snapshot
Postembryonic Axis Formation in Planarians
inferred← citeshttps://doi.org/10.1007/978-90-481-2767-2_2openalex-snapshot
Putative Stem Cell Origins in Solitary Tunicates
inferred← citeshttps://doi.org/10.1007/s00285-026-02459-2openalex-snapshot
A hybrid mathematical framework for morphogenesis and regeneration
inferred← citeshttps://doi.org/10.1007/s00427-012-0426-4openalex-snapshot
Stem cell systems and regeneration in planaria
inferred← citeshttps://doi.org/10.1007/s00427-015-0494-3openalex-snapshot
Protein expression profiling in head fragments during planarian regeneration after amputation
inferred← citeshttps://doi.org/10.1007/s00427-019-00632-wopenalex-snapshot
Divergent Axin and GSK-3 paralogs in the beta-catenin destruction complexes of tapeworms
inferred← citeshttps://doi.org/10.1007/s00427-021-00681-0openalex-snapshot
Effects of GSK3β inhibition in the regeneration of Syllis malaquini (Syllidae, Annelida)
inferred← citeshttps://doi.org/10.1007/s00427-025-00726-8openalex-snapshot
Silencing of β-catenin1 blocks tail regeneration, but does not induce head regeneration in the flatworm Macrostomum lignano
inferred← citeshttps://doi.org/10.1007/s00441-019-03094-8openalex-snapshot
No head regeneration here: regeneration capacity and stem cell dynamics of Theama mediterranea (Polycladida, Platyhelminthes)
inferred← citeshttps://doi.org/10.1007/s10495-009-0445-4openalex-snapshot
Autophagy and apoptosis in planarians
inferred← citeshttps://doi.org/10.1007/s10739-009-9203-2openalex-snapshot
Regeneration: Thomas Hunt Morgan’s Window into Development
inferred← citeshttps://doi.org/10.1007/s12010-016-2342-yopenalex-snapshot
Proteomic Analysis Reveals the Contribution of TGFβ/Smad4 Signaling Pathway to Cell Differentiation During Planarian Tail Regeneration
inferred← citeshttps://doi.org/10.1007/s12035-023-03478-6openalex-snapshot
DjFARP Contributes to the Regeneration and Maintenance of the Brain through Activation of DjRac1 in Dugesia japonica
inferred← citeshttps://doi.org/10.1007/s12217-012-9317-6openalex-snapshot
Space Research Program on Planarian Schmidtea Mediterranea’s Establishment of the Anterior-Posterior Axis in Altered Gravity Conditions
inferred← citeshttps://doi.org/10.1016/b978-0-12-385975-4.00012-7openalex-snapshot
Signaling Pathways and Axis Formation in the Lower Metazoa
inferred← citeshttps://doi.org/10.1016/b978-0-12-391498-9.00011-5openalex-snapshot
Mathematical Modeling of Regenerative Processes
inferred← citeshttps://doi.org/10.1016/b978-0-323-85652-2.00015-4openalex-snapshot
Nutrients seminal role in the development and epigenetic reprogramming during the first 1000 days of life
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How Somatic Adult Tissues Develop Organizer Activity
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Molecular insights into deuterostome evolution from hemichordate developmental biology
inferred← citeshttps://doi.org/10.1016/bs.ctdb.2023.01.003openalex-snapshot
From injury to patterning—MAPKs and Wnt signaling in Hydra
inferred← citeshttps://doi.org/10.1016/bs.ctdb.2023.01.007openalex-snapshot
Wnt signaling in whole-body regeneration
inferred← citeshttps://doi.org/10.1016/j.aanat.2019.07.001openalex-snapshot
Wnt/β-catenin signaling was activated in supporting cells during exposure of the zebrafish lateral line to cisplatin
inferred← citeshttps://doi.org/10.1016/j.bbrc.2020.10.020openalex-snapshot
A novel RhoA-related gene, DjRhoA, contributes to the regeneration of brain and intestine in planarian Dugesia japonica
inferred← citeshttps://doi.org/10.1016/j.bbrc.2022.12.008openalex-snapshot
Actin restricts cell proliferation and promotes differentiation during planarian regeneration
inferred← citeshttps://doi.org/10.1016/j.bbrc.2025.151824openalex-snapshot
The stress-associated small heat shock protein affects stem cell proliferation, differentiation, and tissue-specific transcriptional networks during regeneration in Dugesia japonica
inferred← citeshttps://doi.org/10.1016/j.bpj.2017.04.011openalex-snapshot
Long-Term, Stochastic Editing of Regenerative Anatomy via Targeting Endogenous Bioelectric Gradients
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The Role of Early Bioelectric Signals in the Regeneration of Planarian Anterior/Posterior Polarity
inferred← citeshttps://doi.org/10.1016/j.cdev.2023.203846openalex-snapshot
The Hydra stem cell system – Revisited
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Evo-Devo: Variations on Ancestral Themes
inferred← citeshttps://doi.org/10.1016/j.cell.2008.01.040openalex-snapshot
Slicing across Kingdoms: Regeneration in Plants and Animals
inferred← citeshttps://doi.org/10.1016/j.cell.2009.11.035openalex-snapshot
Wnt Signaling and the Polarity of the Primary Body Axis
inferred← citeshttps://doi.org/10.1016/j.cell.2018.09.021openalex-snapshot
The Cellular and Molecular Basis for Planarian Regeneration
inferred← citeshttps://doi.org/10.1016/j.celrep.2013.07.022openalex-snapshot
Muscle Cells Provide Instructions for Planarian Regeneration
inferred← citeshttps://doi.org/10.1016/j.celrep.2014.12.018openalex-snapshot
β-Catenin-Dependent Control of Positional Information along the AP Body Axis in Planarians Involves a Teashirt Family Member
inferred← citeshttps://doi.org/10.1016/j.celrep.2018.11.004openalex-snapshot
Cellular and Molecular Responses Unique to Major Injury Are Dispensable for Planarian Regeneration
inferred← citeshttps://doi.org/10.1016/j.celrep.2020.108098openalex-snapshot
A Regulatory Program for Initiation of Wnt Signaling during Posterior Regeneration
inferred← citeshttps://doi.org/10.1016/j.celrep.2021.108903openalex-snapshot
The DEAD-box helicase DDX56 is a conserved stemness regulator in normal and cancer stem cells
inferred← citeshttps://doi.org/10.1016/j.celrep.2024.114305openalex-snapshot
Epidermal turnover in the planarian Schmidtea mediterranea involves basal cell extrusion and intestinal digestion
inferred← citeshttps://doi.org/10.1016/j.celrep.2024.114892openalex-snapshot
A genetic and microscopy toolkit for manipulating and monitoring regeneration in Macrostomum lignano
inferred← citeshttps://doi.org/10.1016/j.celrep.2025.116551openalex-snapshot
Multi-omics analyses reveal DjTcf4 critical for proper timing of differentiation in planarian regeneration
inferred← citeshttps://doi.org/10.1016/j.chembiol.2010.11.012openalex-snapshot
A Chemical Genetics Approach Reveals H,K-ATPase-Mediated Membrane Voltage Is Required for Planarian Head Regeneration
inferred← citeshttps://doi.org/10.1016/j.cois.2022.100877openalex-snapshot
Evolution and loss of ß-catenin and TCF-dependent axis specification in insects
inferred← citeshttps://doi.org/10.1016/j.ctrv.2016.06.009openalex-snapshot
Wnt/β-catenin signaling in melanoma: Preclinical rationale and novel therapeutic insights
inferred← citeshttps://doi.org/10.1016/j.cub.2011.01.017openalex-snapshot
A Bmp/Admp Regulatory Circuit Controls Maintenance and Regeneration of Dorsal-Ventral Polarity in Planarians
inferred← citeshttps://doi.org/10.1016/j.cub.2019.11.068openalex-snapshot
STRIPAK Limits Stem Cell Differentiation of a WNT Signaling Center to Control Planarian Axis Scaling
inferred← citeshttps://doi.org/10.1016/j.cub.2022.10.071openalex-snapshot
A Wnt11 and Dishevelled signaling pathway acts prior to injury to control wound polarization for the onset of planarian regeneration
inferred← citeshttps://doi.org/10.1016/j.cub.2025.03.065openalex-snapshot
Developmental onset of planarian whole-body regeneration depends on axis reset
inferred← citeshttps://doi.org/10.1016/j.cytogfr.2009.10.017openalex-snapshot
Integration of BMP and Wnt signaling via vertebrate Smad1/5/8 and Drosophila Mad
inferred← citeshttps://doi.org/10.1016/j.devcel.2009.04.015openalex-snapshot
Regenerative Growth in Drosophila Imaginal Discs Is Regulated by Wingless and Myc
inferred← citeshttps://doi.org/10.1016/j.devcel.2011.06.016openalex-snapshot
The Cellular Basis for Animal Regeneration
inferred← citeshttps://doi.org/10.1016/j.devcel.2012.09.008openalex-snapshot
An RNAi Screen Reveals Intestinal Regulators of Branching Morphogenesis, Differentiation, and Stem Cell Proliferation in Planarians
inferred← citeshttps://doi.org/10.1016/j.devcel.2016.07.012openalex-snapshot
Egf Signaling Directs Neoblast Repopulation by Regulating Asymmetric Cell Division in Planarians
inferred← citeshttps://doi.org/10.1016/j.devcel.2016.08.011openalex-snapshot
Generating Cellular Diversity and Spatial Form: Wnt Signaling and the Evolution of Multicellular Animals
inferred← citeshttps://doi.org/10.1016/j.devcel.2016.12.024openalex-snapshot
Antagonistic Self-Organizing Patterning Systems Control Maintenance and Regeneration of the Anteroposterior Axis in Planarians
inferred← citeshttps://doi.org/10.1016/j.devcel.2018.10.014openalex-snapshot
SoxB1 Activity Regulates Sensory Neuron Regeneration, Maintenance, and Function in Planarians
inferred← citeshttps://doi.org/10.1016/j.devcel.2019.10.021openalex-snapshot
Emergence of a Bilaterally Symmetric Pattern from Chiral Components in the Planarian Epidermis
inferred← citeshttps://doi.org/10.1016/j.devcel.2019.10.022openalex-snapshot
Dynamic Polarization of the Multiciliated Planarian Epidermis between Body Plan Landmarks
inferred← citeshttps://doi.org/10.1016/j.devcel.2025.08.015openalex-snapshot
Proteomics-based multi-omics identifies the roadmap of transcription-translation-protein dynamics in planarian regeneration
inferred← citeshttps://doi.org/10.1016/j.exppara.2016.12.004openalex-snapshot
Evolutionary developmental biology (evo-devo) of cestodes
inferred← citeshttps://doi.org/10.1016/j.gde.2008.06.001openalex-snapshot
Integrating positional information at the level of Smad1/5/8
inferred← citeshttps://doi.org/10.1016/j.gde.2009.05.003openalex-snapshot
Emerging patterns in planarian regeneration
inferred← citeshttps://doi.org/10.1016/j.gde.2015.01.009openalex-snapshot
On the organ trail: insights into organ regeneration in the planarian
inferred← citeshttps://doi.org/10.1016/j.gde.2016.07.009openalex-snapshot
Neoblasts and the evolution of whole-body regeneration
inferred← citeshttps://doi.org/10.1016/j.gep.2008.12.008openalex-snapshot
Expression pattern of the expanded noggin gene family in the planarian Schmidtea mediterranea
inferred← citeshttps://doi.org/10.1016/j.gep.2011.07.004openalex-snapshot
Temporal pattern of the posterior expression of Wingless in Drosophila blastoderm
inferred← citeshttps://doi.org/10.1016/j.gep.2025.119403openalex-snapshot
Wnt/β-catenin signaling pathway regulates the regeneration of the annelid Lumbriculus variegatus
inferred← citeshttps://doi.org/10.1016/j.heliyon.2025.e41833openalex-snapshot
Stem cells (neoblasts) and positional information jointly dominate regeneration in planarians
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2019.01.014openalex-snapshot
Exportin-1 is required for the maintenance of the planarian epidermal lineage
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2020.08.209openalex-snapshot
Cellular and molecular responses-mediated by DjMEK1/2 are necessary for planarian regeneration
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2024.138729openalex-snapshot
FoxO is required for neoblast differentiation during planarian regeneration
inferred← citeshttps://doi.org/10.1016/j.ijpddr.2018.01.001openalex-snapshot
Profiling G protein-coupled receptors of Fasciola hepatica identifies orphan rhodopsins unique to phylum Platyhelminthes
inferred← citeshttps://doi.org/10.1016/j.isci.2026.115640openalex-snapshot
Redox-modulated ERK dynamics support wound-dependent tissue formation during early planarian regeneration
inferred← citeshttps://doi.org/10.1016/j.jid.2020.11.014openalex-snapshot
Regulation of the Wound Healing Response during Aging
inferred← citeshttps://doi.org/10.1016/j.jtbi.2019.110042openalex-snapshot
Cross-inhibition of Turing patterns explains the self-organized regulatory mechanism of planarian fission
inferred← citeshttps://doi.org/10.1016/j.jtbi.2025.112354openalex-snapshot
Emergent stable tissue shapes from the regulatory feedback between morphogens and cell growth
inferred← citeshttps://doi.org/10.1016/j.mod.2011.07.001openalex-snapshot
The role of canonical Wnt signaling in leg regeneration and metamorphosis in the red flour beetle Tribolium castaneum
inferred← citeshttps://doi.org/10.1016/j.mod.2020.103614openalex-snapshot
Regulation of axial and head patterning during planarian regeneration by a commensal bacterium
inferred← citeshttps://doi.org/10.1016/j.pbiomolbio.2018.03.008openalex-snapshot
Bioelectrical control of positional information in development and regeneration: A review of conceptual and computational advances
inferred← citeshttps://doi.org/10.1016/j.semcdb.2018.03.005openalex-snapshot
Planarian stem cell niche, the challenge for understanding tissue regeneration
inferred← citeshttps://doi.org/10.1016/j.semcdb.2018.04.003openalex-snapshot
Planarian regeneration as a model of anatomical homeostasis: Recent progress in biophysical and computational approaches
inferred← citeshttps://doi.org/10.1016/j.semcdb.2018.04.004openalex-snapshot
Regenerative tissue remodeling in planarians – The mysteries of morphallaxis
inferred← citeshttps://doi.org/10.1016/j.semcdb.2018.04.009openalex-snapshot
Post-translational regulation of planarian regeneration
inferred← citeshttps://doi.org/10.1016/j.semcdb.2018.04.014openalex-snapshot
Staying in shape: Planarians as a model for understanding regenerative morphology
inferred← citeshttps://doi.org/10.1016/j.semcdb.2018.05.011openalex-snapshot
The role of the EGFR signaling pathway in stem cell differentiation during planarian regeneration and homeostasis
inferred← citeshttps://doi.org/10.1016/j.semcdb.2021.06.007openalex-snapshot
Composite morphogenesis during embryo development
inferred← citeshttps://doi.org/10.1016/j.semcdb.2025.103632openalex-snapshot
Gradients, waves and nematics: quantitative perspectives on regeneration
inferred← citeshttps://doi.org/10.1016/j.stem.2008.06.013openalex-snapshot
Stem Cells: Time to Check Our Premises
inferred← citeshttps://doi.org/10.1016/j.stem.2008.07.002openalex-snapshot
Molecular Analysis of Stem Cells and Their Descendants during Cell Turnover and Regeneration in the Planarian Schmidtea mediterranea
inferred← citeshttps://doi.org/10.1016/j.stem.2008.08.017openalex-snapshot
Periodic Activation of Wnt/β-Catenin Signaling Enhances Somatic Cell Reprogramming Mediated by Cell Fusion
inferred← citeshttps://doi.org/10.1016/j.tcb.2009.03.007openalex-snapshot
Regeneration, repair and remembering identity: the three Rs of Hox gene expression
inferred← citeshttps://doi.org/10.1016/j.tcb.2011.01.005openalex-snapshot
Planarian stem cells: a simple paradigm for regeneration
inferred← citeshttps://doi.org/10.1016/j.tig.2011.04.004openalex-snapshot
Constitutive gene expression and the specification of tissue identity in adult planarian biology
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.xpro.2025.104214openalex-snapshot
Protocol combining RNA interference and regeneration assays in planarian embryos
inferred← citeshttps://doi.org/10.1016/j.ydbio.2008.02.042openalex-snapshot
β-Catenin is required for the establishment of vegetal embryonic fates in the nemertean, Cerebratulus lacteus
inferred← citeshttps://doi.org/10.1016/j.ydbio.2009.02.004openalex-snapshot
Multiple Wnts are involved in Hydra organizer formation and regeneration
inferred← citeshttps://doi.org/10.1016/j.ydbio.2009.09.015openalex-snapshot
Cell death and tissue remodeling in planarian regeneration
inferred← citeshttps://doi.org/10.1016/j.ydbio.2009.10.033openalex-snapshot
Making heads from tails: Development of a reversed anterior–posterior axis during budding in an acoel
inferred← citeshttps://doi.org/10.1016/j.ydbio.2009.12.012openalex-snapshot
Long-range neural and gap junction protein-mediated cues control polarity during planarian regeneration
inferred← citeshttps://doi.org/10.1016/j.ydbio.2009.12.036openalex-snapshot
β-catenin plays a central role in setting up the head organizer in hydra
inferred← citeshttps://doi.org/10.1016/j.ydbio.2010.01.018openalex-snapshot
Germ layer specification and axial patterning in the embryonic development of the freshwater planarian Schmidtea polychroa
inferred← citeshttps://doi.org/10.1016/j.ydbio.2010.02.037openalex-snapshot
Different requirements for conserved post-transcriptional regulators in planarian regeneration and stem cell maintenance
inferred← citeshttps://doi.org/10.1016/j.ydbio.2010.08.007openalex-snapshot
Expression of secreted Wnt pathway components reveals unexpected complexity of the planarian amputation response
inferred← citeshttps://doi.org/10.1016/j.ydbio.2010.08.034openalex-snapshot
Regeneration and transdetermination: The role of wingless and its regulation
inferred← citeshttps://doi.org/10.1016/j.ydbio.2011.01.032openalex-snapshot
Evolutionary implications of morphogenesis and molecular patterning of the blind gut in the planarian Schmidtea polychroa
inferred← citeshttps://doi.org/10.1016/j.ydbio.2011.03.023openalex-snapshot
EGFR signaling regulates cell proliferation, differentiation and morphogenesis during planarian regeneration and homeostasis
inferred← citeshttps://doi.org/10.1016/j.ydbio.2011.05.669openalex-snapshot
Stem cell-based growth, regeneration, and remodeling of the planarian intestine
inferred← citeshttps://doi.org/10.1016/j.ydbio.2011.07.013openalex-snapshot
Early planarian brain regeneration is independent of blastema polarity mediated by the Wnt/β-catenin pathway
inferred← citeshttps://doi.org/10.1016/j.ydbio.2012.03.010openalex-snapshot
TORC1 is required to balance cell proliferation and cell death in planarians
inferred← citeshttps://doi.org/10.1016/j.ydbio.2013.09.020openalex-snapshot
Planarian MBD2/3 is required for adult stem cell pluripotency independently of DNA methylation
inferred← citeshttps://doi.org/10.1016/j.ydbio.2014.03.016openalex-snapshot
Stem cell-dependent formation of a functional anterior regeneration pole in planarians requires Zic and Forkhead transcription factors
inferred← citeshttps://doi.org/10.1016/j.ydbio.2015.04.021openalex-snapshot
Identification of HECT E3 ubiquitin ligase family genes involved in stem cell regulation and regeneration in planarians
inferred← citeshttps://doi.org/10.1016/j.ydbio.2017.08.024openalex-snapshot
The planarian TCF/LEF factor Smed-tcf1 is required for the regeneration of dorsal-lateral neuronal subtypes
inferred← citeshttps://doi.org/10.1016/j.ydbio.2017.08.030openalex-snapshot
Cellular, ultrastructural and molecular analyses of epidermal cell development in the planarian Schmidtea mediterranea
inferred← citeshttps://doi.org/10.1016/j.ydbio.2019.04.006openalex-snapshot
Insights into regeneration tool box: An animal model approach
inferred← citeshttps://doi.org/10.1016/j.ydbio.2019.10.005openalex-snapshot
Insights into intestinal regeneration signaling mechanisms
inferred← citeshttps://doi.org/10.1016/j.ydbio.2022.01.007openalex-snapshot
Hif1α and Wnt are required for posterior gene expression during Xenopus tropicalis tail regeneration
inferred← citeshttps://doi.org/10.1016/j.ydbio.2022.04.005openalex-snapshot
The role of cnidarian developmental biology in unraveling axis formation and Wnt signaling
inferred← citeshttps://doi.org/10.1016/j.ydbio.2022.04.011openalex-snapshot
DDX24 is required for muscle fiber organization and the suppression of wound-induced Wnt activity necessary for pole re-establishment during planarian regeneration
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.ydbio.2024.06.021openalex-snapshot
Planarian LDB and SSDP proteins scaffold transcriptional complexes for regeneration and patterning
inferred← citeshttps://doi.org/10.1016/j.ydbio.2025.05.017openalex-snapshot
Wnt/β-catenin signaling promotes posterior axial regeneration in non-regenerative tissue of the annelid Capitella teleta
inferred← citeshttps://doi.org/10.1016/j.ydbio.2026.07.013openalex-snapshot
Axial differences in cellular regeneration responses in the annelid Capitella teleta
inferred← citeshttps://doi.org/10.1016/j.zool.2014.04.001openalex-snapshot
Recent identification of an ERK signal gradient governing planarian regeneration
inferred← citeshttps://doi.org/10.1016/s1673-8527(09)60081-3openalex-snapshot
A small scale expression screen identifies tissue specific markers in the Dugesia japonica strain Pek-1
inferred← citeshttps://doi.org/10.1017/s0022149x22000621openalex-snapshot
Planarians to schistosomes: an overview of flatworm cell-types and regulators
inferred← citeshttps://doi.org/10.1038/d41586-019-02376-zopenalex-snapshot
What makes flatworms go to pieces
inferred← citeshttps://doi.org/10.1038/emboj.2011.418openalex-snapshot
Wnt1/βcatenin injury response activates the epicardium and cardiac fibroblasts to promote cardiac repair
inferred← citeshttps://doi.org/10.1038/nature12359openalex-snapshot
The molecular logic for planarian regeneration along the anterior–posterior axis
inferred← citeshttps://doi.org/10.1038/nature12403openalex-snapshot
Restoration of anterior regeneration in a planarian with limited regenerative ability
inferred← citeshttps://doi.org/10.1038/nature12414openalex-snapshot
Reactivating head regrowth in a regeneration-deficient planarian species
inferred← citeshttps://doi.org/10.1038/nature24660openalex-snapshot
Orthogonal muscle fibres have different instructive roles in planarian regeneration
inferred← citeshttps://doi.org/10.1038/ncb0208-122openalex-snapshot
Heads or tails: can Wnt tell which one is up?
inferred← citeshttps://doi.org/10.1038/nrc2389openalex-snapshot
Wnt signalling and its impact on development and cancer
inferred← citeshttps://doi.org/10.1038/nrg2879openalex-snapshot
Advances in understanding tissue regenerative capacity and mechanisms in animals
inferred← citeshttps://doi.org/10.1038/nrm3999openalex-snapshot
Live to die another way: modes of programmed cell death and the signals emanating from dying cells
inferred← citeshttps://doi.org/10.1038/s41467-017-02338-xopenalex-snapshot
Generic wound signals initiate regeneration in missing-tissue contexts
inferred← citeshttps://doi.org/10.1038/s41467-020-16454-8openalex-snapshot
Genome and single-cell RNA-sequencing of the earthworm Eisenia andrei identifies cellular mechanisms underlying regeneration
inferred← citeshttps://doi.org/10.1038/s41467-021-26986-2openalex-snapshot
Hox genes regulate asexual reproductive behavior and tissue segmentation in adult animals
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/s41467-024-52380-9openalex-snapshot
A comparative analysis of planarian genomes reveals regulatory conservation in the face of rapid structural divergence
inferred← citeshttps://doi.org/10.1038/s41467-025-66299-2openalex-snapshot
Wnt signaling restores evolutionary loss of robust foot regeneration rates in Hydra
inferred← citeshttps://doi.org/10.1038/s41467-026-68656-1openalex-snapshot
RoboA reinforces planarian stem cell fate through FoxA and Anosmin1a
inferred← citeshttps://doi.org/10.1038/s41559-023-02221-7openalex-snapshot
Evolutionary dynamics of whole-body regeneration across planarian flatworms
inferred← citeshttps://doi.org/10.1038/s41576-024-00699-wopenalex-snapshot
The origin and evolution of Wnt signalling
inferred← citeshttps://doi.org/10.1038/s41586-019-1478-7openalex-snapshot
Wnt and TGFβ coordinate growth and patterning to regulate size-dependent behaviour
inferred← citeshttps://doi.org/10.1038/s41598-020-79588-1openalex-snapshot
Reactive oxygen species rescue regeneration after silencing the MAPK–ERK signaling pathway in Schmidtea mediterranea
inferred← citeshttps://doi.org/10.1038/s41598-022-17411-9openalex-snapshot
Plasticity of body axis polarity in Hydra regeneration under constraints
inferred← citeshttps://doi.org/10.1039/c1mt00093dopenalex-snapshot
The preferential accumulation of cadmium in the head portion of the freshwater planarian, Dugesia japonica (Platyhelminthes: Turbellaria)
inferred← citeshttps://doi.org/10.1073/pnas.0906823106openalex-snapshot
A wound-induced Wnt expression program controls planarian regeneration polarity
inferred← citeshttps://doi.org/10.1073/pnas.0907464106openalex-snapshot
Planarian Hedgehog/Patched establishes anterior–posterior polarity by regulating Wnt signaling
inferred← citeshttps://doi.org/10.1073/pnas.1012090108openalex-snapshot
Dishevelled is essential for neural connectivity and planar cell polarity in planarians
inferred← citeshttps://doi.org/10.1073/pnas.1016386108openalex-snapshot
Phosphorylation of Grainy head by ERK is essential for wound-dependent regeneration but not for development of an epidermal barrier
inferred← citeshttps://doi.org/10.1073/pnas.1214053110openalex-snapshot
Follistatin antagonizes Activin signaling and acts with Notum to direct planarian head regeneration
inferred← citeshttps://doi.org/10.1073/pnas.2009539118openalex-snapshot
Calcineurin controls proximodistal blastema polarity in zebrafish fin regeneration
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