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Generic and context-dependent gene modulations during Hydra whole body regeneration

https://doi.org/10.1101/587147
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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/bies.200800183openalex-snapshot
Hydra and the evolution of stem cells
inferredcites →https://doi.org/10.1002/dvdy.10221openalex-snapshot
Hydra regeneration and epitheliopeptides
inferredcites →https://doi.org/10.1002/j.1460-2075.1992.tb05233.xopenalex-snapshot
HOM/HOX homeobox genes are present in hydra (Chlorohydra viridissima) and are differentially expressed during regeneration.
inferredcites →https://doi.org/10.1002/jez.1400070102openalex-snapshot
The production of new hydranths in Hydra by the insertion of small grafts
inferredcites →https://doi.org/10.1006/dbio.1996.0321openalex-snapshot
CnNK-2,an NK-2 Homeobox Gene, Has a Role in Patterning the Basal End of the Axis in Hydra
inferredcites →https://doi.org/10.1007/978-0-387-98141-3openalex-snapshot
ggplot2: Elegant Graphics for Data Analysis
inferredcites →https://doi.org/10.1007/bf00289234openalex-snapshot
A theory of biological pattern formation
inferredcites →https://doi.org/10.1007/bf00376156openalex-snapshot
Lithium ions interfere with pattern control in Hydra vulgaris
inferredcites →https://doi.org/10.1007/bf00848589openalex-snapshot
Analysis of head and foot formation inHydra by means of an endogenous inhibitor
inferredcites →https://doi.org/10.1007/bf00868146openalex-snapshot
A new biochemical marker for foot-specific cell differentiation in hydra
inferredcites →https://doi.org/10.1007/bf02108176openalex-snapshot
über Induktion von Embryonalanlagen durch Implantation artfremder Organisatoren
inferredcites →https://doi.org/10.1007/s00427-012-0411-yopenalex-snapshot
Injury-induced asymmetric cell death as a driving force for head regeneration in Hydra
inferredcites →https://doi.org/10.1007/s004270050050openalex-snapshot
Response to insulin and the expression pattern of a gene encoding an insulin receptor homologue suggest a role for an insulin-like molecule in regulating growth and patterning in Hydra
inferredcites →https://doi.org/10.1016/0012-1606(83)90324-xopenalex-snapshot
Hydra transplantation phenomena and the mechanism of Hydra head regeneration
inferredcites →https://doi.org/10.1016/0012-1606(83)90325-1openalex-snapshot
Hydra transplantation phenomena and the mechanism of Hydra head regeneration
inferredcites →https://doi.org/10.1016/0012-1606(90)90360-uopenalex-snapshot
Cell cycle length, cell size, and proliferation rate in hydra stem cells
inferredcites →https://doi.org/10.1016/bs.ctdb.2015.11.002openalex-snapshot
How Somatic Adult Tissues Develop Organizer Activity
inferredcites →https://doi.org/10.1016/j.cell.2005.12.018openalex-snapshot
Embryonic Dorsal-Ventral Signaling: Secreted Frizzled-Related Proteins as Inhibitors of Tolloid Proteinases
inferredcites →https://doi.org/10.1016/j.cell.2006.08.052openalex-snapshot
A Dynamic Epicardial Injury Response Supports Progenitor Cell Activity during Zebrafish Heart Regeneration
inferredcites →https://doi.org/10.1016/j.cell.2008.01.003openalex-snapshot
Evo-Devo: Variations on Ancestral Themes
inferredcites →https://doi.org/10.1016/j.cell.2011.02.015openalex-snapshot
Impulse Control: Temporal Dynamics in Gene Transcription
inferredcites →https://doi.org/10.1016/j.celrep.2016.12.063openalex-snapshot
A Tissue-Mapped Axolotl De Novo Transcriptome Enables Identification of Limb Regeneration Factors
inferredcites →https://doi.org/10.1016/j.devcel.2009.07.014openalex-snapshot
Apoptotic Cells Provide an Unexpected Source of Wnt3 Signaling to Drive Hydra Head Regeneration
inferredcites →https://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
inferredcites →https://doi.org/10.1016/j.diff.2014.03.001openalex-snapshot
Robust G2 pausing of adult stem cells in Hydra
inferredcites →https://doi.org/10.1016/j.jmb.2012.10.003openalex-snapshot
Members of the DAN Family Are BMP Antagonists That Form Highly Stable Noncovalent Dimers
inferredcites →https://doi.org/10.1016/j.mod.2003.12.001openalex-snapshot
Control of foot differentiation in Hydra: in vitro evidence that the NK-2 homeobox factor CnNK-2 autoregulates its own expression and uses pedibin as target gene
inferredcites →https://doi.org/10.1016/j.mod.2005.04.010openalex-snapshot
Control of foot differentiation in Hydra: Phylogenetic footprinting indicates interaction of head, bud and foot patterning systems
inferredcites →https://doi.org/10.1016/j.semcdb.2006.05.005openalex-snapshot
Hydra, a niche for cell and developmental plasticity
inferredcites →https://doi.org/10.1016/j.smim.2014.06.004openalex-snapshot
Injury-induced immune responses in Hydra
inferredcites →https://doi.org/10.1016/j.str.2013.06.005openalex-snapshot
Structure of Protein Related to Dan and Cerberus: Insights into the Mechanism of Bone Morphogenetic Protein Antagonism
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.ydbio.2003.10.031openalex-snapshot
HyBMP5-8b , a BMP5-8 orthologue, acts during axial patterning and tentacle formation in hydra
inferredcites →https://doi.org/10.1016/j.ydbio.2004.07.037openalex-snapshot
The orphan COUP-TF nuclear receptors are markers for neurogenesis from cnidarians to vertebrates
inferredcites →https://doi.org/10.1016/j.ydbio.2006.04.003openalex-snapshot
Dickkopf related genes are components of the positional value gradient in Hydra
inferredcites →https://doi.org/10.1016/j.ydbio.2007.06.013openalex-snapshot
Transgenic stem cells in Hydra reveal an early evolutionary origin for key elements controlling self-renewal and differentiation
inferredcites →https://doi.org/10.1016/j.ydbio.2009.02.004openalex-snapshot
Multiple Wnts are involved in Hydra organizer formation and regeneration
inferredcites →https://doi.org/10.1016/j.ydbio.2010.06.017openalex-snapshot
Planarian regeneration involves distinct stem cell responses to wounds and tissue absence
inferredcites →https://doi.org/10.1016/j.ydbio.2017.09.005openalex-snapshot
β-Catenin acts in a position-independent regeneration response in the simple eumetazoan Hydra
inferredcites →https://doi.org/10.1016/j.zool.2008.09.002openalex-snapshot
Plasticity of epithelial cell shape in response to upstream signals: A whole-organism study using transgenic Hydra
inferredcites →https://doi.org/10.1016/s0092-8674(00)80133-6openalex-snapshot
The Spemann Organizer Signal noggin Binds and Inactivates Bone Morphogenetic Protein 4
inferredcites →https://doi.org/10.1016/s0742-8413(97)00204-1openalex-snapshot
Hydroperoxides Mediate Lithium Effects on Regeneration in Hydra
inferredcites →https://doi.org/10.1016/s0968-0004(98)01211-0openalex-snapshot
Ets transcription factors: nuclear effectors of the Ras–MAP-kinase signaling pathway
inferredcites →https://doi.org/10.1016/s1534-5807(04)00056-5openalex-snapshot
Nodal and BMP2/4 Signaling Organizes the Oral-Aboral Axis of the Sea Urchin Embryo
inferredcites →https://doi.org/10.1038/35101500openalex-snapshot
Morphogen gradient interpretation
inferredcites →https://doi.org/10.1038/nature07039openalex-snapshot
Wound repair and regeneration
inferredcites →https://doi.org/10.1038/nature12037openalex-snapshot
Visualization of an endogenous retinoic acid gradient across embryonic development
inferredcites →https://doi.org/10.1038/nature13666openalex-snapshot
Nodal signalling determines biradial asymmetry in Hydra
inferredcites →https://doi.org/10.1038/nmeth.1701openalex-snapshot
SignalP 4.0: discriminating signal peptides from transmembrane regions
inferredcites →https://doi.org/10.1038/nmeth.4197openalex-snapshot
Salmon provides fast and bias-aware quantification of transcript expression
inferredcites →https://doi.org/10.1038/nrg1347openalex-snapshot
Regionally specific induction by the Spemann–Mangold organizer
inferredcites →https://doi.org/10.1038/nrm3541openalex-snapshot
The role of transcription-independent damage signals in the initiation of epithelial wound healing
inferredcites →https://doi.org/10.1038/s41467-018-08242-2openalex-snapshot
An evolutionarily-conserved Wnt3/β-catenin/Sp5 feedback loop restricts head organizer activity in Hydra
inferredcites →https://doi.org/10.1038/sj.onc.1204036openalex-snapshot
Signal transduction and the Ets family of transcription factors
inferredcites →https://doi.org/10.1073/pnas.0306512101openalex-snapshot
Reactivation of developmental programs: The cAMP-response element-binding protein pathway is involved in hydra head regeneration
inferredcites →https://doi.org/10.1073/pnas.0510163103openalex-snapshot
Transgenic Hydra allow in vivo tracking of individual stem cells during morphogenesis
inferredcites →https://doi.org/10.1073/pnas.0604501104openalex-snapshot
An ancient chordin-like gene in organizer formation of Hydra
inferredcites →https://doi.org/10.1073/pnas.0703331104openalex-snapshot
The evolutionary emergence of cell type-specific genes inferred from the gene expression analysis of Hydra
inferredcites →https://doi.org/10.1073/pnas.071041898openalex-snapshot
Cell autonomous regulation of multiple Dishevelled-dependent pathways by mammalian Nkd
inferredcites →https://doi.org/10.1073/pnas.0900151106openalex-snapshot
BMPs and Chordin regulate patterning of the directive axis in a sea anemone
inferredcites →https://doi.org/10.1073/pnas.101049998openalex-snapshot
Trans-spliced leader addition to mRNAs in a cnidarian
inferredcites →https://doi.org/10.1073/pnas.1018109108openalex-snapshot
Autoregulatory and repressive inputs localize Hydra Wnt3 to the head organizer
inferredcites →https://doi.org/10.1073/pnas.12.9.565openalex-snapshot
Localization of Formative Agencies in Hydra
inferredcites →https://doi.org/10.1073/pnas.1319745110openalex-snapshot
Chordin forms a self-organizing morphogen gradient in the extracellular space between ectoderm and mesoderm in the Xenopus embryo
inferredcites →https://doi.org/10.1073/pnas.1620755114openalex-snapshot
Transcriptomic, proteomic, and metabolomic landscape of positional memory in the caudal fin of zebrafish
inferredcites →https://doi.org/10.1073/pnas.97.9.4493openalex-snapshot
Evolution of Antp-class genes and differential expression of Hydra Hox/paraHox genes in anterior patterning
inferredcites →https://doi.org/10.1086/415724openalex-snapshot
Hydra and the Birth of Experimental Biology 1744. Abraham Trembley's Memoirs Concerning the Polyps. Book I: Some Reflections on Abraham Trembley and His Memoires. Book II: A Translation from the French of Memoires, pour servir a L'histoire d' un genre de polypes d'eau douce, a bras en forme de…
inferredcites →https://doi.org/10.1093/gbe/evt142openalex-snapshot
Punctuated Emergences of Genetic and Phenotypic Innovations in Eumetazoan, Bilaterian, Euteleostome, and Hominidae Ancestors
inferredcites →https://doi.org/10.1093/hmg/10.6.605openalex-snapshot
PTEN inhibits insulin-stimulated MEK/MAPK activation and cell growth by blocking IRS-1 phosphorylation and IRS-1/Grb-2/Sos complex formation in a breast cancer model
inferredcites →https://doi.org/10.1093/molbev/msn154openalex-snapshot
Cilium Evolution: Identification of a Novel Protein, Nematocilin, in the Mechanosensory Cilium of Hydra Nematocytes
inferredcites →https://doi.org/10.1093/molbev/mss134openalex-snapshot
Molecular Signatures of the Three Stem Cell Lineages in Hydra and the Emergence of Stem Cell Function at the Base of Multicellularity
inferredcites →https://doi.org/10.1093/molbev/msv079openalex-snapshot
A Comprehensive Transcriptomic and Proteomic Analysis of Hydra Head Regeneration
inferredcites →https://doi.org/10.1093/nar/gki078openalex-snapshot
The PANTHER database of protein families, subfamilies, functions and pathways
inferredcites →https://doi.org/10.1093/nar/gki418openalex-snapshot
FFAS03: a server for profile-profile sequence alignments
inferredcites →https://doi.org/10.1093/nar/gkt1223openalex-snapshot
Pfam: the protein families database
inferredcites →https://doi.org/10.1093/nar/gky675openalex-snapshot
Impulse model-based differential expression analysis of time course sequencing data
inferredcites →https://doi.org/10.1098/rstb.2015.0040openalex-snapshot
Loss of neurogenesis in Hydra leads to compensatory regulation of neurogenic and neurotransmission genes in epithelial cells
inferredcites →https://doi.org/10.1101/460154openalex-snapshot
Stem cell differentiation trajectories in Hydra resolved at single-cell resolution
inferredcites →https://doi.org/10.1101/gad.187377.112openalex-snapshot
A molecular wound response program associated with regeneration initiation in planarians
inferredcites →https://doi.org/10.1111/j.1440-169x.2011.01250.xopenalex-snapshot
Injury-induced activation of the MAPK/CREB pathway triggers apoptosis-induced compensatory proliferation in hydra head regeneration
inferredcites →https://doi.org/10.1111/j.1525-142x.2010.00412.xopenalex-snapshot
Cloning of noggin gene from hydra and analysis of its functional conservation using Xenopus laevis embryos
inferredcites →https://doi.org/10.1126/science.1248252openalex-snapshot
Construction of a Vertebrate Embryo from Two Opposing Morphogen Gradients
inferredcites →https://doi.org/10.1128/mcb.24.24.10954-10964.2004openalex-snapshot
Ras/Mitogen-Activated Protein Kinase Signaling Activates Ets-1 and Ets-2 by CBP/p300 Recruitment
inferredcites →https://doi.org/10.1146/annurev.cellbio.24.110707.175336openalex-snapshot
Comparative Aspects of Animal Regeneration
inferredcites →https://doi.org/10.1161/circulationaha.117.028252openalex-snapshot
Multicellular Transcriptional Analysis of Mammalian Heart Regeneration
inferredcites →https://doi.org/10.1186/1471-2164-14-797openalex-snapshot
The planarian regeneration transcriptome reveals a shared but temporally shifted regulatory program between opposing head and tail scenarios
inferredcites →https://doi.org/10.1186/gb-2013-14-2-r16openalex-snapshot
A de novo assembly of the newt transcriptome combined with proteomic validation identifies new protein families expressed during tissue regeneration
inferredcites →https://doi.org/10.1186/s13059-014-0550-8openalex-snapshot
Moderated estimation of fold change and dispersion for RNA-seq data with DESeq2
inferredcites →https://doi.org/10.1242/dev.010173openalex-snapshot
Divergent functions of two ancientHydra Brachyuryparalogues suggest specific roles for their C-terminal domains in tissue fate induction
inferredcites →https://doi.org/10.1242/dev.01848openalex-snapshot
Formation of the head organizer in hydra involves the canonical Wnt pathway
inferredcites →https://doi.org/10.1242/dev.02265openalex-snapshot
An ancient Wnt-Dickkopf antagonism inHydra
inferredcites →https://doi.org/10.1242/dev.105.3.521openalex-snapshot
Genetic analysis of developmental mechanisms in hydra XIX. Stimulation of regeneration by injury in the regeneration-deficient mutant strain, reg-16
inferredcites →https://doi.org/10.1242/dev.121.4.1205openalex-snapshot
The cAMP Response Element Binding protein is involved in hydra regeneration
inferredcites →https://doi.org/10.1242/dev.122.6.1941openalex-snapshot
Isolation and characterization of two new morphogenetically active peptides from Hydra vulgaris
inferredcites →https://doi.org/10.1242/dev.126.3.517openalex-snapshot
The novel signal peptides, Pedibin and Hym-346, lower positional value thereby enhancing foot formation in hydra
inferredcites →https://doi.org/10.1242/dev.126.5.999openalex-snapshot
HyBra1, a Brachyury homologue, acts during head formation in Hydra
inferredcites →https://doi.org/10.1242/dev.127.22.4743openalex-snapshot
HyAlx, an aristaless-related gene, is involved in tentacle formation in hydra
inferredcites →https://doi.org/10.1242/dev.129.4.875openalex-snapshot
Characterization of the head organizer in hydra
inferredcites →https://doi.org/10.1242/dev.16.1.91openalex-snapshot
Studies on pattern regulation in hydra
inferredcites →https://doi.org/10.1242/dev.30.3.727openalex-snapshot
Positional information and pattern regulation in hydra: formation of the foot end
inferredcites →https://doi.org/10.1242/dev.78.1.141openalex-snapshot
Genetic analysis of developmental mechanisms in hydra. VIII. Head-activation and head-inhibition potentials of a slow-budding strain (L4)
inferredcites →https://doi.org/10.1242/dev.80.1.155openalex-snapshot
Genetic analysis of developmental mechanisms in hydra
inferredcites →https://doi.org/10.1242/jcs.026096openalex-snapshot
Beyond Wnt inhibition: new functions of secreted Frizzled-related proteins in development and disease
inferredcites →https://doi.org/10.1242/jcs.11.2.557openalex-snapshot
Cell cycle kinetics and development of Hydra attenuata: I. epithelial cells
inferredcites →https://doi.org/10.1242/jcs.114.11.2043openalex-snapshot
Repression of Wnt-5a impairs DDR1 phosphorylation and modifies adhesion and migration of mammary cells
inferredcites →https://doi.org/10.1242/jcs.16.2.349openalex-snapshot
Cell cycle kinetics and development of Hydra attenuata: II. interstitial cells
inferredcites →https://doi.org/10.1242/jeb.21.3-4.147openalex-snapshot
Studies on the Organizer Problem in Pelmatohydra Oligactis: I. The Induction Potency of the Implants and the Nature of the Induced Hydranth
inferredcites →https://doi.org/10.1261/rna.1975210openalex-snapshot
Convergent origins and rapid evolution of spliced leader trans-splicing in Metazoa: Insights from the Ctenophora and Hydrozoa
inferredcites →https://doi.org/10.1371/journal.pone.0105004openalex-snapshot
Transcriptomic Analysis of Tail Regeneration in the Lizard Anolis carolinensis Reveals Activation of Conserved Vertebrate Developmental and Repair Mechanisms
inferredcites →https://doi.org/10.1371/journal.pone.0151823openalex-snapshot
Thrombospondin Type-1 Repeat Domain-Containing Proteins Are Strongly Expressed in the Head Region of Hydra
inferredcites →https://doi.org/10.1387/ijdb.113454abopenalex-snapshot
Hydra, a model system to trace the emergence of boundaries in developing eumetazoans
inferredcites →https://doi.org/10.1387/ijdb.113477tfopenalex-snapshot
Peptide signaling in Hydra
inferredcites →https://doi.org/10.1387/ijdb.123498hsopenalex-snapshot
Transplantation analysis of developmental mechanisms in Hydra
inferredcites →https://doi.org/10.14806/ej.17.1.200openalex-snapshot
Cutadapt removes adapter sequences from high-throughput sequencing reads
inferredcites →https://doi.org/10.3892/ijmm.17.5.795openalex-snapshot
CER1 is a common target of WNT and NODAL signaling pathways in human embryonic stem cells
inferredcites →https://doi.org/10.4161/sgtp.19630openalex-snapshot
RAS/ERK pathway transcriptional regulation through ETS/AP-1 binding sites
inferredcites →https://doi.org/10.48550/arxiv.1601.02213openalex-snapshot
On Clustering Time Series Using Euclidean Distance and Pearson Correlation
inferredcites →https://doi.org/10.5962/bhl.title.64073openalex-snapshot
Mémoires pour servir à l'histoire d'un genre de polypes d'eau douce, à bras en forme de cornes /
inferredcites →https://doi.org/10.7554/elife.25605openalex-snapshot
Reciprocal analyses in zebrafish and medaka reveal that harnessing the immune response promotes cardiac regeneration

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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High regenerative capacity is a general feature within colonial dendrophylliid corals (Anthozoa, Scleractinia)
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/10.1007/978-1-0716-2172-1_34openalex-snapshot
Combining RNAi-Mediated β-Catenin Inhibition and Reaggregation to Study Hydra Whole-Body Regeneration
inferred← citeshttps://doi.org/10.1007/978-1-4939-9732-9_1openalex-snapshot
Combining BrdU-Labeling to Detection of Neuronal Markers to Monitor Adult Neurogenesis in Hydra
inferred← citeshttps://doi.org/10.1007/978-3-030-88084-2_2openalex-snapshot
Self-Organization of Tissues Through Biochemical and Mechanical Signals
inferred← citeshttps://doi.org/10.1007/978-3-032-06766-1_12openalex-snapshot
Hydra at the Crossroads of Evolution: Insights into Cell-type Diversification, Regeneration, and Epigenetic Regulation
inferred← citeshttps://doi.org/10.1007/s00018-021-03760-7openalex-snapshot
Animal regeneration in the era of transcriptomics
inferred← citeshttps://doi.org/10.1016/j.cbpb.2019.110365openalex-snapshot
Comparative analysis of β-hexosaminidase and acid phosphatase from Hydra vulgaris Ind-Pune, H. vulgaris Naukuchiatal and H. magnipapillata sf-1: Localization studies of acid phosphatase and β-hexosaminidase from H. vulgaris Ind-Pune
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.mad.2020.111414openalex-snapshot
The ULK1 kinase, a necessary component of the pro-regenerative and anti-aging machinery in Hydra
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.2019.11.006openalex-snapshot
Boundary maintenance in the ancestral metazoan Hydra depends on histone acetylation
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/s41467-026-73887-3openalex-snapshot
Dynamic cell fate transitions during morphallactic regeneration
inferred← citeshttps://doi.org/10.1038/s41598-021-82489-6openalex-snapshot
Immature symbiotic system between horizontally transmitted green algae and brown hydra
inferred← citeshttps://doi.org/10.1038/s42003-019-0680-3openalex-snapshot
Molecular signature of an ancient organizer regulated by Wnt/β-catenin signalling during primary body axis patterning in Hydra
inferred← citeshttps://doi.org/10.1093/molbev/msae254openalex-snapshot
The Rich Evolutionary History of the Reactive Oxygen Species Metabolic Arsenal Shapes Its Mechanistic Plasticity at the Onset of Metazoan Regeneration
inferred← citeshttps://doi.org/10.1101/2020.07.06.189811openalex-snapshot
Oral Regeneration Is the Default Pathway Triggered by Injury in Hydra
inferred← citeshttps://doi.org/10.1101/2021.12.22.473838openalex-snapshot
The transcription factor Zic4 acts as a transdifferentiation switch
inferred← citeshttps://doi.org/10.1101/2022.10.04.510867openalex-snapshot
Apical-to-basal graded ROS metabolism in intact Hydra leads to distinct levels of injury-induced ROS signaling in apical and basal regenerating tips
inferred← citeshttps://doi.org/10.1101/2024.07.24.604959openalex-snapshot
A whole-body atlas of non-graded BMP signaling activity in a sea anemone
inferred← citeshttps://doi.org/10.1101/2025.11.07.687297openalex-snapshot
Extracellular matrix remodeling supports Hydra vulgaris head regeneration and stem cell invasion
inferred← citeshttps://doi.org/10.1101/cshperspect.a040725openalex-snapshot
Cellular, Metabolic, and Developmental Dimensions of Whole-Body Regeneration in Hydra
inferred← citeshttps://doi.org/10.1126/sciadv.abj6897openalex-snapshot
Mechanical oscillations orchestrate axial patterning through Wnt activation in Hydra
inferred← citeshttps://doi.org/10.1126/sciadv.abo0694openalex-snapshot
The transcription factor Zic4 promotes tentacle formation and prevents epithelial transdifferentiation in Hydra
inferred← citeshttps://doi.org/10.1134/s0006297922030075openalex-snapshot
Studying of Molecular Regulation of Developmental Processes of Lower Metazoans Exemplified by Cnidaria Using High-Throughput Sequencing
inferred← citeshttps://doi.org/10.1186/s12915-025-02150-wopenalex-snapshot
A whole-body atlas of BMP signaling activity in an adult sea anemone
inferred← citeshttps://doi.org/10.1186/s13072-020-00364-6openalex-snapshot
Epigenomic landscape of enhancer elements during Hydra head organizer formation
inferred← citeshttps://doi.org/10.1242/dev.177212openalex-snapshot
Model systems for regeneration: Hydra
inferred← citeshttps://doi.org/10.1242/dev.204725openalex-snapshot
A transcription factor toggle switch determines differentiated epidermal cell identities in Hydra
inferred← citeshttps://doi.org/10.1242/dev.205368openalex-snapshot
Collagen remodeling supports Hydra vulgaris head regeneration and stem cell invasion
inferred← citeshttps://doi.org/10.1371/journal.pone.0230547openalex-snapshot
The polymorphism of Hydra microsatellite sequences provides strain-specific signatures
inferred← citeshttps://doi.org/10.1387/ijdb.210087ylopenalex-snapshot
A screen of kinase inhibitors reveals a potential role of Chk1 in regulating Hydra head regeneration and maintenance
inferred← citeshttps://doi.org/10.31857/s0320972522020075openalex-snapshot
Исследования молекулярной регуляции процессов развития низших многоклеточных на примере стрекающих с использованием технологий высокопроизводительного секвенирования
inferred← citeshttps://doi.org/10.3389/fcell.2021.788117openalex-snapshot
The Aquatic Invertebrate Hydra vulgaris Releases Molecular Messages Through Extracellular Vesicles
inferred← citeshttps://doi.org/10.3390/biomedicines12061274openalex-snapshot
The Wnt/β-catenin/TCF/Sp5/Zic4 Gene Network That Regulates Head Organizer Activity in Hydra Is Differentially Regulated in Epidermis and Gastrodermis
inferred← citeshttps://doi.org/10.3390/cimb47040219openalex-snapshot
Signaling Mechanism of Budding, Proliferation, and Tissue Regeneration in Cnidaria
inferred← citeshttps://doi.org/10.7554/elife.60562openalex-snapshot
Generic injuries are sufficient to induce ectopic Wnt organizers in Hydra
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