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Regeneration in spiralians: evolutionary patterns and developmental processes

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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/cne.20022openalex-snapshot

Ground plan of the polychaete brain—I. Patterns of nerve development during regeneration in Dorvillea bermudensis (Dorvilleidae)

inferredcites →https://doi.org/10.1002/dneu.20993openalex-snapshot

Rapid neural circuit switching mediated by synaptic plasticity during neural morphallactic regeneration

inferredcites →https://doi.org/10.1002/dvdy.10228openalex-snapshot

Allometric scaling and proportion regulation in the freshwater planarian Schmidtea mediterranea

inferredcites →https://doi.org/10.1002/dvdy.21518openalex-snapshot

Morphallactic regeneration as revealed by region‐specific gene expression in the digestive tract of Enchytraeus japonensis (Oligochaeta, Annelida)

inferredcites →https://doi.org/10.1002/jez.1400070402openalex-snapshot

Contributions to the physiology of regeneration. I. Experiments on Podarke obscura

inferredcites →https://doi.org/10.1002/jez.1400540304openalex-snapshot

Regeneration in nemerteans

inferredcites →https://doi.org/10.1002/jez.1400570105openalex-snapshot

Regeneration in nemerteans. II. Regeneration of small sections of the body split or partially split longitudinally

inferredcites →https://doi.org/10.1002/jez.1400670204openalex-snapshot

Regeneration in nemerteans. IV. Cellular changes involved in restitution and reorganization

inferredcites →https://doi.org/10.1002/jez.b.22523openalex-snapshot

Investment choices in post‐embryonic development: Quantifying interactions among growth, regeneration, and asexual reproduction in the annelid Pristina leidyi

inferredcites →https://doi.org/10.1002/jez.b.22572openalex-snapshot

Cell proliferation dynamics in regeneration of the operculum head appendage in the annelid Pomatoceros lamarckii

inferredcites →https://doi.org/10.1002/jmor.1051240406openalex-snapshot

Later stages of regeneration in the polychaete, Nephtys

inferredcites →https://doi.org/10.1006/dbio.2000.9645openalex-snapshot

Bromodeoxyuridine Specifically Labels the Regenerative Stem Cells of Planarians

inferredcites →https://doi.org/10.1007/978-1-4615-3830-1_7openalex-snapshot

Growth, Degrowth and Regeneration as Developmental Phenomena in Adult Freshwater Planarians

inferredcites →https://doi.org/10.1007/978-3-642-79839-9openalex-snapshot

Nervous System Regeneration in the Invertebrates

inferredcites →https://doi.org/10.1007/978-94-011-2775-2_8openalex-snapshot

Pharyngeal regeneration in the land planarian Bipalium kewense

inferredcites →https://doi.org/10.1007/bf00391902openalex-snapshot

Regeneration in the gonochoristic polychaete Ophryotrocha notoglandulata

inferredcites →https://doi.org/10.1007/bf00582076openalex-snapshot

Anteriore und caudale Regeneration bei dem proterandrischen PolychaetenOphryotrocha puerilis Clap. Mecz

inferredcites →https://doi.org/10.1007/bf02161491openalex-snapshot

Experimental studies of the regeneration of Planaria maculata

inferredcites →https://doi.org/10.1007/bf02263782openalex-snapshot

Studien über die Regeneration der Nemertinen

inferredcites →https://doi.org/10.1007/bf02287014openalex-snapshot

Contributions to the physiology of regeneration

inferredcites →https://doi.org/10.1007/s00227-006-0431-0openalex-snapshot

Anterior regeneration in the spionid polychaetes Dipolydora quadrilobata and Pygospio elegans

inferredcites →https://doi.org/10.1007/s00244-004-0041-0openalex-snapshot

Antioxidant Enzymes and Tissue Regeneration in Eurythoe complanata (Polychaeta: Amphinomidae) Exposed to Used Vehicle Crankcase Oil

inferredcites →https://doi.org/10.1007/s00427-006-0069-4openalex-snapshot

The regeneration capacity of the flatworm Macrostomum lignano—on repeated regeneration, rejuvenation, and the minimal size needed for regeneration

inferredcites →https://doi.org/10.1007/s00427-006-0079-2openalex-snapshot

The regeneration capacity of the flatworm Macrostomum lignano–on repeated regeneration, rejuvenation and the minimal size needed for regeneration

inferredcites →https://doi.org/10.1007/s00427-012-0402-zopenalex-snapshot

Activation of Hox genes during caudal regeneration of the polychaete annelid Platynereis dumerilii

inferredcites →https://doi.org/10.1007/s00427-013-0448-6openalex-snapshot

Identification and characterization of a twist ortholog in the polychaete annelid Platynereis dumerilii reveals mesodermal expression of Pdu-twist

inferredcites →https://doi.org/10.1007/s00435-003-0073-4openalex-snapshot

Experiments on anterior regeneration in Eurythoe complanata ("Polychaeta", Amphinomidae): reconfiguration of the nervous system and its function for regeneration

inferredcites →https://doi.org/10.1007/s00441-006-0299-9openalex-snapshot

Regeneration in Macrostomum lignano (Platyhelminthes): cellular dynamics in the neoblast stem cell system

inferredcites →https://doi.org/10.1007/s00441-012-1426-4openalex-snapshot

Proliferation pattern during rostrum regeneration of the symbiotic flatworm Paracatenula galateia: a pulse-chase-pulse analysis

inferredcites →https://doi.org/10.1007/s13127-011-0044-4openalex-snapshot

Higher-level metazoan relationships: recent progress and remaining questions

inferredcites →https://doi.org/10.1016/0016-6480(75)90144-6openalex-snapshot

Hormone independent regeneration in Eulalia viridis (polychaeta-phyllodocidae)

inferredcites →https://doi.org/10.1016/0301-0082(95)00007-iopenalex-snapshot

Neural regeneration in gastropod molluscs

inferredcites →https://doi.org/10.1016/b978-1-4831-9951-1.50008-5openalex-snapshot

Regeneration in Annelids

inferredcites →https://doi.org/10.1016/j.aquaculture.2013.01.035openalex-snapshot

Healing and regeneration of the freshwater pearl mussel Hyriopsis cumingii Lea after donating mantle saibos

inferredcites →https://doi.org/10.1016/j.cell.2009.11.035openalex-snapshot

Wnt Signaling and the Polarity of the Primary Body Axis

inferredcites →https://doi.org/10.1016/j.cub.2006.04.036openalex-snapshot

Early Segregation of Germ and Somatic Lineages during Gonadal Regeneration in the Annelid Enchytraeus japonensis

inferredcites →https://doi.org/10.1016/j.devcel.2011.06.016openalex-snapshot

The Cellular Basis for Animal Regeneration

inferredcites →https://doi.org/10.1016/j.exger.2008.11.007openalex-snapshot

The free-living flatworm Macrostomum lignano: A new model organism for ageing research

inferredcites →https://doi.org/10.1016/j.gde.2009.05.003openalex-snapshot

Emerging patterns in planarian regeneration

inferredcites →https://doi.org/10.1016/j.gep.2007.12.008openalex-snapshot

Exploration of embryonic origins of germline stem cells and neoblasts in Enchytraeus japonensis (Oligochaeta, Annelida)

inferredcites →https://doi.org/10.1016/j.jembe.2006.03.003openalex-snapshot

Regeneration of lost siphon tissues in the tellinacean bivalve Nuttallia olivacea

inferredcites →https://doi.org/10.1016/j.jembe.2013.02.015openalex-snapshot

Octopus arm regeneration: Role of acetylcholinesterase during morphological modification

inferredcites →https://doi.org/10.1016/j.tcb.2011.01.005openalex-snapshot

Planarian stem cells: a simple paradigm for regeneration

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.2010.06.017openalex-snapshot

Planarian regeneration involves distinct stem cell responses to wounds and tissue absence

inferredcites →https://doi.org/10.1016/j.ydbio.2010.08.007openalex-snapshot

Expression of secreted Wnt pathway components reveals unexpected complexity of the planarian amputation response

inferredcites →https://doi.org/10.1016/j.ydbio.2013.04.010openalex-snapshot

Homeogenetic inductive mechanism of segmentation in polychaete tail regeneration

inferredcites →https://doi.org/10.1016/j.ydbio.2013.07.013openalex-snapshot

Posterior elongation in the annelid Platynereis dumerilii involves stem cells molecularly related to primordial germ cells

inferredcites →https://doi.org/10.1017/s0025315400043976openalex-snapshot

Remarks on the Reversible Asymmetry in the Opercula of the Polychæte Hydroides

inferredcites →https://doi.org/10.1017/s0031182000053920openalex-snapshot

Schistosoma mansoni : structural damage and tegumental repair after in vivo treatment with praziquantel

inferredcites →https://doi.org/10.1023/a:1003475324285openalex-snapshot

Inhibition of regeneration in the planarian Dugesia polychroa (Schmidt) by treatment with magnesium chloride: a morphological study of wound closure

inferredcites →https://doi.org/10.1038/078171a0openalex-snapshot

A Monograph of the British Annelids

inferredcites →https://doi.org/10.1038/nature09676openalex-snapshot

Acoelomorph flatworms are deuterostomes related to Xenoturbella

inferredcites →https://doi.org/10.1038/nature09864openalex-snapshot

Phylogenomic analyses unravel annelid evolution

inferredcites →https://doi.org/10.1038/nature10382openalex-snapshot

Phylogenomics reveals deep molluscan relationships

inferredcites →https://doi.org/10.1038/nature10526openalex-snapshot

Resolving the evolutionary relationships of molluscs with phylogenomic tools

inferredcites →https://doi.org/10.1038/nature11924openalex-snapshot

Adult somatic stem cells in the human parasite Schistosoma mansoni

inferredcites →https://doi.org/10.1038/nature12359openalex-snapshot

The molecular logic for planarian regeneration along the anterior–posterior axis

inferredcites →https://doi.org/10.1038/nature12403openalex-snapshot

Restoration of anterior regeneration in a planarian with limited regenerative ability

inferredcites →https://doi.org/10.1038/nature12414openalex-snapshot

Reactivating head regrowth in a regeneration-deficient planarian species

inferredcites →https://doi.org/10.1038/nrg1923openalex-snapshot

Bridging the regeneration gap: genetic insights from diverse animal models

inferredcites →https://doi.org/10.1038/nrg759openalex-snapshot

Not your father's planarian: a classic model enters the era of functional genomics

inferredcites →https://doi.org/10.1073/pnas.0906823106openalex-snapshot

A wound-induced Wnt expression program controls planarian regeneration polarity

inferredcites →https://doi.org/10.1073/pnas.0907931107openalex-snapshot

Latent regeneration abilities persist following recent evolutionary loss in asexual annelids

inferredcites →https://doi.org/10.1073/pnas.93.7.2658openalex-snapshot

Isolation of a Pax-6 homolog from the ribbonworm Lineus sanguineus.

inferredcites →https://doi.org/10.1080/00222930902741669openalex-snapshot

A new higher classification of planarian flatworms (Platyhelminthes, Tricladida)

inferredcites →https://doi.org/10.1080/07924259.1991.9672186openalex-snapshot

Intraspecific Variation in Somatic Cell Turnover and Regenerative Rate in the Freshwater PlanarianDendrocoelum Lacteum

inferredcites →https://doi.org/10.1080/17451000.2012.707323openalex-snapshot

The effect of temperature on the inhalant siphon regeneration ofAmiantis purpurata(Lamarck, 1818) (Bivalvia; Veneridae)

inferredcites →https://doi.org/10.1086/280919openalex-snapshot

Aspects of Regeneration in Annelids

inferredcites →https://doi.org/10.1093/icb/10.2.101openalex-snapshot

Origin of the Regeneration Blastema in Polychaete Annelids

inferredcites →https://doi.org/10.1093/icb/icj051openalex-snapshot

Distribution of segment regeneration ability in the Annelida

inferredcites →https://doi.org/10.1093/icb/icq118openalex-snapshot

Evolutionary Loss of Animal Regeneration: Pattern and Process

inferredcites →https://doi.org/10.1093/icb/icu109openalex-snapshot

Early Events in Annelid Regeneration: A Cellular Perspective

inferredcites →https://doi.org/10.1093/molbev/msu080openalex-snapshot

Illuminating the Base of the Annelid Tree Using Transcriptomics

inferredcites →https://doi.org/10.1093/mollus/65.2.223openalex-snapshot

Recovery from Siphon Damage in Donax vittatus (Da Costa) (Bivalvia: Donacidae)

inferredcites →https://doi.org/10.1098/rspb.1952.0045openalex-snapshot

The respiratory significance of the crown in the polychaete worms Sabella and Myxicola

inferredcites →https://doi.org/10.1098/rspb.2002.2254openalex-snapshot

Ribbon worm relationships: a phylogeny of the phylum Nemertea

inferredcites →https://doi.org/10.1098/rspb.2009.1340openalex-snapshot

MicroRNAs resolve an apparent conflict between annelid systematics and their fossil record

inferredcites →https://doi.org/10.1098/rspb.2012.1943openalex-snapshot

Cost of autotomy drives ontogenetic switching of anti-predator mechanisms under developmental constraints in a land snail

inferredcites →https://doi.org/10.1101/sqb.2008.73.022openalex-snapshot

Germ Cell Specification and Regeneration in Planarians

inferredcites →https://doi.org/10.1111/ivb.12002openalex-snapshot

Characterization of serine proteases of Lumbriculus variegatus and their role in regeneration

inferredcites →https://doi.org/10.1111/j.1096-0031.2006.00128.xopenalex-snapshot

A molecular phylogeny of annelids

inferredcites →https://doi.org/10.1111/j.1096-0031.2011.00376.xopenalex-snapshot

Disentangling ribbon worm relationships: multi‐locus analysis supports traditional classification of the phylum Nemertea

inferredcites →https://doi.org/10.1111/j.1440-169x.2004.00763.xopenalex-snapshot

Nerve development, growth and differentiation during regeneration inEnchytraeus fragmentosusandStylaria lacustris(Oligochaeta)

inferredcites →https://doi.org/10.1111/j.1440-169x.2009.01149.xopenalex-snapshot

Stem cell system in asexual and sexual reproduction of Enchytraeus japonensis (Oligochaeta, Annelida)

inferredcites →https://doi.org/10.1111/j.1440-169x.2012.01328.xopenalex-snapshot

Stem cells in asexual reproduction of Enchytraeus japonensis (Oligochaeta, Annelid): Proliferation and migration of neoblasts

inferredcites →https://doi.org/10.1111/j.1463-6409.2004.00146.xopenalex-snapshot

18S rDNA phylogeny of Clitellata (Annelida)

inferredcites →https://doi.org/10.1111/j.1525-142x.2007.00180.xopenalex-snapshot

Phylogenetic distribution of microRNAs supports the basal position of acoel flatworms and the polyphyly of Platyhelminthes

inferredcites →https://doi.org/10.1111/j.1525-142x.2010.00458.xopenalex-snapshot

Evolution of a novel developmental trajectory: fission is distinct from regeneration in the annelid Pristina leidyi

inferredcites →https://doi.org/10.1111/j.1744-7410.2007.00114.xopenalex-snapshot

Morphology of anterior regeneration in two spionid polychaete species: implications for feeding efficiency

inferredcites →https://doi.org/10.1111/j.1744-7410.2010.00195.xopenalex-snapshot

Regeneration of the visual system in gastropods (Mollusca)

inferredcites →https://doi.org/10.1126/science.1149943openalex-snapshot

Smed- β catenin-1 Is Required for Anteroposterior Blastema Polarity in Planarian Regeneration

inferredcites →https://doi.org/10.1126/science.1150029openalex-snapshot

β-Catenin Defines Head Versus Tail Identity During Planarian Regeneration and Homeostasis

inferredcites →https://doi.org/10.1126/science.1188913openalex-snapshot

Hedgehog Signaling Regulates Segment Formation in the Annelid Platynereis

inferredcites →https://doi.org/10.1126/science.1203983openalex-snapshot

Clonogenic Neoblasts Are Pluripotent Adult Stem Cells That Underlie Planarian Regeneration

inferredcites →https://doi.org/10.1126/science.283.5409.1919openalex-snapshot

Acoel Flatworms: Earliest Extant Bilaterian Metazoans, Not Members of Platyhelminthes

inferredcites →https://doi.org/10.1139/z68-120openalex-snapshot

On regeneration of the tentacular arm of the giant squid Architeuthis dux Steenstrup (Decapoda, Architeuthidae)

inferredcites →https://doi.org/10.1146/annurev.cellbio.20.010403.095114openalex-snapshot

FUNDAMENTALS OF PLANARIAN REGENERATION

inferredcites →https://doi.org/10.1146/annurev.cellbio.24.110707.175336openalex-snapshot

Comparative Aspects of Animal Regeneration

inferredcites →https://doi.org/10.1146/annurev.ecolsys.35.112202.130124openalex-snapshot

The New View of Animal Phylogeny

inferredcites →https://doi.org/10.1155/2012/167265openalex-snapshot

The FlatwormMacrostomum lignanoIs a Powerful Model Organism for Ion Channel and Stem Cell Research

inferredcites →https://doi.org/10.11646/zootaxa.1668.1.8openalex-snapshot

A modern look at the Animal Tree of Life*

inferredcites →https://doi.org/10.1186/1471-2148-7-57openalex-snapshot

Annelid phylogeny and the status of Sipuncula and Echiura

inferredcites →https://doi.org/10.1186/1742-9994-7-22openalex-snapshot

Stem cell proliferation during in vitro development of the model cestode Mesocestoides corti from larva to adult worm

inferredcites →https://doi.org/10.1186/2041-9139-2-10openalex-snapshot

Somatic and germline expression of piwi during development and regeneration in the marine polychaete annelid Capitella teleta

inferredcites →https://doi.org/10.1186/2041-9139-4-14openalex-snapshot

Expression of Hox genes during regeneration of nereid polychaete Alitta (Nereis) virens (Annelida, Lophotrochozoa)

inferredcites →https://doi.org/10.1186/jbiol223openalex-snapshot

Acoel and platyhelminth models for stem-cell research

inferredcites →https://doi.org/10.1242/dev.060764openalex-snapshot

ERK signaling controls blastema cell differentiation during planarian regeneration

inferredcites →https://doi.org/10.1242/dev.082099openalex-snapshot

Amputation induces stem cell mobilization to sites of injury during planarian regeneration

inferredcites →https://doi.org/10.1242/dev.107.1.77openalex-snapshot

Regeneration and pattern formation in planarians: III. Evidence that neoblasts are totipotent stem cells and the source of blastema cells

inferredcites →https://doi.org/10.1242/dev.22.2.279openalex-snapshot

Gut and nerve-cord interaction in sabellid regeneration

inferredcites →https://doi.org/10.1242/dev.47.1.85openalex-snapshot

Induced segmental reorganization in sabellid worms

inferredcites →https://doi.org/10.1242/jeb.046938openalex-snapshot

Effects of tentacle amputation and regeneration on the morphology and activity of the olfactory center of the terrestrial slug Limax valentianus

inferredcites →https://doi.org/10.1242/jeb.204.2.283openalex-snapshot

Hydrobia Ulvae (Gastropoda: Prosobranchia): a New Model for Regeneration Studies

inferredcites →https://doi.org/10.1371/journal.pone.0000717openalex-snapshot

Acoel Flatworms Are Not Platyhelminthes: Evidence from Phylogenomics

inferredcites →https://doi.org/10.1371/journal.pone.0037319openalex-snapshot

What Role Do Annelid Neoblasts Play? A Comparison of the Regeneration Patterns in a Neoblast-Bearing and a Neoblast-Lacking Enchytraeid Oligochaete

inferredcites →https://doi.org/10.1387/ijdb.072414esopenalex-snapshot

Planarian regeneration: achievements and future directions after 20 years of research

inferredcites →https://doi.org/10.1387/ijdb.082790mtopenalex-snapshot

Functional analysis of grimp, a novel gene required for mesodermal cell proliferation at an initial stage of regeneration in Enchytraeus japonensis (Enchytraeidae, Oligochaete)

inferredcites →https://doi.org/10.1387/ijdb.113441mropenalex-snapshot

Evolutionary history of the Tricladida and the Platyhelminthes: an up-to-date phylogenetic and systematic account

inferredcites →https://doi.org/10.1387/ijdb.113442jmopenalex-snapshot

Planarian embryology in the era of comparative developmental biology

inferredcites →https://doi.org/10.1387/ijdb.120056caopenalex-snapshot

Brachyury, Tbx2/3 and sall expression during embryogenesis of the indirectly developing polychaete Hydroides elegans

inferredcites →https://doi.org/10.2307/1535722openalex-snapshot

NOTES ON REGENERATION

inferredcites →https://doi.org/10.2307/1537383openalex-snapshot

ANALYSIS OF THE REGENERATIVE PROCESSES IN NEMERTEANS

inferredcites →https://doi.org/10.2307/3276836openalex-snapshot

Longevity of the Tapeworm, Hymenolepis diminuta

inferredcites →https://doi.org/10.2307/3277128openalex-snapshot

Regeneration of Tetrathyridia of Mesocestoides (Cestoda: Cyclophyllidea) In vivo and In vitro

inferredcites →https://doi.org/10.2307/3278675openalex-snapshot

The Inheritance of X-Irradiation-Induced Effects in the Rat Tapeworm, Hymenolepis diminuta

inferredcites →https://doi.org/10.3354/meps09714openalex-snapshot

Economy of arm autotomy in the mesopelagic squid Octopoteuthis deletron

inferredcites →https://doi.org/10.5281/zenodo.13674442openalex-snapshot

The Morphology And Generic Relationships Of Some Fissiparous heteronemertines

inferredcites →https://doi.org/10.5451/unibas-004256214openalex-snapshot

Homeobox-containing genes in the nemertean "Lineus" : key players in the antero-posterior body patterning and in the specification of the visual structures

What points at this work

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

inferred← citeshttps://doi.org/10.11646/zootaxa.5646.4.1zenodo-depositor-declared

A taxonomic revision of the freshwater monostiliferous hoplonemertean genus Prostoma Dugès, 1828 (Nemertea: Eumonostilifera): a radical solution or an over-lumping?

inferred← citeshttps://doi.org/10.1002/9780470015902.a0022103.pub2openalex-snapshot

Evolutionary Aspects of Annelid Regeneration

inferred← citeshttps://doi.org/10.1002/jez.b.23233openalex-snapshot

Annelids as models of germ cell and gonad regeneration

inferred← citeshttps://doi.org/10.1002/reg2.78openalex-snapshot

Regulation of dorso-ventral polarity by the nerve cord during annelid regeneration: A review of experimental evidence

inferred← citeshttps://doi.org/10.1002/reg2.98openalex-snapshot

Regeneration mechanisms in Syllidae (Annelida)

inferred← citeshttps://doi.org/10.1007/978-1-0716-2172-1_11openalex-snapshot

Studying Annelida Regeneration Using Platynereis dumerilii

inferred← citeshttps://doi.org/10.1007/978-1-0716-2172-1_12openalex-snapshot

Collecting and Culturing Lineus sanguineus to Study Nemertea WBR

inferred← citeshttps://doi.org/10.1007/s00227-016-2854-6openalex-snapshot

Quantitative regeneration in bivalve siphons: difference between short- and long-siphoned species

inferred← citeshttps://doi.org/10.1007/s13127-019-00412-4openalex-snapshot

Recent progress in reconstructing lophotrochozoan (spiralian) phylogeny

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.gde.2016.07.010openalex-snapshot

Developmental and molecular biology of annelid regeneration: a comparative review of recent studies

inferred← citeshttps://doi.org/10.1016/j.jcz.2017.07.004openalex-snapshot

Nervous system regeneration in Typosyllis antoni (Annelida: Syllidae)

inferred← citeshttps://doi.org/10.1016/j.jcz.2017.09.005openalex-snapshot

Rhodope placozophagus (Heterobranchia) a new species of turbellarian-like Gastropoda that preys on placozoans

inferred← citeshttps://doi.org/10.1016/j.ydbio.2018.05.004openalex-snapshot

Regeneration of the germline in the annelid Capitella teleta

inferred← citeshttps://doi.org/10.1016/j.ygeno.2021.02.010openalex-snapshot

Molecular mechanisms of wound healing and regeneration of siphon in the Manila clam Ruditapes philippinarum revealed by transcriptomic analysis

inferred← citeshttps://doi.org/10.1038/s41467-024-54041-3openalex-snapshot

Molecular profiles, sources and lineage restrictions of stem cells in an annelid regeneration model

inferred← citeshttps://doi.org/10.1038/srep12072openalex-snapshot

The making of a branching annelid: an analysis of complete mitochondrial genome and ribosomal data of Ramisyllis multicaudata

inferred← citeshttps://doi.org/10.1086/741621openalex-snapshot

Regeneration and Caudal Segmentation in Phragmatopoma californica (Annelida: Sabellariidae)

inferred← citeshttps://doi.org/10.1093/bfgp/elad038openalex-snapshot

Single-cell transcriptomics refuels the exploration of spiralian biology

inferred← citeshttps://doi.org/10.1093/bfgp/elad043openalex-snapshot

Emerging questions on the mechanisms and dynamics of 3D genome evolution in spiralians

inferred← citeshttps://doi.org/10.1093/g3journal/jkaf164openalex-snapshot

The chromosome-level genome assembly of the slug Deroceras laeve facilitates its use as a comparative model of regeneration

inferred← citeshttps://doi.org/10.1093/gbe/evy144openalex-snapshot

A Revised Spiralian Homeobox Gene Classification Incorporating New Polychaete Transcriptomes Reveals a Diverse TALE Class and a Divergent Hox Gene

inferred← citeshttps://doi.org/10.1093/gbe/evz021openalex-snapshot

JmjC Domain-Encoding Genes Are Conserved in Highly Regenerative Metazoans and Are Associated with Planarian Whole-Body Regeneration

inferred← citeshttps://doi.org/10.1093/oso/9780198786962.003.0005openalex-snapshot

Asexual Reproduction of Marine Invertebrate Embryos and Larvae

inferred← citeshttps://doi.org/10.1098/rspb.2018.2524openalex-snapshot

A phylum-wide survey reveals multiple independent gains of head regeneration in Nemertea

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/10.1111/1365-2435.14525openalex-snapshot

Investment in regeneration versus asexual reproduction is resource‐dependent in a freshwater annelid

inferred← citeshttps://doi.org/10.1111/azo.12487openalex-snapshot

Regeneration and regengrow in multicellular animals derive from the presence of processes of organ metamorphosis and continuous growth in their life cycles

inferred← citeshttps://doi.org/10.1111/brv.12801openalex-snapshot

A pan‐metazoan concept for adult stem cells: the wobbling Penrose landscape

inferred← citeshttps://doi.org/10.1111/brv.12894openalex-snapshot

Integrative biology of injury in animals

inferred← citeshttps://doi.org/10.1111/ivb.12151openalex-snapshot

Phylogenetic distribution of regeneration and asexual reproduction in Annelida: regeneration is ancestral and fission evolves in regenerative clades

inferred← citeshttps://doi.org/10.1111/ivb.12154openalex-snapshot

Sequestration of nematocysts by divergent cnidarian predators: mechanism, function, and evolution

inferred← citeshttps://doi.org/10.1134/s1062359022140151openalex-snapshot

Assessment of the Effect of Valproic Acid on Regeneration in Eisenia fetida

inferred← citeshttps://doi.org/10.1134/s106307402006005xopenalex-snapshot

Variability of Regeneration Mechanisms in Echinoderms

inferred← citeshttps://doi.org/10.1186/s12864-019-6223-yopenalex-snapshot

Comparative transcriptomics in Syllidae (Annelida) indicates that posterior regeneration and regular growth are comparable, while anterior regeneration is a distinct process

inferred← citeshttps://doi.org/10.1186/s12864-023-09602-zopenalex-snapshot

Transcriptomic landscape of posterior regeneration in the annelid Platynereis dumerilii

inferred← citeshttps://doi.org/10.1186/s12864-026-12671-5openalex-snapshot

Transcriptomic analysis of three annelid species: looking for markers of positional information

inferred← citeshttps://doi.org/10.1186/s12983-024-00544-0openalex-snapshot

Explosive regeneration and anamorphic development of legs in the house centipede Scutigera coleoptrata

inferred← citeshttps://doi.org/10.1186/s40851-015-0023-2openalex-snapshot

Morphological investigations of posttraumatic regeneration in Timarete cf. punctata (Annelida: Cirratulidae)

inferred← citeshttps://doi.org/10.1371/journal.pone.0149724openalex-snapshot

A Stable Thoracic Hox Code and Epimorphosis Characterize Posterior Regeneration in Capitella teleta

inferred← citeshttps://doi.org/10.1371/journal.pone.0312407openalex-snapshot

SlugAtlas, a histological and 3D online resource of the land slugs Deroceras laeve and Ambigolimax valentianus

inferred← citeshttps://doi.org/10.1387/ijdb.140154esopenalex-snapshot

Variation in spiralian development: insights from polychaetes

inferred← citeshttps://doi.org/10.1387/ijdb.160321esopenalex-snapshot

The pioneer factor Smed-gata456-1 is required for gut cell differentiation and maintenance in planarians

inferred← citeshttps://doi.org/10.1387/ijdb.170110jhopenalex-snapshot

Beyond the sea: Crepidula atrasolea as a spiralian model system

inferred← citeshttps://doi.org/10.1387/ijdb.180049fsopenalex-snapshot

Elly Tanaka’s passion for exploring animal regeneration

inferred← citeshttps://doi.org/10.1590/2675-2824072.24024openalex-snapshot

Regeneration patterns in Naineris aurantiaca (Muller, 1858) (Annelida, Orbiniidae)

inferred← citeshttps://doi.org/10.2108/zs180203openalex-snapshot

A Population Without Females: Males of Baseodiscus delineatus (Nemertea: Heteronemertea) Reproduce Asexually by Fragmentation

inferred← citeshttps://doi.org/10.3389/fcell.2023.1206157openalex-snapshot

The salamander blastema within the broader context of metazoan regeneration

inferred← citeshttps://doi.org/10.3389/fevo.2021.621686openalex-snapshot

Evolution of Regeneration in Animals: A Tangled Story

inferred← citeshttps://doi.org/10.3389/fmars.2023.1195253openalex-snapshot

Molecular bioinformatic and functional analysis of Enolase4 gene during siphonal autotomy and regeneration of razor clam Solen grandis

inferred← citeshttps://doi.org/10.3390/genes12040506openalex-snapshot

Whole-Body Regeneration in Sponges: Diversity, Fine Mechanisms, and Future Prospects

inferred← citeshttps://doi.org/10.3923/ajsr.2021.32.42openalex-snapshot

Regeneration of the Posterior Segments in the Clam Worm Platynereis dumerilii (Audouin and Milne Edwards, 1833) (Polychaeta, Phyllodocida)

inferred← citeshttps://doi.org/10.6084/m9.figshare.26621959openalex-snapshot

Additional file 1 of Transcriptomic landscape of posterior regeneration in the annelid Platynereis dumerilii

inferred← citeshttps://doi.org/10.6084/m9.figshare.26621962openalex-snapshot

Additional file 2 of Transcriptomic landscape of posterior regeneration in the annelid Platynereis dumerilii

inferred← citeshttps://doi.org/10.6084/m9.figshare.26621965openalex-snapshot

Additional file 3 of Transcriptomic landscape of posterior regeneration in the annelid Platynereis dumerilii

inferred← citeshttps://doi.org/10.6084/m9.figshare.26621968openalex-snapshot

Additional file 4 of Transcriptomic landscape of posterior regeneration in the annelid Platynereis dumerilii

inferred← citeshttps://doi.org/10.6084/m9.figshare.26621971openalex-snapshot

Additional file 5 of Transcriptomic landscape of posterior regeneration in the annelid Platynereis dumerilii

inferred← citeshttps://doi.org/10.6084/m9.figshare.26621974openalex-snapshot

Additional file 6 of Transcriptomic landscape of posterior regeneration in the annelid Platynereis dumerilii

inferred← citeshttps://doi.org/10.6084/m9.figshare.26621977openalex-snapshot

Additional file 7 of Transcriptomic landscape of posterior regeneration in the annelid Platynereis dumerilii

inferred← citeshttps://doi.org/10.6084/m9.figshare.26621980openalex-snapshot

Additional file 8 of Transcriptomic landscape of posterior regeneration in the annelid Platynereis dumerilii

inferred← citeshttps://doi.org/10.6084/m9.figshare.26621983openalex-snapshot

Additional file 9 of Transcriptomic landscape of posterior regeneration in the annelid Platynereis dumerilii

inferred← citeshttps://doi.org/10.6084/m9.figshare.26621986openalex-snapshot

Additional file 10 of Transcriptomic landscape of posterior regeneration in the annelid Platynereis dumerilii

inferred← citeshttps://doi.org/10.6084/m9.figshare.26621989openalex-snapshot

Additional file 11 of Transcriptomic landscape of posterior regeneration in the annelid Platynereis dumerilii

inferred← citeshttps://doi.org/10.6084/m9.figshare.26621992openalex-snapshot

Additional file 12 of Transcriptomic landscape of posterior regeneration in the annelid Platynereis dumerilii

inferred← citeshttps://doi.org/10.6084/m9.figshare.26621998openalex-snapshot

Additional file 13 of Transcriptomic landscape of posterior regeneration in the annelid Platynereis dumerilii

inferred← citeshttps://doi.org/10.6084/m9.figshare.26622001openalex-snapshot

Additional file 14 of Transcriptomic landscape of posterior regeneration in the annelid Platynereis dumerilii

inferred← citeshttps://doi.org/10.6084/m9.figshare.26622004openalex-snapshot

Additional file 15 of Transcriptomic landscape of posterior regeneration in the annelid Platynereis dumerilii

inferred← citeshttps://doi.org/10.6084/m9.figshare.26622007openalex-snapshot

Additional file 16 of Transcriptomic landscape of posterior regeneration in the annelid Platynereis dumerilii

inferred← citeshttps://doi.org/10.6084/m9.figshare.26622013openalex-snapshot

Additional file 17 of Transcriptomic landscape of posterior regeneration in the annelid Platynereis dumerilii

inferred← citeshttps://doi.org/10.6084/m9.figshare.26622016openalex-snapshot

Additional file 18 of Transcriptomic landscape of posterior regeneration in the annelid Platynereis dumerilii

inferred← citeshttps://doi.org/10.6084/m9.figshare.26622019openalex-snapshot

Additional file 19 of Transcriptomic landscape of posterior regeneration in the annelid Platynereis dumerilii

inferred← citeshttps://doi.org/10.6084/m9.figshare.26622022openalex-snapshot

Additional file 20 of Transcriptomic landscape of posterior regeneration in the annelid Platynereis dumerilii

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