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Regeneration mechanisms in Syllidae (Annelida)

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/dvdy.20849openalex-snapshot

Molecular approach to annelid regeneration: cDNA subtraction cloning reveals various novel genes that are upregulated during the large‐scale regeneration of the oligochaete, Enchytraeus japonensis

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/jmor.20316openalex-snapshot

Structure and anterior regeneration of musculature and nervous system inCirratuluscf.cirratus(Cirratulidae, Annelida)

inferredcites →https://doi.org/10.1002/jmor.20496openalex-snapshot

Myoanatomy and anterior muscle regeneration of the fireworm Eurythoe cf. complanata (Annelida: Amphinomidae)

inferredcites →https://doi.org/10.1002/reg2.78openalex-snapshot

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

inferredcites →https://doi.org/10.1002/reg2.94openalex-snapshot

Investigation into the cellular origins of posterior regeneration in the annelid Capitella teleta

inferredcites →https://doi.org/10.1002/reg2.98openalex-snapshot

Regeneration mechanisms in Syllidae (Annelida)

inferredcites →https://doi.org/10.1007/978-94-017-2887-4_3openalex-snapshot

Reproduction of the Syllidae (Annelida: Polychaeta)

inferredcites →https://doi.org/10.1007/bf00848444openalex-snapshot

The effects of prostomium and proventriculus removal on sex determination and gametogenesis inTyposyllis pulchra (Polychaeta: Syllidae)

inferredcites →https://doi.org/10.1007/bf00848485openalex-snapshot

Endocrine mechanisms mediating light-temperature effects on male reproductive activity inTyposyllis prolifera (polychaeta, syllidae)

inferredcites →https://doi.org/10.1007/bf01983542openalex-snapshot

Zur Determination der zeitlichen Verteilung von Fortpflanzungsprozessen in Laborkulturen des PolychaetenTyposyllis prolifera

inferredcites →https://doi.org/10.1007/bf02079006openalex-snapshot

Regeneration and fragmentation in the Syllidian Polychaetes

inferredcites →https://doi.org/10.1007/bf02161891openalex-snapshot

Studies on regulation

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/s004270050318openalex-snapshot

Nervous system dynamics during fragmentation and regeneration in Enchytraeus japonensis (Oligochaeta, Annelida)

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/s10719-017-9778-3openalex-snapshot

Isolation of a methylated mannose-binding protein from terrestrial worm Enchytraeus japonensis

inferredcites →https://doi.org/10.1007/s13127-014-0183-5openalex-snapshot

Description of a new syllid species as a model for evolutionary research of reproduction and regeneration in annelids

inferredcites →https://doi.org/10.1016/b978-0-12-282503-3.50007-9openalex-snapshot

ANNELIDA: POLYCHAETA

inferredcites →https://doi.org/10.1016/j.ccell.2017.02.005openalex-snapshot

Nerve Dependence: From Regeneration to Cancer

inferredcites →https://doi.org/10.1016/j.cub.2003.10.006openalex-snapshot

Arthropod-like Expression Patterns of engrailed and wingless in the Annelid Platynereis dumerilii Suggest a Role in Segment Formation

inferredcites →https://doi.org/10.1016/j.gde.2016.07.010openalex-snapshot

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

inferredcites →https://doi.org/10.1016/j.jcz.2017.07.004openalex-snapshot

Nervous system regeneration in Typosyllis antoni (Annelida: Syllidae)

inferredcites →https://doi.org/10.1016/j.molcel.2015.04.028openalex-snapshot

Choosing the Right Tool for the Job: RNAi, TALEN, or CRISPR

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.2015.06.001openalex-snapshot

Gonad establishment during asexual reproduction in the annelid Pristina leidyi

inferredcites →https://doi.org/10.1016/j.ydbio.2016.07.005openalex-snapshot

FGF and BMP derived from dorsal root ganglia regulate blastema induction in limb regeneration in Ambystoma mexicanum

inferredcites →https://doi.org/10.1016/s1055-7903(03)00095-2openalex-snapshot

Phylogeny and evolution of reproductive modes in Autolytinae (Syllidae, Annelida)

inferredcites →https://doi.org/10.1017/s0025315400010079openalex-snapshot

Stolonization in Myrianida

inferredcites →https://doi.org/10.1017/s0025315400043964openalex-snapshot

Syllidian Miscellany

inferredcites →https://doi.org/10.1017/s0025315400051122openalex-snapshot

Fragmentation in the Genus Autolytus and in other Syllids

inferredcites →https://doi.org/10.1017/s0025315400053960openalex-snapshot

An Internal Factor Controlling Posterior Regeneration in Syllid Polychaetes

inferredcites →https://doi.org/10.1017/s002531541700039xopenalex-snapshot

New observations on reproduction in the branching polychaetes Ramisyllis multicaudata and Syllis ramosa (Annelida: Syllidae: Syllinae)

inferredcites →https://doi.org/10.1023/a:1003732307286openalex-snapshot

Reproduction of the Syllidae (Annelida: Polychaeta)

inferredcites →https://doi.org/10.1038/nature12214openalex-snapshot

Wnt activation in nail epithelium couples nail growth to digit regeneration

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

Bridging the regeneration gap: genetic insights from diverse animal models

inferredcites →https://doi.org/10.1038/srep10771openalex-snapshot

Correction: Corrigendum: Simultaneous submicrometric 3D imaging of the micro-vascular network and the neuronal system in a mouse spinal cord

inferredcites →https://doi.org/10.1038/srep12072openalex-snapshot

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

inferredcites →https://doi.org/10.1046/j.1440-169x.1999.00455.xopenalex-snapshot

Fragmenting oligochaete Enchytraeus japonensis: A new material for regeneration study

inferredcites →https://doi.org/10.1071/it9931551openalex-snapshot

Family revision and cladistic analysis of the Nereidoidea (Polychaeta : Phyllodocida)

inferredcites →https://doi.org/10.1086/275581openalex-snapshot

Bifurcated Annelids

inferredcites →https://doi.org/10.1086/278120openalex-snapshot

Collateral Budding in Annelids of the Genus Trypanosyllis

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

Aspects of Regeneration in Annelids

inferredcites →https://doi.org/10.1093/icb/26.2.433openalex-snapshot

The Role of Light and Endogenous Factors in the Timing of the Reproductive Cycle ofTyposyllis proliferaand some other Polychaetes

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

Distribution of segment regeneration ability in the Annelida

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

Early Events in Annelid Regeneration: A Cellular Perspective

inferredcites →https://doi.org/10.1098/rstb.1923.0003openalex-snapshot

III.—Regeneration and reproduction of the syllid procerastea

inferredcites →https://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

inferredcites →https://doi.org/10.1111/j.1096-0031.2007.00163.xopenalex-snapshot

Phylogeny of Syllidae (Polychaeta) based on combined molecular analysis of nuclear and mitochondrial genes

inferredcites →https://doi.org/10.1111/j.1096-0031.2011.00377.xopenalex-snapshot

Systematics and evolution of syllids (Annelida, Syllidae)

inferredcites →https://doi.org/10.1111/j.1096-3642.1879.tb02356.xopenalex-snapshot

On a Remarkably Branched Syllis, dredged by H.M.S. ‘Challenger.’

inferredcites →https://doi.org/10.1111/j.1096-3642.2011.00800.xopenalex-snapshot

Branching out: a remarkable new branching syllid (Annelida) living in a Petrosia sponge (Porifera: Demospongiae)

inferredcites →https://doi.org/10.1111/j.1440-169x.2007.00919.xopenalex-snapshot

Unifying principles of regeneration I: Epimorphosis versus morphallaxis

inferredcites →https://doi.org/10.1111/j.1463-6409.1997.tb00411.xopenalex-snapshot

Polychaete systematics: Past and present

inferredcites →https://doi.org/10.1111/j.1463-6409.2008.00380.xopenalex-snapshot

Phylogeny of Syllidae (Polychaeta) based on morphological data

inferredcites →https://doi.org/10.1111/j.1469-185x.1952.tb01512.xopenalex-snapshot

REGENERATON AND BUDDING IN WORMS

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/10.1134/s1062360417030079openalex-snapshot

Regeneration of the nervous and muscular system after caudal amputation in the polychaete Alitta virens (Annelida: Nereididae)

inferredcites →https://doi.org/10.1139/z74-020openalex-snapshot

Etude histologique de la régénération pharyngienne de Syllis gracilis Grube (Annélide, Polychète)

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

Comparative Aspects of Animal Regeneration

inferredcites →https://doi.org/10.11646/zootaxa.1840.1.1openalex-snapshot

Syllinae (Polychaeta, Syllidae) from Australia. Part. 2. Genera Inermosyllis, Megasyllis n. gen., Opisthosyllis, and Trypanosyllis

inferredcites →https://doi.org/10.11646/zootaxa.2493.1.3openalex-snapshot

Syllinae (Polychaeta: Syllidae) from Australia. Part 3. Genera Alcyonosyllis, Genus A, Parahaplosyllis, and Trypanosyllis (Trypanobia)

inferredcites →https://doi.org/10.11646/zootaxa.3734.2.4openalex-snapshot

A new species and new record of the commensal genus Alcyonosyllis Glasby & Watson, 2001 and a new species of Parahaplosyllis Hartmann-Schröder, 1990, (Annelida: Syllidae: Syllinae) from Philippines Islands

inferredcites →https://doi.org/10.1186/1471-2164-13-287openalex-snapshot

Transcriptome characterization via 454 pyrosequencing of the annelid Pristina leidyi, an emerging model for studying the evolution of regeneration

inferredcites →https://doi.org/10.1186/2041-9139-4-13openalex-snapshot

Hox gene expression during postlarval development of the polychaete Alitta virens

inferredcites →https://doi.org/10.1186/2041-9139-4-21openalex-snapshot

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

inferredcites →https://doi.org/10.1186/s12862-016-0770-5openalex-snapshot

On the role of the proventricle region in reproduction and regeneration in Typosyllis antoni (Annelida: Syllidae)

inferredcites →https://doi.org/10.1186/s12983-017-0211-3openalex-snapshot

Development of the nervous system in Platynereis dumerilii (Nereididae, Annelida)

inferredcites →https://doi.org/10.1186/s13227-016-0059-1openalex-snapshot

Plasticity and regeneration of gonads in the annelid Pristina leidyi

inferredcites →https://doi.org/10.1186/s40851-015-0023-2openalex-snapshot

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

inferredcites →https://doi.org/10.1201/9781482280159openalex-snapshot

Reproductive Biology and Phylogeny of Annelida

inferredcites →https://doi.org/10.1242/dev.128.14.2781openalex-snapshot

Evolution of regeneration and fission in annelids: insights fromengrailed- andorthodenticle-class gene expression

inferredcites →https://doi.org/10.1242/jcs.58.1.411openalex-snapshot

Ultrastructural analysis of the x, X2X3O sex chromosome system during the spermatogenesis of Tegenaria domestica (arachnida)

inferredcites →https://doi.org/10.1242/jcs.s2-58.231.411openalex-snapshot

Stolon Formation in Certain Species of Trypanosyllis

inferredcites →https://doi.org/10.1387/ijdb.140142abopenalex-snapshot

Regeneration in spiralians: evolutionary patterns and developmental processes

inferredcites →https://doi.org/10.1387/ijdb.140148gbopenalex-snapshot

Segment formation in Annelids: patterns, processes and evolution

inferredcites →https://doi.org/10.1387/ijdb.14756334openalex-snapshot

Segmentation: mono- or polyphyletic?

inferredcites →https://doi.org/10.2108/zs130259openalex-snapshot

Segment Regeneration in the Vestimentiferan Tubeworm, Lamellibrachia satsuma

inferredcites →https://doi.org/10.21411/cbm.a.814b9b30openalex-snapshot

SUR LA RÉGÉNÉRATION D'UN INTESTIN DANS LA ZONE PHARYNGIENNE CHEZ SYLLIS AMICA QUATREFAGES (ANNÉLIDE POLYCHÈTE)

inferredcites →https://doi.org/10.5479/si.00963801.14-852.277openalex-snapshot

Report upon the Annelida Polychaeta of Beaufort, North Carolina

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.5244.4.2zenodo-depositor-declared

Another piece for the syllid puzzle: A new species from Japan and its mitochondrial genome reveal the enigmatic Clavisyllis (Phyllodocida: Syllidae) as a member of Eusyllinae

inferred← citeshttps://doi.org/10.1002/dvdy.751openalex-snapshot

Functional significance of earthworm clitellum in regulating the various biological aspects of cell survival and regeneration

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

Annelids as models of germ cell and gonad regeneration

inferred← citeshttps://doi.org/10.1007/s00227-024-04468-5openalex-snapshot

Effect of temperature and body size on anterior and posterior regeneration in Hermodice carunculata (Polychaeta, Amphinomidae)

inferred← citeshttps://doi.org/10.1007/s00343-021-0378-5openalex-snapshot

Taxonomy and regeneration of a newly recorded Polychaete Capitella teleta (Annelida, Capitellidae) in the coastal water of Shandong, China

inferred← citeshttps://doi.org/10.1007/s00427-024-00713-5openalex-snapshot

Nerves and availability of mesodermal cells are essential for the function of the segment addition zone (SAZ) during segment regeneration in polychaete annelids

inferred← citeshttps://doi.org/10.1007/s12526-020-01046-yopenalex-snapshot

A new species of Syllis Grube, 1850 including transcriptomic data and an updated phylogeny of Syllinae (Annelida: Syllidae)

inferred← citeshttps://doi.org/10.1007/s13258-020-01031-6openalex-snapshot

Identification and expression of adenosine deaminases acting on tRNA (ADAT) during early tail regeneration of the earthworm

inferred← citeshttps://doi.org/10.1016/j.biomaterials.2020.120646openalex-snapshot

Unlocking mammalian regeneration through hypoxia inducible factor one alpha signaling

inferred← citeshttps://doi.org/10.1016/j.ecss.2024.108619openalex-snapshot

Macroalgae traits and seasonality as drivers of polychaete assemblages on macroalgae of tropical sandstone reefs

inferred← citeshttps://doi.org/10.1016/j.gene.2024.148636openalex-snapshot

Profiling microRNAs of earthworm, Perionyx excavatus and deciphering the expression of distinct novel miRNAs regulating epimorphosis regeneration

inferred← citeshttps://doi.org/10.1017/s0025315420000119openalex-snapshot

Atypical reproduction in a syllid worm: the stolon ofSyllis rosea(Annelida, Syllidae) takes care of its offspring

inferred← citeshttps://doi.org/10.1038/s41598-020-68200-1openalex-snapshot

Multiple cryoinjuries modulate the efficiency of zebrafish heart regeneration

inferred← citeshttps://doi.org/10.1073/pnas.2217272120openalex-snapshot

The sea spider Pycnogonum litorale overturns the paradigm of the absence of axial regeneration in molting animals

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.12826openalex-snapshot

Monsters reveal patterns: bifurcated annelids and their implications for the study of development and evolution

inferred← citeshttps://doi.org/10.1111/dgd.12961openalex-snapshot

Regeneration of Lumbriculus variegatus requires post‐amputation production of reactive oxygen species

inferred← citeshttps://doi.org/10.1111/ede.12263openalex-snapshot

Expression of vasa, piwi, and nanos during gametogenesis in Typosyllis antoni (Annelida, Syllidae)

inferred← citeshttps://doi.org/10.1111/ede.12477openalex-snapshot

Secondary‐tail formation during stolonization in the Japanese green syllid, Megasyllis nipponica

inferred← citeshttps://doi.org/10.1111/ede.12492openalex-snapshot

From two segments and beyond: Investigating the onset of regeneration in Syllis malaquini

inferred← citeshttps://doi.org/10.1134/s1062359020030048openalex-snapshot

Morphallaxis versus Epimorphosis? Cellular and Molecular Aspects of Regeneration and Asexual Reproduction in Annelids

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

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

inferred← citeshttps://doi.org/10.1186/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/s12983-021-00396-yopenalex-snapshot

Cellular proliferation dynamics during regeneration in Syllis malaquini (Syllidae, Annelida)

inferred← citeshttps://doi.org/10.1371/journal.pone.0293087openalex-snapshot

New species and record of Dodecaceria (Annelida: Cirratulidae) the Biological Reserve of Rocas Atoll, Brazil, the only atoll in the South Atlantic Ocean

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/zs190058openalex-snapshot

Life Cycle of the Japanese Green Syllid, Megasyllis nipponica (Annelida: Syllidae): Field Collection and Establishment of Rearing System

inferred← citeshttps://doi.org/10.2108/zs200085openalex-snapshot

The Germline Marker Piwi Expressed in the Skin Layer of the Polychaete Perinereis wilsoni After Injury

inferred← citeshttps://doi.org/10.2108/zs250076openalex-snapshot

Beyond Individuality: Developmental and Evolutionary Deviations in Animal Body Plans

inferred← citeshttps://doi.org/10.3389/fcell.2021.780422openalex-snapshot

It Cuts Both Ways: An Annelid Model System for the Study of Regeneration in the Laboratory and in the Classroom

inferred← citeshttps://doi.org/10.3389/fcell.2023.1229613openalex-snapshot

Editorial: Regeneration from cells to limbs: past, present, and future

inferred← citeshttps://doi.org/10.3389/fmars.2022.886009openalex-snapshot

A Tropical Macroalga (Halimeda incrassata) Enhances Diversity and Abundance of Epifaunal Assemblages in Mediterranean Seagrass Meadows

inferred← citeshttps://doi.org/10.3390/biology9090273openalex-snapshot

Characterization of Perionyx excavatus Development and Its Head Regeneration

inferred← citeshttps://doi.org/10.3390/biology9120448openalex-snapshot

Identification and Spatiotemporal Expression of Adenosine Deaminases Acting on RNA (ADAR) during Earthworm Regeneration: Its Possible Implication in Muscle Redifferentiation

inferred← citeshttps://doi.org/10.3390/ijms252211904openalex-snapshot

Nature’s Secret Neuro-Regeneration Pathway in Axolotls, Polychaetes and Planarians for Human Therapeutic Target Pathways

inferred← citeshttps://doi.org/10.3390/jdb11030034openalex-snapshot

Vasa, Piwi, and Pl10 Expression during Sexual Maturation and Asexual Reproduction in the Annelid Pristina longiseta

inferred← citeshttps://doi.org/10.34019/2596-3325.2018.v19.24750openalex-snapshot

Checklist of the species of Syllidae (Annelida: Phyllodocida) recorded in Brazil

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)

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