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Neuropeptides in cnidarians
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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.902300305openalex-snapshot
FMRFamide immunoreactivity in the nervous system of the medusa Polyorchis penicillatus
inferredcites →https://doi.org/10.1002/cne.903260103openalex-snapshot
Nerve ring of the hypostome in Hydra. I. Its structure, development, and maintenance
inferredcites →https://doi.org/10.1002/jez.1402490105openalex-snapshot
Ultrastructural localization of RFamide‐like peptides in neuronal dense‐cored vesicles in the peduncle of Hydra
inferredcites →https://doi.org/10.1002/jnr.1191openalex-snapshot
Regulation of olfactory neurogenesis by amidated neuropeptides
inferredcites →https://doi.org/10.1006/bbrc.1996.1849openalex-snapshot
Isolation of Four Novel Neuropeptides, the Hydra-RFamides I–IV, fromHydra magnipapillata
inferredcites →https://doi.org/10.1006/bbrc.1997.7022openalex-snapshot
Isolation of Three Novel Neuropeptides, the Cyanea-RFamides I–III, from Scyphomedusae
inferredcites →https://doi.org/10.1006/bbrc.1997.7854openalex-snapshot
Molecular Cloning of a Peptidylglycine α-Hydroxylating Monooxygenase from Sea Anemones
inferredcites →https://doi.org/10.1006/bbrc.1998.8831openalex-snapshot
A Novel Neuropeptide, Hym-176, Induces Contraction of the Ectodermal Muscle in Hydra
inferredcites →https://doi.org/10.1006/bbrc.2000.3629openalex-snapshot
Genomic Organization and Splicing Variants of a Peptidylglycine α-Hydroxylating Monooxygenase from Sea Anemones
inferredcites →https://doi.org/10.1006/dbio.1993.1138openalex-snapshot
A Model for Pattern Formation of Hypostome, Tentacles, and Foot in Hydra: How to Form Structures Close to Each Other, How to Form Them at a Distance
inferredcites →https://doi.org/10.1006/dbio.1994.1160openalex-snapshot
Metamorphosin A: A Novel Peptide Controlling Development of the Lower Metazoan Hydractinia echinata (Coelenterata, Hydrozoa)
inferredcites →https://doi.org/10.1006/dbio.1998.9150openalex-snapshot
Expression and Developmental Regulation of the Hydra-RFamide and Hydra-LWamide Preprohormone Genes inHydra:Evidence for Transient Phases of Head Formation
inferredcites →https://doi.org/10.1007/bf00214639openalex-snapshot
Antisera to the sequence Arg-Phe-amide visualize neuronal centralization in hydroid polyps
inferredcites →https://doi.org/10.1007/bf00215186openalex-snapshot
Organization of the nervous system of physonectid siphonophores
inferredcites →https://doi.org/10.1007/bf00289234openalex-snapshot
A theory of biological pattern formation
inferredcites →https://doi.org/10.1007/bf00318692openalex-snapshot
The presence and distribution of Antho-RFamide-like material in scyphomedusae
inferredcites →https://doi.org/10.1007/bf00365801openalex-snapshot
LWamides from Cnidaria constitute a novel family of neuropeptides with morphogenetic activity
inferredcites →https://doi.org/10.1007/bf00493017openalex-snapshot
Bombesin-like immunoreactivity in the nervous system of hydra
inferredcites →https://doi.org/10.1007/bf00493364openalex-snapshot
FMRFamide-like immunoreactivity in the nervous system of hydra
inferredcites →https://doi.org/10.1007/bf00495879openalex-snapshot
Substance P-like immunoreactivity in the nervous system of hydra
inferredcites →https://doi.org/10.1007/bf00496623openalex-snapshot
FMRFamide immunoreactivity is generally occurring in the nervous systems of coelenterates
inferredcites →https://doi.org/10.1007/bf00517133openalex-snapshot
Neurotensin-like immunoreactivity in the nervous system of hydra
inferredcites →https://doi.org/10.1007/s00441-002-0534-yopenalex-snapshot
A new case of neuropeptide coexpression (RGamide and LWamides) in Hydra , found by whole-mount, two-color double-labeling in situ hybridization
inferredcites →https://doi.org/10.1007/s004410000240openalex-snapshot
Two-color double-labeling in situ hybridization of whole-mount Hydra using RNA probes for five different Hydra neuropeptide preprohormones: evidence for colocalization
inferredcites →https://doi.org/10.1016/0006-291x(87)90911-9openalex-snapshot
Cloning and sequence of cDNA encoding a peptide C-terminal α-amidating enzyme from Xenopuslaevis
inferredcites →https://doi.org/10.1016/0006-291x(88)90767-xopenalex-snapshot
Cloning of cDNA encoding a new peptide C-terminal α-amidating enzyme having a putative membrane-spanning domain from Xenopuslaevis skin
inferredcites →https://doi.org/10.1016/0006-291x(91)91700-mopenalex-snapshot
Isolation of L-3-phenyllactyl-Phe-Lys-Ala-NH2 (Antho-KAamide), a novel neuropeptide from sea anemones
inferredcites →https://doi.org/10.1016/0006-291x(92)90491-3openalex-snapshot
Isolation of the neuropeptide
inferredcites →https://doi.org/10.1016/0014-5793(87)81283-8openalex-snapshot
Isolation of the neuropeptide pGlu‐Gly‐Arg‐Phe‐amide from the pennatulid Renilla köllikeri
inferredcites →https://doi.org/10.1016/0014-5793(88)80560-xopenalex-snapshot
Isolation of 2 (Antho‐RWamide II), a novel neuropeptide from sea anemones
inferredcites →https://doi.org/10.1016/0196-9781(85)90417-6openalex-snapshot
Arg-Phe-amide-like peptides in the primitive nervous systems of coelenterates
inferredcites →https://doi.org/10.1016/0196-9781(91)90190-zopenalex-snapshot
Isolation of two novel neuropeptides from sea anemones: The unusual, biologically active L-3-phenyllactyl-Tyr-Arg-Ile-NH2 and its des-phenyllactyl fragment Tyr-Arg-Ile-NH2
inferredcites →https://doi.org/10.1016/0196-9781(92)90040-aopenalex-snapshot
Isolation of Leu-Pro-Pro-Gly-Pro-Leu-Pro-Arg-Pro-NH2 (Antho-RPamide), an protected, biologically active neuropeptide from sea anemones
inferredcites →https://doi.org/10.1016/0306-4522(82)90241-xopenalex-snapshot
Oxytocin/vasopressin-like immunoreactivity is present in the nervous system of hydra
inferredcites →https://doi.org/10.1016/0306-4522(83)90272-5openalex-snapshot
Coexistence of neuropeptides in hydra
inferredcites →https://doi.org/10.1016/0968-0004(90)90126-vopenalex-snapshot
Processing of precursors by dipeptidylaminopeptidases: a case of molecular ticketing
inferredcites →https://doi.org/10.1016/s0014-5793(98)01314-3openalex-snapshot
The structure and expression of a preprohormone of a neuropeptide, Hym‐176 in Hydra magnipapillata
inferredcites →https://doi.org/10.1016/s0021-9258(18)41705-xopenalex-snapshot
Identification of a novel type of processing sites in the precursor for the sea anemone neuropeptide Antho-RFamide (
inferredcites →https://doi.org/10.1016/s0070-2153(08)60742-5openalex-snapshot
Chapter 2 Biological Features and Physical Concepts of Pattern Formation Exemplified By Hydra
inferredcites →https://doi.org/10.1016/s0074-7696(08)61345-5openalex-snapshot
Peptides in the Nervous Systems of Cnidarians: Structure, Function, and Biosynthesis
inferredcites →https://doi.org/10.1021/bi9708747openalex-snapshot
Peptidylglycine α-Hydroxylating Monooxygenase: Active Site Residues, Disulfide Linkages, and a Two-Domain Model of the Catalytic Core
inferredcites →https://doi.org/10.1038/13351openalex-snapshot
Substrate-mediated electron transfer in peptidylglycine alpha-hydroxylating monooxygenase.
inferredcites →https://doi.org/10.1038/35025063openalex-snapshot
WNT signalling molecules act in axis formation in the diploblastic metazoan Hydra
inferredcites →https://doi.org/10.1038/newbio239098a0openalex-snapshot
Regeneration of Hydra from Reaggregated Cells
inferredcites →https://doi.org/10.1042/bj2990431openalex-snapshot
The primary structure of the Pol-RFamide neuropeptide precursor protein from the hydromedusa Polyorchis penicillatus indicates a novel processing proteinase activity
inferredcites →https://doi.org/10.1042/bj3320403openalex-snapshot
Three different prohormones yield a variety of Hydra-RFamide (Arg-Phe-NH2) neuropeptides in Hydra magnipapillata
inferredcites →https://doi.org/10.1046/j.1471-4159.1994.62031214.xopenalex-snapshot
Primary Structure of the Precursor for the Anthozoan Neuropeptide Antho‐RFamide from Renilla köllikeri: Evidence for Unusual Processing Enzymes
inferredcites →https://doi.org/10.1046/j.1471-4159.1997.68031319.xopenalex-snapshot
Molecular Cloning of a Preprohormone from Hydra magnipapillata Containing Multiple Copies of Hydra‐LWamide (Leu‐Trp‐NH2) Neuropeptides: Evidence for Processing at Ser and Asn Residues
inferredcites →https://doi.org/10.1073/pnas.83.24.9817openalex-snapshot
Isolation of pyroGlu-Gly-Arg-Phe-NH2 (Antho-RFamide), a neuropeptide from sea anemones.
inferredcites →https://doi.org/10.1073/pnas.84.11.3628openalex-snapshot
Identification of a mammalian glutaminyl cyclase converting glutaminyl into pyroglutamyl peptides.
inferredcites →https://doi.org/10.1073/pnas.87.14.5410openalex-snapshot
Isolation of L-3-phenyllactyl-Leu-Arg-Asn-NH2 (Antho-RNamide), a sea anemone neuropeptide containing an unusual amino-terminal blocking group.
inferredcites →https://doi.org/10.1073/pnas.88.22.10059openalex-snapshot
Primary structure and functional expression of a glutaminyl cyclase.
inferredcites →https://doi.org/10.1073/pnas.88.6.2555openalex-snapshot
Primary structure of the precursor for the sea anemone neuropeptide Antho-RFamide (less than Glu-Gly-Arg-Phe-NH2).
inferredcites →https://doi.org/10.1073/pnas.92.25.11647openalex-snapshot
Molecular cloning of a preprohormone from sea anemones containing numerous copies of a metamorphosis-inducing neuropeptide: a likely role for dipeptidyl aminopeptidase in neuropeptide precursor processing.
inferredcites →https://doi.org/10.1073/pnas.94.4.1241openalex-snapshot
Systematic isolation of peptide signal molecules regulating development in hydra: LWamide and PW families
inferredcites →https://doi.org/10.1073/pnas.97.22.12127openalex-snapshot
Parameters of self-organization in Hydra aggregates
inferredcites →https://doi.org/10.1093/icb/30.4.907openalex-snapshot
The Elementary Nervous System Revisited
inferredcites →https://doi.org/10.1093/icb/32.1.1openalex-snapshot
Coelenterate Neuropeptides: Structure, Action and Biosynthesis
inferredcites →https://doi.org/10.1096/fasebj.13.6.735openalex-snapshot
A molluscan peptide α‐amidating enzyme precursor that generates five distinct enzymes
inferredcites →https://doi.org/10.1098/rspb.1993.0100openalex-snapshot
The expansion behaviour of sea anemones may be coordinated by two inhibitory neuropeptides, Antho-KAamide and Antho-RIamide
inferredcites →https://doi.org/10.1111/j.1463-6395.1985.tb00840.xopenalex-snapshot
Distribution of Nerve Elements Showing FMRFamide‐like Immunoreactivity in Hydromedusae
inferredcites →https://doi.org/10.1139/z91-116openalex-snapshot
Immunogold labelling of FMRFamide-like neuropeptide in neurons of Aglantha digitale (Hydromedusae: Trachylina)
inferredcites →https://doi.org/10.1146/annurev.ne.15.030192.000421openalex-snapshot
The Biosynthesis of Neuropeptides: Peptide alpha-Amidation
inferredcites →https://doi.org/10.1242/dev.127.5.997openalex-snapshot
A novel neuropeptide, Hym-355, positively regulates neuron differentiation in Hydra
inferredcites →https://doi.org/10.1242/jeb.133.1.157openalex-snapshot
EXCITATORY ACTIONS OF Antho-RFamide, AN ANTHOZOAN NEUROPEPTIDE, ON MUSCLES AND CONDUCTING SYSTEMS IN THE SEA ANEMONE CALLIACTIS PARASITICA
inferredcites →https://doi.org/10.1242/jeb.155.1.669openalex-snapshot
Three Anthozoan Neuropeptides, Antho-RFamide and Antho-RWamides I and II, Modulate Spontaneous Tentacle Contractions in Sea Anemones
inferredcites →https://doi.org/10.1242/jeb.156.1.419openalex-snapshot
EFFECTS OF THREE ANTHOZOAN NEUROPEPTIDES, ANTHO-RWamide I, ANTHO-RWamide II and ANTHO-RFamide, ON SLOW MUSCLES FROM SEA ANEMONES
inferredcites →https://doi.org/10.1242/jeb.164.1.295openalex-snapshot
Opposite Actions of the Anthozoan Neuropeptide Antho-Rnamide on Antagonistic Muscle Groups in Sea Anemones
inferredcites →https://doi.org/10.1523/jneurosci.17-04-01363.1997openalex-snapshot
Neuropeptide Amidation inDrosophila: Separate Genes Encode the Two Enzymes Catalyzing Amidation
inferredcites →https://doi.org/10.2307/1542134openalex-snapshot
Antho-RFamide Immunoreactivity in Neuronal Synaptic and Nonsynaptic Vesicles of Sea Anemones
inferredcites →https://doi.org/10.2307/1542145openalex-snapshot
Ultrastructural Localization of Antho-RWamides I and II at Neuromuscular Synapses in the Gastrodermis and Oral Sphincter Muscle of the Sea Anemone Calliactis parasitica
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.4766191openalex-extracted
Signal-Transduction Proteins from Cassiopea Xamachana: The Scaffolding Protein Cxrack1 Shows Conserved Molecular Signatures and Mrna Quantitation Suggests Differential Expression between Larval and the Subsequent Metamorphic Stages
inferred← citeshttps://doi.org/10.1002/9783527335855.marprod202openalex-snapshot
Cnidaria and Ctenophora–2
inferred← citeshttps://doi.org/10.1002/cne.20108openalex-snapshot
Antho‐RFamide‐containing neurons in the primitive nervous system of the anthozoan Renilla koellikeri
inferred← citeshttps://doi.org/10.1002/cne.20658openalex-snapshot
Bilateral symmetric organization of neural elements in the visual system of a coelenterate, Tripedalia cystophora (Cubozoa)
inferred← citeshttps://doi.org/10.1002/cne.22072openalex-snapshot
Prominent system of RFamide immunoreactive neurons in the rhopalia of box jellyfish (Cnidaria: Cubozoa)
inferred← citeshttps://doi.org/10.1002/cne.25133openalex-snapshot
Neuropeptide expression in the box jellyfish Tripedalia cystophora —New insights into the complexity of a “simple” nervous system
inferred← citeshttps://doi.org/10.1002/dneu.20698openalex-snapshot
Anatomy and development of the nervous system of Nematostella vectensis , an anthozoan cnidarian
inferred← citeshttps://doi.org/10.1002/jez.b.21386openalex-snapshot
New insights on ctenophore neural anatomy: Immunofluorescence study in Pleurobrachia pileus (Müller, 1776)
inferred← citeshttps://doi.org/10.1002/jmor.10838openalex-snapshot
GABA and glutamate immunoreactivity in tentacles of the sea anemone Phymactis papillosa (LESSON 1830)
inferred← citeshttps://doi.org/10.1002/jmor.20617openalex-snapshot
Muscle and nerve net organization in stalked jellyfish ( M edusozoa: Staurozoa)
inferred← citeshttps://doi.org/10.1002/med.70022openalex-snapshot
Pharmacological Potential of Jellyfish Bioactive Peptides: From Neurodegenerative Disorders to Cancers
inferred← citeshttps://doi.org/10.1002/pmic.201100327openalex-snapshot
A mass spectrometry‐based method to screen for α‐amidated peptides
inferred← citeshttps://doi.org/10.1007/978-3-540-75555-5_2openalex-snapshot
Diffuse Nerve Net of Hydra Revealed by NADPH-Diaphorase Histochemical Labeling
inferred← citeshttps://doi.org/10.1007/s00338-010-0634-1openalex-snapshot
Settlement induction of Acropora palmata planulae by a GLW-amide neuropeptide
inferred← citeshttps://doi.org/10.1007/s00427-010-0328-2openalex-snapshot
Structure of the central nervous system of a juvenile acoel, Symsagittifera roscoffensis
inferred← citeshttps://doi.org/10.1007/s00435-012-0146-3openalex-snapshot
An allatotropin-like neuropeptide in Mesostoma ehrenbergii (Rhabdocoela, Platyhelminthes)
inferred← citeshttps://doi.org/10.1007/s00435-013-0188-1openalex-snapshot
Neural system reorganization during metamorphosis in the planula larva of Clava multicornis (Hydrozoa, Cnidaria)
inferred← citeshttps://doi.org/10.1007/s00441-004-1072-6openalex-snapshot
FMRFamide-like immunoreactivity in the sea-fan Eunicella cavolini (Cnidaria: Octocorallia)
inferred← citeshttps://doi.org/10.1007/s10071-023-01833-7openalex-snapshot
Chemical cognition: chemoconnectomics and convergent evolution of integrative systems in animals
inferred← citeshttps://doi.org/10.1007/s10158-009-0095-9openalex-snapshot
Physiological and chemical analysis of neurotransmitter candidates at a fast excitatory synapse in the jellyfish Cyanea capillata (Cnidaria, Scyphozoa)
inferred← citeshttps://doi.org/10.1007/s10158-010-0097-7openalex-snapshot
A review of FMRFamide- and RFamide-like peptides in metazoa
inferred← citeshttps://doi.org/10.1007/s10158-010-0109-7openalex-snapshot
Neuronal cell death during metamorphosis of Hydractina echinata (Cnidaria, Hydrozoa)
inferred← citeshttps://doi.org/10.1007/s10646-006-0121-1openalex-snapshot
Hormonal signaling in cnidarians: do we understand the pathways well enough to know whether they are being disrupted?
inferred← citeshttps://doi.org/10.1007/s10750-004-2637-9openalex-snapshot
Biogenic amine receptors in the sea pansy: activity, molecular structure, and physiological significance
inferred← citeshttps://doi.org/10.1007/s10750-004-2647-7openalex-snapshot
Glutamatergic and GABAnergic control in the tentacle effector systems of Hydra vulgaris
inferred← citeshttps://doi.org/10.1007/s10750-004-2660-xopenalex-snapshot
Cnidarian neurobiology: what does the future hold?
inferred← citeshttps://doi.org/10.1007/s10750-004-2689-xopenalex-snapshot
Neuropeptides and photic behavior in Cnidaria
inferred← citeshttps://doi.org/10.1016/b978-008045046-9.01445-5openalex-snapshot
Invertebrate Neurohormone GPCRs
inferred← citeshttps://doi.org/10.1016/b978-008045046-9.01446-7openalex-snapshot
Neuropeptide Signaling in Invertebrates
inferred← citeshttps://doi.org/10.1016/j.bbapap.2005.08.015openalex-snapshot
Cytochrome b561 protein family: Expanding roles and versatile transmembrane electron transfer abilities as predicted by a new classification system and protein sequence motif analyses
inferred← citeshttps://doi.org/10.1016/j.biosystems.2006.03.008openalex-snapshot
Evolving visual pigments: Hints from the opsin-based proteins in a phylogenetically old “eyeless” invertebrate
inferred← citeshttps://doi.org/10.1016/j.bmc.2008.10.013openalex-snapshot
Substituted hippurates and hippurate analogs as substrates and inhibitors of peptidylglycine α-hydroxylating monooxygenase (PHM)
inferred← citeshttps://doi.org/10.1016/j.cbd.2009.07.001openalex-snapshot
Chemical transmission in the sea anemone Nematostella vectensis: A genomic perspective
inferred← citeshttps://doi.org/10.1016/j.cbi.2008.03.004openalex-snapshot
Acetylcholinesterase activity in Clytia hemisphaerica (Cnidaria)
inferred← citeshttps://doi.org/10.1016/j.cbpa.2006.09.008openalex-snapshot
Cnidarian chemical neurotransmission, an updated overview
inferred← citeshttps://doi.org/10.1016/j.cobeha.2024.101437openalex-snapshot
Dynamics of neural activity in early nervous system evolution
inferred← citeshttps://doi.org/10.1016/j.cub.2017.08.014openalex-snapshot
The Jellyfish Cassiopea Exhibits a Sleep-like State
inferred← citeshttps://doi.org/10.1016/j.ijpara.2016.05.007openalex-snapshot
De novo discovery of neuropeptides in the genomes of parasitic flatworms using a novel comparative approach
inferred← citeshttps://doi.org/10.1016/j.jembe.2011.07.025openalex-snapshot
Coral larvae: From gametes to recruits
inferred← citeshttps://doi.org/10.1016/j.mod.2006.03.002openalex-snapshot
Foot formation in Hydra: A novel gene, anklet, is involved in basal disk formation
inferred← citeshttps://doi.org/10.1016/j.peptides.2015.10.005openalex-snapshot
Molecular cloning, expression analysis and cellular localization of an LFRFamide gene in the cuttlefish Sepiella japonica
inferred← citeshttps://doi.org/10.1016/j.peptides.2016.05.011openalex-snapshot
Somatostatin signaling system as an ancestral mechanism: Myoregulatory activity of an Allatostatin-C peptide in Hydra
inferred← citeshttps://doi.org/10.1016/j.regpep.2012.05.001openalex-snapshot
Mini-review: The evolution of neuropeptide signaling
inferred← citeshttps://doi.org/10.1016/j.tice.2011.07.005openalex-snapshot
Expression of a neuropeptide similar to allatotropin in free living turbellaria (platyhelminthes)
inferred← citeshttps://doi.org/10.1016/j.toxicon.2021.03.005openalex-snapshot
The venom proteome of three common scyphozoan jellyfishes (Chrysaora caliparea, Cyanea nozakii and Lychnorhiza malayensis) (Cnidaria: Scyphozoa) from the coastal waters of India
inferred← citeshttps://doi.org/10.1016/j.ydbio.2009.05.563openalex-snapshot
Origins of neurogenesis, a cnidarian view
inferred← citeshttps://doi.org/10.1016/j.ygcen.2014.07.009openalex-snapshot
Evolution of the AKH/corazonin/ACP/GnRH receptor superfamily and their ligands in the Protostomia
inferred← citeshttps://doi.org/10.1016/j.ygcen.2016.04.025openalex-snapshot
Structural and functional diversity of nonapeptide hormones from an evolutionary perspective: A review
inferred← citeshttps://doi.org/10.1016/j.ygcen.2020.113637openalex-snapshot
G protein-coupled receptor signal transduction and Ca2+ signaling pathways of the allatotropin/orexin system in Hydra
inferred← citeshttps://doi.org/10.1016/j.ygcen.2021.113905openalex-snapshot
Involvement of RFamide neuropeptides in polyp contraction of the adult scleractinian corals Euphyllia ancora and Stylophora pistillata
inferred← citeshttps://doi.org/10.1016/j.zool.2012.07.002openalex-snapshot
FMRF-amide immunoreactivity pattern in the planula and colony of the hydroid Gonothyraea loveni
inferred← citeshttps://doi.org/10.1016/s1096-4959(03)00226-4openalex-snapshot
Ancient signals: peptides and the interpretation of positional information in ancestral metazoans
inferred← citeshttps://doi.org/10.1038/s41559-022-01835-7openalex-snapshot
Mass spectrometry of short peptides reveals common features of metazoan peptidergic neurons
inferred← citeshttps://doi.org/10.1038/s41598-020-66438-3openalex-snapshot
Involvement of GLWamide neuropeptides in polyp contraction of the adult stony coral Euphyllia ancora
inferred← citeshttps://doi.org/10.1038/s41598-025-91048-2openalex-snapshot
Piezo proteins, mechano reception and behaviour in Hydra
inferred← citeshttps://doi.org/10.1086/bblv226n1p29openalex-snapshot
Organization of the Ectodermal Nervous Structures in Jellyfish: Scyphomedusae
inferred← citeshttps://doi.org/10.1086/bblv226n1p41openalex-snapshot
Organization of the Ectodermal Nervous Structures in Medusae: Cubomedusae
inferred← citeshttps://doi.org/10.1086/bblv227n3p274openalex-snapshot
Multiple Conducting Systems in the Cubomedusa Carybdea marsupialis
inferred← citeshttps://doi.org/10.1093/molbev/mss114openalex-snapshot
A "Neural" Enzyme in Nonbilaterian Animals and Algae: Preneural Origins for Peptidylglycine -Amidating Monooxygenase
inferred← citeshttps://doi.org/10.1093/molbev/msy160openalex-snapshot
Xenacoelomorph Neuropeptidomes Reveal a Major Expansion of Neuropeptide Systems during Early Bilaterian Evolution
inferred← citeshttps://doi.org/10.1093/oxfordhb/9780190456757.013.10openalex-snapshot
Neurotransmitters and Neuropeptides of Invertebrates
inferred← citeshttps://doi.org/10.1093/oxfordhb/9780190456757.013.7openalex-snapshot
Cnidarian Neurobiology
inferred← citeshttps://doi.org/10.1098/rstb.2015.0065openalex-snapshot
Evolution of eumetazoan nervous systems: insights from cnidarians
inferred← citeshttps://doi.org/10.1101/gr.6714008openalex-snapshot
Genomics, transcriptomics, and peptidomics of neuropeptides and protein hormones in the red flour beetle Tribolium castaneum
inferred← citeshttps://doi.org/10.1111/j.1600-079x.2012.00994.xopenalex-snapshot
Temporal and histological evaluation of melatonin patterns in a ‘basal’ metazoan
inferred← citeshttps://doi.org/10.1139/cjz-2023-0114openalex-snapshot
Signalling pathway associated with discharge of cnidocyst induced by reduced glutathione in Hydra plagiodesmica (Dioni, 1968)
inferred← citeshttps://doi.org/10.1155/2024/8676010openalex-snapshot
Signal‐Transduction Proteins from Caribbean Cassiopea xamachana: The Scaffolding Protein CxRACK1 Shows Conserved Molecular Signatures and Differential Expression between Larval and the Subsequent Metamorphic Stages
inferred← citeshttps://doi.org/10.1186/1471-2164-13-271openalex-snapshot
Developing the anemone Aiptasia as a tractable model for cnidarian-dinoflagellate symbiosis: the transcriptome of aposymbiotic A. pallida
inferred← citeshttps://doi.org/10.1186/1471-2164-14-509openalex-snapshot
KEGG orthology-based annotation of the predicted proteome of Acropora digitifera: ZoophyteBase - an open access and searchable database of a coral genome
inferred← citeshttps://doi.org/10.1186/1741-7007-8-4openalex-snapshot
Early evolution of the LIM homeobox gene family
inferred← citeshttps://doi.org/10.1186/s12864-019-5514-7openalex-snapshot
De novo transcriptome assembly of the cubomedusa Tripedalia cystophora, including the analysis of a set of genes involved in peptidergic neurotransmission
inferred← citeshttps://doi.org/10.1186/s12864-020-06945-9openalex-snapshot
A comparative genomics study of neuropeptide genes in the cnidarian subclasses Hexacorallia and Ceriantharia
inferred← citeshttps://doi.org/10.1186/s12864-021-08091-2openalex-snapshot
An evolutionary genomics view on neuropeptide genes in Hydrozoa and Endocnidozoa (Myxozoa)
inferred← citeshttps://doi.org/10.1186/s12864-025-12201-9openalex-snapshot
An updated and spatially validated somatic single-cell atlas of Hydractinia symbiolongicarpus
inferred← citeshttps://doi.org/10.1201/b10425-9openalex-snapshot
"A Key Innovation in Animal Evolution, the Emergence of Neurogenesis
inferred← citeshttps://doi.org/10.1242/jeb.00450openalex-snapshot
Central circuitry in the jellyfishAglantha digitaleIV. Pathways coordinating feeding behaviour
inferred← citeshttps://doi.org/10.1242/jeb.043687openalex-snapshot
Do jellyfish have central nervous systems?
inferred← citeshttps://doi.org/10.1242/jeb.110379openalex-snapshot
The nervous system of Xenacoelomorpha: a genomic perspective
inferred← citeshttps://doi.org/10.1242/jeb.162396openalex-snapshot
Neuropeptidergic integration of behavior in Trichoplax adhaerens, an animal without synapses
inferred← citeshttps://doi.org/10.1371/journal.pone.0046513openalex-snapshot
Transcriptomic Analysis of Neuropeptides and Peptide Hormones in the Barnacle Balanus amphitrite: Evidence of Roles in Larval Settlement
inferred← citeshttps://doi.org/10.1371/journal.pone.0052266openalex-snapshot
Melatonin Distribution Reveals Clues to Its Biological Significance in Basal Metazoans
inferred← citeshttps://doi.org/10.1371/journal.pone.0077520openalex-snapshot
Allatotropin: An Ancestral Myotropic Neuropeptide Involved in Feeding
inferred← citeshttps://doi.org/10.1371/journal.pone.0132544openalex-snapshot
Gene Expression Data from the Moon Jelly, Aurelia, Provide Insights into the Evolution of the Combinatorial Code Controlling Animal Sense Organ Development
inferred← citeshttps://doi.org/10.1387/ijdb.120086bgopenalex-snapshot
Hydra, a fruitful model system for 270 years
inferred← citeshttps://doi.org/10.21203/rs.3.rs-3015567/v1openalex-snapshot
Signalling Pathway Associated to Discharge of Cnidocyst Induced by Reduced Glutathione in Hydra
inferred← citeshttps://doi.org/10.2307/1543588openalex-snapshot
Evidence for a Common Pattern of Peptidergic Innervation of Cnidocytes
inferred← citeshttps://doi.org/10.2307/3593133openalex-snapshot
Muscle Organization of the Cubozoan JellyfishTripedalia cystophoraConant 1897
inferred← citeshttps://doi.org/10.23860/thesis-munro-bailey-2014openalex-snapshot
IMMUNOHISTOCHEMICAL LOCALIZATION OF THE NEUROPEPTIDE RFAMIDE IN THE HYPOSTOMAL NERVE NET OF HYDRA VULGARIS
inferred← citeshttps://doi.org/10.3389/fendo.2019.00831openalex-snapshot
Global Neuropeptide Annotations From the Genomes and Transcriptomes of Cubozoa, Scyphozoa, Staurozoa (Cnidaria: Medusozoa), and Octocorallia (Cnidaria: Anthozoa)
inferred← citeshttps://doi.org/10.3389/fendo.2020.00063openalex-snapshot
Expression Analysis of Cnidarian-Specific Neuropeptides in a Sea Anemone Unveils an Apical-Organ-Associated Nerve Net That Disintegrates at Metamorphosis
inferred← citeshttps://doi.org/10.3389/fendo.2022.973862openalex-snapshot
Review: The evolution of peptidergic signaling in Cnidaria and Placozoa, including a comparison with Bilateria
inferred← citeshttps://doi.org/10.3389/fnins.2015.00166openalex-snapshot
Molecular cloning, sequencing and tissue expression of vasotocin and isotocin precursor genes from Ostariophysian catfishes: phylogeny and evolutionary considerations in teleosts
inferred← citeshttps://doi.org/10.3389/fnmol.2010.00011openalex-snapshot
The specification of glycinergic neurons and the role of glycinergic transmission in development
inferred← citeshttps://doi.org/10.3390/molecules20034780openalex-snapshot
QM/MM Calculations with deMon2k
inferred← citeshttps://doi.org/10.3390/molecules25071636openalex-snapshot
An FMRFamide Neuropeptide in Cuttlefish Sepia pharaonis: Identification, Characterization, and Potential Function
inferred← citeshttps://doi.org/10.5983/nl2008jsce.46.122openalex-snapshot
神経ペプチドGLWamideはイシサンゴのポリプ収縮に関与する
inferred← citeshttps://doi.org/10.6084/m9.figshare.13023689openalex-snapshot
Additional file 10 of A comparative genomics study of neuropeptide genes in the cnidarian subclasses Hexacorallia and Ceriantharia
inferred← citeshttps://doi.org/10.6084/m9.figshare.13023692openalex-snapshot
Additional file 11 of A comparative genomics study of neuropeptide genes in the cnidarian subclasses Hexacorallia and Ceriantharia
inferred← citeshttps://doi.org/10.6084/m9.figshare.13023695openalex-snapshot
Additional file 1 of A comparative genomics study of neuropeptide genes in the cnidarian subclasses Hexacorallia and Ceriantharia
inferred← citeshttps://doi.org/10.6084/m9.figshare.13023698openalex-snapshot
Additional file 2 of A comparative genomics study of neuropeptide genes in the cnidarian subclasses Hexacorallia and Ceriantharia
inferred← citeshttps://doi.org/10.6084/m9.figshare.13023701openalex-snapshot
Additional file 3 of A comparative genomics study of neuropeptide genes in the cnidarian subclasses Hexacorallia and Ceriantharia
inferred← citeshttps://doi.org/10.6084/m9.figshare.13023704openalex-snapshot
Additional file 4 of A comparative genomics study of neuropeptide genes in the cnidarian subclasses Hexacorallia and Ceriantharia
inferred← citeshttps://doi.org/10.6084/m9.figshare.13023707openalex-snapshot
Additional file 5 of A comparative genomics study of neuropeptide genes in the cnidarian subclasses Hexacorallia and Ceriantharia
inferred← citeshttps://doi.org/10.6084/m9.figshare.13023710openalex-snapshot
Additional file 6 of A comparative genomics study of neuropeptide genes in the cnidarian subclasses Hexacorallia and Ceriantharia
inferred← citeshttps://doi.org/10.6084/m9.figshare.13023713openalex-snapshot
Additional file 7 of A comparative genomics study of neuropeptide genes in the cnidarian subclasses Hexacorallia and Ceriantharia
inferred← citeshttps://doi.org/10.6084/m9.figshare.13023716openalex-snapshot
Additional file 8 of A comparative genomics study of neuropeptide genes in the cnidarian subclasses Hexacorallia and Ceriantharia
inferred← citeshttps://doi.org/10.6084/m9.figshare.13023719openalex-snapshot
Additional file 9 of A comparative genomics study of neuropeptide genes in the cnidarian subclasses Hexacorallia and Ceriantharia
inferred← citeshttps://doi.org/10.6084/m9.figshare.17104039openalex-snapshot
Additional file 1 of An evolutionary genomics view on neuropeptide genes in Hydrozoa and Endocnidozoa (Myxozoa)
inferred← citeshttps://doi.org/10.6084/m9.figshare.17104042openalex-snapshot
Additional file 2 of An evolutionary genomics view on neuropeptide genes in Hydrozoa and Endocnidozoa (Myxozoa)
inferred← citeshttps://doi.org/10.6084/m9.figshare.17104045openalex-snapshot
Additional file 3 of An evolutionary genomics view on neuropeptide genes in Hydrozoa and Endocnidozoa (Myxozoa)
inferred← citeshttps://doi.org/10.6084/m9.figshare.17104048openalex-snapshot
Additional file 4 of An evolutionary genomics view on neuropeptide genes in Hydrozoa and Endocnidozoa (Myxozoa)
inferred← citeshttps://doi.org/10.6084/m9.figshare.17104051openalex-snapshot
Additional file 5 of An evolutionary genomics view on neuropeptide genes in Hydrozoa and Endocnidozoa (Myxozoa)
inferred← citeshttps://doi.org/10.6084/m9.figshare.17104054openalex-snapshot
Additional file 6 of An evolutionary genomics view on neuropeptide genes in Hydrozoa and Endocnidozoa (Myxozoa)
inferred← citeshttps://doi.org/10.6084/m9.figshare.17104057openalex-snapshot
Additional file 7 of An evolutionary genomics view on neuropeptide genes in Hydrozoa and Endocnidozoa (Myxozoa)
inferred← citeshttps://doi.org/10.6084/m9.figshare.17104060openalex-snapshot
Additional file 8 of An evolutionary genomics view on neuropeptide genes in Hydrozoa and Endocnidozoa (Myxozoa)
inferred← citeshttps://doi.org/10.7554/elife.39742openalex-snapshot
CRISPR knockouts reveal an endogenous role for ancient neuropeptides in regulating developmental timing in a sea anemone
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