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The buds of Oscarella lobularis (Porifera): a new convenient model for sponge cell and developmental biology
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/9780470015902.a0001582.pub2openalex-snapshot
Porifera (Sponges): Recent Knowledge and New Perspectives
inferredcites →https://doi.org/10.1002/bies.080058openalex-snapshot
The Homoscleromorph sponge Oscarella lobularis , a promising sponge model in evolutionary and developmental biology
inferredcites →https://doi.org/10.1002/bies.201700237openalex-snapshot
Understanding Animal Evolution: The Added Value of Sponge Transcriptomics and Genomics
inferredcites →https://doi.org/10.1002/dvdy.20815openalex-snapshot
Predictable mosaic transgene expression in ascidian embryos produced with a simple electroporation device
inferredcites →https://doi.org/10.1002/jez.2006openalex-snapshot
Sponge cell reaggregation: Cellular structure and morphogenetic potencies of multicellular aggregates
inferredcites →https://doi.org/10.1002/jez.b.22830openalex-snapshot
Sewing up the wounds : The epithelial morphogenesis as a central mechanism of calcaronean sponge regeneration
inferredcites →https://doi.org/10.1002/jmor.10506openalex-snapshot
Metamorphosis of cinctoblastula larvae (Homoscleromorpha, porifera)
inferredcites →https://doi.org/10.1002/jmor.1051800103openalex-snapshot
Comparative study of the choanosome of Porifera: 1. The Homoscleromorpha
inferredcites →https://doi.org/10.1006/cbir.1995.1041openalex-snapshot
Genome size and chromosomes in marine sponges [Suberites domuncula, Geodia cydonium]
inferredcites →https://doi.org/10.1006/dbio.2001.0565openalex-snapshot
Morpholino Oligos: Making Sense of Antisense?
inferredcites →https://doi.org/10.1007/978-1-4612-5214-6openalex-snapshot
The Cell Biology of Sponges
inferredcites →https://doi.org/10.1007/978-3-030-30363-1_7openalex-snapshot
A Look Back Over 20 Years of Evo-Devo Studies on Sponges: A Challenged View of Urmetazoa
inferredcites →https://doi.org/10.1007/978-90-481-8575-7openalex-snapshot
The Comparative Embryology of Sponges
inferredcites →https://doi.org/10.1007/bf00397088openalex-snapshot
Cellular organization in the marine demosponge Callyspongia diffusa
inferredcites →https://doi.org/10.1007/s00227-003-1100-1openalex-snapshot
The cellular basis of photobehavior in the tufted parenchymella larva of demosponges
inferredcites →https://doi.org/10.1007/s00227-006-0439-5openalex-snapshot
Asexual reproduction in homoscleromorph sponges (Porifera; Homoscleromorpha)
inferredcites →https://doi.org/10.1007/s00227-012-2100-9openalex-snapshot
Pluri-annual study of the reproduction of two Mediterranean Oscarella species (Porifera, Homoscleromorpha): cycle, sex-ratio, reproductive effort and phenology
inferredcites →https://doi.org/10.1007/s00227-012-2133-0openalex-snapshot
Unique and species-specific microbial communities in Oscarella lobularis and other Mediterranean Oscarella species (Porifera: Homoscleromorpha)
inferredcites →https://doi.org/10.1007/s00359-002-0293-yopenalex-snapshot
Spectral sensitivity in a sponge larva
inferredcites →https://doi.org/10.1007/s00359-006-0165-yopenalex-snapshot
GABA and glutamate specifically induce contractions in the sponge Tethya wilhelma
inferredcites →https://doi.org/10.1007/s00427-008-0242-zopenalex-snapshot
NK homeobox genes with choanocyte-specific expression in homoscleromorph sponges
inferredcites →https://doi.org/10.1007/s00427-012-0399-3openalex-snapshot
Cellular and molecular processes leading to embryo formation in sponges: evidences for high conservation of processes throughout animal evolution
inferredcites →https://doi.org/10.1007/s10750-011-0842-xopenalex-snapshot
No longer Demospongiae: Homoscleromorpha formal nomination as a fourth class of Porifera
inferredcites →https://doi.org/10.1007/s11626-011-9469-5openalex-snapshot
Efforts to develop a cultured sponge cell line: revisiting an intractable problem
inferredcites →https://doi.org/10.1016/j.cub.2015.08.023openalex-snapshot
Dynamic Transport and Cementation of Skeletal Elements Build Up the Pole-and-Beam Structured Skeleton of Sponges
inferredcites →https://doi.org/10.1016/j.cub.2017.02.031openalex-snapshot
A Large and Consistent Phylogenomic Dataset Supports Sponges as the Sister Group to All Other Animals
inferredcites →https://doi.org/10.1016/j.cub.2017.08.054openalex-snapshot
Embracing Uncertainty in Reconstructing Early Animal Evolution
inferredcites →https://doi.org/10.1016/j.cub.2019.02.031openalex-snapshot
Evolution: The Battle of the First Animals
inferredcites →https://doi.org/10.1016/j.jpha.2019.03.008openalex-snapshot
Primmorph extracts and mesohyls of marine sponges inhibit proliferation and migration of hepatocellular carcinoma cells in vitro
inferredcites →https://doi.org/10.1016/j.marenvres.2018.02.020openalex-snapshot
Suspended sediment causes feeding current arrests in situ in the glass sponge Aphrocallistes vastus
inferredcites →https://doi.org/10.1016/j.margen.2015.07.008openalex-snapshot
Comparative analyses of developmental transcription factor repertoires in sponges reveal unexpected complexity of the earliest animals
inferredcites →https://doi.org/10.1016/j.tree.2015.03.003openalex-snapshot
The hidden biology of sponges and ctenophores
inferredcites →https://doi.org/10.1016/j.ydbio.2016.02.026openalex-snapshot
ROCK inhibition abolishes the establishment of the aquiferous system in Ephydatia muelleri (Porifera, Demospongiae)
inferredcites →https://doi.org/10.1016/j.ydbio.2017.06.012openalex-snapshot
Think like a sponge: The genetic signal of sensory cells in sponges
inferredcites →https://doi.org/10.1016/j.ydbio.2017.10.010openalex-snapshot
EvoRegen in animals: Time to uncover deep conservation or convergence of adult stem cell evolution and regenerative processes
inferredcites →https://doi.org/10.1016/s0047-6374(98)00078-5openalex-snapshot
Primmorphs generated from dissociated cells of the sponge Suberites domuncula: a model system for studies of cell proliferation and cell death
inferredcites →https://doi.org/10.1016/s0248-4900(97)86829-3openalex-snapshot
Type IV collagen in sponges, the missing link in basement membrane ubiquity*
inferredcites →https://doi.org/10.1038/nature09201openalex-snapshot
The Amphimedon queenslandica genome and the evolution of animal complexity
inferredcites →https://doi.org/10.1038/nature13881openalex-snapshot
Calcisponges have a ParaHox gene and dynamic expression of dispersed NK homeobox genes
inferredcites →https://doi.org/10.1038/ncomms4905openalex-snapshot
Developmental gene expression provides clues to relationships between sponge and eumetazoan body plans
inferredcites →https://doi.org/10.1038/nmeth.2019openalex-snapshot
Fiji: an open-source platform for biological-image analysis
inferredcites →https://doi.org/10.1038/nrg.2016.127openalex-snapshot
The origin and evolution of cell types
inferredcites →https://doi.org/10.1038/nrm.2017.125openalex-snapshot
Shedding light on the cell biology of extracellular vesicles
inferredcites →https://doi.org/10.1038/s41559-017-0331-3openalex-snapshot
Ctenophore relationships and their placement as the sister group to all other animals
inferredcites →https://doi.org/10.1038/s41559-018-0575-6openalex-snapshot
Early metazoan cell type diversity and the evolution of multicellular gene regulation
inferredcites →https://doi.org/10.1038/s41580-019-0158-7openalex-snapshot
Extracellular vesicles: a new communication paradigm?
inferredcites →https://doi.org/10.1038/s41586-019-1290-4openalex-snapshot
Pluripotency and the origin of animal multicellularity
inferredcites →https://doi.org/10.1038/s41598-019-51282-xopenalex-snapshot
Co-expression of synaptic genes in the sponge Amphimedon queenslandica uncovers ancient neural submodules
inferredcites →https://doi.org/10.1038/s41598-019-53643-yopenalex-snapshot
Breakthrough in Marine Invertebrate Cell Culture: Sponge Cells Divide Rapidly in Improved Nutrient Medium
inferredcites →https://doi.org/10.1038/srep37546openalex-snapshot
An ancient role for nitric oxide in regulating the animal pelagobenthic life cycle: evidence from a marine sponge
inferredcites →https://doi.org/10.1073/pnas.0604065103openalex-snapshot
Early evolution of animal cell signaling and adhesion genes
inferredcites →https://doi.org/10.1073/pnas.1120685109openalex-snapshot
Origin of metazoan cadherin diversity and the antiquity of the classical cadherin/β-catenin complex
inferredcites →https://doi.org/10.1073/pnas.1514789112openalex-snapshot
The ancestral gene repertoire of animal stem cells
inferredcites →https://doi.org/10.1074/jbc.ra117.001325openalex-snapshot
Analysis of a vinculin homolog in a sponge (phylum Porifera) reveals that vertebrate-like cell adhesions emerged early in animal evolution
inferredcites →https://doi.org/10.1083/jcb.201211138openalex-snapshot
Extracellular vesicles: Exosomes, microvesicles, and friends
inferredcites →https://doi.org/10.1093/gbe/evw289openalex-snapshot
The Conservation of the Germline Multipotency Program, from Sponges to Vertebrates: A Stepping Stone to Understanding the Somatic and Germline Origins
inferredcites →https://doi.org/10.1093/icb/icp038openalex-snapshot
Epithelia and integration in sponges
inferredcites →https://doi.org/10.1093/icb/icz122openalex-snapshot
Sponge Behavior and the Chemical Basis of Responses: A Post-Genomic View
inferredcites →https://doi.org/10.1093/molbev/msx058openalex-snapshot
Origin and evolution of the sponge aggregation factor gene family
inferredcites →https://doi.org/10.1093/molbev/msy033openalex-snapshot
Evidence of Signaling and Adhesion Roles for β-Catenin in the Sponge Ephydatia muelleri
inferredcites →https://doi.org/10.1098/rsos.160484openalex-snapshot
The role of cell replacement in benthic–pelagic coupling by suspension feeders
inferredcites →https://doi.org/10.1098/rspb.2019.0831openalex-snapshot
Revisiting metazoan phylogeny with genomic sampling of all phyla
inferredcites →https://doi.org/10.1111/ede.12032openalex-snapshot
The evolution and function of the Pax/ S ix regulatory network in sponges
inferredcites →https://doi.org/10.1111/ede.12060openalex-snapshot
Choanoflagellate and choanocyte collar‐flagellar systems and the assumption of homology
inferredcites →https://doi.org/10.1111/j.1440-169x.2005.00800.xopenalex-snapshot
Isolation of the choanocyte in the fresh water sponge, Ephydatia fluviatilis and its lineage marker, Ef annexin
inferredcites →https://doi.org/10.1111/j.1525-142x.2010.00434.xopenalex-snapshot
Wnt signaling and induction in the sponge aquiferous system: evidence for an ancient origin of the organizer
inferredcites →https://doi.org/10.1111/j.1744-7410.2010.00193.xopenalex-snapshot
Evolutionary emergence of synaptic nervous systems: what can we learn from the non‐synaptic, nerveless Porifera?
inferredcites →https://doi.org/10.1111/j.1744-7410.2010.00196.xopenalex-snapshot
Phototactic responses of larvae from the marine sponges Neopetrosia proxima and Xestospongia bocatorensis (Haplosclerida: Petrosiidae)
inferredcites →https://doi.org/10.1111/j.1749-4877.2009.00167.xopenalex-snapshot
Origin of the neuro‐sensory system: new and expected insights from sponges
inferredcites →https://doi.org/10.1126/science.abj2949openalex-snapshot
Profiling cellular diversity in sponges informs animal cell type and nervous system evolution
inferredcites →https://doi.org/10.1128/genomea.00977-15openalex-snapshot
Draft Genome Sequence of an Alphaproteobacterium Associated with the Mediterranean Sponge Oscarella lobularis
inferredcites →https://doi.org/10.1134/s1062360414040067openalex-snapshot
Sponge cell reaggregation: Mechanisms and dynamics of the process
inferredcites →https://doi.org/10.1139/z05-171openalex-snapshot
Physiology of coordination in sponges
inferredcites →https://doi.org/10.1186/1471-2148-14-3openalex-snapshot
Evolutionary origins of sensation in metazoans: functional evidence for a new sensory organ in sponges
inferredcites →https://doi.org/10.1186/1472-6750-11-67openalex-snapshot
RNA interference in marine and freshwater sponges: actin knockdown in Tethya wilhelma and Ephydatia muelleriby ingested dsRNA expressing bacteria
inferredcites →https://doi.org/10.1186/1741-7007-12-26openalex-snapshot
Evolutionary origin of gastrulation: insights from sponge development
inferredcites →https://doi.org/10.1186/1742-9994-3-7openalex-snapshot
Neuroactive substances specifically modulate rhythmic body contractions in the nerveless metazoon Tethya wilhelma (Demospongiae, Porifera)
inferredcites →https://doi.org/10.1186/2041-9139-3-14openalex-snapshot
Genome-wide analysis of the sox family in the calcareous sponge Sycon ciliatum: multiple genes with unique expression patterns
inferredcites →https://doi.org/10.1186/s12862-014-0230-zopenalex-snapshot
Calcareous sponge genomes reveal complex evolution of α-carbonic anhydrases and two key biomineralization enzymes
inferredcites →https://doi.org/10.1186/s12862-018-1118-0openalex-snapshot
Wnt signaling and polarity in freshwater sponges
inferredcites →https://doi.org/10.1186/s12864-015-1588-zopenalex-snapshot
Deep developmental transcriptome sequencing uncovers numerous new genes and enhances gene annotation in the sponge Amphimedon queenslandica
inferredcites →https://doi.org/10.1186/s12864-018-4715-9openalex-snapshot
New genomic data and analyses challenge the traditional vision of animal epithelium evolution
inferredcites →https://doi.org/10.1186/s13227-016-0042-xopenalex-snapshot
The ontogeny of choanocyte chambers during metamorphosis in the demosponge Amphimedon queenslandica
inferredcites →https://doi.org/10.1186/s13227-016-0050-xopenalex-snapshot
Conserved expression of vertebrate microvillar gene homologs in choanocytes of freshwater sponges
inferredcites →https://doi.org/10.1242/jcs.222406openalex-snapshot
New insights into extracellular vesicle biogenesis and function
inferredcites →https://doi.org/10.1242/jeb.003392openalex-snapshot
Coordinated contractions effectively expel water from the aquiferous system of a freshwater sponge
inferredcites →https://doi.org/10.1242/jeb.039859openalex-snapshot
Evidence for glutamate, GABA and NO in coordinating behaviour in the sponge, Ephydatia muelleri (Demospongiae, Spongillidae)
inferredcites →https://doi.org/10.1242/jeb.049148openalex-snapshot
The contractile sponge epitheliumsensu lato– body contraction of the demospongeTethya wilhelmais mediated by the pinacoderm
inferredcites →https://doi.org/10.1242/jeb.110817openalex-snapshot
Elements of a ‘nervous system’ in sponges
inferredcites →https://doi.org/10.1242/jeb.202.9.1139openalex-snapshot
Impulse conduction in a sponge
inferredcites →https://doi.org/10.1371/journal.pbio.3000363openalex-snapshot
The biology of extracellular vesicles: The known unknowns
inferredcites →https://doi.org/10.1371/journal.pone.0001031openalex-snapshot
Wnt and TGF-β Expression in the Sponge Amphimedon queenslandica and the Origin of Metazoan Embryonic Patterning
inferredcites →https://doi.org/10.1371/journal.pone.0005823openalex-snapshot
WNT/β-Catenin Signalling and Epithelial Patterning in the Homoscleromorph Sponge Oscarella
inferredcites →https://doi.org/10.1371/journal.pone.0014290openalex-snapshot
Molecular Phylogeny Restores the Supra-Generic Subdivision of Homoscleromorph Sponges (Porifera, Homoscleromorpha)
inferredcites →https://doi.org/10.1371/journal.pone.0015040openalex-snapshot
Freshwater Sponges Have Functional, Sealing Epithelia with High Transepithelial Resistance and Negative Transepithelial Potential
inferredcites →https://doi.org/10.1371/journal.pone.0027787openalex-snapshot
The Sponge Pump: The Role of Current Induced Flow in the Design of the Sponge Body Plan
inferredcites →https://doi.org/10.1371/journal.pone.0063976openalex-snapshot
Systematics and Molecular Phylogeny of the Family Oscarellidae (Homoscleromorpha) with Description of Two New Oscarella Species
inferredcites →https://doi.org/10.1371/journal.pone.0113153openalex-snapshot
A New Flow-Regulating Cell Type in the Demosponge Tethya wilhelma – Functional Cellular Anatomy of a Leuconoid Canal System
inferredcites →https://doi.org/10.1371/journal.pone.0134566openalex-snapshot
Oscarella lobularis (Homoscleromorpha, Porifera) Regeneration: Epithelial Morphogenesis and Metaplasia
inferredcites →https://doi.org/10.1371/journal.pone.0212005openalex-snapshot
Secreted frizzled related protein is a target of PaxB and plays a role in aquiferous system development in the freshwater sponge, Ephydatia muelleri
inferredcites →https://doi.org/10.1387/ijdb.072526mpopenalex-snapshot
Heterologous expression of DsRed2 in young sponges (Porifera)
inferredcites →https://doi.org/10.1534/g3.119.400951openalex-snapshot
A Screen for Gene Paralogies Delineating Evolutionary Branching Order of Early Metazoa
inferredcites →https://doi.org/10.1534/genetics.118.301121openalex-snapshot
Establishment of Transgenesis in the Demosponge Suberites domuncula
inferredcites →https://doi.org/10.1590/s1415-475738320150005openalex-snapshot
Evo-devo of non-bilaterian animals
inferredcites →https://doi.org/10.2108/zsj.25.480openalex-snapshot
Sponge Cytogenetics — Mitotic Chromosomes of Ten Species of Freshwater Sponge
inferredcites →https://doi.org/10.2307/1543611openalex-snapshot
Cytological Basis of Photoresponsive Behavior in a Sponge Larva
inferredcites →https://doi.org/10.2307/3593127openalex-snapshot
Endosymbiotic Yeast Maternally Transmitted in a Marine Sponge
inferredcites →https://doi.org/10.32614/r.manualsopenalex-snapshot
R: A Language and Environment for Statistical Computing
inferredcites →https://doi.org/10.3389/fimmu.2018.01486openalex-snapshot
Apoptotic Cell-Derived Extracellular Vesicles: More Than Just Debris
inferredcites →https://doi.org/10.3402/jev.v3.24641openalex-snapshot
Routes and mechanisms of extracellular vesicle uptake
inferredcites →https://doi.org/10.5479/si.00810282.596openalex-snapshot
Thesaurus of sponge morphology
inferredcites →https://doi.org/10.6084/m9.figshare.c.3571566openalex-snapshot
Supplementary material from “The role of cell replacement in benthic–pelagic coupling by suspension feeders”
inferredcites →https://doi.org/10.70675/e20e27ebza00az4c18za8bezff8cc572085eopenalex-snapshot
La reproduction chez Oscarella lobularis (Porifera - Homoscleromorpha) : gènes impliqués et effets de l'environnement
inferredcites →https://doi.org/10.7717/peerj.1211openalex-snapshot
Transdifferentiation is a driving force of regeneration inHalisarca dujardini(Demospongiae, Porifera)
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1007/978-1-0716-0974-3_11openalex-snapshot
In Situ Hybridization Techniques in the Homoscleromorph Sponge Oscarella lobularis
inferred← citeshttps://doi.org/10.1007/978-1-0716-0974-3_5openalex-snapshot
Staining and Tracking Methods for Studying Sponge Cell Dynamics
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/s11626-021-00578-2openalex-snapshot
Cultivation of fractionated cells from a bioactive-alkaloid-bearing marine sponge Axinella sp.
inferred← citeshttps://doi.org/10.1186/s12862-021-01866-xopenalex-snapshot
Evolution of mechanisms controlling epithelial morphogenesis across animals: new insights from dissociation-reaggregation experiments in the sponge Oscarella lobularis
inferred← citeshttps://doi.org/10.3390/genes12040506openalex-snapshot
Whole-Body Regeneration in Sponges: Diversity, Fine Mechanisms, and Future Prospects
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