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Historical introduction, overview, and reproductive biology of the protochordates
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Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/(sici)1098-2795(199709)48:1<137::aid-mrd16>3.0.co;2-yopenalex-snapshot
Ascidian eggs block polyspermy by two independent mechanisms: One at the egg plasma membrane, the other involving the follicle cells
inferredcites →https://doi.org/10.1002/(sici)1098-2795(199901)52:1<99::aid-mrd12>3.0.co;2-nopenalex-snapshot
Self-sterility of eggs induced by exogenous and endogenous protease in the solitary ascidian,Halocynthia roretzi
inferredcites →https://doi.org/10.1002/(sici)1098-2795(200001)55:1<109::aid-mrd15>3.0.co;2-bopenalex-snapshot
Mechanism of the block to hybridization and selfing between the sympatric ascidians Ciona intestinalis and Ciona savignyi
inferredcites →https://doi.org/10.1002/cne.903090402openalex-snapshot
Cell counts and maps in the larval central nervous system of the ascidian ciona intestinalis (L.)
inferredcites →https://doi.org/10.1002/jez.1400020202openalex-snapshot
Mosaic development in ascidian eggs
inferredcites →https://doi.org/10.1002/jez.1401950211openalex-snapshot
Control of spawning in the tunicate Styela plicata by variations in a natural light regime
inferredcites →https://doi.org/10.1002/jez.1402120214openalex-snapshot
The follicular envelope of ascidian eggs: A site of messenger RNA and protein synthesis during early embryogenesis
inferredcites →https://doi.org/10.1002/jez.1402120310openalex-snapshot
Periodic spawning of three types of the ascidian, Halocynthia roretzi (Drasche), under continuous light conditions
inferredcites →https://doi.org/10.1002/jez.1402270120openalex-snapshot
Ascidian one‐half embryos can develop into functional adult ascidians
inferredcites →https://doi.org/10.1002/jez.1402490309openalex-snapshot
Ascidian sperm penetration and the translocation of a cell surface glycosidase
inferredcites →https://doi.org/10.1002/mrd.1120080309openalex-snapshot
Mitochondrial movement during the ascidian sperm reaction
inferredcites →https://doi.org/10.1006/dbio.2002.0772openalex-snapshot
Cyclical Generation and Degeneration of Organs in a Colonial Urochordate Involves Crosstalk between Old and New: A Model for Development and Regeneration
inferredcites →https://doi.org/10.1007/978-1-4613-2255-9_15openalex-snapshot
Sperm Glycosidase as a Plausible Mediator of Sperm Binding to the Vitelline Envelope in Ascidians
inferredcites →https://doi.org/10.1007/978-4-431-66982-1_14openalex-snapshot
Cell Signalings for Activation of Motility and Chemotaxis in the Sperm of Ciona
inferredcites →https://doi.org/10.1007/978-4-431-66982-1_27openalex-snapshot
Maternal Genetic Information Stored in Fertilized Eggs of the Ascidian, Halocynthia roretzi
inferredcites →https://doi.org/10.1007/bf00377219openalex-snapshot
Establishment of self-sterility of eggs in the ovary of the solitary ascidian, Halocynthia roretzi
inferredcites →https://doi.org/10.1007/bf01313478openalex-snapshot
Storage of exogenous sperm by the compound ascidianDiplosoma listerianum
inferredcites →https://doi.org/10.1007/bf03543240openalex-snapshot
The central nervous system, its cellular organisation and development, in the tadpole larva of the ascidian Ciona intestinalis
inferredcites →https://doi.org/10.1016/0012-1606(74)90118-3openalex-snapshot
Microfilaments and the mechanism of light-triggered sperm release in ascidians
inferredcites →https://doi.org/10.1016/0012-1606(79)90293-8openalex-snapshot
Calcium-mediated mitochondrial movement in ascidian sperm during fertilization
inferredcites →https://doi.org/10.1016/0012-1606(81)90322-5openalex-snapshot
Evidence for participation of sperm proteinases in fertilization of the solitary ascidian, Halocynthia roretzi: Effects of protease inhibitors
inferredcites →https://doi.org/10.1016/0012-1606(84)90229-xopenalex-snapshot
The role of actin and myosin in ascidian sperm mitochondrial translocation
inferredcites →https://doi.org/10.1016/0012-1606(90)90088-zopenalex-snapshot
Ultraviolet irradiation during ooplasmic segregation prevents gastrulation, sensory cell induction, and axis formation in the ascidian embryo
inferredcites →https://doi.org/10.1016/0012-1606(90)90353-kopenalex-snapshot
Interspecific hybridization between an anural and urodele ascidian: Differential expression of urodele features suggests multiple mechanisms control anural development
inferredcites →https://doi.org/10.1016/0169-5347(92)90115-ropenalex-snapshot
Fish evolution and systematics: Evidence from Spermatozoa
inferredcites →https://doi.org/10.1016/b978-0-12-282502-6.50014-5openalex-snapshot
CHORDATA: ACRANIA (CEPHALOCHORDATA)
inferredcites →https://doi.org/10.1016/b978-0-12-282505-7.x5001-5openalex-snapshot
Reproduction of Marine Invertebrates
inferredcites →https://doi.org/10.1016/j.biolcel.2003.11.002openalex-snapshot
Fertilisation calcium signals in the ascidian egg
inferredcites →https://doi.org/10.1016/s0022-0981(00)00168-4openalex-snapshot
Light induced larval release of a colonial ascidian
inferredcites →https://doi.org/10.1016/s0065-2881(08)60341-7openalex-snapshot
The Biology of Ascidians
inferredcites →https://doi.org/10.1016/s0065-2881(08)60457-5openalex-snapshot
The Physiology of Ascidians
inferredcites →https://doi.org/10.1016/s0074-7696(02)17016-1openalex-snapshot
Specification of developmental fates in ascidian embryos: Molecular approach to maternal determinants and signaling molecules
inferredcites →https://doi.org/10.1016/s0092-8674(01)00481-0openalex-snapshot
The Ascidian as a Model Organism in Developmental and Evolutionary Biology
inferredcites →https://doi.org/10.1016/s0166-2236(00)01851-8openalex-snapshot
The larval ascidian nervous system: the chordate brain from its small beginnings
inferredcites →https://doi.org/10.1017/cbo9781139567411openalex-snapshot
Histoire naturelle des animaux sans vertèbres
inferredcites →https://doi.org/10.1038/254244a0openalex-snapshot
Chemotaxis of the spermatozoa of Ciona intestinalis
inferredcites →https://doi.org/10.1038/nrg1042openalex-snapshot
The ascidian tadpole larva: comparative molecular development and genomics
inferredcites →https://doi.org/10.1046/j.1432-0436.2001.068001001.xopenalex-snapshot
Ascidian embryos as a model system to analyze expression and function of developmental genes
inferredcites →https://doi.org/10.1073/pnas.032389499openalex-snapshot
Extracellular ubiquitination and proteasome-mediated degradation of the ascidian sperm receptor
inferredcites →https://doi.org/10.1073/pnas.242470599openalex-snapshot
A chemoattractant for ascidian spermatozoa is a sulfated steroid
inferredcites →https://doi.org/10.1073/pnas.96.17.9633openalex-snapshot
Follicle cell proteasome activity and acid extract from the egg vitelline coat prompt the onset of self-sterility in Ciona intestinalis oocytes
inferredcites →https://doi.org/10.1093/icb/22.4.753openalex-snapshot
Asexual Development of Ascidians: Its Biological Significance, Diversity, and Morphogenesis
inferredcites →https://doi.org/10.1093/icb/22.4.775openalex-snapshot
Self or Non—self Recognition in Compound Ascidians
inferredcites →https://doi.org/10.1093/icb/22.4.783openalex-snapshot
Colony Specificity in the Colonial Tunicate Botryllus and the Origins of Vertebrate Immunity
inferredcites →https://doi.org/10.1093/oso/9780198540243.001.0001openalex-snapshot
The Biology of Pelagic Tunicates
inferredcites →https://doi.org/10.1098/rspb.1999.0628openalex-snapshot
Not like Botryllus: indiscriminate post–metamorphic fusion in a compound ascidian
inferredcites →https://doi.org/10.1098/rstb.1931.0006openalex-snapshot
VI. Studies in tunicate development, Part II. - Abbreviation of development in the molgulidæ
inferredcites →https://doi.org/10.1111/j.1096-3642.1990.tb00562.xopenalex-snapshot
Revision of the class Sorberacea (benthic tunicates) with descriptions of seven new species
inferredcites →https://doi.org/10.1111/j.1440-169x.1988.00325.xopenalex-snapshot
Sperm Binding and Penetration during Ascidian Fertilization*
inferredcites →https://doi.org/10.1111/j.1440-169x.1991.00155.xopenalex-snapshot
Possible MIS Production by Follicle Cells in Spontaneous Oocyte Maturation of the Ascidian, Halocynthia roretzi
inferredcites →https://doi.org/10.1111/j.1463-6395.1996.tb01253.xopenalex-snapshot
Ascidian Larvae: The Role of Test Cells in Preventing Hydrophobicity
inferredcites →https://doi.org/10.1126/science.200.4337.64openalex-snapshot
Tunicate Eggs Utilize Ammonium Ions for Flotation
inferredcites →https://doi.org/10.1139/z04-155openalex-snapshot
Amphioxus molecular biology: insights into vertebrate evolution and developmental mechanisms
inferredcites →https://doi.org/10.1139/z04-156openalex-snapshot
Ecology and natural history of the protochordates
inferredcites →https://doi.org/10.1139/z04-157openalex-snapshot
The morphology, behavior, and biomechanics of swimming in ascidian larvae
inferredcites →https://doi.org/10.1139/z04-158openalex-snapshot
Key characters uniting hemichordates and chordates: homologies or homoplasies?
inferredcites →https://doi.org/10.1139/z04-159openalex-snapshot
Eutely, cell lineage, and fate within the ascidian larval nervous system: determinacy or to be determined?
inferredcites →https://doi.org/10.1139/z04-161openalex-snapshot
Rejection patterns in botryllid ascidian immunity: the first tier of allorecognition
inferredcites →https://doi.org/10.1139/z04-162openalex-snapshot
Protochordate body plan and the evolutionary role of larvae: old controversies resolved?
inferredcites →https://doi.org/10.1139/z04-163openalex-snapshot
The nervous system of amphioxus: structure, development, and evolutionary significance
inferredcites →https://doi.org/10.1139/z04-164openalex-snapshot
Environmental factors affecting reproduction and development in ascidians and other protochordates
inferredcites →https://doi.org/10.1139/z04-165openalex-snapshot
Using ascidian embryos to study the evolution of developmental gene regulatory networks
inferredcites →https://doi.org/10.1139/z04-177openalex-snapshot
The nervous system in adult tunicates: current research directions
inferredcites →https://doi.org/10.1139/z04-190openalex-snapshot
A phylogeny of the hemichordates based on morphological characters
inferredcites →https://doi.org/10.1139/z05-010openalex-snapshot
Molecular phylogeny of the protochordates: chordate evolution
inferredcites →https://doi.org/10.1139/z81-203openalex-snapshot
Corella species in the American Pacific Northwest: distinction of C. inflata Huntsman, 1912 from C. willmeriana Herdman, 1898 (Ascidiacea, Phlebobranchia)
inferredcites →https://doi.org/10.1139/z95-198openalex-snapshot
Brooding strategies in solitary ascidians: Corella species from north and south temperate waters
inferredcites →https://doi.org/10.1242/dev.121.10.3457openalex-snapshot
The sperm entry point defines the orientation of the calcium-induced contraction wave that directs the first phase of cytoplasmic reorganization in the ascidian egg
inferredcites →https://doi.org/10.1242/dev.125.5.899openalex-snapshot
The hsp70 protein is involved in the acquisition of gamete self-sterility in the ascidian Ciona intestinalis
inferredcites →https://doi.org/10.1242/dev.126.8.1643openalex-snapshot
A multigene locus containing the Manx and bobcat genes is required for development of chordate features in the ascidian tadpole larva
inferredcites →https://doi.org/10.1242/jcs.s2-25.s1.81openalex-snapshot
The later stages in the development of balanoglossus kowalevskii, with a suggestion as to the affinities of the enteropneusta
inferredcites →https://doi.org/10.2108/zsj.13.241openalex-snapshot
Immunohistology with Antibodies Specific to Test Cells in the Ascidian Ciona intestinalis Suggests Their Role in Larval Tunic Formation
inferredcites →https://doi.org/10.2108/zsj.20.889openalex-snapshot
Gonadal State of Wild Amphioxus Populations and Spawning Success in Captive Conditions during the Breeding Period in Japan
inferredcites →https://doi.org/10.2307/1539783openalex-snapshot
THE GENERAL ECOLOGY AND GROWTH OF A SOLITARY ASCIDIAN, CORELLA WILLMERIANA
inferredcites →https://doi.org/10.2307/1539890openalex-snapshot
THE EFFECT OF LIGHT ON THE SPAWNING OF CIONA INTESTINALIS
inferredcites →https://doi.org/10.2307/1539896openalex-snapshot
LIGHT-INDUCTION OF SHEDDING OF GAMETES IN CIONA INTESTINALIS AND MOLGULA MANHATTENSIS
inferredcites →https://doi.org/10.2307/1540308openalex-snapshot
LARVA RELEASE IN RESPONSE TO LIGHT BY THE COMPOUND ASCIDIANSDISTAPLIA OCCIDENTALISANDMETANDROCARPA TAYLORI
inferredcites →https://doi.org/10.2307/1541757openalex-snapshot
Distributional Consequences of Adhesive Eggs and Anural Development in the Ascidian Molgula pacifica (Huntsman, 1912)
inferredcites →https://doi.org/10.2307/1542799openalex-snapshot
Germ-cell warfare in ascidians: sperm from one species can interfere with the fertilization of a second species
inferredcites →https://doi.org/10.2307/1543025openalex-snapshot
Chemical Mediation of Sperm Activity and Longevity in the Solitary Ascidians Ciona intestinalis and Ascidiella aspersa
inferredcites →https://doi.org/10.2307/1543154openalex-snapshot
Mechanisms of Specification in Ascidian Embryos
inferredcites →https://doi.org/10.2307/1543540openalex-snapshot
Strategies for Sperm Chemotaxis in the Siphonophores and Ascidians: A Numerical Simulation Study
inferredcites →https://doi.org/10.2307/2422543openalex-snapshot
The Invertebrates: Smaller Coelomate Groups.
inferredcites →https://doi.org/10.4052/tigg.4.437openalex-snapshot
The Involvement of Sperm and Egg Glycosidases in Animal Fertilization
inferredcites →https://doi.org/10.5281/zenodo.16047652openalex-snapshot
Loss of the Paternal Mitochondrion during Fertilization
inferredcites →https://doi.org/10.5860/choice.35-3280openalex-snapshot
Embryology: constructing the organism
inferredcites →https://doi.org/10.5962/bhl.title.125513openalex-snapshot
Mémoires sur les animaux sans vertèbres. *1e partie*@Description et classification des animaux invertébrés et articulés, connus sous les noms de crustacés, d'insectes, d'annélides, etc
inferredcites →https://doi.org/10.5962/bhl.title.1824openalex-snapshot
The British Tunicata; an unfinished monograph
inferredcites →https://doi.org/10.5962/bhl.title.4801openalex-snapshot
The organization and cell-lineage of the ascidian egg
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1590/s1984-4689.v41.e23042zenodo-depositor-declared
A synopsis of Tunicata biodiversity in Brazil
inferred← citeshttps://doi.org/10.1002/ece3.1035openalex-snapshot
Two sexes, one body: intra‐ and intersex covariation of gamete phenotypes in simultaneous hermaphrodites
inferred← citeshttps://doi.org/10.1002/ece3.70639openalex-snapshot
Morphological Characteristics, Mitochondrial Genome, and Evolutionary Insights Into a New Sea Squirt From the Beibu Gulf
inferred← citeshttps://doi.org/10.1007/978-3-319-92486-1_15openalex-snapshot
Solitary Ascidians as Model Organisms in Regenerative Biology Studies
inferred← citeshttps://doi.org/10.1007/s00239-010-9372-9openalex-snapshot
Accelerated Evolutionary Rate of Housekeeping Genes in Tunicates
inferred← citeshttps://doi.org/10.1007/s00300-013-1319-3openalex-snapshot
A re-evaluation of morphological characters of the invasive ascidian Corella eumyota reveals two different species at the tip of South America and in the South Shetland Islands, Antarctica
inferred← citeshttps://doi.org/10.1007/s00435-008-0074-4openalex-snapshot
Fine structure of the ventral nerve centre and interspecific identification of individual neurons in the enigmatic Chaetognatha
inferred← citeshttps://doi.org/10.1007/s00436-006-0178-zopenalex-snapshot
Infestation of Lymnaea stagnalis by digenean flukes in the Jeziorak Lake
inferred← citeshttps://doi.org/10.1007/s00442-007-0817-9openalex-snapshot
Spatiotemporal variation in reproductive parameters of yellow-bellied marmots
inferred← citeshttps://doi.org/10.1007/s10682-020-10065-xopenalex-snapshot
Correlational selection on size and development time is inconsistent across early life stages
inferred← citeshttps://doi.org/10.1007/s42991-026-00597-0openalex-snapshot
Within-group kinship and mating system in a cooperative breeder, the northern mole vole (Ellobius talpinus), in the Lower Volga region
inferred← citeshttps://doi.org/10.1016/b978-0-12-407774-4.00002-9openalex-snapshot
Cephalostatins and Ritterazines
inferred← citeshttps://doi.org/10.1016/j.cbpa.2005.11.013openalex-snapshot
Neuroendocrinology of protochordates: Insights from Ciona genomics
inferred← citeshttps://doi.org/10.1016/j.dci.2020.103669openalex-snapshot
Antitumoral compounds from vertebrate sister group: A review of Mediterranean ascidians
inferred← citeshttps://doi.org/10.1016/j.ecss.2016.08.048openalex-snapshot
Biology of the invasive ascidian Ascidiella aspersa in its native habitat: Reproductive patterns and parasite load
inferred← citeshttps://doi.org/10.1016/j.ecss.2022.107883openalex-snapshot
Disembarking in port: Early detection of the ascidian Ascidiella scabra (Müller, 1776) in a SW Atlantic port and forecast of its worldwide environmental suitability
inferred← citeshttps://doi.org/10.1016/j.jembe.2007.08.004openalex-snapshot
Effects of temporal variability of disturbance on the succession in marine fouling communities in northern-central Chile
inferred← citeshttps://doi.org/10.1016/j.rsma.2018.07.001openalex-snapshot
The highly competitive ascidian Didemnum sp. threatens coral reef communities in the Wakatobi Marine National Park, Southeast Sulawesi, Indonesia
inferred← citeshttps://doi.org/10.1016/j.rsma.2020.101430openalex-snapshot
Population genetic structure in the coral reef associated ascidian, Polycarpa aurata, throughout Wallacea, Indonesia
inferred← citeshttps://doi.org/10.1038/s41598-020-68031-0openalex-snapshot
Coupling feeding activity, growth rates and molecular data shows dietetic needs of Ciona robusta (Ascidiacea, Phlebobranchia) in automatic culture plants
inferred← citeshttps://doi.org/10.1038/s43247-024-01607-0openalex-snapshot
Shifts in benthic megafauna communities after glacial retreat in an Antarctic fjord
inferred← citeshttps://doi.org/10.1080/07924259.2021.1927861openalex-snapshot
Invertebrate oogenesis – a review and synthesis: comparative ovarian morphology, accessory cell function and the origins of yolk precursors
inferred← citeshttps://doi.org/10.1086/bblv221n1p43openalex-snapshot
Asexual Propagation and Regeneration in Colonial Ascidians
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780199549429.001.0001openalex-snapshot
Animal Evolution
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780199549429.002.0003openalex-snapshot
Copyright Page
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780199549429.002.0007openalex-snapshot
Contributors
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780199549429.002.0008openalex-snapshot
Introduction
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780199549429.003.0001openalex-snapshot
The earliest fossil record of the animals and its significance
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780199549429.003.0002openalex-snapshot
The Ediacaran emergence of bilaterians: congruence between the genetic and the geological fossil records
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780199549429.003.0003openalex-snapshot
Genomic, phylogenetic, and cell biological insights into metazoan origins
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780199549429.003.0004openalex-snapshot
The mouth, the anus, and the blastopore—open questions about questionable openings
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780199549429.003.0005openalex-snapshot
Origins of metazoan body plans: the larval revolution
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780199549429.003.0006openalex-snapshot
Assembling the spiralian tree of life
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780199549429.003.0007openalex-snapshot
The evolution of nervous system centralization
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780199549429.003.0008openalex-snapshot
The origins and evolution of the Ecdysozoa
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780199549429.003.0009openalex-snapshot
Deciphering deuterostome phylogeny: molecular, morphological, and palaeontological perspectives
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780199549429.003.0010openalex-snapshot
Molecular genetic insights into deuterostome evolution from the direct-developing hemichordateSaccoglossus kowalevskii
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780199549429.003.0011openalex-snapshot
Invertebrate Problematica: kinds, causes, and solutions
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780199549429.003.0012openalex-snapshot
Improvement of molecular phylogenetic inference and the phylogeny of Bilateria
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780199549429.003.0013openalex-snapshot
Beyond linear sequence comparisons: the use of genome-level characters for phylogenetic reconstruction
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780199549429.003.0014openalex-snapshot
The animal in the genome: comparative genomics and evolution
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780199549429.003.0015openalex-snapshot
MicroRNAs and metazoan phylogeny: big trees from little genes
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780199549429.003.0016openalex-snapshot
The evolution of developmental gene networks: lessons from comparative studies on holometabolous insects
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780199549429.003.0017openalex-snapshot
Conserved developmental processes and the evolution of novel traits: wounds, embryos, veins, and butterfly eyespots
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780199549429.003.0018openalex-snapshot
Reassembling animal evolution: a four-dimensional puzzle
inferred← citeshttps://doi.org/10.1093/icb/icj035openalex-snapshot
Coloniality has evolved once in Stolidobranch Ascidians
inferred← citeshttps://doi.org/10.1098/rstb.2007.2246openalex-snapshot
Deciphering deuterostome phylogeny: molecular, morphological and palaeontological perspectives
inferred← citeshttps://doi.org/10.1111/ecog.03018openalex-snapshot
Climate change, glacier retreat and a new ice‐free island offer new insights on Antarctic benthic responses
inferred← citeshttps://doi.org/10.1111/ivb.12013openalex-snapshot
Growing or reproducing in a temperate sea: optimization of resource allocation in a colonial ascidian
inferred← citeshttps://doi.org/10.1111/j.1474-919x.2011.01205.xopenalex-snapshot
Accelerated growth rates in late‐hatched Rhinoceros AukletCerorhinca monoceratachicks depend on food conditions and growth stage: an experimental approach
inferred← citeshttps://doi.org/10.1139/z04-155openalex-snapshot
Amphioxus molecular biology: insights into vertebrate evolution and developmental mechanisms
inferred← citeshttps://doi.org/10.1139/z04-156openalex-snapshot
Ecology and natural history of the protochordates
inferred← citeshttps://doi.org/10.1139/z04-157openalex-snapshot
The morphology, behavior, and biomechanics of swimming in ascidian larvae
inferred← citeshttps://doi.org/10.1139/z04-158openalex-snapshot
Key characters uniting hemichordates and chordates: homologies or homoplasies?
inferred← citeshttps://doi.org/10.1139/z04-159openalex-snapshot
Eutely, cell lineage, and fate within the ascidian larval nervous system: determinacy or to be determined?
inferred← citeshttps://doi.org/10.1139/z04-161openalex-snapshot
Rejection patterns in botryllid ascidian immunity: the first tier of allorecognition
inferred← citeshttps://doi.org/10.1139/z04-162openalex-snapshot
Protochordate body plan and the evolutionary role of larvae: old controversies resolved?
inferred← citeshttps://doi.org/10.1139/z04-163openalex-snapshot
The nervous system of amphioxus: structure, development, and evolutionary significance
inferred← citeshttps://doi.org/10.1139/z04-164openalex-snapshot
Environmental factors affecting reproduction and development in ascidians and other protochordates
inferred← citeshttps://doi.org/10.1139/z04-165openalex-snapshot
Using ascidian embryos to study the evolution of developmental gene regulatory networks
inferred← citeshttps://doi.org/10.1139/z04-177openalex-snapshot
The nervous system in adult tunicates: current research directions
inferred← citeshttps://doi.org/10.1139/z05-010openalex-snapshot
Molecular phylogeny of the protochordates: chordate evolution
inferred← citeshttps://doi.org/10.11606/issn.1984-5154.v21p1-13openalex-snapshot
Um panorama atual sobre a filogenia de Metazoa: conflitos e concordâncias
inferred← citeshttps://doi.org/10.11606/revbio.21.07.10.2021openalex-snapshot
Um panorama atual sobre a filogenia de Metazoa: conflitos e concordâncias
inferred← citeshttps://doi.org/10.1186/1742-9994-4-14openalex-snapshot
A new look at the ventral nerve centre of Sagitta: implications for the phylogenetic position of Chaetognatha (arrow worms) and the evolution of the bilaterian nervous system
inferred← citeshttps://doi.org/10.1186/1742-9994-7-29openalex-snapshot
Invertebrate neurophylogeny: suggested terms and definitions for a neuroanatomical glossary
inferred← citeshttps://doi.org/10.1186/s12983-020-00365-xopenalex-snapshot
Spawning induction, development and culturing of the solitary ascidian Polycarpa mytiligera, an emerging model for regeneration studies
inferred← citeshttps://doi.org/10.1371/journal.pone.0020657openalex-snapshot
Global Diversity of Ascidiacea
inferred← citeshttps://doi.org/10.1371/journal.pone.0186756openalex-snapshot
Benthic colonization in newly ice-free soft-bottom areas in an Antarctic fjord
inferred← citeshttps://doi.org/10.15368/theses.2012.31openalex-snapshot
THE PROTEOMIC RESPONSE OF SEA SQUIRTS (GENUS CIONA CONGENERS) TO HYPOSALINITY STRESS
inferred← citeshttps://doi.org/10.1590/s0073-47212009000100015openalex-snapshot
Sexual and asexual reproduction in Didemnum rodriguesi (Ascidiacea, Didemnidae)
inferred← citeshttps://doi.org/10.18359/rfcb.2129openalex-snapshot
Chaetognatha, Thaliacea, Euphausiacea and Pelagic Polychaeta in the Colombian Pacific Ocean During Two Periods in 1996 (La Niña) and Two Periods in 1997 (El Niño)
inferred← citeshttps://doi.org/10.21608/eajbsz.2018.13429openalex-snapshot
Reproductive Biology of The Solitary Ascidian, Herdmania momus (Ascidiacea: Hemichordta) from Hurghada Coasts, Red Sea, Egypt
inferred← citeshttps://doi.org/10.21608/jbaar.2018.148656openalex-snapshot
Marine pollution by some heavy metals and physiological response of Ruditapes decussatus
inferred← citeshttps://doi.org/10.26686/wgtn.17004652openalex-snapshot
Ecology of Biofouling and Impacts on Mussel Aquaculture: A Case Study with Didemnum Vexillum
inferred← citeshttps://doi.org/10.26686/wgtn.17004652.v1openalex-snapshot
Ecology of Biofouling and Impacts on Mussel Aquaculture: A Case Study with Didemnum Vexillum
inferred← citeshttps://doi.org/10.3354/ab00115openalex-snapshot
Microgeographical differentiation between morphotypes of Trididemnum orbiculatum (Tunicata: Ascidiacea) in southeastern Brazil
inferred← citeshttps://doi.org/10.3354/aei00063openalex-snapshot
Reproductive seasonality of the invasive ascidian Didemnum vexillum in New Zealand and implications for shellfish aquaculture
inferred← citeshttps://doi.org/10.3354/meps10416openalex-snapshot
Early biotic interactions among introduced and native benthic species reveal cryptic predation and shifts in larval behaviour
inferred← citeshttps://doi.org/10.3354/meps14632openalex-snapshot
Palatability of ascidians: a meta-analysis of the predation effect on ascidians
inferred← citeshttps://doi.org/10.3389/fevo.2016.00102openalex-snapshot
From Tropical to Sub-Tropical: Prolonged Reproductive Activity of the Invasive Ascidian Microcosmus exasperatus in the Eastern Mediterranean
inferred← citeshttps://doi.org/10.3389/fmicb.2015.01022openalex-snapshot
Temporal stability of bacterial symbionts in a temperate ascidian
inferred← citeshttps://doi.org/10.3390/md12063608openalex-snapshot
Quinone and Hydroquinone Metabolites from the Ascidians of the Genus Aplidium
inferred← citeshttps://doi.org/10.3390/md16050162openalex-snapshot
Ascidian Toxins with Potential for Drug Development
inferred← citeshttps://doi.org/10.3391/ai.2009.4.1.16openalex-snapshot
Larval recruitment of the invasive colonial ascidian Didemnum vexillum, seasonal water temperatures in New England coastal and offshore waters, and implications for spread of the species
inferred← citeshttps://doi.org/10.3391/ai.2011.6.4.11openalex-snapshot
Induced spawning and culture techniques for the invasive ascidian Didemnum vexillum (Kott, 2002)
inferred← citeshttps://doi.org/10.35229/jaes.1145082openalex-snapshot
Oikopleura (Vexillaria) dioica Fol, 1872 (Sınıf: Appendicularia)’nın Güneydoğu Karadeniz Ekosisteminde Biyometrik Özellikleri, Zamansal ve Alansal Dağılımı
inferred← citeshttps://doi.org/10.4067/s0718-19572017000200012openalex-snapshot
Ciclo reproductivo de la ascidia Pyura chilensis (Urochordata: Ascidiacea) procedente de líneas de cultivo de mitílidos
inferred← citeshttps://doi.org/10.47193/mafis.3922026010406openalex-snapshot
Reproductive strategies of benthic macroinvertebrates at the Argentine shelf-break front, southwestern Atlantic Ocean
inferred← citeshttps://doi.org/10.70675/02a6aa79z3c43z4f51z9498z306596326f97openalex-snapshot
De novo myogenesis and neurogenesis during budding of the colonial ascidian, Botryllus schlosseri
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