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THE DEVELOPMENT OF THE BUD IN BOTRYLLUS
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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/jmor.1050570204openalex-snapshot
Cell division and differentiation in asexual and sexual development
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.4353.1.2zenodo-depositor-declared
Fixation, description and DNA barcode of a neotype for Botryllus schlosseri (Pallas, 1766) (Tunicata, Ascidiacea)
inferred← citeshttps://doi.org/10.5252/zoosystema2020v42a9zenodo-depositor-declared
Botrylloides crystallinus n. sp., a new Botryllinae Adams & Adams, 1858 (Ascidiacea) from Mediterranean Sea
inferred← citeshttps://doi.org/10.1002/(sici)1097-0029(19990215)44:4<269::aid-jemt6>3.0.co;2-kopenalex-snapshot
Cell adhesion in the process of asexual reproduction of tunicates
inferred← citeshttps://doi.org/10.1002/aja.1001940109openalex-snapshot
A cyclical, developmentally‐regulated death phenomenon in a colonial urochordate
inferred← citeshttps://doi.org/10.1002/bies.10123openalex-snapshot
The colonial urochordate Botryllus schlosseri: from stem cells and natural tissue transplantation to issues in evolutionary ecology
inferred← citeshttps://doi.org/10.1002/cne.10097openalex-snapshot
Development of the motor nervous system in ascidians
inferred← citeshttps://doi.org/10.1002/dvdy.10112openalex-snapshot
Cell reorganisation during epithelial fusion and perforation: The case of ascidian branchial fissures
inferred← citeshttps://doi.org/10.1002/dvdy.20583openalex-snapshot
Identification of a novel gene involved in asexual organogenesis in the budding ascidian Botryllus schlosseri
inferred← citeshttps://doi.org/10.1002/dvdy.21037openalex-snapshot
Botryllus schlosseri : A model ascidian for the study of asexual reproduction
inferred← citeshttps://doi.org/10.1002/dvdy.21592openalex-snapshot
Cell proliferation dynamics of somatic and germline tissues during zooidal life span in the colonial tunicate Botryllus primigenus
inferred← citeshttps://doi.org/10.1002/dvdy.22542openalex-snapshot
Germline cell formation and gonad regeneration in solitary and colonial ascidians
inferred← citeshttps://doi.org/10.1002/dvg.22802openalex-snapshot
Sexual and asexual reproduction in the colonial ascidian B otryllus schlosseri
inferred← citeshttps://doi.org/10.1002/dvg.22820openalex-snapshot
Whole‐mount fluorescent in situ hybridization staining of the colonial tunicate B otryllus schlosseri
inferred← citeshttps://doi.org/10.1002/jez.1402070212openalex-snapshot
Sexual differentiation and germ cell transfer in the colonial ascidian Botryllus schlosseri
inferred← citeshttps://doi.org/10.1002/jez.1402200104openalex-snapshot
Induction of malformed zooids and determination of polarity in palleal buds of the polystyelid ascidian, Polyandrocarpa misakiensis
inferred← citeshttps://doi.org/10.1002/jez.1402240204openalex-snapshot
Pattern development in palleal buds of the polystyelid ascidian, Polyandrocarpa misakiensis: Bud grafting induces bilateral asymmetry conversion through polarity reversal
inferred← citeshttps://doi.org/10.1002/jez.1402530209openalex-snapshot
Botryllus schlosseri (tunicata) whole colony irradiation: Do senescent zooid resorption and immunological resorption involve similar recognition events?
inferred← citeshttps://doi.org/10.1002/jez.a.10244openalex-snapshot
Phenotypic plasticity of reproductive effort in a colonial ascidian, Botryllus schlosseri
inferred← citeshttps://doi.org/10.1002/jez.b.21303openalex-snapshot
Whole body regeneration in a colonial ascidian, Botrylloides violaceus
inferred← citeshttps://doi.org/10.1002/jez.b.22940openalex-snapshot
The eventful history of nonembryonic development in tunicates
inferred← citeshttps://doi.org/10.1002/jmor.1051390102openalex-snapshot
Development of polarity and bilateral asymmetry in the palleal bud of Botryllus schlosseri (Pallas)
inferred← citeshttps://doi.org/10.1002/jmor.1051480203openalex-snapshot
Budding by Oozooids in the Polystyelid Ascidian Metandrocarpa Taylori Huntsman
inferred← citeshttps://doi.org/10.1002/jmor.1051480306openalex-snapshot
Studies on the formation of germ cells in a compound ascidian Botryllus, primigenus oka
inferred← citeshttps://doi.org/10.1002/jmor.1051520307openalex-snapshot
Comparative studies on the structure of reproductive organs of four botryllid ascidians
inferred← citeshttps://doi.org/10.1002/jmor.1051570105openalex-snapshot
Comparative studies on the circulatory system of the compound ascidians, Botryllus, Botrylloides and Symplegma
inferred← citeshttps://doi.org/10.1002/jmor.1051730306openalex-snapshot
Pattern development in palleal buds of botryllid ascidians: Relation between parent and its buds in their body axes
inferred← citeshttps://doi.org/10.1002/mrd.22661openalex-snapshot
Gonad development and hermaphroditism in the ascidian Botryllus schlosseri
inferred← citeshttps://doi.org/10.1002/reg2.26openalex-snapshot
Distal regeneration involves the age dependent activity of branchial sac stem cells in the ascidian Ciona intestinalis
inferred← citeshttps://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
inferred← citeshttps://doi.org/10.1007/978-3-642-79847-4_5openalex-snapshot
Histocompatibility Reactions in Invertebrates
inferred← citeshttps://doi.org/10.1007/978-90-481-2767-2openalex-snapshot
Stem Cells in Marine Organisms
inferred← citeshttps://doi.org/10.1007/978-90-481-2767-2_11openalex-snapshot
Stem Cells in Sexual and Asexual Reproduction of Botryllus schlosseri (Ascidiacea, Tunicata): An Overview
inferred← citeshttps://doi.org/10.1007/978-90-481-2767-2_4openalex-snapshot
Stem Cells in Aquatic Invertebrates: Common Premises and Emerging Unique Themes
inferred← citeshttps://doi.org/10.1007/bf00391934openalex-snapshot
Shedding of gametes in the compound ascidian Botryllus primigenus
inferred← citeshttps://doi.org/10.1007/bf00848597openalex-snapshot
The mechanism of anteroposterior cell determination in ascidian palleal buds: A gap of positional values triggers posterior formation
inferred← citeshttps://doi.org/10.1007/bf00848766openalex-snapshot
The role of parental positional information in the determination of antero-posterior polarity during palleal budding in ascidians
inferred← citeshttps://doi.org/10.1007/s00441-003-0738-9openalex-snapshot
Apoptosis and phosphatidylserine-mediated recognition during the take-over phase of the colonial life-cycle in the ascidian Botryllus schlosseri
inferred← citeshttps://doi.org/10.1007/s10126-004-5067-9openalex-snapshot
Development of Panel of Monoclonal Antibodies Specific to Urochordate Cell Surface Antigens
inferred← citeshttps://doi.org/10.1007/s11626-009-9179-4openalex-snapshot
Further portrayal of epithelial monolayers emergent de novo from extirpated ascidians palleal buds
inferred← citeshttps://doi.org/10.1007/s11626-010-9357-4openalex-snapshot
De novo emerged stemness signatures in epithelial monolayers developed from extirpated palleal buds
inferred← citeshttps://doi.org/10.1007/s11626-997-0058-6openalex-snapshot
Initiation of epithelial cell cultures from palleal buds of Botryllus schlosseri, a colonial tunicate
inferred← citeshttps://doi.org/10.1016/0012-1606(75)90088-3openalex-snapshot
Determination of polarity and bilateral asymmetry in palleal and vascular buds of the ascidian Botryllus schlosseri
inferred← citeshttps://doi.org/10.1016/0012-1606(79)90211-2openalex-snapshot
Muscle cell differentiation in the ascidian heart
inferred← citeshttps://doi.org/10.1016/0012-1606(84)90236-7openalex-snapshot
Morphogenetic tissue interactions during posterior commitment in palleal buds of the polystyelid ascidian, Polyandrocarpa misakiensis
inferred← citeshttps://doi.org/10.1016/0012-1606(86)90041-2openalex-snapshot
Mitosis and body patterning during morphallactic development of palleal buds in ascidians
inferred← citeshttps://doi.org/10.1016/j.cell.2005.10.026openalex-snapshot
Stem Cells Are Units of Natural Selection in a Colonial Ascidian
inferred← citeshttps://doi.org/10.1016/j.cellbi.2005.08.013openalex-snapshot
Development of monoclonal antibodies specific to urochordate intracellular epitopes
inferred← citeshttps://doi.org/10.1016/j.dci.2003.08.007openalex-snapshot
Continuous development precludes radioprotection in a colonial ascidian
inferred← citeshttps://doi.org/10.1016/j.dci.2009.10.005openalex-snapshot
Hovering between death and life: Natural apoptosis and phagocytes in the blastogenetic cycle of the colonial ascidian Botryllus schlosseri
inferred← citeshttps://doi.org/10.1016/j.fsi.2020.09.006openalex-snapshot
BsTLR1: A new member of the TLR family of recognition proteins from the colonial ascidian Botryllus schlosseri
inferred← citeshttps://doi.org/10.1016/j.imbio.2010.10.011openalex-snapshot
Immune roles of a rhamnose-binding lectin in the colonial ascidian Botryllus schlosseri
inferred← citeshttps://doi.org/10.1016/j.ydbio.2004.05.029openalex-snapshot
Telomerase maintained in self-renewing tissues during serial regeneration of the urochordate Botryllus schlosseri
inferred← citeshttps://doi.org/10.1016/j.ydbio.2006.08.055openalex-snapshot
Suppression of programmed cell death regulates the cyclical degeneration of organs in a colonial urochordate
inferred← citeshttps://doi.org/10.1016/j.ydbio.2008.08.023openalex-snapshot
The role of Nanos homologue in gametogenesis and blastogenesis with special reference to male germ cell formation in the colonial ascidian, Botryllus primigenus
inferred← citeshttps://doi.org/10.1016/j.ydbio.2012.11.006openalex-snapshot
Phagocyte dynamics in a highly regenerative urochordate: Insights into development and host defense
inferred← citeshttps://doi.org/10.1016/j.ydbio.2015.07.017openalex-snapshot
Evolution of the chordate regeneration blastema: Differential gene expression and conserved role of notch signaling during siphon regeneration in the ascidian Ciona
inferred← citeshttps://doi.org/10.1016/j.ydbio.2016.05.016openalex-snapshot
Redeployment of germ layers related TFs shows regionalized expression during two non-embryonic developments
inferred← citeshttps://doi.org/10.1016/j.ydbio.2017.01.012openalex-snapshot
Vascular budding in Symplegma brakenhielmi and the evolution of coloniality in styelid ascidians
inferred← citeshttps://doi.org/10.1016/j.ydbio.2018.09.009openalex-snapshot
Sixty years of experimental studies on the blastogenesis of the colonial tunicate Botryllus schlosseri
inferred← citeshttps://doi.org/10.1016/j.ydbio.2025.08.013openalex-snapshot
Germ cell formation and reproduction in tunicates
inferred← citeshttps://doi.org/10.1016/j.ydbio.2025.10.002openalex-snapshot
Botryllus humilis: A promising new ascidian model for aging, stem cell dynamics, and whole-body regeneration
inferred← citeshttps://doi.org/10.1017/9781139939867.011openalex-snapshot
Senescence in Modular Animals
inferred← citeshttps://doi.org/10.1017/s0025315425100611openalex-snapshot
Asexual reproduction and regenerative responses of botryllid ascidians to salinity and temperature variations
inferred← citeshttps://doi.org/10.1038/s41598-018-23749-wopenalex-snapshot
De novo draft assembly of the Botrylloides leachii genome provides further insight into tunicate evolution
inferred← citeshttps://doi.org/10.1073/pnas.1606276113openalex-snapshot
Developmental cell death programs license cytotoxic cells to eliminate histocompatible partners
inferred← citeshttps://doi.org/10.1080/01688170.1986.10510242openalex-snapshot
Developmental pattern of colonies in the polystyelid ascidian,Polyandrocarpa misakiensis
inferred← citeshttps://doi.org/10.1080/07924259.1995.9672447openalex-snapshot
Oogenesis and oocyte envelope differentiation in the viviparous ascidianBotrylloides violaceus
inferred← citeshttps://doi.org/10.1080/11250005509439204openalex-snapshot
Osservazioni sullo sviluppo, l'accrescimento e la riproduzione diBotryllus schlosseri(Pallas), in condizioni di laboratorio
inferred← citeshttps://doi.org/10.1080/11250005609439244openalex-snapshot
Effetti dell'estirpazione delle gemme sulla durata del ciclo vitale inBotryllus Schlosseri(Pallas)
inferred← citeshttps://doi.org/10.1080/11250006609440508openalex-snapshot
Aspetti e problemi della vita coloniale
inferred← citeshttps://doi.org/10.1080/11250007009436927openalex-snapshot
Sviluppo e Differenziamento del Tubo Digerente Nel Blastozooide Dell'ascidia ColonialeBotryllus Schlossebi(Pallas)
inferred← citeshttps://doi.org/10.1080/11250007109429158openalex-snapshot
The Circulatory System in the Blastozooid of the Colonial Ascidian Botryllus Schlosseri (Pallas)
inferred← citeshttps://doi.org/10.1080/11250007409430119openalex-snapshot
Observations on the Life Cycle ofBotryllus Schlosseri(Pallas) (Ascidiacea) in the Venetian Lagoon
inferred← citeshttps://doi.org/10.1080/11250007609430146openalex-snapshot
Hibernation of the Colonial AscidianBotrylloides Leachi(Savigny): Histological Observations
inferred← citeshttps://doi.org/10.1080/11250008409439481openalex-snapshot
Combined effects of temperature and salinity on sexual reproduction and colonial growth ofBotryllus schlosseri(Tunicata)
inferred← citeshttps://doi.org/10.1080/11250009609356159openalex-snapshot
New data on phagocytes and phagocytosis in the compound ascidian Botryllus schlosseri (Tunicata, Ascidiacea)
inferred← citeshttps://doi.org/10.1086/692841openalex-snapshot
Hematological Analysis of the Ascidian Botrylloides leachii (Savigny, 1816) During Whole-Body Regeneration
inferred← citeshttps://doi.org/10.1086/bblv221n1p43openalex-snapshot
Asexual Propagation and Regeneration in Colonial Ascidians
inferred← citeshttps://doi.org/10.1093/g3journal/jkad181openalex-snapshot
De novo genome assembly and comparative genomics for the colonial ascidian Botrylloides violaceus
inferred← citeshttps://doi.org/10.1093/zoolinnean/zlaa023openalex-snapshot
Toward a resolution of the cosmopolitanBotryllus schlosserispecies complex (Ascidiacea, Styelidae): mitogenomics and morphology of clade E (Botryllus gaiae)
inferred← citeshttps://doi.org/10.1096/fj.06-7337comopenalex-snapshot
Striving for normality: whole body regeneration through a series of abnormal generations
inferred← citeshttps://doi.org/10.1098/rspb.1994.0165openalex-snapshot
Alloimmune hierarchies and stress-induced reversals in the resorption of chimeric protochordate colonies
inferred← citeshttps://doi.org/10.1101/2020.05.31.126409openalex-snapshot
Evolution of colonial life history in styelids tunicates involves changes in complexity patterns
inferred← citeshttps://doi.org/10.1101/2023.07.10.548363openalex-snapshot
De novo genome assembly and comparative genomics for the colonial ascidian Botrylloides violaceus
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/j.1440-169x.1992.00463.xopenalex-snapshot
Ascidian Budding as a Transdifferentiation‐Like System: Multipotent Epithelium is not Undifferentiated
inferred← citeshttps://doi.org/10.1111/j.1440-169x.2007.00972.xopenalex-snapshot
Multipotent epithelial cells in the process of regeneration and asexual reproduction in colonial tunicates
inferred← citeshttps://doi.org/10.1111/j.1440-169x.2010.01196.xopenalex-snapshot
Piwi‐expressing hemoblasts serve as germline stem cells during postembryonic germ cell specification in colonial ascidian, Botryllus primigenus
inferred← citeshttps://doi.org/10.1111/j.1463-6395.1993.tb01226.xopenalex-snapshot
Egg Envelope Cytodifferentiation in the Colonial Ascidian Botryllus schlosseri (Tunicata)
inferred← citeshttps://doi.org/10.1111/j.1463-6395.1994.tb01115.xopenalex-snapshot
Ultrastructural Study of Oogenesis in the Compound Ascidian Botryllus schlosseri(Tunicata)
inferred← citeshttps://doi.org/10.1111/j.1469-185x.1951.tb01207.xopenalex-snapshot
REGENERATION AND BUDDING IN TUNICATES
inferred← citeshttps://doi.org/10.1111/j.1558-5646.1988.tb02510.xopenalex-snapshot
LIFE‐HISTORY VARIATION WITHIN A POPULATION OF THE COLONIAL ASCIDIAN BOTRYLLUS SCHLOSSERI. I. THE GENETIC AND ENVIRONMENTAL CONTROL OF SEASONAL VARIATION
inferred← citeshttps://doi.org/10.1139/z04-161openalex-snapshot
Rejection patterns in botryllid ascidian immunity: the first tier of allorecognition
inferred← citeshttps://doi.org/10.11606/t.41.2020.tde-24092019-095624openalex-snapshot
Developmental modularity in the colonial ascidian Symplegma: individual intercommunication, colony hematopoiesis, and environmental factors involved in coloniality
inferred← citeshttps://doi.org/10.1186/s13227-016-0047-5openalex-snapshot
Temporally and spatially dynamic germ cell niches in Botryllus schlosseri revealed by expression of a TGF-beta family ligand and vasa
inferred← citeshttps://doi.org/10.1186/s13227-019-0116-7openalex-snapshot
Modular co-option of cardiopharyngeal genes during non-embryonic myogenesis
inferred← citeshttps://doi.org/10.1186/s13227-019-0125-6openalex-snapshot
Regulation and evolution of muscle development in tunicates
inferred← citeshttps://doi.org/10.1186/s13227-021-00185-yopenalex-snapshot
Whole body regeneration and developmental competition in two botryllid ascidians
inferred← citeshttps://doi.org/10.1201/9781003217503-21openalex-snapshot
Botryllus schlosseri—A Model Colonial Species in Basic and Applied Studies
inferred← citeshttps://doi.org/10.1201/b10425-20openalex-snapshot
Redefining Stem Cells and Assembling Germ Plasm
inferred← citeshttps://doi.org/10.1242/dev.00804openalex-snapshot
Mechanisms of germ cell specification across the metazoans: epigenesis and preformation
inferred← citeshttps://doi.org/10.1242/dev.113.3.995openalex-snapshot
Budding-specific lectin induced in epithelial cells is an extracellular matrix component for stem cell aggregation in tunicates
inferred← citeshttps://doi.org/10.1242/jcs.s3-88.4.393openalex-snapshot
The Developmental Cycle of Botrylloides
inferred← citeshttps://doi.org/10.1242/jeb.00899openalex-snapshot
In vitrodelayed senescence of extirpated buds from zooids of the colonial tunicateBotryllus schlosseri
inferred← citeshttps://doi.org/10.1371/journal.pbio.0050071openalex-snapshot
Systemic Bud Induction and Retinoic Acid Signaling Underlie Whole Body Regeneration in the Urochordate Botrylloides leachi
inferred← citeshttps://doi.org/10.18353/crustacea.31.0_39openalex-snapshot
Interna structure and nucleus formation in Sacculina polygenea (Crustacea: Cirripedia: Rhizocephala: Sacculinidae)
inferred← citeshttps://doi.org/10.18353/crustacea.33.0_61openalex-snapshot
Development of primordial externae in the colonial interna of Polyascus polygenea (Crustacea: Cirripedia: Rhizocephala)
inferred← citeshttps://doi.org/10.20944/preprints202008.0459.v1openalex-snapshot
Colonial Life-history: A Major Evolutionary Transition, Involving Modularization of Multicellular Individuals and Heterochrony (Miniaturization and Adultation)
inferred← citeshttps://doi.org/10.2108/jsz.17.281openalex-snapshot
Advantage or Disadvantage. Is Asexual Reproduction Beneficial to Survival of the Tunicate, Polyandrocarpa misakiensis?
inferred← citeshttps://doi.org/10.2108/zsj.18.397openalex-snapshot
Studies on the Structure of the Brooding Organs of Two Botryllid Ascidians, Botryllus delicatus and Botryllus sexiens
inferred← citeshttps://doi.org/10.2108/zsj.23.245openalex-snapshot
In VitroCulture of Mesenchymal Lineage Cells Established from the Colonial Tunicate Botryllus primigenus
inferred← citeshttps://doi.org/10.2108/zsj.24.542openalex-snapshot
Body Muscle-Cell Differentiation from Coelomic Stem Cells in Colonial Tunicates
inferred← citeshttps://doi.org/10.2108/zsj.27.96openalex-snapshot
Natural Apoptosis During the Blastogenetic Cycle of the Colonial Ascidian Botryllus schlosseri : A Morphological Analysis
inferred← citeshttps://doi.org/10.2307/1538173openalex-snapshot
ASEXUAL REPRODUCTION IN THE COLONIAL TUNICATE, BOTRYLLUS SCHLOSSERI (PALLAS) SAVIGNY, WITH SPECIAL REFERENCE TO THE DEVELOPMENTAL HISTORY OF INTERSIPHONAL BANDS OF PIGMENT CELLS
inferred← citeshttps://doi.org/10.2307/1540579openalex-snapshot
BUDDING, SEXUAL REPRODUCTION, AND DEGENERATION IN THE COLONIAL ASCIDIAN,SYMPLEGMA REPTANS
inferred← citeshttps://doi.org/10.2307/1541365openalex-snapshot
COORDINATION OF COMPOUND ASCIDIANS BY EPITHELIAL CONDUCTION IN THE COLONIAL BLOOD VESSELS
inferred← citeshttps://doi.org/10.2307/1541621openalex-snapshot
DEVELOPMENT OF SPATIAL ORGANIZATION IN PALLEAL BUDS OF THE COMPOUND ASCIDIAN, SYMPLEGMA REPTANS
inferred← citeshttps://doi.org/10.2307/1543168openalex-snapshot
Development Basis of Phenotypic Variation in Egg Production in a Colonial Ascidian: Primary Oocyte Production Versus Oocyte Development
inferred← citeshttps://doi.org/10.2307/1543525openalex-snapshot
Delayed Insemination Results in Embryo Mortality in a Brooding Ascidian
inferred← citeshttps://doi.org/10.3354/meps002303openalex-snapshot
Combined Effects of Temperature and Salinity on Colonies of Botryllus schlosseri and Botfylloides leachi (Ascidiacea) from the Venetian Lagoon
inferred← citeshttps://doi.org/10.3390/biology11081106openalex-snapshot
How Metabolic Rate Relates to Cell Size
inferred← citeshttps://doi.org/10.46569/20.500.12680/kp78gn64popenalex-snapshot
Genetic Distribution and Regenarative Capacity of Botrylloides Diegensis and Botrylloides Niger
inferred← citeshttps://doi.org/10.5134/175997openalex-snapshot
OOZOOID FORMATION IN THE ASCIDIAN BOTRYLLOIDES VIOLACEUS
inferred← citeshttps://doi.org/10.5962/bhl.title.1020openalex-snapshot
Methods for obtaining and handling marine eggs and embryos [by] Donald P. Costello and Catherine Henley
inferred← citeshttps://doi.org/10.5962/bhl.title.1023openalex-snapshot
Methods for obtaining and handling marine eggs and embryos [by] D.P. Costello [and others
inferred← citeshttps://doi.org/10.70675/536ee4c3ze8e7z4184z9cccz681f8501b7d1openalex-snapshot
Bourgeonnement vasale : caractérisation d’une nouvelle forme de développement non-embryonnaire dans l’ascidie colonial Polyandrocarpa zorritensis
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