Modification of ciliary beating in sea urchin larvae induced by neurotransmitters: beat-plane rotation and control of frequency fluctuation

STUDIES ON CILIA

Satir, P. (1968) · The Journal of Cell Biology · doi:10.1083/jcb.39.1.77 · Cited by 556 · see citing works

Swimming and Flying in Nature

Wu, T. Y.-T., Brokaw, C. J., & Brennen, C. E. (1975) · Springer eBooks · doi:10.1007/978-1-4757-1326-8 · Cited by 485 · see citing works

The Physiology of Cilia and Mucociliary Interactions

Satir, P., & Sleigh, M. A. (1990) · Annual Review of Physiology · doi:10.1146/annurev.ph.52.030190.001033 · Cited by 239 · see citing works

SUSPENSION FEEDING BY MARINE INVERTEBRATE LARVAE: CLEARANCE OF PARTICLES BY CILIATED BANDS OF A ROTIFER, PLUTEUS, AND TROCHOPHORE

Strathmann, R. R., Jahn, T. L., & Fonseca, J. R. (1972) · Biological Bulletin · doi:10.2307/1540326 · Cited by 210 · see citing works

Calcium-Induced Contraction of the Rhizoplast of a Quadriflagellate Green Alga

Salisbury, J. L., & Floyd, G. L. (1978) · Science · doi:10.1126/science.202.4371.975 · Cited by 185 · see citing works

cAMP-stimulated phosphorylation of an axonemal polypeptide that copurifies with the 22S dynein arm regulates microtubule translocation velocity and swimming speed in Paramecium.

Hamasaki, T., Barkalow, K. L., Richmond, J., & Satir, P. (1991) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.88.18.7918 · Cited by 184 · see citing works

Direct Measurements of Sliding Between Outer Doublet Microtubules in Swimming Sperm Flagella

Brokaw, C. J. (1989) · Science · doi:10.1126/science.2928796 · Cited by 163 · see citing works

Basal body reorientation mediated by a Ca2+-modulated contractile protein.

McFadden, G. I., Schulze, D., Surek, B., Salisbury, J. L., & Melkonian, M. (1987) · The Journal of Cell Biology · doi:10.1083/jcb.105.2.903 · Cited by 141 · see citing works

Factors Affecting Ciliary Activity on the Gill of the Mussel Mytilus edulis

Aiello, E. (1960) · Physiological Zoology · doi:10.1086/physzool.33.2.30152299 · Cited by 140 · see citing works

The pair of central tubules rotates during ciliary beat in Paramecium

Omoto, C. K., & Kung, C. (1979) · Nature · doi:10.1038/279532a0 · Cited by 119 · see citing works

Ciliary reversal without rotation of axonemal structures in ctenophore comb plates.

Tamm, S. L., & Tamm, S. (1981) · The Journal of Cell Biology · doi:10.1083/jcb.89.3.495 · Cited by 117 · see citing works

Microtubule sliding in swimming sperm flagella: direct and indirect measurements on sea urchin and tunicate spermatozoa [published erratum appears in J Cell Biol 1991 Nov;115(4):1204]

Brokaw, C. J. (1991) · The Journal of Cell Biology · doi:10.1083/jcb.114.6.1201 · Cited by 102 · see citing works

Effect of vanadate on gill cilia: Switching mechanism in ciliary beat

Wais‐Steider, J., & Satir, P. (1979) · Journal of Supramolecular Structure · doi:10.1002/jss.400110309 · Cited by 83 · see citing works

Dynein from serotonin-activated cilia and flagella: extraction characteristics and distinct sites for cAMP-dependent protein phosphorylation

Stephens, R. E., & Prior, G. (1992) · Journal of Cell Science · doi:10.1242/jcs.103.4.999 · Cited by 83 · see citing works

The relation between the orientation of the central fibrils and the direction of beat in cilia of Opalina

Tamm, S. L., & Horridge, G. A. (1970) · Proceedings of the Royal Society B Biological Sciences · doi:10.1098/rspb.1970.0020 · Cited by 79 · see citing works

Electrical Activity associated with Ciliary Reversal in an Echinoderm Larva

Mackie, G. O., Spencer, A. N., & Strathmann, R. R. (1969) · Nature · doi:10.1038/2231384a0 · Cited by 65 · see citing works

Development Of Cell Junctions In Seaurchin Embryos

Spiegel, E., & Howard, L. (1983) · Journal of Cell Science · doi:10.1242/jcs.62.1.27 · Cited by 51 · see citing works

Regulation of ciliary movement in sea urchin embryos: Dopamine and 5-HT change the swimming behaviour

Mogami, Y., Watanabe, K., Chieko, O., Akemi, K., & Baba, S. A. (1992) · Comparative Biochemistry and Physiology Part C Comparative Pharmacology · doi:10.1016/0742-8413(92)90269-d · Cited by 41 · see citing works

Rotating the plane of imposed vibration can rotate the plane of flagellar beating in sea-urchin sperm without twisting the axoneme

Shingyoji, C., Katada, J., Takahashi, K., & Gibbons, I. R. (1991) · Journal of Cell Science · doi:10.1242/jcs.98.2.175 · Cited by 35 · see citing works

VARIABLE PERIODICITY IN THE RHIZOPLAST OF NAEGLERIA FLAGELLATES

Simpson, P. A., & Dingle, A. D. (1971) · The Journal of Cell Biology · doi:10.1083/jcb.51.1.323 · Cited by 33 · see citing works

Regular steps in bending cilia during the effective stroke

Baba, S. A. (1979) · Nature · doi:10.1038/282717a0 · Cited by 29 · see citing works

Negative Geotaxis in Sea Urchin Larvae: a Possible Role of Mechanoreception in the Late Stages of Development

Mogami, Y., Oobayashi, C., Yamaguchi, T., Ogiso, Y., & Baba, S. A. (1988) · Journal of Experimental Biology · doi:10.1242/jeb.137.1.141 · Cited by 26 · see citing works

Stimulation ofSpisulasperm motility by 5-hydroxytryptamine analogs

Kadam, A. L., & KOIDE, S. S. (1990) · Invertebrate Reproduction & Development · doi:10.1080/07924259.1990.9672085 · Cited by 26 · see citing works

Mechanisms and controls of microtubule sliding in cilia.

Satir, P. (1982) · PubMed · Cited by 25 · see citing works

Reconstitution of Metachronal Waves in Ciliated Cortical Sheets of Paramecium: II. Asymmetry of the Ciliary Movements

Okamoto, K.-I., & Nakaoka, Y. (1994) · Journal of Experimental Biology · doi:10.1242/jeb.192.1.73 · Cited by 19 · see citing works

Reconstitution of Metachronal Waves in Ciliated Cortical Sheets of Paramecium: I. Wave Stabilities

Okamoto, K.-I., & Nakaoka, Y. (1994) · Journal of Experimental Biology · doi:10.1242/jeb.192.1.61 · Cited by 19 · see citing works

Developmental changes in Ca2+ sensitivity of sea-urchin embryo cilia

Degawa, M., Mogami, Y., & Baba, S. A. (1986) · Comparative Biochemistry and Physiology Part A Physiology · doi:10.1016/0300-9629(86)90466-4 · Cited by 15 · see citing works

Three-dimensional recording and measurement of swimming paths of micro-organisms with two synchronized monochrome cameras

Baba, S. A., Inomata, S., Ooya, M., Mogami, Y., & Izumi-Kurotani, A. (1991) · Review of Scientific Instruments · doi:10.1063/1.1142103 · Cited by 14 · see citing works

Depolarization‐controlled parameters of the ciliary cycle and axonemal function

Sugino, K., & Machemer, H. (1990) · Cell Motility and the Cytoskeleton · doi:10.1002/cm.970160405 · Cited by 14 · see citing works

High time‐resolution analysis of transient bending patterns during ciliary responses following electric stimulation in sea urchin embryos

Baba, S. A., & Mogami, Y. (1987) · Cell Motility and the Cytoskeleton · doi:10.1002/cm.970070303 · Cited by 14 · see citing works

Five Different States of Ciliary Activity in the Epaulette of Echinoplutei

Mogami, Y., Fujima, K., & Baba, S. A. (1991) · Journal of Experimental Biology · doi:10.1242/jeb.155.1.65 · Cited by 12 · see citing works

Aspects of differentiation and function of cilia and adjacent structures of the sea urchin larva.

Immers, J., & Lundgren, B. (1972) · PubMed · Cited by 9 · see citing works

RECONSTITUTION OF METACHRONAL WAVES IN CILIATED CORTICAL SHEETS OF PARAMECIUM

Okamoto, K., & Nakaoka, Y. (1994) · Cited by 8 · see citing works

Beating of Cilia of Sea Urchin Embryos: A Critical Comparison of the Normal and Reversed Beating of Cilia of Isolated Cells

Mogami, Y., Sekiguchi, S., & Baba, S. A. (1993) · Journal of Experimental Biology · doi:10.1242/jeb.175.1.251 · Cited by 7 · see citing works

Cholinesterase inhibition and impacts on behavior of the Asian clam, Corbicula fluminea, after exposure to an organophosphate insecticide

Cooper, N. L., & Bidwell, J. R. (2005) · Aquatic Toxicology · doi:10.1016/j.aquatox.2005.09.012 · Cited by 113 · see citing works

Origin and early evolution of neural circuits for the control of ciliary locomotion

Jékely, G. (2011) · Proceedings of the Royal Society B: Biological Sciences · doi:10.1098/rspb.2010.2027 · Cited by 103 · see citing works

Expression of tryptophan 5‐hydroxylase gene during sea urchin neurogenesis and role of serotonergic nervous system in larval behavior

Yaguchi, S., & Katow, H. (2003) · The Journal of Comparative Neurology · doi:10.1002/cne.10865 · Cited by 87 · see citing works

Neuronal coordination of motile cilia in locomotion and feeding

Marinković, M., Berger, J., & Jékely, G. (2019) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2019.0165 · Cited by 67 · see citing works

A novel serotonin-secreting cell type regulates ciliary motility in the mucociliary epidermis of <i>Xenopus</i> tadpoles

Walentek, P., Bogusch, S., Thumberger, T., Vick, P., Dubaissi, E., Beyer, T., Blum, M., & Schweickert, A. (2014) · Development · doi:10.1242/dev.102343 · Cited by 61 · see citing works

Serotonin Increases Cilia-Driven Particle Transport via an Acetylcholine-Independent Pathway in the Mouse Trachea

König, P., Krain, B., Krasteva‐Christ, G., & Kummer, W. (2009) · PLoS ONE · doi:10.1371/journal.pone.0004938 · Cited by 57 · see citing works

Neural control of the velum in larvae of the gastropod,<i>Ilyanassa obsoleta</i>

Braubach, O. R., Dickinson, A. J. G., Evans, C. C. E., & Croll, R. P. (2006) · Journal of Experimental Biology · doi:10.1242/jeb.02556 · Cited by 56 · see citing works

Ciliary and Flagellar Structure and Function—Their Regulations by Posttranslational Modifications of Axonemal Tubulin

Konno, A., Setou, M., & Ikegami, K. (2012) · International review of cytology · doi:10.1016/b978-0-12-394305-7.00003-3 · Cited by 47 · see citing works

A Chemical Screen Identifies Class A G-Protein Coupled Receptors As Regulators of Cilia

Avasthi, P. P., Marley, A., Lin, H., Gregori‐Puigjané, E., Shoichet, B. K., von Zastrow, M., & Marshall, W. F. (2012) · ACS Chemical Biology · doi:10.1021/cb200349v · Cited by 45 · see citing works

Time and Extent of Ciliary Response to Particles in a Non-Filtering Feeding Mechanism

Strathmann, R. R. (2007) · Biological Bulletin · doi:10.2307/25066587 · Cited by 44 · see citing works

Effect of serotonin on ciliary beating and intracellular calcium concentration in identified populations of embryonic ciliary cells

Doran, S. A., Koss, R., Tran, C. H. T., Christopher, K. J., Gallin, W. J., & Goldberg, J. I. (2004) · Journal of Experimental Biology · doi:10.1242/jeb.00924 · Cited by 36 · see citing works

Neural correlates of settlement in veliger larvae of the gastropod, C repidula fornicata

Penniman, J. R., Doll, M. K., & Pires, A. (2013) · Invertebrate Biology · doi:10.1111/ivb.12014 · Cited by 33 · see citing works

Serotonergic Nervous System of Two Macrostomid Species: Recent or Ancient Divergence?

Ladurner, P., Mair, G. R., Reiter, D., Salvenmoser, W., & Rieger, R. M. (1997) · Invertebrate Biology · doi:10.2307/3226895 · Cited by 33 · see citing works

Ontogenetic changes in larval swimming and orientation of pre-competent sea urchin Arbacia punctulata in turbulence

Wheeler, J. D., Chan, K. Y. K., Anderson, E. J., & Mullineaux, L. S. (2016) · Journal of Experimental Biology · doi:10.1242/jeb.129502 · Cited by 31 · see citing works

Surface flow for colonial integration in reef-building corals

Bouderlique, T., Petersen, J., Faure, L., Abed‐Navandi, D., Bouchnita, A., Mueller, B., Nazarov, M., Englmaier, L., Tesarova, M., Frade, P. R., et al. (2022) · Current Biology · doi:10.1016/j.cub.2022.04.054 · Cited by 31 · see citing works

Serotonin stimulates [Ca2+]i elevation in ciliary ectodermal cells of echinoplutei through a serotonin receptor cell network in the blastocoel

Katow, H., Yaguchi, S., & Kyozuka, K. (2007) · Journal of Experimental Biology · doi:10.1242/jeb.02666 · Cited by 31 · see citing works

Respiratory Biology of Animals

Perry, S. F., Lambertz, M., & Schmitz, A. (2019) · doi:10.1093/oso/9780199238460.001.0001 · Cited by 27 · see citing works

Development of the γ-amino butyric acid (GABA)-ergic signaling system and its role in larval swimming in sea urchin

Katow, H., Abe, K., Katow, T., Zamani, A., & Abe, H. (2013) · Journal of Experimental Biology · doi:10.1242/jeb.074856 · Cited by 27 · see citing works

Molecular and cellular architecture of the larval sensory organ in the cnidarian Nematostella vectensis

Gilbert, E., Teeling, C., Lebedeva, T. S., Pedersen, S., Chrismas, N. A. M., Genikhovich, G., & Modepalli, V. (2022) · Development · doi:10.1242/dev.200833 · Cited by 26 · see citing works

First description of the serotonergic nervous system in a bdelloid rotifer: Macrotrachela quadricornifera Milne 1886 (Philodinidae)

Leasi, F., Pennati, R., & Ricci, C. N. (2008) · Zoologischer Anzeiger · doi:10.1016/j.jcz.2008.10.002 · Cited by 25 · see citing works

Planktonic sea urchin larvae change their swimming direction in response to strong photoirradiation

Yaguchi, S., Taniguchi, Y., Suzuki, H., Kamata, M., & Yaguchi, J. (2022) · PLoS Genetics · doi:10.1371/journal.pgen.1010033 · Cited by 23 · see citing works

Comparative Neurobiology of Biogenic Amines in Animal Models in Deuterostomes

D’Aniello, E., Paganos, P., Anishchenko, E., D’Aniello, S., & Arnone, M. I. (2020) · Frontiers in Ecology and Evolution · doi:10.3389/fevo.2020.587036 · Cited by 22 · see citing works

The urochordate larva and archichordate organization: chordate origin and anagenesis revisited†

Salvini-Plawen, L. V. (2009) · Journal of Zoological Systematics & Evolutionary Research · doi:10.1111/j.1439-0469.1998.tb00832.x · Cited by 20 · see citing works

Extensive presence of serotonergic cells and fibers in the peripheral nervous system of lampreys

Barreiro‐Iglesias, A., Aldegunde, M., Anadón, R., & Rodicio, M. C. (2008) · The Journal of Comparative Neurology · doi:10.1002/cne.21914 · Cited by 18 · see citing works

Acetylcholinesterase and dopamine inhibition suppress the filtration rate, burrowing behaviours, and immunological responses induced by bisphenol A in the hemocytes and gills of date mussels, Lithophaga lithophaga

Elkader, H. A. E. A., & Al‐Shami, A. S. (2024) · Aquatic Toxicology · doi:10.1016/j.aquatox.2024.106971 · Cited by 16 · see citing works

Effects of the dynein inhibitor ciliobrevin on the flagellar motility of sea urchin spermatozoa

Wada, Y., Baba, S. A., & Kamimura, S. (2015) · Cytoskeleton · doi:10.1002/cm.21218 · Cited by 16 · see citing works

Dopamine modulation of Ca2+ dependent Cl- current regulates ciliary beat frequency controlling locomotion inTritonia diomedea

Woodward, O. M., & Willows, A. O. D. (2006) · Journal of Experimental Biology · doi:10.1242/jeb.02312 · Cited by 15 · see citing works

Nervous control of ciliary beating by Cl-, Ca2+ and calmodulin inTritonia diomedea

Woodward, O. M., & Willows, A. O. D. (2006) · Journal of Experimental Biology · doi:10.1242/jeb.02377 · Cited by 14 · see citing works

microRNA‐124 regulates Notch and NeuroD1 to mediate transition states of neuronal development

Konrad, K. D., & Song, J. L. (2022) · Developmental Neurobiology · doi:10.1002/dneu.22902 · Cited by 14 · see citing works

Effects of monocrotophos pesticide on serotonin metabolism during early development in the sea urchin, Hemicentrotus pulcherrimus

Xu, L., Tian, H., Wang, W., & Ru, S. (2012) · Environmental Toxicology and Pharmacology · doi:10.1016/j.etap.2012.06.014 · Cited by 14 · see citing works

Comparative study of serotonin-like immunoreactivity in the branchial basket, digestive tract, and nervous system in tunicates

Braun, K.-P., & Stach, T. (2016) · Zoomorphology · doi:10.1007/s00435-016-0317-8 · Cited by 14 · see citing works

Near future ocean acidification modulates the physiological impact of fluoxetine at environmental concentration on larval urchins

Lo, H. K. A., Chua, V. A., & Chan, K. Y. K. (2021) · The Science of The Total Environment · doi:10.1016/j.scitotenv.2021.149709 · Cited by 13 · see citing works

Detergent-extracted Volvox model exhibits an anterior–posterior gradient in flagellar Ca 2+ sensitivity

Ueki, N., & Wakabayashi, K. (2018) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1715489115 · Cited by 13 · see citing works

Immunohistochemical and ultrastructural properties of the larval ciliary band-associated strand in the sea urchin Hemicentrotus pulcherrimus

Katow, H., Katow, T., Yoshida, H., Kiyomoto, M., & Uemura, I. (2016) · Frontiers in Zoology · doi:10.1186/s12983-016-0159-8 · Cited by 12 · see citing works

Inhibitory effects of neurotoxin β-N-methylamino-L-alanine on fertilization and early development of the sea urchin Lytechinus pictus

Li, A., Espinoza, J., & Hamdoun, A. M. (2020) · Aquatic Toxicology · doi:10.1016/j.aquatox.2020.105425 · Cited by 11 · see citing works

Non-directional Photoreceptors in the Pluteus of Strongylocentrotus purpuratus

Valero‐Gracia, A., Petrone, L., Oliveri, P., Nilsson, D., & Arnone, M. I. (2016) · Frontiers in Ecology and Evolution · doi:10.3389/fevo.2016.00127 · Cited by 11 · see citing works

Initial report of γ-aminobutyric acidergic locomotion regulatory system and its 3-mercaptopropionic acid-sensitivity in metamorphic juvenile of sea urchin, Hemicentrotus pulcherrimus

Katow, H., Yoshida, H., & Kiyomoto, M. (2020) · Scientific Reports · doi:10.1038/s41598-020-57567-w · Cited by 10 · see citing works

Dynamics and emergence of metachronal waves in the ciliary band of a metazoan larva

Poon, R. N., Jékely, G., & Wan, K. Y. (2025) · Science Advances · doi:10.1126/sciadv.adw4067 · Cited by 9 · see citing works

Effects of neurotransmitter receptor antagonists on sea urchin righting behavior and tube foot motility

McDonald, M., Griffin, N. P., Howell, E., Li, D., Harnew-Spradley, S., Rodriguez, P., Lancaster, A., Umutoni, F., Besh, J., & Shelley, C. (2022) · Journal of Experimental Biology · doi:10.1242/jeb.243076 · Cited by 9 · see citing works

Vertical distribution of echinoid larvae in pH stratified water columns

Maboloc, E. A., Batzel, G. O., Grünbaum, D., & Chan, K. Y. K. (2020) · Marine Biology · doi:10.1007/s00227-019-3629-7 · Cited by 8 · see citing works

Molecular and Cellular Characterization of the TH Pathway in the Sea Urchin Strongylocentrotus purpuratus

Cocurullo, M., Paganos, P., Wood, N. J., Arnone, M. I., & Oliveri, P. (2023) · Cells · doi:10.3390/cells12020272 · Cited by 7 · see citing works

Roles of Ca2+and protein kinase C in the excitatory response to serotonin in embryonic molluscan ciliary cells

Doran, S. A., & Goldberg, J. I. (2006) · Canadian Journal of Physiology and Pharmacology · doi:10.1139/y06-010 · Cited by 7 · see citing works

Spontaneous intersibling polymorphism in the development of dopaminergic neuroendocrine cells in sea urchin larvae: impacts on the expansion of marine benthic species

Obukhova, A. L., Khabarova, M. Y., Semenova, M. N., Starunov, V. V., Voronezhskaya, E. E., & Ivashkin, E. G. (2024) · Frontiers in Neuroscience · doi:10.3389/fnins.2024.1348999 · Cited by 5 · see citing works

Involvement of Huntingtin in Development and Ciliary Beating Regulation of Larvae of the Sea Urchin, Hemicentrotus pulcherrimus

Katow, H., Katow, T., Yoshida, H., & Kiyomoto, M. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22105116 · Cited by 4 · see citing works

Monocrotophos, an organophosphorus insecticide, disrupts the expression of HpNetrin and its receptor neogenin during early development in the sea urchin (Hemicentrotus pulcherrimus)

Zhang, X., Xu, L., Tian, H., Wang, C., Wang, W., & Ru, S. (2017) · NeuroToxicology · doi:10.1016/j.neuro.2017.06.010 · Cited by 3 · see citing works

Distribution and evolution of serotonin-like immunoreactive cells in Thaliacea (Tunicata)

Braun, K., & Stach, T. (2018) · Zoomorphology · doi:10.1007/s00435-018-0416-9 · Cited by 3 · see citing works

Fast mechanosensitive and Ca2+-dependent reorientation of motile cilia basal bodies in the placozoan Trichoplax

Léria, M., Barthélémy-Requin, M., Daroueche, M.-M., Richard, F., Brouilly, N., Hill, R., Bivic, A. L., Pasini, A., & Clément, R. (2026) · Current Biology · doi:10.1016/j.cub.2026.04.054 · Cited by 2 · see citing works

Structure, function, and evolution of respiratory proteins

Perry, S. F., Lambertz, M., & Schmitz, A. (2019) · Oxford University Press eBooks · doi:10.1093/oso/9780199238460.003.0004 · Cited by 2 · see citing works

Development of flexible ciliary actuators and their application to mobile robots

Kimura, H., Kataoka, M., Higashi, T., & Norio, I. N. O. U. (2015) · Journal of Aero Aqua Bio-mechanisms · doi:10.5226/jabmech.4.71 · Cited by 2 · see citing works

Neural Development in Invertebrates

Croll, R. P. (2016) · Wiley eBooks · doi:10.1002/9781118316757.ch11 · Cited by 2 · see citing works

Sensory perception in marine larvae

Modepalli, V. (2025) · Advances in marine biology · doi:10.1016/bs.amb.2025.09.003 · Cited by 1 · see citing works

Respiratory faculties of aquatic invertebrates

Perry, S. F., Lambertz, M., & Schmitz, A. (2019) · Oxford University Press eBooks · doi:10.1093/oso/9780199238460.003.0006 · Cited by 1 · see citing works

The evolution of air-breathing respiratory faculties in invertebrates

Perry, S. F., Lambertz, M., & Schmitz, A. (2019) · Oxford University Press eBooks · doi:10.1093/oso/9780199238460.003.0010 · Cited by 1 · see citing works

Respiratory faculties of amphibious and terrestrial craniotes

Perry, S. F., Lambertz, M., & Schmitz, A. (2019) · Oxford University Press eBooks · doi:10.1093/oso/9780199238460.003.0012 · Cited by 1 · see citing works

Respiratory faculties of amphibious and terrestrial invertebrates

Perry, S. F., Lambertz, M., & Schmitz, A. (2019) · Oxford University Press eBooks · doi:10.1093/oso/9780199238460.003.0007 · Cited by 1 · see citing works

Mechanosensory cells and swimming behaviour of embryos of the sea urchin Strongylocentrotus purpuratus.

Volnoukhin, M. (2010) · Summit (Simon Fraser University) · Cited by 1 · see citing works

Behavioral responses of invertebrate larvae to water column cues

Wheeler, J. D. (2016) · doi:10.1575/1912/7756 · Cited by 1 · see citing works

A primer on respiratory physiology

Perry, S. F., Lambertz, M., & Schmitz, A. (2019) · Oxford University Press eBooks · doi:10.1093/oso/9780199238460.003.0003

The evolution of water-breathing respiratory faculties in craniotes

Perry, S. F., Lambertz, M., & Schmitz, A. (2019) · Oxford University Press eBooks · doi:10.1093/oso/9780199238460.003.0014

Control of breathing in craniotes

Perry, S. F., Lambertz, M., & Schmitz, A. (2019) · Oxford University Press eBooks · doi:10.1093/oso/9780199238460.003.0013

Respiratory faculties of aquatic craniotes

Perry, S. F., Lambertz, M., & Schmitz, A. (2019) · Oxford University Press eBooks · doi:10.1093/oso/9780199238460.003.0011

The evolution of water-breathing respiratory faculties in invertebrates

Perry, S. F., Lambertz, M., & Schmitz, A. (2019) · Oxford University Press eBooks · doi:10.1093/oso/9780199238460.003.0009

Control of breathing in invertebrates

Perry, S. F., Lambertz, M., & Schmitz, A. (2019) · Oxford University Press eBooks · doi:10.1093/oso/9780199238460.003.0008

Coping with extremes

Perry, S. F., Lambertz, M., & Schmitz, A. (2019) · Oxford University Press eBooks · doi:10.1093/oso/9780199238460.003.0005

A very brief history of respiratory biology

Perry, S. F., Lambertz, M., & Schmitz, A. (2019) · Oxford University Press eBooks · doi:10.1093/oso/9780199238460.003.0002

Ocean acidification modulates the impact of fluoxetine on larval behaviors of non-target organisms

Chua, V. A. (2021) · Works - Scholarship, Research, & Creative Expression (Swarthmore College)

The bottom line

Perry, S. F., Lambertz, M., & Schmitz, A. (2019) · Oxford University Press eBooks · doi:10.1093/oso/9780199238460.003.0016

Prolegomena

Perry, S. F., Lambertz, M., & Schmitz, A. (2019) · Oxford University Press eBooks · doi:10.1093/oso/9780199238460.003.0001

The evolution of air-breathing respiratory faculties in craniotes

Perry, S. F., Lambertz, M., & Schmitz, A. (2019) · Oxford University Press eBooks · doi:10.1093/oso/9780199238460.003.0015

Epigraph

(2019) · Oxford University Press eBooks · doi:10.1093/oso/9780199238460.002.0008

Copyright Page

(2019) · Oxford University Press eBooks · doi:10.1093/oso/9780199238460.002.0003

Dedication

(2019) · Oxford University Press eBooks · doi:10.1093/oso/9780199238460.002.0004

Preface

(2019) · Oxford University Press eBooks · doi:10.1093/oso/9780199238460.002.0005

Control of ciliary beating by neurotransmitters in sea urchin larvae

和田, 祐. (1997) · Institutional Repositories DataBase (IRDB)

Control of ciliary beating by neurotransmitters in sea urchin larvae(ウニ幼生繊毛打の神経伝達物質による調節)

和田祐子 (1997) · doi:10.11501/3131959

Ciliary Movement of Sea-urchin Embryos

Shiba, K., Mogami, Y., & Baba, S. A. (2002) · Cited by 17 · see citing works

Regulation of ciliary movement in sea urchin embryos: Dopamine and 5-HT change the swimming behaviour

Mogami, Y., Watanabe, K., Chieko, O., Akemi, K., & Baba, S. A. (1992) · Comparative Biochemistry and Physiology Part C Comparative Pharmacology · doi:10.1016/0742-8413(92)90269-d · Cited by 41 · see citing works

Pharmacological control of ciliary activity in the young sea urchin larva : cholinergic and monoaminergic effects and the role of calcium and cyclic nucleotides

Soliman, S. M. (1983)