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

R: A Language and Environment for Statistical Computing

R Core Team (2000) · doi:10.32614/r.manuals · Cited by 355,706 · see citing works

Fiji: an open-source platform for biological-image analysis

Schindelin, J., Arganda-Carreras, I., Frise, E., Kaynig, V., Longair, M., Pietzsch, T., Preibisch, S., Rueden, C., Saalfeld, S., Schmid, B., et al. (2012) · Nature Methods · doi:10.1038/nmeth.2019 · Cited by 66,890 · see citing works

A review of central 5-HT receptors and their function

Barnes, N. M., & Sharp, T. (1999) · Neuropharmacology · doi:10.1016/s0028-3908(99)00010-6 · Cited by 3,150 · see citing works

The expanded biology of serotonin

Berger, M., Gray, J. A., & Roth, B. L. (2009) · Annual Review of Medicine · doi:10.1146/annurev.med.60.042307.110802 · Cited by 2,100 · see citing works

Feature point tracking and trajectory analysis for video imaging in cell biology

Sbalzarini, I. F., & Koumoutsakos, P. (2005) · Journal of Structural Biology · doi:10.1016/j.jsb.2005.06.002 · Cited by 1,403 · see citing works

Early development of Xenopus laevis : a laboratory manual

Sive, H. L., Grainger, R. M., & Harland, R. M. (2000) · Medical Entomology and Zoology · Cited by 1,222 · see citing works

New Neurons Follow the Flow of Cerebrospinal Fluid in the Adult Brain

Sawamoto, K., Wichterle, H., González-Pérez, Ó., Cholfin, J. A., Yamada, M., Spassky, N., Murcia, N. S., García‐Verdugo, J. M., Marín, Ó., Rubenstein, J. L. R., et al. (2006) · Science · doi:10.1126/science.1119133 · Cited by 803 · see citing works

Nodal Flow and the Generation of Left-Right Asymmetry

Hirokawa, N., Tanaka, Y., Okada, Y., & Takeda, S. (2006) · Cell · doi:10.1016/j.cell.2006.03.002 · Cited by 576 · see citing works

Foxj1 transcription factors are master regulators of the motile ciliogenic program

Yu, X., Ng, C. P., Habacher, H., & Roy, S. (2008) · Nature Genetics · doi:10.1038/ng.263 · Cited by 495 · see citing works

Cerberus-like is a secreted factor with neuralizing activity expressed in the anterior primitive endoderm of the mouse gastrula

Belo, J. A., Bouwmeester, T., Leyns, L., Kertesz, N., Gallo, M., Follettie, M., & De Robertis, E. M. (1997) · Mechanisms of Development · doi:10.1016/s0925-4773(97)00125-1 · Cited by 460 · see citing works

Ependymal cells: biology and pathology

Bigio, M. R. D. (2009) · Acta Neuropathologica · doi:10.1007/s00401-009-0624-y · Cited by 381 · see citing works

Morphogenesis of the murine node and notochordal plate

Sulik, K., Dehart, D. B., Inagaki, T., Carson, J. L., Vrablic, T., Gesteland, K., & Schoenwolf, G. C. (1994) · Developmental Dynamics · doi:10.1002/aja.1002010309 · Cited by 338 · see citing works

The forkhead protein Foxj1 specifies node-like cilia in Xenopus and zebrafish embryos

Stubbs, J. L., Oishi, I., Izpisúa Belmonte, J. C., & Kintner, C. (2008) · Nature Genetics · doi:10.1038/ng.267 · Cited by 327 · see citing works

Serotonin Signaling Is a Very Early Step in Patterning of the Left-Right Axis in Chick and Frog Embryos

Fukumoto, T., Kema, I. P., & Levin, M. G. (2005) · Current Biology · doi:10.1016/j.cub.2005.03.044 · Cited by 249 · see citing works

Localization of 5-HT6 receptors at the plasma membrane of neuronal cilia in the rat brain

Brailov, I., Bancila, M., Brisorgueil, M.-J., Miquel, M.-C., Hamon, M., & Vergé, D. (2000) · Brain Research · doi:10.1016/s0006-8993(00)02519-1 · Cited by 245 · see citing works

Multicilin promotes centriole assembly and ciliogenesis during multiciliate cell differentiation

Stubbs, J. L., Vladar, E. K., Axelrod, J. D., & Kintner, C. R. (2012) · Nature Cell Biology · doi:10.1038/ncb2406 · Cited by 241 · see citing works

Clara cell: Progenitor for the bronchiolar epithelium

Reynolds, S. D., & Malkinson, A. M. (2009) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2009.09.002 · Cited by 220 · see citing works

The two faces of serotonin in bone biology

Ducy, P. F., & Karsenty, G. (2010) · The Journal of Cell Biology · doi:10.1083/jcb.201006123 · Cited by 214 · see citing works

Functional facets of the pulmonary neuroendocrine system

Linnoila, R. I. (2006) · Laboratory Investigation · doi:10.1038/labinvest.3700412 · Cited by 207 · see citing works

Review article: intestinal serotonin signalling in irritable bowel syndrome

Mawe, G. M., Coates, M. D., & Moses, P. L. (2006) · Alimentary Pharmacology & Therapeutics · doi:10.1111/j.1365-2036.2006.02858.x · Cited by 205 · see citing works

Inhibition of Serotonin Synthesis by Para-Chlorophenylalanine in Patients with the Carcinoid Syndrome

Engelman, K., Lovenberg, W. M., & Sjoerdsma, A. (1967) · New England Journal of Medicine · doi:10.1056/nejm196711232772101 · Cited by 199 · see citing works

Cystic Fibrosis and Other Respiratory Diseases of Impaired Mucus Clearance

Livraghi-Butrico, A., & Randell, S. H. (2007) · Toxicologic Pathology · doi:10.1080/01926230601060025 · Cited by 196 · see citing works

Planar cell polarity signaling, cilia and polarized ciliary beating

Wallingford, J. B. (2010) · Current Opinion in Cell Biology · doi:10.1016/j.ceb.2010.07.011 · Cited by 191 · see citing works

Mucus structure and properties in cystic fibrosis

Rubin, B. K. (2007) · Paediatric Respiratory Reviews · doi:10.1016/j.prrv.2007.02.004 · Cited by 172 · see citing works

Spatio-temporal expression of tryptophan hydroxylase isoforms in murine and human brain: Convergent data from Tph2 knockout mice

Gutknecht, L., Kriegebaum, C., Waider, J., Schmitt, A. G., & Lesch, K. (2009) · European Neuropsychopharmacology · doi:10.1016/j.euroneuro.2008.12.005 · Cited by 170 · see citing works

Medullary serotonin neurons and central CO2 chemoreception

Corcoran, A. E., Hodges, M. R., Wu, Y., Wang, W., Wylie, C. J., Deneris, E. S., & Richerson, G. B. (2009) · Respiratory Physiology & Neurobiology · doi:10.1016/j.resp.2009.04.014 · Cited by 155 · see citing works

Life without Peripheral Serotonin: Insights from Tryptophan Hydroxylase 1 Knockout Mice Reveal the Existence of Paracrine/Autocrine Serotonergic Networks

Amireault, P., Sibon, D., & Côté, F. (2012) · ACS Chemical Neuroscience · doi:10.1021/cn300154j · Cited by 155 · see citing works

The role of serotonin in intestinal luminal sensing and secretion

Hansen, M. B., & Witte, A. ‐. (2008) · Acta Physiologica · doi:10.1111/j.1748-1716.2008.01870.x · Cited by 144 · see citing works

Hypoxia‐induced secretion of serotonin from intact pulmonary neuroepithelial bodies in neonatal rabbit

Fu, X., Nurse, C. A., Wong, V. S. C., & Cutz, E. (2002) · The Journal of Physiology · doi:10.1113/jphysiol.2001.013071 · Cited by 137 · see citing works

5-Hydroxytryptamine metabolism in early embryogenesis, and the development of brain and retinal tissues. A review

Baker, P. C., & Quay, W. B. (1969) · Brain Research · doi:10.1016/0006-8993(69)90001-8 · Cited by 134 · see citing works

Recent advances and contraversies on the role of pulmonary neuroepithelial bodies as airway sensors

Cutz, E., Pan, J., Yeger, H., Domnik, N. J., & Fisher, J. T. (2012) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2012.09.003 · Cited by 130 · see citing works

Radial intercalation of ciliated cells during Xenopus skin development

Stubbs, J. L., Davidson, L. A., Keller, R. E., & Kintner, C. R. (2006) · Development · doi:10.1242/dev.02417 · Cited by 128 · see citing works

Identification of novel ciliogenesis factors using a new in vivo model for mucociliary epithelial development

Hayes, J. M., Kim, S. K., Abitua, P. B., Park, T. J., Herrington, E. R., Kitayama, A., Grow, M. W., Ueno, N., & Wallingford, J. B. (2007) · Developmental Biology · doi:10.1016/j.ydbio.2007.09.031 · Cited by 120 · see citing works

Specification of ion transport cells in theXenopuslarval skin

Quigley, I. K., Stubbs, J. L., & Kintner, C. R. (2011) · Development · doi:10.1242/dev.055699 · Cited by 120 · see citing works

Morphology and electrophysiology of neurons innervating the ciliated locomotor epithelium in Lymnaea stagnalis (L.)

Syed, N. I., & Winlow, W. (1989) · Comparative Biochemistry and Physiology Part A Physiology · doi:10.1016/0300-9629(89)90024-8 · Cited by 118 · see citing works

Disorders of Ciliary Motility

Cowan, M. J., Gladwin, M. T., & Shelhamer, J. H. (2001) · The American Journal of the Medical Sciences · doi:10.1097/00000441-200101000-00002 · Cited by 103 · see citing works

Embryonic frog epidermis: a model for the study of cell-cell interactions in the development of mucociliary disease

Dubaissi, E., & Papalopulu, N. (2011) · Disease Models & Mechanisms · doi:10.1242/dmm.006494 · Cited by 102 · see citing works

Pulmonary neuroendocrine cells (PNEC) and neuroepithelial bodies (NEB): chemoreceptors and regulators of lung development

Lommel, A. V. (2001) · Paediatric Respiratory Reviews · doi:10.1053/prrv.2000.0126 · Cited by 102 · see citing works

Intracellular pathways regulating ciliary beating of rat brain ependymal cells

Nguyen, T., Chin, W., O'Brien, J. A., Verdugo, P., & Berger, A. J. (2001) · The Journal of Physiology · doi:10.1111/j.1469-7793.2001.0131j.x · Cited by 98 · see citing works

Understanding ciliated epithelia: The power of Xenopus

Werner, M. E., & Mitchell, B. J. (2011) · genesis · doi:10.1002/dvg.20824 · Cited by 94 · see citing works

Efficient mucociliary transport relies on efficient regulation of ciliary beating

Braiman, A., & Priel, Z. (2008) · Respiratory Physiology & Neurobiology · doi:10.1016/j.resp.2008.05.010 · Cited by 83 · see citing works

A secretory cell type develops alongside multiciliated cells, ionocytes and goblet cells, and provides a protective, anti-infective function in the frog embryonic mucociliary epidermis

Dubaissi, E., Rousseau, K., Lea, R., Soto, X., Nardeosingh, S., Schweickert, A., Amaya, E., Thornton, D. J., & Papalopulu, N. (2014) · Development · doi:10.1242/dev.102426 · Cited by 81 · see citing works

Cloning of two tryptophan hydroxylase genes expressed in the diencephalon of the developing zebrafish brain

Bellipanni, G., Rink, E., & Bally‐Cuif, L. (2002) · Mechanisms of Development · doi:10.1016/s0925-4773(03)00119-9 · Cited by 79 · see citing works

Serotoninergic Receptors on Human Airway Epithelial Cells

Bayer, H., Müller, T., Myrtek, D., Sorichter, S., Ziegenhagen, M. W., Norgauer, J., Zissel, G., & Idzko, M. (2006) · American Journal of Respiratory Cell and Molecular Biology · doi:10.1165/rcmb.2006-0151oc · Cited by 75 · see citing works

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

Wada, Y., Mogami, Y., & Baba, S. A. (1997) · Journal of Experimental Biology · doi:10.1242/jeb.200.1.9 · Cited by 73 · see citing works

The neuronal primary cilium—an extrasynaptic signaling device

Whitfield, J. F. (2004) · Cellular Signalling · doi:10.1016/j.cellsig.2003.12.002 · Cited by 64 · see citing works

Serotonin Signaling Is Required for Wnt-Dependent GRP Specification and Leftward Flow in Xenopus

Beyer, T., Danilchik, M. V., Thumberger, T., Vick, P., Tisler, M., Schneider, I., Bogusch, S., Andre, P., Ulmer, B. M., Walentek, P., et al. (2011) · Current Biology · doi:10.1016/j.cub.2011.11.027 · Cited by 62 · see citing works

Ciliary beat co-ordination by calcium

Schmid, A., & Salathe, M. A. (2011) · Biology of the Cell · doi:10.1042/bc20100120 · Cited by 60 · see citing works

Serotonergic sensory-motor neurons mediate a behavioral response to hypoxia in pond snail embryos

Kuang, S., Doran, S. A., Wilson, R. J. A., Goss, G. G., & Goldberg, J. I. (2002) · Journal of Neurobiology · doi:10.1002/neu.10071 · Cited by 60 · 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

Regulation of tryptophan hydroxylase expression by a retinal circadian oscillator in vitro

Green, C. B., Cahill, G. M., & Besharse, J. C. (1995) · Brain Research · doi:10.1016/0006-8993(95)00166-n · Cited by 50 · 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

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

The role of serotonin in mucociliary transport system in the ciliated epithelium of frog palatine mucosa

Maruyama, I., Inagaki, M., & Momose, K. (1984) · European Journal of Pharmacology · doi:10.1016/0014-2999(84)90053-0 · Cited by 31 · see citing works

Biogenic Amines Stimulate Regeneration of Cilia in Tetrahymena thermophila1

CASTRODAD, F. A., Renaud, F. L., Ortiz, J. R., & Phillips, D. M. (1988) · The Journal of Protozoology · doi:10.1111/j.1550-7408.1988.tb04340.x · Cited by 26 · see citing works

Neuronal control of pedal sole cilia in the pond snail Lymnaea stagnalis appressa

Longley, R. D., & Peterman, M. (2012) · Journal of Comparative Physiology A · doi:10.1007/s00359-012-0770-x · Cited by 19 · see citing works

Glycogen metabolism in rat ependymal primary cultures: Regulation by serotonin

Verleysdonk, S., Kistner, S., Pfeiffer-Guglielmi, B., Wellard, J., Lupescu, A., Laske-Ernst, J. K., Lang, F. J. W., Rapp, M., & Hamprecht, B. (2005) · Brain Research · doi:10.1016/j.brainres.2005.08.045 · Cited by 18 · see citing works

Xenopus laevis embryo development: Arrest of epidermal cell differentiation by the chelating agent 1,10-phenanthroline

Montorzi, M., Burgos, M. H., & Falchuk, K. H. (2000) · Molecular Reproduction and Development · doi:10.1002/(sici)1098-2795(200001)55:1 · Cited by 14 · see citing works

Identification and evolutionary implications of neurotransmitter–ciliary interactions underlying the behavioral response to hypoxia inLymnaea stagnalisembryos

Goldberg, J. I., Rich, D. R., Muruganathan, S. P., Liu, M. B., Pon, J. R., Tam, R., Diefenbach, T. J., & Kuang, S. (2011) · Journal of Experimental Biology · doi:10.1242/jeb.053009 · Cited by 14 · see citing works

The effects of heat shock on the morphology and protein synthesis of the epidermis of Xenopus laevis larvae.

Nickells, R. W., Cavey, M. J., & Browder, L. W. (1988) · The Journal of Cell Biology · doi:10.1083/jcb.106.3.905 · Cited by 7 · see citing works

Cilia and Human Disease

Albee, A. J., & Dutcher, S. K. (2012) · Encyclopedia of Life Sciences · doi:10.1002/9780470015902.a0022544 · Cited by 3 · see citing works

miR-34/449 miRNAs are required for motile ciliogenesis by repressing CP110

Song, R., Walentek, P., Sponer, N., Klimke, A., Lee, J. S., Dixon, G., Harland, R., Wan, Y., Lishko, P., Lize, M., et al. (2014) · Nature · doi:10.1038/nature13413 · Cited by 222 · see citing works

Frog Skin Innate Immune Defences: Sensing and Surviving Pathogens

Varga, J. F. A., Bui-Marinos, M. P., & Katzenback, B. A. (2019) · Frontiers in Immunology · doi:10.3389/fimmu.2018.03128 · Cited by 214 · see citing works

Xenbase, the Xenopus model organism database; new virtualized system, data types and genomes

Karpinka, J. B., Fortriede, J. D., Burns, K. A., James‐Zorn, C., Ponferrada, V. G., Lee, J., Karimi, K., Zorn, A. M., & Vize, P. D. (2014) · Nucleic Acids Research · doi:10.1093/nar/gku956 · Cited by 134 · see citing works

Multiciliated Cells in Animals

Meunier, A., & Azimzadeh, J. (2016) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a028233 · Cited by 117 · see citing works

Gastric pouches and the mucociliary sole: setting the stage for nervous system evolution

Arendt, D., Benito-Gutierrez, E., Brunet, T., & Marlow, H. (2015) · Philosophical Transactions of the Royal Society B: Biological Sciences · doi:10.1098/rstb.2015.0286 · Cited by 112 · see citing works

Ciliomotor circuitry underlying whole-body coordination of ciliary activity in the Platynereis larva

Verasztó, C., Ueda, N., Bezares-Calderón, L. A., Panzera, A., Williams, E. A., Shahidi, R., & Jékely, G. (2017) · eLife · doi:10.7554/elife.26000 · Cited by 113 · see citing works

Xenopus: An Undervalued Model Organism to Study and Model Human Genetic Disease

Blum, M., & Ott, T. (2018) · Cells Tissues Organs · doi:10.1159/000490898 · Cited by 88 · see citing works

What we can learn from a tadpole about ciliopathies and airway diseases: Using systems biology in Xenopus to study cilia and mucociliary epithelia

Walentek, P., & Quigley, I. K. (2017) · genesis · doi:10.1002/dvg.23001 · Cited by 85 · see citing works

A secretory cell type develops alongside multiciliated cells, ionocytes and goblet cells, and provides a protective, anti-infective function in the frog embryonic mucociliary epidermis

Dubaissi, E., Rousseau, K., Lea, R., Soto, X., Nardeosingh, S., Schweickert, A., Amaya, E., Thornton, D. J., & Papalopulu, N. (2014) · Development · doi:10.1242/dev.102426 · Cited by 81 · see citing works

Ciliary transcription factors and miRNAs precisely regulate Cp110 levels required for ciliary adhesions and ciliogenesis

Walentek, P., Quigley, I. K., Sun, D. I., Sajjan, U. K., Kintner, C. R., & Harland, R. M. (2016) · eLife · doi:10.7554/elife.17557 · Cited by 68 · 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

ΔN-Tp63 Mediates Wnt/β-Catenin-Induced Inhibition of Differentiation in Basal Stem Cells of Mucociliary Epithelia

Haas, M., Gómez-Vázquez, J. L., Sun, D. I., Tran, H. T., Brislinger-Engelhardt, M. M., Tasca, A., Shomroni, O., Vleminckx, K., & Walentek, P. (2019) · Cell Reports · doi:10.1016/j.celrep.2019.08.063 · Cited by 63 · see citing works

Control of vertebrate core PCP protein localization and dynamics by Prickle2

Butler, M. T., & Wallingford, J. B. (2015) · Development · doi:10.1242/dev.121384 · Cited by 58 · see citing works

The involvement of PCP proteins in radial cell intercalations during Xenopus embryonic development

Ossipova, O., Chu, C.-W., Fillatre, J., Brott, B., Itoh, K., & Sokol, S. (2015) · Developmental Biology · doi:10.1016/j.ydbio.2015.06.013 · Cited by 52 · see citing works

BMP signalling controls the construction of vertebrate mucociliary epithelia

Cibois, M., Luxardi, G., Chevalier, B., Thomé, V., Mercey, O., Zaragosi, L., Barbry, P., Pasini, A., Marcet, B., & Kodjabachian, L. (2015) · Development · doi:10.1242/dev.118679 · Cited by 52 · see citing works

ERK7 regulates ciliogenesis by phosphorylating the actin regulator CapZIP in cooperation with Dishevelled

Miyatake, K., Kusakabe, M., Takahashi, C., & Nishida, E. (2015) · Nature Communications · doi:10.1038/ncomms7666 · Cited by 44 · see citing works

Functional characterization of the mucus barrier on the Xenopus tropicalis skin surface

Dubaissi, E., Rousseau, K., Hughes, G. W., Ridley, C. E., Grencis, R. K., Roberts, I. S., & Thornton, D. J. (2018) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1713539115 · Cited by 43 · see citing works

Multiciliated cells use filopodia to probe tissue mechanics during epithelial integration in vivo

Ventura, G., Amiri, A., Thiagarajan, R., Tolonen, M., Doostmohammadi, A., & Sedzinski, J. (2022) · Nature Communications · doi:10.1038/s41467-022-34165-0 · Cited by 41 · see citing works

ATP4a is required for development and function of the Xenopus mucociliary epidermis – a potential model to study proton pump inhibitor-associated pneumonia

Walentek, P., Beyer, T., Hagenlocher, C., Müller, C., Feistel, K., Schweickert, A., Harland, R. M., & Blum, M. (2015) · Developmental Biology · doi:10.1016/j.ydbio.2015.03.013 · Cited by 38 · see citing works

Tissue mechanics drives regeneration of a mucociliated epidermis on the surface of Xenopus embryonic aggregates

Kim, H. Y., Jackson, T. R., Stuckenholz, C., & Davidson, L. A. (2020) · Nature Communications · doi:10.1038/s41467-020-14385-y · Cited by 32 · see citing works

Xenopus epidermal and endodermal epithelia as models for mucociliary epithelial evolution, disease, and metaplasia

Walentek, P. (2021) · genesis · doi:10.1002/dvg.23406 · Cited by 31 · see citing works

Signaling Control of Mucociliary Epithelia: Stem Cells, Cell Fates, and the Plasticity of Cell Identity in Development and Disease

Walentek, P. (2021) · Cells Tissues Organs · doi:10.1159/000514579 · Cited by 25 · see citing works

A single-cell, time-resolved profiling of Xenopus mucociliary epithelium reveals nonhierarchical model of development

Lee, J., Møller, A. F., Chae, S., Bussek, A., Park, T. J., Kim, Y., Lee, H., Pers, T. H., Kwon, T., Sedzinski, J., et al. (2023) · Science Advances · doi:10.1126/sciadv.add5745 · Cited by 22 · see citing works

Fluid Mechanics of Mosaic Ciliated Tissues

Boselli, F., Jullien, J., Lauga, E., & Goldstein, R. E. (2021) · Physical Review Letters · doi:10.1103/physrevlett.127.198102 · Cited by 24 · see citing works

Mucociliary Wnt signaling promotes cilia biogenesis and beating

Seidl, C., Silva, F. D., Zhang, K., Wohlgemuth, K., Omran, H., & Niehrs, C. (2023) · Nature Communications · doi:10.1038/s41467-023-36743-2 · Cited by 24 · see citing works

The Frog Xenopus as a Model to Study Joubert Syndrome: The Case of a Human Patient With Compound Heterozygous Variants in PIBF1

Ott, T., Kaufmann, L. T., Granzow, M., Hinderhofer, K., Bartram, C. R., Theiß, S., Seitz, A., Paramasivam, N., Schulz, A., Moog, U., et al. (2019) · Frontiers in Physiology · doi:10.3389/fphys.2019.00134 · Cited by 21 · see citing works

The Xenopus animal cap transcriptome: building a mucociliary epithelium

Angerilli, A., Smialowski, P., & Rupp, R. A. W. (2018) · Nucleic Acids Research · doi:10.1093/nar/gky771 · Cited by 18 · see citing works

Manipulating and Analyzing Cell Type Composition of the Xenopus Mucociliary Epidermis

Walentek, P. (2018) · Methods in molecular biology · doi:10.1007/978-1-4939-8784-9_18 · Cited by 20 · see citing works

Quantitative optical coherence tomography imaging of intermediate flow defect phenotypes in ciliary physiology and pathophysiology

Huang, B. K., Gamm, U. A., Jonas, S., Khokha, M. K., & Choma, M. A. (2015) · Journal of Biomedical Optics · doi:10.1117/1.jbo.20.3.030502 · Cited by 18 · see citing works

The Scf/Kit pathway implements self-organized epithelial patterning

Chuyen, A., Rulquin, C., Daian, F., Thomé, V., Clément, R., Kodjabachian, L., & Pasini, A. (2021) · Developmental Cell · doi:10.1016/j.devcel.2021.02.026 · Cited by 18 · see citing works

Simple Method To Characterize the Ciliary Proteome of Multiciliated Cells

Sim, H. J., Yun, S., Kim, H. E., Kwon, K. Y., Kim, G., Yun, S., Kim, B. G., Myung, K., Park, T. J., & Kwon, T. (2019) · Journal of Proteome Research · doi:10.1021/acs.jproteome.9b00589 · Cited by 16 · see citing works

Na+/H+ Exchangers Are Required for the Development and Function of Vertebrate Mucociliary Epithelia

Sun, D. I., Tasca, A., Haas, M., Baltazar, G., Harland, R. M., Finkbeiner, W. E., & Walentek, P. (2018) · Cells Tissues Organs · doi:10.1159/000492973 · Cited by 16 · see citing works

ATP4 and ciliation in the neuroectoderm and endoderm of Xenopus embryos and tadpoles

Walentek, P., Hagenlocher, C., Beyer, T., Müller, C., Feistel, K., Schweickert, A., Harland, R. M., & Blum, M. (2015) · Data in Brief · doi:10.1016/j.dib.2015.04.003 · Cited by 14 · see citing works

Cilia-localized GID/CTLH ubiquitin ligase complex regulates protein homeostasis of sonic hedgehog signaling components

Hantel, F., Liu, H., Fechtner, L., Neuhaus, H., Ding, J., Arlt, D., Walentek, P., Villavicencio‐Lorini, P., Gerhardt, C., Hollemann, T., et al. (2022) · Journal of Cell Science · doi:10.1242/jcs.259209 · Cited by 13 · see citing works

Xenopus: An alternative model system for identifying muco-active agents

Sim, H. J., Kim, S., Myung, K., Kwon, T., Lee, H., & Park, T. J. (2018) · PLoS ONE · doi:10.1371/journal.pone.0193310 · Cited by 13 · see citing works

The role of nitric oxide during embryonic epidermis development ofXenopus laevis

Tománková, S., Abaffy, P., & Radek Sindelka, E. (2017) · Biology Open · doi:10.1242/bio.023739 · Cited by 12 · see citing works

Planar Cell Polarity in Ciliated Epithelia

Walentek, P., Boutin, C., & Kodjabachian, L. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-802438-6.00007-3 · Cited by 11 · see citing works

Revealing non-trivial information structures in aneural biological tissues via functional connectivity

Blackiston, D. J., Dromiack, H. T., Grasso, C., Varley, T. F., Moore, D. G., Srinivasan, K., Sporns, O., Bongard, J., Levin, M. G., & Walker, S. I. (2025) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1012149 · Cited by 10 · see citing works

Male reproductive tract cilia beat to a different drummer

Rosenfeld, C. S. (2019) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1900112116 · Cited by 10 · see citing works

The Xenopus Embryo: An Ideal Model System to Study Human Ciliopathies

Schweickert, A., & Feistel, K. (2015) · Current Pathobiology Reports · doi:10.1007/s40139-015-0074-2 · Cited by 10 · see citing works

AI-enabled drug prediction and gene network analysis reveal therapeutic use of vorinostat for Rett Syndrome in preclinical models

Novak, R., Lin, T., Kaushal, S., Sperry, M. M., Vigneault, F., Gardner, E., Loomba, S., Shcherbina, K., Keshari, V., Dinis, A., et al. (2025) · Communications Medicine · doi:10.1038/s43856-025-00975-8 · Cited by 8 · see citing works

Unraveling spatial cellular pattern by computational tissue shuffling

Laruelle, E., Spassky, N., & Genovesio, A. (2020) · Communications Biology · doi:10.1038/s42003-020-01323-3 · Cited by 8 · see citing works

Serotonin and MucXS release by small secretory cells depend on Xpod, a SSC specific marker gene

Kurrle, Y., Kunesch, K., Bogusch, S., & Schweickert, A. (2019) · genesis · doi:10.1002/dvg.23344 · Cited by 6 · see citing works

Temporal Notch signaling and Hes-mediated competitive de-repression regulate mucociliary cell fates in XenopusPreprint

Brislinger-Engelhardt, M. M., Hansen, M., Litwin, T., Haas, M., Andricek, A., Lorenz, F., Temporal-Plo, A., Bowden, S. A., Hägele, S., Weber, D., et al. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.02.15.528675 · Cited by 6 · see citing works

Calcium transients regulate the apical emergence of basally located progenitors during Xenopus skin development

Christodoulou, N., & Skourides, P. A. (2025) · Nature Communications · doi:10.1038/s41467-025-61610-7 · Cited by 5 · 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

Foxi1 regulates multipotent mucociliary progenitors and ionocyte specification through transcriptional and epigenetic mechanisms

Bowden, S. A., Brislinger-Engelhardt, M. M., Hansen, M., Andricek, A., Temporal-Plo, A., Weber, D., Hägele, S., Lorenz, F., Litwin, T., Kreutz, C., et al. (2026) · PLoS Biology · doi:10.1371/journal.pbio.3003583 · Cited by 4 · see citing works

Actin Depolymerizing Factor Destrin Regulates Cilia Development and Function during Vertebrate Embryogenesis

Kim, Y., Lee, H.-K., Park, K., Ismail, T., Lee, H., & Lee, H. (2024) · Development & Reproduction · doi:10.12717/dr.2024.28.3.109 · Cited by 2 · see citing works

A microscopical and ultrastructural analysis of the embryonic epidermis of the pool frog, Pelophylax lessonae (Camerano, 1882) (Anura: Ranidae)

Semeraro, D., Mentino, D., Rossi, R., Scillitani, G., Guglielmi, M. V., & Mastrodonato, M. (2024) · The European Zoological Journal · doi:10.1080/24750263.2024.2422089 · Cited by 2 · see citing works

Mucociliary cell type compositions - bridging the gap between genes and emergent tissue functions

Walentek, P. (2025) · Cells and Development · doi:10.1016/j.cdev.2025.204019 · Cited by 2 · see citing works

Interspecific comparisons of anuran embryonic epidermal landscapes and energetic trade‐offs in response to changes in salinity

Whitfield, K., & Crespi, E. J. (2025) · Developmental Dynamics · doi:10.1002/dvdy.70016 · Cited by 2 · see citing works

Mechanics of cell integration in vivoPreprint

Ventura, G., Amiri, A., Thiagarajan, R., Tolonen, M., Doostmohammadi, A., & Sedzinski, J. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.11.18.469090 · Cited by 2 · see citing works

Effects of Metallic Nanoparticles Treatments on the Development of the Pool Frog, Pelophylax lessonae (Amphibia: Ranidae)

Semeraro, D., Mentino, D., Rossi, R., Blasi, C. D., Guglielmi, M. V., Scillitani, G., & Mastrodonato, M. (2025) · Microscopy Research and Technique · doi:10.1002/jemt.70098 · Cited by 1 · see citing works

Engineered Living Systems With Self‐Organizing Neural Networks: From Anatomy to Behavior and Gene Expression

Fotowat, H., O’Neill, L., Pio‐Lopez, L., Sperry, M. M., Erickson, P., Lin, T. G., & Levin, M. G. (2026) · Advanced Science · doi:10.1002/advs.202508967 · Cited by 1 · see citing works

Self-Organizing Neural Networks in Novel Moving Bodies: Anatomical, Behavioral, and Transcriptional Characterization of a Living Construct with a Nervous SystemPreprint

Fotowat, H., O’Neill, L., Pio‐Lopez, L., Sperry, M. M., Erickson, P., Lin, T., & Levin, M. G. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.04.14.648732 · Cited by 1 · see citing works

Mechanics of cell integration in vivoPreprint

Ventura, G., Amiri, A., Thiagarajan, R., Tolonen, M., Doostmohammadi, A., & Sedzinski, J. (2021) · arXiv (Cornell University) · doi:10.48550/arxiv.2111.12740

Development of Peripheral Innervation in the Frog Xenopus Laevis

Gandhi, M. A. (2014) · UWM Digital Commons (University of Wisconsin–Milwaukee)

Crb3 is required to organize the apical domain of multiciliated cells

Burcklé, C., Raitière, J., Michaux, G., Kodjabachian, L., & Bivic, A. L. (2023) · Journal of Cell Science · doi:10.1242/jcs.261046

Multi scale study of three conserved centriolar effectors of ciliated epithelia

Nommick, A. (2021) · doi:10.70675/0371981az05eez4db7z9ee5zec03e9c86a3e

Molecular and cellular basis of pattern establishment in a vertebrate epithelium

Chuyen, A. (2020) · doi:10.70675/952292a9z3a2bz442fzb547ze3e304a159d0

Experiments and simulations to understand cilia-driven flows and their protective role in Xenopus

Baby, A. (2023) · theses.fr (ABES) · doi:10.70675/becb6094z4cc2z4e0bzbb94z2ca2283753f6

Serotonin and MucXS release by small secretory cells depend on Xpod, a SSC specific marker gene

Kurrle, Y., Kunesch, K., Bogusch, S., & Schweickert, A. (2019) · genesis · doi:10.1002/dvg.23344 · Cited by 6 · see citing works

Serotonin inhibits ciliary transport in esophagus of the nudibranch mollusk, Tritonia diomedea

Pavlova, G. A., Willows, A. O. D., & Gaston, M. R. (1999) · Acta Biologica Hungarica · doi:10.1007/bf03543040 · Cited by 11 · see citing works

The role of serotonin in mucociliary transport system in the ciliated epithelium of frog palatine mucosa

Maruyama, I., Inagaki, M., & Momose, K. (1984) · European Journal of Pharmacology · doi:10.1016/0014-2999(84)90053-0 · Cited by 31 · see citing works

Embryonic frog epidermis: a model for the study of cell-cell interactions in the development of mucociliary disease

Dubaissi, E., & Papalopulu, N. (2011) · Disease Models & Mechanisms · doi:10.1242/dmm.006494 · Cited by 102 · 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