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A positive feedback mechanism governs the polarity and motion of motile cilia

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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/ar.1091620209openalex-snapshot
Development of order during ciliogenesis
inferredcites →https://doi.org/10.1002/jez.1400500302openalex-snapshot
Experimental studies on the ciliary action of amphibian embryos
inferredcites →https://doi.org/10.1002/path.1652openalex-snapshot
Cilia‐related diseases
inferredcites →https://doi.org/10.1006/bbrc.2001.5221openalex-snapshot
Effects of Flow Patterns on Endothelial Cell Migration into a Zone of Mechanical Denudation
inferredcites →https://doi.org/10.1006/dbio.1993.1312openalex-snapshot
Planar Polarity in the Ciliated Epidermis of Xenopus Embryos
inferredcites →https://doi.org/10.1006/dbio.2002.0537openalex-snapshot
Mesendoderm Extension and Mantle Closure in Xenopus laevis Gastrulation: Combined Roles for Integrin α5β1, Fibronectin, and Tissue Geometry
inferredcites →https://doi.org/10.1007/bf02079527openalex-snapshot
Entwicklungsmechanische Untersuchungen über die Wimperbewegung des Ectoderms von Amphibienlarven
inferredcites →https://doi.org/10.1016/b978-0-12-677202-9.50019-8openalex-snapshot
Biophysical Behavior of Red Cells in Suspensions
inferredcites →https://doi.org/10.1038/79951openalex-snapshot
Effective targeted gene ‘knockdown’ in zebrafish
inferredcites →https://doi.org/10.1126/science.1119133openalex-snapshot
New Neurons Follow the Flow of Cerebrospinal Fluid in the Adult Brain
inferredcites →https://doi.org/10.1126/science.3883488openalex-snapshot
Flow Effects on Prostacyclin Production by Cultured Human Endothelial Cells
inferredcites →https://doi.org/10.1128/mcb.22.17.6298-6305.2002openalex-snapshot
Male Infertility, Impaired Sperm Motility, and Hydrocephalus in Mice Deficient in Sperm-Associated Antigen 6
inferredcites →https://doi.org/10.1128/mcb.24.18.7958-7964.2004openalex-snapshot
Mice Deficient in the Axonemal Protein Tektin-t Exhibit Male Infertility and Immotile-Cilium Syndrome Due to Impaired Inner Arm Dynein Function
inferredcites →https://doi.org/10.1146/annurev.physiol.69.040705.141301openalex-snapshot
Genetic Defects in Ciliary Structure and Function
inferredcites →https://doi.org/10.1183/09031936.98.12040982openalex-snapshot
Primary ciliary dyskinesia: diagnosis and standards of care
inferredcites →https://doi.org/10.1242/jcs.s2-38.152.465openalex-snapshot
Memoirs: Notes on the Ciliation of the Ectoderm of the Amphibian Embryo
inferredcites →https://doi.org/10.2174/1566524054553496openalex-snapshot
New Developments in the Field of Cystic Kidney Diseases
inferredcites →https://doi.org/10.3109/2000-1967-010openalex-snapshot
Transmission Electron Microscopy in the Diagnosis of Primary Ciliary Dyskinesia

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.2139/ssrn.3275291openalex-extracted
Emergence of Bilateral Symmetry from Chiral Components in the Planarian Epidermis
inferred← citeshttps://doi.org/10.2139/ssrn.3371408openalex-extracted
CTENO64 is Required for Coordinated Paddling of Ciliary Comb Plate in Ctenophores
inferred← citeshttps://doi.org/10.1002/9781118492833.ch7openalex-snapshot
Induction and Differentiation of theXenopusCiliated Embryonic Epidermis
inferred← citeshttps://doi.org/10.1002/bies.70107openalex-snapshot
Linking Planar Cell Polarity to Mechanotransduction During Morphogenesis
inferred← citeshttps://doi.org/10.1002/cm.20498openalex-snapshot
A role for central spindle proteins in cilia structure and function
inferred← citeshttps://doi.org/10.1002/cm.21496openalex-snapshot
The small molecule AMBMP disrupts microtubule growth, ciliogenesis, cell polarity, and cell migration
inferred← citeshttps://doi.org/10.1002/cm.70056openalex-snapshot
A Cell Type‐Specific Role for Tubb6 in Ciliogenesis of Xenopus Epidermal Multiciliated Cells
inferred← citeshttps://doi.org/10.1002/dvdy.22564openalex-snapshot
The planar cell polarity pathway in vertebrate development
inferred← citeshttps://doi.org/10.1002/dvdy.22756openalex-snapshot
Axonemal positioning and orientation in three‐dimensional space for primary cilia: What is known, what is assumed, and what needs clarification
inferred← citeshttps://doi.org/10.1002/dvdy.24024openalex-snapshot
Fused (Stk36) is a ciliary protein required for central pair assembly and motile cilia orientation in the mammalian oviduct
inferred← citeshttps://doi.org/10.1002/dvdy.283openalex-snapshot
Developmental origins of mechanical homeostasis in the aorta
inferred← citeshttps://doi.org/10.1002/dvg.20824openalex-snapshot
Understanding ciliated epithelia: The power of Xenopus
inferred← citeshttps://doi.org/10.1002/dvg.23001openalex-snapshot
What we can learn from a tadpole about ciliopathies and airway diseases: Using systems biology in Xenopus to study cilia and mucociliary epithelia
inferred← citeshttps://doi.org/10.1002/dvg.23406openalex-snapshot
Xenopus epidermal and endodermal epithelia as models for mucociliary epithelial evolution, disease, and metaplasia
inferred← citeshttps://doi.org/10.1002/humu.23261openalex-snapshot
Mutation of serine/threonine protein kinase 36 ( STK36 ) causes primary ciliary dyskinesia with a central pair defect
inferred← citeshttps://doi.org/10.1002/jcp.29594openalex-snapshot
Differential phosphorylation regulates the shear stress‐induced polar activity of Rho‐specific guanine nucleotide dissociation inhibitor α
inferred← citeshttps://doi.org/10.1002/lary.26983openalex-snapshot
Absence or mislocalization of DNAH5 is a characteristic marker for motile ciliary abnormality in nasal polyps
inferred← citeshttps://doi.org/10.1002/mrd.23650openalex-snapshot
Structures and functions of cilia during vertebrate embryo development
inferred← citeshttps://doi.org/10.1002/term.3220openalex-snapshot
Airway ciliated cells regenerated on collagen sponge implants acquire planar polarities towards nearby edges of implanted areas
inferred← citeshttps://doi.org/10.1007/978-1-4614-5372-7_1openalex-snapshot
Bioinspired Nanoscale Water Channel and its Potential Applications
inferred← citeshttps://doi.org/10.1007/978-1-61779-513-8_15openalex-snapshot
Establishment of Respiratory Air–Liquid Interface Cultures and Their Use in Studying Mucin Production, Secretion, and Function
inferred← citeshttps://doi.org/10.1007/978-3-030-23173-6_7openalex-snapshot
Positioning of the Centrosome and Golgi Complex
inferred← citeshttps://doi.org/10.1007/978-3-030-23173-6_8openalex-snapshot
Centriole Positioning: Not Just a Little Dot in the Cell
inferred← citeshttps://doi.org/10.1007/978-3-642-28502-8_25openalex-snapshot
Microfluidic Phenotyping of Cilia-Driven Mixing for the Assessment of Respiratory Diseases
inferred← citeshttps://doi.org/10.1007/978-4-431-53933-9_12openalex-snapshot
Epithelial Organization of Adult Neurogenic Germinal Niches
inferred← citeshttps://doi.org/10.1007/978-94-007-5808-7_7openalex-snapshot
Motile Cilia and Brain Function: Ependymal Motile Cilia Development, Organization, Function and Their Associated Pathologies
inferred← citeshttps://doi.org/10.1007/s00018-010-0323-9openalex-snapshot
Centrioles: active players or passengers during mitosis?
inferred← citeshttps://doi.org/10.1007/s00018-014-1784-zopenalex-snapshot
Microscale imaging of cilia-driven fluid flow
inferred← citeshttps://doi.org/10.1007/s00381-025-06951-wopenalex-snapshot
Emerging insights into primary ciliary dyskinesia-associated hydrocephalus: a scoping review
inferred← citeshttps://doi.org/10.1007/s00424-008-0475-8openalex-snapshot
Flow modulates centriole movements in tubular epithelial cells
inferred← citeshttps://doi.org/10.1007/s00441-017-2611-2openalex-snapshot
Toolbox in a tadpole: Xenopus for kidney research
inferred← citeshttps://doi.org/10.1007/s11538-008-9296-3openalex-snapshot
An Integrative Computational Model of Multiciliary Beating
inferred← citeshttps://doi.org/10.1007/s13238-010-0098-7openalex-snapshot
Cilia in cell signaling and human disorders
inferred← citeshttps://doi.org/10.1007/s40139-015-0074-2openalex-snapshot
The Xenopus Embryo: An Ideal Model System to Study Human Ciliopathies
inferred← citeshttps://doi.org/10.1016/b978-0-12-394311-8.00009-1openalex-snapshot
Atypical Cadherins Celsr1–3 and Planar Cell Polarity in Vertebrates
inferred← citeshttps://doi.org/10.1016/b978-0-12-394592-1.00010-7openalex-snapshot
Celsr1–3 Cadherins in PCP and Brain Development
inferred← citeshttps://doi.org/10.1016/b978-0-12-397944-5.00010-9openalex-snapshot
Using Xenopus Skin to Study Cilia Development and Function
inferred← citeshttps://doi.org/10.1016/b978-0-12-802438-6.00007-3openalex-snapshot
Planar Cell Polarity in Ciliated Epithelia
inferred← citeshttps://doi.org/10.1016/b978-0-12-821618-7.00209-1openalex-snapshot
Cilia and Flagella
inferred← citeshttps://doi.org/10.1016/b978-0-323-38944-0.00005-xopenalex-snapshot
Ciliary Motion
inferred← citeshttps://doi.org/10.1016/bs.ctdb.2015.11.036openalex-snapshot
Mechanotransduction During Vertebrate Neurulation
inferred← citeshttps://doi.org/10.1016/bs.mcb.2015.01.016openalex-snapshot
Observing planar cell polarity in multiciliated mouse airway epithelial cells
inferred← citeshttps://doi.org/10.1016/bs.mcb.2015.01.018openalex-snapshot
In vivo investigation of cilia structure and function using Xenopus
inferred← citeshttps://doi.org/10.1016/bs.mcb.2015.03.001openalex-snapshot
In vivo examination of the cortical cytoskeleton in multiciliated cells using electron tomography
inferred← citeshttps://doi.org/10.1016/bs.mcb.2015.03.015openalex-snapshot
Centriole biogenesis and function in multiciliated cells
inferred← citeshttps://doi.org/10.1016/bs.mcb.2022.12.015openalex-snapshot
Analysis of motility and mucociliary function of tracheal epithelial cilia
inferred← citeshttps://doi.org/10.1016/j.ajhg.2018.12.009openalex-snapshot
Lack of GAS2L2 Causes PCD by Impairing Cilia Orientation and Mucociliary Clearance
inferred← citeshttps://doi.org/10.1016/j.bbadis.2011.05.005openalex-snapshot
Polycystic kidney disease: The complexity of planar cell polarity and signaling during tissue regeneration and cyst formation
inferred← citeshttps://doi.org/10.1016/j.biopsych.2023.11.004openalex-snapshot
Cilia and Extracellular Vesicles in Brain Development and Disease
inferred← citeshttps://doi.org/10.1016/j.bpj.2021.01.041openalex-snapshot
Induction of ciliary orientation by matrix patterning and characterization of mucociliary transport
inferred← citeshttps://doi.org/10.1016/j.cbpa.2007.10.003openalex-snapshot
Can we build synthetic, multicellular systems by controlling developmental signaling in space and time?
inferred← citeshttps://doi.org/10.1016/j.cdev.2022.203791openalex-snapshot
Mechanical strain breaks planar symmetry in embryonic epithelia via polarized microtubules
inferred← citeshttps://doi.org/10.1016/j.ceb.2007.11.009openalex-snapshot
Cilia orientation and the fluid mechanics of development
inferred← citeshttps://doi.org/10.1016/j.ceb.2010.07.011openalex-snapshot
Planar cell polarity signaling, cilia and polarized ciliary beating
inferred← citeshttps://doi.org/10.1016/j.ceb.2023.102286openalex-snapshot
Mechanisms and functions of multiciliary coordination
inferred← citeshttps://doi.org/10.1016/j.cell.2011.10.052openalex-snapshot
Coordinated Ciliary Beating Requires Odf2-Mediated Polarization of Basal Bodies via Basal Feet
inferred← citeshttps://doi.org/10.1016/j.celrep.2016.01.069openalex-snapshot
c21orf59/kurly Controls Both Cilia Motility and Polarization
inferred← citeshttps://doi.org/10.1016/j.cub.2009.04.018openalex-snapshot
The PCP Pathway Instructs the Planar Orientation of Ciliated Cells in the Xenopus Larval Skin
inferred← citeshttps://doi.org/10.1016/j.cub.2010.01.012openalex-snapshot
Xenopus
inferred← citeshttps://doi.org/10.1016/j.cub.2012.01.031openalex-snapshot
Proteomic Analysis of Mammalian Primary Cilia
inferred← citeshttps://doi.org/10.1016/j.cub.2012.09.046openalex-snapshot
Microtubules Enable the Planar Cell Polarity of Airway Cilia
inferred← citeshttps://doi.org/10.1016/j.cub.2012.10.030openalex-snapshot
Planar Cell Polarity: Microtubules Make the Connection with Cilia
inferred← citeshttps://doi.org/10.1016/j.cub.2014.08.047openalex-snapshot
Multiciliated Cells
inferred← citeshttps://doi.org/10.1016/j.cub.2015.06.063openalex-snapshot
Zeta-Tubulin Is a Member of a Conserved Tubulin Module and Is a Component of the Centriolar Basal Foot in Multiciliated Cells
inferred← citeshttps://doi.org/10.1016/j.cub.2015.09.015openalex-snapshot
Mechanical Strain Determines the Axis of Planar Polarity in Ciliated Epithelia
inferred← citeshttps://doi.org/10.1016/j.cub.2015.09.042openalex-snapshot
Planar Polarity: Forcing Cells Into Line
inferred← citeshttps://doi.org/10.1016/j.cub.2019.08.059openalex-snapshot
CTENO64 Is Required for Coordinated Paddling of Ciliary Comb Plate in Ctenophores
inferred← citeshttps://doi.org/10.1016/j.cub.2019.08.067openalex-snapshot
Animal Evolution: The Hidden Biology of the Ctenophore Cilium
inferred← citeshttps://doi.org/10.1016/j.cub.2022.09.061openalex-snapshot
Two distinct compartments of a ctenophore comb plate provide structural and functional integrity for the motility of giant multicilia
inferred← citeshttps://doi.org/10.1016/j.cub.2026.04.054openalex-snapshot
Fast mechanosensitive and Ca2+-dependent reorientation of motile cilia basal bodies in the placozoan Trichoplax
inferred← citeshttps://doi.org/10.1016/j.ddmec.2013.12.001openalex-snapshot
Planar cell polarity (PCP) and Wnt signaling in renal disease
inferred← citeshttps://doi.org/10.1016/j.devcel.2013.12.003openalex-snapshot
Making the Connection: Ciliary Adhesion Complexes Anchor Basal Bodies to the Actin Cytoskeleton
inferred← citeshttps://doi.org/10.1016/j.devcel.2018.04.007openalex-snapshot
Mechanical Strain Determines Cilia Length, Motility, and Planar Position in the Left-Right Organizer
inferred← citeshttps://doi.org/10.1016/j.devcel.2018.08.009openalex-snapshot
WDR5 Stabilizes Actin Architecture to Promote Multiciliated Cell Formation
inferred← citeshttps://doi.org/10.1016/j.devcel.2019.10.021openalex-snapshot
Emergence of a Bilaterally Symmetric Pattern from Chiral Components in the Planarian Epidermis
inferred← citeshttps://doi.org/10.1016/j.devcel.2019.10.022openalex-snapshot
Dynamic Polarization of the Multiciliated Planarian Epidermis between Body Plan Landmarks
inferred← citeshttps://doi.org/10.1016/j.devcel.2020.09.015openalex-snapshot
Comparative Super-Resolution Mapping of Basal Feet Reveals a Modular but Distinct Architecture in Primary and Motile Cilia
inferred← citeshttps://doi.org/10.1016/j.devcel.2020.09.016openalex-snapshot
Super-Resolution Microscopy and FIB-SEM Imaging Reveal Parental Centriole-Derived, Hybrid Cilium in Mammalian Multiciliated Cells
inferred← citeshttps://doi.org/10.1016/j.diff.2011.10.007openalex-snapshot
Planar polarity of ependymal cilia
inferred← citeshttps://doi.org/10.1016/j.diff.2011.11.012openalex-snapshot
Inversin, Wnt signaling and primary cilia
inferred← citeshttps://doi.org/10.1016/j.gde.2010.04.002openalex-snapshot
Translation of anterior–posterior polarity into left–right polarity in the mouse embryo
inferred← citeshttps://doi.org/10.1016/j.gde.2019.04.006openalex-snapshot
Biology of multiciliated cells
inferred← citeshttps://doi.org/10.1016/j.gde.2020.05.011openalex-snapshot
From biomechanics to mechanobiology: Xenopus provides direct access to the physical principles that shape the embryo
inferred← citeshttps://doi.org/10.1016/j.isci.2026.114771openalex-snapshot
Directional alignment of different cell types organizes planar cell polarity
inferred← citeshttps://doi.org/10.1016/j.jaci.2010.05.046openalex-snapshot
Ciliary dysfunction and ultrastructural abnormalities are features of severe asthma
inferred← citeshttps://doi.org/10.1016/j.jsb.2020.107680openalex-snapshot
Multi-scale alignment of respiratory cilia and its relation to mucociliary function
inferred← citeshttps://doi.org/10.1016/j.jtbi.2011.06.016openalex-snapshot
Effect of localization, length and orientation of chondrocytic primary cilium on murine growth plate organization
inferred← citeshttps://doi.org/10.1016/j.mehy.2023.111079openalex-snapshot
Role of ependymal cilia impairment in syringomyelia formation and its potential mechanism
inferred← citeshttps://doi.org/10.1016/j.mod.2011.07.004openalex-snapshot
Regulation of basal body and ciliary functions by Diversin
inferred← citeshttps://doi.org/10.1016/j.molmed.2010.05.004openalex-snapshot
Cystic kidney disease: the role of Wnt signaling
inferred← citeshttps://doi.org/10.1016/j.mtadv.2022.100216openalex-snapshot
Airborne toxicological assessment: The potential of lung-on-a-chip as an alternative to animal testing
inferred← citeshttps://doi.org/10.1016/j.protis.2013.04.003openalex-snapshot
Epiplasmins and Epiplasm in Paramecium: The Building of a Submembraneous Cytoskeleton
inferred← citeshttps://doi.org/10.1016/j.semcdb.2009.09.016openalex-snapshot
Planar cell polarity and cilia
inferred← citeshttps://doi.org/10.1016/j.semcdb.2015.05.002openalex-snapshot
Spatial and temporal aspects of Wnt signaling and planar cell polarity during vertebrate embryonic development
inferred← citeshttps://doi.org/10.1016/j.semcdb.2016.03.012openalex-snapshot
Tissue morphodynamics: Translating planar polarity cues into polarized cell behaviors
inferred← citeshttps://doi.org/10.1016/j.semcdb.2016.05.011openalex-snapshot
On the role of mechanics in driving mesenchymal-to-epithelial transitions
inferred← citeshttps://doi.org/10.1016/j.semcdb.2017.07.014openalex-snapshot
Seven pass Cadherins CELSR1-3
inferred← citeshttps://doi.org/10.1016/j.semcdb.2020.07.005openalex-snapshot
On being the right shape: Roles for motile cilia and cerebrospinal fluid flow in body and spine morphology
inferred← citeshttps://doi.org/10.1016/j.semcdb.2025.103651openalex-snapshot
Mammalian motile cilia: Structure, formation, organization, and function
inferred← citeshttps://doi.org/10.1016/j.tcb.2008.08.004openalex-snapshot
Dishevelled links basal body docking and orientation in ciliated epithelial cells
inferred← citeshttps://doi.org/10.1016/j.tig.2013.09.001openalex-snapshot
Roles of cilia, fluid flow, and Ca2+ signaling in breaking of left–right symmetry
inferred← citeshttps://doi.org/10.1016/j.tins.2016.05.004openalex-snapshot
Planar Organization of Multiciliated Ependymal (E1) Cells in the Brain Ventricular Epithelium
inferred← citeshttps://doi.org/10.1016/j.ydbio.2007.09.031openalex-snapshot
Identification of novel ciliogenesis factors using a new in vivo model for mucociliary epithelial development
inferred← citeshttps://doi.org/10.1016/j.ydbio.2009.05.373openalex-snapshot
Dishevelled controls apical docking and planar polarization of basal bodies in ciliated epithelial cells
inferred← citeshttps://doi.org/10.1016/j.ydbio.2010.07.013openalex-snapshot
Bbs8, together with the planar cell polarity protein Vangl2, is required to establish left–right asymmetry in zebrafish
inferred← citeshttps://doi.org/10.1016/j.ydbio.2013.05.004openalex-snapshot
Xenopus laevis nucleotide binding protein 1 (xNubp1) is important for convergent extension movements and controls ciliogenesis via regulation of the actin cytoskeleton
inferred← citeshttps://doi.org/10.1016/j.ydbio.2015.03.013openalex-snapshot
ATP4a is required for development and function of the Xenopus mucociliary epidermis – a potential model to study proton pump inhibitor-associated pneumonia
inferred← citeshttps://doi.org/10.1016/j.ydbio.2015.07.013openalex-snapshot
Huntingtin is required for ciliogenesis and neurogenesis during early Xenopus development
inferred← citeshttps://doi.org/10.1016/j.ydbio.2020.08.009openalex-snapshot
Nervous system and tissue polarity dynamically adapt to new morphologies in planaria
inferred← citeshttps://doi.org/10.1016/j.ydbio.2026.10.005openalex-snapshot
Epilepsy-associated potassium channel KCNT1 is required for multiciliated cell specification in Xenopus
inferred← citeshttps://doi.org/10.1016/s0070-2153(08)00801-6openalex-snapshot
Basal bodies platforms for building cilia.
inferred← citeshttps://doi.org/10.1016/s0070-2153(08)00808-9openalex-snapshot
Chapter Eight Primary Cilia in Planar Cell Polarity Regulation of the Inner Ear
inferred← citeshttps://doi.org/10.1017/jfm.2024.600openalex-snapshot
Hydrodynamic coupling of a cilia–mucus system in Herschel–Bulkley flows
inferred← citeshttps://doi.org/10.1038/emboj.2013.3openalex-snapshot
Kif3a interacts with Dynactin subunit p150Glued to organize centriole subdistal appendages
inferred← citeshttps://doi.org/10.1038/nature07883openalex-snapshot
Fused has evolved divergent roles in vertebrate Hedgehog signalling and motile ciliogenesis
inferred← citeshttps://doi.org/10.1038/ncb0410-314openalex-snapshot
Cilia self-organize in response to planar cell polarity and flow
inferred← citeshttps://doi.org/10.1038/ncb2040openalex-snapshot
Coupling between hydrodynamic forces and planar cell polarity orients mammalian motile cilia
inferred← citeshttps://doi.org/10.1038/ncb2241openalex-snapshot
Control of vertebrate multiciliogenesis by miR-449 through direct repression of the Delta/Notch pathway
inferred← citeshttps://doi.org/10.1038/ncb3524openalex-snapshot
Multiscale force sensing in development
inferred← citeshttps://doi.org/10.1038/ncomms5888openalex-snapshot
Basal foot MTOC organizes pillar MTs required for coordination of beating cilia
inferred← citeshttps://doi.org/10.1038/ncomms9388openalex-snapshot
PTEN regulates cilia through Dishevelled
inferred← citeshttps://doi.org/10.1038/ng.104openalex-snapshot
Dishevelled controls apical docking and planar polarization of basal bodies in ciliated epithelial cells
inferred← citeshttps://doi.org/10.1038/ng.2007.54openalex-snapshot
Ciliary proteins link basal body polarization to planar cell polarity regulation
inferred← citeshttps://doi.org/10.1038/ng.267openalex-snapshot
The forkhead protein Foxj1 specifies node-like cilia in Xenopus and zebrafish embryos
inferred← citeshttps://doi.org/10.1038/nn.2555openalex-snapshot
Lack of cadherins Celsr2 and Celsr3 impairs ependymal ciliogenesis, leading to fatal hydrocephalus
inferred← citeshttps://doi.org/10.1038/nrm.2017.11openalex-snapshot
Planar cell polarity in development and disease
inferred← citeshttps://doi.org/10.1038/nrm.2017.21openalex-snapshot
The development and functions of multiciliated epithelia
inferred← citeshttps://doi.org/10.1038/nrm2185openalex-snapshot
Go with the flow
inferred← citeshttps://doi.org/10.1038/nrn3525openalex-snapshot
Shaping the nervous system: role of the core planar cell polarity genes
inferred← citeshttps://doi.org/10.1038/s41467-018-04676-wopenalex-snapshot
Ependymal cilia beating induces an actin network to protect centrioles against shear stress
inferred← citeshttps://doi.org/10.1038/s41467-022-29741-3openalex-snapshot
Microridge-like structures anchor motile cilia
inferred← citeshttps://doi.org/10.1038/s41467-025-61610-7openalex-snapshot
Calcium transients regulate the apical emergence of basally located progenitors during Xenopus skin development
inferred← citeshttps://doi.org/10.1038/s41467-025-67086-9openalex-snapshot
A protein complex in the extreme distal tip of vertebrate motile cilia controls their organization, length, and function
inferred← citeshttps://doi.org/10.1038/s41467-026-70661-3openalex-snapshot
DEUP1 functions as a scaffold for basal foot integrity and planar polarity in multiciliated cells
inferred← citeshttps://doi.org/10.1038/s41567-020-0923-8openalex-snapshot
Multi-scale spatial heterogeneity enhances particle clearance in airway ciliary arrays
inferred← citeshttps://doi.org/10.1038/s41567-020-0980-zopenalex-snapshot
Active mucus–cilia hydrodynamic coupling drives self-organization of human bronchial epithelium
inferred← citeshttps://doi.org/10.1038/s41598-017-10822-zopenalex-snapshot
Calaxin establishes basal body orientation and coordinates movement of monocilia in sea urchin embryos
inferred← citeshttps://doi.org/10.1038/s41598-020-64695-wopenalex-snapshot
Hydrodynamic model of directional ciliary-beat organization in human airways
inferred← citeshttps://doi.org/10.1038/s42003-019-0462-yopenalex-snapshot
Calaxin is required for cilia-driven determination of vertebrate laterality
inferred← citeshttps://doi.org/10.1038/s42003-026-09827-0openalex-snapshot
Cilia-driven surface currents characterize specific cnidarian groups and lifecycle stages
inferred← citeshttps://doi.org/10.1038/s44319-024-00066-0openalex-snapshot
Dual-color live imaging unveils stepwise organization of multiple basal body arrays by cytoskeletons
inferred← citeshttps://doi.org/10.1038/srep16506openalex-snapshot
Sperm Associated Antigen 6 (SPAG6) Regulates Fibroblast Cell Growth, Morphology, Migration and Ciliogenesis
inferred← citeshttps://doi.org/10.1038/srep45870openalex-snapshot
Cilia distribution and polarity in the epithelial lining of the mouse middle ear cavity
inferred← citeshttps://doi.org/10.1039/b817409aopenalex-snapshot
Bio-mimetic silicone cilia for microfluidic manipulation
inferred← citeshttps://doi.org/10.1039/b920392copenalex-snapshot
Microbristle in gels: Toward all-polymer reconfigurable hybrid surfaces
inferred← citeshttps://doi.org/10.1039/c0nr00304bopenalex-snapshot
Signal transmission, conversion and multiplication by polar molecules confined in nanochannels
inferred← citeshttps://doi.org/10.1039/c3lc50571eopenalex-snapshot
A novel approach to quantifying ciliary physiology: microfluidic mixing driven by a ciliated biological surface
inferred← citeshttps://doi.org/10.1039/c5lc00633copenalex-snapshot
Flow-induced stress on adherent cells in microfluidic devices
inferred← citeshttps://doi.org/10.1039/c9sm01672dopenalex-snapshot
Controllable directional deformation of micro-pillars actuated by a magnetic field
inferred← citeshttps://doi.org/10.1042/ebc20180029openalex-snapshot
Coordination of eukaryotic cilia and flagella
inferred← citeshttps://doi.org/10.1055/s-0035-1546748openalex-snapshot
Primary Ciliary Dyskinesia
inferred← citeshttps://doi.org/10.1063/1.4901930openalex-snapshot
A microfluidic device to apply shear stresses to polarizing ciliated airway epithelium using air flow
inferred← citeshttps://doi.org/10.1073/pnas.0909465106openalex-snapshot
Regulation of ciliary polarity by the APC/C
inferred← citeshttps://doi.org/10.1073/pnas.1404988111openalex-snapshot
A dual role for planar cell polarity genes in ciliated cells
inferred← citeshttps://doi.org/10.1073/pnas.1910065117openalex-snapshot
Entrainment of mammalian motile cilia in the brain with hydrodynamic forces
inferred← citeshttps://doi.org/10.1073/pnas.2302624120openalex-snapshot
Scanning electron microscopy of human islet cilia
inferred← citeshttps://doi.org/10.1073/pnas.2605383123openalex-snapshot
Successful oocyte transport through the oviduct does not depend on the longitudinal alignment of oviduct epithelial folds
inferred← citeshttps://doi.org/10.1083/jcb.200710162openalex-snapshot
Mutations in Hydin impair ciliary motility in mice
inferred← citeshttps://doi.org/10.1083/jcb.201106110openalex-snapshot
Actin and microtubules drive differential aspects of planar cell polarity in multiciliated cells
inferred← citeshttps://doi.org/10.1083/jcb.201204072openalex-snapshot
Control of vertebrate intraflagellar transport by the planar cell polarity effector Fuz
inferred← citeshttps://doi.org/10.1083/jcb.201502043openalex-snapshot
The polarity protein Inturned links NPHP4 to Daam1 to control the subapical actin network in multiciliated cells
inferred← citeshttps://doi.org/10.1083/jcb.201601023openalex-snapshot
Multiciliated cell basal bodies align in stereotypical patterns coordinated by the apical cytoskeleton
inferred← citeshttps://doi.org/10.1083/jcb.201706058openalex-snapshot
CLAMP/Spef1 regulates planar cell polarity signaling and asymmetric microtubule accumulation in the Xenopus ciliated epithelia
inferred← citeshttps://doi.org/10.1083/jcb.201811147openalex-snapshot
Developmentally regulated GTP-binding protein 1 modulates ciliogenesis via an interaction with Dishevelled
inferred← citeshttps://doi.org/10.1083/jcb.202303052openalex-snapshot
JNK regulates ciliogenesis through the interflagellar transport complex and actin networks
inferred← citeshttps://doi.org/10.1083/jcb.202307150openalex-snapshot
Formation and function of multiciliated cells
inferred← citeshttps://doi.org/10.1091/mbc.e15-07-0474openalex-snapshot
Ccdc11 is a novel centriolar satellite protein essential for ciliogenesis and establishment of left–right asymmetry
inferred← citeshttps://doi.org/10.1091/mbc.e22-10-0468-topenalex-snapshot
Basal bodies bend in response to ciliary forces
inferred← citeshttps://doi.org/10.1091/mbc.e22-11-0508openalex-snapshot
Basal body organization and cell geometry during the cell cycle in Tetrahymena thermophila
inferred← citeshttps://doi.org/10.1093/biosci/biu173openalex-snapshot
Mechanobiology of Ciliogenesis
inferred← citeshttps://doi.org/10.1093/hmg/ddn045openalex-snapshot
Acute kidney injury and aberrant planar cell polarity induce cyst formation in mice lacking renal cilia
inferred← citeshttps://doi.org/10.1093/icb/icad106openalex-snapshot
Perspectives on Principles of Cellular Behavior from the Biophysics of Protists
inferred← citeshttps://doi.org/10.1093/jmicro/dfy147openalex-snapshot
Live cell imaging of dynamic behaviors of motile cilia and primary cilium
inferred← citeshttps://doi.org/10.1093/molehr/gaab009openalex-snapshot
Motility of efferent duct cilia aids passage of sperm cells through the male reproductive system
inferred← citeshttps://doi.org/10.1093/ndt/gfs524openalex-snapshot
The ciliary flow sensor and polycystic kidney disease
inferred← citeshttps://doi.org/10.1098/rsif.2013.0571openalex-snapshot
Emergence of polar order and cooperativity in hydrodynamically coupled model cilia
inferred← citeshttps://doi.org/10.1098/rstb.2019.0152openalex-snapshot
Motile cilia hydrodynamics: entrainment versus synchronization when coupling through flow
inferred← citeshttps://doi.org/10.1101/2022.03.27.486007openalex-snapshot
“Two-story building” of a ctenophore comb plate provides structural and functional integrity for motility of giant multicilia
inferred← citeshttps://doi.org/10.1101/2023.01.24.525309openalex-snapshot
Crb3 stabilizes activated Ezrin-Radixin-Moesin to organize the apical domain of multiciliated cells
inferred← citeshttps://doi.org/10.1101/2023.09.13.557556openalex-snapshot
Left-right asymmetry is formed in the basal bodies of the mouse node cilia in a cilia motility-dependent manner
inferred← citeshttps://doi.org/10.1101/2025.02.19.638730openalex-snapshot
Ciliated cell domains with locally coordinated ciliary motion generate a mosaic of microflows in the brain’s lateral ventricles
inferred← citeshttps://doi.org/10.1101/2025.03.13.643176openalex-snapshot
RPGR regulates motile cilia by interfering with actin dynamics
inferred← citeshttps://doi.org/10.1101/2025.08.22.671430openalex-snapshot
Fast calcium-dependent reorientation of motile cilia basal bodies in the simple metazoan, Trichoplax
inferred← citeshttps://doi.org/10.1101/487330openalex-snapshot
Super-resolution Molecular Map of Basal Foot Reveals Novel Cilium in Airway Multiciliated Cells
inferred← citeshttps://doi.org/10.1101/668459openalex-snapshot
Synchronization of mammalian motile cilia in the brain with hydrodynamic forces
inferred← citeshttps://doi.org/10.1101/735332openalex-snapshot
Spatial Intra- and Intercellular Alignment of Respiratory Cilia and its Relation to Function
inferred← citeshttps://doi.org/10.1101/cshperspect.a002964openalex-snapshot
Planar Cell Polarity Signaling: The Developing Cell's Compass
inferred← citeshttps://doi.org/10.1101/cshperspect.a027813openalex-snapshot
Role of Polarity Proteins in the Generation and Organization of Apical Surface Protrusions
inferred← citeshttps://doi.org/10.1101/cshperspect.a028233openalex-snapshot
Multiciliated Cells in Animals
inferred← citeshttps://doi.org/10.1101/gad.1810409openalex-snapshot
The hydrolethalus syndrome protein HYLS-1 links core centriole structure to cilia formation
inferred← citeshttps://doi.org/10.1111/ahg.12519openalex-snapshot
Uncovering cilia function in glial development
inferred← citeshttps://doi.org/10.1111/jeu.12794openalex-snapshot
High Diversity of Testate Amoebae (Amoebozoa, Arcellinida) Detected by HTS Analyses in a New England Fen using Newly Designed Taxon‐specific Primers
inferred← citeshttps://doi.org/10.1111/jeu.12880openalex-snapshot
Ciliate cortical organization and dynamics for cell motility: Comparing ciliates and vertebrates
inferred← citeshttps://doi.org/10.1126/sciadv.add5745openalex-snapshot
A single-cell, time-resolved profiling of Xenopus mucociliary epithelium reveals nonhierarchical model of development
inferred← citeshttps://doi.org/10.1126/scitranslmed.aay0071openalex-snapshot
A quantitative super-resolution imaging toolbox for diagnosis of motile ciliopathies
inferred← citeshttps://doi.org/10.1142/s0217979211102198openalex-snapshot
EFFECT OF POSITIVE FEEDBACK WITH THRESHOLD CONTROL ON STOCHASTIC RESONANCE OF BI-STABLE SYSTEMS
inferred← citeshttps://doi.org/10.1146/annurev-cellbio-100818-125436openalex-snapshot
Mechanics of Anteroposterior Axis Formation in Vertebrates
inferred← citeshttps://doi.org/10.1146/annurev-conmatphys-031115-011451openalex-snapshot
Realizing the Physics of Motile Cilia Synchronization with Driven Colloids
inferred← citeshttps://doi.org/10.1146/annurev-genet-112414-055224openalex-snapshot
Conservation of Planar Polarity Pathway Function Across the Animal Kingdom
inferred← citeshttps://doi.org/10.1146/annurev.physiol.70.113006.100621openalex-snapshot
Polycystins and Primary Cilia: Primers for Cell Cycle Progression
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