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Specification of ion transport cells in theXenopuslarval skin
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1006/dbio.1995.1279openalex-snapshot
Efficient Hormone-Inducible Protein Function in Xenopus laevis
inferredcites →https://doi.org/10.1006/dbio.2001.0565openalex-snapshot
Morpholino Oligos: Making Sense of Antisense?
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/10.1007/978-1-60327-483-8_31openalex-snapshot
A Method for Generating Transgenic Frog Embryos
inferredcites →https://doi.org/10.1007/bf00339641openalex-snapshot
The active absorption of ions in some freshwater animals
inferredcites →https://doi.org/10.1007/bf02952317openalex-snapshot
Zur Kenntniss des Baues der Schleimdrüsen
inferredcites →https://doi.org/10.1007/s002329900221openalex-snapshot
The H + Pump in Frog Skin ( Rana esculenta ): Identification and Localization of a V-ATPase
inferredcites →https://doi.org/10.1007/s00360-002-0276-xopenalex-snapshot
Proton pump activity is required for active uptake of chloride in isolated amphibian skin exposed to freshwater
inferredcites →https://doi.org/10.1007/s00424-007-0382-4openalex-snapshot
V-ATPase functions in normal and disease processes
inferredcites →https://doi.org/10.1007/s00424-009-0657-zopenalex-snapshot
Regulated acid–base transport in the collecting duct
inferredcites →https://doi.org/10.1016/j.bbamem.2003.07.002openalex-snapshot
Proton pump-driven cutaneous chloride uptake in anuran amphibia
inferredcites →https://doi.org/10.1016/j.cbpa.2007.06.416openalex-snapshot
New insights into fish ion regulation and mitochondrion-rich cells
inferredcites →https://doi.org/10.1016/j.ydbio.2007.04.044openalex-snapshot
Foxi3 transcription factors and Notch signaling control the formation of skin ionocytes from epidermal precursors of the zebrafish embryo
inferredcites →https://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
inferredcites →https://doi.org/10.1016/j.ydbio.2007.12.022openalex-snapshot
Long- and short-range signals control the dynamic expression of an animal hemisphere-specific gene in Xenopus
inferredcites →https://doi.org/10.1016/s0091-679x(08)60307-6openalex-snapshot
Appendix G: In Situ Hybridization: An Improved Whole-Mount Method for Xenopus Embryos
inferredcites →https://doi.org/10.1016/s0925-4773(02)00046-1openalex-snapshot
A highly conserved novel family of mammalian developmental transcription factors related to Drosophila grainyhead
inferredcites →https://doi.org/10.1038/5022openalex-snapshot
Mutations in the gene encoding B1 subunit of H+-ATPase cause renal tubular acidosis with sensorineural deafness
inferredcites →https://doi.org/10.1038/ng1082openalex-snapshot
Non-polarized targeting of AE1 causes autosomal dominant distal renal tubular acidosis
inferredcites →https://doi.org/10.1038/sj.emboj.7601272openalex-snapshot
Epididymal expression of the forkhead transcription factor Foxi1 is required for male fertility
inferredcites →https://doi.org/10.1046/j.1523-1755.2002.00671.xopenalex-snapshot
Regulation of the expression of the Cl-/anion exchanger pendrin in mouse kidney by acid-base status
inferredcites →https://doi.org/10.1073/pnas.071516798openalex-snapshot
Pendrin, encoded by the Pendred syndrome gene, resides in the apical region of renal intercalated cells and mediates bicarbonate secretion
inferredcites →https://doi.org/10.1073/pnas.1010364107openalex-snapshot
Deletion of hensin/DMBT1 blocks conversion of β- to α-intercalated cells and induces distal renal tubular acidosis
inferredcites →https://doi.org/10.1093/nar/28.4.e12openalex-snapshot
A simplified method of generating transgenic Xenopus
inferredcites →https://doi.org/10.1095/biolreprod.105.043752openalex-snapshot
Distinct Expression Patterns of Different Subunit Isoforms of the V-ATPase in the Rat Epididymis1
inferredcites →https://doi.org/10.1097/01.asn.0000099375.74789.abopenalex-snapshot
Localization and Regulation of the ATP6V0A4 (a4) Vacuolar H+-ATPase Subunit Defective in an Inherited Form of Distal Renal Tubular Acidosis
inferredcites →https://doi.org/10.1097/01.mnh.0000168390.04520.06openalex-snapshot
Recent advances in our understanding of intercalated cells
inferredcites →https://doi.org/10.1097/01.mnh.0000172727.82993.aaopenalex-snapshot
Role of hensin in mediating the adaptation of the cortical collecting duct to metabolic acidosis
inferredcites →https://doi.org/10.1101/gad.3.8.1099openalex-snapshot
Notch is required for successive cell decisions in the developing Drosophila retina.
inferredcites →https://doi.org/10.1101/gad.991602openalex-snapshot
Mastermind mediates chromatin-specific transcription and turnover of the Notch enhancer complex
inferredcites →https://doi.org/10.1111/j.1365-2443.2005.00884.xopenalex-snapshot
Heterodimerization with LBP‐1b is necessary for nuclear localization of LBP‐1a and LBP‐1c
inferredcites →https://doi.org/10.1111/j.1365-2443.2009.01344.xopenalex-snapshot
Transactivation activity of LBP‐1 proteins and their dimerization in living cells
inferredcites →https://doi.org/10.1111/j.1748-1716.1937.tb01583.xopenalex-snapshot
Osmotic regulation in the frog (R. esculenta) by active absorption of chloride ions
inferredcites →https://doi.org/10.1113/expphysiol.1996.sp003955openalex-snapshot
Role of mitochondria‐rich cells in epithelial chloride uptake
inferredcites →https://doi.org/10.1128/mcb.14.3.1776openalex-snapshot
Characterization of a Family of Related Cellular Transcription Factors Which Can Modulate Human Immunodeficiency Virus Type 1 Transcription In Vitro
inferredcites →https://doi.org/10.1128/mcb.24.16.7113-7129.2004openalex-snapshot
Defective Extraembryonic Angiogenesis in Mice Lacking LBP-1a, a Member of the grainyhead Family of Transcription Factors
inferredcites →https://doi.org/10.1152/ajpcell.1996.270.6.c1571openalex-snapshot
Plasticity in epithelial polarity of renal intercalated cells: targeting of the H(+)-ATPase and band 3
inferredcites →https://doi.org/10.1152/ajprenal.00037.2002openalex-snapshot
Immunocytochemical localization of pendrin in intercalated cell subtypes in rat and mouse kidney
inferredcites →https://doi.org/10.1152/ajprenal.00340.2006openalex-snapshot
New insights into the regulation of V-ATPase-dependent proton secretion
inferredcites →https://doi.org/10.1152/ajprenal.1999.277.6.f957openalex-snapshot
Cellular and subcellular immunolocalization of ClC-5 channel in mouse kidney: colocalization with H+-ATPase
inferredcites →https://doi.org/10.1159/000104159openalex-snapshot
Differential Localization of Vacuolar H+-ATPases Containing a1, a2, a3, or a4 (ATP6V0A1-4) Subunit Isoforms Along the Nephron
inferredcites →https://doi.org/10.1172/jci0213292openalex-snapshot
Acid incubation reverses the polarity of intercalated cell transporters, an effect mediated by hensin
inferredcites →https://doi.org/10.1172/jci13292openalex-snapshot
Acid incubation reverses the polarity of intercalated cell transporters, an effect mediated by hensin
inferredcites →https://doi.org/10.1172/jci200420665openalex-snapshot
Distal renal tubular acidosis in mice that lack the forkhead transcription factor Foxi1
inferredcites →https://doi.org/10.1172/jci38416openalex-snapshot
Inactivation of Notch signaling in the renal collecting duct causes nephrogenic diabetes insipidus in mice
inferredcites →https://doi.org/10.1186/gb-2002-3-6-software0001openalex-snapshot
Software and methods for oligonucleotide and cDNA array data analysis
inferredcites →https://doi.org/10.1242/dev.00376openalex-snapshot
Lack of pendrin expression leads to deafness and expansion of the endolymphatic compartment in inner ears ofFoxi1null mutant mice
inferredcites →https://doi.org/10.1242/dev.01865openalex-snapshot
Xema, afoxi-class gene expressed in the gastrula stageXenopusectoderm, is required for the suppression of mesendoderm
inferredcites →https://doi.org/10.1242/dev.02417openalex-snapshot
Radial intercalation of ciliated cells during Xenopus skin development
inferredcites →https://doi.org/10.1242/dev.02768openalex-snapshot
FoxI1e activates ectoderm formation and controls cell position in theXenopusblastula
inferredcites →https://doi.org/10.1242/dev.124.3.693openalex-snapshot
The Xenopus homolog of Drosophila Suppressor of Hairless mediates Notch signaling during primary neurogenesis
inferredcites →https://doi.org/10.1242/dmm.006494openalex-snapshot
Embryonic frog epidermis: a model for the study of cell-cell interactions in the development of mucociliary disease
inferredcites →https://doi.org/10.1242/jeb.199.11.2345openalex-snapshot
Mitochondria-Rich, Proton-Secreting Epithelial Cells
inferredcites →https://doi.org/10.1242/jeb.200.2.247openalex-snapshot
The Key Role of the H+ V-ATPase in Acid–Base Balance and Na+ Transport Processes in Frog Skin
inferredcites →https://doi.org/10.1371/journal.pone.0000302openalex-snapshot
A Positive Regulatory Loop between foxi3a and foxi3b Is Essential for Specification and Differentiation of Zebrafish Epidermal Ionocytes
inferredcites →https://doi.org/10.1371/journal.pone.0004471openalex-snapshot
The Forkhead Transcription Factor Foxi1 Is a Master Regulator of Vacuolar H+-ATPase Proton Pump Subunits in the Inner Ear, Kidney and Epididymis
inferredcites →https://doi.org/10.1371/journal.pone.0011702openalex-snapshot
Modulation of CP2 Family Transcriptional Activity by CRTR-1 and Sumoylation
inferredcites →https://doi.org/10.1385/1-59259-270-8:393openalex-snapshot
A Method for Generating Transgenic Frog Embryos
inferredcites →https://doi.org/10.1387/ijdb.092877mjopenalex-snapshot
Zebrafish grainyhead-like1 is a common marker of different non-keratinocyte epidermal cell lineages, which segregate from each other in a Foxi3-dependent manner
inferredcites →https://doi.org/10.1530/rep.1.00964openalex-snapshot
Expression of ion transport-associated proteins in human efferent and epididymal ducts
inferredcites →https://doi.org/10.1681/asn.2006101072openalex-snapshot
Distal Renal Tubular Acidosis in Mice Lacking the AE1 (Band3) Cl−/HCO3 − Exchanger (slc4a1)
inferredcites →https://doi.org/10.1681/asn.2006101076openalex-snapshot
Origin and Fate of Pendrin-Positive Intercalated Cells in Developing Mouse Kidney
inferredcites →https://doi.org/10.1681/asn.v1271327openalex-snapshot
Intrarenal and Cellular Localization of CLC-K2 Protein in the Mouse Kidney
inferredcites →https://doi.org/10.2353/ajpath.2010.090389openalex-snapshot
Remodeling of the Fetal Collecting Duct Epithelium
inferredcites →https://doi.org/10.3791/1229openalex-snapshot
Zebrafish Whole Mount High-Resolution Double Fluorescent In Situ Hybridization
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.4581585openalex-extracted
Developmental Expression Patterns of Carbonic Anhydrase 2 (Ca2) Gene in Xenopus Tropicalis
inferred← citeshttps://doi.org/10.1002/9781118492833.ch7openalex-snapshot
Induction and Differentiation of theXenopusCiliated Embryonic Epidermis
inferred← citeshttps://doi.org/10.1002/bdrc.20215openalex-snapshot
Development of zebrafish epidermis
inferred← citeshttps://doi.org/10.1002/dvdy.23706openalex-snapshot
ΔNp63 is regulated by BMP4 signaling and is required for early epidermal development in Xenopus
inferred← citeshttps://doi.org/10.1002/dvdy.23826openalex-snapshot
Rab11 regulates planar polarity and migratory behavior of multiciliated cells in Xenopus embryonic epidermis
inferred← citeshttps://doi.org/10.1002/dvdy.70016openalex-snapshot
Interspecific comparisons of anuran embryonic epidermal landscapes and energetic trade‐offs in response to changes in salinity
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.23344openalex-snapshot
Serotonin and MucXS release by small secretory cells depend on Xpod, a SSC specific marker gene
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/jemt.70098openalex-snapshot
Effects of Metallic Nanoparticles Treatments on the Development of the Pool Frog, Pelophylax lessonae (Amphibia: Ranidae)
inferred← citeshttps://doi.org/10.1007/978-1-4939-8784-9_18openalex-snapshot
Manipulating and Analyzing Cell Type Composition of the Xenopus Mucociliary Epidermis
inferred← citeshttps://doi.org/10.1007/978-3-319-51436-9_7openalex-snapshot
Development and Diseases of the Collecting Duct System
inferred← citeshttps://doi.org/10.1007/s00360-024-01545-5openalex-snapshot
The origins of gas exchange and ion regulation in fish gills: evidence from structure and function
inferred← citeshttps://doi.org/10.1007/s00424-014-1669-xopenalex-snapshot
Renal acid-base regulation: new insights from animal models
inferred← citeshttps://doi.org/10.1007/s00424-020-02423-zopenalex-snapshot
Adaptive response of the murine collecting duct to alkali loading
inferred← citeshttps://doi.org/10.1007/s00439-016-1660-zopenalex-snapshot
Expanding the clinical and genetic heterogeneity of hereditary disorders of connective tissue
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/b978-0-12-381462-3.00054-9openalex-snapshot
The SLC4 Anion Exchanger Gene Family
inferred← citeshttps://doi.org/10.1016/b978-0-12-405945-0.00011-9openalex-snapshot
Early Development of Epidermis and Neural Tissue
inferred← citeshttps://doi.org/10.1016/b978-0-12-802438-6.00001-2openalex-snapshot
Cell Polarity in Oocyte Development
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/b978-0-323-35214-7.00110-4openalex-snapshot
Urinary Acidification
inferred← citeshttps://doi.org/10.1016/bs.ctdb.2020.08.001openalex-snapshot
Building a ciliated epithelium: Transcriptional regulation and radial intercalation of multiciliated cells
inferred← citeshttps://doi.org/10.1016/j.cdev.2025.204019openalex-snapshot
Mucociliary cell type compositions - bridging the gap between genes and emergent tissue functions
inferred← citeshttps://doi.org/10.1016/j.celrep.2019.08.063openalex-snapshot
ΔN-Tp63 Mediates Wnt/β-Catenin-Induced Inhibition of Differentiation in Basal Stem Cells of Mucociliary Epithelia
inferred← citeshttps://doi.org/10.1016/j.celrep.2021.109556openalex-snapshot
Tubulin acetylation promotes penetrative capacity of cells undergoing radial intercalation
inferred← citeshttps://doi.org/10.1016/j.celrep.2022.110663openalex-snapshot
A mesenchymal to epithelial switch in Fgf10 expression specifies an evolutionary-conserved population of ionocytes in salivary glands
inferred← citeshttps://doi.org/10.1016/j.cub.2020.03.013openalex-snapshot
Centriole Number and the Accumulation of Microtubules Modulate the Timing of Apical Insertion during Radial Intercalation
inferred← citeshttps://doi.org/10.1016/j.devcel.2014.03.015openalex-snapshot
Polarized Wnt Signaling Regulates Ectodermal Cell Fate in Xenopus
inferred← citeshttps://doi.org/10.1016/j.devcel.2017.02.008openalex-snapshot
Planarian Epidermal Stem Cells Respond to Positional Cues to Promote Cell-Type Diversity
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.2021.02.026openalex-snapshot
The Scf/Kit pathway implements self-organized epithelial patterning
inferred← citeshttps://doi.org/10.1016/j.exer.2019.04.010openalex-snapshot
Molecular markers for corneal epithelial cells in larval vs. adult Xenopus frogs
inferred← citeshttps://doi.org/10.1016/j.febslet.2013.05.007openalex-snapshot
Cell biology of the intercalated cell in the kidney
inferred← citeshttps://doi.org/10.1016/j.gep.2021.119213openalex-snapshot
Eya1 protein distribution during embryonic development of Xenopus laevis
inferred← citeshttps://doi.org/10.1016/j.heliyon.2023.e14568openalex-snapshot
CFTR High Expresser Cells in cystic fibrosis and intestinal diseases
inferred← citeshttps://doi.org/10.1016/j.jcf.2019.09.010openalex-snapshot
Regeneration of airway epithelial cells to study rare cell states in cystic fibrosis
inferred← citeshttps://doi.org/10.1016/j.prrv.2023.04.005openalex-snapshot
Airway epithelial development and function: A key player in asthma pathogenesis?
inferred← citeshttps://doi.org/10.1016/j.semnephrol.2019.04.004openalex-snapshot
Molecular Pathophysiology of Acid-Base Disorders
inferred← citeshttps://doi.org/10.1016/j.toxlet.2025.111813openalex-snapshot
Predicting acute developmental toxicity of chemicals in embryos of the African clawed frog (Xenopus laevis): Calibration and validation of regression-based quantitative structure activity relationship models for hazard assessment of chemicals in anuran amphibians
inferred← citeshttps://doi.org/10.1016/j.xpro.2021.100928openalex-snapshot
A live-imaging protocol to track cell movement in the Xenopus embryo
inferred← citeshttps://doi.org/10.1016/j.ydbio.2014.02.019openalex-snapshot
Ephrin-B2 governs morphogenesis of endolymphatic sac and duct epithelia in the mouse inner ear
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.2017.02.007openalex-snapshot
Elf5 is a principal cell lineage specific transcription factor in the kidney that contributes to Aqp 2 and Avpr 2 gene expression
inferred← citeshttps://doi.org/10.1016/j.ydbio.2020.08.005openalex-snapshot
Foxi1 inactivation rescues loss of principal cell fate selection in Hes1-deficient kidneys but does not ensure maintenance of principal cell gene expression
inferred← citeshttps://doi.org/10.1016/j.ymthe.2019.02.019openalex-snapshot
Recent Developments in mRNA-Based Protein Supplementation Therapy to Target Lung Diseases
inferred← citeshttps://doi.org/10.1021/acs.jproteome.9b00589openalex-snapshot
Simple Method To Characterize the Ciliary Proteome of Multiciliated Cells
inferred← citeshttps://doi.org/10.1038/ncb2406openalex-snapshot
Multicilin promotes centriole assembly and ciliogenesis during multiciliate cell differentiation
inferred← citeshttps://doi.org/10.1038/ncomms7017openalex-snapshot
mab21-l3 regulates cell fate specification of multiciliate cells and ionocytes
inferred← citeshttps://doi.org/10.1038/ncomms7666openalex-snapshot
ERK7 regulates ciliogenesis by phosphorylating the actin regulator CapZIP in cooperation with Dishevelled
inferred← citeshttps://doi.org/10.1038/nrm3723openalex-snapshot
Cell intercalation from top to bottom
inferred← citeshttps://doi.org/10.1038/s41385-020-00370-7openalex-snapshot
Cellular and functional heterogeneity of the airway epithelium
inferred← citeshttps://doi.org/10.1038/s41392-021-00709-xopenalex-snapshot
Multimodal single-cell omics analysis identifies epithelium–immune cell interactions and immune vulnerability associated with sex differences in COVID-19
inferred← citeshttps://doi.org/10.1038/s41467-020-14385-yopenalex-snapshot
Tissue mechanics drives regeneration of a mucociliated epidermis on the surface of Xenopus embryonic aggregates
inferred← citeshttps://doi.org/10.1038/s41467-020-16239-zopenalex-snapshot
Dissecting the cellular specificity of smoking effects and reconstructing lineages in the human airway epithelium
inferred← citeshttps://doi.org/10.1038/s41467-022-34165-0openalex-snapshot
Multiciliated cells use filopodia to probe tissue mechanics during epithelial integration in vivo
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/s41577-020-00477-9openalex-snapshot
Regulation of immune responses by the airway epithelial cell landscape
inferred← citeshttps://doi.org/10.1038/s41586-018-0393-7openalex-snapshot
A revised airway epithelial hierarchy includes CFTR-expressing ionocytes
inferred← citeshttps://doi.org/10.1038/s41586-018-0394-6openalex-snapshot
A single-cell atlas of the airway epithelium reveals the CFTR-rich pulmonary ionocyte
inferred← citeshttps://doi.org/10.1038/s41586-022-05331-7openalex-snapshot
Ion regulation at gills precedes gas exchange and the origin of vertebrates
inferred← citeshttps://doi.org/10.1038/s41598-023-30603-1openalex-snapshot
Transcriptomic profile comparison reveals conservation of ionocytes across multiple organs
inferred← citeshttps://doi.org/10.1038/s44320-026-00212-xopenalex-snapshot
Single-cell morphodynamics predict cell fate decisions during mucociliary epithelial differentiation
inferred← citeshttps://doi.org/10.1038/srep03217openalex-snapshot
The medaka mutation tintachina sheds light on the evolution of V-ATPase B subunits in vertebrates
inferred← citeshttps://doi.org/10.1042/bcj20220572openalex-snapshot
Respiratory epithelial cell types, states and fates in the era of single-cell RNA-sequencing
inferred← citeshttps://doi.org/10.1042/bst20200745openalex-snapshot
A ‘tad’ of hope in the fight against airway disease
inferred← citeshttps://doi.org/10.1073/pnas.1221496110openalex-snapshot
Renal intercalated cells are rather energized by a proton than a sodium pump
inferred← citeshttps://doi.org/10.1080/24750263.2024.2422089openalex-snapshot
A microscopical and ultrastructural analysis of the embryonic epidermis of the pool frog, Pelophylax lessonae (Camerano, 1882) (Anura: Ranidae)
inferred← citeshttps://doi.org/10.1083/jcb.201312045openalex-snapshot
Radial intercalation is regulated by the Par complex and the microtubule-stabilizing protein CLAMP/Spef1
inferred← citeshttps://doi.org/10.1089/hum.2020.013openalex-snapshot
Viral Vectors, Animal Models, and Cellular Targets for Gene Therapy of Cystic Fibrosis Lung Disease
inferred← citeshttps://doi.org/10.1093/med/9780199592548.003.0024openalex-snapshot
Renal acid–base homeostasis
inferred← citeshttps://doi.org/10.1093/nar/gky771openalex-snapshot
The Xenopus animal cap transcriptome: building a mucociliary epithelium
inferred← citeshttps://doi.org/10.1101/2020.04.22.055483openalex-snapshot
The SCF/KIT pathway implements self-organised epithelial patterning by cell movement
inferred← citeshttps://doi.org/10.1101/2021.11.18.469090openalex-snapshot
Mechanics of cell integration in vivo
inferred← citeshttps://doi.org/10.1101/2023.02.15.528675openalex-snapshot
Temporal Notch signaling and Hes-mediated competitive de-repression regulate mucociliary cell fates in Xenopus
inferred← citeshttps://doi.org/10.1101/2025.01.13.632850openalex-snapshot
A single-cell transcriptomic map of the Xenopus mesonephros reveals conserved nephron patterning across vertebrate kidney forms
inferred← citeshttps://doi.org/10.1101/cshperspect.a035733openalex-snapshot
A Synthesis Concerning Conservation and Divergence of Cell Types across Epithelia
inferred← citeshttps://doi.org/10.1101/gad.243832.114openalex-snapshot
Multicilin drives centriole biogenesis via E2f proteins
inferred← citeshttps://doi.org/10.1126/sciadv.1700523openalex-snapshot
A tail of two voltages: Proteomic comparison of the three electric organs of the electric eel
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/10.1146/annurev-pathol-042420-094031openalex-snapshot
Cystic Fibrosis and the Cells of the Airway Epithelium: What Are Ionocytes and What Do They Do?
inferred← citeshttps://doi.org/10.1152/physiol.00008.2011openalex-snapshot
Differentiation of Intercalated Cells in the Kidney
inferred← citeshttps://doi.org/10.1159/000492973openalex-snapshot
Na+/H+ Exchangers Are Required for the Development and Function of Vertebrate Mucociliary Epithelia
inferred← citeshttps://doi.org/10.1159/000514579openalex-snapshot
Signaling Control of Mucociliary Epithelia: Stem Cells, Cell Fates, and the Plasticity of Cell Identity in Development and Disease
inferred← citeshttps://doi.org/10.1164/rccm.202205-1010leopenalex-snapshot
De Novo Generation of Pulmonary Ionocytes from Normal and Cystic Fibrosis Human Induced Pluripotent Stem Cells
inferred← citeshttps://doi.org/10.1186/s12931-020-01442-9openalex-snapshot
Cell-specific expression of lung disease risk-related genes in the human small airway epithelium
inferred← citeshttps://doi.org/10.1186/s12931-024-02800-7openalex-snapshot
In vitro platform to model the function of ionocytes in the human airway epithelium
inferred← citeshttps://doi.org/10.1242/bio.023739openalex-snapshot
The role of nitric oxide during embryonic epidermis development ofXenopus laevis
inferred← citeshttps://doi.org/10.1242/dev.102343openalex-snapshot
A novel serotonin-secreting cell type regulates ciliary motility in the mucociliary epidermis of Xenopus tadpoles
inferred← citeshttps://doi.org/10.1242/dev.102426openalex-snapshot
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
inferred← citeshttps://doi.org/10.1242/dev.118679openalex-snapshot
BMP signalling controls the construction of vertebrate mucociliary epithelia
inferred← citeshttps://doi.org/10.1242/dev.121384openalex-snapshot
Control of vertebrate core PCP protein localization and dynamics by Prickle2
inferred← citeshttps://doi.org/10.1242/dev.202809openalex-snapshot
Environmental and molecular control of tissue-specific ionocyte differentiation in zebrafish
inferred← citeshttps://doi.org/10.1242/jcs.261046openalex-snapshot
Crb3 is required to organize the apical domain of multiciliated cells
inferred← citeshttps://doi.org/10.1371/journal.pbio.3003583openalex-snapshot
Foxi1 regulates multipotent mucociliary progenitors and ionocyte specification through transcriptional and epigenetic mechanisms
inferred← citeshttps://doi.org/10.1371/journal.pgen.1006538openalex-snapshot
Rfx2 Stabilizes Foxj1 Binding at Chromatin Loops to Enable Multiciliated Cell Gene Expression
inferred← citeshttps://doi.org/10.1371/journal.pone.0023746openalex-snapshot
Acquisition of glial cells missing 2 Enhancers Contributes to a Diversity of Ionocytes in Zebrafish
inferred← citeshttps://doi.org/10.1681/asn.2012121183openalex-snapshot
Salt and Pepper Distribution of Cell Types in the Collecting Duct
inferred← citeshttps://doi.org/10.1681/asn.2013070764openalex-snapshot
Adam10 Mediates the Choice between Principal Cells and Intercalated Cells in the Kidney
inferred← citeshttps://doi.org/10.1681/asn.2018040440openalex-snapshot
Endogenous Notch Signaling in Adult Kidneys Maintains Segment-Specific Epithelial Cell Types of the Distal Tubules and Collecting Ducts to Ensure Water Homeostasis
inferred← citeshttps://doi.org/10.17077/etd.vys5pbkropenalex-snapshot
Characterization of a Cdc42 effector protein (Cep4l) and a novel role for Cdc42 in xenopus neurogenesis and Fgf signaling
inferred← citeshttps://doi.org/10.2215/cjn.08880914openalex-snapshot
Collecting Duct Intercalated Cell Function and Regulation
inferred← citeshttps://doi.org/10.3390/genes14030597openalex-snapshot
Distribution and Expression of Pulmonary Ionocyte-Related Factors CFTR, ATP6V0D2, and ATP6V1C2 in the Lungs of Yaks at Different Ages
inferred← citeshttps://doi.org/10.3390/ijms19102852openalex-snapshot
Neglected Functions of TFCP2/TFCP2L1/UBP1 Transcription Factors May Offer Valuable Insights into Their Mechanisms of Action
inferred← citeshttps://doi.org/10.3390/ijms252413431openalex-snapshot
Integrating Single-Cell RNA-Seq and ATAC-Seq Analysis Reveals Uterine Cell Heterogeneity and Regulatory Networks Linked to Pimpled Eggs in Chickens
inferred← citeshttps://doi.org/10.48550/arxiv.2111.12740openalex-snapshot
Mechanics of cell integration in vivo
inferred← citeshttps://doi.org/10.6084/m9.figshare.25698161openalex-snapshot
Additional file 1 of In vitro platform to model the function of ionocytes in the human airway epithelium
inferred← citeshttps://doi.org/10.6084/m9.figshare.25698435openalex-snapshot
Additional file 2 of In vitro platform to model the function of ionocytes in the human airway epithelium
inferred← citeshttps://doi.org/10.6084/m9.figshare.26712356openalex-snapshot
Additional file 3 of In vitro platform to model the function of ionocytes in the human airway epithelium
inferred← citeshttps://doi.org/10.64898/2025.12.15.694399openalex-snapshot
Spatial gene expression maps in vertebrate limbs display conserved and regenerative species-specific features within connective tissue
inferred← citeshttps://doi.org/10.64898/2026.05.08.723674openalex-snapshot
Gluconeogenesis and glycogen metabolism in the epidermis and endoderm of Xenopus tropicalis embryos and larvae
inferred← citeshttps://doi.org/10.64898/2026.07.22.740112openalex-snapshot
Mucus cell and ionocyte precursors migrate between epithelial cells to disperse through the zebrafish epidermis
inferred← citeshttps://doi.org/10.70675/0371981az05eez4db7z9ee5zec03e9c86a3eopenalex-snapshot
Multi scale study of three conserved centriolar effectors of ciliated epithelia
inferred← citeshttps://doi.org/10.70675/59922945z5cb5z4a25za7c9z46e1e95003feopenalex-snapshot
Le microRNA miR-449 contrôle le développement des cellules multiciliées dans l' épithélium mucociliaire de l' amphibien Xenopus laevis en agissant sur des multiples gènes cibles
inferred← citeshttps://doi.org/10.70675/67876ef0zf5dcz40acza191z2631d60927b2openalex-snapshot
Catching cellular heterogeneity and differentiation dynamics of normal and pathological airway epithelia through single cell transcriptional profiling
inferred← citeshttps://doi.org/10.70675/6e115649zd82ez404azba02zb48dd44c464fopenalex-snapshot
Role of SLC6A14 in cystic fibrosis lung pathophysiology
inferred← citeshttps://doi.org/10.70675/952292a9z3a2bz442fzb547ze3e304a159d0openalex-snapshot
Molecular and cellular basis of pattern establishment in a vertebrate epithelium
inferred← citeshttps://doi.org/10.70675/f8595ff5z98e1z4dcez9387z0d1292e3feccopenalex-snapshot
Contribution des gènes des loci 5q11 et 11q23 à la multiciliogenèse et régulation de l’équilibre mucociliaire de l’épithélium des voies respiratoires au cours de la régénération in vitro
inferred← citeshttps://doi.org/10.7554/elife.24265openalex-snapshot
Transcription factor TFCP2L1 patterns cells in the mouse kidney collecting ducts
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