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Claudin extracellular domains determine paracellular charge selectivity and resistance but not tight junction fibril architecture
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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/(sici)1521-2254(199909/10)1:5<372::aid-jgm61>3.0.co;2-topenalex-snapshot
Controlling genes with tetracyclines
inferredcites →https://doi.org/10.1007/bf01870332openalex-snapshot
Morphological factors influencing transepithelial permeability: A model for the resistance of theZonula Occludens
inferredcites →https://doi.org/10.1007/bf01871696openalex-snapshot
Distribution and characteristics of the occluding junctions in a monolayer of a cell line (MDCK) derived from canine kidney
inferredcites →https://doi.org/10.1007/bf02431979openalex-snapshot
The mechanism of cation permeation in rabbit gallbladder
inferredcites →https://doi.org/10.1007/s002320010031openalex-snapshot
Occludin Localization at the Tight Junction Requires the Second Extracellular Loop
inferredcites →https://doi.org/10.1007/s00418-001-0359-xopenalex-snapshot
Formation of tight junction strands by expression of claudin-1 mutants in their ZO-1 binding site in MDCK cells
inferredcites →https://doi.org/10.1016/0005-2736(68)90033-3openalex-snapshot
Effects of pH and polyvalent cations on the selective permeability of gall-bladder epithelium to monovalent ions
inferredcites →https://doi.org/10.1016/s0171-9335(99)80086-7openalex-snapshot
Claudin-1 contributes to the epithelial barrier function in MDCK cells
inferredcites →https://doi.org/10.1073/pnas.96.2.511openalex-snapshot
Claudin multigene family encoding four-transmembrane domain protein components of tight junction strands
inferredcites →https://doi.org/10.1074/jbc.m106013200openalex-snapshot
Interleukin-2 Receptor β Subunit-dependent and -independent Regulation of Intestinal Epithelial Tight Junctions
inferredcites →https://doi.org/10.1083/jcb.141.7.1539openalex-snapshot
Claudin-1 and -2: Novel Integral Membrane Proteins Localizing at Tight Junctions with No Sequence Similarity to Occludin
inferredcites →https://doi.org/10.1083/jcb.143.2.391openalex-snapshot
A Single Gene Product, Claudin-1 or -2, Reconstitutes Tight Junction Strands and Recruits Occludin in Fibroblasts
inferredcites →https://doi.org/10.1083/jcb.147.6.1351openalex-snapshot
Direct Binding of Three Tight Junction-Associated Maguks, Zo-1, Zo-2, and Zo-3, with the Cooh Termini of Claudins
inferredcites →https://doi.org/10.1083/jcb.153.2.263openalex-snapshot
Conversion of Zonulae Occludentes from Tight to Leaky Strand Type by Introducing Claudin-2 into Madin-Darby Canine Kidney I Cells
inferredcites →https://doi.org/10.1083/jcb.58.2.390openalex-snapshot
FRACTURE FACES OF ZONULAE OCCLUDENTES FROM "TIGHT" AND "LEAKY" EPITHELIA
inferredcites →https://doi.org/10.1152/ajpcell.00038.2002openalex-snapshot
Claudins create charge-selective channels in the paracellular pathway between epithelial cells
inferredcites →https://doi.org/10.1152/ajpcell.1981.240.3.c96openalex-snapshot
Occluding junctions in cultured epithelial monolayers
inferredcites →https://doi.org/10.1152/ajpgi.1981.241.4.g275openalex-snapshot
Barrier function of epithelia
inferredcites →https://doi.org/10.1152/ajprenal.0021.2001openalex-snapshot
Claudin-2 is selectively expressed in proximal nephron in mouse kidney
inferredcites →https://doi.org/10.1152/ajprenal.1986.250.4.f734openalex-snapshot
Occluding junctions in a renal cell line (LLC-PK1) with characteristics of proximal tubular cells
inferredcites →https://doi.org/10.1172/jci12464openalex-snapshot
Regulated expression of claudin-4 decreases paracellular conductance through a selective decrease in sodium permeability
inferredcites →https://doi.org/10.1242/jcs.109.9.2287openalex-snapshot
Occludin is a functional component of the tight junction
inferredcites →https://doi.org/10.1242/jcs.113.19.3387openalex-snapshot
Inducible expression of claudin-1-myc but not occludin-VSV-G results in aberrant tight junction strand formation in MDCK cells
inferredcites →https://doi.org/10.1681/asn.v134875openalex-snapshot
Differential Expression Patterns of Claudins, Tight Junction Membrane Proteins, in Mouse Nephron Segments
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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inferred← citeshttps://doi.org/10.1002/j.2040-4603.2012.tb00420.xopenalex-snapshot
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Differentiating Between Tight Junction-Dependent and Tight Junction-Independent Intestinal Barrier Loss In Vivo
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Na+/K+-ATPase Drives Most Asymmetric Transports and Modulates the Phenotype of Epithelial Cells
inferred← citeshttps://doi.org/10.1007/978-1-61779-185-7_15openalex-snapshot
Identification of Claudins by Western Blot and Immunofluorescence in Different Cell Lines and Tissues
inferred← citeshttps://doi.org/10.1007/978-1-61779-185-7_9openalex-snapshot
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Postnatal Renal Maturation
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Na+/K+-ATPase Drives Most Asymmetric Transports and Modulates the Phenotype of Epithelial Cells
inferred← citeshttps://doi.org/10.1007/978-3-030-97204-2_6openalex-snapshot
Tight Junctions in the Inflamed Gut
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inferred← citeshttps://doi.org/10.1007/978-3-642-27843-3_76-1openalex-snapshot
Renal Tubular Development
inferred← citeshttps://doi.org/10.1007/978-3-642-27843-3_85-1openalex-snapshot
Postnatal Renal Maturation
inferred← citeshttps://doi.org/10.1007/978-3-662-43596-0_76openalex-snapshot
Renal Tubular Development
inferred← citeshttps://doi.org/10.1007/978-3-662-52972-0_34openalex-snapshot
Disorders of Calcium and Magnesium Metabolism
inferred← citeshttps://doi.org/10.1007/978-94-007-6028-8_2openalex-snapshot
The Distribution of Tight Junctions and Junctional Proteins in the Human Body
inferred← citeshttps://doi.org/10.1007/s00018-015-1987-yopenalex-snapshot
Molecular basis of claudin-17 anion selectivity
inferred← citeshttps://doi.org/10.1007/s00232-004-0673-zopenalex-snapshot
The Cytoplasmic Tails of Claudins Can Influence Tight Junction Barrier Properties through Effects on Protein Stability
inferred← citeshttps://doi.org/10.1007/s00232-005-0772-5openalex-snapshot
Aldosterone Reduces Crypt Colon Permeability during Low-Sodium Adaptation
inferred← citeshttps://doi.org/10.1007/s00232-005-0807-yopenalex-snapshot
Critical Role of Tight Junctions in Drug Delivery across Epithelial and Endothelial Cell Layers
inferred← citeshttps://doi.org/10.1007/s00232-005-0831-yopenalex-snapshot
Epithelial Fluid Transport: Protruding Macromolecules and Space Charges Can Bring about Electro-Osmotic Coupling at the Tight Junctions
inferred← citeshttps://doi.org/10.1007/s00232-010-9312-zopenalex-snapshot
Epithelial Barrier Resistance is Increased by the Divalent Cation Zinc in Cultured MDCKII Epithelial Monolayers
inferred← citeshttps://doi.org/10.1007/s00281-015-0516-2openalex-snapshot
Glial regulation of the blood-brain barrier in health and disease
inferred← citeshttps://doi.org/10.1007/s00345-019-03017-wopenalex-snapshot
Claudin-1 upregulation is associated with favorable tumor features and a reduced risk for biochemical recurrence in ERG-positive prostate cancer
inferred← citeshttps://doi.org/10.1007/s00418-007-0374-7openalex-snapshot
Bile duct ligation in the rat causes upregulation of ZO-2 and decreased colocalization of claudins with ZO-1 and occludin
inferred← citeshttps://doi.org/10.1007/s00418-008-0424-9openalex-snapshot
Tight junctions and the modulation of barrier function in disease
inferred← citeshttps://doi.org/10.1007/s00424-005-0023-8openalex-snapshot
Nucleotide regulation of paracellular Cl− permeability in natural rabbit airway epithelium
inferred← citeshttps://doi.org/10.1007/s00424-012-1097-8openalex-snapshot
Hypertonicity augments bullfrog taste nerve responses to inorganic salts
inferred← citeshttps://doi.org/10.1007/s00428-005-0120-2openalex-snapshot
Differential expression of claudin-2 in normal human tissues and gastrointestinal carcinomas
inferred← citeshttps://doi.org/10.1007/s00441-004-1010-7openalex-snapshot
Changes in the distribution of ZO-1, occludin, and claudins in the rat uterine epithelium during the estrous cycle
inferred← citeshttps://doi.org/10.1007/s00441-005-0135-7openalex-snapshot
Endothelia of term human placentae display diminished expression of tight junction proteins during preeclampsia
inferred← citeshttps://doi.org/10.1007/s00441-005-1101-0openalex-snapshot
Contribution of claudin-5 to barrier properties in tight junctions of epithelial cells
inferred← citeshttps://doi.org/10.1007/s00441-008-0621-9openalex-snapshot
Double gene deletion reveals lack of cooperation between claudin 11 and claudin 14 tight junction proteins
inferred← citeshttps://doi.org/10.1007/s00467-007-0569-0openalex-snapshot
Developmental changes in proximal tubule NaCl transport
inferred← citeshttps://doi.org/10.1007/s00467-011-1824-yopenalex-snapshot
Claudins in renal physiology and disease
inferred← citeshttps://doi.org/10.1007/s00726-025-03479-wopenalex-snapshot
Exploring claudin proteins: from sequence motifs to their impact on tight junction-mediated signaling pathways
inferred← citeshttps://doi.org/10.1007/s10157-011-0491-4openalex-snapshot
Claudins and renal salt transport
inferred← citeshttps://doi.org/10.1007/s11934-012-0289-2openalex-snapshot
The Role of Claudin in Hypercalciuric Nephrolithiasis
inferred← citeshttps://doi.org/10.1007/s12576-019-00688-3openalex-snapshot
Factors inhibiting intestinal calcium absorption: hormones and luminal factors that prevent excessive calcium uptake
inferred← citeshttps://doi.org/10.1016/b978-0-12-381462-3.00012-4openalex-snapshot
Intercellular Junctions
inferred← citeshttps://doi.org/10.1016/b978-0-12-381462-3.00020-3openalex-snapshot
Structural Organization of the Mammalian Kidney
inferred← citeshttps://doi.org/10.1016/b978-0-12-381462-3.00061-6openalex-snapshot
Mechanisms and Disorders of Magnesium Metabolism
inferred← citeshttps://doi.org/10.1016/b978-0-12-382026-6.00038-5openalex-snapshot
Tight Junctions and the Intestinal Barrier
inferred← citeshttps://doi.org/10.1016/b978-0-12-382026-6.00049-xopenalex-snapshot
Structure–function Relationships in the Pancreatic Acinar Cell
inferred← citeshttps://doi.org/10.1016/b978-0-12-382026-6.00065-8openalex-snapshot
Water Transport in the Gastrointestinal Tract
inferred← citeshttps://doi.org/10.1016/b978-0-12-397175-3.00046-6openalex-snapshot
Lactation and its Hormonal Control
inferred← citeshttps://doi.org/10.1016/b978-0-12-809954-4.00025-6openalex-snapshot
Tight Junctions and the Intestinal Barrier
inferred← citeshttps://doi.org/10.1016/b978-0-12-809954-4.00055-4openalex-snapshot
Water Transport in the Gastrointestinal Tract
inferred← citeshttps://doi.org/10.1016/b978-0-12-811114-7.00027-xopenalex-snapshot
Structural and biophysical properties of tight junctions
inferred← citeshttps://doi.org/10.1016/b978-0-12-814635-4.00004-8openalex-snapshot
Paracellular Cation Channel
inferred← citeshttps://doi.org/10.1016/b978-0-12-815389-5.00043-5openalex-snapshot
Intercellular junctions and cell–matrix interactions
inferred← citeshttps://doi.org/10.1016/b978-0-12-819509-3.00014-6openalex-snapshot
The blood brain barrier
inferred← citeshttps://doi.org/10.1016/b978-0-12-820466-5.00004-1openalex-snapshot
Physiology of the biological barriers
inferred← citeshttps://doi.org/10.1016/b978-0-323-04883-5.50036-2openalex-snapshot
Disorders of Magnesium Metabolism
inferred← citeshttps://doi.org/10.1016/b978-012088394-3/50055-6openalex-snapshot
Structure–Function Relations in the Pancreatic Acinar Cell
inferred← citeshttps://doi.org/10.1016/b978-012088394-3/50064-7openalex-snapshot
Tight Junctions and the Intestinal Barrier
inferred← citeshttps://doi.org/10.1016/b978-012088394-3/50075-1openalex-snapshot
Water Transport in the Gastrointestinal Tract
inferred← citeshttps://doi.org/10.1016/b978-012088488-9.50023-1openalex-snapshot
Structural Organization of the Mammalian Kidney
inferred← citeshttps://doi.org/10.1016/b978-012088488-9.50064-4openalex-snapshot
Mechanisms and Disorders of Magnesium Metabolism
inferred← citeshttps://doi.org/10.1016/b978-012515400-0/50062-2openalex-snapshot
Lactation and Its Hormonal Control
inferred← citeshttps://doi.org/10.1016/j.acthis.2008.07.003openalex-snapshot
Ovarian hormones control the changing expression of claudins and occludin in rat uterine epithelial cells during early pregnancy
inferred← citeshttps://doi.org/10.1016/j.addr.2004.08.004openalex-snapshot
Applications of imaging techniques to studies of epithelial tight junctions
inferred← citeshttps://doi.org/10.1016/j.addr.2011.07.004openalex-snapshot
Spiral progression in the development of absorption enhancers based on the biology of tight junctions
inferred← citeshttps://doi.org/10.1016/j.ajpath.2011.05.017openalex-snapshot
Claudin-4 Levels Are Associated with Intact Alveolar Fluid Clearance in Human Lungs
inferred← citeshttps://doi.org/10.1016/j.ajpath.2013.01.013openalex-snapshot
Bifidobacteria Stabilize Claudins at Tight Junctions and Prevent Intestinal Barrier Dysfunction in Mouse Necrotizing Enterocolitis
inferred← citeshttps://doi.org/10.1016/j.anl.2011.07.004openalex-snapshot
The mRNA of claudins is expressed in the endolymphatic sac epithelia
inferred← citeshttps://doi.org/10.1016/j.bbamem.2007.07.012openalex-snapshot
Adherens and tight junctions: Structure, function and connections to the actin cytoskeleton
inferred← citeshttps://doi.org/10.1016/j.bbamem.2007.09.001openalex-snapshot
Tight junction and polarity interaction in the transporting epithelial phenotype
inferred← citeshttps://doi.org/10.1016/j.bbamem.2007.10.018openalex-snapshot
Structure and function of claudins
inferred← citeshttps://doi.org/10.1016/j.bbamem.2008.07.004openalex-snapshot
Tight junction claudins and the kidney in sickness and in health
inferred← citeshttps://doi.org/10.1016/j.bbamem.2010.07.014openalex-snapshot
Claudin-3 acts as a sealing component of the tight junction for ions of either charge and uncharged solutes
inferred← citeshttps://doi.org/10.1016/j.bbamem.2020.183339openalex-snapshot
Ruffles and spikes: Control of tight junction morphology and permeability by claudins
inferred← citeshttps://doi.org/10.1016/j.bbamem.2020.183344openalex-snapshot
Channel functions of claudins in the organization of biological systems
inferred← citeshttps://doi.org/10.1016/j.bbcan.2011.04.001openalex-snapshot
Junctions gone bad: Claudins and loss of the barrier in cancer
inferred← citeshttps://doi.org/10.1016/j.bbrep.2015.11.004openalex-snapshot
Curcumin, bisdemethoxycurcumin and dimethoxycurcumin complexed with cyclodextrins have structure specific effect on the paracellular integrity of lung epithelia in vitro
inferred← citeshttps://doi.org/10.1016/j.biomaterials.2015.03.007openalex-snapshot
Mode of action of claudin peptidomimetics in the transient opening of cellular tight junction barriers
inferred← citeshttps://doi.org/10.1016/j.cbpa.2009.11.025openalex-snapshot
Claudin-15 and -25b expression in the intestinal tract of Atlantic salmon in response to seawater acclimation, smoltification and hormone treatment
inferred← citeshttps://doi.org/10.1016/j.cbpa.2015.04.017openalex-snapshot
Functional dynamics of claudin expression in Japanese medaka (Oryzias latipes): Response to environmental salinity
inferred← citeshttps://doi.org/10.1016/j.cbpa.2016.05.014openalex-snapshot
Regulation of gill claudin paralogs by salinity, cortisol and prolactin in Mozambique tilapia (Oreochromis mossambicus)
inferred← citeshttps://doi.org/10.1016/j.csbj.2022.10.038openalex-snapshot
Multiscale modelling of claudin-based assemblies: A magnifying glass for novel structures of biological interfaces
inferred← citeshttps://doi.org/10.1016/j.ejcb.2010.01.003openalex-snapshot
The protoplasmic or exoplasmic face association of tight junction particles cannot predict paracellular permeability or heterotypic claudin compatibility
inferred← citeshttps://doi.org/10.1016/j.ejps.2006.01.009openalex-snapshot
Primary porcine proximal tubular cells as a model for transepithelial drug transport in human kidney
inferred← citeshttps://doi.org/10.1016/j.gene.2013.03.123openalex-snapshot
Analysis of CLDN14 gene in deaf Moroccan patients with non-syndromic hearing loss
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2020.01.168openalex-snapshot
Cell junction proteins: Crossing the glomerular filtration barrier in diabetic nephropathy
inferred← citeshttps://doi.org/10.1016/j.ijpharm.2006.02.004openalex-snapshot
Ciprofloxacin permeability and its active secretion through rat small intestine in vitro
inferred← citeshttps://doi.org/10.1016/j.immuni.2009.09.012openalex-snapshot
The Gut Immune Barrier and the Blood-Brain Barrier: Are They So Different?
inferred← citeshttps://doi.org/10.1016/j.jaci.2009.05.038openalex-snapshot
Intestinal barrier function: Molecular regulation and disease pathogenesis
inferred← citeshttps://doi.org/10.1016/j.jcf.2007.01.001openalex-snapshot
Bioelectric effects of quinine on polarized airway epithelial cells
inferred← citeshttps://doi.org/10.1016/j.jconrel.2021.08.014openalex-snapshot
M01 as a novel drug enhancer for specifically targeting the blood-brain barrier.
inferred← citeshttps://doi.org/10.1016/j.jconrel.2025.114314openalex-snapshot
Claudin 5-binding small molecule transiently opens the blood-brain barrier and safely enhances brain drug delivery
inferred← citeshttps://doi.org/10.1016/j.jid.2019.06.145openalex-snapshot
Peptides Derived from the Tight Junction Protein CLDN1 Disrupt the Skin Barrier and Promote Responsiveness to an Epicutaneous Vaccine
inferred← citeshttps://doi.org/10.1016/j.jmb.2008.06.009openalex-snapshot
Kinetics of Adhesion Mediated by Extracellular Loops of Claudin-2 as Revealed by Single-Molecule Force Spectroscopy
inferred← citeshttps://doi.org/10.1016/j.jmb.2014.10.020openalex-snapshot
Model for the Architecture of Claudin-Based Paracellular Ion Channels through Tight Junctions
inferred← citeshttps://doi.org/10.1016/j.jpedsurg.2016.09.011openalex-snapshot
Intestinal barrier dysfunction in human necrotizing enterocolitis
inferred← citeshttps://doi.org/10.1016/j.lfs.2007.01.063openalex-snapshot
Chronic metabolic acidosis upregulated claudin mRNA expression in the duodenal enterocytes of female rats
inferred← citeshttps://doi.org/10.1016/j.lfs.2011.02.002openalex-snapshot
Claudin-2 knockdown decreases matrix metalloproteinase-9 activity and cell migration via suppression of nuclear Sp1 in A549 cells
inferred← citeshttps://doi.org/10.1016/j.margen.2013.05.001openalex-snapshot
Phylogenetic revision of the claudin gene family
inferred← citeshttps://doi.org/10.1016/j.mce.2016.10.034openalex-snapshot
Claudin-31 contributes to corticosteroid-induced alterations in the barrier properties of the gill epithelium
inferred← citeshttps://doi.org/10.1016/j.mod.2005.03.009openalex-snapshot
The zebrafish gene claudinj is essential for normal ear function and important for the formation of the otoliths
inferred← citeshttps://doi.org/10.1016/j.molimm.2007.09.003openalex-snapshot
n-3 polyunsaturated fatty acids prevent disruption of epithelial barrier function induced by proinflammatory cytokines
inferred← citeshttps://doi.org/10.1016/j.prp.2005.05.005openalex-snapshot
The expression of five different claudins in invasive breast carcinomas: Comparison of pT1pN1 and pT1pN0 tumors
inferred← citeshttps://doi.org/10.1016/j.reprotox.2018.08.013openalex-snapshot
Cellular junctions in the epididymis, a critical parameter for understanding male reproductive toxicology
inferred← citeshttps://doi.org/10.1016/j.semcdb.2015.04.008openalex-snapshot
Conceptual barriers to understanding physical barriers
inferred← citeshttps://doi.org/10.1016/j.semcdb.2015.04.009openalex-snapshot
Claudins: Gatekeepers of lung epithelial function
inferred← citeshttps://doi.org/10.1016/j.semcdb.2015.04.010openalex-snapshot
Assembly and function of claudins: Structure–function relationships based on homology models and crystal structures
inferred← citeshttps://doi.org/10.1016/j.talo.2024.100289openalex-snapshot
Gut-liver interaction study on an all-polydimethylsiloxane microfluidic device integrating intestinal paracellular permeability assay
inferred← citeshttps://doi.org/10.1016/j.xphs.2015.11.040openalex-snapshot
Why Does the Intestine Lack Basolateral Efflux Transporters for Cationic Compounds? A Provocative Hypothesis
inferred← citeshttps://doi.org/10.1016/j.yexcr.2007.01.026openalex-snapshot
ZO-2 silencing in epithelial cells perturbs the gate and fence function of tight junctions and leads to an atypical monolayer architecture
inferred← citeshttps://doi.org/10.1016/j.yexcr.2007.03.010openalex-snapshot
Oncostatin M induces upregulation of claudin-2 in rodent hepatocytes coinciding with changes in morphology and function of tight junctions
inferred← citeshttps://doi.org/10.1016/j.yexcr.2008.05.015openalex-snapshot
Probing effects of pH change on dynamic response of Claudin-2 mediated adhesion using single molecule force spectroscopy
inferred← citeshttps://doi.org/10.1016/j.yexcr.2017.03.036openalex-snapshot
Contributions of intestinal epithelial barriers to health and disease
inferred← citeshttps://doi.org/10.1016/s0002-9440(10)61243-6openalex-snapshot
Transforming Growth Factor-β Regulation of Epithelial Tight Junction Proteins Enhances Barrier Function and Blocks Enterohemorrhagic Escherichia coli O157:H7-Induced Increased Permeability
inferred← citeshttps://doi.org/10.1016/s0072-9752(08)01910-6openalex-snapshot
Chapter 10 Vascular endothelium and the blood–brain barrier
inferred← citeshttps://doi.org/10.1016/s1063-5823(10)65004-1openalex-snapshot
Structure–Function Studies of the Claudin Pore
inferred← citeshttps://doi.org/10.1016/s1063-5823(10)65005-3openalex-snapshot
The Investigation of cis- and trans-Interactions Between Claudins
inferred← citeshttps://doi.org/10.1016/s1063-5823(10)65007-7openalex-snapshot
Claudins and Renal Magnesium Handling
inferred← citeshttps://doi.org/10.1016/s1937-6448(10)79001-8openalex-snapshot
Functions of Claudin Tight Junction Proteins and Their Complex Interactions in Various Physiological Systems
inferred← citeshttps://doi.org/10.1017/cbo9780511541537.013openalex-snapshot
Interactions of enteric bacteria with the intestinal mucosa
inferred← citeshttps://doi.org/10.1021/acs.analchem.8b05237openalex-snapshot
Induced Proton Perturbation for Sensitive and Selective Detection of Tight Junction Breakdown
inferred← citeshttps://doi.org/10.1021/acs.jpcb.5b09977openalex-snapshot
Molecular Architecture of the Blood Brain Barrier Tight Junction Proteins–A Synergistic Computational and In Vitro Approach
inferred← citeshttps://doi.org/10.1021/acs.jpcb.8b06484openalex-snapshot
Molecular Dynamics Simulations of Ion Selectivity in a Claudin-15 Paracellular Channel
inferred← citeshttps://doi.org/10.1021/acs.langmuir.0c00877openalex-snapshot
Paracellular Gatekeeping: What Does It Take for an Ion to Pass Through a Tight Junction Pore?
inferred← citeshttps://doi.org/10.1021/acschemneuro.2c00139openalex-snapshot
Computational Assessment of Different Structural Models for Claudin-5 Complexes in Blood–Brain Barrier Tight Junctions
inferred← citeshttps://doi.org/10.1021/mp3000937openalex-snapshot
A Peptidomimetic Tight Junction Modulator To Improve Regional Analgesia
inferred← citeshttps://doi.org/10.1038/labinvest.2016.118openalex-snapshot
Gluten-induced symptoms in diarrhea-predominant irritable bowel syndrome are associated with increased myosin light chain kinase activity and claudin-15 expression
inferred← citeshttps://doi.org/10.1038/labinvest.3700050openalex-snapshot
A porous defense: the leaky epithelial barrier in intestinal disease
inferred← citeshttps://doi.org/10.1038/labinvest.3700316openalex-snapshot
Inflammatory processes have differential effects on claudins 2, 3 and 4 in colonic epithelial cells
inferred← citeshttps://doi.org/10.1038/ng.538openalex-snapshot
Mutations in VIPAR cause an arthrogryposis, renal dysfunction and cholestasis syndrome phenotype with defects in epithelial polarization
inferred← citeshttps://doi.org/10.1038/nri2653openalex-snapshot
Intestinal mucosal barrier function in health and disease
inferred← citeshttps://doi.org/10.1038/onc.2008.344openalex-snapshot
Tight junction-based epithelial microenvironment and cell proliferation
inferred← citeshttps://doi.org/10.1038/s41467-019-08760-7openalex-snapshot
Morphologic determinant of tight junctions revealed by claudin-3 structures
inferred← citeshttps://doi.org/10.1038/s41467-023-41999-9openalex-snapshot
Claudin-23 reshapes epithelial tight junction architecture to regulate barrier function
inferred← citeshttps://doi.org/10.1038/s41598-023-28045-wopenalex-snapshot
Multiple plasma membrane reporters discern LHFPL5 region that blocks trafficking to the plasma membrane
inferred← citeshttps://doi.org/10.1038/sj.emboj.7600605openalex-snapshot
E‐cadherin is essential for in vivo epidermal barrier function by regulating tight junctions
inferred← citeshttps://doi.org/10.1038/srep35857openalex-snapshot
Formaldehyde impairs transepithelial sodium transport
inferred← citeshttps://doi.org/10.1039/c3mb70271eopenalex-snapshot
Activation mechanism of claudin-4 by ephrin type-A receptor 2: a molecular dynamics approach
inferred← citeshttps://doi.org/10.1039/c9me00177hopenalex-snapshot
Predicting selectivity of paracellular pores for biomimetic applications
inferred← citeshttps://doi.org/10.1039/d3lc00855jopenalex-snapshot
Horizontal and vertical microchamber platforms for evaluation of the paracellular permeability of an epithelial cell monolayer
inferred← citeshttps://doi.org/10.1042/bj20140431openalex-snapshot
Molecular and structural transmembrane determinants critical for embedding claudin-5 into tight junctions reveal a distinct four-helix bundle arrangement
inferred← citeshttps://doi.org/10.1042/bj20150148openalex-snapshot
Probing thecis-arrangement of prototype tight junction proteins claudin-1 and claudin-3
inferred← citeshttps://doi.org/10.1073/pnas.0306924101openalex-snapshot
Disease-causing mutant WNK4 increases paracellular chloride permeability and phosphorylates claudins
inferred← citeshttps://doi.org/10.1073/pnas.0907724106openalex-snapshot
Claudin-16 and claudin-19 interaction is required for their assembly into tight junctions and for renal reabsorption of magnesium
inferred← citeshttps://doi.org/10.1073/pnas.1009399107openalex-snapshot
Claudin-4 forms paracellular chloride channel in the kidney and requires claudin-8 for tight junction localization
inferred← citeshttps://doi.org/10.1074/jbc.m110.146621openalex-snapshot
Calcium Inhibits Paracellular Sodium Conductance through Claudin-2 by Competitive Binding
inferred← citeshttps://doi.org/10.1074/jbc.m110.195578openalex-snapshot
Claudin-2 Forms Homodimers and Is a Component of a High Molecular Weight Protein Complex
inferred← citeshttps://doi.org/10.1074/jbc.m113.484238openalex-snapshot
Conserved Aromatic Residue Confers Cation Selectivity in Claudin-2 and Claudin-10b
inferred← citeshttps://doi.org/10.1074/jbc.m113.531012openalex-snapshot
Claudin-3 and Claudin-5 Protein Folding and Assembly into the Tight Junction Are Controlled by Non-conserved Residues in the Transmembrane 3 (TM3) and Extracellular Loop 2 (ECL2) Segments
inferred← citeshttps://doi.org/10.1074/jbc.m113.536888openalex-snapshot
Comprehensive Cysteine-scanning Mutagenesis Reveals Claudin-2 Pore-lining Residues with Different Intrapore Locations
inferred← citeshttps://doi.org/10.1074/jbc.m115.646695openalex-snapshot
Structural Basis of a Key Factor Regulating the Affinity between the Zonula Occludens First PDZ Domain and Claudins
inferred← citeshttps://doi.org/10.1074/jbc.m408122200openalex-snapshot
Extracellular Signal-regulated Kinases 1/2 Control Claudin-2 Expression in Madin-Darby Canine Kidney Strain I and II Cells
inferred← citeshttps://doi.org/10.1074/jbc.m703547200openalex-snapshot
Regulation of Heterotypic Claudin Compatibility
inferred← citeshttps://doi.org/10.1080/08958378.2021.1956021openalex-snapshot
Effects of ozone and particulate matter on airway epithelial barrier structure and function: a review of in vitro and in vivo studies
inferred← citeshttps://doi.org/10.1080/10408398.2018.1486284openalex-snapshot
Modulation of gastrointestinal barrier and nutrient transport function in farm animals by natural plant bioactive compounds – A comprehensive review
inferred← citeshttps://doi.org/10.1080/21688370.2017.1361899openalex-snapshot
Claudins in morphogenesis: Forming an epithelial tube
inferred← citeshttps://doi.org/10.1080/21688370.2021.1926190openalex-snapshot
The blood–brain and gut–vascular barriers: from the perspective of claudins
inferred← citeshttps://doi.org/10.1080/21688370.2022.2077620openalex-snapshot
Tight junctions: from molecules to gastrointestinal diseases
inferred← citeshttps://doi.org/10.1080/21688370.2025.2459963openalex-snapshot
Size-selective permeation-enhancing modulation of the tight junction by receptor-binding domains of Clostridium perfringens enterotoxin and Clostridium perfringens iota-toxin
inferred← citeshttps://doi.org/10.1083/jcb.200309134openalex-snapshot
Sinuous is a Drosophila claudin required for septate junction organization and epithelial tube size control
inferred← citeshttps://doi.org/10.1083/jcb.201010065openalex-snapshot
Occludin S408 phosphorylation regulates tight junction protein interactions and barrier function
inferred← citeshttps://doi.org/10.1085/jgp.200810154openalex-snapshot
Molecular Basis for Cation Selectivity in Claudin-2–based Paracellular Pores: Identification of an Electrostatic Interaction Site
inferred← citeshttps://doi.org/10.1085/jgp.201711868openalex-snapshot
Molecular determination of claudin-15 organization and channel selectivity
inferred← citeshttps://doi.org/10.1085/jgp.202513824openalex-snapshot
Molecular dynamics analyses of CLDN15 pore size and charge selectivity
inferred← citeshttps://doi.org/10.1089/ars.2013.5706openalex-snapshot
Redox-Sensitive Structure and Function of the First Extracellular Loop of the Cell–Cell Contact Protein Claudin-1: Lessons from Molecular Structure to Animals
inferred← citeshttps://doi.org/10.1091/mbc.e04-06-0465openalex-snapshot
Multiple Protein Interactions Involving Proposed Extracellular Loop Domains of the Tight Junction Protein Occludin
inferred← citeshttps://doi.org/10.1091/mbc.e04-12-1089openalex-snapshot
Actin Depolymerization Disrupts Tight Junctions via Caveolae-mediated Endocytosis
inferred← citeshttps://doi.org/10.1091/mbc.e07-04-0308openalex-snapshot
Transcriptional Modulation of Genes Encoding Structural Characteristics of Differentiating Enterocytes During Development of a Polarized Epithelium In Vitro
inferred← citeshttps://doi.org/10.1091/mbc.e09-08-0734openalex-snapshot
Tight Junction–associated MARVEL Proteins MarvelD3, Tricellulin, and Occludin Have Distinct but Overlapping Functions
inferred← citeshttps://doi.org/10.1091/mbc.e13-06-0298openalex-snapshot
JAM-A associates with ZO-2, afadin, and PDZ-GEF1 to activate Rap2c and regulate epithelial barrier function
inferred← citeshttps://doi.org/10.1091/mbc.e16-10-0698openalex-snapshot
Visualizing the dynamic coupling of claudin strands to the actin cytoskeleton through ZO-1
inferred← citeshttps://doi.org/10.1093/brain/awac461openalex-snapshot
Variants in CLDN5 cause a syndrome characterized by seizures, microcephaly and brain calcifications
inferred← citeshttps://doi.org/10.1093/carcin/bgl120openalex-snapshot
DNA-methylation-dependent alterations of claudin-4 expression in human bladder carcinoma
inferred← citeshttps://doi.org/10.1093/ckj/sfv081openalex-snapshot
Familial hypomagnesaemia with hypercalciuria and nephrocalcinosis: clinical and molecular characteristics
inferred← citeshttps://doi.org/10.1093/jn/nxaa025openalex-snapshot
An Amino Acid–Based Oral Rehydration Solution Regulates Radiation-Induced Intestinal Barrier Disruption in Mice
inferred← citeshttps://doi.org/10.1093/med/9780199592548.003.0040openalex-snapshot
Approach to the patient with hypomagnesaemia
inferred← citeshttps://doi.org/10.1093/ndt/gfq006openalex-snapshot
Differential expression of claudin tight junction proteins in the human cortical nephron
inferred← citeshttps://doi.org/10.1096/fj.07-8319comopenalex-snapshot
Formation of tight junction: determinants of homophilic interaction between classic claudins
inferred← citeshttps://doi.org/10.1096/fj.202100960ropenalex-snapshot
AKAP9 supports spermatogenesis through its effects on microtubule and actin cytoskeletons in the rat testis
inferred← citeshttps://doi.org/10.1097/00075197-200211000-00012openalex-snapshot
Intestinal barrier function
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