Claudin-1, claudin-2 and claudin-11 are present in tight junctions of choroid plexus epithelium of the mouse

A Single Gene Product, Claudin-1 or -2, Reconstitutes Tight Junction Strands and Recruits Occludin in Fibroblasts

Furuse, M., Sasaki, H., Fujimoto, K., & Tsukita, S. (1998) · The Journal of Cell Biology · doi:10.1083/jcb.143.2.391 · Cited by 962

Endothelial Claudin

Morita, K., Sasaki, H., Furuse, M., & Tsukita, S. (1999) · The Journal of Cell Biology · doi:10.1083/jcb.147.1.185 · Cited by 867

Conversion of Zonulae Occludentes from Tight to Leaky Strand Type by Introducing Claudin-2 into Madin-Darby Canine Kidney I Cells

Furuse, M., Furuse, K., Sasaki, H., & Tsukita, S. (2001) · The Journal of Cell Biology · doi:10.1083/jcb.153.2.263 · Cited by 712

CNS Myelin and Sertoli Cell Tight Junction Strands Are Absent in Osp/Claudin-11 Null Mice

Gow, A., Southwood, C. M., Li, J. S., Pariali, M., Riordan, G. P., Brodie, S. E., Danias, J., Bronstein, J. M., Kachar, B., & Lazzarini, R. A. (1999) · Cell · doi:10.1016/s0092-8674(00)81553-6 · Cited by 702

Clostridium perfringens Enterotoxin Fragment Removes Specific Claudins from Tight Junction Strands

Sonoda, N., Furuse, M., Sasaki, H., Yonemura, S., Katahira, J., Horiguchi, Y., & Tsukita, S. (1999) · The Journal of Cell Biology · doi:10.1083/jcb.147.1.195 · Cited by 612

Occludin and claudins in tight-junction strands: leading or supporting players?

Tsukita, S., & Furuse, M. (1999) · Trends in Cell Biology · doi:10.1016/s0962-8924(99)01578-0 · Cited by 592

Claudin-1 and claudin-5 expression and tight junction morphology are altered in blood vessels of human glioblastoma multiforme

Liebner, S., Fischmann, A., Rascher, G., Duffner, F., Grote, E.-H., Kalbacher, H., & Wolburg, H. (2000) · Acta Neuropathologica · doi:10.1007/s004010000180 · Cited by 490

Pores in the Wall

Tsukita, S., & Furuse, M. (2000) · The Journal of Cell Biology · doi:10.1083/jcb.149.1.13 · Cited by 458

Molecular Physiology and Pathophysiology of Tight Junctions I. Tight junction structure and function: lessons from mutant animals and proteins

Mitic, L. L., Itallie, C. M. V., & Anderson, J. M. (2000) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.2000.279.2.g250 · Cited by 452

Claudin-11/OSP-based Tight Junctions of Myelin Sheaths in Brain and Sertoli Cells in Testis

Morita, K., Sasaki, H., Fujimoto, K., Furuse, M., & Tsukita, S. (1999) · The Journal of Cell Biology · doi:10.1083/jcb.145.3.579 · Cited by 444

The temporospatial expression of peripheral myelin protein 22 at the developing blood‐nerve and blood‐brain barriers

Roux, K. J., Amici, S. A., & Notterpek, L. (2004) · Journal of Comparative Neurology · doi:10.1002/cne.20154 · Cited by 34

Directional Fluid Transport across Organ–Blood Barriers: Physiology and Cell BiologyPreprint

Caceres, P. S., Benedicto, I., Lehmann, G. L., & Rodriguez-Boulan, E. J. (2016) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a027847 · Cited by 35

Claudin-5a is essential for the functional formation of both zebrafish blood-brain barrier and blood-cerebrospinal fluid barrier

Li, Y., Wang, C., Zhang, L., Chen, B., Mo, Y., & Zhang, J. (2022) · Fluids and Barriers of the CNS · doi:10.1186/s12987-022-00337-9 · Cited by 32

Efflux Mechanisms in the Central Nervous System: A Powerful Influence on Drug Distribution within the Brain

Begley, D. J. (2004) · Elsevier eBooks · doi:10.1016/b978-012639011-7/50013-9 · Cited by 34

Corrigendum: Inflammatory and Microbiota-Related Regulation of the Intestinal Epithelial Barrier

Barbara, G., Barbaro, M. R., Fuschi, D., Palombo, M., Falangone, F., Cremon, C., Marasco, G., & Stanghellini, V. (2021) · Frontiers in Nutrition · doi:10.3389/fnut.2021.790387 · Cited by 41

Characterization of immortalized choroid plexus epithelial cell lines for studies of transport processes across the blood-cerebrospinal fluid barrier

Kläs, J., Wolburg, H., Terasaki, T., Fricker, G., & Reichel, V. (2010) · Cerebrospinal Fluid Research · doi:10.1186/1743-8454-7-11 · Cited by 33

Physiology of the Blood–Brain Barrier and Mechanisms of Transport Across the BBB

Lalatsa, A., & Butt, A. M. (2018) · Elsevier eBooks · doi:10.1016/b978-0-12-812218-1.00003-8 · Cited by 34

Immunolocalization of tight junction proteins in blood vessels in human germinal matrix and cortex

Anstrom, J. A., Thore, C. R., Moody, D. M., & Brown, W. R. (2006) · Histochemistry and Cell Biology · doi:10.1007/s00418-006-0232-z · Cited by 31

A new in vitro model for blood?cerebrospinal fluid barrier transport studies: an immortalized choroid plexus epithelial cell line derived from the tsA58 SV40 large T-antigen gene transgenic rat

Hosoya, K., Hori, S., Ohtsuki, S., & Terasaki, T. (2004) · Advanced Drug Delivery Reviews · doi:10.1016/j.addr.2004.07.013 · Cited by 30

Presence of claudins mRNA in the brain

Lamas, M., González‐Mariscal, L., & Gutiérrez, R. (2002) · Molecular Brain Research · doi:10.1016/s0169-328x(02)00328-5 · Cited by 30

Regulatory volume increase in epithelial cells isolated from the mouse fourth ventricle choroid plexus involves Na+–H+ exchange but not Na+–K+–2Cl− cotransport

Hughes, A. L. H., Пахомова, А. Н., & Brown, P. D. N. (2010) · Brain Research · doi:10.1016/j.brainres.2009.12.094 · Cited by 29

Tight Junctions in the Blood–Brain Barrier

Wolburg, H., Lippoldt, A., & Ebnet, K. (2002) · Springer eBooks · doi:10.1007/978-0-387-30380-2_1 · Cited by 30

Convection-enhanced delivery for treatment of brain tumors

Ferguson, S. D., Foster, K. A., & Yamini, B. (2007) · Expert Review of Anticancer Therapy · doi:10.1586/14737140.7.12s.s79 · Cited by 27

Targeting modulation of the choroid plexus blood-CSF barrier and CSF hypersecretion via lipid nanoparticle-mediated co-delivery of siRNA and resveratrol

Wang, Q., Xia, X., Zhang, H., Li, Y., Zhu, L., Shi, Y., Tang, Y., Cheng, J., Hui, X., & Gao, H. (2025) · Nature Communications · doi:10.1038/s41467-025-61543-1 · Cited by 29

Targeting the Choroid Plexuses for Protein Drug Delivery

Bryniarski, M. A., Ren, T., Rizvi, A. R., Snyder, A. M., & Morris, M. E. (2020) · Pharmaceutics · doi:10.3390/pharmaceutics12100963 · Cited by 28

The Blood–Brain Barrier: Much More Than a Selective Access to the Brain

Sánchez-Cano, F., Hernández‐Kelly, L. C., & Ortega, A. (2021) · Neurotoxicity Research · doi:10.1007/s12640-021-00431-0 · Cited by 30

Dual function of the choroid plexus: Cerebrospinal fluid production and control of brain ion homeostasis

MacAulay, N., & Toft‐Bertelsen, T. L. (2023) · Cell Calcium · doi:10.1016/j.ceca.2023.102797 · Cited by 25

Emerging Multifunctional Roles of Claudin Tight Junction Proteins in Bone

Alshbool, F. Z., & Mohan, S. (2014) · Endocrinology · doi:10.1210/en.2014-1173 · Cited by 26

Na+ dependent acid-base transporters in the choroid plexus; insights from slc4 and slc9 gene deletion studies

Christensen, H., Nguyen, A. T., Pedersen, F. D., & Damkier, H. H. (2013) · Frontiers in Physiology · doi:10.3389/fphys.2013.00304 · Cited by 26

Advancing brain barriers RNA sequencing: guidelines from experimental design to publication

Francisco, D. M. F., Marchetti, L., Rodríguez‐Lorenzo, S., Frías-Anaya, E., de Figueiredo, R. M., BtRAIN Network, Heymans, M., Culot, M., Santa-Maria, A. R., Deli, M. A., et al. (2020) · Fluids and Barriers of the CNS · doi:10.1186/s12987-020-00207-2 · Cited by 24

Targeting choroid plexus epithelium as a novel therapeutic strategy for hydrocephalus

Yang, Y., He, J. W., Wang, Y.-C., Wang, C., Tan, C., Liao, J., Tong, L., & Xiao, G. (2022) · Journal of Neuroinflammation · doi:10.1186/s12974-022-02500-3 · Cited by 26

Emergence of the brain-border immune niches and their contribution to the development of neurodegenerative diseases

Tan, L. Y., Cunliffe, G., Hogan, M. P., Yeo, X. Y., Oh, C., Jin, B., Kang, J., Park, J., Kwon, M., Kim, M., et al. (2024) · Frontiers in Immunology · doi:10.3389/fimmu.2024.1380063 · Cited by 23

Basal Sodium-Dependent Vitamin C Transporter 2 polarization in choroid plexus explant cells in normal or scorbutic conditions

Ulloa, V., Saldivia, N., Ferrada, L., Salazar, K., Martínez, F., Silva-Álvarez, C., Magdalena, R., Oviedo, M. J., Montecinos, H., Torres‐Vergara, P., et al. (2019) · Scientific Reports · doi:10.1038/s41598-019-50772-2 · Cited by 23

The Lyme disease bacterium, Borrelia burgdorferi, stimulates an inflammatory response in human choroid plexus epithelial cells

Thompson, D., Sorenson, J., Greenmyer, J. R., Brissette, C. A., & Watt, J. A. (2020) · PLoS ONE · doi:10.1371/journal.pone.0234993 · Cited by 24

Multiscale modelling of claudin-based assemblies: A magnifying glass for novel structures of biological interfaces

Berselli, A., Benfenati, F., Maragliano, L., & Alberini, G. (2022) · Computational and Structural Biotechnology Journal · doi:10.1016/j.csbj.2022.10.038 · Cited by 21

Aging alters the expression of trophic factors and tight junction proteins in the mouse choroid plexus

Sadanandan, J., Sathyanesan, M., & Newton, S. S. (2024) · Fluids and Barriers of the CNS · doi:10.1186/s12987-024-00574-0 · Cited by 21

Reduction of chromatin assembly factor 1 p60 and C21orf2 protein, encoded on chromosome 21, in Down Syndrome brain

Shim, K.-S., Bergelson, J. M., Furuse, M., Ovod, V., Krude, T., & Lübec, G. (2003) · Journal of neural transmission. Supplementum · doi:10.1007/978-3-7091-6721-2_10 · Cited by 20

Persistence of tight junctions and changes in apical structures and protein expression in choroid plexus epithelium of rats after short-term head-down tilt

Masseguin, C., Mani-Ponset, L., Herbuté, S., Tixier‐Vidal, A., & Gabrion, J. (2002) · Journal of Neurocytology · doi:10.1023/a:1015008308515 · Cited by 20

Claudin-11 in health and disease: implications for myelin disorders, hearing, and fertility

Gjervan, S. C., Ozgoren, O. K., Gow, A., Stöckler‐Ipsiroglu, S., & Pouladi, M. A. (2024) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2023.1344090 · Cited by 20

Micelle-Based Drug Delivery for Brain Tumors

Gothwal, A., Khan, I., Kesharwani, P., Chourasia, M. K., & Gupta, U. D. (2018) · Elsevier eBooks · doi:10.1016/b978-0-12-812218-1.00011-7 · Cited by 18

OSP/claudin‐11‐induced EAE in mice is mediated by pathogenic T cells primarily governed by OSP192Y residue of major encephalitogenic region OSP179–207

Kaushansky, N., Hemo, R., Eisenstein, M., & Ben‐Nun, A. (2007) · European Journal of Immunology · doi:10.1002/eji.200636965 · Cited by 18

The development and function of the brain barriers – an overlooked consideration for chemical toxicity

Bell, K. S., & O’Shaughnessy, K. L. (2022) · Frontiers in Toxicology · doi:10.3389/ftox.2022.1000212 · Cited by 18

Transporters, Ion Channels, and Junctional Proteins in Choroid Plexus Epithelial Cells

Ueno, M., Chiba, Y., Murakami, R., Miyai, Y., Matsumoto, K., Wakamatsu, K., Nakagawa, T., Takebayashi, G., Uemura, N., Yanase, K., et al. (2024) · Biomedicines · doi:10.3390/biomedicines12040708 · Cited by 16

Nanotechnology Based Targeted Drug Delivery: Current Status and Future Prospects for Drug Development

Sharma, S., & Singh, A. (2011) · InTech eBooks · doi:10.5772/28902 · Cited by 16

Spatial expression of claudin family members in various organs of mice

Hwang, I., Yang, H. J., KANG, H.-S., Ahn, C., Lee, G., Hong, E., An, B., & Jeung, E. (2014) · Molecular Medicine Reports · doi:10.3892/mmr.2014.2031 · Cited by 16

Review of functional in vitro models of the blood-cerebrospinal fluid barrier in leukaemia research

Erb, U., Schwerk, C., Schroten, H., & Karremann, M. (2019) · Journal of Neuroscience Methods · doi:10.1016/j.jneumeth.2019.108478 · Cited by 15

Proteins of the Tight Junction in the Blood-Brain Barrier

Bauer, H., Traweger, A., & BAUER, H. (2004) · Elsevier eBooks · doi:10.1016/b978-012639011-7/50005-x · Cited by 15

Cell-Penetrating Peptides-Mediated Therapeutic Agents Delivery into the Central Nervous System

Wei, Y., Bao, H., Wang, L., Cao, Y., Liu, Z., Zhu, X., Chen, T., Wu, A., & Li, J. (2024) · ACS Materials Letters · doi:10.1021/acsmaterialslett.4c00397 · Cited by 13

Mouse Models of Human Claudin-Associated Disorders: Benefits and Limitations

Seker, M., Fernández‐Rodríguez, C., Martínez‐Cruz, L. A., & Müller, D. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms20215504 · Cited by 13

Les plexus choroïdes : une interface dynamique entre sang et liquide cephalo-rachidien

Strazielle, N., Mutin, M., & Ghersi‐Egea, J. (2005) · Morphologie · doi:10.1016/s1286-0115(05)83244-8 · Cited by 12

Nanostructures Overcoming the Blood-Brain Barrier: Physiological Considerations and Mechanistic Issues

Lalatsa, A., Schätzlein, A. G., & Uchegbu, I. F. (2012) · Royal Society of Chemistry eBooks · doi:10.1039/9781849735292-00329 · Cited by 12

The role of claudin-2 in kidney function and dysfunction

Nyimanu, D., Behm, C. V., Choudhury, S., & Yu, A. S. L. (2023) · Biochemical Society Transactions · doi:10.1042/bst20220639 · Cited by 11

Shifting from ependyma to choroid plexus epithelium and the changing expressions of aquaporin‐1 and aquaporin‐4

Mack, A. F., Bihlmaier, R., & Deffner, F. (2023) · The Journal of Physiology · doi:10.1113/jp284196 · Cited by 11

Structure of the Mammalian Choroid Plexus

Damkier, H. H., & Prætorius, J. (2020) · Physiology in health and disease · doi:10.1007/978-1-0716-0536-3_1 · Cited by 10

Expression of tight junction proteins and transporters for xenobiotic metabolism at the blood–CSF barrier during development in the nonhuman primate (P. hamadryas)

Ek, C. J., D’Angelo, B., Lehner, C., Nathanielsz, P. W., Li, C., & Mallard, C. E. (2015) · Reproductive Toxicology · doi:10.1016/j.reprotox.2015.06.047 · Cited by 11

Drug resistance in glioblastoma: from chemo- to immunotherapy

Sharma, S., Chepurna, O. M., & Sun, T. (2023) · Cancer Drug Resistance · doi:10.20517/cdr.2023.82 · Cited by 11

Nano-biohybrids with cell-penetrating peptides: A molecular trojans for glioblastoma precision medicine

Phatale, V., Khairnar, P., Shukla, S., Puri, N., Sahane, P., & Srivastava, S. (2025) · International Journal of Pharmaceutics · doi:10.1016/j.ijpharm.2025.126077 · Cited by 11

Lactoferrin deficiency during lactation increases the risk of depressive-like behavior in adult mice

Wang, W., Cheng, Z., Wang, X., An, Q., Huang, K., Dai, Y., Meng, Q., & Zhang, Y. (2023) · BMC Biology · doi:10.1186/s12915-023-01748-2 · Cited by 10

The Neuropathogenesis of Acanthamoeba encephalitis: Barriers to Overcome

Khan, N. A. (2011) · Journal of Cell Science & Therapy · doi:10.4172/2157-7013.s3-001 · Cited by 10

A Comparative Transcriptome Analysis of Human and Porcine Choroid Plexus Cells in Response to Streptococcus suis Serotype 2 Infection Points to a Role of Hypoxia

Lauer, A. N., Scholtysik, R., Beineke, A., Baums, C. G., Klose, K., Valentin‐Weigand, P., Ishikawa, H., Schroten, H., Klein‐Hitpaß, L., & Schwerk, C. (2021) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2021.639620 · Cited by 10

Region Specific Differences of Claudin-5 Expression in Pediatric Intracranial Ependymomas: Potential Prognostic Role in Supratentorial Cases

Virág, J., Haberler, C., Baksa, G., Piurkó, V., Hegedűs, Z., Reiniger, L., Bálint, K., Chocholous, M., Kiss, A., Lotz, G., et al. (2016) · Pathology & Oncology Research · doi:10.1007/s12253-016-0084-3 · Cited by 9

Pathophysiology of the choroid plexus in brain diseases

Mihaljević, S., Michalicová, A., Bhide, M., & Kováč, A. (2021) · General Physiology and Biophysics · doi:10.4149/gpb_2021032 · Cited by 9

Tight Junctions and the Blood-Brain Barrier

Wolburg, H., Lippoldt, A., & Ebnet, K. (2007) · Springer eBooks · doi:10.1007/0-387-36673-3_13 · Cited by 9

Bacillus coagulans and Clostridium butyricum synergistically alleviate depression in a chronic unpredictable mild stress mouse model through altering gut microbiota and prefrontal cortex gene expression

Xu, J., Zhou, L., Chen, Z., Wang, Y., Xu, F., Kuang, Q. F., Zhang, Y., & Zheng, H. (2024) · Frontiers in Pharmacology · doi:10.3389/fphar.2024.1393874 · Cited by 8

Claudins 1, 11 and twist in meningiomas

Soini, Y., Rauramaa, T. H., Alafuzoff, I. I., Sandell, P., & Kärjä, V. J. (2010) · Histopathology · doi:10.1111/j.1365-2559.2010.03538.x · Cited by 8

RPE Polarity and Barrier Function

Rizzolo, L. J. (2020) · Springer eBooks · doi:10.1007/978-3-030-28384-1_2 · Cited by 7

Single-cell analysis of mesenchymal cells in permeable neural vasculature reveals novel diverse subpopulations of fibroblasts

Bastedo, W. E., Scott, R. W., Arostegui, M., & Underhill, T. M. (2024) · Fluids and Barriers of the CNS · doi:10.1186/s12987-024-00535-7 · Cited by 6

The Blood–Brain Barrier in the Human Glioma

Rascher-Eggstein, G., Liebner, S., & Wolburg, H. (2004) · Elsevier eBooks · doi:10.1016/b978-012639011-7/50031-0 · Cited by 7

Treatment with Glycyrrhiza glabra Extract Induces Anxiolytic Effects Associated with Reduced Salt Preference and Changes in Barrier Protein Gene Expression

Murck, H., Karailiev, P., Karailievova, L., Puhova, A., & Ježová, D. (2024) · Nutrients · doi:10.3390/nu16040515 · Cited by 6

Effect of a two-week treatment with a low dose of 2,2′4,4′,5,5′-hexachlorobiphenyl (PCB153) on tight junction protein expression in ovine choroid plexus during long and short photoperiods

Szczepkowska, A., Lagaraine, C., Robert, V., Dufourny, L., Thiéry, J., & Skipor, J. (2013) · Neurotoxicology and Teratology · doi:10.1016/j.ntt.2013.03.061 · Cited by 6

Regulation of cell-cell adhesion and actin cytoskeleton in non-transformed and transformed epithelial cells

Palovuori, R. (2003) · Cited by 6

Blood Retinal Barrier

Phillips, B. E., Antonetti, D. A., & Berkowitz, B. A. (2007) · Springer eBooks · doi:10.1007/978-3-540-29542-6_8 · Cited by 6

Chinese bayberry extract regulates the permeability of blood–cerebrospinal fluid barrier and ameliorates experimental colitis-related brain comorbidities in mice

Huang, Z., Yan, J., Liu, Y., Fan, F., Liu, T., Yin, Y., Li, J., Li, X., & Zheng, Y. (2024) · Food Quality and Safety · doi:10.1093/fqsafe/fyae028 · Cited by 5

Mechanisms of cerebrospinal fluid secretion by the choroid plexus epithelium: Application to various intracranial pathologies

Johnsen, L. Ø., Friis, K. A., Møller‐Madsen, M. K., & Damkier, H. H. (2024) · Clinical Anatomy · doi:10.1002/ca.24199 · Cited by 5

Blood–neural barrier: Overview and latest progress

Sano, Y., & Kanda, T. (2013) · Clinical and Experimental Neuroimmunology · doi:10.1111/cen3.12021 · Cited by 6

Balancing act: The dual role of claudin‐2 in disease

Wu, S., Gao, J., Han, Y., Zhang, W., Li, X., Kong, D., Wang, H., & Zuo, L. (2025) · Annals of the New York Academy of Sciences · doi:10.1111/nyas.15311 · Cited by 4

MMSpa is a deep learning-based tool that enhances the identification of spatial domains in spatial transcriptomics studies

Liu, Y., Zhai, Y., Zhang, P., Zou, Q., & Luo, X. (2026) · PLoS Biology · doi:10.1371/journal.pbio.3003580 · Cited by 4

E-Cadherin Is Expressed in Epithelial Cells of the Choroid Plexus in Human and Mouse Brains

Takebayashi, G., Chiba, Y., Wakamatsu, K., Murakami, R., Miyai, Y., Matsumoto, K., Uemura, N., Yanase, K., Shirakami, G., Ogino, Y., et al. (2023) · Current Issues in Molecular Biology · doi:10.3390/cimb45100492 · Cited by 4

In Vitro Investigation of the Blood–Cerebrospinal Fluid Barrier Properties

Strazielle, N., & Ghersi‐Egea, J. (2005) · CRC Press eBooks · doi:10.1201/9781420023404.ch23 · Cited by 3

Nanomedicines for Delivery Across the Blood–Brain Barrier

Lalatsa, A., Das, D., & Osouli-Bostanabad, K. (2024) · Springer eBooks · doi:10.1007/978-3-031-59478-6_11 · Cited by 2

Effects of valproate on the entry of inert hydrophilic markers and expression of tight junction associated genes in the neonatal brain and choroid plexus of a rat model of epilepsy (GAERS)

Qiu, F., Dzięgielewska, K. M., Habgood, M. D., Huang, Y., & Saunders, N. R. (2025) · Fluids and Barriers of the CNS · doi:10.1186/s12987-025-00667-4 · Cited by 2

The Claudin 11 Gene

Gow, A. (2004) · Elsevier eBooks · doi:10.1016/b978-012439510-7/50075-9 · Cited by 2

The Blood-Brain Barrier in EAE

Engelhardt, B., & Wolburg, H. (2008) · Springer eBooks · doi:10.1007/0-387-25518-4_20 · Cited by 2

Structure of the Blood Brain Barrier and the Role of Transporters in the movement of substrates across the barriersPreprint

Singh, A., & Vellapandian, C. (2022) · Qeios · doi:10.32388/5giw6a · Cited by 2

A quantitative measure of choroid plexus contrast enhancement strongly relates to markers of diffuse brain tissue injury in multiple sclerosisPreprint

Senthil, S., Tagge, I., Fetco, D., Hsieh, C. H., Assemlal, H.-E., Karimaghaloo, Z., Fetco, E., Moore, G. R. W., Arnold, D. L., Rudko, D. A., et al. (2025) · medRxiv · doi:10.1101/2025.03.26.25324694 · Cited by 2

Growth Factors and the Choroid Plexus: Their Role in Posthemorrhagic Hydrocephalus

Ye, H., Miao, W., Keep, R. F., & Xiang, J. (2025) · Biomedicines · doi:10.3390/biomedicines13061366 · Cited by 1

Interactions between the immune and nervous systems

Kilpatrick, T. J., Ransohoff, R. M., & Wesselingh, S. L. (2009) · Cambridge University Press eBooks · doi:10.1017/cbo9781139195805.002 · Cited by 1

An Overview of Human Choroid Plexus Structure and Transport Functions

Prætorius, J., & Damkier, H. H. (2025) · Current human cell research and applications · doi:10.1007/978-981-97-9495-9_2 · Cited by 1

Blood–Brain Barrier and Blood–Nerve Barrier

Sano, Y., & Kanda, T. (2016) · Springer eBooks · doi:10.1007/978-4-431-55594-0_4 · Cited by 1

Challenges of Brain Drug Delivery and G-Technology as One of Solution

Garg, S., Dwivedi, A., Saini, P., Pareek, A. K., & Trivedi, S. (2013) · Research and reviews : journal of pharmacy and pharmaceutical sciences · Cited by 1

Ion Transport in the Choroid Plexus Epithelium

Johnsen, L. Ø., Damkier, H. H., & Prætorius, J. (2020) · Physiology in health and disease · doi:10.1007/978-3-030-55310-4_10 · Cited by 1

Immunociblage du cerveau par des nanocapsules lipidiques

Béduneau, A. (2007) · OpenGrey (Institut de l'Information Scientifique et Technique) · Cited by 1

Role of SPAK-NKCC1 Signaling Cascade in the Choroid Plexus Blood-CSF Barrier Damage After StrokePreprint

Wang, J., Liu, R., Hasan, M. N., Fischer, S. G., Como, M., Fiesler, V. M., Begum, G., Chen, Y., Bhuiyan, M. I. H., Dong, S., et al. (2021) · Research Square · doi:10.21203/rs.3.rs-1189368/v1 · Cited by 1

Mechanisms for Extracellular Matrix-Dependent Blood-Brain Barrier Dysfunction

Hoettles, B. A. (2021) · doi:10.18122/td/1903/boisestate · Cited by 1

Functional and Genetic Analysis of Choroid Plexus Development in Zebrafish

Henson, H. E. (2014) · doi:10.21007/etd.cghs.2014.0134 · Cited by 1

Effect of bilirubin on expression and localization of PGP and Mrp1 in the central nervous system

Gazzin, S. (2008) · OpenstarTs (Univeristy of Trieste https://www.units.it/)

Inflammation in the immature brain: The role of Toll like receptors

Stridh, L. (2011) · Gothenburg University Publications Electronic Archive (Gothenburg University)

Developmental Changes in Choroid Plexus Epithelium: A Review

Mahajan, T., & Ganguly, S. (2015) · International Journal of Contemporary Pathology · doi:10.5958/2395-1184.2015.00036.4

The Neuropathogenesis of Acanthamoeba encephalitis: Barriers to

Khan, O., & Siddiqui, R. (2011)

Junctional Proteins of the Blood–CSF Barrier

Galla, H., & Angelow, S. (2005) · CRC Press eBooks · doi:10.1201/9781420023404.ch3

Negotiating the brain barriers:

Engelhardt, B. (2009) · Cambridge University Press eBooks · doi:10.1017/cbo9781139195805.005

Lactoferrin Feeding Deficiency during Lactation Increases the Risk of Depression in Adult Mice by Affecting Microbiota-Gut-Brain Axis DevelopmentPreprint

Wang, W., Cheng, Z., Wang, X., An, Q., Huang, K., Dai, Y., Meng, Q., & Zhang, Y. (2022) · Research Square · doi:10.21203/rs.3.rs-1883790/v1

Probable Hydrocephalus Decompensation after Immunization with Pentavalent Vaccine: Case Report and Literature Review

Caixeta, T. H., Silva, G. J., Fürstenau, C. R., & do Amaral, L. R. (2022) · Arquivos Brasileiros de Neurocirurgia Brazilian Neurosurgery · doi:10.1055/s-0042-1742429

Cerebrospinal fluid physiology

Shapey, J., & Toma, A. K. (2022) · Elsevier eBooks · doi:10.1016/b978-0-12-819509-3.00011-0

Transport of ions across the choroid plexus epithelium

Johnsen, L. Ø., Friis, K. A., & Damkier, H. H. (2022) · Elsevier eBooks · doi:10.1016/b978-0-12-819509-3.00010-9

Lactoferrin feeding deficiency during lactation increases the risk of depression in adult mice by affecting microbiota-gut-brain axis developmentPreprint

Wang, W., Cheng, Z., Wang, X., Qin, A., Huang, K., Dai, Y., Meng, Q., & Zhang, Y. (2022) · Research Square · doi:10.21203/rs.3.rs-1883790/v2

RPE-Polarität und Barrierefunktion

Rizzolo, L. J. (2024) · Springer eBooks · doi:10.1007/978-3-031-35055-9_2

Changes in the Blood Choroid Plexus Barrier in Response to Transient Receptor Potential, Vanilloid 4 Channel Activation

Blazer‐Yost, B. L., & Halm, D. R. (2025) · Current human cell research and applications · doi:10.1007/978-981-97-9495-9_5

Etude des interfaces sang/cerveau dans la région tubérale de l'hypothalamus médiobasal (rôle des tanycytes de l'éminence médiane)

Mullier, A., & Bouret, S. G. (2009) · OpenGrey (Institut de l'Information Scientifique et Technique)

Additional file 1 of Lactoferrin deficiency during lactation increases the risk of depressive-like behavior in adult mice

Wang, W., Cheng, Z., Wang, X., An, Q., Huang, K., Dai, Y., Meng, Q., & Zhang, Y. (2023) · Figshare · doi:10.6084/m9.figshare.24472477

Claudin-1, -2 and -3 Are Selectively Expressed in the Epithelia of the Choroid Plexus of the Mouse from Early Development and into Adulthood While Claudin-5 is Restricted to Endothelial Cells

Steinemann, A., Galm, I., Chip, S., Nitsch, C., & Maly, I. P. (2016) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2016.00016 · Cited by 62

Organization of choroid plexus epithelial and endothelial cell tight junctions and regulation of claudin-1, -2 and -5 expression by protein kinase C

Lippoldt, A., Liebner, S., Andbjer, B., Kalbacher, H., Wolburg, H., Haller, H. G., & Fuxé, K. (2000) · Neuroreport · doi:10.1097/00001756-200005150-00015 · Cited by 123

MOLECULAR NEUROSCIENCE NEUROREPORT Organization of choroid plexus epithelial

Liebner, C. S., Andbjer, B., Kalbacher, H., Wolburg, H., Haller, H. G., & Fuxe, K. (2000)

Investigations into the Function of Claudin-11 Tight Junctions in CNS Myelin

Denninger, A. R. (2016)

MOESM5 of Claudin-12 is not required for blood–brain barrier tight junction function

Dias, M. C., Coisne, C., Baden, P., Enzmann, G. U., Garrett, L., Becker, L., Hölter, S., Angelis, M. H. D., Deutsch, U., & Engelhardt, B. (2019) · Figshare · doi:10.6084/m9.figshare.9808868