Tight junctions/adherens junctions: basic structure and function

JUNCTIONAL COMPLEXES IN VARIOUS EPITHELIA

Farquhar, M. G., & Palade, G. E. (1963) · The Journal of Cell Biology · doi:10.1083/jcb.17.2.375 · Cited by 3,637 · see citing works

Convergence of Wnt, ß-Catenin, and Cadherin Pathways

Nelson, W. J., & Nusse, R. (2004) · Science · doi:10.1126/science.1094291 · Cited by 2,515 · see citing works

Size-selective loosening of the blood-brain barrier in claudin-5–deficient mice

Nitta, T., Hata, M., Gotoh, S., Seo, Y., Sasaki, H., Hashimoto, N., Furuse, M., & Tsukita, S. (2003) · The Journal of Cell Biology · doi:10.1083/jcb.200302070 · Cited by 1,917 · see citing works

Regulation of cadherin-mediated adhesion in morphogenesis

Gumbiner, B. M. (2005) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm1699 · Cited by 1,523 · see citing works

Claudin-based tight junctions are crucial for the mammalian epidermal barrier

Furuse, M., Hata, M., Furuse, K., Yoshida, Y., Haratake, A., Sugitani, Y., Noda, T., Kubo, A., & Tsukita, S. (2002) · The Journal of Cell Biology · doi:10.1083/jcb.200110122 · Cited by 1,512 · see citing works

The tight junction: a multifunctional complex

Schneeberger, E. E., & Lynch, R. D. (2004) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00558.2003 · Cited by 1,401 · see citing works

Complex Phenotype of Mice Lacking Occludin, a Component of Tight Junction Strands

Saitou, M., Furuse, M., Sasaki, H., Schulzke, J.-D., Fromm, M., Takano, H., Noda, T., & Tsukita, S. (2000) · Molecular Biology of the Cell · doi:10.1091/mbc.11.12.4131 · Cited by 1,195 · see citing works

Cadherins in development: cell adhesion, sorting, and tissue morphogenesisPreprint

Halbleib, J. M., & Nelson, W. J. (2006) · Genes & Development · doi:10.1101/gad.1486806 · Cited by 1,063 · see citing works

Myosin-dependent junction remodelling controls planar cell intercalation and axis elongation

Bertet, C., Sulak, L., & Lecuit, T. (2004) · Nature · doi:10.1038/nature02590 · Cited by 1,025 · see citing works

Deconstructing the Cadherin-Catenin-Actin Complex

Yamada, S., Pokutta, S., Drees, F., Weis, W. I., & Nelson, W. J. (2005) · Cell · doi:10.1016/j.cell.2005.09.020 · Cited by 1,022 · see citing works

Asymmetric cell divisions promote stratification and differentiation of mammalian skin

Lechler, T., & Fuchs, E. (2005) · Nature · doi:10.1038/nature03922 · Cited by 998 · see citing works

α-Catenin Is a Molecular Switch that Binds E-Cadherin-β-Catenin and Regulates Actin-Filament Assembly

Drees, F., Pokutta, S., Yamada, S., Nelson, W. J., & Weis, W. I. (2005) · Cell · doi:10.1016/j.cell.2005.09.021 · Cited by 986 · see citing works

Signalling to and from tight junctions

Matter, K., & Balda, M. S. (2003) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm1055 · Cited by 887 · see citing works

ZO-1 and ZO-2 Independently Determine Where Claudins Are Polymerized in Tight-Junction Strand Formation

Umeda, K., Ikenouchi, J., Katahira-Tayama, S., Furuse, K., Sasaki, H., Nakayama, M., Matsui, T., Tsukita, S., Furuse, M., & Tsukita, S. (2006) · Cell · doi:10.1016/j.cell.2006.06.043 · Cited by 825 · see citing works

Tricellulin constitutes a novel barrier at tricellular contacts of epithelial cells

Ikenouchi, J., Furuse, M., Furuse, K., Sasaki, H., Tsukita, S., & Tsukita, S. (2005) · The Journal of Cell Biology · doi:10.1083/jcb.200510043 · Cited by 787 · see citing works

Tight Junctions and Cell Polarity

Shin, K., Fogg, V. C., & Margolis, B. L. (2006) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev.cellbio.22.010305.104219 · Cited by 745 · see citing works

High-Throughput Mapping of a Dynamic Signaling Network in Mammalian Cells

Barrios‐Rodiles, M., Brown, K. R., Ozdamar, B., Bose, R., Liu, Z., Donovan, R. S., Shinjo, F., Liu, Y., Dembowy, J., Taylor, I. W., et al. (2005) · Science · doi:10.1126/science.1105776 · Cited by 726 · see citing works

Adaptation of core mechanisms to generate cell polarity

Nelson, W. J. (2003) · Nature · doi:10.1038/nature01602 · Cited by 716 · see citing works

Involvement of ZO-1 in Cadherin-based Cell Adhesion through Its Direct Binding to α Catenin and Actin Filaments

Itoh, M., Nagafuchi, A., Moroi, S., & Tsukita, S. (1997) · The Journal of Cell Biology · doi:10.1083/jcb.138.1.181 · Cited by 677 · see citing works

Balancing cell adhesion and Wnt signaling, the key role of β-catenin

Brembeck, F. H., Rosário, M., & Birchmeier, W. (2005) · Current Opinion in Genetics & Development · doi:10.1016/j.gde.2005.12.007 · Cited by 668 · see citing works

Regulated expression of claudin-4 decreases paracellular conductance through a selective decrease in sodium permeability

Itallie, C. M. V., Rahner, C., & Anderson, J. M. (2001) · Journal of Clinical Investigation · doi:10.1172/jci12464 · Cited by 593 · see citing works

Claudins create charge-selective channels in the paracellular pathway between epithelial cells

Colegio, O. R., Itallie, C. M. V., McCrea, H. J., Rahner, C., & Anderson, J. M. (2002) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00038.2002 · Cited by 545 · see citing works

Claudins in occluding junctions of humans and flies

Furuse, M., & Tsukita, S. (2006) · Trends in Cell Biology · doi:10.1016/j.tcb.2006.02.006 · Cited by 525 · see citing works

Junctional adhesion molecules (JAMs): more molecules with dual functions?

Ebnet, K., Suzuki, A., Ohno, S., & Vestweber, D. (2003) · Journal of Cell Science · doi:10.1242/jcs.00930 · Cited by 501 · see citing works

E‐cadherin is essential for in vivo epidermal barrier function by regulating tight junctions

Tunggal, J. A., Helfrich, I., Schmitz, A., Schwarz, H., Günzel, D., Fromm, M., Kemler, R., Krieg, T., & Niessen, C. M. (2005) · The EMBO Journal · doi:10.1038/sj.emboj.7600605 · Cited by 491 · cited 2× · see citing works

Hyperproliferation and Defects in Epithelial Polarity upon Conditional Ablation of α-Catenin in Skin

Vasioukhin, V., Bauer, C., Degenstein, L., Wise, B., & Fuchs, E. (2001) · Cell · doi:10.1016/s0092-8674(01)00246-x · Cited by 435 · see citing works

Claudin-1 gene mutations in neonatal sclerosing cholangitis associated with ichthyosis: A tight junction disease

Hadj-Rabia, S., Baala, L., Vabres, P., Hamel‐Teillac, D., Jacquemin, E., Fabrè, M., Lyonnet, S., Prost, Y. D., Münnich, A., Hadchouel, M., et al. (2004) · Gastroenterology · doi:10.1053/j.gastro.2004.07.022 · Cited by 426 · see citing works

p120-Catenin and p190RhoGAP Regulate Cell-Cell Adhesion by Coordinating Antagonism between Rac and Rho

Wildenberg, G. A., Dohn, M. R., Carnahan, R. H., Davis, M. A., Lobdell, N. A., Settleman, J. E., & Reynolds, A. B. (2006) · Cell · doi:10.1016/j.cell.2006.09.046 · Cited by 422 · see citing works

Epithelial myosin light chain kinase-dependent barrier dysfunction mediates T cell activation-induced diarrhea in vivo

Clayburgh, D. R. (2005) · Journal of Clinical Investigation · doi:10.1172/jci24970 · Cited by 419 · see citing works

Mammalian formin-1 participates in adherens junctions and polymerization of linear actin cables

Kobielak, A., Pasolli, H. A., & Fuchs, E. V. (2003) · Nature Cell Biology · doi:10.1038/ncb1075 · Cited by 401 · see citing works

Cadherin-mediated cell adhesion and tissue segregation: qualitative and quantitative determinants

Duguay, D., Foty, R. A., & Steinberg, M. S. (2003) · Developmental Biology · doi:10.1016/s0012-1606(02)00016-7 · Cited by 389 · see citing works

The roles of catenins in the cadherin-mediated cell adhesion: functional analysis of E-cadherin-alpha catenin fusion molecules.

Nagafuchi, A., Ishihara, S., & Tsukita, S. (1994) · The Journal of Cell Biology · doi:10.1083/jcb.127.1.235 · Cited by 386 · see citing works

Rap1: a key regulator in cell-cell junction formation

Kooistra, M. R. H., Dubé, N., & Bos, J. L. (2006) · Journal of Cell Science · doi:10.1242/jcs.03306 · Cited by 321 · see citing works

Knockdown of occludin expression leads to diverse phenotypic alterations in epithelial cells

Yu, A. S. L., McCarthy, K. M., Francis, S. A., McCormack, J. M., Lai, J., Rogers, R. A., Lynch, R. D., & Schneeberger, E. E. (2005) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00581.2004 · Cited by 307 · see citing works

Desmoplakin is essential in epidermal sheet formation

Vasioukhin, V. I., Bowers, E., Bauer, C. R., Degenstein, L., & Fuchs, E. V. (2001) · Nature Cell Biology · doi:10.1038/ncb1201-1076 · Cited by 304 · see citing works

Afadin

Ikeda, W., Nakanishi, H., Miyoshi, J., Mandai, K., Ishizaki, H., Tanaka, M., Togawa, A., Takahashi, K. P., Nishioka, H., Yoshida, H., et al. (1999) · The Journal of Cell Biology · doi:10.1083/jcb.146.5.1117 · Cited by 302 · see citing works

Isolation and functional characterization of the actin‐binding region in the tight junction protein ZO‐1

Fanning, A. S., Ma, T. Y., & Anderson, J. M. (2002) · The FASEB Journal · doi:10.1096/fj.02-0121fje · Cited by 296 · see citing works

The mammalian Scribble polarity protein regulates epithelial cell adhesion and migration through E-cadherin

Qin, Y., Capaldo, C., Gumbiner, B. M., & Macara, I. G. (2005) · The Journal of Cell Biology · doi:10.1083/jcb.200506094 · Cited by 285 · see citing works

Tricellulin is a tight-junction protein necessary for hearing

Riazuddin, S., Ahmed, Z. M., Fanning, A. S., Lagziel, A., Kitajiri, S.-I., Ramzan, K., Khan, S. N., Chattaraj, P., Friedman, P. L., Anderson, J. M., et al. (2006) · The American Journal of Human Genetics · doi:10.1086/510022 · Cited by 283 · see citing works

The epidermal barrier function is dependent on the serine protease CAP1/Prss8

Leyvraz, C., Charles, R., Rubera, I., Guitard, M., Rotman, S., Breiden, B., Sandhoff, K., & Hümmler, E. (2005) · The Journal of Cell Biology · doi:10.1083/jcb.200501038 · Cited by 272 · see citing works

p120-Catenin Mediates Inflammatory Responses in the Skin

Pérez‐Moreno, M., Davis, M. A., Wong, E., Pasolli, H. A., Reynolds, A. B., & Fuchs, E. V. (2006) · Cell · doi:10.1016/j.cell.2005.11.043 · Cited by 264 · see citing works

Cloning of the ALL-1 fusion partner, the AF-6 gene, involved in acute myeloid leukemias with the t(6;11) chromosome translocation.

Prasad, R., Gu, Y., Alder, H., Nakamura, T., Canaani, O. D., Saito, H., Huebner, K., Gale, R. P., Nowell̀, P. C., & Kuriyama, K. (1993) · PubMed · Cited by 257 · see citing works

aPKC kinase activity is required for the asymmetric differentiation of the premature junctional complex during epithelial cell polarization

Suzuki, A., Ishiyama, C., Hashiba, K., Shimizu, M., Ebnet, K., & Ohno, S. (2002) · Journal of Cell Science · doi:10.1242/jcs.00032 · Cited by 251 · see citing works

Spermatid differentiation requires the assembly of a cell polarity complex downstream of junctional adhesion molecule-C

Gliki, G., Ebnet, K., Aurrand‐Lions, M., Imhof, B. A., & Adams, R. H. (2004) · Nature · doi:10.1038/nature02877 · Cited by 241 · see citing works

Permeability barrier dysfunction in transgenic mice overexpressing claudin 6

Turksen, K., & Troy, T.-C. (2002) · Development · doi:10.1242/dev.129.7.1775 · Cited by 230 · see citing works

Binding of GEF-H1 to the Tight Junction-Associated Adaptor Cingulin Results in Inhibition of Rho Signaling and G1/S Phase Transition

Aijaz, S., D’Atri, F., Citi, S., Balda, M. S., & Matter, K. (2005) · Developmental Cell · doi:10.1016/j.devcel.2005.03.003 · Cited by 226 · see citing works

Setting up a selective barrier at the apical junction complex

Anderson, J. M., Van Itallie, C. M., & Fanning, A. S. (2004) · Current Opinion in Cell Biology · doi:10.1016/j.ceb.2004.01.005 · Cited by 215 · see citing works

V-src kinase shifts the cadherin-based cell adhesion from the strong to the weak state and beta catenin is not required for the shift.

Takeda, H., Nagafuchi, A., Yonemura, S., Tsukita, S., Behrens, J., Birchmeier, W., & Tsukita, S. (1995) · The Journal of Cell Biology · doi:10.1083/jcb.131.6.1839 · Cited by 212 · see citing works

Absence of the tight junctional protein AF-6 disrupts epithelial cell–cell junctions and cell polarity during mouse development

Zhadanov, A. B., Provance, D. W., Speer, C. A., Coffin, J. D., Goss, D., Blixt, J. A., Reichert, C. M., & Mercer, J. A. (1999) · Current Biology · doi:10.1016/s0960-9822(99)80392-3 · Cited by 208 · see citing works

Cadherin-mediated cell sorting not determined by binding or adhesion specificity

Niessen, C. M., & Gumbiner, B. M. (2002) · The Journal of Cell Biology · doi:10.1083/jcb.200108040 · Cited by 200 · see citing works

Conditional targeting of E-cadherin in skin: Insights into hyperproliferative and degenerative responses

Tinkle, C. L., Lechler, T., Pasolli, H. A., & Fuchs, E. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0307437100 · Cited by 193 · see citing works

p120-ctn: A nexus for contextual signaling via Rho GTPases

Anastasiadis, P. Z. (2006) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2006.08.040 · Cited by 192 · see citing works

Can 1000 Reviews Be Wrong? Actin, α-Catenin, and Adherens Junctions

Gates, J., & Peifer, M. A. (2005) · Cell · doi:10.1016/j.cell.2005.11.009 · Cited by 182 · see citing works

Regulation of E-cadherin Endocytosis by Nectin through Afadin, Rap1, and p120ctn

Hoshino, T., Sakisaka, T., Baba, T., Yamada, T., Kimura, T., & Takai, Y. (2005) · Journal of Biological Chemistry · doi:10.1074/jbc.m414447200 · Cited by 171 · see citing works

Arp2/3 Activity Is Necessary for Efficient Formation of E-cadherin Adhesive Contacts

Verma, S., Shewan, A. M., Scott, J. A., Helwani, F., den Elzen, N. R., Miki, H., Takenawa, T., & Yap, A. S. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.m404814200 · Cited by 161 · see citing works

E‐cadherin controls adherens junctions in the epidermis and the renewal of hair follicles

Young, P., Boussadia, O., Halfter, H., Grose, R., Berger, P., Leone, D. P., Robenek, H., Charnay, P., Kemler, R., & Suter, U. (2003) · The EMBO Journal · doi:10.1093/emboj/cdg560 · Cited by 156 · see citing works

Role of p120-catenin in cadherin trafficking

Xiao, K., Oas, R. G., Chiasson, C. M., & Kowalczyk, A. P. (2006) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2006.07.005 · Cited by 144 · see citing works

The challenges of abundance: epithelial junctions and small GTPase signalling

Braga, V. M. M., & Yap, A. S. (2005) · Current Opinion in Cell Biology · doi:10.1016/j.ceb.2005.08.012 · Cited by 139 · see citing works

Links between α-catenin, NF-κB, and squamous cell carcinoma in skin

Kobielak, A., & Fuchs, E. V. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0510422103 · Cited by 124 · see citing works

Role of aPKC Isoforms and Their Binding Partners Par3 and Par6 in Epidermal Barrier Formation

Helfrich, I., Schmitz, A., Zigrino, P., Michels, C., Haase, I., Bivic, A. L., Leitges, M., & Niessen, C. M. (2006) · Journal of Investigative Dermatology · doi:10.1038/sj.jid.5700621 · Cited by 112 · see citing works

Interneurite affinity is regulated by heterophilic nectin interactions in concert with the cadherin machinery

Togashi, H., Miyoshi, J., Honda, T., Sakisaka, T., Takai, Y., & Takeichi, M. (2006) · The Journal of Cell Biology · doi:10.1083/jcb.200601089 · Cited by 110 · see citing works

Roles and modes of action of nectins in cell–cell adhesion

Irie, K., Shimizu, K., Sakisaka, T., Ikeda, W., & Takai, Y. (2004) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2004.09.002 · Cited by 109 · see citing works

Regulatory mechanisms required for DE-cadherin function in cell migration and other types of adhesion

Pacquelet, A., & Rørth, P. (2005) · The Journal of Cell Biology · doi:10.1083/jcb.200506131 · Cited by 107 · see citing works

Tight Junction Proteins in the Skin

Brandner, J. M., Kief, S., Wladykowski, E., Houdek, P., & Moll, I. (2006) · Skin Pharmacology and Physiology · doi:10.1159/000091973 · Cited by 93 · see citing works

Disruption of the cingulin gene does not prevent tight junction formation but alters gene expression

Guillemot, L., Hammar, E. B., Kaister, C., Ritz, J., Caille, D., Jond, L., Bauer, C. R., Meda, P., & Citi, S. (2004) · Journal of Cell Science · doi:10.1242/jcs.01399 · Cited by 88 · see citing works

Microbial strategies to target, cross or disrupt epithelia

Sousa, S., Lecuit, M., & Cossart, P. (2005) · Current Opinion in Cell Biology · doi:10.1016/j.ceb.2005.08.013 · Cited by 86 · see citing works

Roles and modes of action of nectins in cell–cell adhesion

IRIE, K., Shimizu, K., Sakisaka, T., et al. (2004) · Seminars in Cell and Developmental Biology · doi:10.1016/s1084-9521(04)00088-6 · Cited by 83 · see citing works

Sealing the live part of the skin: The integrated meshwork of desmosomes, tight junctions and curvilinear ridge structures in the cells of the uppermost granular layer of the human epidermis

Schlüter, H., Wepf, R. A., Moll, I., & Franke, W. W. (2004) · European Journal of Cell Biology · doi:10.1078/0171-9335-00434 · Cited by 80 · see citing works

Cinderella no longer: α-catenin steps out of cadherin's shadow

Scott, J. A., & Yap, A. S. (2006) · Journal of Cell Science · doi:10.1242/jcs.03267 · Cited by 56 · see citing works

Regulation of epithelial wound closure and intercellular adhesion by interaction of AF6 with actin cytoskeleton

Lorger, M., & Moelling, K. (2006) · Journal of Cell Science · doi:10.1242/jcs.03027 · Cited by 53 · see citing works

Progesterone triggers rapid transmembrane calcium influx and/or calcium mobilization from endoplasmic reticulum, via a pertussis-insensitive G-protein in granulosa cells in relation to luteinization process

Machelon, V., Mercier‐Nomé, F., Grosse, B., & Lieberherr, M. (1996) · Journal of Cellular Biochemistry · doi:10.1002/(sici)1097-4644(19960616)61:4 · Cited by 52 · see citing works

ZOning out Tight Junctions

Shin, K., & Margolis, B. L. (2006) · Cell · doi:10.1016/j.cell.2006.08.005 · Cited by 42 · see citing works

Postnatal Lethality of P-Cadherin/Desmoglein 3 Double Knockout Mice: Demonstration of a Cooperative Effect of these Cell Adhesion Molecules in Tissue Homeostasis of Stratified Squamous Epithelia

Lenox, J. M., Koch, P. J., Mahoney, M. G., Lieberman, M. K., Stanley, J. R., & Radice, G. L. (2000) · Journal of Investigative Dermatology · doi:10.1046/j.1523-1747.2000.00976.x · Cited by 21 · see citing works

Collective cell migration in morphogenesis, regeneration and cancer

Friedl, P., & Gilmour, D. T. (2009) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm2720 · Cited by 2,668 · see citing works

Atopic dermatitis: a disease of altered skin barrier and immune dysregulation

Boguniewicz, M., & Leung, D. Y. M. (2011) · Immunological Reviews · doi:10.1111/j.1600-065x.2011.01027.x · Cited by 1,081 · see citing works

Regulation of Intestinal Barrier Function by Microbial Metabolites

Ghosh, S., Whitley, C. S., Haribabu, B., & Jala, V. R. (2021) · Cellular and Molecular Gastroenterology and Hepatology · doi:10.1016/j.jcmgh.2021.02.007 · Cited by 835 · see citing works

Tight junction defects in patients with atopic dermatitis

Benedetto, A. D., Rafaels, N. M., McGirt, L. Y., Ivanov, A. I., Georas, S. N., Cheadle, C., Berger, A. E., Zhang, K., Vidyasagar, S., Yoshida, T., et al. (2010) · Journal of Allergy and Clinical Immunology · doi:10.1016/j.jaci.2010.10.018 · Cited by 750 · see citing works

Skin tissue generation by laser cell printing

Koch, L., Deiwick, A., Schlie, S., Michael, S., Gruene, M., Coger, V., Zychlinski, D., Schambach, A., Reimers, K., Vogt, P. M., et al. (2012) · Biotechnology and Bioengineering · doi:10.1002/bit.24455 · Cited by 611 · see citing works

Transcriptional regulation of cell polarity in EMT and cancer

Moreno‐Bueno, G., Portillo, F., & Cano, A. (2008) · Oncogene · doi:10.1038/onc.2008.346 · Cited by 610 · see citing works

The Horizon of Materiobiology: A Perspective on Material-Guided Cell Behaviors and Tissue Engineering

Li, Y., Xiao, Y., & Liu, C. (2017) · Chemical Reviews · doi:10.1021/acs.chemrev.6b00654 · Cited by 600 · see citing works

Immunopathogenesis of Chronic Rhinosinusitis and Nasal Polyposis

Schleimer, R. P. (2016) · Annual Review of Pathology Mechanisms of Disease · doi:10.1146/annurev-pathol-052016-100401 · Cited by 548 · see citing works

Deconstructing the skin: cytoarchitectural determinants of epidermal morphogenesis

Simpson, C. L., Patel, D. M., & Green, K. J. (2011) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm3175 · Cited by 516 · see citing works

Oral Mucosal Epithelial Cells

Groeger, S., & Meyle, J. (2019) · Frontiers in Immunology · doi:10.3389/fimmu.2019.00208 · Cited by 473 · see citing works

Epithelial barrier function: At the front line of asthma immunology and allergic airway inflammation

Georas, S. N., & Rezaee, F. (2014) · Journal of Allergy and Clinical Immunology · doi:10.1016/j.jaci.2014.05.049 · Cited by 467 · see citing works

Enteric Pathogens and Their Toxin-Induced Disruption of the Intestinal Barrier through Alteration of Tight Junctions in Chickens

Awad, W., Hess, C., & Hess, M. (2017) · Toxins · doi:10.3390/toxins9020060 · Cited by 397 · see citing works

Cell Migration

Trepat, X., Chen, Z., & Jacobson, K. (2012) · Comprehensive physiology · doi:10.1002/cphy.c110012 · Cited by 475 · see citing works

Causes of epidermal filaggrin reduction and their role in the pathogenesis of atopic dermatitis

Thyssen, J. P., & Kežić, S. (2014) · Journal of Allergy and Clinical Immunology · doi:10.1016/j.jaci.2014.06.014 · Cited by 398 · see citing works

Potential use of tight junction modulators to reversibly open membranous barriers and improve drug delivery

Deli, M. A. (2008) · Biochimica et Biophysica Acta (BBA) - Biomembranes · doi:10.1016/j.bbamem.2008.09.016 · Cited by 385 · see citing works

Calcium regulation of keratinocyte differentiation

Bikle, D. D., Xie, Z., & Tu, C. (2012) · Expert Review of Endocrinology & Metabolism · doi:10.1586/eem.12.34 · Cited by 327 · see citing works

Atopic Dermatitis: A Disease Caused by Innate Immune Defects?

Benedetto, A. D., Agnihothri, R. V., McGirt, L. Y., Bankova, L. G., & Beck, L. A. (2008) · Journal of Investigative Dermatology · doi:10.1038/jid.2008.259 · Cited by 326 · see citing works

EMT and stemness: flexible processes tuned by alternative splicing in development and cancer progression

Pradella, D., Naro, C., Sette, C., & Ghigna, C. (2017) · Molecular Cancer · doi:10.1186/s12943-016-0579-2 · Cited by 325 · see citing works

Mechanisms of the Epithelial–Mesenchymal Transition by TGF-β

Wendt, M. K., Allington, T. M., & Schiemann, W. P. (2009) · Future Oncology · doi:10.2217/fon.09.90 · Cited by 318 · see citing works

Anatomy and Organization of Human Skin

McGrath, J. A., Eady, R. A. J., & Pope, F. M. (2004) · Wiley eBooks · doi:10.1002/9780470750520.ch3 · Cited by 314 · see citing works

An update on the genetics of atopic dermatitis: Scratching the surface in 2009

Barnes, K. C. (2010) · Journal of Allergy and Clinical Immunology · doi:10.1016/j.jaci.2009.11.008 · Cited by 310 · see citing works

EMT and EndMT: Emerging Roles in Age-Related Macular Degeneration

Shu, D. Y., Butcher, E. R., & Saint‐Geniez, M. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21124271 · Cited by 293 · see citing works

The gut microbiome and hypertension

O’Donnell, J. A., Zheng, T., Méric, G., & Marques, F. Z. (2023) · Nature Reviews Nephrology · doi:10.1038/s41581-022-00654-0 · Cited by 294 · see citing works

Polar Targeting and Endocytic Recycling in Auxin-Dependent Plant Development

Kleine‐Vehn, J., & Friml, J. (2008) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev.cellbio.24.110707.175254 · Cited by 275 · see citing works

Exchange Protein Directly Activated by cAMP (epac): A Multidomain cAMP Mediator in the Regulation of Diverse Biological Functions

Schmidt, M., Dekker, F. J., & Maarsingh, H. (2013) · Pharmacological Reviews · doi:10.1124/pr.110.003707 · Cited by 268 · see citing works

Microbial translocation and microbiome dysbiosis in HIV-associated immune activation

Zevin, A. S., McKinnon, L. R., Burgener, A., & Klatt, N. R. (2015) · Current Opinion in HIV and AIDS · doi:10.1097/coh.0000000000000234 · Cited by 266 · see citing works

Claudins in intestines

Lü, Z., Ding, L., Lu, Q., & Chen, Y. (2013) · Tissue Barriers · doi:10.4161/tisb.24978 · Cited by 268 · see citing works

Neurovascular Unit: a Focus on Pericytes

Sá-Pereira, I., Brites, D. M. T. O., & Brito, M. A. (2012) · Molecular Neurobiology · doi:10.1007/s12035-012-8244-2 · Cited by 267 · see citing works

Genetic and Transcriptomic Bases of Intestinal Epithelial Barrier Dysfunction in Inflammatory Bowel Disease

Vancamelbeke, M., Vanuytsel, T., Farré, R., Verstockt, S., Ferrante, M., Assche, G. V., Rutgeerts, P. J., Schuit, F. C., Vermeire, S., Arijs, I., et al. (2017) · Inflammatory Bowel Diseases · doi:10.1097/mib.0000000000001246 · Cited by 270 · see citing works

Mechanosensation of Tight Junctions Depends on ZO-1 Phase Separation and Flow

Schwayer, C., Shamipour, S., Pranjic-Ferscha, K., Schauer, A., Balda, M. S., Tada, M., Matter, K., & Heisenberg, C. (2019) · Cell · doi:10.1016/j.cell.2019.10.006 · Cited by 263 · see citing works

Intercellular Junction Assembly, Dynamics, and HomeostasisPreprint

Green, K. J., Getsios, S., Troyanovsky, S. M., & Godsel, L. M. (2009) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a000125 · Cited by 259 · see citing works

Claudin-1 regulates intestinal epithelial homeostasis through the modulation of Notch-signalling

Pope, J. L., Bhat, A. A., Sharma, A. K., Ahmad, R., Krishnan, M., Washington, M. K., Beauchamp, R. D., Singh, A. B., & Dhawan, P. (2013) · Gut · doi:10.1136/gutjnl-2012-304241 · Cited by 264 · see citing works

Heat stress directly impairs gut integrity and recruits distinct immune cell populations into the bovine intestine

Koch, F., Thom, U., Albrecht, E., Weikard, R., Nolte, W., Kuhla, B., & Kuehn, C. (2019) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1820130116 · Cited by 257 · see citing works

Skin Basement Membrane: The Foundation of Epidermal Integrity—BM Functions and Diverse Roles of Bridging Molecules Nidogen and Perlecan

Breitkreutz, D., Koxholt, I., Thiemann, K., & Nischt, R. (2013) · BioMed Research International · doi:10.1155/2013/179784 · Cited by 241 · see citing works

The functionality of prebiotics as immunostimulant: Evidences from trials on terrestrial and aquatic animals

Nawaz, A., Javaid, A. B., Irshad, S., Hoseinifar, S. H., & Xiong, H. (2018) · Fish & Shellfish Immunology · doi:10.1016/j.fsi.2018.03.004 · Cited by 244 · see citing works

Epithelial barrier and oral bacterial infection

Groeger, S. E., & Meyle, J. (2015) · Periodontology 2000 · doi:10.1111/prd.12094 · Cited by 229 · see citing works

Deconstructing the mechanisms and consequences of TGF-β-induced EMT during cancer progression

Wendt, M. K., Tian, M., & Schiemann, W. P. (2011) · Cell and Tissue Research · doi:10.1007/s00441-011-1199-1 · Cited by 212 · see citing works

Skin barrier defects in atopic dermatitis

Agrawal, R., & Woodfolk, J. A. (2014) · Current Allergy and Asthma Reports · doi:10.1007/s11882-014-0433-9 · Cited by 201 · see citing works

The TRPV4 Channel Contributes to Intercellular Junction Formation in Keratinocytes

Sokabe, T., Fukumi-Tominaga, T., Yonemura, S., Mizuno, A., & Tominaga, M. (2010) · Journal of Biological Chemistry · doi:10.1074/jbc.m110.103606 · Cited by 198 · see citing works

Mesenchymal Stem Cells Transmigrate Between and Directly Through Tumor Necrosis Factor‐α‐Activated Endothelial Cells Via Both Leukocyte‐Like and Novel Mechanisms

Teo, G. S. L., Ankrum, J. A., Martinelli, R., Boetto, S. E., Simms, K., Sciuto, T. E., Dvořàk, A. M., Karp, J. M., & Carman, C. V. (2012) · Stem Cells · doi:10.1002/stem.1198 · Cited by 196 · see citing works

Respiratory microbiome and epithelial interactions shape immunity in the lungs

Invernizzi, R., Lloyd, C. M., & Molyneaux, P. L. (2020) · Immunology · doi:10.1111/imm.13195 · Cited by 195 · see citing works

Mechanisms of endothelial cell migration

Michaelis, U. R. (2014) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-014-1678-0 · Cited by 191 · see citing works

Interleukin-4 and interleukin-13 cause barrier dysfunction in human airway epithelial cells

Saatian, B., Rezaee, F., DeSando, S. A., Emo, J. A., Chapman, T., Knowlden, S. A., & Georas, S. N. (2013) · Tissue Barriers · doi:10.4161/tisb.24333 · Cited by 190 · see citing works

The etiopathogenesis of atopic dermatitis: barrier disruption, immunological derangement, and pruritus

Rerknimitr, P., Otsuka, A., Nakashima, C., & Kabashima, K. (2017) · Inflammation and Regeneration · doi:10.1186/s41232-017-0044-7 · Cited by 187 · see citing works

Cardiac cell–cell junctions in health and disease: Electrical versus mechanical coupling

Noorman, M., van der Heyden, M. A. G., van Veen, T. A. B., Cox, M. G. P. J., Hauer, R. N. W., de Bakker, J. M. T., & van Rijen, H. V. M. (2009) · Journal of Molecular and Cellular Cardiology · doi:10.1016/j.yjmcc.2009.03.016 · Cited by 186 · see citing works

Resolving cadherin interactions and binding cooperativity at the single-molecule level

Zhang, Y., Sivasankar, S., Nelson, W. J., & Chu, S. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0811350106 · Cited by 181 · see citing works

Breaking Barriers. New Insights into Airway Epithelial Barrier Function in Health and Disease

Rezaee, F., & Georas, S. N. (2014) · American Journal of Respiratory Cell and Molecular Biology · doi:10.1165/rcmb.2013-0541rt · Cited by 172 · see citing works

Wound healing revised: A novel reepithelialization mechanism revealed by in vitro and in silico models

Safferling, K., Sütterlin, T., Westphal, K., Ernst, C., Breuhahn, K., James, M., Jäger, D., Halama, N., & Grabe, N. (2013) · The Journal of Cell Biology · doi:10.1083/jcb.201212020 · Cited by 172 · see citing works

Activation of Epidermal Toll-Like Receptor 2 Enhances Tight Junction Function: Implications for Atopic Dermatitis and Skin Barrier Repair

Kuo, I., Carpenter-Mendini, A. B., Yoshida, T., McGirt, L. Y., Ivanov, A. I., Barnes, K. C., Gallo, R. L., Borkowski, A. W., Yamasaki, K., Leung, D. Y. M., et al. (2012) · Journal of Investigative Dermatology · doi:10.1038/jid.2012.437 · Cited by 171 · see citing works

Adhesive and Signaling Functions of Cadherins and Catenins in Vertebrate DevelopmentPreprint

Stępniak-Konieczna, E., Radice, G. L., & Vasioukhin, V. I. (2009) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a002949 · Cited by 167 · see citing works

Epithelial Barrier Dysfunction in Chronic Respiratory Diseases

Carlier, F. M., Fays, C. D., & Pilette, C. (2021) · Frontiers in Physiology · doi:10.3389/fphys.2021.691227 · Cited by 168 · see citing works

Vinculin phosphorylation differentially regulates mechanotransduction at cell–cell and cell–matrix adhesions

Bays, J., Peng, X. L., Tolbert, C. E., Guilluy, C., Angell, A. E., Pan, Y., Superfine, R., Burridge, K., & DeMali, K. A. (2014) · The Journal of Cell Biology · doi:10.1083/jcb.201309092 · Cited by 164 · see citing works

Basement membranes in skin: unique matrix structures with diverse functions?

Breitkreutz, D., Mirancea, N., & Nischt, R. (2009) · Histochemistry and Cell Biology · doi:10.1007/s00418-009-0586-0 · Cited by 160 · see citing works

Role of epithelial–mesenchymal transition in proliferative vitreoretinopathy

Tamiya, S., & Kaplan, H. J. (2015) · Experimental Eye Research · doi:10.1016/j.exer.2015.02.008 · Cited by 160 · see citing works

Alteration of Tight Junction Proteins Is an Early Event in Psoriasis

Kirschner, N., Poetzl, C., Driesch, P. V. D., Wladykowski, E., Moll, I., Behne, M. J., & Brandner, J. M. (2009) · American Journal Of Pathology · doi:10.2353/ajpath.2009.080973 · Cited by 158 · see citing works

Calcium - a central regulator of keratinocyte differentiation in health and disease

Elsholz, F., Harteneck, C., Muller, W., & Friedland, K. (2014) · European Journal of Dermatology · doi:10.1684/ejd.2014.2452 · Cited by 157 · see citing works

Cell–cell junction formation: The role of Rap1 and Rap1 guanine nucleotide exchange factors

Pannekoek, W., Kooistra, M. R. H., Zwartkruis, F. J. T., & Bos, J. L. (2008) · Biochimica et Biophysica Acta (BBA) - Biomembranes · doi:10.1016/j.bbamem.2008.12.010 · Cited by 156 · see citing works

Influence of Th2 Cytokines on the Cornified Envelope, Tight Junction Proteins, and β-Defensins in Filaggrin-Deficient Skin Equivalents

Hönzke, S., Wallmeyer, L., Ostrowski, A., Radbruch, M., Mundhenk, L., Schäfer‐Korting, M., & Hedtrich, S. (2015) · Journal of Investigative Dermatology · doi:10.1016/j.jid.2015.11.007 · Cited by 154 · see citing works

Mechanical Forces in the Skin: Roles in Tissue Architecture, Stability, and Function

Biggs, L. C., Kim, C. S. K., Miroshnikova, Y. A., & Wickström, S. A. (2019) · Journal of Investigative Dermatology · doi:10.1016/j.jid.2019.06.137 · Cited by 151 · see citing works

Resveratrol induces chemosensitization to 5-fluorouracil through up-regulation of intercellular junctions, Epithelial-to-mesenchymal transition and apoptosis in colorectal cancer

Buhrmann, C., Shayan, P., Kraehe, P., Popper, B., Goel, A., & Shakibaei, M. (2015) · Biochemical Pharmacology · doi:10.1016/j.bcp.2015.08.105 · Cited by 148 · see citing works

Constitutively active Stat3 enhances neu-mediated migration and metastasis in mammary tumors via upregulation of Cten

Barbieri, I., Pensa, S., Pannellini, T., Quaglino, E., Maritano, D., Demaria, M., Voster, A., Turkson, J., Cavallo, F., Watson, C. J., et al. (2010) · Cancer Research · doi:10.1158/0008-5472.can-09-2840 · Cited by 148 · see citing works

Cell polarity signaling in the plasticity of cancer cell invasiveness

Gandalovičová, A., Vomastek, T., Rösel, D., & Brábek, J. (2016) · Oncotarget · doi:10.18632/oncotarget.7214 · Cited by 149 · see citing works

Physiological Effects of Dietary Amino Acids on Gut Health and Functions of Swine

Yang, Z., & Liao, S. F. (2019) · Frontiers in Veterinary Science · doi:10.3389/fvets.2019.00169 · Cited by 145 · see citing works

Barrier Dysfunction Caused by Environmental Proteases in the Pathogenesis of Allergic Diseases

Takai, T., & Ikeda, S. (2011) · Allergology International · doi:10.2332/allergolint.10-rai-0273 · Cited by 142 · see citing works

Matrix metalloproteinase 13 modulates intestinal epithelial barrier integrity in inflammatory diseases by activating TNF

Vandenbroucke, R. E., Dejonckheere, E., Hauwermeiren, F. V., Lodens, S., Rycke, R. M. D., Wonterghem, E. V., Staes, A., Gevaert, K., López-Otı́n, C., & Libert, C. (2013) · EMBO Molecular Medicine · doi:10.1002/emmm.201202100 · Cited by 140 · see citing works

Ineffective esophageal motility: Concepts, future directions, and conclusions from the Stanford 2018 symposium

Gyawali, C. P., Sifrim, D. A., Carlson, D. A., Hawn, M. T., Katzka, D. A., Pandolfino, J. E., Penagini, R., Roman, S., Savarino, E. V., Tatum, R. P., et al. (2019) · Neurogastroenterology & Motility · doi:10.1111/nmo.13584 · Cited by 135 · see citing works

Epidermal Differentiation in Barrier Maintenance and Wound Healing

Wikramanayake, T. C., Stojadinović, O., & Tomic‐Canic, M. (2014) · Advances in Wound Care · doi:10.1089/wound.2013.0503 · Cited by 130 · see citing works

ALX4 dysfunction disrupts craniofacial and epidermal development

Kayserili, H., Uz, E., Niessen, C. M., Vargel, İ., Alanay, Y., Tunçbi̇lek, G., Yigit, G., Uyguner, Z. O., Candan, Ş., Okur, H., et al. (2009) · Human Molecular Genetics · doi:10.1093/hmg/ddp391 · Cited by 132 · see citing works

Role of E-cadherin in the Pathogenesis of Gastroesophageal Reflux Disease

Jovov, B., Que, J., Tobey, N. A., Djukic, Z., Hogan, B. L. M., & Orlando, R. C. (2011) · The American Journal of Gastroenterology · doi:10.1038/ajg.2011.102 · Cited by 130 · see citing works

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Goodarzi, P., Falahzadeh, K., Nematizadeh, M., Farazandeh, P., Payab, M., Larijani, B. A., Tayanloo-Beik, A., & Arjmand, B. (2018) · Advances in experimental medicine and biology · doi:10.1007/5584_2018_226 · Cited by 131 · see citing works

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Erickson, E., Leydon, C., & Thibeault, S. L. (2014) · Journal of Speech Language and Hearing Research · doi:10.1044/2014_jslhr-s-13-0283 · Cited by 128 · see citing works

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Judkins, T. C., Archer, D. L., Kramer, D. C., & Solch-Ottaiano, R. J. (2020) · Current Gastroenterology Reports · doi:10.1007/s11894-019-0740-3 · Cited by 134 · see citing works

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Popoff, M. R., & Geny, B. (2009) · Biochimica et Biophysica Acta (BBA) - Biomembranes · doi:10.1016/j.bbamem.2009.01.011 · Cited by 127 · see citing works

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Kiatsurayanon, C., Niyonsaba, F., Smithrithee, R., Akiyama, T., Ushio, H., Hara, M., Okumura, K., Ikeda, S., & Ogawa, H. (2014) · Journal of Investigative Dermatology · doi:10.1038/jid.2014.143 · Cited by 126 · see citing works

IL-22 Increases Permeability of Intestinal Epithelial Tight Junctions by Enhancing Claudin-2 Expression

Wang, Y., Mumm, J. B., Herbst, R., Kolbeck, R., & Wang, Y. (2017) · The Journal of Immunology · doi:10.4049/jimmunol.1700152 · Cited by 125 · see citing works

Activation of SIRT1 ameliorates LPS-induced lung injury in mice via decreasing endothelial tight junction permeability

Fu, C., Hao, S., Xu, X., Zhou, J., Liu, Z., Lu, H., Wang, L., Jin, W., & Li, S. (2018) · Acta Pharmacologica Sinica · doi:10.1038/s41401-018-0045-3 · Cited by 125 · see citing works

Metformin protects against intestinal barrier dysfunction via AMPKα1‐dependent inhibition of JNK signalling activation

Deng, J., Zeng, L., Lai, X., Li, J., Liu, L., Lin, Q., & Chen, Y. (2017) · Journal of Cellular and Molecular Medicine · doi:10.1111/jcmm.13342 · Cited by 124 · see citing works

Mutations in PVRL4, Encoding Cell Adhesion Molecule Nectin-4, Cause Ectodermal Dysplasia-Syndactyly Syndrome

Brancati, F., Fortugno, P., Bottillo, I., Lopez, M., Josselin, E., Boudghène-Stambouli, O., Agolini, E., Bernardini, L., Bellacchio, E., Iannicelli, M., et al. (2010) · The American Journal of Human Genetics · doi:10.1016/j.ajhg.2010.07.003 · Cited by 123 · see citing works

Importance of transient receptor potential vanilloid 4 (TRPV4) in epidermal barrier function in human skin keratinocytes

Kida, N., Sokabe, T., Kashio, M., Haruna, K., Mizuno, Y., Suga, Y., Nishikawa, K., Kanamaru, A., Hongo, M., Oba, A., et al. (2012) · Pflügers Archiv - European Journal of Physiology · doi:10.1007/s00424-012-1081-3 · Cited by 121 · see citing works

Skin barrier in atopic dermatitis: beyond filaggrin

Zaniboni, M. C., ­Samorano, L. P., Orfali, R. L., & Aoki, V. (2016) · Anais Brasileiros de Dermatologia · doi:10.1590/abd1806-4841.20164412 · Cited by 121 · see citing works

Vinculin-dependent Cadherin mechanosensing regulates efficient epithelial barrier formation

Twiss, F., le Duc, Q., van der Horst, S. E. M., Tabdili, H., van der Krogt, G. N. M., Wang, N., Rehmann, H., Huveneers, S., Leckband, D. E., & de Rooij, J. (2012) · Biology Open · doi:10.1242/bio.20122428 · Cited by 119 · see citing works

Role of Lgl/Dlg/Scribble in the regulation of epithelial junction, polarity and growth

Yamanaka, T. (2008) · Frontiers in bioscience · doi:10.2741/3182 · Cited by 116 · see citing works

Skin barrier in atopic dermatitis

Kezic, S. (2014) · Frontiers in Bioscience · doi:10.2741/4225 · Cited by 115 · see citing works

Lasers as an approach for promoting drug delivery via skin

Lin, C.-H., Aljuffali, I. A., & Fang, J. (2014) · Expert Opinion on Drug Delivery · doi:10.1517/17425247.2014.885501 · Cited by 114 · see citing works

Exposure to Lipopolysaccharide and/or Unconjugated Bilirubin Impair the Integrity and Function of Brain Microvascular Endothelial Cells

Cardoso, F. L., Kittel, Á., Veszelka, S., Palmela, I., Tóth, A. E., Brites, D. M. T. O., Deli, M. A., & Brito, M. A. (2012) · PLoS ONE · doi:10.1371/journal.pone.0035919 · Cited by 111 · see citing works

The Blood-Aqueous Barrier in Health and Disease

Coca‐Prados, M. (2014) · Journal of Glaucoma · doi:10.1097/ijg.0000000000000107 · Cited by 106 · see citing works

Methodologies in creating skin substitutes

Nicholas, M. N., Jeschke, M. G., & Amini‐Nik, S. (2016) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-016-2252-8 · Cited by 106 · see citing works

Reductions in claudin-1 may enhance susceptibility to herpes simplex virus 1 infections in atopic dermatitis

Benedetto, A. D., Slifka, M. K., Rafaels, N. M., Kuo, I., Georas, S. N., Boguniewicz, M., Hata, T. R., Schneider, L. C., Hanifin, J. M., Gallo, R. L., et al. (2011) · Journal of Allergy and Clinical Immunology · doi:10.1016/j.jaci.2011.02.014 · Cited by 104 · see citing works

Molecular Carcinogenesis of Canine Mammary Tumors

Klopfleisch, R., von Euler, H., Sarli, G., Pinho, S. S., Gärtner, F., & Gruber, A. D. (2010) · Veterinary Pathology · doi:10.1177/0300985810390826 · Cited by 103 · see citing works

The Human Cathelicidin LL-37 Host Defense Peptide Upregulates Tight Junction-Related Proteins and Increases Human Epidermal Keratinocyte Barrier Function

Akiyama, T., Niyonsaba, F., Kiatsurayanon, C., Nguyen, T. T., Ushio, H., Fujimura, T., Ueno, T., Okumura, K., Ogawa, H., & Ikeda, S. (2014) · Journal of Innate Immunity · doi:10.1159/000362789 · Cited by 102 · see citing works

Melatonin decreases duodenal epithelial paracellular permeability via a nicotinic receptor–dependent pathway in rats in vivo

Sommansson, A., Nylander, O., & Sjöblom, M. (2012) · Journal of Pineal Research · doi:10.1111/jpi.12013 · Cited by 102 · see citing works

Epithelial cell polarity and tumorigenesis: new perspectives for cancer detection and treatment

Coradini, D., Casarsa, C., & Oriana, S. (2011) · Acta Pharmacologica Sinica · doi:10.1038/aps.2011.20 · Cited by 101 · see citing works

Epithelial integrity, junctional complexes, and biomarkers associated with intestinal functions

Alizadeh, A., Akbari, P., Garssen, J., Fink‐Gremmels, J., & Braber, S. (2021) · Tissue Barriers · doi:10.1080/21688370.2021.1996830 · Cited by 100 · see citing works

Eczema Herpeticum: Clinical and Pathophysiological Aspects

Damour, A., Garcia, M., Sénéschal, J., Lévêque, N., & Bodet, C. (2019) · Clinical Reviews in Allergy & Immunology · doi:10.1007/s12016-019-08768-3 · Cited by 101 · see citing works

Characterization of Ovine Nectin-4, a Novel Peste des Petits Ruminants Virus Receptor

Birch, J., Juleff, N. D., Heaton, M. P., Kalbfleisch, T., Kijas, J., & Bailey, D. (2013) · Journal of Virology · doi:10.1128/jvi.02792-12 · Cited by 98 · see citing works

Co-culture of human alveolar epithelial (hAELVi) and macrophage (THP-1) cell lines

Kletting, S. (2017) · ALTEX · doi:10.14573/altex.1607191 · Cited by 97 · see citing works

Polyinosinic:polycytidylic acid induces protein kinase D–dependent disassembly of apical junctions and barrier dysfunction in airway epithelial cells

Rezaee, F., Meednu, N., Emo, J. A., Saatian, B., Chapman, T. J., Naydenov, N. G., Benedetto, A. D., Beck, L. A., Ivanov, A. I., & Georas, S. N. (2011) · Journal of Allergy and Clinical Immunology · doi:10.1016/j.jaci.2011.08.035 · Cited by 97 · see citing works

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Zhang, F., Zarkada, G., Yi, S., & Eichmann, A. (2020) · Frontiers in Physiology · doi:10.3389/fphys.2020.00509 · Cited by 92 · see citing works

Abnormal Epithelial Cell Polarity and Ectopic Epidermal Growth Factor Receptor (EGFR) Expression Induced in Emx2 KO Embryonic Gonads

Kusaka, M., Fukui, Y., Ogawa, H., Miyabayashi, K., Baba, T., Shima, Y., Sugiyama, N., Sugimoto, Y., Okuno, Y., Kodama, R., et al. (2010) · Endocrinology · doi:10.1210/en.2010-0915 · Cited by 95 · see citing works

The Interaction of Streptococcus pneumoniae with Plasmin Mediates Transmigration across Endothelial and Epithelial Monolayers by Intercellular Junction Cleavage

Attali, C., Durmort, C., Vernet, T., & Guilmi, A. M. D. (2008) · Infection and Immunity · doi:10.1128/iai.00184-08 · Cited by 95 · see citing works

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Brandner, J. M., Haftek, M., & Niessen, C. M. (2010) · The Open Dermatology Journal · doi:10.2174/1874372201004010014 · Cited by 43 · see citing works

Open Access Adherens Junctions, Desmosomes and Tight Junctions in Epidermal Barrier Function

Brandner, J. M., Haftek, M., & Niessen, C. M. (2016)

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Michels, C., Aghdam, S. Y., & Niessen, C. M. (2009) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2009.04443.x · Cited by 20 · see citing works

Tight junctions in the skin

Morita, K., & Miyachi, Y. (2003) · Journal of Dermatological Science · doi:10.1016/s0923-1811(03)00038-0 · Cited by 65 · see citing works

Adherens Junctions, Desmosomes and Tight Junctions in Epidermal Barrier Function~!2009-10-24~!2009-12-10~!2010-04-23~!

Brandner, J. M., Haftek, M., & Niessen, C. M. (2010) · The Open Dermatology Journal · doi:10.2174/1874372201004020014 · Cited by 25 · see citing works