Nutritional Keys for Intestinal Barrier Modulation

Extracellular vesicles: Exosomes, microvesicles, and friends

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Changes of Intestinal Functions in Liver Cirrhosis

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Functional interactions between the gut microbiota and host metabolism

Tremaroli, V., & Bäckhed, F. (2012) · Nature · doi:10.1038/nature11552 · Cited by 4,387 · see citing works

Intestinal mucosal barrier function in health and disease

Turner, J. R. (2009) · Nature reviews. Immunology · doi:10.1038/nri2653 · Cited by 3,952 · see citing works

Gut Microbiota from Twins Discordant for Obesity Modulate Metabolism in Mice

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Duodenal Infusion of Donor Feces for Recurrent <i>Clostridium difficile</i>

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Intestinal epithelial cells: regulators of barrier function and immune homeostasis

Peterson, L. W., & Artis, D. (2014) · Nature reviews. Immunology · doi:10.1038/nri3608 · Cited by 3,191 · see citing works

Systematic review and meta-analysis

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Occludin: a novel integral membrane protein localizing at tight junctions.

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Dietary modulation of the human colonic microbiota: updating the concept of prebiotics

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Celiac Disease

Green, P. H. R., Jones, R., & Green, P. H. R. (2006) · Cited by 2,465 · see citing works

Psychosomatic medicine in Germany: more timely than ever

Zipfel, S., Herzog, W., Kruse, J., & Henningsen, P. (2016) · Psychotherapy and Psychosomatics · doi:10.1159/000447701 · Cited by 2,323 · see citing works

Claudin-1 and -2: Novel Integral Membrane Proteins Localizing at Tight Junctions with No Sequence Similarity to Occludin

Furuse, M., Fujita, K., Hiiragi, T., Fujimoto, K., & Tsukita, S. (1998) · The Journal of Cell Biology · doi:10.1083/jcb.141.7.1539 · Cited by 2,100 · see citing works

Intestinal barrier function: molecular regulation and disease pathogenesis

Groschwitz, K. R., & Hogan, S. P. (2009) · Journal of Allergy and Clinical Immunology · doi:10.1016/j.jaci.2009.05.038 · Cited by 1,775 · see citing works

Regional specialization within the intestinal immune system

Mowat, A. M., & Agace, W. W. (2014) · Nature reviews. Immunology · doi:10.1038/nri3738 · Cited by 1,769 · see citing works

Intestinal permeability – a new target for disease prevention and therapy

Bischoff, S. C., Barbara, G., Buurman, W., Ockhuizen, T., Schulzke, J.-D., Serino, M., Tilg, H., Watson, A., & Wells, J. M. (2014) · BMC Gastroenterology · doi:10.1186/s12876-014-0189-7 · Cited by 1,755 · see citing works

Dysbiosis of the gut microbiota in disease

Carding, S., Verbeke, K., Vipond, D. T., Corfe, B. M., & Owen, L. J. (2015) · Microbial Ecology in Health &amp; Disease · doi:10.3402/mehd.v26.26191 · Cited by 1,710 · see citing works

Bacteria as vitamin suppliers to their host: A gut microbiota perspective

LeBlanc, J. G., Milani, C., de Giori, G. S., Sesma, F., van Sinderen, D., & Ventura, M. (2013) · Current Opinion in Biotechnology · doi:10.1016/j.copbio.2012.08.005 · Cited by 1,613 · see citing works

CX 3 CR1-Mediated Dendritic Cell Access to the Intestinal Lumen and Bacterial Clearance

Niess, J. H., Brand, S., Gu, X., Landsman, L., Jung, S., McCormick, B. A., Vyas, J. M., Boes, M. L., Ploegh, H. L., Fox, J. G., et al. (2005) · Science · doi:10.1126/science.1102901 · Cited by 1,609 · see citing works

Adherens and tight junctions: Structure, function and connections to the actin cytoskeleton

Hartsock, A., & Nelson, W. J. (2007) · Biochimica et Biophysica Acta (BBA) - Biomembranes · doi:10.1016/j.bbamem.2007.07.012 · Cited by 1,559 · see citing works

Claudins and the Modulation of Tight Junction Permeability

Günzel, D., & Yu, A. S. L. (2013) · Physiological Reviews · doi:10.1152/physrev.00019.2012 · Cited by 1,456 · see citing works

Increased intestinal permeability and tight junction alterations in nonalcoholic fatty liver disease

Miele, L., Valenza, V., La Torre, G., Montalto, M., Cammarota, G., Ricci, R., Mascianà, R., Forgione, A., Gabrieli, M. L., Perotti, G., et al. (2009) · Hepatology · doi:10.1002/hep.22848 · Cited by 1,434 · see citing works

Anatomical basis of tolerance and immunity to intestinal antigens

Mowat, A. M. (2003) · Nature reviews. Immunology · doi:10.1038/nri1057 · Cited by 1,414 · see citing works

Junctional Adhesion Molecule, a Novel Member of the Immunoglobulin Superfamily That Distributes at Intercellular Junctions and Modulates Monocyte Transmigration

Martín-Padura, I., Lostaglio, S., Schneemann, M., Williams, L., Romano, M., Fruscella, P., Panzeri, C., Stoppacciaro, A., Ruco, L., Villa, A., et al. (1998) · The Journal of Cell Biology · doi:10.1083/jcb.142.1.117 · Cited by 1,387 · see citing works

Regulation of intestinal epithelial permeability by tight junctions

Suzuki, T. (2012) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-012-1070-x · Cited by 1,365 · see citing works

Interaction between Phenolics and Gut Microbiota: Role in Human Health

Selma, M. V., Espín, J. C., & Tomás-Barberán, F. A. (2009) · Journal of Agricultural and Food Chemistry · doi:10.1021/jf902107d · Cited by 1,324 · see citing works

Secretory IgA's complex roles in immunity and mucosal homeostasis in the gut

Mantis, N. J., Rol, N., & Corthésy, B. (2011) · Mucosal Immunology · doi:10.1038/mi.2011.41 · Cited by 1,283 · see citing works

Induction of phase I, II and III drug metabolism/transport by xenobiotics

Xu, C., Li, C. Y.-T., & Kong, A. T. (2005) · Archives of Pharmacal Research · doi:10.1007/bf02977789 · Cited by 1,272 · see citing works

Regulation of Tight Junction Permeability by Intestinal Bacteria and Dietary Components1,2

Ulluwishewa, D., Anderson, R. C., McNabb, W. C., Moughan, P. J., Wells, J. M., & Roy, N. C. (2011) · The Journal of Nutrition · doi:10.3945/jn.110.135657 · Cited by 1,177 · see citing works

Irritable Bowel Syndrome

Chey, W. D., Kurlander, J. E., & Eswaran, S. L. (2015) · JAMA · doi:10.1001/jama.2015.0954 · Cited by 1,086 · see citing works

Physiology and function of the tight junction

Anderson, J. M., & Van Itallie, C. M. (2009) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a002584 · Cited by 1,059 · see citing works

Probiotics, Prebiotics, and Synbiotics

de Vrese, M., & Schrezenmeir, J. (2008) · Advances in biochemical engineering, biotechnology · doi:10.1007/10_2008_097 · Cited by 1,033 · see citing works

Treating Clostridium difficile infection with fecal microbiota transplantation

Bakken, J. S., Borody, T., Brandt, L. J., Brill, J. V., Demarco, D. C., Franzos, M. A., Kelly, C., Khoruts, A., Louie, T., Martinelli, L. P., et al. (2011) · Clinical Gastroenterology and Hepatology · doi:10.1016/j.cgh.2011.08.014 · Cited by 1,003 · see citing works

Goblet cells deliver luminal antigen to CD103+ dendritic cells in the small intestine

Mcdole, J. R., Wheeler, L. W., McDonald, K. G., Wang, B., Konjufca, V. H., Knoop, K. A., Newberry, R. D., & Miller, M. J. (2012) · Nature · doi:10.1038/nature10863 · Cited by 976 · see citing works

Tight Junction Pore and Leak Pathways: A Dynamic Duo

Shen, L., Weber, C. R., Raleigh, D. R., Yu, D., & Turner, J. R. (2011) · Annual Review of Physiology · doi:10.1146/annurev-physiol-012110-142150 · Cited by 867 · see citing works

Intestinal Permeability Regulation by Tight Junction: Implication on Inflammatory Bowel Diseases

Lee, S. H. (2015) · Intestinal Research · doi:10.5217/ir.2015.13.1.11 · Cited by 810 · 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

Cytokine regulation of tight junctions

Capaldo, C., & Nusrat, A. (2008) · Biochimica et Biophysica Acta (BBA) - Biomembranes · doi:10.1016/j.bbamem.2008.08.027 · Cited by 724 · see citing works

Dynamic imaging of dendritic cell extension into the small bowel lumen in response to epithelial cell TLR engagement

Chieppa, M., Rescigno, M., Huang, A. Y.-C., & Germain, R. N. (2006) · The Journal of Experimental Medicine · doi:10.1084/jem.20061884 · Cited by 711 · see citing works

Intestinal epithelial cells secrete exosome–like vesicles

van Niel, G., Raposo, G., Candalh, C., Boussac, M., Hershberg, R. M., Cerf–Bensussan, N., & Heyman, M. (2001) · Gastroenterology · doi:10.1053/gast.2001.26263 · Cited by 698 · see citing works

Bile acids as regulatory molecules

Hylemon, P. B., Zhou, H., Pandak, W. M., Ren, S., Gil, G., & Dent, P. (2009) · Journal of Lipid Research · doi:10.1194/jlr.r900007-jlr200 · Cited by 694 · see citing works

Transcytosis: Crossing Cellular Barriers

TUMA, P. L., & HUBBARD, A. L. (2003) · Physiological Reviews · doi:10.1152/physrev.00001.2003 · Cited by 681 · see citing works

Influence of red wine polyphenols and ethanol on the gut microbiota ecology and biochemical biomarkers

Queipo-Ortuño, M. I., Boto-Ordóñez, M., Murri, M., Gomez-Zumaquero, J. M., Clemente-Postigo, M., Estruch, R., Cardona Diaz, F., Andrés-Lacueva, C., & Tinahones, F. J. (2012) · The American Journal of Clinical Nutrition · doi:10.3945/ajcn.111.027847 · Cited by 671 · see citing works

Novel role of the vitamin D receptor in maintaining the integrity of the intestinal mucosal barrier

Kong, J., Zhang, Z., Musch, M. W., Ning, G., Sun, J., Hart, J., Bissonnette, M., & Li, Y. C. (2007) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.00398.2007 · Cited by 669 · see citing works

Oral tolerance to food protein

Pabst, O., & Mowat, A. M. (2012) · Mucosal Immunology · doi:10.1038/mi.2012.4 · Cited by 656 · see citing works

Alterations in intestinal permeability

Arrieta, M., Bistritz, L., & Meddings, J. B. (2006) · Gut · doi:10.1136/gut.2005.085373 · Cited by 634 · see citing works

Oral, Capsulized, Frozen Fecal Microbiota Transplantation for Relapsing <i>Clostridium difficile</i> Infection

Youngster, I., Russell, G. H., Pindar, C., Ziv-Baran, T., Sauk, J., & Hohmann, E. L. (2014) · JAMA · doi:10.1001/jama.2014.13875 · Cited by 629 · see citing works

IL-1β Causes an Increase in Intestinal Epithelial Tight Junction Permeability

Al-Sadi, R. M., & Ma, T. Y. (2007) · The Journal of Immunology · doi:10.4049/jimmunol.178.7.4641 · Cited by 601 · see citing works

Chitosans as Absorption Enhancers for Poorly Absorbable Drugs 2: Mechanism of Absorption Enhancement

Schipper, N. G. M., Olsson, S., Hoogstraate, J. A., deBoer, A. G., Vårum, K. M., & Artursson, P. (1997) · Pharmaceutical Research · doi:10.1023/a:1012160102740 · Cited by 588 · see citing works

Collaboration of epithelial cells with organized mucosal lymphoid tissues

Neutra, M. R., Mantis, N. J., & Kraehenbühl, J.-P. (2001) · Nature Immunology · doi:10.1038/ni1101-1004 · Cited by 580 · see citing works

Gliadin Induces an Increase in Intestinal Permeability and Zonulin Release by Binding to the Chemokine Receptor CXCR3

Lammers, K. M., Lu, R., Brownley, J., Lu, B., Gerard, C. J., Thomas, K., Rallabhandi, P., Shea‐Donohue, T., Tamiz, A. P., Alkan, Ş. Ş., et al. (2008) · Gastroenterology · doi:10.1053/j.gastro.2008.03.023 · Cited by 545 · see citing works

Intestinal barrier: An interface between health and disease

Farhadi, A., Banan, A., Fields, J. Z., & Keshavarzian, A. (2003) · Journal of Gastroenterology and Hepatology · doi:10.1046/j.1440-1746.2003.03032.x · Cited by 532 · see citing works

Fecal microbiota transplantation as therapy for inflammatory bowel disease: A systematic review and meta-analysis

Colman, R. J., & Rubin, D. T. (2014) · Journal of Crohn's and Colitis · doi:10.1016/j.crohns.2014.08.006 · Cited by 475 · see citing works

A clinical review

Siegel, I. M. (1978) · Muscle & Nerve · doi:10.1002/mus.880010603 · Cited by 455 · see citing works

Increased intestinal permeability precedes clinical onset of type 1 diabetes

Bosi, E., Molteni, L., Radaelli, M. G., Folini, L., Fermo, I., Bazzigaluppi, E., Piemonti, L., Pastore, M. R., & Paroni, R. C. (2006) · Diabetologia · doi:10.1007/s00125-006-0465-3 · Cited by 444 · see citing works

Effects of probiotic bacteria on diarrhea, lipid metabolism, and carcinogenesis: a review of papers published between 1988 and 1998

de Roos, N. M., & Katan, M. (2000) · American Journal of Clinical Nutrition · doi:10.1093/ajcn/71.2.405 · Cited by 437 · see citing works

Intestinal Inflammation and Mucosal Barrier Function

de Medina, F. S., Romero‐Calvo, I., Mascaraque, C., & Martínez‐Augustin, O. (2014) · Inflammatory Bowel Diseases · doi:10.1097/mib.0000000000000204 · Cited by 435 · see citing works

Central Role of the Gut Epithelial Barrier in the Pathogenesis of Chronic Intestinal Inflammation: Lessons Learned from Animal Models and Human Genetics

Pastorelli, L., Salvo, C. D., Mercado, J. R., Vecchi, M. L., & Pizarro, T. T. (2013) · Frontiers in Immunology · doi:10.3389/fimmu.2013.00280 · Cited by 434 · see citing works

Claudin-2, a component of the tight junction, forms a paracellular water channel

Rosenthal, R., Milatz, S., Krug, S. M., Oelrich, B., Schulzke, J., Amasheh, S., Günzel, D., & Fromm, M. (2010) · Journal of Cell Science · doi:10.1242/jcs.060665 · Cited by 419 · see citing works

A guide to Ussing chamber studies of mouse intestine

Clarke, L. L. (2009) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.90649.2008 · Cited by 419 · see citing works

Multiple facets of intestinal permeability and epithelial handling of dietary antigens

Ménard, S., Cerf–Bensussan, N., & Heyman, M. (2010) · Mucosal Immunology · doi:10.1038/mi.2010.5 · Cited by 410 · see citing works

The density of small tight junction pores varies among cell types and is increased by expression of claudin-2

Itallie, C. M. V., Holmes, J. C., Bridges, A. S., Gookin, J. L., Coccaro, M. R., Proctor, W. R., Colegio, O. R., & Anderson, J. M. (2008) · Journal of Cell Science · doi:10.1242/jcs.021485 · Cited by 410 · see citing works

Roles of short-chain fatty acids receptors, GPR41 and GPR43 on colonic functions.

Tazoe, H., Otomo, Y., Kaji, I., Tanaka, R., Si, K., & Kuwahara, A. (2008) · PubMed · Cited by 406 · see citing works

Tyrosine phosphorylation and dissociation of occludin–ZO-1 and E-cadherin–β-catenin complexes from the cytoskeleton by oxidative stress

Rao, R., Basuroy, S., Rao, V. U., KARNAKY, K. J., & Gupta, A. K. (2002) · Biochemical Journal · doi:10.1042/bj20011804 · Cited by 402 · see citing works

Impedance-based cell monitoring: barrier properties and beyond

Benson, K., Cramer, S., & Galla, H. (2013) · Fluids and Barriers of the CNS · doi:10.1186/2045-8118-10-5 · Cited by 402 · see citing works

The capacity of nondigestible carbohydrates to stimulate fecal bifidobacteria in healthy humans: a double-blind, randomized, placebo-controlled, parallel-group, dose-response relation study

Bouhnik, Y., Raskine, L., Simoneau, G., Vicaut, É., Neut, C., Flourié, B., Brouns, F. J. P. H., & Bornet, F. R. J. (2004) · American Journal of Clinical Nutrition · doi:10.1093/ajcn/80.6.1658 · Cited by 402 · see citing works

Mechanisms of Disease: the role of intestinal barrier function in the pathogenesis of gastrointestinal autoimmune diseases

Fasano, A., & Shea-Donohue, T. (2005) · Nature Clinical Practice Gastroenterology &amp; Hepatology · doi:10.1038/ncpgasthep0259 · Cited by 399 · see citing works

Molecular mechanism of tumor necrosis factor-alpha modulation of intestinal epithelial tight junction barrier.

Ye, D., Ma, I., & Ma, T. (2006) · American Journal of Physiology - Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.00318.2005 · Cited by 395 · see citing works

Colon-specific delivery of a probiotic-derived soluble protein ameliorates intestinal inflammation in mice through an EGFR-dependent mechanism

Yan, F., Cao, H., Cover, T. L., Washington, M. K., Shi, Y., Liu, L., Chaturvedi, R., Peek, R. M., Wilson, K. T., & Polk, D. B. (2011) · Journal of Clinical Investigation · doi:10.1172/jci44031 · Cited by 376 · see citing works

Tumor necrosis factor-alpha (TNFα) regulates the epithelial barrier in the human intestinal cell line HT-29/B6

Schmitz, H., Fromm, M., Bentzel, C. J., Scholz, P., Detjen, K. M., Mankertz, J., Bode, H., Epple, H., Riecken, E., & Schulzke, J. (1999) · Journal of Cell Science · doi:10.1242/jcs.112.1.137 · Cited by 375 · see citing works

Intestinal microbiota and diet in IBS: causes, consequences, or epiphenomena?

Rajilić-Stojanović, M., Jonkers, D. M., Salonen, A., Hanevik, K., Raes, J., Jalanka, J., de Vos, W. M., Manichanh, C., Golic, N., Enck, P., et al. (2015) · American Journal of Gastroenterology · doi:10.1038/ajg.2014.427 · Cited by 359 · see citing works

Prebiotic carbohydrates modify the mucosa associated microflora of the human large bowel

Langlands, S. J. (2004) · Gut · doi:10.1136/gut.2003.037580 · Cited by 359 · see citing works

Physiological concentrations of short-chain fatty acids immediately suppress colonic epithelial permeability

Suzuki, T., Yoshida, S., & Hara, H. (2008) · British Journal Of Nutrition · doi:10.1017/s0007114508888733 · Cited by 356 · see citing works

The intestinal epithelial barrier in the control of homeostasis and immunity

Rescigno, M. (2011) · Trends in Immunology · doi:10.1016/j.it.2011.04.003 · Cited by 346 · see citing works

Intestinal permeability: functional assessment and significance

Travis, S. P. L., & Menzies, I. S. (1992) · Clinical Science · doi:10.1042/cs0820471 · Cited by 343 · see citing works

Transfer of extracellular vesicles during immune cell‐cell interactions

Gutiérrez‐Vázquez, C., Villarroya‐Beltri, C., Mittelbrunn, M., & Sánchez‐Madrid, F. (2012) · Immunological Reviews · doi:10.1111/imr.12013 · Cited by 325 · see citing works

Secretory IgA mediates retrotranscytosis of intact gliadin peptides via the transferrin receptor in celiac disease

Matysiak‐Budnik, T., Moura, I. C., Arcos‐Fajardo, M., Lebreton, C., Ménard, S., Candalh, C., Ben-Khalifa, K., Dugave, C., Tamouza, H., van Niel, G., et al. (2007) · The Journal of Experimental Medicine · doi:10.1084/jem.20071204 · Cited by 312 · see citing works

Quercetin Enhances Intestinal Barrier Function through the Assembly of Zonnula Occludens-2, Occludin, and Claudin-1 and the Expression of Claudin-4 in Caco-2 Cells

Suzuki, T., & Hara, H. (2009) · Journal of Nutrition · doi:10.3945/jn.108.100867 · Cited by 303 · see citing works

Dendritic Cells Shuttle Microbes Across Gut Epithelial Monolayers

Rescigno, M., Rotta, G., Valzasina, B., & Ricciardi-Castagnoli, P. (2001) · Immunobiology · doi:10.1078/0171-2985-00094 · Cited by 296 · see citing works

Modulating immune responses with probiotic bacteria

Matsuzaki, T., & Chin, J. (2000) · Immunology and Cell Biology · doi:10.1046/j.1440-1711.2000.00887.x · Cited by 292 · see citing works

Microbiota-dependent sequelae of acute infection compromise tissue-specific immunity

Fonseca, D. M. D., Hand, T. W., Han, S.-J., Gerner, M. Y., Zaretsky, A. G., Byrd, A. L., Harrison, O. J., Ortiz, A. M., Quinones, M., Trinchieri, G., et al. (2015) · Cell · doi:10.1016/j.cell.2015.08.030 · Cited by 281 · see citing works

Identification and Analysis of Multivalent Proteolytically Resistant Peptides from Gluten: Implications for Celiac Sprue

Shan, L., Qiao, S., Arentz–Hansen, H., Molberg, Ø., Gm, G., Sollid, L. M., & Khosla, C. (2005) · Journal of Proteome Research · doi:10.1021/pr050173t · Cited by 274 · see citing works

T84-Intestinal Epithelial Exosomes Bear MHC Class II/Peptide Complexes Potentiating Antigen Presentation by Dendritic Cells

Mallegol, J., van Niel, G., Lebreton, C., Lepelletier, Y., Candalh, C., Dugave, C., Heath, J. K., Raposo, G., Cerf–Bensussan, N., & Heyman, M. (2007) · Gastroenterology · doi:10.1053/j.gastro.2007.02.043 · Cited by 271 · see citing works

Intestinal Permeation and Gastrointestinal Disease

DeMeo, M. T., Mutlu, E., Keshavarzian, A., & Tobin, M. C. (2002) · Journal of Clinical Gastroenterology · doi:10.1097/00004836-200204000-00003 · Cited by 269 · see citing works

Ethanol modulation of intestinal epithelial tight junction barrier

Ma, T. Y., Nguyen, D., Bui, V., Nguyen, H. B., & Hoa, N. T. (1999) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.1999.276.4.g965 · Cited by 261 · see citing works

Oral oligofructose‐enriched inulin supplementation in acute ulcerative colitis is well tolerated and associated with lowered faecal calprotectin

Casellas, F., Borruel, N., Torrejón, A., Varela, E., Antolı́n, M., Guarner, F., & Malagelada, J. (2007) · Alimentary Pharmacology & Therapeutics · doi:10.1111/j.1365-2036.2007.03288.x · Cited by 260 · see citing works

Impairment of the Intestinal Barrier by Ethanol Involves Enteric Microflora and Mast Cell Activation in Rodents

Ferrier, L., Bérard, F., Debrauwer, L., Chabo, C., Langella, P., Bueno, L. P., & Fioramonti, J. (2006) · American Journal Of Pathology · doi:10.2353/ajpath.2006.050617 · Cited by 247 · see citing works

Molecular mechanisms for regulation of intestinal calcium absorption by vitamin D and other factors

Fleet, J. C., & Schoch, R. D. (2010) · Critical Reviews in Clinical Laboratory Sciences · doi:10.3109/10408363.2010.536429 · Cited by 242 · see citing works

Use of probiotics in gastrointestinal disorders: what to recommend?

Verna, E. C., & Lucak, S. L. (2010) · Therapeutic Advances in Gastroenterology · doi:10.1177/1756283x10373814 · Cited by 242 · see citing works

Tight Junctions, Intestinal Permeability, and Autoimmunity

Visser, J. T. J., Rozing, J., Sapone, A., Lammers, K. M., & Fasano, A. (2009) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2009.04037.x · Cited by 240 · see citing works

Dietary phenolic compounds: inhibition of Na+-dependent D-glucose uptake in rat intestinal brush border membrane vesicles.

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TNFα-induced and berberine-antagonized tight junction barrier impairment via tyrosine kinase, Akt and NFκB signaling

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Sodium Caprate Elicits Dilatations in Human Intestinal Tight Junctions and Enhances Drug Absorption by the Paracellular Route

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