Autocrine regulation of epithelial permeability by hypoxia: Role for polarized release of tumor necrosis factor α

The Pathophysiology of Tumor Necrosis Factors

VASSALLI, P. (1992) · Annual Review of Immunology · doi:10.1146/annurev.iy.10.040192.002211 · Cited by 1,874

The inducing role of tumor necrosis factor in the development of bactericidal granulomas during BCG infection

Kindler, V., Sappino, A., Grau, G. E., Piguet, P., & VASSALLI, P. (1989) · Cell · doi:10.1016/0092-8674(89)90676-4 · Cited by 1,239

A distinct array of proinflammatory cytokines is expressed in human colon epithelial cells in response to bacterial invasion.

Jung, H. C., Eckmann, L., Yang, S. K., Panja, A. B., Fierer, J., Morzycka-Wroblewska, E., & Kagnoff, M. F. (1995) · Journal of Clinical Investigation · doi:10.1172/jci117676 · Cited by 1,197

Thalidomide selectively inhibits tumor necrosis factor alpha production by stimulated human monocytes.

Sampaio, E. P., Sarno, E. N., Gallily, R., Cohn, Z. A., & Kaplan, G. (1991) · The Journal of Experimental Medicine · doi:10.1084/jem.173.3.699 · Cited by 1,191

Two populations of Ia-like molecules on a human B cell line.

Lampson, L. A., & Levy, R. (1980) · The Journal of Immunology · doi:10.4049/jimmunol.125.1.293 · Cited by 1,102

Thalidomide exerts its inhibitory action on tumor necrosis factor alpha by enhancing mRNA degradation.

Moreira, A. L., Sampaio, E. P., Zmuidzinas, A., Frindt, P., Smith, K. A., & Kaplan, G. (1993) · The Journal of Experimental Medicine · doi:10.1084/jem.177.6.1675 · Cited by 1,041

Characterization of receptors for human tumour necrosis factor and their regulation by γ-interferon

Aggarwal, B. B., Eessalu, T. E., & Hass, P. E. (1985) · Nature · doi:10.1038/318665a0 · Cited by 876

Tumour necrosis factor as immunomodulator and mediator of monocyte cytotoxicity induced by itself, γ-interferon and interleukin-1

Philip, R., & Epstein, L. B. (1986) · Nature · doi:10.1038/323086a0 · Cited by 762

Increased Intestinal Permeability in Patients with Crohn's Disease and Their Relatives

Hollander, D., Vadheim, C. M., Brettholz, E., Petersen, G. M., Delahunty, T., & Rotter, J. I. (1986) · Annals of Internal Medicine · doi:10.7326/0003-4819-105-6-883 · Cited by 762

Interferon-gamma directly affects barrier function of cultured intestinal epithelial monolayers.

Madara, J. L., & Stafford, J. (1989) · Journal of Clinical Investigation · doi:10.1172/jci113938 · Cited by 758

Intestinal barrier function and metabolic/liver diseases

Ghosh, S. S., Wang, J., Yannie, P. J., & Ghosh, S. (2020) · Liver Research · doi:10.1016/j.livres.2020.03.002 · Cited by 49

Hydroxylase-dependent regulation of the NF-κB pathway

Scholz, C. C., & Taylor, C. T. (2013) · Biological Chemistry · doi:10.1515/hsz-2012-0338 · Cited by 46

Alpha-1-antitrypsin Therapy Ameliorates Acute Colitis and Chronic Murine Ileitis

Collins, C. B., Aherne, C. M., Ehrentraut, S., Gerich, M. E., McNamee, E. N., McManus, M. C., Lebsack, M. D. P., Jedlicka, P., Azam, T., de Zoeten, E. F., et al. (2013) · Inflammatory Bowel Diseases · doi:10.1097/mib.0b013e31829292aa · Cited by 44

Antisense Oligonucleotides to poly(ADP-ribose) Polymerase-2 Ameliorate Colitis in Interleukin-10-Deficient Mice

Popoff, I., Jijon, H. B., Monia, B. P., Tavernini, M. M., Ma, M., McKay, R., & Madsen, K. L. (2002) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1124/jpet.102.039768 · Cited by 44

Therapeutic Targets for Hypoxia-Elicited Pathways

Taylor, C. T., & Colgan, S. P. (1999) · Pharmaceutical Research · doi:10.1023/a:1011936016833 · Cited by 44

Epithelial Barrier Regulation by Hypoxia-Inducible Factor

Glover, L. E., & Colgan, S. P. (2017) · Annals of the American Thoracic Society · doi:10.1513/annalsats.201608-610mg · Cited by 43

Hypoxia-inducible factor as a bridge between healthy barrier function, wound healing, and fibrosis

Steiner, C. A., Cartwright, I. M., Taylor, C. T., & Colgan, S. P. (2022) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00227.2022 · Cited by 45

Involvement of HIF-1α in MLCK-dependent Endothelial Barrier Dysfunction in Hypoxia

Qi, H., Wang, P., Liu, C., Li, M., Wang, S., Huang, Y., & Wang, F. (2011) · Cellular Physiology and Biochemistry · doi:10.1159/000327951 · Cited by 42

Tight Junctions and the Intestinal Barrier

Ma, T. Y., Nighot, P. K., & Al–Sadi, R. (2018) · Elsevier eBooks · doi:10.1016/b978-0-12-809954-4.00025-6 · Cited by 42

Hepatocellular transport and gastrointestinal absorption of lanthanum in chronic renal failure

Bervoets, A., Behets, G. J. S., Schryvers, D., Roels, F., Yang, Z., Verberckmoes, S. C., Damment, S. J. P., Dauwe, S. E. H., Mubiana, V. K., Blust, R., et al. (2008) · Kidney International · doi:10.1038/ki.2008.571 · Cited by 41

Bile canalicular barrier function and expression of tight-junctional molecules in rat hepatocytes during common bile duct ligation

Takakuwa, Y., Kokai, Y., Sasaki, K., Chiba, H., Tobioka, H., Mori, M., & Sawada, N. (2001) · Cell and Tissue Research · doi:10.1007/s00441-001-0489-4 · Cited by 41

Metabolic Stress Evokes Decreases in Epithelial Barrier Function

Lewis, K. J., & McKay, D. M. (2009) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2009.04036.x · Cited by 39

ABSENCE OF FUNCTIONAL PEROXISOME PROLIFERATOR-ACTIVATED RECEPTOR-α ENHANCED ILEUM PERMEABILITY DURING EXPERIMENTAL COLITIS

Mazzon, E., & Cuzzocrea, S. (2007) · Shock · doi:10.1097/shk.0b013e318033eb29 · Cited by 38

Bile Mediates Intestinal Pathology in Endotoxemia in Rats

Jackson, G. D. F., Dai, Y., & Sewell, W. A. (2000) · Infection and Immunity · doi:10.1128/iai.68.8.4714-4719.2000 · Cited by 38

Expression of cytokine and chemokine mRNA and secretion of tumor necrosis factor-α by gallbladder epithelial cells: Response to bacterial lipopolysaccharides

Savard, C. E., Blinman, T. A., Choi, H., Lee, S., Pandol, S. J., & Lee, S. P. (2002) · BMC Gastroenterology · doi:10.1186/1471-230x-2-23 · Cited by 38

Monocyte/macrophages evoke epithelial dysfunction: indirect role of tumor necrosis factor-α

Zareie, M., McKay, D. M., Kovarik, G. G., & Perdue, M. H. (1998) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.1998.275.4.c932 · Cited by 38

Cellular Stress Responses and Gut Microbiota in Inflammatory Bowel Disease

Cao, S. “. (2018) · Gastroenterology Research and Practice · doi:10.1155/2018/7192646 · Cited by 37

Airway surface liquid composition in mice

Cowley, E. A., Govindaraju, K., Guilbault, C., Radzioch, D., & Eidelman, D. H. (2000) · American Journal of Physiology-Lung Cellular and Molecular Physiology · doi:10.1152/ajplung.2000.278.6.l1213 · Cited by 37

REVIEW: Small Bowel Review: Normal Physiology Part 2

Thomson, A. B. R., Keelan, M., Thiesen, A., Clandinin, M. T., Ropeleski, M. J., & Wild, G. (2001) · Digestive Diseases and Sciences · doi:10.1023/a:1012746622735 · Cited by 36

Regulation of intestinal epithelial function: a link between opportunities for macromolecular drug delivery and inflammatory bowel disease

Siccardi, D., Turner, J. R., & Mrsny, R. J. (2004) · Advanced Drug Delivery Reviews · doi:10.1016/j.addr.2004.08.005 · Cited by 35

Adenosine A1 Receptors Promote Vasa Vasorum Endothelial Cell Barrier Integrity via Gi and Akt-Dependent Actin Cytoskeleton Remodeling

Umapathy, N. S., Kaczmarek, E., Fatteh, N., Burns, N., Lucas, R., Stenmark, K. R., Verin, A. D., & Gerasimovskaya, E. V. (2013) · PLoS ONE · doi:10.1371/journal.pone.0059733 · Cited by 32

Restoration of dysregulated intestinal barrier and inflammatory regulation through synergistically ameliorating hypoxia and scavenging reactive oxygen species using ceria nanozymes in ulcerative colitis

Zhang, Y., Lei, H., Wang, P., Zhou, Q., Yu, J., Leng, X., Ma, R., Wang, D., Dong, K., Xing, J., et al. (2023) · Biomaterials Research · doi:10.1186/s40824-023-00412-8 · Cited by 34

Differentiation of human colon tissue in culture: Effects of calcium on trans-epithelial electrical resistance and tissue cohesive properties

McClintock, S. D., Dame, M. K., Richter, A., Attili, D., Silvestri, S. S., Berner, M. M., Bohm, M. S., Karpoff, K., McCarthy, C. L., Spence, J. R., et al. (2020) · PLoS ONE · doi:10.1371/journal.pone.0222058 · Cited by 31

Exacerbation of DSS ‐induced colitis in mice lacking kinin B 1 receptors through compensatory up‐regulation of kinin B 2 receptors: the role of tight junctions and intestinal homeostasis

Marcon, R., Claudino, R., Dutra, R. C., Bento, A., Schmidt, E., Bouzon, Z., Sordi, R., Morais, R., Pesquero, J. B., & Calixto, J. Β. (2012) · British Journal of Pharmacology · doi:10.1111/j.1476-5381.2012.02136.x · Cited by 30

IFN-γ Attenuates Hypoxia-Inducible Factor (HIF) Activity in Intestinal Epithelial Cells through Transcriptional Repression of HIF-1β

Glover, L. E., Irizarry, K., Scully, M. M., Campbell, E. L., Bowers, B., Aherne, C. M., Kominsky, D. J., MacManus, C. F., & Colgan, S. P. (2011) · The Journal of Immunology · doi:10.4049/jimmunol.1001442 · Cited by 30

Tumour necrosis factor alpha potentiates ion secretion induced by histamine in a human intestinal epithelial cell line and in mouse colon: involvement of the phospholipase D pathway

Oprins, J. C. J. (2002) · Gut · doi:10.1136/gut.50.3.314 · Cited by 29

Modulation of hypoxia-inducible factor-1α/cyclo-oxygenase-2 pathway associated with attenuation of intestinal mucosa inflammatory damage by Acanthopanax senticosus polysaccharides in lipopolysaccharide-challenged piglets

Fan, C., Han, J., Liu, X., Zhang, F., Long, Y., & Xie, Q. (2019) · British Journal Of Nutrition · doi:10.1017/s0007114519001363 · Cited by 27

Does increased serum d-lactate mean subclinical hyperpermeability of intestinal barrier in middle-aged nonobese males with OSA?

Heizati, M., Li, N., Shao, L., Yao, X., Wang, Y., Hong, J., Zhou, L., Zhang, D., Chang, G., & Abulikemu, S. (2017) · Medicine · doi:10.1097/md.0000000000009144 · Cited by 27

Chemically mimicked hypoxia modulates gene expression and protein levels of the sodium calcium exchanger in HEK 293 cell line via HIF-1α

Hudecová, S., Lencesova, L., Csáderová, L., Sirová, M., Cholujová, D., & Cagala, M. (2011) · General Physiology and Biophysics · doi:10.4149/gpb_2011_02_196 · Cited by 26

The Pivotal Role of Tumor Necrosis Factor-?? in Signaling Apoptosis in Intestinal Epithelial Cells under Shock Conditions

Diebel, L. N., Liberati, D. M., Baylor, A. E., Brown, W. J., & Diglio, C. A. (2005) · The Journal of Trauma: Injury, Infection, and Critical Care · doi:10.1097/01.ta.0000162727.30897.c8 · Cited by 26

Immunological activities are modulated by enteral administration of an elemental diet in mice

Menezes, J. S., Andrade, M. C., Senra, B., Rodrigues, V. S., Vaz, N. M., & Faria, A. M. C. (2006) · Clinical Nutrition · doi:10.1016/j.clnu.2006.01.005 · Cited by 25

Regulation of intestinal epithelial gene expression in hypoxia

Taylor, C. T. (2004) · Kidney International · doi:10.1111/j.1523-1755.2004.761_12.x · Cited by 25

SUMOylation Attenuates Sensitivity toward Hypoxia- or Desferroxamine-Induced Injury by Modulating Adaptive Responses in Salivary Epithelial Cells

Nguyen, H., Chen, J.-L., Zhong, J., Kim, K., Crandall, E. D., Borok, Z., Chen, Y., & Ann, D. K. (2006) · American Journal Of Pathology · doi:10.2353/ajpath.2006.050782 · Cited by 24

Effects of Heat Shock and Hypoxia on Neonatal Neutrophil Lipopolysaccharide Responses: Altered Apoptosis, Toll-Like Receptor-4 and CD11b Expression Compared with Adults

Molloy, E. J., O’Neill, A., Doyle, B. T., Grantham, J. J., Taylor, C. T., Sheridan‐Pereira, M., Fitzpatrick, J. M., Webb, D. W., & Watson, R. W. G. (2006) · Neonatology · doi:10.1159/000091743 · Cited by 23

My gut feeling says rest: Increased intestinal permeability contributes to chronic diseases in high-intensity exercisers

Houten, J. M. V., Wessells, R. J., Lujan, H. L., & DiCarlo, S. E. (2015) · Medical Hypotheses · doi:10.1016/j.mehy.2015.09.018 · Cited by 23

Regulation of protein phosphatase 1γ activity in hypoxia through increased interaction with NIPP1: Implications for cellular metabolism

Comerford, K. M., Leonard, M. O., Cummins, E. P., Fitzgerald, K. T., Beullens, M., Bollen, M., & Taylor, C. T. (2006) · Journal of Cellular Physiology · doi:10.1002/jcp.20726 · Cited by 23

The Role of the Epithelial Barrier in Inflammatory Bowel Disease

Nieuwenhuis, E. E. S., & Blumberg, R. S. (2006) · Advances in experimental medicine and biology · doi:10.1007/0-387-33778-4_7 · Cited by 22

Activated endothelial cells elicit paracrine induction of epithelial chloride secretion. 6-Keto-PGF1alpha is an epithelial secretagogue.

Blume, E. D., Taylor, C. T., Lennon, P., Stahl, G. L., & Colgan, S. P. (1998) · Journal of Clinical Investigation · doi:10.1172/jci3465 · Cited by 22

Microvascular Effects of Oral Interleukin-6 on Ischemia/Reperfusion in the Murine Small Intestine

Rollwagen, F. M., Li, Y., Pacheco, N. D., Dick, E. J., & Kang, Y. (2000) · American Journal Of Pathology · doi:10.1016/s0002-9440(10)64987-5 · Cited by 22

Adrenomedullin improves intestinal epithelial barrier function by downregulating myosin light chain phosphorylation in ulcerative colitis rats

Yi, Z.-F., Fan, H., Liu, X., TANG, Q., ZUO, D., & Yang, J. (2015) · Molecular Medicine Reports · doi:10.3892/mmr.2015.3887 · Cited by 21

Hypoxic signal transduction in critical illness

Bertges, D. J., Fink, M. P., & Delude, R. L. (2000) · Critical Care Medicine · doi:10.1097/00003246-200004001-00009 · Cited by 21

Vagal afferent input from the acid-challenged rat stomach to the brainstem: Enhancement by interleukin-1β

Holzer, P. D., Danzer, M., Schicho, R., Samberger, C., Painsipp, E., & Lippe, I. T. (2004) · Neuroscience · doi:10.1016/j.neuroscience.2004.07.040 · Cited by 20

Intestinal Lymphoepithelial Communication

Shanahan, F. (1999) · Advances in experimental medicine and biology · doi:10.1007/978-1-4615-4143-1_1 · Cited by 20

Immunologically Mediated Transport of Ions and Macromolecules

Yu, L. C., & Perdue, M. H. (2000) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2000.tb05248.x · Cited by 20

Huangshui Polysaccharide Exerts Intestinal Barrier Protective Effects through the TLR4/MyD88/NF-κB and MAPK Signaling Pathways in Caco-2 Cells

Huo, J., Pei, W., Liu, G., Sun, W., Wu, J., Huang, M., Lü, W., Sun, J., & Sun, B. (2023) · Foods · doi:10.3390/foods12030450 · Cited by 19

Role of peroxisome proliferator-activated receptor-α in ileum tight junction alteration in mouse model of restraint stress

Mazzon, E., Crisafulli, C., Galuppo, M., & Cuzzocrea, S. (2009) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.00023.2009 · Cited by 19

Hypoxia Augments Cerebral Inflammation in a Dextran Sulfate Sodium-Induced Colitis Mouse Model

Han, Y., Ding, L., Cheng, X., Zhao, M., Zhao, T., Guo, L., Li, X., Geng, Y., Fan, M., Liao, H., et al. (2020) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2020.611764 · Cited by 18

A pea (Pisum sativum L.) seed albumin extract prevents colonic DSS induced dysbiosis in mice

Aranda‐Olmedo, I., Ruiz, R., Peinado, M. J., & Rubio, L. A. (2017) · Journal of Functional Foods · doi:10.1016/j.jff.2017.05.038 · Cited by 17

Artificial Digestion of Polydisperse Copper Oxide Nanoparticles: Investigation of Effects on the Human In Vitro Intestinal Co-Culture Model Caco-2/HT29-MTX

Büttner, J., Schneider, T. L., Westermann, M., & Glei, M. (2022) · Toxics · doi:10.3390/toxics10030130 · Cited by 16

Bacterial Infections in Acute on Chronic Liver Failure

Incicco, S., Angeli, P., & Piano, S. S. (2023) · Clinics in Liver Disease · doi:10.1016/j.cld.2023.03.013 · Cited by 16

The roles of migrasomes in immunity, barriers, and diseases

Cai, C., & Shen, J. (2024) · Acta Biomaterialia · doi:10.1016/j.actbio.2024.09.013 · Cited by 16

Small Bowel Review: Part II

Thomson, A., Keelan, M., Thiesen, A., Clandinin, M. T., Ropeleski, M., & Wild, G. (2001) · Canadian Journal of Gastroenterology · doi:10.1155/2001/949167 · Cited by 15

Intrarectal administration of oxygenated perfluorodecalin promotes healing of murine colitis by targeting inflammatory hypoxia

Hindryckx, P., Devisscher, L., Laukens, D., Venken, K., Peeters, H., & Vos, M. D. (2011) · Laboratory Investigation · doi:10.1038/labinvest.2011.102 · Cited by 14

A Dual Protective Effect of Intestinal Remote Ischemic Conditioning in a Rat Model of Total Hepatic Ischemia

Czigány, Z., Hata, K., Lai, W., Schwandt, T., Yamamoto, Y., Üemoto, S., & Tolba, R. H. (2019) · Journal of Clinical Medicine · doi:10.3390/jcm8101546 · Cited by 13

Expression of apoptosis-related proteins in rat with induced colitis

D’Argenio, G., Farrace, M. G., Cosenza, V., Ritis, F. D., Valle, N. D., Manguso, F., & Piacentini, M. (2004) · International Journal of Colorectal Disease · doi:10.1007/s00384-004-0585-5 · Cited by 13

Regulation of Hypoxia-Inducible Factor 1 in Enterocytic Cells

Bertges, D. J., Berg, S., Fink, M. P., & Delude, R. L. (2002) · Journal of Surgical Research · doi:10.1006/jsre.2002.6439 · Cited by 13

Targeting Hypoxia to Augment Mucosal Barrier Function

Kelly, C. J. (2012) · Journal of Epithelial Biology & Pharmacology · doi:10.2174/1875044301205010067 · Cited by 13

Parallel induction of epithelial surface-associated chemokine and proteoglycan by cellular hypoxia: implications for neutrophil activation

Furuta, G. T., Dzus, A. L., Taylor, C. T., & Colgan, S. P. (2000) · Journal of Leukocyte Biology · doi:10.1189/jlb.68.2.251 · Cited by 12

Endothelial and Epithelial Barriers in Graft-Versus-Host Disease

Nalle, S. C., & Turner, J. R. (2013) · Advances in experimental medicine and biology · doi:10.1007/978-1-4614-4711-5_5 · Cited by 10

No Static at All

Graham, W. V., Marchiando, A. M., Shen, L., & Turner, J. R. (2009) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2009.04050.x · Cited by 10

Role of tight junctions in the occurrence of cancer invasion and metastasis

Mori, M., Sawada, N., Kokai, Y., & Satoh, M. (1999) · Medical Molecular Morphology · doi:10.1007/pl00021461 · Cited by 10

Nutritional stimulation of the autonomic nervous system

Luyer, M. D. P. (2011) · World Journal of Gastroenterology · doi:10.3748/wjg.v17.i34.3859 · Cited by 10

Hyperosmotic Stress Induces the Expression of Organic Osmolyte Transporters in Porcine Intestinal Cells and Betaine Exerts a Protective Effect on the Barrier Function

Angelis, E. D., Borghetti, P., Passeri, B., Cavalli, V., Ferrari, L., Andrani, M., Martelli, P. R., & Saleri, R. (2024) · Biomedicines · doi:10.3390/biomedicines12102391 · Cited by 9

Hypoxia/Reoxygenation Effects on Ion Transport across Rat Colonic Epithelium

Schindele, S., Pouokam, E., & Diener, M. (2016) · Frontiers in Physiology · doi:10.3389/fphys.2016.00247 · Cited by 9

Induction of Nitric Oxide Synthase and Subsequent Production of Nitric Oxide Not Involved in Interferon-γ-induced Hyperpermeability of Caco-2 Intestinal Epithelial Monolayers

SATAKE, M., Watanabe, H., Miyamoto, Y., & Shimizu, M. (2001) · Bioscience Biotechnology and Biochemistry · doi:10.1271/bbb.65.428 · Cited by 9

Microbiota, immunity and immunologically-mediated diseases

Hogenová, H. T., Zakostelska, Z. J., Petanová, J., & Kverka, M. (2019) · Vnitřní lékařství · doi:10.36290/vnl.2019.022 · Cited by 8

Cholera Toxin Potentiates Influences of IFN-γ Through Activation of NF-κB and Release of Tumor Necrosis Factor-α

Blumberg, R. S., Pitman, R. S., Taylor, C. T., & Colgan, S. P. (2005) · Journal of Interferon & Cytokine Research · doi:10.1089/jir.2005.25.209 · Cited by 8

Suppression of NF-κB/p65 Inhibits the Proliferation in Oral Squamous Cancer Cells

Anbo, N., Ogi, K., Sogabe, Y., Shimanishi, M., Kaneko, T., Dehari, H., Miyazaki, A., & Hiratsuka, H. (2013) · Journal of Cancer Therapy · doi:10.4236/jct.2013.44100 · Cited by 6

Cytokines and Epithelial Function

Colgan, S. P., Furuta, G. T., & Taylor, C. T. (2014) · ASM Press eBooks · doi:10.1128/9781555817848.ch4 · Cited by 6

Epithelia and Gastrointestinal Function

Turner, J. R. (2015) · Wiley eBooks · doi:10.1002/9781118512074.ch18 · Cited by 6

Boosting the hypoxia-induced adaptive response in inflammatory bowel disease: A novel concept of treatment

Hindryckx, P., Laukens, D., & Vos, M. D. (2010) · Inflammatory Bowel Diseases · doi:10.1002/ibd.21589 · Cited by 5

Bioelectric, tissue, and molecular characteristics of the gastric mucosa at different times of ischemia

Peña-Mercado, E., Mario, G.-L., Patiño-Morales, C. C., Montecillo-Aguado, M. R., Sara, H.-Y., & Beltran-Vargas, N. E. (2021) · Experimental Biology and Medicine · doi:10.1177/15353702211021601 · Cited by 5

Preclinical Study of DCD and Normothermic Perfusion for Visceral Transplantation

Serradilla, J. J., Moreno, A. M. A., Talayero, P., Burgos, P., Machuca, M., Ortega, O. C., Vallejo, M. T., Bolívar, F. J. R., Bueno, A., Sánchez, A., et al. (2023) · Transplant International · doi:10.3389/ti.2023.11518 · Cited by 3

Identification of Cyclic AMP Response Element-Binding Protein-Dependent Transcriptional Responses in Hypoxia by Microarray Analysis

Leonard, M. O., O'Reilly, S., Comerford, K. M., & Taylor, C. T. (2004) · Methods in enzymology on CD-ROM/Methods in enzymology · doi:10.1016/s0076-6879(04)81033-4 · Cited by 3

Inflammation and inflammatory bowel disease

Mathew, C. G. (2005) · Encyclopedia of Genetics, Genomics, Proteomics and Bioinformatics · doi:10.1002/047001153x.g105316 · Cited by 3

Modulation of Intestinal Disorders by Claudin-2 and Occludin Via Canonical and Noncanonical Mechanisms

Sweat, Y. Y., Abtahi, S., Chánez-Paredes, S. D., Raju, P., Zuo, L., Shashikanth, N., Kuo, W., & Turner, J. R. (2022) · Springer eBooks · doi:10.1007/978-3-030-97204-2_5 · Cited by 2

The Effects of Chronic Hypoxia on Inflammation and Pulmonary Vascular Function

Stenmark, K. R., Pugliese, S. C., Poth, J. M., Frid, M. G., Gerasimovskaya, E. V., Nozik‐Grayck, E., & Kasmi, K. C. E. (2015) · Springer eBooks · doi:10.1007/978-3-319-23594-3_5 · Cited by 1

The Actions of Ursodeoxycholic Acid and its derivatives on Colonic Epithelial Transport and Barrier Function

Kelly, O. (2014) · Figshare · doi:10.25419/rcsi.10807235

Interplay between Pathogenic and Immune Regulatory Mechanisms in G-alpha-i2 deficient colitis

Götlind, Y.-Y. C. (2011) · Gothenburg University Publications Electronic Archive (Gothenburg University)

Small intestinal pathology

Okolo, C. N., & Surawicz, C. M. (1999) · Current Opinion in Gastroenterology · doi:10.1097/00001574-199903000-00009

TESIS PARA OPTAR AL GRADO DE DOCTOR DE

de Medicina, D., & de Medicina, F. (2015)

HANS H. USSING DISTINGUISHED LECTURESHIP OF THE EPITHELIAL TRANSPORT GROUP, 2015

Ussing, B., Herrmann, J. R., & Turner, J. R. (2016)

Butyrate and the colonic epithelial barrier: prevention of bacterial transcytosis

Lewis, K. J. (2009) · Libraries and Cultural Resources (University of Calgary) · doi:10.11575/prism/16948

Colonic Ischemia

Karhausen, J., & Taylor, C. T. (2004) · Encyclopedia of Gastroenterology · doi:10.1016/b0-12-386860-2/00149-0

Additional file 1 of Restoration of dysregulated intestinal barrier and inflammatory regulation through synergistically ameliorating hypoxia and scavenging reactive oxygen species using ceria nanozymes in ulcerative colitis

Zhang, Y., Lei, H., Wang, P., Zhou, Q., Yu, J., Leng, X., Ma, R., Wang, D., Dong, K., Xing, J., et al. (2023) · Figshare · doi:10.6084/m9.figshare.23803085

Réponses cellulaires du système adénosinergique à la dysoxie

Bruzzese, L. (2015) · theses.fr (ABES) · doi:10.70675/e916fde4zdb3fz48f1z8a4bz90efc70e27af

Nouveaux aspects dans la prise en charge de la cirrhose

Weil, D. (2019) · theses.fr (ABES) · doi:10.70675/4a4d8249z67c4z42e5zad08zc3d08f49b5d2

E-cadherin acts as a dynamic switch in epithelial regeneration in inflammatory bowel disease

Girma, B., Ayansola, H., Chen, J., Kim, J., Miko, C., Gruskin, Z. L., & Jin, Y. (2026) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.00044.2026

98/04300 A multi-product cogeneration system using combined coal gasification and combustion

(1998) · Fuel and Energy Abstracts · doi:10.1016/s0140-6701(98)94295-3 · Cited by 1

98/04295 Measurement of corrosion damage in coal-fired combined cycle power systems

(1998) · Fuel and Energy Abstracts · doi:10.1016/s0140-6701(98)94290-4 · Cited by 1

98/04294 Mass transfer influences on the design of selective catalytic reduction (SCR) monolithic reactors

(1998) · Fuel and Energy Abstracts · doi:10.1016/s0140-6701(98)94289-8 · Cited by 1

Effect of interferon-gamma on intestinal barrier function of epithelial cells under hypoxia

Liang, H., Wang, W., Yang, Y., Sun, L., & Yang, H. (2012) · Zhonghua shiyan waike zazhi · doi:10.3760/cma.j.issn.1001-9030.2012.05.041

Regulation of Hypoxia Inducible Factor in Intestinal Epithelial Cells in Inflammation

Irizarry, K., Glover, L. E., & Colgan, S. P. (2008) · The FASEB Journal · doi:10.1096/fasebj.22.1_supplement.328.11