Relevant bibliographies by topics / Claudin-5

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  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers

Academic literature on the topic 'Claudin-5'

Author: Grafiati
Published: 4 June 2021
Last updated: 6 February 2022

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Journal articles on the topic "Claudin-5"

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Kiuchi-Saishin, Yumiko, Shimpei Gotoh, Mikio Furuse, Akiko Takasuga, Yasuo Tano, and Shoichiro Tsukita. "Differential Expression Patterns of Claudins, Tight Junction Membrane Proteins, in Mouse Nephron Segments." Journal of the American Society of Nephrology 13, no. 4 (2002): 875–86. http://dx.doi.org/10.1681/asn.v134875.

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ABSTRACT. As the first step in understanding the physiologic functions of claudins (tight junction integral membrane proteins) in nephrons, the expression of claudin-1 to -16 in mouse kidneys was examined by Northern blotting. Among these claudins, only claudin-6, -9, -13, and -14 were not detectable. Claudin-5 and -15 were detected only in endothelial cells. Polyclonal antibodies specific for claudin-7 and -12 were not available. Therefore, the distributions of claudin-1, -2, -3, -4, -8, -10, -11, and -16 in nephron segments were examined with immunofluorescence microscopy. For identification
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Jakab, Csaba, Judit Halász, Attila Szász, et al. "Expression and localisation of claudin-1,-2,-3,-4,-5,-7 and-10 proteins in the normal canine mammary gland." Acta Veterinaria Hungarica 56, no. 3 (2008): 341–52. http://dx.doi.org/10.1556/avet.56.2008.3.8.

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The recently identified claudins are dominant components of tight junctions, responsible for cell adhesion, polarity and paracellular permeability. Certain claudins have been shown to have relevance in tumour development. The aim of the present study was to analyse the expression of claudin-1,-2,-3,-4,-5,-7 and-10 in normal canine mammary glands. Samples from the inguinal mammary regions of 20 non-castrated, 1–13 years old female dogs were studied. Immunohistochemical analysis was performed on conventional specimens and tissue microarrays. The results of the immunohistochemical reactions detec
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Markov, Alexander G., Arina A. Fedorova, Violetta V. Kravtsova, et al. "Circulating Ouabain Modulates Expression of Claudins in Rat Intestine and Cerebral Blood Vessels." International Journal of Molecular Sciences 21, no. 14 (2020): 5067. http://dx.doi.org/10.3390/ijms21145067.

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The ability of exogenous low ouabain concentrations to affect claudin expression and therefore epithelial barrier properties was demonstrated previously in cultured cell studies. We hypothesized that chronic elevation of circulating ouabain in vivo can affect the expression of claudins and tight junction permeability in different tissues. We tested this hypothesis in rats intraperitoneally injected with ouabain (1 μg/kg) for 4 days. Rat jejunum, colon and brain frontal lobes, which are variable in the expressed claudins and tight junction permeability, were examined. Moreover, the porcine jeju
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Ahn, C., D. Lee, and E. B. Jeung. "216 HORMONAL REGULATION OF CLAUDIN-4 TIGHT JUNCTION MOLECULE IN MOUSE PLACENTA." Reproduction, Fertility and Development 27, no. 1 (2015): 198. http://dx.doi.org/10.1071/rdv27n1ab216.

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Tight junctions (TJ) are composed of a branching network of sealing strands. TJ regulate paracellular conductance and ionic selectivity. TJ components include the peripheral protein ZO-1, junctional adhesion molecules (JAM) and the integral proteins such as occludin and claudin. Claudins are a family of proteins that are the most important components in the tight junctions. The established paracellular transport barriers that control transportation of molecules within intercellular space. The present study focused on the expression of claudin, suggesting as major working molecules in the parac
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Daugherty, Brandy L., Madalina Mateescu, Anand S. Patel, et al. "Developmental regulation of claudin localization by fetal alveolar epithelial cells." American Journal of Physiology-Lung Cellular and Molecular Physiology 287, no. 6 (2004): L1266—L1273. http://dx.doi.org/10.1152/ajplung.00423.2003.

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Tight junction proteins in the claudin family regulate epithelial barrier function. We examined claudin expression by human fetal lung (HFL) alveolar epithelial cells cultured in medium containing dexamethasone, 8-bromo-cAMP, and isobutylmethylxanthanine (DCI), which promotes alveolar epithelial cell differentiation to a type II phenotype. At the protein level, HFL cells expressed claudin-1, claudin-3, claudin-4, claudin-5, claudin-7, and claudin-18, where levels of expression varied with culture conditions. DCI-treated differentiated HFL cells cultured on permeable supports formed tight trans
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Chen, Stephen P., Beiyun Zhou, Brigham C. Willis, et al. "Effects of transdifferentiation and EGF on claudin isoform expression in alveolar epithelial cells." Journal of Applied Physiology 98, no. 1 (2005): 322–28. http://dx.doi.org/10.1152/japplphysiol.00681.2004.

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Rat alveolar epithelial type II cells grown on polycarbonate filters form high-resistance monolayers and concurrently acquire many phenotypic properties of type I cells. Treatment with EGF has previously been shown to increase transepithelial resistance across alveolar epithelial cell (AEC) monolayers. We investigated changes in claudin expression in primary cultured AEC during transdifferentiation to the type I cell-like phenotype ( days 0, 1, and 8), and on day 5 in culture ± EGF (10 ng/ml) from day 0 or day 4. Claudins 4 and 7 were increased, whereas claudins 3 and 5 were decreased, on late
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Ohta, Hiromitsu, Shigeki Chiba, Masahito Ebina, Mikio Furuse, and Toshihiro Nukiwa. "Altered expression of tight junction molecules in alveolar septa in lung injury and fibrosis." American Journal of Physiology-Lung Cellular and Molecular Physiology 302, no. 2 (2012): L193—L205. http://dx.doi.org/10.1152/ajplung.00349.2010.

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The dysfunction of alveolar barriers is a critical factor in the development of lung injury and subsequent fibrosis, but the underlying molecular mechanisms remain poorly understood. To clarify the pathogenic roles of tight junctions in lung injury and fibrosis, we examined the altered expression of claudins, the major components of tight junctions, in the lungs of disease models with pulmonary fibrosis. Among the 24 known claudins, claudin-1, claudin-3, claudin-4, claudin-7, and claudin-10 were identified as components of airway tight junctions. Claudin-5 and claudin-18 were identified as com
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András, Ibolya E., Hong Pu, Jing Tian, et al. "Signaling Mechanisms of HIV-1 Tat-Induced Alterations of Claudin-5 Expression in Brain Endothelial Cells." Journal of Cerebral Blood Flow & Metabolism 25, no. 9 (2005): 1159–70. http://dx.doi.org/10.1038/sj.jcbfm.9600115.

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Exposure of brain microvascular endothelial cells (BMEC) to human immunodeficiency virus-1 (HIV-1) Tat protein can decrease expression and change distribution of tight junction proteins, including claudin-5. Owing to the importance of claudin-5 in maintaining the blood–brain barrier (BBB) integrity, the present study focused on the regulatory mechanisms of Tat-induced alterations of claudin-5 mRNA and protein levels. Real-time reverse-transcription-polymerase chain reaction revealed that claudin-5 mRNA was markedly diminished in BMEC exposed to Tat. However, U0126 (an inhibitor of mitogen-acti
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Abuazza, Ghazala, Amy Becker, Scott S. Williams, et al. "Claudins 6, 9, and 13 are developmentally expressed renal tight junction proteins." American Journal of Physiology-Renal Physiology 291, no. 6 (2006): F1132—F1141. http://dx.doi.org/10.1152/ajprenal.00063.2006.

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The adult proximal tubule is a low-resistance epithelium where there are high rates of both active transcellular and passive paracellular NaCl transport. We have previously demonstrated that the neonatal rabbit and rat proximal tubule have substantively different passive paracellular transport properties than the adult proximal tubule, which results in a maturational change in the paracellular passive flux of ions. Neonatal proximal tubules have a higher PNa/PCl ratio and lower chloride and bicarbonate permeabilities than adult proximal tubules. Claudins are a large family of proteins which ar
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Ahn, C., J. S. Lee, and E. B. Jeung. "128 EXPRESSIONS OF MOUSE TIGHT JUNCTION MOLECULES IN PLACENTA – CLAUDINS AND OTHER PARACELLULAR TRANSPORT MOLECULES." Reproduction, Fertility and Development 26, no. 1 (2014): 178. http://dx.doi.org/10.1071/rdv26n1ab128.

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Tight junctions (TJ) are composed of a branching network of sealing strands. Tight junctions regulate paracellular conductance and ionic selectivity. The TJ components include the peripheral protein ZO-1, junctional adhesion molecules (JAM), and integral proteins, such as occludin and claudin. Claudins, a family of proteins, are the most important components in TJ. They establish paracellular transport barriers, which control transportation of molecules within intercellular space. The current study focused on expression of claudin, suggesting claudin as a major working molecule in the paracell
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Dissertations / Theses on the topic "Claudin-5"

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Zhang, Bo. "The Role of Claudin-5 on Xenopus Heart Development." NCSU, 2008. http://www.lib.ncsu.edu/theses/available/etd-12172008-131757/.

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Claudin-5 is an important member of the claudin gene family. The expression of claudin-5 in the heart of Xenopus laevis was determined by whole mount in situ hybridization. RNA over expression and knock down experiments demonstrated that claudin-5 is critical for heart development. Meanwhile, claudin-5 down regulated bone morphogenetic protein 4 (BMP4) expression in early stage through upregulating chordin (chd). In addition, other pathways such as estrogen hormone and transforming growth factor-β (TGF-β) may also affect claudin-5 activity. The results show that claudin-5 plays an important
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Escudero-Esparza, Astrid. "Role of Claudin-5 in the progression of human breast cancer." Thesis, Cardiff University, 2010. http://orca.cf.ac.uk/55020/.

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A key step in metastasis is the interaction and penetration of the vascular endothelium by cancer cells. Tight Junctions (TJ) are located between the cancer epithelial cells themselves functioning in an adhesive manner, and between the endothelial cells. They represent a critical barrier which the cancer cells must overcome in order to penetrate and initiate metastasis. The Claudin family are TJ proteins expressed in both endothelial and epithelial cells. They participate in the formation of tissue barriers between different tissue compartments by regulating the efflux of molecules through TJ
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Nitta, Takehiro. "Size-selective loosening of the blood-brain barrier in claudin-5-deficient mice." Kyoto University, 2004. http://hdl.handle.net/2433/148267.

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Tscheik, Christian [Verfasser]. "Transiente Öffnung der Blut-Hirnschranke für kleine Moleküle durch Claudin-5-Modulatoren / Christian Tscheik." Berlin : Freie Universität Berlin, 2015. http://d-nb.info/1077768273/34.

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Kondo, Nobuyuki. "Thrombin induces rapid disassembly of claudin-5 from the tight junction of endothelial cells." Kyoto University, 2010. http://hdl.handle.net/2433/120612.

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Sanford, Jamie Lynn. "Analysis of the cell junction proteins CASK and claudin-5 in skeletal and cardiac muscle." Connect to this title online, 2005. http://rave.ohiolink.edu/etdc/view?acc%5Fnum=osu1117553681.

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Thesis (Ph. D.)--Ohio State University, 2005.<br>Title from first page of PDF file. Document formatted into pages; contains xv, 188 p.; also includes graphics (some col.) Includes bibliographical references (p. 166-188). Available online via OhioLINK's ETD Center
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Röhrs, Lena [Verfasser]. "Untersuchungen der Blut-Hoden-Schranke während der Rekrudeszenz der Spermatogenese nach Downregulation mittels eines slow release GnRH-Implantates beim Rüden : Expression von Connexin 43, Occludin, Claudin-3, -5 und -11 / Lena Röhrs." Gießen : Universitätsbibliothek, 2014. http://d-nb.info/1068275855/34.

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Scheffer, David [Verfasser], Carola [Gutachter] Förster, Srikanth [Gutachter] Karnati, and Philip [Gutachter] Tovote. "Einfluss einer Dexamethason/Bortezomib-Kombinationstherapie auf den Glukokortikoidrezeptor und die Tight Junction-Moleküle Claudin-5 und Occludin in Endothelzellen der Blut-Hirn-Schranke in experimentellen Modellen des Schädel-Hirn-Traumas / David Scheffer ; Gutachter: Carola Förster, Srikanth Karnati, Philip Tovote." Würzburg : Universität Würzburg, 2020. http://d-nb.info/1223851362/34.

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Zaniboni, Mariana Colombini. "Estudo da expressão de filagrina e claudinas 1 e 4 em indivíduos adultos com dermatite atópica." Universidade de São Paulo, 2015. http://www.teses.usp.br/teses/disponiveis/5/5133/tde-11082015-160618/.

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Introdução: A dermatite atópica (DA) é uma doença cutânea inflamatória crônica que cursa em surtos. Possui manifestação clínica variável, mas o prurido e a xerose são características frequentes, e pode estar associada a outras manifestações extra-cutâneas de atopia. Pacientes com DA apresentam maior risco de infecções por bactérias e vírus, destacando-se a erupção variceliforme de Kaposi, causada por herpes simples. A DA mostra-se como exemplo de dermatose com comprometimento da barreira cutânea, aliado a disfunção imunológica. São descritas alterações das proteínas da barreira cutânea na DA (
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Drujont, Lucile. "Étude de nouveaux acteurs de l'immunité de type 17 à travers l'exploration du rôle des canaux ioniques TMEM176A et B dans les cellules RORγt+". Nantes, 2016. https://archive.bu.univ-nantes.fr/pollux/show/show?id=36471303-ef4e-453c-94a1-59fb808e17a9.

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Le récepteur nucléaire d'hormone RORγt est un facteur de transcription clé qui orchestre la différenciation des cellules Th17 mais aussi définit les cellules TγƠ17 et les Cellules Lymphoïdes Innées du groupe 3 (ILC3s). Notre avons identifié TMEM176B, une protéine à quatre domaines transmembranaires qui interagit avec son homologue TMEM176A de structure identique. Des expériences d'électrophysiologie ont révélé que TMEM176A et B fonctionnent comme des canaux ioniques et peuvent s'hétérodimériser. Ces deux homologues font partie des rares cibles directes de RORγt. Nous avons prouvé que ces deux
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Books on the topic "Claudin-5"

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Blyton, Enid. Claudine at St. Clare's. Egmont, 2005.

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Blyton, Enid. Claudine at St. Clare's. Egmont, 1996.

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Tamar, Erika. YOU CANT CHOOSE YOUR FAMILY PARTY OF FIVE CLAUDIA 5 (Party of 5). Aladdin, 1997.

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Mostow, Debra. TOO COOL FOR SCHOOL PARTY OF FIVE CLAUDIA 2 (Party of 5). Aladdin, 1997.

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Speregen, Devra Newberger. The TROUBLE WITH GUYS PARTY OF FIVE CLAUDIA 6 (Party of 5). Aladdin, 1997.

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Momigliano, Arnaldo, Theodore John Cadoux, and Ernst Badian. Claudius Marcellus (5), Marcus, nephew of Augustus, 42–23 bce. Oxford University Press, 2016. http://dx.doi.org/10.1093/acrefore/9780199381135.013.1632.

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Suetonius. The Lives Of The Twelve Caesars, Volume 4 & 5: Caligula & Claudius. IndyPublish, 2006.

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Suetonius. The Lives Of The Twelve Caesars, Volume 4 & 5: Caligula & Claudius. IndyPublish, 2006.

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Boldo (Peumus boldus Mol.) Avances en la investigación para el desarrollo de modelos productivos sustentables. INFOR : FIA, 2018. http://dx.doi.org/10.52904/20.500.12220/27297.

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Capítulo 1. Antecedentes Generales. Benedetti, Susana; Morales, Carolina y Soto, Daniel -- Capítulo 2. Caracterización de las Formaciones Naturales. Benedetti, Susana y Morales, Carolina -- Capítulo 3. Caracterización de los Compuestos Activos de Boldo. Benedetti, Susana -- Capítulo 4. Evaluación de Diversidad Genética y Búsqueda de Marcadores Moleculares Asociados a la Producción de Metabolitos en Genotipos Seleccionados de Boldo. Hasbun, Rodrigo; González, Jorge; Benedetti, Susana y Molina María Paz -- Capítulo 5. Producción de Plantas y Propagación de Boldo. García, Edison y González, Marta
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Stillufsen, Heather. Claudia You're on Your Way to an Amazing Future: Day Planner - Personalized Notebook with Your Girls' Name - First Name Notebook Journals to Write in for Women, Diary for Girls - Birthday, Best Friend, Mom, Dad, Office Gift - 8. 5 X11. Independently Published, 2020.

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Book chapters on the topic "Claudin-5"

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Coutinho-Camillo, Cláudia Malheiros, Silvia Vanessa Lourenço, and Fernando Augusto Soares. "Claudin-5 and Cancer Metastasis." In Cancer Metastasis - Biology and Treatment. Springer Netherlands, 2013. http://dx.doi.org/10.1007/978-94-007-6028-8_11.

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Stamatovic, Svetlana M., Richard F. Keep, and Anuska V. Andjelkovic. "Tracing the Endocytosis of Claudin-5 in Brain Endothelial Cells." In Methods in Molecular Biology. Humana Press, 2011. http://dx.doi.org/10.1007/978-1-61779-185-7_22.

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Cooper, Itzik, Katayun Cohen-Kashi-Malina, and Vivian I. Teichberg. "Claudin-5 Expression in In Vitro Models of the Blood–Brain Barrier." In Methods in Molecular Biology. Humana Press, 2011. http://dx.doi.org/10.1007/978-1-61779-185-7_25.

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András, Ibolya E., and Michal Toborek. "HIV-1-Induced Alterations of Claudin-5 Expression at the Blood–Brain Barrier Level." In Methods in Molecular Biology. Humana Press, 2011. http://dx.doi.org/10.1007/978-1-61779-185-7_26.

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Yang, Yi, and Gary A. Rosenberg. "MMP-Mediated Disruption of Claudin-5 in the Blood–Brain Barrier of Rat Brain After Cerebral Ischemia." In Methods in Molecular Biology. Humana Press, 2011. http://dx.doi.org/10.1007/978-1-61779-185-7_24.

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Isacke, Clare M., and Michael A. Horton. "Claudin-5." In The Adhesion Molecule FactsBook. Elsevier, 2000. http://dx.doi.org/10.1016/b978-012356505-1/50098-8.

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Patricia Rendón-Huerta, Erika, Carlos Abraham García-García, and Luis Felipe Montaño Estrada. "Effect of Helicobacter pylori on Tight Junctions in Gastric Epithelia." In Helicobacter pylori - From First Isolation to 2020 [Working Title]. IntechOpen, 2021. http://dx.doi.org/10.5772/intechopen.96607.

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Molecular complexes grouped under the names of tight, adherent or gap junction regulate the flow of water, ions and macromolecules through epithelium paracellular spaces. The main constituents of tight junctions are claudins, a family of 26 different proteins whose expression and distribution are tissue specific but varies in tumors. A change in claudin 1, 3, 4, 5, 6, 7, 9 and 18 expression, that contributes to lose epithelial cohesion, has been associated to enhanced cell proliferation, migration, and invasiveness in gastric neoplastic tissue. Chronic inflammation process induced by H. pylori infection, a major risk factor for gastric cancer development, disrupts tight junctions via CagA gene, Cag pathogenicity island, and VacA, but the effect upon the epithelial barrier of H. pylori lipopolysaccharides or H. pylori-induced up-regulation of mTOR and ERK signaling pathways by microRNA-100 establishes new concepts of proof.
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Armstrong, Tyler D., Usa Suwannasual, Conner L. Kennedy, et al. "Exposure to Traffic-Generated Pollutants Exacerbates the Expression of Factors Associated with the Pathophysiology of Alzheimer’s Disease in Aged C57BL/6 Wild-Type Mice." In Advances in Alzheimer’s Disease. IOS Press, 2021. http://dx.doi.org/10.3233/aiad210017.

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Background: Multiple studies report a strong correlation between traffic-generated air pollution-exposure and detrimental outcomes in the central nervous system (CNS), including Alzheimer’s disease (AD). Incidence of AD is rapidly increasing and, worldwide, many live in regions where pollutants exceed regulatory standards. Thus, it is imperative to identify environmental pollutants that contribute to AD, and the mechanisms involved. Objective: We investigated the effects of mixed gasoline and diesel engine emissions (MVE) on the expression of factors involved in progression of AD in the hippocampus and cerebrum in a young versus aged mouse model. Methods: Young (2 months old) and aged (18 months old) male C57BL/6 mice were exposed to either MVE (300 μg/m3 PM) or filtered air (FA) for 6 h/d, 7 d/wk, for 50 d. Immunofluorescence and RT-qPCR were used to quantify oxidative stress (8-OHdG) and expression of amyloid-β protein precursor (AβPP), β secretase (BACE1), amyloid-β (Aβ), aryl hydrocarbon receptor (AhR), cytochrome P450 (CYP) 1B1, angiotensin-converting enzyme (ACE1), and angiotensin II type 1 (AT1) receptor in the cerebrum and hippocampus, in addition to cerebral microvascular tight junction (TJ) protein expression. Results: We observed age-related increases in oxidative stress, AhR, CYP1B1, Aβ, BACE1, and AT1 receptor in the CA1 region of the hippocampus, and elevation of cerebral AβPP, AhR, and CYP1B1 mRNA, associated with decreased cerebral microvascular TJ protein claudin-5. MVE-exposure resulted in further promotion of oxidative stress, and significant increases in AhR, CYP1B1, BACE1, ACE1, and Aβ, compared to the young and aged FA-exposed mice. Conclusion: Such findings suggest that MVE-exposure exacerbates the expression of factors in the CNS associated with AD pathogenesis in aged populations.
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"5. Typologie der praefationes Claudians." In Claudians praefationes. B. G. Teubner, 1999. http://dx.doi.org/10.1515/9783110961249.187.

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"Production Notice." In Terence: Phormio, edited by Robert Maltby. Liverpool University Press, 2012. http://dx.doi.org/10.3828/liverpool/9780856686061.003.1008.

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Here begins Terence’s Phormio; performed at the Roman Games during the curule aedileship of Lucius Postumius Albinus and Lucius Cornelius Merula; produced by Lucius Ambivius Turpio and Lucius Atilius of Praeneste; music composed by Flaccus, slave of Claudius, for unequal pipes throughout; (5) Greek original ...
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Conference papers on the topic "Claudin-5"

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Bulgarelli, Adriana, Silvia V. Lourenço, Cláudia M. Coutinho-Camillo, et al. "Abstract 5009: The expression pattern of claudin-1, claudin-3, claudin-4, claudin-5 and claudin-7 in penile squamous cell carcinoma." In Proceedings: AACR 102nd Annual Meeting 2011‐‐ Apr 2‐6, 2011; Orlando, FL. American Association for Cancer Research, 2011. http://dx.doi.org/10.1158/1538-7445.am2011-5009.

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Jang, An_Soo, Vincent J. Concel, Kiflai Bein, et al. "Endothelial Dysfunction And Claudin 5 Regulation During Acrolein-induced Lung Injury." In American Thoracic Society 2010 International Conference, May 14-19, 2010 • New Orleans. American Thoracic Society, 2010. http://dx.doi.org/10.1164/ajrccm-conference.2010.181.1_meetingabstracts.a3607.

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chen, weiguo, Joe G. Garcia, and Jeffrey R. Jacobson. "Endothelial Cell Barrier Regulation By Simvastatin Is Mediated By Claudin-5." In American Thoracic Society 2011 International Conference, May 13-18, 2011 • Denver Colorado. American Thoracic Society, 2011. http://dx.doi.org/10.1164/ajrccm-conference.2011.183.1_meetingabstracts.a3759.

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Chen, Weiguo, Joe G. N. Garcia, and Jeffrey R. Jacobson. "Simvastatin Induces Upregulation Of Claudin-5 And Rearrangement Of Endothelial Tight Junctions." In American Thoracic Society 2010 International Conference, May 14-19, 2010 • New Orleans. American Thoracic Society, 2010. http://dx.doi.org/10.1164/ajrccm-conference.2010.181.1_meetingabstracts.a3429.

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Armstrong, Susan M., Jayesh Tigdi, Changsen Wang, Theo Moraes, and Warren L. Lee. "Influenza Infects Human Microvascular Endothelium Leading To Microvascular Leak: Role Of Apoptosis And Claudin-5." In American Thoracic Society 2012 International Conference, May 18-23, 2012 • San Francisco, California. American Thoracic Society, 2012. http://dx.doi.org/10.1164/ajrccm-conference.2012.185.1_meetingabstracts.a3662.

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Virág, József, Gábor Baksa, Zsuzsa Schaff, József Tímár, Miklós Garami, and Balázs Hegedũs. "Abstract 854: Claudin-5 expression in tumor cells is a potential prognostic marker in pediatric ependymoma." In Proceedings: AACR 101st Annual Meeting 2010‐‐ Apr 17‐21, 2010; Washington, DC. American Association for Cancer Research, 2010. http://dx.doi.org/10.1158/1538-7445.am10-854.

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Dunlap, SM, LJ Chiao, L. Nogueria, et al. "S6-5: Obesity Drives Epithelial-to-Mesenchymal Transition and Tumor Progression in a Novel Claudin-Low Mammary Cancer Model." In Abstracts: Thirty-Fourth Annual CTRC‐AACR San Antonio Breast Cancer Symposium‐‐ Dec 6‐10, 2011; San Antonio, TX. American Association for Cancer Research, 2011. http://dx.doi.org/10.1158/0008-5472.sabcs11-s6-5.

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Escudero-Esparza, A., T. Martin, and W. Jiang. "The Role of Claudin- 5 and the Paracellular Barrier Function in Endothelial Cells during Invasion of Breast Cancer Cells." In Abstracts: Thirty-Second Annual CTRC‐AACR San Antonio Breast Cancer Symposium‐‐ Dec 10‐13, 2009; San Antonio, TX. American Association for Cancer Research, 2009. http://dx.doi.org/10.1158/0008-5472.sabcs-09-6170.

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Konieczna, Sylwia, Michael Ohlmeyer, and J. Paul Spiers. "P12 Role of protein phosphatase 2a inhibition in modulation of claudin- 5 and ve-cadherin in human brain microvascular endothelial cells." In Scottish Cardiovascular Forum – 23rd annual meeting, University of Strathclyde, Saturday 1st February 2020. BMJ Publishing Group Ltd and British Cardiovascular Society, 2020. http://dx.doi.org/10.1136/heartjnl-2020-scf.22.

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Romanov, Victor, Terry Whyard, Wayne C. Waltzer, and Theodore Gabig. "Abstract 1817: Development of claudin-3 and claudin-4-targeted antiprostate cancer prodrug." In Proceedings: AACR Annual Meeting 2014; April 5-9, 2014; San Diego, CA. American Association for Cancer Research, 2014. http://dx.doi.org/10.1158/1538-7445.am2014-1817.

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