JNJ26993135 + BML-111 decreases permeability and enhances ZO-1 and claudin-1 induced by PAF but does not change TEER. by Kameljit K. Kalsi (16496511)

VSL#3 decreases epithelial paracellular permeability in a TNF-dependent manner on ilea from pre-inflamed SAMP mice. by Daniele Corridoni (148198)

Immunohistochemical staining and analysis of NF-κB activation in cytokine- and α-MSH-treated Caco-2 cells. by Judit Váradi (507449)

The effect of α-MSH treatment on the permeability of cytokine treated Caco-2 monolayers. by Judit Váradi (507449)

Secretion of IL-6 and IL-8 in Caco-2 cells treated with cytokines and α-MSH. by Judit Váradi (507449)

The effect of different concentrations of α-MSH on the electrical resistance of cytokine treated Caco-2 monolayers. by Judit Váradi (507449)

Dose- and time-dependent effect of IFN-γ and TNF-α on benzamil-sensitive <i>I</i>_sc and TEER in HBECs. by Anusree Sasidharan (19226521)

Dose- and time-dependent effect of IL-13, IL-4, and TGF-β1 on benzamil-sensitive <i>I</i>_sc and TEER in HBECs. by Anusree Sasidharan (19226521)

<i>L.</i><i>interrogans</i> induces afadin degradation in infected RPTECs through different strain-dependent mechanisms. by Tetsuya Kakita (4922584)

Effects of 1,25(OH)₂D₃ on transendothelial electrical resistance (TEER) in bEnd.3 cells under hypoxia/reoxygenation (H/R). by Soonmi Won (713581)

P2X7 modulates migration and the epithelial-mesenchymal phenotype. by José David Nuñez-Ríos (18823719)

Depleting extracellular ATP reverts the mesenchymal phenotype of ovarian carcinoma cell lines. by José David Nuñez-Ríos (18823719)

Changes in TEER and permeability of EA.hy926 cells exposed to EVs or pellets from infected or uninfected macrophages. by Myriam Lucia Velandia-Romero (8259726)

AA-T but not AA-NC increases benzamil-sensitive <i>I</i>_sc in IL-13-treated HBECs. by Anusree Sasidharan (19226521)

WNV infection of HMBVE cells, but not of leukocytes, mediates the disruption of the <i>in vitro</i> BBB model. by Kelsey Roe (309298)

“…<p>The effect of leukocyte migration on the permeability of the <i>in vitro</i> BBB model was determined by TEER measurements. (<b>A)</b> WNV infected monocytes (2.5 x 10⁵) at 24 hrs after infection were added in the upper compartment of the uninfected BBB model and permeability was measured at 2 and 4 hrs after incubation. …”