PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
23761298-9	2013	Additionally, PFOS decreased the expression of junction proteins in Sertoli cells, which was further confirmed by in vivo results that PFOS decreased or dislocated junction proteins (i.e., ZO-1, occludin, claudin-11, and connexin-43) and increased proteins related to the MAPK signaling pathway (i.e., Erk and p38), whereas basal ectoplasmic specialization proteins did not change.	perfluorooctane sulfonic acid	135-139	occludin	Mus musculus	195-203	
31706766-6	2020	PFOS significantly decreased the expression of TJ-related proteins (ZO-1, Claudin-5, Claudin-11, Occludin) in endothelial cells and disrupted BBB, which subsequently led PFOS to astrocytes and increased the expression of the proteins related to astrocytic damages (Aquaporin 4 and S100beta).	perfluorooctane sulfonic acid	0-4	occludin	Mus musculus	97-105	
29990813-8	2018	Several testicular genes, which are sensitive to PFOS exposure, were also detected using Western blotting, and included steroidogenic proteins, STAR, CYP11A1, CYP17A1, and 3beta-HSD and cell junction proteins, occludin, beta-catenin, and connexin 43; however, none were changed after 6:2 Cl-PFAES exposure.	perfluorooctane sulfonic acid	49-53	occludin	Mus musculus	210-218	
27818224-7	2016	Our results demonstrated that PFOS dose-dependently increased BTB permeability, p38/ATF2 phosphorylation and MMP9 expression, paralleled by decrease in BTB junction protein Occludin and Connexin43 expression.	perfluorooctane sulfonic acid	30-34	occludin	Mus musculus	173-181	
27818224-8	2016	Additionally, similar to the in vivo results, treatment of PFOS time-dependently increased Sertoli cell-based BTB permeability, phosphorylated-p38/ATF2 level, translocation of ATF2 into the nucleus and MMP9 expression/activity, paralleled by decrease in Occludin and Connexin43 expression.	perfluorooctane sulfonic acid	59-63	occludin	Mus musculus	254-262