PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
30538149-5	2019	During this time period, HO-1 induction fully prevented the pro-oxidant tert-butylhydroperoxide (tBuOOH)-induced drop in bile flow, and in the biliary excretion of bile salts and glutathione, the two main driving forces of bile flow; this was associated with preservation of the membrane localization of their respective canalicular transporters, bile salt export pump (Bsep) and multidrug resistance-associated protein 2 (Mrp2), which are otherwise endocytosed by OS.	tert-Butylhydroperoxide	72-95	ATP binding cassette subfamily B member 11	Rattus norvegicus	347-368	
30538149-5	2019	During this time period, HO-1 induction fully prevented the pro-oxidant tert-butylhydroperoxide (tBuOOH)-induced drop in bile flow, and in the biliary excretion of bile salts and glutathione, the two main driving forces of bile flow; this was associated with preservation of the membrane localization of their respective canalicular transporters, bile salt export pump (Bsep) and multidrug resistance-associated protein 2 (Mrp2), which are otherwise endocytosed by OS.	tert-Butylhydroperoxide	72-95	ATP binding cassette subfamily B member 11	Rattus norvegicus	370-374	
30538149-5	2019	During this time period, HO-1 induction fully prevented the pro-oxidant tert-butylhydroperoxide (tBuOOH)-induced drop in bile flow, and in the biliary excretion of bile salts and glutathione, the two main driving forces of bile flow; this was associated with preservation of the membrane localization of their respective canalicular transporters, bile salt export pump (Bsep) and multidrug resistance-associated protein 2 (Mrp2), which are otherwise endocytosed by OS.	tert-Butylhydroperoxide	97-103	ATP binding cassette subfamily B member 11	Rattus norvegicus	347-368	
30538149-5	2019	During this time period, HO-1 induction fully prevented the pro-oxidant tert-butylhydroperoxide (tBuOOH)-induced drop in bile flow, and in the biliary excretion of bile salts and glutathione, the two main driving forces of bile flow; this was associated with preservation of the membrane localization of their respective canalicular transporters, bile salt export pump (Bsep) and multidrug resistance-associated protein 2 (Mrp2), which are otherwise endocytosed by OS.	tert-Butylhydroperoxide	97-103	ATP binding cassette subfamily B member 11	Rattus norvegicus	370-374	
27913845-1	2017	In previous studies, we showed that the pro-oxidant model agent tert-butyl hydroperoxide (tBuOOH) induces alterations in hepatocanalicular secretory function by activating Ca2+-dependent protein kinase C isoforms (cPKC), via F-actin disorganization followed by endocytic internalization of canalicular transporters relevant to bile formation (Mrp2, Bsep).	tert-Butylhydroperoxide	64-88	ATP binding cassette subfamily B member 11	Rattus norvegicus	349-353	
16452108-4	2006	tBOOH-induced bile salt secretory failure was accompanied by internalization of the canalicular bile salt export pump (Bsep), and disarrangement of cytoskeletal F-actin.	tert-Butylhydroperoxide	0-5	ATP binding cassette subfamily B member 11	Rattus norvegicus	96-117	
16452108-4	2006	tBOOH-induced bile salt secretory failure was accompanied by internalization of the canalicular bile salt export pump (Bsep), and disarrangement of cytoskeletal F-actin.	tert-Butylhydroperoxide	0-5	ATP binding cassette subfamily B member 11	Rattus norvegicus	119-123