PMID-sentid	Pub_year	Sent_text	compound_name	comp_offset	prot_official_name	organism	prot_offset
35151725-5	2022	Following PCB and OH-PCB exposure, significant changes in mRNA expression of NIS, TPO, and TG were observed.	oh-pcb	18-24	thyroid peroxidase	Gallus gallus	82-85
16006569-10	2005	In conclusion, glucuronidation activities of UGT1A1, UGT1A6, and UGT2B1 toward OH-PCBs is relative to expression of the isoforms in each tissue, and glucuronidation intensity of the isoforms is relative to the structure of the OH-PCB to be glucuronidated.	oh-pcb	79-85	UDP glucuronosyltransferase family 1 member A1	Rattus norvegicus	45-51
16006569-10	2005	In conclusion, glucuronidation activities of UGT1A1, UGT1A6, and UGT2B1 toward OH-PCBs is relative to expression of the isoforms in each tissue, and glucuronidation intensity of the isoforms is relative to the structure of the OH-PCB to be glucuronidated.	oh-pcb	79-85	UDP glucuronosyltransferase family 1 member A6	Rattus norvegicus	53-59
16006569-10	2005	In conclusion, glucuronidation activities of UGT1A1, UGT1A6, and UGT2B1 toward OH-PCBs is relative to expression of the isoforms in each tissue, and glucuronidation intensity of the isoforms is relative to the structure of the OH-PCB to be glucuronidated.	oh-pcb	79-85	UDP glucuronosyltransferase family 2 member B17	Rattus norvegicus	65-71
11351435-6	2001	Maximum plasma VTG of 0.048 mg/ml in the highest dose (50 mg/kg) of OH-PCB 61 was approximately 100-fold lower than natural estrogens and OH-PCB 30.	oh-pcb	68-74	LOC100136735	Oncorhynchus mykiss	15-18
11351435-6	2001	Maximum plasma VTG of 0.048 mg/ml in the highest dose (50 mg/kg) of OH-PCB 61 was approximately 100-fold lower than natural estrogens and OH-PCB 30.	oh-pcb	138-144	LOC100136735	Oncorhynchus mykiss	15-18
11351435-10	2001	Differences in plasma VTG induction by OH-PCB 30 and OH-PCB 61 support in vitro predictions that the degree and position of chlorination are important for ER activation.	oh-pcb	39-45	LOC100136735	Oncorhynchus mykiss	22-25
11351435-10	2001	Differences in plasma VTG induction by OH-PCB 30 and OH-PCB 61 support in vitro predictions that the degree and position of chlorination are important for ER activation.	oh-pcb	53-59	LOC100136735	Oncorhynchus mykiss	22-25
23584369-6	2013	The ability of OH-PCBs to serve as substrates for human cytosolic sulfotransferase 1A1 (hSULT1A1) was assessed by OH-PCB-dependent formation of adenosine-3",5"-diphosphate, an end product of the sulfation reaction.	oh-pcb	15-21	sulfotransferase family 1A member 1	Homo sapiens	88-96
23584369-9	2013	All OH-PCB precursors for these sulfates were found to be substrates for hSULT1A1.	oh-pcb	4-10	sulfotransferase family 1A member 1	Homo sapiens	73-81
18414928-7	2009	For estrogen receptor beta (ERbeta), the mRNA expression pattern was OH-PCB-metabolite congener-specific.	oh-pcb	69-75	estrogen receptor 2a	Salmo salar	4-26
17207528-4	2007	Our data show that OH-PCB congeners and EE2, decreased AhRalpha and ARNT transcript levels, and CYP1A1, UGT and GST gene expressions, together with CYP3A gene expression.	oh-pcb	19-25	cytochrome P450 3A27	Salmo salar	148-153
20060147-3	2010	The levels of VTG production in hepatocytes of male X. laevis exposed to six kinds of OH-PCB isomers (2"-OH-CB30, 3"-OH-CB30, 4"-OH-CB30, 4"-OH-CB50, 4"-OH-CB61 4"-OH-CB65) were significantly higher as compared to the control group (p<0.05).	oh-pcb	86-92	a1-a	Xenopus laevis	14-17
20060147-7	2010	The OH-PCB structures of high rank order in the VTG-assay had no chlorine substituted phenolic ring.	oh-pcb	4-10	a1-a	Xenopus laevis	48-51