PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
27543355-9	2016	[3H]-GlySar and [3H]-l-His uptake receded to approximately 30% in the presence of His-Leu-LPV supporting the PepT1/PHT1 mediated uptake process.	Tritium	1-3	solute carrier family 15 member 1	Homo sapiens	109-114	
30135242-3	2018	The hiPSC-IECs showed the transport activities of P-glycoprotein (P-gp), breast cancer resistance protein (BCRP), and peptide transporter 1 (PEPT1), revealed by using their probe substrates ([3H]digoxin, sulfasalazine, and [14C]glycylsarcosine), and the metabolic activities of CYP3A4, CES2, and CES1, which were clarified using their probe substrates (midazolam, irinotecan, and temocapril).	Tritium	192-194	solute carrier family 15 member 1	Homo sapiens	118-139	
30135242-3	2018	The hiPSC-IECs showed the transport activities of P-glycoprotein (P-gp), breast cancer resistance protein (BCRP), and peptide transporter 1 (PEPT1), revealed by using their probe substrates ([3H]digoxin, sulfasalazine, and [14C]glycylsarcosine), and the metabolic activities of CYP3A4, CES2, and CES1, which were clarified using their probe substrates (midazolam, irinotecan, and temocapril).	Tritium	192-194	solute carrier family 15 member 1	Homo sapiens	141-146	
28705621-6	2017	In Caco-2 cell monolayer model, competition between functionalized nanoparticles and [3H]Glycylsarcosine, a strong substrate of PepT1, reduced [3H]Glycylsarcosine transport from 22 to 46%.	Tritium	86-88	solute carrier family 15 member 1	Homo sapiens	128-133	
28705621-6	2017	In Caco-2 cell monolayer model, competition between functionalized nanoparticles and [3H]Glycylsarcosine, a strong substrate of PepT1, reduced [3H]Glycylsarcosine transport from 22 to 46%.	Tritium	144-146	solute carrier family 15 member 1	Homo sapiens	128-133	
27543355-9	2016	[3H]-GlySar and [3H]-l-His uptake receded to approximately 30% in the presence of His-Leu-LPV supporting the PepT1/PHT1 mediated uptake process.	Tritium	1-4	solute carrier family 15 member 1	Homo sapiens	109-114	
14725353-7	2003	RESULTS: At pH 6.0, H57K-, H57R-, H121K-, and H121R-hPepT1 led to a 97%, 90%, 45%, and 75% decrease in [3H]Gly-Sar uptake into HEK293 cells, respectively.	Tritium	104-106	solute carrier family 15 member 1	Homo sapiens	52-58	
9811478-5	1998	Wild type or mutagenized human PepT1 cDNA was transfected into human embryonic kidney (HEK293) cells, and the uptake of tritiated glycylsarcosine [3H]-(Gly-Sar) was measured.	Tritium	147-149	solute carrier family 15 member 1	Homo sapiens	31-36	
14661916-5	2003	RESULTS: In HeLa/hPept1 cells, [3H]Gly-Sar uptake was significantly inhibited by Lys-FITC-OCH3 (74%) but not by FITC-Val-OCH3 (22%).	Tritium	32-34	solute carrier family 15 member 1	Homo sapiens	17-23	
11741253-3	2001	The hPepT1-GFP fusion construct was then transfected into Caco-2 and HeLa cells, and drug inhibition was studied by inhibiting 3H-Gly-Sar uptake.	Tritium	127-129	solute carrier family 15 member 1	Homo sapiens	4-10	
9753615-2	1998	A significant increase in the uptake of [3H]vacv by Xenopus laevis oocytes injected with human intestinal peptide transporter (hPepT1) cRNA compared to the uptake by water injected oocytes indicated that vacv was translocated by hPepT1.	Tritium	40-43	solute carrier family 15 member 1	Homo sapiens	127-133	
9753615-2	1998	A significant increase in the uptake of [3H]vacv by Xenopus laevis oocytes injected with human intestinal peptide transporter (hPepT1) cRNA compared to the uptake by water injected oocytes indicated that vacv was translocated by hPepT1.	Tritium	40-43	solute carrier family 15 member 1	Homo sapiens	229-235	
9735340-4	1998	[3H]Gly-sar uptake in cells transiently transfected with Y167A-hPepT1 was abolished completely, even though the level of Y167A-hPepT1 expression by Western blot analysis and cell surface expression by immunofluorescence microscopy was similar to those of the wild type.	Tritium	1-3	solute carrier family 15 member 1	Homo sapiens	63-69	
9126331-3	1997	Functional expression of PepT1 was determined in different recombinant clones by flux studies employing the radiolabeled dipeptide 3H-(D)-Phe-(L)-Ala. One clone (GS-PepT1) displayed high level functional expression that was pH dependent and saturable with an app.	Tritium	131-133	solute carrier family 15 member 1	Homo sapiens	25-30