PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
9730903-0	1998	D1 dopamine receptor agonists mediate activation of p38 mitogen-activated protein kinase and c-Jun amino-terminal kinase by a protein kinase A-dependent mechanism in SK-N-MC human neuroblastoma cells.	sk-n-mc	166-173	mitogen-activated protein kinase 14	Homo sapiens	52-55	
9730903-0	1998	D1 dopamine receptor agonists mediate activation of p38 mitogen-activated protein kinase and c-Jun amino-terminal kinase by a protein kinase A-dependent mechanism in SK-N-MC human neuroblastoma cells.	sk-n-mc	166-173	mitogen-activated protein kinase 8	Homo sapiens	93-120	
9730903-2	1998	We found that the D1 dopamine receptor agonist SKF38393 induced similar time- and dose-related activation of p38 MAPK and c-Jun amino-terminal kinase (JNK), whereas extracellular signal-regulated kinase activity was not affected by D1 dopamine receptor stimulation.	2,3,4,5-Tetrahydro-7,8-dihydroxy-1-phenyl-1H-3-benzazepine	47-55	mitogen-activated protein kinase 14	Homo sapiens	109-112	
9730903-2	1998	We found that the D1 dopamine receptor agonist SKF38393 induced similar time- and dose-related activation of p38 MAPK and c-Jun amino-terminal kinase (JNK), whereas extracellular signal-regulated kinase activity was not affected by D1 dopamine receptor stimulation.	2,3,4,5-Tetrahydro-7,8-dihydroxy-1-phenyl-1H-3-benzazepine	47-55	Jun proto-oncogene, AP-1 transcription factor subunit	Homo sapiens	122-127	
9730903-2	1998	We found that the D1 dopamine receptor agonist SKF38393 induced similar time- and dose-related activation of p38 MAPK and c-Jun amino-terminal kinase (JNK), whereas extracellular signal-regulated kinase activity was not affected by D1 dopamine receptor stimulation.	2,3,4,5-Tetrahydro-7,8-dihydroxy-1-phenyl-1H-3-benzazepine	47-55	mitogen-activated protein kinase 8	Homo sapiens	151-154	
9730903-3	1998	Maximal stimulation of p38 MAPK and JNK was observed after a 15-min incubation with 100 microM SKF38393.	2,3,4,5-Tetrahydro-7,8-dihydroxy-1-phenyl-1H-3-benzazepine	95-103	mitogen-activated protein kinase 14	Homo sapiens	23-26	
9730903-3	1998	Maximal stimulation of p38 MAPK and JNK was observed after a 15-min incubation with 100 microM SKF38393.	2,3,4,5-Tetrahydro-7,8-dihydroxy-1-phenyl-1H-3-benzazepine	95-103	mitogen-activated protein kinase 8	Homo sapiens	36-39	
9730903-7	1998	Furthermore, dibutyryl-cAMP mimicked SKF38393-mediated stimulation of p38 MAPK and JNK.	Bucladesine	13-27	mitogen-activated protein kinase 14	Homo sapiens	70-73	
9730903-7	1998	Furthermore, dibutyryl-cAMP mimicked SKF38393-mediated stimulation of p38 MAPK and JNK.	Bucladesine	13-27	mitogen-activated protein kinase 8	Homo sapiens	83-86	
9730903-7	1998	Furthermore, dibutyryl-cAMP mimicked SKF38393-mediated stimulation of p38 MAPK and JNK.	2,3,4,5-Tetrahydro-7,8-dihydroxy-1-phenyl-1H-3-benzazepine	37-45	mitogen-activated protein kinase 14	Homo sapiens	70-73	
9730903-7	1998	Furthermore, dibutyryl-cAMP mimicked SKF38393-mediated stimulation of p38 MAPK and JNK.	2,3,4,5-Tetrahydro-7,8-dihydroxy-1-phenyl-1H-3-benzazepine	37-45	mitogen-activated protein kinase 8	Homo sapiens	83-86