PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
15229233-2	2004	Phosphorylated (phospho)-ERK was examined immunohistochemically after both single and repeated (i.e., sensitizing) doses of the partial D1-dopamine (DA) receptor agonist SKF-38393 (2,3,4,5-tetrahydro-7,8-dihydroxy-1-phenyl-1H-3-benazepine HCl) to adult rats lesioned as neonates (neonate lesioned) with 6-hydroxydopamine.	2,3,4,5-Tetrahydro-7,8-dihydroxy-1-phenyl-1H-3-benzazepine	170-179	Eph receptor B1	Rattus norvegicus	25-28	
30930179-1	2019	The D1 dopamine receptor agonist, SKF-38393, induces cytotoxicity in striatal dopaminergic neurons via an extracellular signal-regulated kinase (ERK) signaling cascade.	2,3,4,5-Tetrahydro-7,8-dihydroxy-1-phenyl-1H-3-benzazepine	34-43	Eph receptor B1	Rattus norvegicus	106-143	
30930179-1	2019	The D1 dopamine receptor agonist, SKF-38393, induces cytotoxicity in striatal dopaminergic neurons via an extracellular signal-regulated kinase (ERK) signaling cascade.	2,3,4,5-Tetrahydro-7,8-dihydroxy-1-phenyl-1H-3-benzazepine	34-43	Eph receptor B1	Rattus norvegicus	145-148	
30930179-13	2019	These results suggest that SKF-38393 induces neurotoxicity by activation of the sustained ERK-Bad-Bax system.	2,3,4,5-Tetrahydro-7,8-dihydroxy-1-phenyl-1H-3-benzazepine	27-36	Eph receptor B1	Rattus norvegicus	90-93	
30930179-0	2019	Repeated treatments with the D1 dopamine receptor agonist SKF-38393 modulate cell viability via sustained ERK-Bad-Bax activation in dopaminergic neuronal cells.	2,3,4,5-Tetrahydro-7,8-dihydroxy-1-phenyl-1H-3-benzazepine	58-67	Eph receptor B1	Rattus norvegicus	106-109	
29232769-9	2018	AT-403 reduced the ERK phosphorylation induced by SKF38393 in vitro and by levodopa in vivo.	2,3,4,5-Tetrahydro-7,8-dihydroxy-1-phenyl-1H-3-benzazepine	50-58	Eph receptor B1	Rattus norvegicus	19-22	
15229233-5	2004	At 36 d, an additional injection of SKF-38393 to sensitized rats restored phospho-ERK to maximal levels only in MPC when examined 7 d later.	2,3,4,5-Tetrahydro-7,8-dihydroxy-1-phenyl-1H-3-benzazepine	36-45	Eph receptor B1	Rattus norvegicus	82-85	
23152595-2	2012	In striatal slices of naive rodents, N/OFQ (0.1-1 mum) prevented the increase of ERK phosphorylation and the loss of depotentiation of synaptic plasticity induced by the D1 receptor agonist SKF38393 in spiny neurons.	2,3,4,5-Tetrahydro-7,8-dihydroxy-1-phenyl-1H-3-benzazepine	190-198	Eph receptor B1	Rattus norvegicus	81-84