PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
22125116-3	2012	Zymosan and/or PMA (Phorbol 12-myristate 13-acetate)-induced recruitment of p47(phox) and p67(phox) to the membrane fraction was normal for both mutants.	Tetradecanoylphorbol Acetate	15-18	CD33 molecule	Homo sapiens	90-93	
22125116-3	2012	Zymosan and/or PMA (Phorbol 12-myristate 13-acetate)-induced recruitment of p47(phox) and p67(phox) to the membrane fraction was normal for both mutants.	Tetradecanoylphorbol Acetate	20-51	CD33 molecule	Homo sapiens	90-93	
21705328-4	2011	Small interfering RNA (siRNA) experiments indicated that knocking down the NADPH oxidase components e.g. Rac1, p22(phox), p67(phox), and NOXO1 in A549 cells impaired TPA-induced MnSOD expression.	Tetradecanoylphorbol Acetate	166-169	CD33 molecule	Homo sapiens	122-125	
15698597-16	2005	L-cystathionine and N-acetyl-L-cysteine suppressed fMLP- and PMA-induced superoxide generation by the inhibition of translocation to membrane of p47(phox) and p67(phox).	Tetradecanoylphorbol Acetate	61-64	CD33 molecule	Homo sapiens	159-162	
16846837-8	2006	These results suggest that Tau-Cl inhibits PMA-elicited O(2)(-) production in PLB-985 granulocytes by inhibiting phosphorylation of p47(phox) and translocation of p47(phox) and p67(phox), eventually blocking the assembly of NADPH oxidase complex.	Tetradecanoylphorbol Acetate	43-46	CD33 molecule	Homo sapiens	177-180	
16846837-6	2006	Translocation of p47(phox), p67(phox) and Rac was increased in response to PMA, and Tau-Cl inhibited the PMA-stimulated translocation of p47(phox) and p67(phox) to plasma membrane without affecting the translocation of Rac.	Tetradecanoylphorbol Acetate	75-78	CD33 molecule	Homo sapiens	28-31	
16254825-5	2005	FMLP-induced tyrosyl phosphorylation or PMA-induced serine/threonine phosphorylation and the translocation of the cytosolic proteins p47(phox) and p67(phox) to the cell membrane were suppressed in parallel to the suppression of the stimulus-induced superoxide generation.	Tetradecanoylphorbol Acetate	40-43	CD33 molecule	Homo sapiens	147-150	
12693948-11	2003	Indeed, PD98059 and SB203580, two selective inhibitors of MEK1/2 and p38MAPK, respectively, inhibited p67(PHOX) phosphorylation in fMLP- and PMA-stimulated neutrophils, with additive effects, thus suggesting that they also target different sites in vivo.	Tetradecanoylphorbol Acetate	141-144	CD33 molecule	Homo sapiens	102-105	
11056390-3	2000	When human polymorphonuclear leukocytes (PMNs) were stimulated with phorbol myristate acetate (PMA), p40(phox) was translocated to the membrane along with p67(phox), and not was released into the cytosol.	Tetradecanoylphorbol Acetate	68-93	CD33 molecule	Homo sapiens	155-158	
11056390-3	2000	When human polymorphonuclear leukocytes (PMNs) were stimulated with phorbol myristate acetate (PMA), p40(phox) was translocated to the membrane along with p67(phox), and not was released into the cytosol.	Tetradecanoylphorbol Acetate	95-98	CD33 molecule	Homo sapiens	155-158	
8257426-8	1993	That the phosphorylated p67 protein we identified in immunoprecipitation experiments was p67phox was confirmed by the observation that no phosphorylated band of 67 kDa was immunoprecipitated from the cytosol and membranes of PMA-stimulated neutrophils from a p67phox-deficient chronic granulomatous disease patient.	Tetradecanoylphorbol Acetate	225-228	CD33 molecule	Homo sapiens	24-27	
7948035-7	1994	The amounts of p47-phox and p67-phox translocated to the plasma membrane in response to phorbol myristate acetate (PMA) increased with increasing amounts of cytochrome b-558 in the membrane.	Tetradecanoylphorbol Acetate	88-113	CD33 molecule	Homo sapiens	28-31	
7948035-7	1994	The amounts of p47-phox and p67-phox translocated to the plasma membrane in response to phorbol myristate acetate (PMA) increased with increasing amounts of cytochrome b-558 in the membrane.	Tetradecanoylphorbol Acetate	115-118	CD33 molecule	Homo sapiens	28-31	
9202043-5	1997	In this study, we found that activation of human neutrophils with formyl-methionyl-leucyl-phenylalanine (fMLP), a chemotactic peptide, or phorbol myristate acetate (PMA), a stimulator of protein kinase C (PKC), resulted in the phosphorylation of p67(phox).	Tetradecanoylphorbol Acetate	165-168	CD33 molecule	Homo sapiens	246-249	
9202043-5	1997	In this study, we found that activation of human neutrophils with formyl-methionyl-leucyl-phenylalanine (fMLP), a chemotactic peptide, or phorbol myristate acetate (PMA), a stimulator of protein kinase C (PKC), resulted in the phosphorylation of p67(phox).	Tetradecanoylphorbol Acetate	165-168	CD33 molecule	Homo sapiens	250-254	
9202043-10	1997	PMA-induced phosphorylation of p67(phox) was strongly inhibited by the PKC inhibitor GF109203X.	Tetradecanoylphorbol Acetate	0-3	CD33 molecule	Homo sapiens	31-40	
8407934-6	1993	After activation of neutrophils with phorbol 12-myristate 13-acetate or formyl-methionyl-leucyl-phenylalanine, Rac was translocated from the cytosol to the plasma membrane, and this translocation corresponded temporally with the translocation of p47-phox and p67-phox and with the generation of superoxide.	Tetradecanoylphorbol Acetate	37-68	CD33 molecule	Homo sapiens	259-262	
1985107-6	1991	In two patients with p47-phox deficiency, p67-phox failed to translocate, whereas p47-phox was detected in the particulate fraction of PMA-stimulated neutrophils from two patients deficient in p67-phox.	Tetradecanoylphorbol Acetate	135-138	CD33 molecule	Homo sapiens	193-196