PMID-sentid	Pub_year	Sent_text	comp_official_name	comp_offset	protein_name	organism	prot_offset
3030265-1	1986	In an attempt to identify the nature of guanine nucleotide binding protein(s) (G-protein) involved in the acetylcholine (ACh)-induced (muscarinic) response of pig coronary-artery smooth muscle, we studied the effect of ADP-ribosylation of specific membrane protein(s) catalysed by islet-activating protein (IAP; pertussis toxin).	Acetylcholine	121-124	CD47 molecule	Sus scrofa	307-310
3030265-2	1986	The ACh-stimulated and guanine nucleotide-dependent activities of phosphatidylinositol 4,5-bisphosphate (PIP2) phosphodiesterase (PDE), assessed by the production of inositol 1,4,5-trisphosphate (IP3) from exogenously applied PIP2, were not modified, in either IAP-treated or non-treated cell homogenates used as the enzyme source.	Acetylcholine	4-7	CD47 molecule	Sus scrofa	261-264
3030265-2	1986	The ACh-stimulated and guanine nucleotide-dependent activities of phosphatidylinositol 4,5-bisphosphate (PIP2) phosphodiesterase (PDE), assessed by the production of inositol 1,4,5-trisphosphate (IP3) from exogenously applied PIP2, were not modified, in either IAP-treated or non-treated cell homogenates used as the enzyme source.	Guanine Nucleotides	23-41	CD47 molecule	Sus scrofa	261-264
3030265-2	1986	The ACh-stimulated and guanine nucleotide-dependent activities of phosphatidylinositol 4,5-bisphosphate (PIP2) phosphodiesterase (PDE), assessed by the production of inositol 1,4,5-trisphosphate (IP3) from exogenously applied PIP2, were not modified, in either IAP-treated or non-treated cell homogenates used as the enzyme source.	phosphatidylinositol 4,5	66-90	CD47 molecule	Sus scrofa	261-264
21944178-4	2011	Following baseline observations, high intra-abdominal pressure (IAP) with intraperitoneal nitrogen inflation was induced in all 6 pigs.	Nitrogen	90-98	CD47 molecule	Sus scrofa	64-67
18297407-2	2008	The result of analysis by flow cytometry after reaction with mouse-anti-human CD47 and caprine-anti-mouse IgG-FITC reagents indicated that the CD47 quantity on RBCs changed correlatively with the course of PE.	Fluorescein-5-isothiocyanate	110-114	CD47 molecule	Sus scrofa	143-147
8118422-4	1993	In contrast, the cultured with low glucose concentrations induced the increases of both islet activating protein (IAP)-catalyzed ADP-ribosylation of Gi alpha and Na+/glucose cotransport activity.	Glucose	35-42	CD47 molecule	Sus scrofa	88-112
8118422-4	1993	In contrast, the cultured with low glucose concentrations induced the increases of both islet activating protein (IAP)-catalyzed ADP-ribosylation of Gi alpha and Na+/glucose cotransport activity.	Glucose	35-42	CD47 molecule	Sus scrofa	114-117
1964035-1	1990	Islet-activating protein (IAP), one of the pertussis toxins, serving [alpha-32P]nicotinamide adenine dinucleotide (NAD) as a substrate for ADP ribosylation, radiolabelled a specific pig epidermal membrane protein.	[alpha-32p]nicotinamide adenine dinucleotide	69-113	CD47 molecule	Sus scrofa	0-24
1964035-1	1990	Islet-activating protein (IAP), one of the pertussis toxins, serving [alpha-32P]nicotinamide adenine dinucleotide (NAD) as a substrate for ADP ribosylation, radiolabelled a specific pig epidermal membrane protein.	[alpha-32p]nicotinamide adenine dinucleotide	69-113	CD47 molecule	Sus scrofa	26-29
1964035-1	1990	Islet-activating protein (IAP), one of the pertussis toxins, serving [alpha-32P]nicotinamide adenine dinucleotide (NAD) as a substrate for ADP ribosylation, radiolabelled a specific pig epidermal membrane protein.	nadide	115-118	CD47 molecule	Sus scrofa	0-24
1964035-1	1990	Islet-activating protein (IAP), one of the pertussis toxins, serving [alpha-32P]nicotinamide adenine dinucleotide (NAD) as a substrate for ADP ribosylation, radiolabelled a specific pig epidermal membrane protein.	nadide	115-118	CD47 molecule	Sus scrofa	26-29
1964035-2	1990	The IAP-specific substrate was detectable by sodium dodecyl sulphate-polyacrylamide gel electrophoresis as a single band corresponding to a molecular weight of 40 kDa.	Sodium Dodecyl Sulfate	45-68	CD47 molecule	Sus scrofa	4-7
1964035-2	1990	The IAP-specific substrate was detectable by sodium dodecyl sulphate-polyacrylamide gel electrophoresis as a single band corresponding to a molecular weight of 40 kDa.	polyacrylamide	69-83	CD47 molecule	Sus scrofa	4-7
1964035-3	1990	The ADP ribosylation catalysed by IAP was inhibited by the addition of Mg2+ to the reaction mixture.	Adenosine Diphosphate	4-7	CD47 molecule	Sus scrofa	34-37
1964035-3	1990	The ADP ribosylation catalysed by IAP was inhibited by the addition of Mg2+ to the reaction mixture.	magnesium ion	71-75	CD47 molecule	Sus scrofa	34-37
1964035-5	1990	Following IAP pretreatment of intact pig epidermis, the epidermal receptor adenylate cyclase responses were markedly increased; all the stimulatory receptor adenylate cyclase responses (beta-adrenergic, prostaglandin E, adenosine and histamine responses) were significantly increased.	Prostaglandins E	203-218	CD47 molecule	Sus scrofa	10-13
1964035-5	1990	Following IAP pretreatment of intact pig epidermis, the epidermal receptor adenylate cyclase responses were markedly increased; all the stimulatory receptor adenylate cyclase responses (beta-adrenergic, prostaglandin E, adenosine and histamine responses) were significantly increased.	Adenosine	220-229	CD47 molecule	Sus scrofa	10-13
1964035-5	1990	Following IAP pretreatment of intact pig epidermis, the epidermal receptor adenylate cyclase responses were markedly increased; all the stimulatory receptor adenylate cyclase responses (beta-adrenergic, prostaglandin E, adenosine and histamine responses) were significantly increased.	Histamine	234-243	CD47 molecule	Sus scrofa	10-13
1964035-7	1990	Forskolin-induced cyclic AMP accumulation was slightly increased after IAP pretreatment, but this was not statistically significant.	Colforsin	0-9	CD47 molecule	Sus scrofa	71-74
3030265-2	1986	The ACh-stimulated and guanine nucleotide-dependent activities of phosphatidylinositol 4,5-bisphosphate (PIP2) phosphodiesterase (PDE), assessed by the production of inositol 1,4,5-trisphosphate (IP3) from exogenously applied PIP2, were not modified, in either IAP-treated or non-treated cell homogenates used as the enzyme source.	Phosphatidylinositol 4,5-Diphosphate	105-109	CD47 molecule	Sus scrofa	261-264
3030265-3	1986	In intact tissues, pretreatment with up to 100 ng of IAP/ml inhibited neither the ACh-induced decrease in the amount of inositol phospholipids nor the increase in the amounts of phosphatidic acid and of inositol phosphates.	Acetylcholine	82-85	CD47 molecule	Sus scrofa	53-56
3030265-3	1986	In intact tissues, pretreatment with up to 100 ng of IAP/ml inhibited neither the ACh-induced decrease in the amount of inositol phospholipids nor the increase in the amounts of phosphatidic acid and of inositol phosphates.	Phosphatidylinositols	120-142	CD47 molecule	Sus scrofa	53-56
3030265-3	1986	In intact tissues, pretreatment with up to 100 ng of IAP/ml inhibited neither the ACh-induced decrease in the amount of inositol phospholipids nor the increase in the amounts of phosphatidic acid and of inositol phosphates.	Phosphatidic Acids	178-195	CD47 molecule	Sus scrofa	53-56
3030265-3	1986	In intact tissues, pretreatment with up to 100 ng of IAP/ml inhibited neither the ACh-induced decrease in the amount of inositol phospholipids nor the increase in the amounts of phosphatidic acid and of inositol phosphates.	Inositol Phosphates	203-222	CD47 molecule	Sus scrofa	53-56
3030265-4	1986	IAP treatment increased the amount of cyclic AMP accumulated by isoprenaline.	Cyclic AMP	38-48	CD47 molecule	Sus scrofa	0-3
3030265-4	1986	IAP treatment increased the amount of cyclic AMP accumulated by isoprenaline.	Isoproterenol	64-76	CD47 molecule	Sus scrofa	0-3
24931767-9	2014	Brain CD47 levels were lower in the ipsilateral white and gray matter in pigs which had deferoxamine treatment.	Deferoxamine	88-100	CD47 molecule	Sus scrofa	6-10
24931767-11	2014	Deferoxamine and iron may modulate CD47 expression.	Deferoxamine	0-12	CD47 molecule	Sus scrofa	35-39
24931767-11	2014	Deferoxamine and iron may modulate CD47 expression.	Iron	17-21	CD47 molecule	Sus scrofa	35-39
8118422-4	1993	In contrast, the cultured with low glucose concentrations induced the increases of both islet activating protein (IAP)-catalyzed ADP-ribosylation of Gi alpha and Na+/glucose cotransport activity.	Adenosine Diphosphate	129-132	CD47 molecule	Sus scrofa	88-112
8118422-4	1993	In contrast, the cultured with low glucose concentrations induced the increases of both islet activating protein (IAP)-catalyzed ADP-ribosylation of Gi alpha and Na+/glucose cotransport activity.	Adenosine Diphosphate	129-132	CD47 molecule	Sus scrofa	114-117
1319725-4	1992	The IAP component of pertussis toxin blocked the inhibitory action of InP-gly on cAMP accumulation by reconstituted thyroid follicles (RTF), suggesting the participation of Gi protein.	Glycine	74-77	CD47 molecule	Sus scrofa	4-7
1319725-4	1992	The IAP component of pertussis toxin blocked the inhibitory action of InP-gly on cAMP accumulation by reconstituted thyroid follicles (RTF), suggesting the participation of Gi protein.	Cyclic AMP	81-85	CD47 molecule	Sus scrofa	4-7
1319725-5	1992	But the same treatment with IAP was without effect on iodine metabolism, suggesting that there is a second target for InP-gly, more distal than Gi protein, or coupled to another G protein which is insensitive to the toxin.	Glycine	122-125	CD47 molecule	Sus scrofa	28-31