PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
17890383-8	2008	Including SP-B (1% wt/wt) appears to induce the formation of elongated strands of interacting threads with the fluid phosphatidylglycerols (PG).	Phosphatidylglycerols	117-138	surfactant protein B	Homo sapiens	10-14	
17890383-8	2008	Including SP-B (1% wt/wt) appears to induce the formation of elongated strands of interacting threads with the fluid phosphatidylglycerols (PG).	Phosphatidylglycerols	140-142	surfactant protein B	Homo sapiens	10-14	
17890383-11	2008	Agarose gel electrophoresis studies demonstrated that the aggregation induced by SP-B blocked migration of PG-coated NP.	Phosphatidylglycerols	107-109	surfactant protein B	Homo sapiens	81-85	
15628884-7	2005	SP-Br also mimicked the behavior of native SP-B in lipid-protein films subjected to dynamic compression-expansion cycling in a captive bubble surfactometer, but only in the presence of phosphatidylglycerol (PG), the main anionic phospholipid in surfactant.	Phosphatidylglycerols	185-205	surfactant protein B	Homo sapiens	0-4	
15628884-7	2005	SP-Br also mimicked the behavior of native SP-B in lipid-protein films subjected to dynamic compression-expansion cycling in a captive bubble surfactometer, but only in the presence of phosphatidylglycerol (PG), the main anionic phospholipid in surfactant.	Phosphatidylglycerols	207-209	surfactant protein B	Homo sapiens	0-4	
7696261-9	1995	At near-physiological ionic strength, SP-B showed selectivity for phosphatidylglycerol.	Phosphatidylglycerols	66-86	surfactant protein B	Homo sapiens	38-42	
9100011-0	1997	Pulmonary surfactant protein SP-B interacts similarly with dipalmitoylphosphatidylglycerol and dipalmitoylphosphatidylcholine in phosphatidylcholine/phosphatidylglycerol mixtures.	Phosphatidylglycerols	70-90	surfactant protein B	Homo sapiens	29-33	
11923286-9	2002	For the first time direct observations by atomic force microscopy show (i) that a certain minimal concentration of SP-B is required for the formation of layered protrusions upon film compression, (ii) that protrusion height depends on whether the phospholipids contain an unsaturated fatty acyl chain, and (iii) that protrusion height also depends on whether the unsaturated acyl chain is present in phosphatidylcholine or in phosphatidylglycerol.	Phosphatidylglycerols	426-446	surfactant protein B	Homo sapiens	115-119	
10696076-7	2000	Both SP-B-deficient and CLD infants had markedly decreased phosphatidylglycerol content of lavage and tissue compared with normal lung, whereas synthetic rates for phospholipids, including phosphatidylglycerol, were normal.	Phosphatidylglycerols	59-79	surfactant protein B	Homo sapiens	5-9	
1606172-3	1992	The Wilhelmy surface plate technique was utilized to investigate the interaction between pure SP-B in the bulk phase (0.9% NaCl/1.5 mM CaCl2) and preformed DPPC or phosphatidylglycerol (PG) monolayers.	Phosphatidylglycerols	164-184	surfactant protein B	Homo sapiens	94-98	
1896249-3	1991	The data demonstrate that several peptides, ranging from 17 to 45 residues in length, matching the carboxy-terminal sequence of the SP-B protein, when appropriately recombined with the phospholipid dipalmitoylphosphatidylcholine and phosphatidylglycerol (3:1), are capable of producing a synthetic surfactant with biophysical and biologic activity approaching that of human surfactant derived from amniotic fluid.	Phosphatidylglycerols	233-253	surfactant protein B	Homo sapiens	132-136