PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
14504179-9	2003	Jejunal apoA-I synthesis and plasma apoA-I levels were increased 2- to 3-fold in mice receiving DMPC but not soy or egg lecithin.	Dimyristoylphosphatidylcholine	96-100	apolipoprotein A-I	Mus musculus	8-14	
14504179-5	2003	Eight weeks later, HDL cholesterol levels and apoA-I levels were markedly increased in the mice that received DMPC.	Dimyristoylphosphatidylcholine	110-114	apolipoprotein A-I	Mus musculus	46-52	
14504179-9	2003	Jejunal apoA-I synthesis and plasma apoA-I levels were increased 2- to 3-fold in mice receiving DMPC but not soy or egg lecithin.	Dimyristoylphosphatidylcholine	96-100	apolipoprotein A-I	Mus musculus	36-42	
14504179-10	2003	CONCLUSIONS: DMPC (but not lecithin) raises HDL cholesterol and apoA-I, improves HDL function, and prevents lesions or causes their regression in apoE-null mice.	Dimyristoylphosphatidylcholine	13-17	apolipoprotein A-I	Mus musculus	64-70	
10858447-7	2000	When complexed with dimyristoylphosphatidylcholine, the N-terminal and C-terminal CNBr fragments of apoA-I each bound to SR-BI in a saturable, high affinity manner, and each cross-linked efficiently to mSR-BI.	Dimyristoylphosphatidylcholine	20-50	apolipoprotein A-I	Mus musculus	100-106	
10543393-4	1999	Normal apoA-I and apoA-I(R151C)Paris cleared DMPC emulsions at equal rates.	Dimyristoylphosphatidylcholine	45-49	apolipoprotein A-I	Mus musculus	7-13	
10543393-4	1999	Normal apoA-I and apoA-I(R151C)Paris cleared DMPC emulsions at equal rates.	Dimyristoylphosphatidylcholine	45-49	apolipoprotein A-I	Mus musculus	18-24	
10064737-4	1999	However, both apoA-I(P165R) and apoA-I(R160L)Oslo showed a reduced capacity to clear a turbid emulsion of dimyristoylphosphatidylcholine (DMPC).	Dimyristoylphosphatidylcholine	106-136	apolipoprotein A-I	Mus musculus	14-20	
10064737-4	1999	However, both apoA-I(P165R) and apoA-I(R160L)Oslo showed a reduced capacity to clear a turbid emulsion of dimyristoylphosphatidylcholine (DMPC).	Dimyristoylphosphatidylcholine	106-136	apolipoprotein A-I	Mus musculus	14-19	
10064737-4	1999	However, both apoA-I(P165R) and apoA-I(R160L)Oslo showed a reduced capacity to clear a turbid emulsion of dimyristoylphosphatidylcholine (DMPC).	Dimyristoylphosphatidylcholine	138-142	apolipoprotein A-I	Mus musculus	14-20	
10064737-4	1999	However, both apoA-I(P165R) and apoA-I(R160L)Oslo showed a reduced capacity to clear a turbid emulsion of dimyristoylphosphatidylcholine (DMPC).	Dimyristoylphosphatidylcholine	138-142	apolipoprotein A-I	Mus musculus	14-19	
8428938-9	1993	In the present study, all apoA-I.DMPC complexes except those containing apoA-I(Pro165-->Arg) promoted cholesterol efflux as effectively as those containing normal apoA-I.	Dimyristoylphosphatidylcholine	33-37	apolipoprotein A-I	Mus musculus	26-32	
8428938-10	1993	Cholesterol efflux from adipocytes obtained after 180 min of incubation with apoA-I(Pro165-->Arg).DMPC complexes was decreased by 30% although this variant was bound to adipocytes with normal affinity.	Dimyristoylphosphatidylcholine	101-105	apolipoprotein A-I	Mus musculus	77-83	
8428938-11	1993	By contrast, apoA-I(Lys107-->Met).DMPC complexes were decreased in their binding affinity compared to normal apoA-I.DMPC complexes but normally promoted cholesterol efflux.	Dimyristoylphosphatidylcholine	37-41	apolipoprotein A-I	Mus musculus	13-19	
8428938-11	1993	By contrast, apoA-I(Lys107-->Met).DMPC complexes were decreased in their binding affinity compared to normal apoA-I.DMPC complexes but normally promoted cholesterol efflux.	Dimyristoylphosphatidylcholine	37-41	apolipoprotein A-I	Mus musculus	112-118	
8428938-11	1993	By contrast, apoA-I(Lys107-->Met).DMPC complexes were decreased in their binding affinity compared to normal apoA-I.DMPC complexes but normally promoted cholesterol efflux.	Dimyristoylphosphatidylcholine	119-123	apolipoprotein A-I	Mus musculus	13-19	
8808496-2	1996	Analyses of re-isolated ox-LDL showed that apo A-I was transferred from DMPC/apo A-I to ox-LDL, which accounted for 10% of the total protein of ox-LDL.	Dimyristoylphosphatidylcholine	72-76	apolipoprotein A-I	Mus musculus	43-50	
8808496-2	1996	Analyses of re-isolated ox-LDL showed that apo A-I was transferred from DMPC/apo A-I to ox-LDL, which accounted for 10% of the total protein of ox-LDL.	Dimyristoylphosphatidylcholine	72-76	apolipoprotein A-I	Mus musculus	77-84	
8428938-12	1993	Incubation of mouse peritoneal macrophages with apoA-I(Pro165-->Arg).DMPC complexes did also result in a 30% decreased efflux of radiolabeled cholesterol if compared to rHDL with the normal allele product from the same donor.	Dimyristoylphosphatidylcholine	72-76	apolipoprotein A-I	Mus musculus	48-54	
32810603-8	2020	CONCLUSION: Studies of DMPC microsolubilization show that proline residues are essential to the optimal interaction of APOA1 with membranes, the initial step in cholesterol efflux and HDL production.	Dimyristoylphosphatidylcholine	23-27	apolipoprotein A-I	Mus musculus	119-124