1.杨振华，酶的测定，见：叶应妩，李健斋，王玉琛主编。临床实验诊断学，北京：人民卫生出版社，1991，588～466

　　2.Paltarf F,Wagner E,Stereospecificity of Lipaseenzymatic hydrolyosis of enantiomeric aldyldiacyl and dialdylacylglyerols bylipoprotein lipase.Biochim Biophys Acta,1976,431:359-362

　　3.DeebSS.Peng R.Structure of the human lipoprotein lipase gene.Biochemistry,1989,1169:582-4134

　　4.GotodaT,et al.Anewly identified null allelic mutation in the human lipoproteinlipase(LPL)gene of a compornd heterozygote with familial LPLdeficienacy,Biochys Acta,1992,1169:582-586

　　5.OkabeT,Yorifaji H,et al .Pulmonary macrophage:Amajor source of lipoprtein lipase inthe lung.Biochim Biophys Res Commun,1984,125:273-278

　　6.OkaK,George T,Stocks J,et al.Nucleotide sequence of PvuⅡpoolymorphic site at the humanlipoprotein lipase gene locus .Nuceic Acids Research,1990,18:5407-5411

　　7.ChuatJ,Raisonnier A,Etienne J,et al.The lipoprotein lipase-encodigng humangene:sequence from intron-6 to intron-9 and presence in intron-7 of a40-million-year-old Alu sequence.Gene,1992,110:257-261

　　8.GotodaT,Yamada N,Murase T,et al .Detection of three separate DNA polymorphisms in thehuman lipoprotein lipase gene by gene amplfication and restriction endonucleasedigestion.J Lipid Res,1992,33:1067-1072

　　9.RajK,Edward W,Ruth M,et al .DNA variants at the LPLgene locus associate withangiographically defined severity of atherosclerosis and serum lipoproteinlevels in a welsh poprlation.Arteriosclerosis and Thrombosis,1994,14:1090-1097

　　10.RobertA,Andrew J,Liling T,et al .Agene-gender interaction affecting plasmalipoproteins in a genetic isoalate,Arteriosclerosis andThrombosis,1994,14671-677

　　11.YangC,et al.Lecithin:cholesterol acyltransferase.J Biol Chem,1987,262:3086-3091

　　12.Alberts J,Adolphson J,Chen C,et al.Radiommunoassay of human plasma lecithincholesterol acyltransferase.J Clin Invest,1981,67:141-148

　　13.McleanJ et al .Cloning and expression of human lecithin cholesterol transferase cDNA,Proc Natl Acad Sci USA ,1986,83:2335-2339

　　14.Glomset.J.Norum K,Gjone E,et al.Lecithin:cholesterol acyltransferase deficiency.In:TheMetabolic Basis of Inherited Disease.McGraw Hill ,New Youk,1983,643-654

　　15.GlomsetJ.The plama lecithin cholesterol acyltransferase reaction.J LipidRes,1968,9:156-167

　　16.HolmqusitZ,Carlson L.Normalization of high density lipoprotein in fish eye diseaseplasma by purified normal human lecithin cholesterol acyltransferase .Lipids,1988,23:225-229

　　17.ZilversmitD B.Atherogenic nature of triglycerides .postprandial lipidemia andtriglyceride-rich remnant.Clin Chem,1995,41:153-158

　　18.TakagiA, et al.Molecular strdies on primary lipoprotein lipase(LPL)deficiency:onebase deltion (G916)in exon 5 of LPL gene causes no detectable LPL protein dueto the absence of LPLmessenger RNA transcript.Jclin Invest,1992,41:153-158

　　19.JingamiR,Brown M,Goldstein J,et al .Partial deletion of membrane-bound domain of3-hydroxy-3methylglu-taryl coenzyme a reductase eliminates sterol enhanceddegradation and prevents formation of crystalloid endoplasmic reticulum,JcellBiol,1987,104:1693

　　20.GoldsteirJ,Brown M,Regulation of the mevalonate pathway.Nature ,1990,343:425-430

　　21.EastC,Grundy S,Bilheimer D,et al.Preliminary report:Treatment of ytpe 3hyperlipidemia with mevinolin.Metabolism,1986,35:97098-,104:1693

　　22.阵上久人，HMGCoa Reductaseとそのinhibiter .最新医学，1992，47：82-90