1[1]Brook-Wilson A, Marcil M, Clee SM, et al. Mutation in ABC1 in Tangier disease and familial high-density lipoprotein deficiency. Nat Genet, 1999, 22: 336-346
2[2]Bodzioch M, Orso E, Klucken J, et al. The gene encoding ATP-binding cassette transporter 1 is mutated in Trangier disease. Nat Genet, 1999, 22: 347-352
3[3]Rust S, Rosier M, Funke H, et al. Trangier disease is caused by muations in gene enconding ATP binding cassette transporter 1. Nat Genet, 1999, 22: 352-355
4[4]Marcil M, Brook-Wilson A, Clee SM, et al. Mutaion in the ABC1gene in familiar HDL deficiency with defective cholesterol efflux. Lancet, 1999, 354: 1 341-346
6[6]Francis GA, Kaopp RH, Oram JF. Defective removal of cellular cholesterol and phospholipids by apolipoprotein A-1 in Trangier disease. J Clin Invest, 1995, 96: 78-87
7[7]Santamarina-Fojo S, Peterson K, Knapper C, et al. Complete genomic sequence of human ABCA1gene: Analysis of human and mouse ATP-binding cassette A promoter. Proc Natl Acad Sci USA, 2000, 97: 7 987-992
8[8]Eckardstein AV, Nofer JR, Assmann G. High density lipoproeins and atherolerosis role of cholesterol efflux and reverse cholesterol transport. Arterioscler Thromb Vasc Biol, 2001, 21: 13-27
9[9]Vaisman BL, Lambert G, Amar M, et al. ABCA1 overexpression leads to hyperalphalipoproteinemia and increased biliary cholesterol excretion in transgenic mice. J Clin Invest, 2001, 108: 303-309
10[10]Oram JF, Lawn RM, Garvin MR, et al. ABCA1is the camp-inducible apolipoprotein receptor that mediates cholesterol secretion from macrophages. J Biol Chem, 2000, 275: 34 508-511