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23. A family with complete deficiency of plasma cholesteryl ester transfer protein activities. Makita H, Tsuji M, Furuya Y, Tsuchihashi K, Akita H, Chiba H. Intern Med; 1994 Jul; 33(7):432-6. PubMed ID: 7949644 [Abstract] [Full Text] [Related]
27. Cholesteryl ester transfer protein deficiency caused by a nonsense mutation detected in the patient's macrophage mRNA. Gotoda T, Kinoshita M, Shimano H, Harada K, Shimada M, Ohsuga J, Teramoto T, Yazaki Y, Yamada N. Biochem Biophys Res Commun; 1993 Jul 15; 194(1):519-24. PubMed ID: 8333866 [Abstract] [Full Text] [Related]
28. Molecular genetic study of Finns with hypoalphalipoproteinemia and hyperalphalipoproteinemia: a novel Gly230 Arg mutation (LCAT[Fin]) of lecithin:cholesterol acyltransferase (LCAT) accounts for 5% of cases with very low serum HDL cholesterol levels. Miettinen HE, Gylling H, Tenhunen J, Virtamo J, Jauhiainen M, Huttunen JK, Kantola I, Miettinen TA, Kontula K. Arterioscler Thromb Vasc Biol; 1998 Apr 15; 18(4):591-8. PubMed ID: 9555865 [Abstract] [Full Text] [Related]
40. Relation of polymorphisms in the cholesteryl ester transfer protein gene to transfer protein activity and plasma lipoprotein levels in alcohol drinkers. Hannuksela ML, Liinamaa MJ, Kesäniemi YA, Savolainen MJ. Atherosclerosis; 1994 Sep 30; 110(1):35-44. PubMed ID: 7857368 [Abstract] [Full Text] [Related] Page: [Previous] [Next] [New Search]