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Multiple dysfunctions of two apolipoprotein A-I variants, apoA-I(R160L)Oslo and apoA-I(P165R), that are associated with hypoalphalipoproteinemia in heterozygous carriers.
J Lipid Res. 1999 Mar;40(3):486-94.
J Lipid Res. 1999.
PMID: 10064737
Free article.
Heterozygosity for apolipoprotein A-I(R160L)Oslo is associated with low levels of high density lipoprotein cholesterol and HDL-subclass LpA-I/A-II but normal levels of HDL-subclass LpA-I.
Leren TP, Bakken KS, Daum U, Ose L, Berg K, Assmann G, von Eckardstein A.
Leren TP, et al. Among authors: daum u.
J Lipid Res. 1997 Jan;38(1):121-31.
J Lipid Res. 1997.
PMID: 9034206
Free article.
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A natural apolipoprotein A-I variant, apoA-I (L141R)Pisa, interferes with the formation of alpha-high density lipoproteins (HDL) but not with the formation of pre beta 1-HDL and influences efflux of cholesterol into plasma.
Miccoli R, Zhu Y, Daum U, Wessling J, Huang Y, Navalesi R, Assmann G, von Eckardstein A.
Miccoli R, et al. Among authors: daum u.
J Lipid Res. 1997 Jun;38(6):1242-53.
J Lipid Res. 1997.
PMID: 9215551
Free article.
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Apolipoprotein A-I (R151C)Paris is defective in activation of lecithin: cholesterol acyltransferase but not in initial lipid binding, formation of reconstituted lipoproteins, or promotion of cholesterol efflux.
Daum U, Langer C, Duverger N, Emmanuel F, Benoit P, Denèfle P, Chirazi A, Cullen P, Pritchard PH, Bruckert E, Assmann G, von Eckardstein A.
Daum U, et al.
J Mol Med (Berl). 1999 Aug;77(8):614-22. doi: 10.1007/s001099900034.
J Mol Med (Berl). 1999.
PMID: 10543393
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