Miettinen TA - Search Results

1

Two different allelic mutations in a Finnish family with lecithin:cholesterol acyltransferase deficiency.

Miettinen H, Gylling H, Ulmanen I, Miettinen TA, Kontula K. Miettinen H, et al. Among authors: miettinen ta. Arterioscler Thromb Vasc Biol. 1995 Apr;15(4):460-7. doi: 10.1161/01.atv.15.4.460. Arterioscler Thromb Vasc Biol. 1995. PMID: 7749857

2

Aging and genetic variation of plasma apolipoproteins. Relative loss of the apolipoprotein E4 phenotype in centenarians.

Louhija J, Miettinen HE, Kontula K, Tikkanen MJ, Miettinen TA, Tilvis RS. Louhija J, et al. Among authors: miettinen he, miettinen ta. Arterioscler Thromb. 1994 Jul;14(7):1084-9. doi: 10.1161/01.atv.14.7.1084. Arterioscler Thromb. 1994. PMID: 8018664

3

Regulation of serum cholesterol level in middle-aged and elderly men. Relation of cholesterol absorption and synthesis to lipoprotein metabolism.

Gylling H, Strandberg T, Tilvis R, Miettinen TA. Gylling H, et al. Among authors: miettinen ta. Arterioscler Thromb. 1994 May;14(5):694-700. doi: 10.1161/01.atv.14.5.694. Arterioscler Thromb. 1994. PMID: 8172847

4

Deletion of exon 15 of the LDL receptor gene is associated with a mild form of familial hypercholesterolemia. FH-Espoo.

Koivisto PV, Koivisto UM, Kovanen PT, Gylling H, Miettinen TA, Kontula K. Koivisto PV, et al. Among authors: miettinen ta. Arterioscler Thromb. 1993 Nov;13(11):1680-8. doi: 10.1161/01.atv.13.11.1680. Arterioscler Thromb. 1993. PMID: 8218110

5

Postabsorptive retinyl palmitate removal is retarded in lecithin-cholesterol acyltransferase deficiency.

Gylling H, Miettinen TA. Gylling H, et al. Among authors: miettinen ta. Eur J Clin Invest. 1993 May;23(5):302-6. doi: 10.1111/j.1365-2362.1993.tb00778.x. Eur J Clin Invest. 1993. PMID: 8354337

6

Polymorphisms of the genes encoding apoproteins A-I, B, C-III, and E and LDL receptor, and cholesterol and LDL metabolism during increased cholesterol intake. Common alleles of the apoprotein E gene show the greatest regulatory impact.

Gylling H, Kontula K, Koivisto UM, Miettinen HE, Miettinen TA. Gylling H, et al. Among authors: miettinen he, miettinen ta. Arterioscler Thromb Vasc Biol. 1997 Jan;17(1):38-44. doi: 10.1161/01.atv.17.1.38. Arterioscler Thromb Vasc Biol. 1997. PMID: 9012635

7

Apolipoprotein A-IFin. Dominantly inherited hypoalphalipoproteinemia due to a single base substitution in the apolipoprotein A-I gene.

Miettinen HE, Gylling H, Miettinen TA, Viikari J, Paulin L, Kontula K. Miettinen HE, et al. Among authors: miettinen ta. Arterioscler Thromb Vasc Biol. 1997 Jan;17(1):83-90. doi: 10.1161/01.atv.17.1.83. Arterioscler Thromb Vasc Biol. 1997. PMID: 9012641

8

Familial moderate hypercholesterolemia caused by Asp235-->Glu mutation of the LDL receptor gene and co-occurrence of a de novo deletion of the LDL receptor gene in the same family.

Koivisto UM, Gylling H, Miettinen TA, Kontula K. Koivisto UM, et al. Among authors: miettinen ta. Arterioscler Thromb Vasc Biol. 1997 Jul;17(7):1392-9. doi: 10.1161/01.atv.17.7.1392. Arterioscler Thromb Vasc Biol. 1997. PMID: 9261272

9

Apolipoprotein A-IFIN (Leu159-->Arg) mutation affects lecithin cholesterol acyltransferase activation and subclass distribution of HDL but not cholesterol efflux from fibroblasts.

Miettinen HE, Jauhiainen M, Gylling H, Ehnholm S, Palomäki A, Miettinen TA, Kontula K. Miettinen HE, et al. Among authors: miettinen ta. Arterioscler Thromb Vasc Biol. 1997 Nov;17(11):3021-32. doi: 10.1161/01.atv.17.11.3021. Arterioscler Thromb Vasc Biol. 1997. PMID: 9409289

10

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. Miettinen HE, et al. Among authors: miettinen ta. Arterioscler Thromb Vasc Biol. 1998 Apr;18(4):591-8. doi: 10.1161/01.atv.18.4.591. Arterioscler Thromb Vasc Biol. 1998. PMID: 9555865

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