Compounds > arginine

arginine and Hyperlipoproteinemia

arginine has been researched along with Hyperlipoproteinemia in 4 studies

Research

Studies (4)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's3 (75.00)18.2507
2000's1 (25.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Breuer, ML; Havekes, LM; Hofker, MH; van der Boom, H; van der Zee, A; van Dijk, KW; van Gorp, PJ; van Vlijmen, BJ; van't Hof, HB1
Coetzee, GA; de Villiers, WJ; Henderson, HE; Marais, AD; van der Westhuyzen, DR1
Gylling, H; Huttunen, JK; Jauhiainen, M; Kantola, I; Kontula, K; Miettinen, HE; Miettinen, TA; Tenhunen, J; Virtamo, J1
Arner, P; Ehrenborg, E; Eriksson, P; Hamsten, A; Large, V; Ruotolo, G; Skogsberg, J1

Other Studies

4 other study(ies) available for arginine and Hyperlipoproteinemia

ArticleYear
In the absence of endogenous mouse apolipoprotein E, apolipoprotein E*2(Arg-158 --> Cys) transgenic mice develop more severe hyperlipoproteinemia than apolipoprotein E*3-Leiden transgenic mice.
    The Journal of biological chemistry, 1996, Nov-29, Volume: 271, Issue:48

    Topics: Animals; Apolipoproteins E; Arginine; Cells, Cultured; Cysteine; Genes, Dominant; Heymann Nephritis Antigenic Complex; Hyperlipoproteinemias; Lipoproteins, LDL; Lipoproteins, VLDL; Membrane Glycoproteins; Mice; Mice, Knockout; Mice, Transgenic; Receptors, LDL

1996
The apolipoprotein E2 (Arg145Cys) mutation causes autosomal dominant type III hyperlipoproteinemia with incomplete penetrance.
    Arteriosclerosis, thrombosis, and vascular biology, 1997, Volume: 17, Issue:5

    Topics: Adolescent; Adult; Apolipoprotein E2; Apolipoproteins E; Arginine; Cholesterol, HDL; Cysteine; Female; Heterozygote; Homozygote; Humans; Hyperlipoproteinemias; Male; Middle Aged; Pedigree; Point Mutation; Polymorphism, Restriction Fragment Length; Restriction Mapping; Sequence Analysis, DNA; Triglycerides

1997
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.
    Arteriosclerosis, thrombosis, and vascular biology, 1998, Volume: 18, Issue:4

    Topics: Adult; Arginine; Carrier Proteins; Cholesterol Ester Transfer Proteins; Cholesterol Esters; Cholesterol, HDL; Cholesterol, LDL; Finland; Glycine; Glycoproteins; Humans; Hyperlipoproteinemias; Male; Mutation; Pedigree; Phosphatidylcholine-Sterol O-Acyltransferase; Polymerase Chain Reaction; Tangier Disease

1998
The Q/E27 polymorphism in the beta2-adrenoceptor gene is associated with increased body weight and dyslipoproteinaemia involving triglyceride-rich lipoproteins.
    Journal of internal medicine, 2000, Volume: 247, Issue:6

    Topics: Adult; Alleles; Arginine; Body Weight; Cholesterol; Cholesterol, VLDL; Genotype; Glutamic Acid; Glutamine; Glycine; Humans; Hyperlipoproteinemias; Male; Middle Aged; Mutation; Polymorphism, Genetic; Receptors, Adrenergic, beta-2; Sweden; Triglycerides

2000