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NTIS 바로가기Atherosclerosis, v.153 no.2, 2000년, pp.461 - 468
Frikke-Schmidt, Ruth (Department of Clinical Biochemistry, Herlev University Hospital, DK-2730 Herlev, Denmark) , Wittrup, Hans H (Department of Clinical Biochemistry, Herlev University Hospital, DK-2730 Herlev, Denmark) , Tybjærg-Hansen, Anne (Department of Clinical Biochemistry, Herlev University Hospital, DK-2730 Herlev, Denmark) , Meinertz, Hans (Department of Medicine B, Division of Cardiology, Copenhagen University Hospital, DK-2100 Copenhagen, Denmark) , Schnohr, Peter (The Copenhagen City Heart Study, Bispebjerg University Hospital, DK-2400, Copenhagen NV, Denmark) , Nordestgaard, Børge G (The Copenhagen City Heart Study, Bispebjerg University Hospital, DK-2400, Copenhagen NV, Denmark)
AbstractExcept for the rare ε22 genotype it remains largely unsettled whether apolipoprotein E genotype influences an individual's referral to lipid clinics. To test this hypothesis, we compared genotype distributions among 156 hypercholesterolemic and 83 hypertriglyceridemic patients attendi...
Proc. Natl. Acad. Sci. USA Paik 82 3445 1985 10.1073/pnas.82.10.3445 Nucleotide sequence and structure of the human apolipoprotein E gene
J. Biol. Chem. Das 260 6240 1985 10.1016/S0021-9258(18)88963-3 Isolation, characterization, and mapping to chromosome 19 of the human apolipoprotein E gene
Mahley 1953 1995 The Metabolic and Molecular Bases of Inherited Disease Type III hyperlipoproteinemia (dysbetalipoproteinemia): the role of apolipoprotein E in normal and abnormal lipoprotein metabolism
Curr. Opin. Lipidol. de Knijff 7 59 1996 10.1097/00041433-199604000-00002 Apolipoprotein E as a risk factor for coronary heart disease: a genetic and molecular biology approach
Arterioscler. Thromb. Vasc. Biol. Boer 17 1675 1997 10.1161/01.ATV.17.9.1675 Interactions between lifestyle-related factors and the apoE polymorphism on plasma lipids and apolipoproteins. The EARS study
Clin. Genet. Utermann 14 351 1978 10.1111/j.1399-0004.1978.tb02101.x Polymorphism of apolipoprotein E. I. Methodological aspects and diagnosis of hyperlipoproteinemia type III without ultracentrifugation
Clin. Genet. Utermann 15 37 1979 10.1111/j.1399-0004.1979.tb02027.x Polymorphism of apolipoprotein E. II. Genetics of hyperlipoproteinemia type III
Clin. Genet. Utermann 15 63 1979 10.1111/j.1399-0004.1979.tb02028.x Polymorphism of apolipoprotein E. III. Effect of a single polymorphic gene locus on plasma lipid levels in man
Am. J. Hum. Genet. Reilly 49 1155 1991 The gender-specific apolipoprotein E genotype influence on the distribution of lipids and apolipoproteins in the population of Rochester, MN. I. Pleiotropic effects on means and variances
J. Lipid Res. Dallongeville 33 447 1992 10.1016/S0022-2275(20)41611-6 Modulation of plasma triglyceride levels by apoE phenotype: a meta-analysis
Am. J. Hum. Genet. Reilly 51 1311 1992 The gender-specific apolipoprotein E genotype influence on the distribution of plasma lipids and apolipoproteins in the population of Rochester, MN. II. Regression relationships with concomitants
Am. J. Hum. Genet. Reilly 55 1001 1994 The gender-specific apolipoprotein E genotype influence on the distribution of plasma lipids and apolipoproteins in the population of Rochester, MN. III. Correlations and covariances
Arterioscler. Thromb. Luc 14 1412 1994 10.1161/01.ATV.14.9.1412 Impact of apolipoprotein E polymorphism on lipoproteins and risk of myocardial infarction. The ECTIM Study
Kane 1853 1995 The Metabolic and Molecular Bases for Inherited Diseases Disorders of the biogenesis and secretion of lipoproteins containing the B apolipoproteins
Goldstein 1981 1995 The Metabolic and Molecular Bases of Inherited Disease Familial hypercholesterolemia
Brunzell 1913 1995 The Metabolic and Molecular Bases of Inherited disease Familial lipoprotein lipase deficiency and other causes of the chylomicronemia syndrome
Breslow 2031 1995 The Metabolic and Molecular Bases of Inherited Disease Familial disorders of high-density lipoprotein metabolism
Scand. J. Soc. Med. Suppl. Appleyard 41 1 1989 The Copenhagen City Heart Study. Østerbroundersøgelsen. A book of tables with data from the first examination (1976-1978) and a 5 year follow-up (1981-1983). The Copenhagen City Heart Study Group
J. Clin. Invest. Wittrup 99 1606 1997 10.1172/JCI119323 A common substitution (asn291ser) in lipoprotein lipase is associated with increased risk of ischemic heart disease
J. Clin. Invest. Tybjærg-Hansen 99 3034 1997 10.1172/JCI119499 A common mutation (G-455→A) in the β-fibrinogen promoter is an independent predictor of plasma fibrinogen, but not of ischemic heart disease
N. Eng. J. Med. Tybjærg-Hansen 338 1577 1998 10.1056/NEJM199805283382203 Association of mutations in the apolipoprotein B gene with hypercholesterolemia and the risk of ischemic heart disease
Ann. Intern. Med. Agerholm-Larsen 127 346 1997 10.7326/0003-4819-127-5-199709010-00002 ACE gene polymorphism as a risk factor for ischemic cerebrovascular disease
Circulation Nordestgaard 96 1737 1997 10.1161/01.CIR.96.6.1737 Heterozygous lipoprotein lipase deficiency. Frequency in the general population, effect on plasma lipid levels, and risk of ischemic heart disease
J. Lipid Res. Hixson 31 545 1990 10.1016/S0022-2275(20)43176-1 Restriction isotyping of human apolipoprotein E by gene amplification and cleavage with HhaI
Clin. Chem. Friedewald 18 499 1972 10.1093/clinchem/18.6.499 Estimation of the concentration of low-density lipoprotein cholesterol in plasma, without use of the preparative ultracentrifuge
1998 Base System User's Guide and Professional Statistics, release 8.0
Snedecor 253 1980 Statistical Methods The random effects model
Arterioscler. Thromb. Vasc. Biol. Tonstad 15 1009 1995 10.1161/01.ATV.15.8.1009 Determinants of lipid levels among children with heterozygous familial hypercholesterolemia in Norway
Lancet Ghiselli 2 405 1982 10.1016/S0140-6736(82)90439-1 Phenotype study of apolipoprotein E isoforms in hyperlipoproteinaemic patients
Hum. Genet. Utermann 65 232 1984 10.1007/BF00286508 Apolipoprotein E phenotypes and hyperlipidemia
Clin. Chem. Assmann 30 641 1984 10.1093/clinchem/30.5.641 Apolipoprotein E polymorphism and hyperlipidemia
Arterioscler. Thromb. Ferrieres 14 1553 1994 10.1161/01.ATV.14.10.1553 Apolipoprotein E polymorphism and heterozygous familial hypercholesterolemia. Sex-specific effects
Arteriosclerosis Lussier-Cacan 5 639 1985 10.1161/01.ATV.5.6.639 Apo E allele frequency in primary endogenous hypertriglyceridemia (type IV) with and without hyperapobetalipoproteinemia
Clin. Chem. Leren 27 458 1985 Increased frequency of the apolipoprotein E-4 isoform in male subjects with multifactorial hypercholesterolemia
Eur. J. Epidemiol. Davignon 8 Suppl. I 10 1992 10.1007/BF00145344 Phenotypic heterogeneity associated with defective apolipoprotein B-100 and occurrence of the familial hypercholesterolemia phenotype in the absence of an LDL receptor defect within a Canadian kindred
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