نتایج جستجو برای: apo e4 polymorphism

تعداد نتایج: 117403  

2005
Helena Gylling Katriina Aalto-Setala Kimmo Kontula

The aim of the present study was to evaluate the effect of variation of different gene loci separately and in concert on lipid metabolism in heterozygous familial hypercholesterolemia (FH). We assayed a unique low density lipoprotein (LDL) receptor gene defect (designated as FH-Helsinki), the Xba I polymorphism of the apolipoprotein (apo) B, phenotypes of the apo E, and determined the levels of...

Journal: :Frontiers in bioscience : a journal and virtual library 2002
Joseph F Clark Daniel A Huri Janice Carrozzella Edward C Jauch Pritesh Mehta Daniel Heaton Susan J Biehle Joseph P Broderick

Apo E, and its respective isoforms, have been linked to outcome and survival in cerebral vascular and cardiovascular diseases. The effectiveness of intravenous tPA in patients with acute ischemic stroke appears to be enhanced in patients who have an Apo E2 phenotype. The ability of Apo E isoproteins (endogenous Apo E isoproteins or exogenous Apo E isoproteins) to modulate tPA-induced clot lysis...

Journal: :Chinese medical journal 1992
T F Ashavaid Seema P Todur K G Nair

Apolipoprotein E is a constituent of various lipoproteins and plays an important role in the transport of cholesterol and other lipids among cells of various tissues. The gene is polymorphic with three alleles (epsilon2, epsilon3, and epsilon4) coding for isoforms E2, E3, and E4 and having different binding affinities for the apo E receptors. While the epsilon2 allele is associated with elevate...

2004
Erinn Jochimsen

The relationship between apolipoprotein E4 (Apo E4) and the occurrence of Alzheimer’s Disease is well known; however, the biochemical mechanism behind this association is not well characterized. This research project examines the potential differences in mercury binding between free Apo E2 and Apo E4 isoforms. An equilibrium dialysis chamber is used to monitor the movement and binding of mercur...

Journal: :Clinical chemistry 1995
M K Bolla L Haddad S E Humphries A F Winder I N Day

Molecular epidemiological research has identified the association of a common apolipoprotein E (apo E) isoform (E4 as opposed to E3), with risk both of coronary artery disease and of Alzheimer dementia. In addition, the role of apo E genotype (usually E2/E2) in Type III hyperlipidemia is well known. However, both for diagnostic and research purposes, apo E genotyping is cumbersome. The preferre...

Journal: :The Journal of clinical investigation 1991
T Demant D Bedford C J Packard J Shepherd

This study examined apolipoprotein (apo) B metabolism in normolipemic subjects homozygous for the apo E2 (n = 4), apo E3 (n = 5), or apo E4 (n = 5) phenotype. Radioiodinated very low density lipoprotein (VLDL1) (ultracentrifuge flotation rate [Sf] 60-400) and VLDL2 (Sf 20-60) were injected into volunteers and the conversion of apo B was followed through intermediate density lipoprotein (IDL) to...

Journal: :Clinical chemistry 1995
G Siest T Pillot A Régis-Bailly B Leininger-Muller J Steinmetz M M Galteau S Visvikis

The human apolipoprotein (apo) E gene is polymorphic, with three common alleles (epsilon 2, epsilon 3, epsilon 4) coding for three isoforms (E2, E3, E4). The isoforms differ from each other by a single amino acid substitution, and also differ in their binding affinity for the four apo E receptors. Apo E polymorphism is an important determinant of risk for the development of cardiovascular and A...

Journal: :The British journal of nutrition 2008
Markku J Nissinen Helena Gylling Tatu A Miettinen

The impact of apo E phenotypes on applicability of relative cholesterol synthesis (lathosterol:cholesterol) and absorption (ratios of cholestanol, campesterol and sitosterol to cholesterol) during diets of various cholesterol and fat content is unclear. We examined and compared with each other both relative and absolute synthesis and absorption among twenty-nine men, of whom eight, nine and twe...

2015
Sinem Yalcintepe Ozturk Ozdemir Servet Ozden Hacivelioglu Cisem Akurut Evrim Koc Ahmet Uludag Emine Cosar Fatma Silan

The aim of this study was to investigate the possible role of multiple inherited thrombophilic gene variations in women with unexplained spontaneous abortions. For this purpose, the Factor V Leiden (FVL) (rs6025), Prothrombin G20210A (rs1799963), MTHFR C677T (rs1801133), PAI-1 4G/5G (rs1799889), ACE I/D (rs1799752), eNOS E298D (rs1799983), and Apo E E2/E3/E4 (rs429358) polymorphisms were genoty...

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