نتایج جستجو برای: apolipoprotein ecoronary atherosclerosispolymorphismrestriction isotyping

تعداد نتایج: 23036  

Journal: :research in molecular medicine 0
mohammad askari cellular and molecular research center, tehran university of medical sciences, tehran, iran amin reza nikpoor department of immunology, faculty of medicine, mashhad university of medical sciences, mashhad, iran. hajar aryan fazeli-sanati genetic laboratory, tehran, iran hamid ghaedi department of medical genetics, shahid beheshti university of medical sciences, tehran, iran. javad akhtari immunogenetics research center, faculty of medicine, mazandaran university of medical sciences, sari, iran asaad azarnejad department of medical biotechnology, tehran university of medical sciences, tehran, iran

background: we aimed here to investigate the association between alleles and genotypes of apoe and age-related macular degeneration (amd) development. materials and methods: after ophthalmological examination, 120 patients with confirmed amd and 120 healthy controls were enrolled in the study. the polymorphic segment of apoe gene was pcr-amplified and sequenced to determine the frequency distri...

Journal: :The Journal of biological chemistry 1982
F van't Hooft R J Havel

High density lipoproteins of rat blood plasma were labeled in vitro with radioiodinated apolipoprotein E and biologically with [3H]cholesteryl esters. These two components, present in high density lipoproteins separated from serum of normal or cholesterol-fed rats by molecular sieve chromatography, were removed slowly from perfused livers and the labeled apolipoprotein E was also removed slowly...

Journal: :Journal of lipid research 1990
M E Bouma I Beucler M Pessah C Heinzmann A J Lusis H Y Naim T Ducastelle B Leluyer J Schmitz R Infante

We describe here two patients, M. P. and S. L., with recessive abetalipoproteinemia. Analysis of restriction fragments of DNA from both patients using cDNA probes spanning the entire apolipoprotein B gene revealed no major insertions or deletions. Further, as defined by restriction fragment length polymorphism, abetalipoproteinemia, in these patients, did not appear associated with particular a...

Journal: :journal of nutritional sciences and dietetics 0
laleh keramat department of cellular and molecular nutrition, school of nutritional sciences and dietetics, tehran university of medical sciences, tehran, iran mohammadreza eshraghian department of biostatistics and epidemiology, school of public health, tehran university of medical sciences, tehran, iran mahmoud djalali department of cellular and molecular nutrition, school of nutritional sciences and dietetics, tehran university of medical sciences, tehran, iran gity sotoudeh department of community nutrition, school of nutritional sciences and dietetics, tehran university of medical sciences, tehran, iran haleh sadrzadeh-yeganeh department of community nutrition, school of nutritional sciences and dietetics, tehran university of medical sciences, tehran, iran fariba koohdani department of cellular and molecular nutrition, school of nutritional sciences and dietetics, and diabetes research center, endocrinology and metabolism clinical sciences institute, tehran university of medical sciences, tehran, iran

b a ckground: the objective was to investigate the relationship between serum interleukin-18 (il-18), pentraxin 3 (ptx3), and high-sensitivity c-reactive protein (hs-crp) levels with body mass index (bmi) and abdominal obesity and also the interaction between genetic variants of apolipoprotein a-ii (apo a-ii) and obesity on the levels of these factors in type 2 diabetes patients (t2d). m ethods...

Journal: :medical journal of islamic republic of iran 0
v hadavi from the department of human genetics & anthropology, school of public health & institute of public health research, tehran university of medical sciences, p.d.box 14155-6446, tehran dd farhud from the department of human genetics & anthropology, school of public health & institute of public health research, tehran university of medical sciences, p.d.box 14155-6446, tehran mh sanati the national research center for genetic engineering and biotechnology, tehran sm nabavi the shahed medical university, m seyedian tehran university of medical sciences, roozbeh hospital m hushmand the national research center for genetic engineering and biotechnology

multiple sclerosis (ms) is a chronic inflammatory disorder of the central nervous system, with a complex etiology that includes a strong genetic component. the chromosome 19q 13 region surrounding the apolipoprotein e (apoe) gene has shown consistent evidence of involvement in ms. in a cross-sectional study, to show the apoe genotype and allele frequency in the ms population of iran in comparis...

Journal: :Arteriosclerosis and thrombosis : a journal of vascular biology 1994
J Louhija H E Miettinen K Kontula M J Tikkanen T A Miettinen R S Tilvis

We determined the common polymorphism of apolipoprotein E (E2, E3, and E4), apolipoprotein B Xba I polymorphism, and apolipoprotein C-III Sst I polymorphism in almost all Finnish centenarians alive in 1991 (n = 179/185). Plasma lipid and lipoprotein levels in different apolipoprotein genotypes were also measured. In comparison with younger Finnish populations studied previously, the frequency o...

2002
Carl Franzblau

The expression of apolipoprotein E in cultured neonatal rabbit aortic smooth muscle cells was examined. Northern blot analysis determined that there was a single RNA transcript of approximately 1.2 kb. Moreover, a polyclonal antibody against rabbit apolipoprotein E was prepared in a goat and used in immunoprecipitations to demonstrate that the cultured cells secreted apolipoprotein E into the m...

Journal: :Journal of lipid research 1997
A J Mendez

It is becoming increasingly accepted that removal of cellular cholesterol occurs by at least two pathways, one involving the well-described aqueous diffusion mechanism and another promoted by lipid-free apolipoproteins. We compared the contribution of apolipoprotein-dependent and -independent pathways, taking into consideration the influence of cellular metabolism, on cholesterol efflux promote...

Journal: :Brain : a journal of neurology 2012
Robert M Koffie Tadafumi Hashimoto Hwan-Ching Tai Kevin R Kay Alberto Serrano-Pozo Daniel Joyner Steven Hou Katherine J Kopeikina Matthew P Frosch Virginia M Lee David M Holtzman Bradley T Hyman Tara L Spires-Jones

The apolipoprotein E ε4 gene is the most important genetic risk factor for sporadic Alzheimer's disease, but the link between this gene and neurodegeneration remains unclear. Using array tomography, we analysed >50000 synapses in brains of 11 patients with Alzheimer's disease and five non-demented control subjects and found that synapse loss around senile plaques in Alzheimer's disease correlat...

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