目的：研究极低密度脂蛋白对SD大鼠系膜细胞的促增殖作用。
Objective: To study the proliferation promotion effect of very low density lipoprotein on mesangial cells of SD rats.
本文研究了小鼠腹腔巨噬细胞极低密度脂蛋白（VLDL）受体的调节。
The regulation of the VLDL receptor on mouse peritoneal macrophages was studied.
极低密度脂蛋白一种脂蛋白，含有大量脂质到蛋白质，并带有从肝脏到组织的大部分胆固醇。
A lipoprotein containing a very large proportion of lipids to protein and carrying most cholesterol from the liver to the tissues.
非诺贝特和烟酸对非酒精脂肪肝患者肝内甘油三酯含量，极低密度脂蛋白动力学，胰岛素活性的影响。
Effect of Fenofibrate and Niacin on Intrahepatic Triglyceride Content, Very Low-Density Lipoprotein Kinetics, and Insulin Action in Obese Subjects with Nonalcoholic Fatty Liver Disease.
目的探讨人肾小球系膜细胞脂蛋白脂酶（LPL）的表达情况以及极低密度脂蛋白（VLDL）对其表达的影响。
Objective To study the expression of lipoprotein lipase(LPL) in human glomerular mesangial cells and the effect of very low-density lipoprotein(VLDL) on the expression of LPL.
实验表明SVM在稳定性上优于BP网络，而且在对极低密度脂蛋白（VLDL）类别回归估计的精确度上也比BP网络要好。
The experiments show that the proposed SVM-based method is better than the BP network based method in stability and accuracy, especially for the measurements of the VLDL cholesterol levels.
目的：观察极低密度脂蛋白受体(VLDL -R)的两种亚型在糖尿病患者脂肪组织中的分布和表达，以探讨其变化及意义。
AIM: to observe the distribution and expression of two subtypes of very low density lipoprotein receptor (VLDL r) in diabetic adipose tissues to investigate their changes and significance.
建立具有正常极低密度脂蛋白（VLDL）受体结合功能的小分子受体片段模型并借助此模型研究VLDL受体与配体结合的作用机制。
The purpose of the paper is to build a module of small molecular receptor fragments charactering normal VLDL-R binding function and study the mechanism of VLDL-R binding to ligand.
所得极低密度脂蛋白（VLDL）及低密度脂蛋白（LDL）经琼脂糖电泳、聚丙烯酰胺电泳（PAGE）及载脂蛋白SDS-聚丙烯酰胺电泳（SDS-PAGE）鉴定纯度良好。
The purity of isolated VLDL and LDL was confirmed by the lipoprotein electrophoresis on agarose gel and PAGE and by the apolipoprotein electrophoresis on SDS-PAGE.
所得极低密度脂蛋白（VLDL）及低密度脂蛋白（LDL）经琼脂糖电泳、聚丙烯酰胺电泳（PAGE）及载脂蛋白SDS-聚丙烯酰胺电泳（SDS-PAGE）鉴定纯度良好。
The purity of isolated VLDL and LDL was confirmed by the lipoprotein electrophoresis on agarose gel and PAGE and by the apolipoprotein electrophoresis on SDS-PAGE.
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