نتایج جستجو برای: 3 hydroxy 3 methylglutaryl coa reductase hmgcr cholesterol cholesterol 7α hydroxylase

تعداد نتایج: 1946999  

Journal: :Journal of lipid research 1983
P E Van Zuiden S K Erickson A D Cooper

The effect of remnant lipoproteins on hepatic 3-hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) reductase and hepatic very low density lipoprotein (VLDL) secretion was studied in the perfused rat liver and in vivo. As had been observed previously, when the liver was perfused with a lipid-free medium, HMG-CoA reductase activity increased about twofold after 150 min, and this increase could be prev...

Journal: :The EMBO journal 2000
E S Istvan M Palnitkar S K Buchanan J Deisenhofer

3-hydroxy-3-methylglutaryl-CoA reductase (HMGR) catalyzes the formation of mevalonate, the committed step in the biosynthesis of sterols and isoprenoids. The activity of HMGR is controlled through synthesis, degradation and phosphorylation to maintain the concentration of mevalonate-derived products. In addition to the physiological regulation of HMGR, the human enzyme has been targeted success...

2011
Kyung-Soo Chang Hyun-Jung Jo

Replication of hepatitis C virus (HCV) is regulated by statin, one of 3-hydroxy-3-methylglutaryl CoA reducatase (HMG CoA reductase) inhibitors that block mevalonate pathway and cholesterol biosyntheis, which has been used usefully for health improvement and disease control in clinic. In order to know which statin can be used to inhibit HCV replication, we examined the effects of HCV genotype 1b...

Journal: :Arteriosclerosis and thrombosis : a journal of vascular biology 1994
L Karayan S Qiu C Betard R Dufour G Roederer A Minnich J Davignon J Genest

The 10-kb deletion ("French Canadian mutation") of the low-density lipoprotein (LDL) receptor gene is the most common mutation causing familial hypercholesterolemia among subjects of French Canadian descent. In affected subjects, it results in a null allele of the LDL receptor gene and provides a unique opportunity to examine single-allele regulation of this gene in humans. We sought to ascerta...

2016
Jae Hoon Cha Sun Rim Kim Hyun Joong Kang Myung Hwan Kim Ae Wha Ha Woo Kyoung Kim

BACKGROUND/OBJECTIVES Corn silk (CS) extract contains large amounts of maysin, which is a major flavonoid in CS. However, studies regarding the effect of CS extract on cholesterol metabolism is limited. Therefore, the purpose of this study was to determine the effect of CS extract on cholesterol metabolism in C57BL/6J mouse fed high-fat diets. MATERIALS/METHODS Normal-fat group fed 7% fat die...

Journal: :American journal of physiology. Gastrointestinal and liver physiology 2001
E Hall P Hylemon Z Vlahcevic D Mallonee K Valerie N Avadhani W Pandak

In the liver, sterol 27-hydroxylase (CYP27) participates in the classic and alternative pathways of bile acid biosynthesis from cholesterol (Chol). In extrahepatic tissues, CYP27 converts intracellular Chol to 27-hydroxycholesterol (27OH-Chol), which may regulate the activity of 3-hydroxy-3-methylglutaryl CoA reductase (HMG-CoA-R). This study attempts to better define the role of CYP27 in the m...

Journal: :Human molecular genetics 2014
Chi-Yi Yu Elizabeth Theusch Kathleen Lo Lara M Mangravite Devesh Naidoo Mariya Kutilova Marisa W Medina

3-hydroxy-3-methylglutaryl-Coenzyme A reductase (HMGCR) encodes the rate-limiting enzyme in the cholesterol biosynthesis pathway and is inhibited by statins, a class of cholesterol-lowering drugs. Expression of an alternatively spliced HMGCR transcript lacking exon 13, HMGCR13(-), has been implicated in the variation of plasma LDL-cholesterol (LDL-C) and is the single most informative molecular...

2014
Wei Jiang Jing-Jie Tang Hong-Hua Miao Yu-Xiu Qu Jie Qin Jie Xu Jinbo Yang Bo-Liang Li Bao-Liang Song

Somatic cell genetics is a powerful approach for unraveling the regulatory mechanism of cholesterol metabolism. However, it is difficult to identify the mutant gene(s) due to cells are usually mutagenized chemically or physically. To identify important genes controlling cholesterol biosynthesis, an unbiased forward genetics approach named validation-based insertional mutagenesis (VBIM) system w...

Journal: :Journal of lipid research 1998
S B Patel A Honda G Salen

Sitosterolemia (phytosterolemia) is a rare autosomal recessively inherited disorder that is characterized by premature coronary artery disease, xanthomas, and increased plasma plant sterols and 5alpha-stanols. Affected individuals show an increased absorption of both cholesterol and sitosterol from the diet, decreased bile clearance of these sterols and their metabolites resulting in markedly e...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید