Heterozygous lipoprotein lipase deficiency due to a missense mutation as the cause of impaired triglyceride tolerance with multiple lipoprotein abnormalities.
about
The thyromimetic T-0681 protects from atherosclerosis.FABP4 plasma levels are increased in familial combined hyperlipidemia.Linkage of low-density lipoprotein size to the lipoprotein lipase gene in heterozygous lipoprotein lipase deficiencyRecessive inheritance of obesity in familial non-insulin-dependent diabetes mellitus, and lack of linkage to nine candidate genes.Lipoprotein lipase as a candidate target for cancer prevention/therapyGenetics of LDL particle heterogeneity: from genetic epidemiology to DNA-based variations.Severe hypertriglyceridemia, reduced high density lipoprotein, and neonatal death in lipoprotein lipase knockout mice. Mild hypertriglyceridemia with impaired very low density lipoprotein clearance in heterozygotesApolipoprotein E polymorphism influences postprandial retinyl palmitate but not triglyceride concentrationsBiochemistry and pathophysiology of intravascular and intracellular lipolysis.Lipoprotein lipase deficiency is associated with elevated acylation stimulating protein plasma levels.Effects of simvastatin 20 mg/d on serum lipid profiles in Japanese hyperlipidemic patients: A prospective, open-label pilot study.Association of Rare and Common Variation in the Lipoprotein Lipase Gene With Coronary Artery Disease.Relative hypoglycemia and hyperinsulinemia in mice with heterozygous lipoprotein lipase (LPL) deficiency. Islet LPL regulates insulin secretion.Adenovirus-mediated rescue of lipoprotein lipase-deficient mice. Lipolysis of triglyceride-rich lipoproteins is essential for high density lipoprotein maturation in mice.Metabolic and anti-inflammatory benefits of eccentric endurance exercise - a pilot study.The effect of smoking on post-heparin lipoprotein and hepatic lipase, cholesteryl ester transfer protein and lecithin:cholesterol acyl transferase activities in human plasma.Lipid and lipoprotein analysis of cats with lipoprotein lipase deficiency.COOH-terminal disruption of lipoprotein lipase in mice is lethal in homozygotes, but heterozygotes have elevated triglycerides and impaired enzyme activity.Hypertriglyceridemia and insulin resistance.
P2860
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P2860
Heterozygous lipoprotein lipase deficiency due to a missense mutation as the cause of impaired triglyceride tolerance with multiple lipoprotein abnormalities.
description
1993 nî lūn-bûn
@nan
1993 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
1993 թվականի փետրվարին հրատարակված գիտական հոդված
@hy
1993年の論文
@ja
1993年論文
@yue
1993年論文
@zh-hant
1993年論文
@zh-hk
1993年論文
@zh-mo
1993年論文
@zh-tw
1993年论文
@wuu
name
Heterozygous lipoprotein lipas ...... ple lipoprotein abnormalities.
@ast
Heterozygous lipoprotein lipas ...... ple lipoprotein abnormalities.
@en
type
label
Heterozygous lipoprotein lipas ...... ple lipoprotein abnormalities.
@ast
Heterozygous lipoprotein lipas ...... ple lipoprotein abnormalities.
@en
prefLabel
Heterozygous lipoprotein lipas ...... ple lipoprotein abnormalities.
@ast
Heterozygous lipoprotein lipas ...... ple lipoprotein abnormalities.
@en
P2093
P2860
P356
P1476
Heterozygous lipoprotein lipas ...... iple lipoprotein abnormalities
@en
P2093
B Paulweber
E Brandstätter
F Sandhofer
J R Patsch
P2860
P304
P356
10.1172/JCI116222
P407
P577
1993-02-01T00:00:00Z