Apoa5 Q139X truncation predisposes to late-onset hyperchylomicronemia due to lipoprotein lipase impairment.
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Molecular processes that handle -- and mishandle -- dietary lipidsApolipoprotein A-V gene therapy for disease prevention / treatment:a critical analysisInfluence of apolipoprotein A-V on the metabolic fate of triacylglycerolAPOA5 Ala315>Val, identified in patients with severe hypertriglyceridemia, is a common mutation with no major effects on plasma lipid levelsPost-heparin LPL activity measurement using VLDL as a substrate: a new robust method for routine assessment of plasma triglyceride lipolysis defectsThe C terminus of apolipoprotein A-V modulates lipid-binding activity.Atherogenesis and metabolic dysregulation in LDL receptor-knockout rats.Lipoprotein lipase activity and mass, apolipoprotein C-II mass and polymorphisms of apolipoproteins E and A5 in subjects with prior acute hypertriglyceridaemic pancreatitisApolipoprotein A5 and lipoprotein lipase interact to modulate anthropometric measures in Hispanics of Caribbean origin.Novel LMF1 nonsense mutation in a patient with severe hypertriglyceridemiaGPIHBP1: an endothelial cell molecule important for the lipolytic processing of chylomicrons.The N-terminus of apolipoprotein A-V adopts a helix bundle molecular architecture.Interactions between the APOA5 -1131T>C and the FEN1 10154G>T polymorphisms on ω6 polyunsaturated fatty acids in serum phospholipids and coronary artery disease.Intravenous injection of apolipoprotein A-V reconstituted high-density lipoprotein decreases hypertriglyceridemia in apoav-/- mice and requires glycosylphosphatidylinositol-anchored high-density lipoprotein-binding protein 1.APOA5 Q97X mutation identified through homozygosity mapping causes severe hypertriglyceridemia in a Chilean consanguineous family.Biogenesis of apolipoprotein A-V and its impact on VLDL triglyceride secretion.Association between CETP, MLXIPL, and TOMM40 polymorphisms and serum lipid levels in a Latvian population.Lipoprotein lipase: from gene to obesity.Type 1 hyperlipoproteinemia and recurrent acute pancreatitis due to lipoprotein lipase antibody in a young girl with Sjogren's syndrome.The role of CREB-H transcription factor in triglyceride metabolism.Give me A5 for lipoprotein hydrolysis!Determinants of plasma apolipoprotein A-V and APOA5 gene transcripts in humans.ApoE2-associated hypertriglyceridemia is ameliorated by increased levels of apoA-V but unaffected by apoC-III deficiencyEvaluation of seven common lipid associated loci in a large Indian sib pair study.Structural and functional analysis of APOA5 mutations identified in patients with severe hypertriglyceridemia.Intracellular lipid droplet targeting by apolipoprotein A-V requires the carboxyl-terminal segmentGene transfer of apolipoprotein A-V improves the hypertriglyceridemic phenotype of apoa5 (-/-) mice.The APOA5 rs662799 polymorphism is associated with dyslipidemia and the severity of coronary heart disease in Chinese women.An APOA5 3' UTR variant associated with plasma triglycerides triggers APOA5 downregulation by creating a functional miR-485-5p binding site.Apolipoprotein A-V N-terminal domain lipid interaction properties in vitro explain the hypertriglyceridemic phenotype associated with natural truncation mutants.Association of APOA5 rs662799 and rs3135506 polymorphisms with arterial hypertension in Moroccan patients.The complex genetic basis of plasma triglycerides.The pathophysiology of intestinal lipoprotein production.Apolipoprotein A-V association with intracellular lipid droplets.Apolipoprotein A-V, triglycerides and risk of coronary artery disease: the prospective Epic-Norfolk Population Study.The carboxyl-terminal segment of apolipoprotein A-V undergoes a lipid-induced conformational change.Dietary oxidized linoleic acid lowers triglycerides via APOA5/APOClll dependent mechanisms.Association of APOA5 T1131C polymorphism and risk of coronary artery disease.Dietary capsanthin, the main carotenoid in paprika (Capsicum annuum), alters plasma high-density lipoprotein-cholesterol levels and hepatic gene expression in rats.Hypertriglyceridaemia and low plasma HDL in a patient with apolipoprotein A-V deficiency due to a novel mutation in the APOA5 gene.
P2860
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P2860
Apoa5 Q139X truncation predisposes to late-onset hyperchylomicronemia due to lipoprotein lipase impairment.
description
2005 nî lūn-bûn
@nan
2005 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2005 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
2005年の論文
@ja
2005年論文
@yue
2005年論文
@zh-hant
2005年論文
@zh-hk
2005年論文
@zh-mo
2005年論文
@zh-tw
2005年论文
@wuu
name
Apoa5 Q139X truncation predisp ...... lipoprotein lipase impairment.
@ast
Apoa5 Q139X truncation predisp ...... lipoprotein lipase impairment.
@en
Apoa5 Q139X truncation predisp ...... lipoprotein lipase impairment.
@nl
type
label
Apoa5 Q139X truncation predisp ...... lipoprotein lipase impairment.
@ast
Apoa5 Q139X truncation predisp ...... lipoprotein lipase impairment.
@en
Apoa5 Q139X truncation predisp ...... lipoprotein lipase impairment.
@nl
prefLabel
Apoa5 Q139X truncation predisp ...... lipoprotein lipase impairment.
@ast
Apoa5 Q139X truncation predisp ...... lipoprotein lipase impairment.
@en
Apoa5 Q139X truncation predisp ...... lipoprotein lipase impairment.
@nl
P2093
P2860
P356
P1476
Apoa5 Q139X truncation predisp ...... lipoprotein lipase impairment.
@en
P2093
Agnès Sassolas
Bruno Verges
Christophe Marçais
Jamila Fruchart-Najib
Jocelyne Drai
Laurence Perrot
Len A Pennacchio
Micheline Merlin
Philippe Moulin
Stéphane Billon
P2860
P304
P356
10.1172/JCI24471
P407
P577
2005-10-01T00:00:00Z