Bile acid metabolism in hereditary forms of hypertriglyceridemia: evidence for an increased synthesis rate in monogenic familial hypertriglyceridemia.
about
Human apical sodium-dependent bile salt transporter gene (SLC10A2) is regulated by the peroxisome proliferator-activated receptor alphaFarnesoid X receptor: a master regulator of hepatic triglyceride and glucose homeostasisRole of the intestinal bile acid transporters in bile acid and drug dispositionInhibition of intestinal bile acid transporter Slc10a2 improves triglyceride metabolism and normalizes elevated plasma glucose levels in miceHypertriglyceridemia and cholesteryl ester transfer protein interact to dramatically alter high density lipoprotein levels, particle sizes, and metabolism. Studies in transgenic miceBile acid metabolites in serum: intraindividual variation and associations with coronary heart disease, metabolic syndrome and diabetes mellitusImpaired activation of adipocyte lipolysis in familial combined hyperlipidemiaImpact of nutrient excess and endothelial nitric oxide synthase on the plasma metabolite profile in mice.Deciphering the nuclear bile acid receptor FXR paradigm.Physical activity as a determinant of fecal bile acid levels.Ethnic differences in the prevalence of polymorphisms in CYP7A1, CYP7B1 AND CYP27A1 enzymes involved in cholesterol metabolism.Genetically defined hyperlipidemia.Mechanisms of triglyceride metabolism in patients with bile acid diarrhea.High-Molecular-Weight β-Glucan Decreases Serum Cholesterol Differentially Based on the CYP7A1 rs3808607 Polymorphism in Mildly Hypercholesterolemic Adults.1994 Mack-Forster Award Lecture. Review. Studies on the regulation of hepatic cholesterol metabolism in humans.Increased production of apolipoprotein B-containing lipoproteins in the absence of hyperlipidemia in transgenic mice expressing cholesterol 7alpha-hydroxylase.Stimulation of cholesterol synthesis and hepatic lipogenesis in patients with severe malabsorption.Targeted deletion of the ileal bile acid transporter eliminates enterohepatic cycling of bile acids in mice.A synthetic farnesoid X receptor (FXR) agonist promotes cholesterol lowering in models of dyslipidemia.Translocation-arrested apolipoprotein B evades proteasome degradation via a sterol-sensitive block in ubiquitin conjugation.Dexamethasone exposure of neonatal rats modulates biliary lipid secretion and hepatic expression of genes controlling bile acid metabolism in adulthood without interfering with primary bile acid kinetics.Activation of the farnesoid X receptor improves lipid metabolism in combined hyperlipidemic hamsters.Pronounced variation in bile acid synthesis in humans is related to gender, hypertriglyceridaemia and circulating levels of fibroblast growth factor 19.Characterizing Factors Associated With Differences in FGF19 Blood Levels and Synthesis in Patients With Primary Bile Acid Diarrhea.
P2860
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P2860
Bile acid metabolism in hereditary forms of hypertriglyceridemia: evidence for an increased synthesis rate in monogenic familial hypertriglyceridemia.
description
1987 nî lūn-bûn
@nan
1987 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
1987 թվականի օգոստոսին հրատարակված գիտական հոդված
@hy
1987年の論文
@ja
1987年論文
@yue
1987年論文
@zh-hant
1987年論文
@zh-hk
1987年論文
@zh-mo
1987年論文
@zh-tw
1987年论文
@wuu
name
Bile acid metabolism in heredi ...... familial hypertriglyceridemia.
@ast
Bile acid metabolism in heredi ...... familial hypertriglyceridemia.
@en
Bile acid metabolism in heredi ...... familial hypertriglyceridemia.
@nl
type
label
Bile acid metabolism in heredi ...... familial hypertriglyceridemia.
@ast
Bile acid metabolism in heredi ...... familial hypertriglyceridemia.
@en
Bile acid metabolism in heredi ...... familial hypertriglyceridemia.
@nl
prefLabel
Bile acid metabolism in heredi ...... familial hypertriglyceridemia.
@ast
Bile acid metabolism in heredi ...... familial hypertriglyceridemia.
@en
Bile acid metabolism in heredi ...... familial hypertriglyceridemia.
@nl
P2093
P2860
P356
P1476
Bile acid metabolism in heredi ...... familial hypertriglyceridemia.
@en
P2093
J D Brunzell
K S Hershon
P2860
P304
P356
10.1073/PNAS.84.15.5434
P407
P577
1987-08-01T00:00:00Z