Postprandial Lipoprotein Metabolism in Familial Hypobetalipoproteinemia

Postprandial Lipoprotein Metabolism in Familial Hypobetalipoproteinemia

Objective: Familial hypobetalipoproteinemia (FHBL) is an autosomal codominantly inherited disorder of lipoprotein metabolism characterized by decreased plasma concentrations of low-density lipoprotein-cholesterol and apolipoprotein (apo) B. We examined the effect of truncated apoB variants (

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Bibliographische Detailangaben
Veröffentlicht in:The journal of clinical endocrinology and metabolism 2007-04, Vol.92 (4), p.1474-1478
Hauptverfasser: Hooper, Amanda J., Robertson, Ken, Barrett, P. Hugh R., Parhofer, Klaus G., van Bockxmeer, Frank M., Burnett, John R.
Format: Artikel
Sprache:eng
Schlagworte:
Adult
Apolipoprotein B-48 - blood
Apolipoprotein B-48 - genetics
Biological and medical sciences
Blood Chemical Analysis
Body Mass Index
Dietary Fats
Endocrinopathies
Fundamental and applied biological sciences. Psychology
Humans
Hypobetalipoproteinemias - blood
Kinetics
Lipids - blood
Lipoproteins - blood
Medical sciences
Models, Biological
Postprandial Period
Vertebrates: endocrinology
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Beschreibung
Zusammenfassung:Objective: Familial hypobetalipoproteinemia (FHBL) is an autosomal codominantly inherited disorder of lipoprotein metabolism characterized by decreased plasma concentrations of low-density lipoprotein-cholesterol and apolipoprotein (apo) B. We examined the effect of truncated apoB variants (
ISSN:0021-972X
1945-7197
DOI:10.1210/jc.2006-1998