Overexpression of apolipoprotein CII causes hypertriglyceridemia in transgenic mice.

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Hypertriglyceridemia in Transgenic Mice

We have generated transgenic mice expressing the human apolipoprotein CII (apoCI ) gene under the transcriptional control of the human cytochrome P450 IA1 (CYPIAl) promoter. Human apoCIt transgenic (HuCIITg) mice exhibited significant basal expression of the transgene (plasma apoCIl level = 26.1±4 mg/dl) and showed further induction of transgene expression after treatment with fl-naphthoflavone...

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Detection of mutations in the apolipoprotein CII gene by denaturing gradient gel electrophoresis. Identification of the splice site variant apolipoprotein CII-Hamburg in a patient with severe hypertriglyceridemia.

Familial apolipoprotein (apo) CII deficiency is a rare autosomal recessive inborn error of metabolism clinically resembling lipoprotein lipase deficiency. A number of mutations of the apo CII gene are known to date; they are located in the promoter region, the coding exons, or in the splice junctions. We present a simple assay based on PCR and denaturing gradient gel electrophoresis, which allo...

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Resistant Hypertriglyceridemia in a Patient With High Plasma Levels of Apolipoprotein CII

With High Plasma Levels of Apolipoprotein CII To the Editor: Human apolipoprotein CII (apo CII) consists of 79 amino acid residues and is required as a cofactor in the hydrolysis of triacylglycerides of chylomicrons and VLDL by lipoprotein lipase.1,2 Familial apo CII deficiency is an autosomal recessive genetic disorder characterized by fasting hypertriglyceridemia and an accumulation of chylom...

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Resistant hypertriglyceridemia in a patient with high plasma levels of apolipoprotein CII.

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Demonstration of Apolipoprotein CII in Guinea Pigs

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ژورنال

عنوان ژورنال: Journal of Clinical Investigation

سال: 1994

ISSN: 0021-9738

DOI: 10.1172/jci117151