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Cholesteryl Ester Transfer Protein Deficiency

Known as: HALP1, Hyperalphalipoproteinemia, CETP Deficiency 
An autosomal dominant genetic condition caused by mutation(s) in the CETP gene, encoding cholesteryl ester transfer protein. Affected individuals may… Expand
National Institutes of Health

Papers overview

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Highly Cited
2004
Highly Cited
2004
Our purpose was to compare HDL subpopulations, as determined by nondenaturing two-dimensional gel electrophoresis followed by… Expand
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Highly Cited
2001
Highly Cited
2001
The discovery of the ABCA1 lipid transporter has generated interest in modulating human plasma HDL levels and atherogenic risk by… Expand
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Highly Cited
1998
Highly Cited
1998
BACKGROUND Use of genetic analysis may improve the predictive value of risk factors for disease. A high plasma level of high… Expand
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Highly Cited
1997
Highly Cited
1997
Low levels of HDL cholesterol have been clearly demonstrated to be associated with an increased incidence of coronary heart… Expand
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Highly Cited
1995
Highly Cited
1995
Hyperalphalipoproteinemia (HALP) has been regarded as a beneficial state accompanied by a longevity syndrome. However, we… Expand
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Highly Cited
1995
Highly Cited
1995
The cholesteryl ester transfer protein (CETP) transfers lipids among lipoprotein particles and plays a central role in… Expand
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Review
1995
Review
1995
Plasma cholesteryl ester transfer protein plays a central role in lipoprotein metabolism by exchanging cholesteryl esters with… Expand
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Highly Cited
1993
Highly Cited
1993
Deficiency of the cholesteryl ester transfer protein (CETP) in humans is characterized by markedly elevated plasma concentrations… Expand
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Highly Cited
1990
Highly Cited
1990
This study characterized the plasma lipoproteins of familial hyperalphalipoproteinemic patients with or without deficiency of… Expand
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Highly Cited
1987
Highly Cited
1987
High density lipoprotein (HDL) is the major plasma lipoprotein found in mice fed normal laboratory chow containing 4% fat. When… Expand
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