Total deficiency of plasma cholesteryl ester transfer protein in subjects homozygous and heterozygous for the intron 14 splicing defect

This publication has 14 references indexed in Scilit:

• Organization of the human cholesteryl ester transfer protein gene
  Biochemistry, 1990
• Molecular basis of lipid transfer protein deficiency in a family with increased high-density lipoproteins
  Nature, 1989
• Mutations of the low density lipoprotein receptor in Japanese kindreds with familial hypercholesterolemia
  Human Genetics, 1988
• Small polydisperse low density lipoproteins in familial hyperalphalipoproteinemia with complete deficiency of cholesteryl ester transfer activity
  Atherosclerosis, 1988
• Cloning and sequencing of human cholesteryl ester transfer protein cDNA
  Nature, 1987
• Enzymatic Amplification of β-Globin Genomic Sequences and Restriction Site Analysis for Diagnosis of Sickle Cell Anemia
  Science, 1985
• Rate of Cholesteryl Ester Transfer between High and Low Density Lipoproteins in Human Serum and a Case with Decreased Transfer Rate in Association with Hyperalphalipoproteinemia1
  The Journal of Biochemistry, 1985
• Deficiency of serum cholesteryl-ester transfer activity in patients with familial hyperalphalipoproteinaemia
  Atherosclerosis, 1985
• A catalogue of splice junction sequences
  Nucleic Acids Research, 1982
• Lipoprotein-Polyanion-Metal Interactions1 1This investigation was supported in part by U. S. Public Health Service Research Grant HE-02965, and Training Grant TI HE-5273 and PO-AM 13430.
  Published by Elsevier ,1973