Analysis of apolipoprotein A-I, lecithin:cholesterol acyltransferase and glucocerebrosidase genes in hypoalphalipoproteinemia

This publication has 19 references indexed in Scilit:

• Cholesterol efflux regulatory protein, Tangier disease and familial high-density lipoprotein deficiency
  Current Opinion in Lipidology, 2000
• A novel DNA polymorphism (4886C>T) in the human LCAT gene
  Human Mutation, 2000
• β-glucocerebrosidase gene locus as a link for Gaucher's disease and familial hypo-α-lipoproteinaemia
  The Lancet, 1998
• Intestinal apolipoprotein AI gene transcription is regulated by multiple distinct DNA elements and is synergistically activated by the orphan nuclear receptor, hepatocyte nuclear factor 4.
  Journal of Clinical Investigation, 1995
• An apolipoprotein CIII haplotype protective against hypertriglyceridemia is specified by promoter and 3' untranslated region polymorphisms.
  Proceedings of the National Academy of Sciences, 1993
• Human lecithin-cholesterol acyltransferase gene: complete gene sequence and sites of expression
  Nucleic Acids Research, 1986
• Isolation and DNA Sequence of Full-Length cDNA and of the Entire Gene for Human Apolipoprotein AI—Discovery of a New Genetic Polymorphism in the apo AI Gene
  DNA, 1984
• Gene structure of human apolipoprotein Al
  Nucleic Acids Research, 1983
• DNA POLYMORPHISM ADJACENT TO HUMAN APOPROTEIN A-1 GENE: RELATION TO HYPERTRIGLYCERIDAEMIA
  The Lancet, 1983
• THE TROMSØHEART-STUDY
  The Lancet, 1977