Mutations in the ABC 1 gene in familial HDL deficiency with defective cholesterol efflux

This publication has 31 references indexed in Scilit:

• Gapped BLAST and PSI-BLAST: a new generation of protein database search programs
  Nucleic Acids Research, 1997
• Alteration of Substrate Specificity by Mutations at the His⁶¹ Position in Predicted Transmembrane Domain 1 of Human MDR1/P-Glycoprotein
  Biochemistry, 1997
• Severe Familial HDL Deficiency in French-Canadian Kindreds
  Arteriosclerosis, Thrombosis, and Vascular Biology, 1995
• A lipoprotein lipase mutation (Asn291Ser) is associated with reduced HDL cholesterol levels in premature atherosclerosis
  Nature Genetics, 1995
• HDL-Mediated Efflux of Intracellular Cholesterol Is Impaired in Fibroblasts From Tangier Disease Patients
  Arteriosclerosis, Thrombosis, and Vascular Biology, 1995
• CLUSTAL W: improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choice
  Nucleic Acids Research, 1994
• Familial HDL deficiency due to marked hypercatabolism of normal apoA-I.
  Arteriosclerosis and Thrombosis: A Journal of Vascular Biology, 1993
• Characterization of apolipoprotein A-I- and A-II-containing lipoproteins in a new case of high density lipoprotein deficiency resembling Tangier disease and their effects on intracellular cholesterol efflux.
  Journal of Clinical Investigation, 1993
• Lipoprotein cholesterol, apolipoprotein A-I and B and lipoprotein (a) abnormalities in men with premature coronary artery disease
  Journal of the American College of Cardiology, 1992
• Lipoprotein abnormalities associated with a familial deficiency of hepatic lipase
  Atherosclerosis, 1982