Hua Han

Association of a Novel 3-Amino Acid Deletion Mutation of Apolipoprotein E (Apo E Tokyo) with Lipoprotein Glomerulopathy

T. Saruta, J. Sasaki, S. Oikawa, 1999, Nephron.

A novel two nucleotide deletion in the apolipoprotein A-I gene, apoA-I Shinbashi, associated with high density lipoprotein deficiency, corneal opacities, planar xanthomas, and premature coronary artery disease.

J. Sasaki, S. Mochizuki, A. Endo, 2004, Atherosclerosis.

Compound heterozygosity for an apolipoprotein A1 gene promoter mutation and a structural nonsense mutation with apolipoprotein A1 deficiency.

Wei Huang, J. Sasaki, K. Arakawa, 1999, Arteriosclerosis, thrombosis, and vascular biology.

A novel mutant, ApoA-I nichinan (Glu235-->0), is associated with low HDL cholesterol levels and decreased cholesterol efflux from cells.

J. Sasaki, K. Arakawa, S. Horiuchi, 1999, Arteriosclerosis, thrombosis, and vascular biology.

A single amino acid deletion in the carboxy terminal of apolipoprotein A-I impairs lipid binding and cellular interaction.

Wei Huang, J. Sasaki, K. Arakawa, 2000, Arteriosclerosis, thrombosis, and vascular biology.