Akira Honda

Abnormal cholesterol biosynthesis in sitosterolaemia and the Smith-Lemli-Opitz syndrome

A. Honda, Guorong Xu, G. Tint, 1996, Journal of Inherited Metabolic Disease.

Defective conversion of 7-dehydrocholesterol to cholesterol in cultured skin fibroblasts from Smith-Lemli-Opitz syndrome homozygotes.

A. Honda, G. Tint, A. Batta, 1995, Journal of lipid research.

Down-regulation of cholesterol biosynthesis in sitosterolemia: diminished activities of acetoacetyl-CoA thiolase, 3-hydroxy-3-methylglutaryl-CoA synthase, reductase, squalene synthase, and 7-dehydrocholesterol delta7-reductase in liver and mononuclear leukocytes.

A. Honda, G. Tint, A. Batta, 1998, Journal of lipid research.

Accurate detection of Smith–Lemli–Opitz syndrome carriers by measurement of the rate of reduction of the ergosterol C-7 double bond in cultured skin fibroblasts

A. Honda, G. Tint, A. Batta, 1998, Journal of Inherited Metabolic Disease.

Screening for abnormal cholesterol biosynthesis in the Smith-Lemli-Opitz syndrome: rapid determination of plasma 7-dehydrocholesterol by ultraviolet spectrometry.

A. Honda, G. Tint, A. Batta, 1997, American journal of medical genetics.

Fetal demise with Smith–Lemli–Opitz syndrome confirmed by tissue sterol analysis and the absence of measurable 7‐dehydrocholesterol Δ7‐reductase activity in chorionic villi

R. Steiner, K. Gibson, A. Honda, 2000, Prenatal diagnosis.