Ching Yin Lee

Compound heterozygosity at the sphingomyelin phosphodiesterase-1 (SMPD1) gene is associated with low HDL cholesterol

J. Genest, M. Marcil, C. Bernard, 2003, Human Genetics.

Cholesterol trapping in Niemann-Pick disease type B fibroblasts can be relieved by expressing the phosphotyrosine binding domain of GULP.

R. S. Kiss, J. Genest, M. Denis, 2013, Journal of clinical lipidology.

Carboxyl-terminal disulfide bond of acid sphingomyelinase is critical for its secretion and enzymatic function.

I. Iatan, I. Wada, C. Lazure, 2007, Biochemistry.

ESI-MS quantitation of increased sphingomyelin in Niemann-Pick disease type B HDLs⃞s⃞ The online version of this article (available at http://www.jlr.org) contains an additional figure and two tables. Published, JLR Papers in Press, March 1, 2005. DOI 10.1194/jlr.M500011-JLR200

A. Lesimple, O. Mamer, J. Genest, 2005, Journal of Lipid Research.

Increased sphingomyelin content impairs HDL biogenesis and maturation in human Niemann-Pick disease type B Published, JLR Papers in Press, November 30, 2005.

A. Lesimple, O. Mamer, J. Genest, 2006, Journal of Lipid Research.

Cellular cholesterol efflux is modulated by phospholipid-derived signaling molecules in familial HDL deficiency/Tangier disease fibroblasts.

J. Genest, M. Marcil, S. Mott, 2001, Journal of lipid research.