Authors:
Gergov, M
Boucher, B
Ojanpera, I
Vuori, E
Citation: M. Gergov et al., Toxicological screening of urine for drugs by liquid chromatography/time-of-flight mass spectrometry with automated target library search based on elemental formulas, RAP C MASS, 15(8), 2001, pp. 521-526
Authors:
Haidar, B
Mott, S
Boucher, B
Lee, CY
Marcil, M
Genest, J
Citation: B. Haidar et al., Cellular cholesterol efflux is modulated by phospholipid-derived signalingmolecules in familial HDL deficiency/Tangier disease fibroblasts, J LIPID RES, 42(2), 2001, pp. 249-257
Authors:
Clee, SM
Kastelein, JJP
van Dam, M
Marcil, M
Roomp, K
Zwarts, KY
Collins, JA
Roelants, R
Tamasawa, N
Stulc, T
Suda, T
Ceska, R
Boucher, B
Rondeau, C
DeSouich, C
Brooks-Wilson, A
Molhuizen, HOF
Frohlich, J
Genest, J
Hayden, MR
Citation: Sm. Clee et al., Age and residual cholesterol efflux affect HDL cholesterol levels and coronary artery disease in ABCA1 heterozygotes, J CLIN INV, 106(10), 2000, pp. 1263-1270
Authors:
Mott, S
Yu, L
Marcil, M
Boucher, B
Rondeau, C
Genest, J
Citation: S. Mott et al., Decreased cellular cholesterol efflux is a common cause of familial hypoalphalipoproteinemia: role of the ABCA1 gene mutations, ATHEROSCLER, 152(2), 2000, pp. 457-468
Authors:
Marcil, M
Yu, L
Krimbou, L
Boucher, B
Oram, JF
Cohn, JS
Genest, J
Citation: M. Marcil et al., Cellular cholesterol transport and efflux in fibroblasts are abnormal in subjects with familial HDL deficiency, ART THROM V, 19(1), 1999, pp. 159-169
Authors:
Marcil, M
Brooks-Wilson, A
Clee, SM
Roomp, K
Zhang, LH
Yu, L
Collins, JA
van Dam, M
Molhuizen, HOF
Loubster, O
Ouellette, BFF
Sensen, CW
Fichter, K
Mott, S
Denis, M
Boucher, B
Pimstone, S
Genest, J
Kastelein, JJP
Hayden, MR
Citation: M. Marcil et al., Mutations in the ABC1 gene in familial HDL deficiency with defective cholesterol efflux, LANCET, 354(9187), 1999, pp. 1341-1346
Authors:
Yu, L
Heere-Ress, E
Boucher, B
Defesche, JC
Kastelein, J
Lavoie, MA
Genest, J
Citation: L. Yu et al., Familial hypercholesterolemia. Acceptor splice site (G -> C) mutation in intron 7 of the LDL-R gene: alternate RNA editing causes exon 8 skipping or a premature stop codon in exon 8. LDL-RHonduras-1 [LDL-R1061(-1) G -> C], ATHEROSCLER, 146(1), 1999, pp. 125-131