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Results: 1-9 |
Results: 9
Cellular cholesterol efflux is modulated by phospholipid-derived signalingmolecules in familial HDL deficiency/Tangier disease fibroblasts
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
Interaction of lecithin : cholesterol acyltransferase (LCAT)center dot alpha(2)-macroglobulin complex with low density lipoprotein receptor-related protein (LRP) - Evidence for an alpha(2)-macroglobulin/LRP receptor-mediatedsystem participating in LCAT clearance
Authors: Krimbou, L Marcil, M Davignon, J Genest, J
Citation: L. Krimbou et al., Interaction of lecithin : cholesterol acyltransferase (LCAT)center dot alpha(2)-macroglobulin complex with low density lipoprotein receptor-related protein (LRP) - Evidence for an alpha(2)-macroglobulin/LRP receptor-mediatedsystem participating in LCAT clearance, J BIOL CHEM, 276(35), 2001, pp. 33241-33248
Mutations in ABC1 in Tangier disease and familiar high-density lipoproteindeficiency
Authors: Marcil, M Brooks-Wilson, A Kastelein, J Hayden, M Genest, J
Citation: M. Marcil et al., Mutations in ABC1 in Tangier disease and familiar high-density lipoproteindeficiency, M S-MED SCI, 16(3), 2000, pp. 421-423
Age and residual cholesterol efflux affect HDL cholesterol levels and coronary artery disease in ABCA1 heterozygotes
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
Decreased cellular cholesterol efflux is a common cause of familial hypoalphalipoproteinemia: role of the ABCA1 gene mutations
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
High density lipoproteins in health and in disease
Authors: Genest, J Marcil, M Denis, M Yu, L
Citation: J. Genest et al., High density lipoproteins in health and in disease, J INVES MED, 47(1), 1999, pp. 31-42
Cellular cholesterol transport and efflux in fibroblasts are abnormal in subjects with familial HDL deficiency
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
Mutations in ABC1 in Tangier disease and familial high-density lipoproteindeficiency
Authors: Brooks-Wilson, A Marcil, M Clee, SM Zhang, LH Roomp, K van Dam, M Yu, L Brewer, C Collins, JA Molhuizen, HOF Loubser, O Ouelette, BFF Fichter, K Ashbourne-Excoffon, KJD Sensen, CW Scherer, S Mott, S Denis, M Martindale, D Frohlich, J Morgan, K Koop, B Pimstone, S Kastelein, JJP Genest, J Hayden, MR
Citation: A. Brooks-wilson et al., Mutations in ABC1 in Tangier disease and familial high-density lipoproteindeficiency, NAT GENET, 22(4), 1999, pp. 336-345
Mutations in the ABC1 gene in familial HDL deficiency with defective cholesterol efflux
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
Risultati: 1-9 |