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Results: 1-8 |
Results: 8
Human ABCA1 BAC transgenic mice show increased high density lipoprotein cholesterol and apoAI-dependent efflux stimulated by an internal promoter containing liver X receptor response elements in intron 1
Authors: Singaraja, RR Bocher, V James, ER Clee, SM Zhang, LH Leavitt, BR Tan, B Brooks-Wilson, A Kwok, A Bissada, N Yang, YZ Liu, GQ Tafuri, SR Fievet, C Wellington, CL Staels, B Hayden, MR
Citation: Rr. Singaraja et al., Human ABCA1 BAC transgenic mice show increased high density lipoprotein cholesterol and apoAI-dependent efflux stimulated by an internal promoter containing liver X receptor response elements in intron 1, J BIOL CHEM, 276(36), 2001, pp. 33969-33979
Common genetic variation in ABCA1 is associated with altered lipoprotein levels and a modified risk for coronary artery disease
Authors: Clee, SM Zwinderman, AH Engert, JC Zwarts, KY Molhuizen, HOF Roomp, K Jukema, JW van Wijland, M van Dam, M Hudson, TJ Brooks-Wilson, A Genest, J Kastelein, JJ Hayden, MR
Citation: Sm. Clee et al., Common genetic variation in ABCA1 is associated with altered lipoprotein levels and a modified risk for coronary artery disease, CIRCULATION, 103(9), 2001, pp. 1198-1205
Two genes that map to the STSL locus cause sitosterolemia: genomic structure and spectrum of mutations involving sterolin-1 and sterolin-2, encoded by ABCG5 and ABCG8, respectively
Authors: Lu, KM Lee, MH Hazard, S Brooks-Wilson, A Hidaka, H Kojima, H Ose, L Stalenhoef, AFH Mietinnen, T Bjorkhem, I Bruckert, E Pandya, A Brewer, HB Salen, G Dean, M Srivastava, A Patel, SB
Citation: Km. Lu et al., Two genes that map to the STSL locus cause sitosterolemia: genomic structure and spectrum of mutations involving sterolin-1 and sterolin-2, encoded by ABCG5 and ABCG8, respectively, AM J HU GEN, 69(2), 2001, pp. 278-290
Cholesterol efflux regulatory protein, Tangier disease and familial high-density lipoprotein deficiency
Authors: Hayden, MR Clee, SM Brooks-Wilson, A Genest, J Attie, A Kastelein, JJP
Citation: Mr. Hayden et al., Cholesterol efflux regulatory protein, Tangier disease and familial high-density lipoprotein deficiency, CURR OP LIP, 11(2), 2000, pp. 117-122
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
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: 1-8 |