MPI-INF D3 Publications

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  1. Truncation mutations in ABCA1 suppress normal upregulation of full-length ABCA1 by 9-cis-retinoic acid and 22-R-hydroxycholesterol
    Cheryl L. Wellington, Yu-Zhou Yang, Stephen Zhou, Susanne M. Clee, Bing Tan, Kenichi Hirano, K.Y. Zwarts, Anita Kwok, Allison Gelfer, Michel Marcil, Scott Newman, Kirsten Roomp, Roshni Singaraja, Jennifer A. Collins, Lin-Hua Zhang, Albert K. Groen, Kees Hovingh, Alison Brownlie, Sherrie Tafuri, Jacques Jr Genest, J.J.P. Kastelein, and Michael R. Hayden
    Journal of Lipid Research 43 (11): 1939-1949, 2002
  2. Age and residual cholesterol efflux affect HDL cholesterol levels and coronary artery disease in ABCA1 heterozygotes
    Susanne M. Clee, J.J.P. Kastelein, M van Dam, Michel Marcil, Kirsten Roomp, K.Y. Zwarts, Jennifer A. Collins, R Roelants, N Tamasawa, T Stulc, T Suda, R Ceska, B Boucher, C Rondeau, C DeSouich, A Brooks-Wilson, H.O. Molhuizen, J Frohlich, Jacques Jr Genest, and Michael R. Hayden
    Journal of Clinical Investigation 106 (10): 1263-70, 2000
  3. Mutations in ABC1 in Tangier disease and familial high-density lipoprotein
    A Brooks-Wilson, Michel Marcil, Susanne M. Clee, Lin-Hua Zhang, Kirsten Roomp, M van Dam, L Yu, C Brewer, Jennifer A. Collins, H.O. Molhuizen, O Loubser, B.F. Ouelette, K Fichter, K.J. Ashbourne-Excoffon, C.W. Sensen, S Scherer, S Mott, M Denis, D Martindale, J Frohlich, K Morgan, B Koop, S Pimstone, J.J.P. Kastelein, and Michael R. Hayden
    Nature Genetics 22 (4): 336-45, 1999
  4. Mutations in the ABC1 gene in familial HDL deficiency with defective cholesterol efflux
    Michel Marcil, A. Brooks-Wilson, Susanne M. Clee, Kirsten Roomp, Lin-Hua Zhang, L. Yu, Jennifer A. Collins, M. van Dam, H. O. Molhuizen, O. Loubser, B. F. Ouelette, C. W. Sensen, K. Fichter, S. Mott, M. Denis, B. Boucher, S. Pimstone, Jacques Genest, J. J. P. Kastelein, and Michael R. Hayden
    The Lancet 354 (9187): 1341-6, 1999