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MPI-INF D3 Publications, generated: 23:04, 22 October 2019

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Your search returned the following 6 documents:

  1. K.Y. Zwarts, Susanne M. Clee, A.H. Zwinderman, J.C. Engert, Roshni Singaraja, O Loubser, E James, Kirsten Roomp, T.J. Hudson, J.W. Jukema, J.J.P. Kastelein, and Michael R. Hayden
    ABCA1 regulatory variants influence coronary artery disease independent of effects on plasma lipid levels
    Clinical Genetics 61 (2): 115-125, 2002
  2. 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
    Truncation mutations in ABCA1 suppress normal upregulation of full-length ABCA1 by 9-cis-retinoic acid and 22-R-hydroxycholesterol
    Journal of Lipid Research 43 (11): 1939-1949, 2002
  3. Susanne M. Clee, A.H. Zwinderman, J.C. Engert, K.Y. Zwarts, H.O. Molhuizen, Kirsten Roomp, J.W. Jukema, M van Wijland, M van Dam, T.J. Hudson, A Brooks-Wilson, Jacques Jr Genest, J.J.P. Kastelein, and Michael R. Hayden
    Common genetic variation in ABCA1 is associated with altered lipoprotein levels and a modified risk for coronary artery disease
    Circulation 103 (9): 1198-205, 2001
  4. 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
    Age and residual cholesterol efflux affect HDL cholesterol levels and coronary artery disease in ABCA1 heterozygotes
    Journal of Clinical Investigation 106 (10): 1263-70, 2000
  5. 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
    Mutations in ABC1 in Tangier disease and familial high-density lipoprotein
    Nature Genetics 22 (4): 336-45, 1999
  6. 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
    Mutations in the ABC1 gene in familial HDL deficiency with defective cholesterol efflux
    The Lancet 354 (9187): 1341-6, 1999