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MPI-INF D3 Publications, generated: 11:00, 20 October 2019

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Your search returned the following 3 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. 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
  3. 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