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MPI-INF D3 Publications, generated: 5:01, 18 October 2019

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Your search returned the following 4 documents:

  1. R. Alan Harris, Ting Wang, Cristian Coarfa, Raman P. Nagarajan, Chibo Hong, Sara L. Downey, Brett E. Johnson, Shaun D. Fouse, Allen Delaney, Yongjun Zhao, Adam Olshen, Tracy Ballinger, Xin Zhou, Kevin J. Forsberg, Junchen Gu, Lorigail Echipare, Heriette O'Geen, Ryan Lister, Mattia Pelizzola, Yuanxin Xi, Charles B. Epstein, Bradley E. Bernstein, R. David Hawkins, Bing Ren, Wen-Yu Chung, Hongcang Gu, Christoph Bock, Andreas Gnirke, Michael Q. Zhang, David Haussler, Joseph R. Ecker, Wei Li, Peggy J. Farnham, Robert a. Waterland, Alexander Meissner, Marco A. Marra, Martin Hirst, Aleksandar Milosavljevic, and Joseph F. Costello
    Comparison of sequencing-based methods to profile DNA methylation and identification of monoallelic epigenetic modifications
    Nature Biotechnology 28 (10): 1097-1105, 2010
  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. 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
  4. 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