Rezultati pretrage - Michelle C Redman

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  1. 1
    High-throughput, pooled sequencing identifies mutations in NUBPL and FOXRED1 in human complex I deficiency

    High-throughput, pooled sequencing identifies mutations in NUBPL and FOXRED1 in human complex I deficiency od Sarah E. Calvo, Elena J. Tucker, Alison G. Compton, Denise M. Kirby, Gabriel Crawford, Noël P. Burtt, Manuel A. Rivas, Candace Guiducci, Damien L. Bruno, Olga Goldberger, Michelle C Redman, Esko Wiltshire, Callum Wilson, David Altshuler, Stacey B. Gabriel, Mark J. Daly, David R. Thorburn, Vamsi K. Mootha

    Izdano 2010
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  2. 2
    Exome sequencing identifies recurrent SPOP, FOXA1 and MED12 mutations in prostate cancer

    Exome sequencing identifies recurrent SPOP, FOXA1 and MED12 mutations in prostate cancer od Christopher E. Barbieri, Sylvan C. Baca, Michael S. Lawrence, Francesca Demichelis, Mirjam Blattner, Jean‐Philippe Theurillat, Thomas A. White, Petar Stojanov, Eliezer M. Van Allen, Nicolas Stransky, Elizabeth Nickerson, Sung-Suk Chae, Gunther Boysen, Daniel Auclair, Robert C. Onofrio, Kyung Park, Naoki Kitabayashi, Theresa Y. MacDonald, Karen L. Sheikh, Terry Vuong, Candace Guiducci, Kristian Cibulskis, Andrey Sivachenko, Scott L. Carter, Gordon Saksena, Douglas Voet, Wasay M Hussain, Alex H. Ramos, Wendy Winckler, Michelle C Redman, Kristin Ardlie, Ashutosh Tewari, Juan Miguel Mosquera, Niels J. Rupp, Peter J. Wild, Holger Moch, Colm Morrissey, Peter S. Nelson, Philip W. Kantoff, Stacey Gabriel, Todd R. Golub, Matthew Meyerson, Eric S. Lander, Gad Getz, Mark A. Rubin, Levi A. Garraway

    Izdano 2012
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