-
- Blanka Leber
- Clinical Cooperation Unit Molecular Hematology/Oncology, German Cancer Research Center and Department of Internal Medicine V, University of Heidelberg, 69120 Heidelberg, Germany.
-
- Bettina Maier
- Clinical Cooperation Unit Molecular Hematology/Oncology, German Cancer Research Center and Department of Internal Medicine V, University of Heidelberg, 69120 Heidelberg, Germany.
-
- Florian Fuchs
- Division of Signaling and Functional Genomics, German Cancer Research Center and University of Heidelberg, Medical Faculty Mannheim, 69120 Heidelberg, Germany.
-
- Jing Chi
- Clinical Cooperation Unit Molecular Hematology/Oncology, German Cancer Research Center and Department of Internal Medicine V, University of Heidelberg, 69120 Heidelberg, Germany.
-
- Phillip Riffel
- Clinical Cooperation Unit Molecular Hematology/Oncology, German Cancer Research Center and Department of Internal Medicine V, University of Heidelberg, 69120 Heidelberg, Germany.
-
- Simon Anderhub
- Clinical Cooperation Unit Molecular Hematology/Oncology, German Cancer Research Center and Department of Internal Medicine V, University of Heidelberg, 69120 Heidelberg, Germany.
-
- Ludmila Wagner
- Clinical Cooperation Unit Molecular Hematology/Oncology, German Cancer Research Center and Department of Internal Medicine V, University of Heidelberg, 69120 Heidelberg, Germany.
-
- Anthony D. Ho
- Department of Internal Medicine V, University of Heidelberg, 69120 Heidelberg, Germany.
-
- Jeffrey L. Salisbury
- Tumor Biology Program and Department of Biochemistry and Molecular Biology, Mayo Clinic, Rochester, MN 55905, USA.
-
- Michael Boutros
- Division of Signaling and Functional Genomics, German Cancer Research Center and University of Heidelberg, Medical Faculty Mannheim, 69120 Heidelberg, Germany.
-
- Alwin Krämer
- Clinical Cooperation Unit Molecular Hematology/Oncology, German Cancer Research Center and Department of Internal Medicine V, University of Heidelberg, 69120 Heidelberg, Germany.
この論文をさがす
説明
<jats:p>Identified in an RNA interference screen, proteins that prevent spindle multipolarity in human cancer cells may prove to be promising drug targets.</jats:p>
収録刊行物
-
- Science Translational Medicine
-
Science Translational Medicine 2 (33), 33ra8-, 2010-05-26
American Association for the Advancement of Science (AAAS)