A human genome-wide loss-of-function screen identifies effective chikungunya antiviral drugs.

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Published in Nat Commun on May 12, 2016

Authors

Alexander Karlas1,2, Stefano Berre3,4, Thérèse Couderc3,4, Margus Varjak5, Peter Braun1,2, Michael Meyer2, Nicolas Gangneux3,4, Liis Karo-Astover5, Friderike Weege1, Martin Raftery6, Günther Schönrich6, Uwe Klemm7, Anne Wurzlbauer8, Franz Bracher8, Andres Merits5, Thomas F Meyer1,2, Marc Lecuit3,4,9

Author Affiliations

1: Max Planck Institute for Infection Biology, Department of Molecular Biology, Charitéplatz 1, 10117 Berlin, Germany.
2: Steinbeis Innovation gGmbH, Center for Systems Biomedicine, Haydnallee 21, 14612 Falkensee, Germany.
3: Institut Pasteur, Biology of Infection Unit, 28 rue du Dr. Roux, 75015 Paris, France.
4: Inserm U1117, 28 rue du Dr. Roux, 75015 Paris, France.
5: Institute of Technology, University of Tartu, Nooruse 1, 50411 Tartu, Estonia.
6: Institute of Virology, Charité University Medicine, Charitéplatz 1, 10117 Berlin, Germany.
7: Max Planck Institute for Infection Biology, Core Facility Experimental Animals, Charitéplatz 1, 10117 Berlin, Germany.
8: Ludwig-Maximilians-University, Department of Pharmacy-Center for Drug Research, Butenandtstraße 5-13, 81377 Munich, Germany.
9: Paris Descartes University, Sorbonne Paris Cité, Division of Infectious Diseases and Tropical Medicine, Necker-Enfants Malades University Hospital, Institut Imagine, 149, rue de Sèvres 75743 Paris, France.

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