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Research Paper
Selective inhibitors of trypanosomal uridylyl transferase RET1 establish druggability of RNA post-transcriptional modifications
Amy CordingThe Gurdon Institute, University of Cambridge, Cambridge, UK
, Michael GormallyDepartment of Chemistry, University of Cambridge, Cambridge, UK;Cancer Research UK Cambridge Institute, Li Ka Shing Center, Cambridge, UK;National Center for Advancing Translational Sciences, National Institutes of Health, Bethesda, MD, USA
, Peter J. BondBioinformatics Institute (A*STAR), Singapore;Department of Biological Sciences, National University of Singapore, Singapore
, Mark CarringtonDepartment of Biochemistry, Cambridge, UK
, Shankar BalasubramanianDepartment of Chemistry, University of Cambridge, Cambridge, UK;Cancer Research UK Cambridge Institute, Li Ka Shing Center, Cambridge, UK
, Eric A. MiskaThe Gurdon Institute, University of Cambridge, Cambridge, UKCorrespondence[email protected] [email protected]
& Beth ThomasDepartment of Chemistry, University of Cambridge, Cambridge, UKCorrespondence[email protected] [email protected]
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Pages 611-619
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Received 23 Oct 2015, Accepted 23 Dec 2015, Published online: 27 May 2016
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Selective inhibitors of trypanosomal uridylyl transferase RET1 establish druggability of RNA post-transcriptional modifications
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Selective inhibitors of trypanosomal uridylyl transferase RET1 establish druggability of RNA post-transcriptional modifications
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Selective inhibitors of trypanosomal uridylyl transferase RET1 establish druggability of RNA post-transcriptional modifications
Source:
Figshare
Selective inhibitors of trypanosomal uridylyl transferase RET1 establish druggability of RNA post-transcriptional modifications
Source:
Figshare
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