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FRET-based assay using a three-way junction DNA substrate to identify inhibitors of human cytomegalovirus pUL89 endonuclease activity
Yan Wang,
Robert J. Geraghty
Center for Drug Design
Research output
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Contribution to journal
›
Article
›
peer-review
3
Scopus citations
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Dive into the research topics of 'FRET-based assay using a three-way junction DNA substrate to identify inhibitors of human cytomegalovirus pUL89 endonuclease activity'. Together they form a unique fingerprint.
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Medicine & Life Sciences
terminase
100%
Endonucleases
94%
Cytomegalovirus
78%
Viral Genome
44%
Viral DNA
44%
DNA
43%
Virus Replication
39%
6-bromoindirubin-3'-oxime
36%
High-Throughput Screening Assays
27%
Fluorescence Resonance Energy Transfer
26%
Product Packaging
22%
Sepharose
20%
Inhibitory Concentration 50
17%
Libraries
17%
Antiviral Agents
16%
Gels
16%
Acids
14%
Proteins
14%
Enzyme-Linked Immunosorbent Assay
13%
Genome
13%
Chemical Compounds
High Throughput Screening
84%
IC50
54%
Immunosorbent
52%
Resonance Energy
49%
Agarose
41%
Cleavage
26%
Protein
16%
Acid
13%