2.1.1.56 Breast Neoplasms http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=30991934&form=6&db=m Oncogenic PIK3CA mutations increase dependency on the mRNA cap methyltransferase, RNMT, in breast cancer cells. causal interaction,ongoing research,therapeutic application,unassigned 3,2,4,0 2.1.1.56 Bronchitis http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=20573827&form=6&db=m The cellular RNA helicase DDX1 interacts with coronavirus nonstructural protein 14 and enhances viral replication. diagnostic usage,therapeutic application,unassigned 3,1,0 2.1.1.56 Coinfection http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=24778195&form=6&db=m A highly conserved region between amino acids 221 and 266 of dengue virus non-structural protein 1 is a major epitope region in infected patients. causal interaction,diagnostic usage,ongoing research,unassigned 1,3,2,0 2.1.1.56 Coinfection http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=33245437&form=6&db=m Use of whole blood over plasma enhances the detection of dengue virus RNA: possible utility in dengue vaccine trials. diagnostic usage,unassigned 1,0 2.1.1.56 Coma http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=31891331&form=6&db=m Thrombotic thrombocytopenic purpura in a 2.5-year-old boy with dengue infection: a rare complication. causal interaction,unassigned 3,0 2.1.1.56 COVID-19 http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=32567979&form=6&db=m Structure-based virtual screening and molecular dynamics simulation of SARS-CoV-2 Guanine-N7 methyltransferase (nsp14) for identifying antiviral inhibitors against COVID-19. therapeutic application,unassigned 4,0 2.1.1.56 COVID-19 http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=32907334&form=6&db=m Repurposing of FDA-Approved Toremifene to Treat COVID-19 by Blocking the Spike Glycoprotein and NSP14 of SARS-CoV-2. causal interaction,therapeutic application,unassigned 3,4,0 2.1.1.56 COVID-19 http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=33619486&form=6&db=m Probing the SAM Binding Site of SARS-CoV-2 nsp14 in vitro Using SAM Competitive Inhibitors Guides Developing Selective bi-substrate Inhibitors. causal interaction,therapeutic application,unassigned 3,4,0 2.1.1.56 COVID-19 http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=34192965&form=6&db=m Probing the SAM Binding Site of SARS-CoV-2 Nsp14 In Vitro Using SAM Competitive Inhibitors Guides Developing Selective Bisubstrate Inhibitors. causal interaction,therapeutic application,unassigned 3,4,0 2.1.1.56 COVID-19 http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=34198328&form=6&db=m Identifying SARS-CoV-2 antiviral compounds by screening for small molecule inhibitors of Nsp14 RNA cap methyltransferase. causal interaction,therapeutic application,unassigned 4,4,0