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| Spike protein D614G and RdRp P323L: the SARS-CoV-2 mutations associated with severity of COVID-19 |
| Subrata K. Biswas, Sonchita R. Mudi |
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Genomics Inform. 2020;18(4):e44 Published online December 7, 2020 DOI: https://doi.org/10.5808/GI.2020.18.4.e44 |
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Spike protein D614G and RdRp P323L: the SARS-CoV-2 mutations associated with severity of COVID-19 Genomics & Informatics. 2020;18(4):e44  Chern-Simons Topology Geometrics for the generation of the RoccustyrnaTM molecule, a ligand targeting COVID-19-SARS-COV-2 SPIKE D614G binding sites . 2020; The D614G mutations in the SARS-CoV-2 spike protein: Implications for viral infectivity, disease severity and vaccine design Biochemical and Biophysical Research Communications. 2021;538:104-107 AI-Quantum Phases on Chern-Simons Topological Geometrics for the Generation of A Ligand Targeting COVID-19-SARS-COV-2 SPIKE D614G Binding Sites. . 2021; HUMAN SARS CoV-2 SPIKE PROTEIN MUTATIONS . 2020; HUMAN SARS CoV-2 SPIKE PROTEIN MUTATIONS . 2020; Could the D614G substitution in the SARS-CoV-2 spike (S) protein be associated with higher COVID-19 mortality? International Journal of Infectious Diseases. 2020;96:459-460 Spike Protein Mutations Detected in Currently Circulating Strains SARS-CoV-2 Spike Protein Convergent Evolution. 2021;27-54 D614G substitution at the hinge region enhances the stability of trimeric SARS-CoV-2 spike protein . 2021; Repurposing Therapeutics for COVID-19: Supercomputer-Based Docking to the SARS-CoV-2 Viral Spike Protein and Viral Spike Protein-Human ACE2 Interface . 2020; |
