Every reference with a DOI in the deposited reference list resolved to a known
work in Crossref or DataCite at the dated check, and none carried a retraction,
withdrawal, or removal notice.
The 58 checked references that resolve
resolves10.1126/science.1085952Characterization of a Novel Coronavirus Associated with Severe Acute Respiratory Syndrome
resolves10.1177/11779322211020316DGraph Clusters Flaviviruses and β-Coronaviruses According to Their Hosts, Disease Type, and Human Cell Receptors
resolves10.1016/j.cell.2020.06.025Structures of Human Antibodies Bound to SARS-CoV-2 Spike Reveal Common Epitopes and Recurrent Features of Antibodies
resolves10.1016/j.cell.2020.06.043Tracking Changes in SARS-CoV-2 Spike: Evidence that D614G Increases Infectivity of the COVID-19 Virus
resolves10.1101/2020.12.21.20248640Emergence and rapid spread of a new severe acute respiratory syndrome-related coronavirus 2 (SARS-CoV-2) lineage with multiple spike mutations in South Africa
resolves10.1101/2021.03.24.436620B.1.526 SARS-CoV-2 variants identified in New York City are neutralized by vaccine-elicited and therapeutic monoclonal antibodies
resolves10.1038/s41591-021-01270-4Neutralization of SARS-CoV-2 spike 69/70 deletion, E484K and N501Y variants by BNT162b2 vaccine-elicited sera
resolves10.1126/science.abg6105Neutralization of SARS-CoV-2 lineage B.1.1.7 pseudovirus by BNT162b2 vaccine–elicited human sera
resolves10.1016/j.chom.2021.02.003Comprehensive mapping of mutations in the SARS-CoV-2 receptor-binding domain that affect recognition by polyclonal human plasma antibodies
resolves10.1126/science.abe8499SARS-CoV-2 D614G variant exhibits efficient replication ex vivo and transmission in vivo
resolves10.1016/j.cell.2020.08.012Deep Mutational Scanning of SARS-CoV-2 Receptor Binding Domain Reveals Constraints on Folding and ACE2 Binding
resolves10.7554/eLife.61312Escape from neutralizing antibodies by SARS-CoV-2 spike protein variants
resolves10.1016/j.chom.2021.01.014Identification of SARS-CoV-2 spike mutations that attenuate monoclonal and serum antibody neutralization
resolves10.1126/science.abc6952A neutralizing human antibody binds to the N-terminal domain of the Spike protein of SARS-CoV-2
resolves10.1126/science.abe1502Structural analysis of full-length SARS-CoV-2 spike protein from an advanced vaccine candidate
resolves10.1080/21645515.2020.1740560Potential for developing a SARS-CoV receptor-binding domain (RBD) recombinant protein as a heterologous human vaccine against coronavirus infectious disease (COVID)-19
resolves10.3389/fimmu.2020.576622The SARS-CoV-2 Spike Glycoprotein Biosynthesis, Structure, Function, and Antigenicity: Implications for the Design of Spike-Based Vaccine Immunogens
resolves10.1038/s41598-021-83761-5Serine 477 plays a crucial role in the interaction of the SARS-CoV-2 spike protein with the human receptor ACE2
resolves10.1126/science.abc5881Structural basis for neutralization of SARS-CoV-2 and SARS-CoV by a potent therapeutic antibody
resolves10.3389/fimmu.2021.647934A Structural Landscape of Neutralizing Antibodies Against SARS-CoV-2 Receptor Binding Domain
resolves10.1101/2021.06.23.449568Increased lung cell entry of B.1.617.2 and evasion of antibodies induced by infection and BNT162b2 vaccination
resolves10.1101/gr.1239303Cytoscape: A Software Environment for Integrated Models of Biomolecular Interaction Networks
resolves10.1002/gch2.1018Data, disease and diplomacy: GISAID's innovative contribution to global health
resolves10.1093/nar/gkh340MUSCLE: multiple sequence alignment with high accuracy and high throughput
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