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Times Cited
Times Co-cited
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Clinical features of patients infected with 2019 novel coronavirus in Wuhan, China.
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Crystal structure of SARS-CoV-2 nucleocapsid protein RNA binding domain reveals potential unique drug targeting sites.
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A SARS-CoV-2 protein interaction map reveals targets for drug repurposing.
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Nucleocapsid protein of SARS-CoV-2 phase separates into RNA-rich polymerase-containing condensates.
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Structure of the SARS coronavirus nucleocapsid protein RNA-binding dimerization domain suggests a mechanism for helical packaging of viral RNA.
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Phosphoregulation of Phase Separation by the SARS-CoV-2 N Protein Suggests a Biophysical Basis for its Dual Functions.
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The SARS-CoV-2 nucleocapsid phosphoprotein forms mutually exclusive condensates with RNA and the membrane-associated M protein.
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Remdesivir and chloroquine effectively inhibit the recently emerged novel coronavirus (2019-nCoV) in vitro.
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Oligomerization of the carboxyl terminal domain of the human coronavirus 229E nucleocapsid protein.
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The FDA-approved drug ivermectin inhibits the replication of SARS-CoV-2 in vitro.
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Epidemiological and clinical characteristics of 99 cases of 2019 novel coronavirus pneumonia in Wuhan, China: a descriptive study.
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Angiotensin-converting enzyme 2 is a functional receptor for the SARS coronavirus.
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Analysis of multimerization of the SARS coronavirus nucleocapsid protein.
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The coronavirus nucleocapsid protein is dynamically associated with the replication-transcription complexes.
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8
Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.