Deciphering COVID-19 host transcriptomic complexity and variations for therapeutic discovery against new variants. Xing et al.
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Fab RVFV-268
Fab RVFV-268 Descriptor: CITRIC ACID, Heavy chain Fab268, Light chain Fab268 Authors: Hulswit, R.J.G, Bowden, T.A, Stass, R. Deposit date: 2022-08-30 Release date: 2023-09-06 Last modified: 2026-03-04
Protein Data Bank Japan2026-03-04 更新50
Group deposition for crystallographic fragment screening of Coxsackievirus A16 (G-10) 2A protease -- Crystal structure of Coxsackievirus A16 (G-10) 2A protease in complex with Z57473948 (A71EV2A-x1292)
Group deposition for crystallographic fragment screening of Coxsackievirus A16 (G-10) 2A protease -- Crystal structure of Coxsackievirus A16 (G-10) 2A protease in complex with Z57473948 (A71EV2A-x1292
Protein Data Bank Japan2024-10-16 更新20
Data for Figs 1, S2 and S3.
Human cytomegalovirus (HCMV) is an important pathogen for which new antiviral drugs are needed. HCMV, like other herpesviruses, encodes a nuclear egress complex (NEC) composed of two subunits, UL50 an
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Study of the transcriptome of golden hamsters infected with SARS-CoV-2
In this study, we used young (2-month-old) and aged (22-month-old) golden hamsters infected with SARS-CoV-2. We compared lung pathology and transcriptional responses after infection at two time points
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Additional file 1 of Identifying FDA-approved drugs with multimodal properties against COVID-19 using a data-driven approach and a lung organoid model of SARS-CoV-2 entry
Additional file 1: Table S1. Genes differentially expressed in lung cancer cells after exposure to SARS-CoV-2. Source: Blanco-Melo et al. (2020). Table S2. Connectivity mapping results generated by qu
Figshare2021-10-05 更新10



