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1
The sequence at Spike S1/S2 site enables cleavage by furin and phospho-regulation in SARS-CoV2 but not in SARS-CoV1 or MERS-CoV
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The sequence at Spike S1/S2 site enables cleavage by furin and phospho-regulation in SARS-CoV2 but not in SARS-CoV1 or MERS-CoV

Scientific reports, 2020-10, Vol.10 (1), p.16944-16944, Article 16944 [Peer Reviewed Journal]

The Author(s) 2020 ;ISSN: 2045-2322 ;EISSN: 2045-2322 ;DOI: 10.1038/s41598-020-74101-0 ;PMID: 33037310

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2
Analysis of the SARS-CoV-2 spike protein glycan shield reveals implications for immune recognition
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Analysis of the SARS-CoV-2 spike protein glycan shield reveals implications for immune recognition

Scientific reports, 2020-09, Vol.10 (1), p.14991-14991, Article 14991 [Peer Reviewed Journal]

The Author(s) 2020. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;The Author(s) 2020 ;ISSN: 2045-2322 ;EISSN: 2045-2322 ;DOI: 10.1038/s41598-020-71748-7 ;PMID: 32929138

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3
Genome-wide analysis of SARS-CoV-2 virus strains circulating worldwide implicates heterogeneity
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Genome-wide analysis of SARS-CoV-2 virus strains circulating worldwide implicates heterogeneity

Scientific reports, 2020-08, Vol.10 (1), p.14004, Article 14004 [Peer Reviewed Journal]

The Author(s) 2020. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;The Author(s) 2020. corrected publication 2021. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;The Author(s) 2020, corrected publication 2021 ;ISSN: 2045-2322 ;EISSN: 2045-2322 ;DOI: 10.1038/s41598-020-70812-6 ;PMID: 32814791

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4
Evolutionary and structural analyses of SARS-CoV-2 D614G spike protein mutation now documented worldwide
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Evolutionary and structural analyses of SARS-CoV-2 D614G spike protein mutation now documented worldwide

Scientific reports, 2020-08, Vol.10 (1), p.14031-14031, Article 14031 [Peer Reviewed Journal]

The Author(s) 2020. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;The Author(s) 2020 ;ISSN: 2045-2322 ;EISSN: 2045-2322 ;DOI: 10.1038/s41598-020-70827-z ;PMID: 32820179

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5
An in silico deep learning approach to multi-epitope vaccine design: a SARS-CoV-2 case study
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An in silico deep learning approach to multi-epitope vaccine design: a SARS-CoV-2 case study

Scientific reports, 2021-02, Vol.11 (1), p.3238-21, Article 3238 [Peer Reviewed Journal]

The Author(s) 2021. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;The Author(s) 2021 ;ISSN: 2045-2322 ;EISSN: 2045-2322 ;DOI: 10.1038/s41598-021-81749-9 ;PMID: 33547334

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6
Site specific N- and O-glycosylation mapping of the spike proteins of SARS-CoV-2 variants of concern
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Site specific N- and O-glycosylation mapping of the spike proteins of SARS-CoV-2 variants of concern

Scientific reports, 2023-06, Vol.13 (1), p.10053-10053, Article 10053 [Peer Reviewed Journal]

2023. The Author(s). ;The Author(s) 2023. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;The Author(s) 2023 ;ISSN: 2045-2322 ;EISSN: 2045-2322 ;DOI: 10.1038/s41598-023-33088-0 ;PMID: 37344512

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7
Regional and temporal coordinated mutation patterns in SARS-CoV-2 spike protein revealed by a clustering and network analysis
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Regional and temporal coordinated mutation patterns in SARS-CoV-2 spike protein revealed by a clustering and network analysis

Scientific reports, 2022-01, Vol.12 (1), p.1128-1128, Article 1128 [Peer Reviewed Journal]

2022. The Author(s). ;The Author(s) 2022. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;The Author(s) 2022 ;ISSN: 2045-2322 ;EISSN: 2045-2322 ;DOI: 10.1038/s41598-022-04950-4 ;PMID: 35064154

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8
A platform incorporating trimeric antigens into self-assembling nanoparticles reveals SARS-CoV-2-spike nanoparticles to elicit substantially higher neutralizing responses than spike alone
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A platform incorporating trimeric antigens into self-assembling nanoparticles reveals SARS-CoV-2-spike nanoparticles to elicit substantially higher neutralizing responses than spike alone

Scientific reports, 2020-10, Vol.10 (1), p.18149, Article 18149 [Peer Reviewed Journal]

This is a U.S. Government work and not under copyright protection in the US; foreign copyright protection may apply 2020. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;This is a U.S. Government work and not under copyright protection in the US; foreign copyright protection may apply 2020 ;ISSN: 2045-2322 ;EISSN: 2045-2322 ;DOI: 10.1038/s41598-020-74949-2 ;PMID: 33097791

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9
High affinity nanobodies block SARS-CoV-2 spike receptor binding domain interaction with human angiotensin converting enzyme
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High affinity nanobodies block SARS-CoV-2 spike receptor binding domain interaction with human angiotensin converting enzyme

Scientific reports, 2020-12, Vol.10 (1), p.22370-13, Article 22370 [Peer Reviewed Journal]

This is a U.S. Government work and not under copyright protection in the US; foreign copyright protection may apply 2020. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;This is a U.S. Government work and not under copyright protection in the US; foreign copyright protection may apply 2020 ;ISSN: 2045-2322 ;EISSN: 2045-2322 ;DOI: 10.1038/s41598-020-79036-0 ;PMID: 33353972

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10
Genomic mutations and changes in protein secondary structure and solvent accessibility of SARS-CoV-2 (COVID-19 virus)
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Genomic mutations and changes in protein secondary structure and solvent accessibility of SARS-CoV-2 (COVID-19 virus)

Scientific reports, 2021-02, Vol.11 (1), p.3487-3487, Article 3487 [Peer Reviewed Journal]

The Author(s) 2021. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;The Author(s) 2021 ;ISSN: 2045-2322 ;EISSN: 2045-2322 ;DOI: 10.1038/s41598-021-83105-3 ;PMID: 33568759

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11
Global dynamics of SARS-CoV-2 clades and their relation to COVID-19 epidemiology
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Global dynamics of SARS-CoV-2 clades and their relation to COVID-19 epidemiology

Scientific reports, 2021-04, Vol.11 (1), p.8435-8435, Article 8435 [Peer Reviewed Journal]

The Author(s) 2021. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;The Author(s) 2021 ;ISSN: 2045-2322 ;EISSN: 2045-2322 ;DOI: 10.1038/s41598-021-87713-x ;PMID: 33875719

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12
Structural and functional comparison of SARS-CoV-2-spike receptor binding domain produced in Pichia pastoris and mammalian cells
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Structural and functional comparison of SARS-CoV-2-spike receptor binding domain produced in Pichia pastoris and mammalian cells

Scientific reports, 2020-12, Vol.10 (1), p.21779-21779, Article 21779 [Peer Reviewed Journal]

The Author(s) 2020. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;The Author(s) 2020 ;ISSN: 2045-2322 ;EISSN: 2045-2322 ;DOI: 10.1038/s41598-020-78711-6 ;PMID: 33311634

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13
Rapid production of SARS-CoV-2 receptor binding domain (RBD) and spike specific monoclonal antibody CR3022 in Nicotiana benthamiana
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Rapid production of SARS-CoV-2 receptor binding domain (RBD) and spike specific monoclonal antibody CR3022 in Nicotiana benthamiana

Scientific reports, 2020-10, Vol.10 (1), p.17698-17698, Article 17698 [Peer Reviewed Journal]

The Author(s) 2020 ;ISSN: 2045-2322 ;EISSN: 2045-2322 ;DOI: 10.1038/s41598-020-74904-1 ;PMID: 33077899

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14
Functional analysis of potential cleavage sites in the MERS-coronavirus spike protein
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Functional analysis of potential cleavage sites in the MERS-coronavirus spike protein

Scientific reports, 2018-11, Vol.8 (1), p.16597-11, Article 16597 [Peer Reviewed Journal]

2018. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;The Author(s) 2018 ;ISSN: 2045-2322 ;EISSN: 2045-2322 ;DOI: 10.1038/s41598-018-34859-w ;PMID: 30413791

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15
COVID-19 patient serum less potently inhibits ACE2-RBD binding for various SARS-CoV-2 RBD mutants
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COVID-19 patient serum less potently inhibits ACE2-RBD binding for various SARS-CoV-2 RBD mutants

Scientific reports, 2022-05, Vol.12 (1), p.7168-7168, Article 7168 [Peer Reviewed Journal]

2022. The Author(s). ;The Author(s) 2022. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;The Author(s) 2022 ;ISSN: 2045-2322 ;EISSN: 2045-2322 ;DOI: 10.1038/s41598-022-10987-2 ;PMID: 35505068

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16
Rapidly identifying new coronavirus mutations of potential concern in the Omicron variant using an unsupervised learning strategy
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Rapidly identifying new coronavirus mutations of potential concern in the Omicron variant using an unsupervised learning strategy

Scientific reports, 2022-11, Vol.12 (1), p.19089-19089, Article 19089 [Peer Reviewed Journal]

2022. The Author(s). ;The Author(s) 2022 ;ISSN: 2045-2322 ;EISSN: 2045-2322 ;DOI: 10.1038/s41598-022-23342-2 ;PMID: 36352021

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17
Structural and functional modelling of SARS-CoV-2 entry in animal models
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Structural and functional modelling of SARS-CoV-2 entry in animal models

Scientific reports, 2020-09, Vol.10 (1), p.15917-15917, Article 15917 [Peer Reviewed Journal]

The Author(s) 2020 ;ISSN: 2045-2322 ;EISSN: 2045-2322 ;DOI: 10.1038/s41598-020-72528-z ;PMID: 32985513

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18
The global population of SARS-CoV-2 is composed of six major subtypes
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The global population of SARS-CoV-2 is composed of six major subtypes

Scientific reports, 2020-10, Vol.10 (1), p.18289-18289, Article 18289 [Peer Reviewed Journal]

The Author(s) 2020. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;The Author(s) 2020 ;ISSN: 2045-2322 ;EISSN: 2045-2322 ;DOI: 10.1038/s41598-020-74050-8 ;PMID: 33106569

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19
Sequence analysis of SARS-CoV-2 genome reveals features important for vaccine design
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Sequence analysis of SARS-CoV-2 genome reveals features important for vaccine design

Scientific reports, 2020-09, Vol.10 (1), p.15643-15643, Article 15643 [Peer Reviewed Journal]

This is a U.S. Government work and not under copyright protection in the US; foreign copyright protection may apply 2020. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;This is a U.S. Government work and not under copyright protection in the US; foreign copyright protection may apply 2020 ;ISSN: 2045-2322 ;EISSN: 2045-2322 ;DOI: 10.1038/s41598-020-72533-2 ;PMID: 32973171

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20
Identification and validation of 174 COVID-19 vaccine candidate epitopes reveals low performance of common epitope prediction tools
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Identification and validation of 174 COVID-19 vaccine candidate epitopes reveals low performance of common epitope prediction tools

Scientific reports, 2020-11, Vol.10 (1), p.20465-20465, Article 20465 [Peer Reviewed Journal]

The Author(s) 2020. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;The Author(s) 2020 ;ISSN: 2045-2322 ;EISSN: 2045-2322 ;DOI: 10.1038/s41598-020-77466-4 ;PMID: 33235258

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