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1
Innate immune response to SARS-CoV-2 infection contributes to neuronal damage in human iPSC-derived peripheral neurons
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Innate immune response to SARS-CoV-2 infection contributes to neuronal damage in human iPSC-derived peripheral neurons

Journal of medical virology, 2024-02, Vol.96 (2) [Peer Reviewed Journal]

ISSN: 0146-6615 ;ISSN: 1096-9071 ;EISSN: 1096-9071 ;DOI: 10.1002/jmv.29455

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2
Pharmacological inhibition of bromodomain and extra-terminal proteins induces an NRF-2-mediated antiviral state that is subverted by SARS-CoV-2 infection
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Pharmacological inhibition of bromodomain and extra-terminal proteins induces an NRF-2-mediated antiviral state that is subverted by SARS-CoV-2 infection

PLoS pathogens, 2023-09, Vol.19 (9), p.e1011657-e1011657 [Peer Reviewed Journal]

Copyright: © 2023 Mhlekude et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. ;COPYRIGHT 2023 Public Library of Science ;2023 Mhlekude et al 2023 Mhlekude et al ;ISSN: 1553-7374 ;ISSN: 1553-7366 ;EISSN: 1553-7374 ;DOI: 10.1371/journal.ppat.1011657 ;PMID: 37747932

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3
The Tetraspanin CD81 Is a Host Factor for Chikungunya Virus Replication
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Article
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The Tetraspanin CD81 Is a Host Factor for Chikungunya Virus Replication

mBio, 2022-06, Vol.13 (3), p.e0073122-e0073122 [Peer Reviewed Journal]

Copyright © 2022 Lasswitz et al. ;Copyright © 2022 Lasswitz et al. 2022 Lasswitz et al. ;ISSN: 2150-7511 ;ISSN: 2161-2129 ;EISSN: 2150-7511 ;DOI: 10.1128/mbio.00731-22 ;PMID: 35612284

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4
Characterization of the Filovirus-Resistant Cell Line SH-SY5Y Reveals Redundant Role of Cell Surface Entry Factors
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Characterization of the Filovirus-Resistant Cell Line SH-SY5Y Reveals Redundant Role of Cell Surface Entry Factors

Viruses, 2019-03, Vol.11 (3), p.275 [Peer Reviewed Journal]

2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;2019 by the authors. 2019 ;ISSN: 1999-4915 ;EISSN: 1999-4915 ;DOI: 10.3390/v11030275 ;PMID: 30893855

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5
Interdependent Impact of Lipoprotein Receptors and Lipid-Lowering Drugs on HCV Infectivity
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Article
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Interdependent Impact of Lipoprotein Receptors and Lipid-Lowering Drugs on HCV Infectivity

Cells (Basel, Switzerland), 2021-06, Vol.10 (7), p.1626 [Peer Reviewed Journal]

2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;2021 by the authors. 2021 ;ISSN: 2073-4409 ;EISSN: 2073-4409 ;DOI: 10.3390/cells10071626 ;PMID: 34209751

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6
Impaired immune response mediated by prostaglandin E2 promotes severe COVID-19 disease
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Impaired immune response mediated by prostaglandin E2 promotes severe COVID-19 disease

PloS one, 2021-08, Vol.16 (8), p.e0255335-e0255335 [Peer Reviewed Journal]

COPYRIGHT 2021 Public Library of Science ;2021 Ricke-Hoch et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;2021 Ricke-Hoch et al 2021 Ricke-Hoch et al ;ISSN: 1932-6203 ;EISSN: 1932-6203 ;DOI: 10.1371/journal.pone.0255335 ;PMID: 34347801

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7
The matrix metalloproteinase ADAM10 supports hepatitis C virus entry and cell-to-cell spread via its sheddase activity
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The matrix metalloproteinase ADAM10 supports hepatitis C virus entry and cell-to-cell spread via its sheddase activity

PLoS pathogens, 2023-11, Vol.19 (11), p.e1011759-e1011759 [Peer Reviewed Journal]

COPYRIGHT 2023 Public Library of Science ;ISSN: 1553-7374 ;ISSN: 1553-7366 ;EISSN: 1553-7374 ;DOI: 10.1371/journal.ppat.1011759

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8
Repurposing screen identifies novel candidates for broad-spectrum coronavirus antivirals and druggable host targets
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Article
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Repurposing screen identifies novel candidates for broad-spectrum coronavirus antivirals and druggable host targets

Antimicrobial agents and chemotherapy, 2024-03, Vol.68 (3) [Peer Reviewed Journal]

ISSN: 1098-6596 ;ISSN: 0066-4804 ;EISSN: 1098-6596 ;DOI: 10.1128/aac.01210-23

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9
Filovirus Antiviral Activity of Cationic Amphiphilic Drugs Is Associated with Lipophilicity and Ability To Induce Phospholipidosis
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Article
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Filovirus Antiviral Activity of Cationic Amphiphilic Drugs Is Associated with Lipophilicity and Ability To Induce Phospholipidosis

Antimicrobial agents and chemotherapy, 2020-07, Vol.64 (8) [Peer Reviewed Journal]

Copyright © 2020 American Society for Microbiology. ;Copyright © 2020 American Society for Microbiology. 2020 American Society for Microbiology ;ISSN: 0066-4804 ;EISSN: 1098-6596 ;DOI: 10.1128/AAC.00143-20 ;PMID: 32513799

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10
Fluvastatin mitigates SARS-CoV-2 infection in human lung cells
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Article
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Fluvastatin mitigates SARS-CoV-2 infection in human lung cells

iScience, 2021-12, Vol.24 (12), p.103469-103469, Article 103469 [Peer Reviewed Journal]

2021 The Author(s) ;2021 The Author(s). ;2021 The Author(s) 2021 ;ISSN: 2589-0042 ;EISSN: 2589-0042 ;DOI: 10.1016/j.isci.2021.103469 ;PMID: 34812415

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11
The matrix metalloproteinase ADAM10 supports hepatitis C virus entry and cell-to-cell spread via its sheddase activity
Material Type:
Article
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The matrix metalloproteinase ADAM10 supports hepatitis C virus entry and cell-to-cell spread via its sheddase activity

PLoS pathogens, 2023-11, Vol.19 (11), p.e1011759 [Peer Reviewed Journal]

ISSN: 1553-7366 ;EISSN: 1553-7374 ;DOI: 10.1371/journal.ppat.1011759

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12
Impaired immune response mediated by prostaglandin E2 promotes severe COVID-19 disease
Material Type:
Article
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Impaired immune response mediated by prostaglandin E2 promotes severe COVID-19 disease

PloS one, 2021-01, Vol.16 (8), p.e0255335 [Peer Reviewed Journal]

EISSN: 1932-6203 ;DOI: 10.1371/journal.pone.0255335

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13
Pharmacological inhibition of bromodomain and extra-terminal proteins induces an NRF-2-mediated antiviral state that is subverted by SARS-CoV-2 infection
Material Type:
Article
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Pharmacological inhibition of bromodomain and extra-terminal proteins induces an NRF-2-mediated antiviral state that is subverted by SARS-CoV-2 infection

Digital Resources/Online E-Resources

14
Innate immune response to SARS-1 CoV-2 infection contributes to neuronal damage in human iPSC-derived peripheral neurons
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Article
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Innate immune response to SARS-1 CoV-2 infection contributes to neuronal damage in human iPSC-derived peripheral neurons

bioRxiv, 2022-11

2022. This article is published under http://creativecommons.org/licenses/by-nc-nd/4.0/ (“the License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;DOI: 10.1101/2022.11.18.517047

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15
Structure-based discovery of inhibitors of the SARS-CoV-2 Nsp14 N7-methyltransferase
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Article
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Structure-based discovery of inhibitors of the SARS-CoV-2 Nsp14 N7-methyltransferase

bioRxiv, 2023-01

2023. This article 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. ;DOI: 10.1101/2023.01.12.523677

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16
Pharmacological inhibition of bromodomain and extra-terminal proteins induces NRF-2-mediated inhibition of SARS-CoV-2 replication and is subject to viral antagonism
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Article
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Pharmacological inhibition of bromodomain and extra-terminal proteins induces NRF-2-mediated inhibition of SARS-CoV-2 replication and is subject to viral antagonism

bioRxiv, 2022-09

2022. This article is published under http://creativecommons.org/licenses/by-nd/4.0/ (“the License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;DOI: 10.1101/2022.09.22.508962

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  1. Peer-reviewed Journals (12)

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