(Q37358618)

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Identification of Nafamostat as a Potent Inhibitor of Middle East Respiratory Syndrome Coronavirus S Protein-Mediated Membrane Fusion Using the Split-Protein-Based Cell-Cell Fusion Assay.

scientific article published on 22 August 2016

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21 March 2020

Identification of Nafamostat as a Potent Inhibitor of Middle East Respiratory Syndrome Coronavirus S Protein-Mediated Membrane Fusion Using the Split-Protein-Based Cell-Cell Fusion Assay (English)

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21 March 2020

Middle East respiratory syndrome coronavirus

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based on heuristic

inferred from title

Middle East respiratory syndrome

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based on heuristic

inferred from title

4

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21 March 2020

Mizuki Yamamoto

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Mizuki Yamamoto

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ORCID Public Data File 2021

Shutoku Matsuyama

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Shutoku Matsuyama

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Yasushi Kawaguchi

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Yasushi Kawaguchi

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Xiao Li

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21 March 2020

Jun-Ichiro Inoue

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21 March 2020

Zene Matsuda

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21 March 2020

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21 October 2016

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21 March 2020

Antimicrobial Agents and Chemotherapy

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21 March 2020

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21 March 2020

6532-6539

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21 March 2020

11

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21 March 2020

The epidemiology of Middle East respiratory syndrome coronavirus in the Kingdom of Saudi Arabia, 2012-2015.

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Cross host transmission in the emergence of MERS coronavirus

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MERS coronavirus: diagnostics, epidemiology and transmission

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Bat-to-human: spike features determining 'host jump' of coronaviruses SARS-CoV, MERS-CoV, and beyond

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Using a split luciferase assay (SLA) to measure the kinetics of cell-cell fusion mediated by herpes simplex virus glycoproteins

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Dual Split Protein (DSP) Assay to Monitor Cell-Cell Membrane Fusion

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Host cell proteases: Critical determinants of coronavirus tropism and pathogenesis

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Host cell entry of Middle East respiratory syndrome coronavirus after two-step, furin-mediated activation of the spike protein

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Transmembrane serine protease TMPRSS2 activates hepatitis C virus infection

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Co-expression of foreign proteins tethered to HIV-1 envelope glycoprotein on the cell surface by introducing an intervening second membrane-spanning domain

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Middle East respiratory syndrome coronavirus (MERS-CoV): evidence and speculations.

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Role of the spike glycoprotein of human Middle East respiratory syndrome coronavirus (MERS-CoV) in virus entry and syncytia formation

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Middle East respiratory syndrome coronavirus infection mediated by the transmembrane serine protease TMPRSS2.

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Dual split protein-based fusion assay reveals that mutations to herpes simplex virus (HSV) glycoprotein gB alter the kinetics of cell-cell fusion induced by HSV entry glycoproteins

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TMPRSS2 activates the human coronavirus 229E for cathepsin-independent host cell entry and is expressed in viral target cells in the respiratory epithelium

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Identifiers

10.1128/AAC.01043-16

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21 March 2020

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Europe PubMed Central

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21 March 2020

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21 March 2020

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