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

PloS one, 2013-10, Vol.8 (10), p.e76469

2013

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CD209L (L-SIGN) Is a Receptor for Severe Acute Respiratory Syndrome Coronavirus

Proceedings of the National Academy of Sciences - PNAS, 2004-11, Vol.101 (44), p.15748-15753

2004

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Mutational Analysis of Aminopeptidase N, a Receptor for Several Group 1 Coronaviruses, Identifies Key Determinants of Viral Host Range

Journal of Virology, 2007-02, Vol.81 (3), p.1261-1273

2007

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Aromatic Amino Acids in the Juxtamembrane Domain of Severe Acute Respiratory Syndrome Coronavirus Spike Glycoprotein Are Important for Receptor-Dependent Virus Entry and Cell-Cell Fusion

Journal of Virology, 2008-03, Vol.82 (6), p.2883-2894

2008

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The N-Terminal Domain of the Murine Coronavirus Spike Glycoprotein Determines the CEACAM1 Receptor Specificity of the Virus Strain

Journal of Virology, 2003-01, Vol.77 (2), p.841-850

2003

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The N-Terminal Region of the Murine Coronavirus Spike Glycoprotein Is Associated with the Extended Host Range of Viruses from Persistently Infected Murine Cells

Journal of Virology, 2004-09, Vol.78 (17), p.9073-9083

2004

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Receptor-Dependent Coronavirus Infection of Dendritic Cells

Journal of Virology, 2004-05, Vol.78 (10), p.5486-5490

2004

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Molecular Determinants of Species Specificity in the Coronavirus Receptor Aminopeptidase N (CD13): Influence of N-Linked Glycosylation

Journal of Virology, 2001-10, Vol.75 (20), p.9741-9752

2001

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Human coronavirus 229E can use CD209L (L-SIGN) to enter cells

Advances in experimental medicine and biology, 2006, Vol.581, p.265

2006

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Amino acid substitutions and an insertion in the spike glycoprotein extend the host range of the murine coronavirus MHV-A59

Virology (New York, N.Y.), 2004-07, Vol.324 (2), p.510-524

2004

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Human aminopeptidase N is a receptor for human coronavirus 229E

Nature (London), 1992-06, Vol.357 (6377), p.420-422

1992

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Human angiotensin-converting enzyme 2 (ACE2) is a receptor for human respiratory coronavirus NL63

Advances in experimental medicine and biology, 2006, Vol.581, p.285

2006

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Molecular interactions of group 1 coronaviruses with feline APN

Advances in experimental medicine and biology, 2006, Vol.581, p.289

2006

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Human Coronavirus 229E Infects Polarized Airway Epithelia from the Apical Surface

Journal of Virology, 2000-10, Vol.74 (19), p.9234-9239

2000

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Substitutions of conserved amino acids in the receptor-binding domain of the spike glycoprotein affect utilization of murine CEACAM1a by the murine coronavirus MHV-A59

Virology (New York, N.Y.), 2005-03, Vol.334 (1), p.98-110

2005

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Rat coronavirus infection of primary rat alveolar epithelial cells

Advances in experimental medicine and biology, 2006, Vol.581, p.351

2006

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Mutational Analysis of the Virus and Monoclonal Antibody Binding Sites in MHVR, the Cellular Receptor of the Murine Coronavirus Mouse Hepatitis Virus Strain A59

Journal of Virology, 1998-03, Vol.72 (3), p.1941-1948

1998

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Synergistic inhibition of SARS-coronavirus replication by type I and type II IFN

Advances in experimental medicine and biology, 2006, Vol.581, p.503

2006

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Mustela vison ACE2 functions as a receptor for SARS-coronavirus

Advances in experimental medicine and biology, 2006, Vol.581, p.507

2006

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The nsp2 proteins of mouse hepatitis virus and SARS coronavirus are dispensable for viral replication

Advances in experimental medicine and biology, 2006, Vol.581, p.67

2006

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SARS-CoV, but not HCoV-NL63, utilizes cathepsins to infect cells: viral entry

Advances in experimental medicine and biology, 2006, Vol.581, p.335

2006

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Feline aminopeptidase N serves as a receptor for feline, canine, porcine, and human coronaviruses in serogroup I

Journal of Virology, 1996-12, Vol.70 (12), p.8669-8674

1996

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SARS coronavirus accessory ORFs encode luxury functions

Advances in experimental medicine and biology, 2006, Vol.581, p.149

2006

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Genetic evolution of human coronavirus OC43 in neural cell culture

Advances in experimental medicine and biology, 2006, Vol.581, p.499

2006

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Use of a PRRSV infectious clone to evaluate in vitro quasispecies evolution

Advances in experimental medicine and biology, 2006, Vol.581, p.435

2006

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

CD209L (L-SIGN) Is a Receptor for Severe Acute Respiratory Syndrome Coronavirus

Mutational Analysis of Aminopeptidase N, a Receptor for Several Group 1 Coronaviruses, Identifies Key Determinants of Viral Host Range

Aromatic Amino Acids in the Juxtamembrane Domain of Severe Acute Respiratory Syndrome Coronavirus Spike Glycoprotein Are Important for Receptor-Dependent Virus Entry and Cell-Cell Fusion

The N-Terminal Domain of the Murine Coronavirus Spike Glycoprotein Determines the CEACAM1 Receptor Specificity of the Virus Strain

The N-Terminal Region of the Murine Coronavirus Spike Glycoprotein Is Associated with the Extended Host Range of Viruses from Persistently Infected Murine Cells

Receptor-Dependent Coronavirus Infection of Dendritic Cells

Molecular Determinants of Species Specificity in the Coronavirus Receptor Aminopeptidase N (CD13): Influence of N-Linked Glycosylation

Human coronavirus 229E can use CD209L (L-SIGN) to enter cells

Amino acid substitutions and an insertion in the spike glycoprotein extend the host range of the murine coronavirus MHV-A59

Human aminopeptidase N is a receptor for human coronavirus 229E

Human angiotensin-converting enzyme 2 (ACE2) is a receptor for human respiratory coronavirus NL63

Molecular interactions of group 1 coronaviruses with feline APN

Human Coronavirus 229E Infects Polarized Airway Epithelia from the Apical Surface

Substitutions of conserved amino acids in the receptor-binding domain of the spike glycoprotein affect utilization of murine CEACAM1a by the murine coronavirus MHV-A59

Rat coronavirus infection of primary rat alveolar epithelial cells

Mutational Analysis of the Virus and Monoclonal Antibody Binding Sites in MHVR, the Cellular Receptor of the Murine Coronavirus Mouse Hepatitis Virus Strain A59

Synergistic inhibition of SARS-coronavirus replication by type I and type II IFN

Mustela vison ACE2 functions as a receptor for SARS-coronavirus

The nsp2 proteins of mouse hepatitis virus and SARS coronavirus are dispensable for viral replication

SARS-CoV, but not HCoV-NL63, utilizes cathepsins to infect cells: viral entry

Feline aminopeptidase N serves as a receptor for feline, canine, porcine, and human coronaviruses in serogroup I

SARS coronavirus accessory ORFs encode luxury functions

Genetic evolution of human coronavirus OC43 in neural cell culture

Use of a PRRSV infectious clone to evaluate in vitro quasispecies evolution

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