(Q40243132)

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Highly conserved regions within the spike proteins of human coronaviruses 229E and NL63 determine recognition of their respective cellular receptors

scientific article published on September 2006

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Europe PubMed Central

PMC publication ID

18 September 2017

Highly conserved regions within the spike proteins of human coronaviruses 229E and NL63 determine recognition of their respective cellular receptors (English)

1 reference

Europe PubMed Central

PMC publication ID

18 September 2017

2

1 reference

Europe PubMed Central

PMC publication ID

18 September 2017

Andrew J. Rennekamp

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Andrew J Rennekamp

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Andrea Marzi

9

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Stefan Pöhlmann

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Stefan Pöhlmann

11

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author name string

Heike Hofmann

1

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Europe PubMed Central

PMC publication ID

18 September 2017

Chawaree Chaipan

4

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Europe PubMed Central

PMC publication ID

18 September 2017

Thomas Gramberg

5

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Europe PubMed Central

PMC publication ID

18 September 2017

Elke Heck

6

1 reference

Europe PubMed Central

PMC publication ID

18 September 2017

Martina Geier

7

1 reference

Europe PubMed Central

PMC publication ID

18 September 2017

Anja Wegele

8

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Europe PubMed Central

PMC publication ID

18 September 2017

Paul Bates

10

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Europe PubMed Central

PMC publication ID

18 September 2017

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publication date

1 September 2006

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Europe PubMed Central

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18 September 2017

Journal of Virology

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Europe PubMed Central

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18 September 2017

80

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Europe PubMed Central

PMC publication ID

18 September 2017

17

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Europe PubMed Central

PMC publication ID

18 September 2017

8639-8652

1 reference

Europe PubMed Central

PMC publication ID

18 September 2017

Lack of association between infection with a novel human coronavirus (HCoV), HCoV-NH, and Kawasaki disease in Taiwan

1 reference

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SARS coronavirus, but not human coronavirus NL63, utilizes cathepsin L to infect ACE2-expressing cells

1 reference

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1 reference

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Human coronavirus NL63 is not detected in the respiratory tracts of children with acute Kawasaki disease

1 reference

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Bats are natural reservoirs of SARS-like coronaviruses

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Structure of SARS coronavirus spike receptor-binding domain complexed with receptor

1 reference

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Croup is associated with the novel coronavirus NL63

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Human coronavirus NL63, France

1 reference

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Inhibitors of cathepsin L prevent severe acute respiratory syndrome coronavirus entry

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LSECtin interacts with filovirus glycoproteins and the spike protein of SARS coronavirus

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Multiple organ infection and the pathogenesis of SARS.

1 reference

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A crucial role of angiotensin converting enzyme 2 (ACE2) in SARS coronavirus-induced lung injury

1 reference

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Human coronavirus NL63 employs the severe acute respiratory syndrome coronavirus receptor for cellular entry

1 reference

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Endosomal proteolysis of the Ebola virus glycoprotein is necessary for infection

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A novel pancoronavirus RT-PCR assay: frequent detection of human coronavirus NL63 in children hospitalized with respiratory tract infections in Belgium

1 reference

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Human coronavirus NL63 infection in Canada

1 reference

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Evidence of a novel human coronavirus that is associated with respiratory tract disease in infants and young children

1 reference

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Characterization and complete genome sequence of a novel coronavirus, coronavirus HKU1, from patients with pneumonia

1 reference

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22 September 2017

Genome structure and transcriptional regulation of human coronavirus NL63

1 reference

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22 September 2017

CD209L (L-SIGN) is a receptor for severe acute respiratory syndrome coronavirus

1 reference

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22 September 2017

DC-SIGN and DC-SIGNR interact with the glycoprotein of Marburg virus and the S protein of severe acute respiratory syndrome coronavirus

1 reference

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22 September 2017

Efficient replication of severe acute respiratory syndrome coronavirus in mouse cells is limited by murine angiotensin-converting enzyme 2.

1 reference

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Highly infectious SARS-CoV pseudotyped virus reveals the cell tropism and its correlation with receptor expression

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Susceptibility to SARS coronavirus S protein-driven infection correlates with expression of angiotensin converting enzyme 2 and infection can be blocked by soluble receptor

1 reference

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S protein of severe acute respiratory syndrome-associated coronavirus mediates entry into hepatoma cell lines and is targeted by neutralizing antibodies in infected patients

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Tissue distribution of ACE2 protein, the functional receptor for SARS coronavirus. A first step in understanding SARS pathogenesis.

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pH-dependent entry of severe acute respiratory syndrome coronavirus is mediated by the spike glycoprotein and enhanced by dendritic cell transfer through DC-SIGN

1 reference

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22 September 2017

Amino acids 270 to 510 of the severe acute respiratory syndrome coronavirus spike protein are required for interaction with receptor

1 reference

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How Viruses Enter Animal Cells

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A previously undescribed coronavirus associated with respiratory disease in humans

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SARS--beginning to understand a new virus

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Identification of a new human coronavirus

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Characterization of severe acute respiratory syndrome-associated coronavirus (SARS-CoV) spike glycoprotein-mediated viral entry

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Raji B cells, misidentified as THP-1 cells, stimulate DC-SIGN-mediated HIV transmission

1 reference

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Expression cloning of functional receptor used by SARS coronavirus

1 reference

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The severe acute respiratory syndrome

1 reference

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A 193-amino acid fragment of the SARS coronavirus S protein efficiently binds angiotensin-converting enzyme 2

1 reference

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Angiotensin-converting enzyme 2 is a functional receptor for the SARS coronavirus

1 reference

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Cathepsin B Is Inhibited in Mutant Cells Selected during Persistent Reovirus Infection

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A story of two ACEs

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Human coronavirus 229E: receptor binding domain and neutralization by soluble receptor at 37 degrees C.

1 reference

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Identification of a receptor-binding domain of the spike glycoprotein of human coronavirus HCoV-229E.

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Open reading frame UL26 of human cytomegalovirus encodes a novel tegument protein that contains a strong transcriptional activation domain

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Mutant cells selected during persistent reovirus infection do not express mature cathepsin L and do not support reovirus disassembly.

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Human immunodeficiency virus infection of CD4-bearing cells occurs by a pH-independent mechanism

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Receptor and viral determinants of SARS-coronavirus adaptation to human ACE2.

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The pH independence of mammalian retrovirus infection

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Detection of human coronavirus-NL63 in children in Japan

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Severe acute respiratory syndrome

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1 October 2018

Identifiers

10.1128/JVI.00560-06

1 reference

Europe PubMed Central

PMC publication ID

18 September 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

18 September 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

18 September 2017

ResearchGate publication ID

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