Insights from the association of SARS-CoV S-protein with its receptor, ACE2. (Q36622004)

15 August 2017

2 references

22 October 2022

Insights from the association of SARS-CoV S-protein with its receptor, ACE2. (English)

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15 August 2017

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1 reference

Wenhui Li

1

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Michael Farzan

series ordinal

3

object named as

Michael Farzan

1 reference

15 August 2017

Hyeryun Choe

2

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PubMed ID

17037532

15 August 2017

language of work or name

English

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publication date

1 January 2006

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Advances in Experimental Medicine and Biology

15 August 2017

2 references

15 August 2017

22 October 2022

581

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15 August 2017

209-218

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A previously undescribed coronavirus associated with respiratory disease in humans

15 August 2017

1 reference

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Retroviruses pseudotyped with the severe acute respiratory syndrome coronavirus spike protein efficiently infect cells expressing angiotensin-converting enzyme 2.

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Persistent infection of SARS coronavirus in colonic cells in vitro.

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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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Antibodies to SARS coronavirus in civets

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The SARS-CoV S glycoprotein: expression and functional characterization

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

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Hydrolysis of biological peptides by human angiotensin-converting enzyme-related carboxypeptidase

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

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Localization of neutralizing epitopes and the receptor-binding site within the amino-terminal 330 amino acids of the murine coronavirus spike protein

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Evasion of antibody neutralization in emerging severe acute respiratory syndrome coronaviruses

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Angiotensin-converting enzyme 2 protects from severe acute lung failure.

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Aetiology: Koch's postulates fulfilled for SARS virus

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Identification of immunodominant sites on the spike protein of severe acute respiratory syndrome (SARS) coronavirus: implication for developing SARS diagnostics and vaccines.

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Severe acute respiratory syndrome coronavirus-like virus in Chinese horseshoe bats

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

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Laboratory diagnosis of four recent sporadic cases of community-acquired SARS, Guangdong Province, China

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Identification of a new human coronavirus

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

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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

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

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Identification of a novel coronavirus in bats

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Molecular evolution analysis and geographic investigation of severe acute respiratory syndrome coronavirus-like virus in palm civets at an animal market and on farms

1 reference

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

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Evaluation of human monoclonal antibody 80R for immunoprophylaxis of severe acute respiratory syndrome by an animal study, epitope mapping, and analysis of spike variants

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Surveillance on severe acute respiratory syndrome associated coronavirus in animals at a live animal market of Guangzhou in 2004

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

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A human homolog of angiotensin-converting enzyme. Cloning and functional expression as a captopril-insensitive carboxypeptidase

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Receptor-binding domain of severe acute respiratory syndrome coronavirus spike protein contains multiple conformation-dependent epitopes that induce highly potent neutralizing antibodies

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Several members of the mouse carcinoembryonic antigen-related glycoprotein family are functional receptors for the coronavirus mouse hepatitis virus-A59

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Civets are equally susceptible to experimental infection by two different severe acute respiratory syndrome coronavirus isolates

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Bovine coronavirus uses N-acetyl-9-O-acetylneuraminic acid as a receptor determinant to initiate the infection of cultured cells

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

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Bats are natural reservoirs of SARS-like coronaviruses

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Mice susceptible to SARS coronavirus

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Human aminopeptidase N is a receptor for human coronavirus 229E

1 reference

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10.1007/978-0-387-33012-9_36

Identifiers

DOI

0 references

0 references

1 reference

PubMed ID

17037532