A recombinant baculovirus-expressed S glycoprotein vaccine elicits high titers of SARS-associated coronavirus (SARS-CoV) neutralizing antibodies in mice (Q40312310)

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scientific article published on 9 February 2006

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English	A recombinant baculovirus-expressed S glycoprotein vaccine elicits high titers of SARS-associated coronavirus (SARS-CoV) neutralizing antibodies in mice	scientific article published on 9 February 2006

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

19 September 2017

A recombinant baculovirus-expressed S glycoprotein vaccine elicits high titers of SARS-associated coronavirus (SARS-CoV) neutralizing antibodies in mice (English)

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Europe PubMed Central

PubMed publication ID

19 September 2017

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author name string

Zhimin Zhou

1

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Europe PubMed Central

PubMed publication ID

19 September 2017

Penny Post

2

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Europe PubMed Central

PubMed publication ID

19 September 2017

Rick Chubet

3

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Europe PubMed Central

PubMed publication ID

19 September 2017

Katherine Holtz

4

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Europe PubMed Central

PubMed publication ID

19 September 2017

Clifton McPherson

5

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Europe PubMed Central

PubMed publication ID

19 September 2017

Martin Petric

6

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Europe PubMed Central

PubMed publication ID

19 September 2017

Manon Cox

7

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Europe PubMed Central

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19 September 2017

language of work or name

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publication date

9 February 2006

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Europe PubMed Central

PubMed publication ID

19 September 2017

number of pages

8

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19 September 2017

24

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19 September 2017

17

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Europe PubMed Central

PubMed publication ID

19 September 2017

3624-3631

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Europe PubMed Central

PubMed publication ID

19 September 2017

SARS-Associated Coronavirus

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https://pubmed.ncbi.nlm.nih.gov/16497416

12 December 2020

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Identification of a critical neutralization determinant of severe acute respiratory syndrome (SARS)-associated coronavirus: importance for designing SARS vaccines

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https://pubmed.ncbi.nlm.nih.gov/16497416

12 December 2020

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The SARS-CoV S glycoprotein

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https://pubmed.ncbi.nlm.nih.gov/16497416

12 December 2020

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The SARS-CoV S glycoprotein: expression and functional characterization

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https://pubmed.ncbi.nlm.nih.gov/16497416

12 December 2020

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A single immunization with a rhabdovirus-based vector expressing severe acute respiratory syndrome coronavirus (SARS-CoV) S protein results in the production of high levels of SARS-CoV-neutralizing antibodies

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https://pubmed.ncbi.nlm.nih.gov/16497416

12 December 2020

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The development of vaccines against SARS corona virus in mice and SCID-PBL/hu mice

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https://pubmed.ncbi.nlm.nih.gov/16497416

12 December 2020

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Receptor-binding domain of SARS-CoV spike protein induces highly potent neutralizing antibodies: implication for developing subunit vaccine

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https://pubmed.ncbi.nlm.nih.gov/16497416

12 December 2020

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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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https://pubmed.ncbi.nlm.nih.gov/16497416

12 December 2020

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A DNA vaccine induces SARS coronavirus neutralization and protective immunity in mice

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https://pubmed.ncbi.nlm.nih.gov/16497416

12 December 2020

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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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https://pubmed.ncbi.nlm.nih.gov/16497416

12 December 2020

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Synthesis and characterization of a native, oligomeric form of recombinant severe acute respiratory syndrome coronavirus spike glycoprotein

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https://pubmed.ncbi.nlm.nih.gov/16497416

12 December 2020

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Identification of two neutralizing regions on the severe acute respiratory syndrome coronavirus spike glycoprotein produced from the mammalian expression system.

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https://pubmed.ncbi.nlm.nih.gov/16497416

12 December 2020

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Adenoviral expression of a truncated S1 subunit of SARS-CoV spike protein results in specific humoral immune responses against SARS-CoV in rats

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https://pubmed.ncbi.nlm.nih.gov/16497416

12 December 2020

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The molecular biology of coronaviruses

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https://pubmed.ncbi.nlm.nih.gov/16497416

12 December 2020

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A novel coronavirus associated with severe acute respiratory syndrome

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https://pubmed.ncbi.nlm.nih.gov/16497416

12 December 2020

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Augmentation of immune responses to SARS coronavirus by a combination of DNA and whole killed virus vaccines

1 reference

https://pubmed.ncbi.nlm.nih.gov/16497416

12 December 2020

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Recombinant modified vaccinia virus Ankara expressing the spike glycoprotein of severe acute respiratory syndrome coronavirus induces protective neutralizing antibodies primarily targeting the receptor binding region.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16497416

12 December 2020

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A double-inactivated whole virus candidate SARS coronavirus vaccine stimulates neutralising and protective antibody responses

1 reference

https://pubmed.ncbi.nlm.nih.gov/16497416

12 December 2020

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/16497416

12 December 2020

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/16497416

12 December 2020

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Identification of a novel coronavirus in patients with severe acute respiratory syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/16497416

12 December 2020

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/16497416

12 December 2020

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Contributions of the structural proteins of severe acute respiratory syndrome coronavirus to protective immunity

1 reference

https://pubmed.ncbi.nlm.nih.gov/16497416

12 December 2020

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/16497416

12 December 2020

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/16497416

12 December 2020

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Severe acute respiratory syndrome coronavirus spike protein expressed by attenuated vaccinia virus protectively immunizes mice

1 reference

https://pubmed.ncbi.nlm.nih.gov/16497416

12 December 2020

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Neutralizing antibody and protective immunity to SARS coronavirus infection of mice induced by a soluble recombinant polypeptide containing an N-terminal segment of the spike glycoprotein

1 reference

https://pubmed.ncbi.nlm.nih.gov/16497416

12 December 2020

based on heuristic

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Characterization of a novel coronavirus associated with severe acute respiratory syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/16497416

12 December 2020

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SARS coronavirus spike polypeptide DNA vaccine priming with recombinant spike polypeptide from Escherichia coli as booster induces high titer of neutralizing antibody against SARS coronavirus.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16497416

12 December 2020

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Severe acute respiratory syndrome

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https://pubmed.ncbi.nlm.nih.gov/16497416

12 December 2020

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Inactivated SARS-CoV vaccine elicits high titers of spike protein-specific antibodies that block receptor binding and virus entry

1 reference

https://pubmed.ncbi.nlm.nih.gov/16497416

12 December 2020

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/16497416

12 December 2020

based on heuristic

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The Genome sequence of the SARS-associated coronavirus

1 reference

https://pubmed.ncbi.nlm.nih.gov/16497416

12 December 2020

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Coronavirus as a possible cause of severe acute respiratory syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/16497416

12 December 2020

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Construction of a eukaryotic expression plasmid encoding partial S gene fragments of the SARS-CoV and its potential utility as a DNA vaccine

1 reference

https://pubmed.ncbi.nlm.nih.gov/16497416

12 December 2020

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Identifiers

10.1016/J.VACCINE.2006.01.059

1 reference

Europe PubMed Central

PubMed publication ID

19 September 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

19 September 2017

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