Epithelial cells lining salivary gland ducts are early target cells of severe acute respiratory syndrome coronavirus infection in the upper respiratory tracts of rhesus macaques (Q35076542)

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English	Epithelial cells lining salivary gland ducts are early target cells of severe acute respiratory syndrome coronavirus infection in the upper respiratory tracts of rhesus macaques	scientific article

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scholarly article

1 reference

6 August 2017

Epithelial cells lining salivary gland ducts are early target cells of severe acute respiratory syndrome coronavirus infection in the upper respiratory tracts of rhesus macaques (English)

1 reference

6 August 2017

1 reference

based on heuristic

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author name string

Li Liu

1

1 reference

6 August 2017

Qiang Wei

2

1 reference

6 August 2017

Xavier Alvarez

3

1 reference

6 August 2017

Haibo Wang

4

1 reference

6 August 2017

Yanhua Du

5

1 reference

6 August 2017

Hua Zhu

6

1 reference

6 August 2017

Hong Jiang

7

1 reference

6 August 2017

Jingying Zhou

8

1 reference

6 August 2017

Pokman Lam

9

1 reference

6 August 2017

Linqi Zhang

10

1 reference

6 August 2017

Andrew Lackner

11

1 reference

6 August 2017

Chuan Qin

12

1 reference

6 August 2017

Zhiwei Chen

13

1 reference

6 August 2017

language of work or name

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publication date

2 February 2011

1 reference

6 August 2017

Journal of Virology

1 reference

6 August 2017

85

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6 August 2017

4025-4030

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6 August 2017

8

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6 August 2017

Exacerbated innate host response to SARS-CoV in aged non-human primates

1 reference

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8 July 2018

Early Upregulation of Acute Respiratory Distress Syndrome-Associated Cytokines Promotes Lethal Disease in an Aged-Mouse Model of Severe Acute Respiratory Syndrome Coronavirus Infection

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MyD88 is required for protection from lethal infection with a mouse-adapted SARS-CoV.

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Rhesus angiotensin converting enzyme 2 supports entry of severe acute respiratory syndrome coronavirus in Chinese macaques

1 reference

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The SARS-CoV ferret model in an infection-challenge study.

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A novel subset of putative stem/progenitor CD34+Oct-4+ cells is the major target for SARS coronavirus in human lung.

1 reference

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Severe acute respiratory syndrome coronavirus infection in vaccinated ferrets

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Molecular pathology in the lungs of severe acute respiratory syndrome patients

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Molecular pathogenesis of severe acute respiratory syndrome

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Cynomolgus macaque as an animal model for severe acute respiratory syndrome

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Time course and cellular localization of SARS-CoV nucleoprotein and RNA in lungs from fatal cases of SARS.

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Bats are natural reservoirs of SARS-like coronaviruses

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Single amino acid substitutions in the severe acute respiratory syndrome coronavirus spike glycoprotein determine viral entry and immunogenicity of a major neutralizing domain.

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Multiple organ infection and the pathogenesis of SARS.

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

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An animal model of SARS produced by infection of Macaca mulatta with SARS coronavirus

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8 July 2018

Aged BALB/c mice as a model for increased severity of severe acute respiratory syndrome in elderly humans

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8 July 2018

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.

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Severe acute respiratory syndrome coronavirus infection of golden Syrian hamsters

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Generation of synthetic severe acute respiratory syndrome coronavirus pseudoparticles: implications for assembly and vaccine production

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8 July 2018

Macaque model for severe acute respiratory syndrome

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8 July 2018

Detection of SARS-associated coronavirus in throat wash and saliva in early diagnosis

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8 July 2018

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

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

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The cytoplasmic body component TRIM5alpha restricts HIV-1 infection in Old World monkeys

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8 July 2018

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

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Coronavirus as a possible cause of severe acute respiratory syndrome

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A novel coronavirus associated with severe acute respiratory syndrome

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Quantitative mRNA expression profiling of ACE 2, a novel homologue of angiotensin converting enzyme

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12 December 2020

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10.1128/JVI.02292-10

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6 August 2017

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6 August 2017

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6 August 2017

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