SARS-CoV-2 ORF3b Is a Potent Interferon Antagonist Whose Activity Is Increased by a Naturally Occurring Elongation Variant (Q99561921)

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24 September 2020

title

SARS-CoV-2 ORF3b Is a Potent Interferon Antagonist Whose Activity Is Increased by a Naturally Occurring Elongation Variant (English)

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24 September 2020

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ORF3b protein [SARS-CoV-2]

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based on heuristic

inferred from abstract

variant of SARS-CoV-2

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based on heuristic

inferred from title

follows

SARS-CoV-2 ORF3b is a potent interferon antagonist whose activity is further increased by a naturally occurring elongation variant

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author name string

Yoriyuki Konno

1

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24 September 2020

Izumi Kimura

2

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24 September 2020

Keiya Uriu

3

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24 September 2020

Masaya Fukushi

4

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24 September 2020

Takashi Irie

5

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24 September 2020

Yoshio Koyanagi

6

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24 September 2020

Daniel Sauter

7

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24 September 2020

Robert J Gifford

8

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24 September 2020

USFQ-COVID19 Consortium

9

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24 September 2020

So Nakagawa

10

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24 September 2020

Kei Sato

11

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24 September 2020

publication date

4 September 2020

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24 September 2020

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24 September 2020

volume

32

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issue

12

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page(s)

108185

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The proximal origin of SARS-CoV-2

24 September 2020

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Discovery of a rich gene pool of bat SARS-related coronaviruses provides new insights into the origin of SARS coronavirus

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The Severe Acute Respiratory Syndrome Coronavirus Nucleocapsid Inhibits Type I Interferon Production by Interfering with TRIM25-Mediated RIG-I Ubiquitination

25 December 2020

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25 December 2020

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Severe acute respiratory syndrome coronavirus open reading frame (ORF) 3b, ORF 6, and nucleocapsid proteins function as interferon antagonists

25 December 2020

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25 December 2020

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25 December 2020

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25 December 2020

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25 December 2020

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25 December 2020

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HIV-1 competition experiments in humanized mice show that APOBEC3H imposes selective pressure and promotes virus adaptation

25 December 2020

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25 December 2020

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25 December 2020

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25 December 2020

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25 December 2020

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25 December 2020

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25 December 2020

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25 December 2020

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25 December 2020

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25 December 2020

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10.1016/J.CELREP.2020.108185

25 December 2020

Identifiers

DOI

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24 September 2020

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