Opposing activities of IFITM proteins in SARS‐CoV‐2 infection-Reference-Cited by-同舟云学术

Opposing activities of IFITM proteins in SARS‐CoV‐2 infection

Published:2020-12-21 Issue:3 Volume:40 Page:
ISSN:0261-4189
Container-title:The EMBO Journal
language:en
Short-container-title:EMBO J

Author:

Shi Guoli¹,Kenney Adam D²³,Kudryashova Elena³⁴,Zani Ashley²³,Zhang Lizhi²³,Lai Kin Kui¹,Hall‐Stoodley Luanne²,Robinson Richard T²,Kudryashov Dmitri S³⁴^ORCID,Compton Alex A¹^ORCID,Yount Jacob S²³^ORCID

Affiliation:

1. HIV Dynamics and Replication Program Center for Cancer ResearchNational Cancer InstituteFrederick MD USA

2. Department of Microbial Infection and Immunity The Ohio State University College of Medicine Columbus OH USA

3. Viruses and Emerging Pathogens Program Infectious Diseases Institute The Ohio State University Columbus OH USA

4. Department of Chemistry and Biochemistry The Ohio State University Columbus OH USA

Funder

National Institutes of Health

National Institute of Allergy and Infectious Diseases

National Heart, Lung, and Blood Institute

National Institute of General Medical Sciences

National Science Foundation

Publisher

EMBO

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,Molecular Biology,General Neuroscience

Link

https://onlinelibrary.wiley.com/doi/pdf/10.15252/embj.2020106501

Reference44 articles.

1. SNP-mediated disruption of CTCF binding at the IFITM3 promoter is associated with risk of severe influenza in humans

2. IFITM-Family Proteins: The Cell's First Line of Antiviral Defense

3. Bat IFITM3 restriction depends on S-palmitoylation and a polymorphic site within the CD225 domain

4. TMPRSS2 Activates the Human Coronavirus 229E for Cathepsin-Independent Host Cell Entry and Is Expressed in Viral Target Cells in the Respiratory Epithelium

5. Syncytia formation by SARS‐CoV‐2‐infected cells

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