The structure and functions of coronavirus genomic 3′ and 5′ ends-Reference-Cited by-同舟云学术

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The structure and functions of coronavirus genomic 3′ and 5′ ends

Published:2015-08 Issue: Volume:206 Page:120-133
ISSN:0168-1702
Container-title:Virus Research
language:en
Short-container-title:Virus Research

Author:

Yang Dong,Leibowitz Julian L.

Funder

National Institutes of Health

CST*R Institute of the Texas A&M Health Science Center

Publisher

Elsevier BV

Subject

Cancer Research,Infectious Diseases,Virology

Reference152 articles.

1. Acute and persistent infection of human neural cell lines by human coronavirus OC43;Arbour;J. Virol.,1999

2. Interactions between coronavirus nucleocapsid protein and viral RNAs: implications for viral transcription;Baric;J. Virol.,1988

3. Subgenomic negative-strand RNA function during mouse hepatitis virus infection;Baric;J. Virol.,2000

4. The severe acute respiratory syndrome coronavirus Nsp15 protein is an endoribonuclease that prefers manganese as a cofactor;Bhardwaj;J. Virol.,2004

5. The primary structure and expression of the second open reading frame of the polymerase gene of the coronavirus MHV-A59; a highly conserved polymerase is expressed by an efficient ribosomal frameshifting mechanism;Bredenbeek;Nucleic Acids Res.,1990

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