MicroRNA gga-miR-130b Suppresses Infectious Bursal Disease Virus Replication via Targeting of the Viral Genome and Cellular Suppressors of Cytokine Signaling 5
Author:
Affiliation:
1. State Key Laboratory of Agrobiotechnology, Beijing, China
2. Key Laboratory of Animal Epidemiology and Zoonosis, Ministry of Agriculture, Beijing, China
3. College of Veterinary Medicine, China Agricultural University, Beijing, China
Abstract
Funder
Earmarked Fund for Modern Argo-industry Technology Research System
National Natural Science Foundation of China
Publisher
American Society for Microbiology
Subject
Virology,Insect Science,Immunology,Microbiology
Link
https://journals.asm.org/doi/pdf/10.1128/JVI.01646-17
Reference81 articles.
1. Development and large-scale use of recombinant VP2 vaccine for the prevention of infectious bursal disease of chickens
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3. The characterization and molecular cloning of the double-stranded RNA genome of an Australian strain of infectious bursal disease virus
4. Self-guanylylation of birnavirus VP1 does not require an intact polymerase activity site
5. VP1 of infectious bursal disease virus is an RNA-dependent RNA polymerase
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