Construction of a Full-Length Infectious Clone Derived from Type O Foot-and-Mouth Disease Virus Isolated in South Korea for Vaccine Development with High Antigen Productivity. [PDF]
Vaccines (Basel)Kim JY +6 more
europepmc +1 more source
Ribosomal protein L35 negatively regulates FMDV replication by recruiting AMFR to promote the ubiquitination and degradation of VP2. [PDF]
J VirolShao W +11 more
europepmc +1 more source
Development and immunogenicity of adenoviral Fc-fused FMDV virus-like particle vaccine in swine. [PDF]
Vet QPark JY +9 more
europepmc +1 more source
Characterization of a Virus Rescued from a Full-Length Infectious Clone Derived from the Type A Foot-and-Mouth Disease Virus Isolated in South Korea. [PDF]
VirusesKim JY +6 more
europepmc +1 more source
Oral β-D-glucan potentiates systemic immune responses to intramuscular foot-and-mouth disease vaccination. [PDF]
Front Vet SciKim HW +5 more
europepmc +1 more source
Retrospective study of tongue gangrene in Egyptian buffaloes and its surgical management. [PDF]
Ir Vet JAbass M +4 more
europepmc +1 more source
Systematic review and meta-analysis of the effectiveness of polypeptide, virus-like particles, and viral vector vaccines for foot-and-mouth disease (2020-2025). [PDF]
Sci RepElrashedy A +6 more
europepmc +1 more source
DDX56 cooperates with FMDV 3A to enhance FMDV replication by inhibiting the phosphorylation of IRF3
Cellular Signalling, 2019 The components of foot-and-mouth disease virus (FMDV) interact with host cellular proteins to promote self-replication and evade the host immune response. Previous studies have shown that FMDV 3A, 2C and 2B proteins interact with host cellular proteins involved in FMDV replication.
Dan Li
exaly +3 more sources