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Fuquan Zhang

Researcher at Institute for Animal Health

Publications -  13
Citations -  460

Fuquan Zhang is an academic researcher from Institute for Animal Health. The author has contributed to research in topics: Virus & Foot-and-mouth disease virus. The author has an hindex of 8, co-authored 13 publications receiving 366 citations.

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Journal ArticleDOI

African swine fever virus proteins involved in evading host defence systems.

TL;DR: It is predicted that half to two-thirds of the approximately 150 genes encoded by ASFV are not essential for replication in cells but have an important role for virus survival and transmission in its hosts.
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The African Swine Fever Virus DP71L Protein Recruits the Protein Phosphatase 1 Catalytic Subunit To Dephosphorylate eIF2α and Inhibits CHOP Induction but Is Dispensable for These Activities during Virus Infection

TL;DR: It is hypothesized that ASFV has other mechanisms to prevent the eIF2α phosphorylation and the subsequent protein synthesis inhibition, and it is demonstrated that DP71L causes dephosphorylation of eukaryotic translation initiation factor 2 alpha (eIF2 α) in resting cells and during chemical-induced endoplasmic reticulum stress and acts to enhance expression of cotransfected reporter genes.
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Differential Persistence of Foot-and-Mouth Disease Virus in African Buffalo Is Related to Virus Virulence.

TL;DR: It is shown that the virus persists for up to 400 days in buffaloes and that there is competition between viruses during mixed infections, which may provide a mechanism for the dominance of particular viruses in an ecosystem.
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Macrophage Transcriptional Responses following In Vitro Infection with a Highly Virulent African Swine Fever Virus Isolate

TL;DR: A porcine microarray containing 2,880 cDNAs was used to investigate the response of macrophages to infection by a virulent African swine fever virus (ASFV) isolate, Malawi LIL20/1, and revealed differences between these two ASFV isolates in the amounts of these cytokines secreted from infected cells.
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Vaccination with coxsackievirus B3 virus-like particles elicits humoral immune response and protects mice against myocarditis

TL;DR: It is demonstrated thatCVB3 capsid proteins expressed in insect cells have the intrinsic capacity to assemble into non-infectious VLP, which afforded protection from CVB3 infection to mice when used as a vaccine.