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Yongqiang Wang

Researcher at Harbin Veterinary Research Institute

Publications -  118
Citations -  2123

Yongqiang Wang is an academic researcher from Harbin Veterinary Research Institute. The author has contributed to research in topics: Virus & Infectious bursal disease. The author has an hindex of 24, co-authored 110 publications receiving 1688 citations.

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Molecular epidemiology of avian leukosis virus subgroup J in layer flocks in China

TL;DR: Results suggested that the env gene, E element, and U3 region in the ALV-J layer isolates have evolved rapidly and were significantly different from those of the ALv-J broiler isolates.
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Novel variant strains of infectious bursal disease virus isolated in China.

TL;DR: This study identified the pandemic nature of the novel variant IBDVs for the first time but also discovered the distinct molecular epidemiological characteristics of these viruses, which will contribute more to the control of the disease.
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Protection of chickens from infectious laryngotracheitis with a recombinant fowlpox virus expressing glycoprotein B of infectious laryngotracheitis virus

TL;DR: In this paper, a recombinant fowlpox virus expressing glycoprotein B (gB) of the infectious laryngotracheitis virus (ILTV) was constructed and compared after challenge with a lethal dose of virulent ILTV.
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Naturally occurring mutations at residues 253 and 284 in VP2 contribute to the cell tropism and virulence of very virulent infectious bursal disease virus

TL;DR: Dual evidence from natural and rescued strains identified that the cell tropism of vvIBDV to CEF cells was determined by the combined VP2 mutations Q253H and A284T, but not by single mutation, which were mainly responsible for the virulence of IBDV.
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Development of an antigen-capture ELISA for the detection of avian leukosis virus p27 antigen

TL;DR: An antigen-capture enzyme-linked immunosorbent assay employing monoclonal and polyclonal antibodies against p27 detected the virus in the albumin and cloacal swabs of naturally infected chickens and the results were confirmed by PCR, indicating that the AC-ELISA was a suitable method for the detection of ALV.