Jian-hua Zhou

Jian-hua Zhou


Research Focus & Metrics

Academic Career Length

9Years (2018-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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31 May 2018 in Genes & Genomics
Verified
Journal Article
Closed access
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XMXiao-xia Ma
Xiao-xia Ma
YWYi-Ning Wang
Yi-Ning Wang
XCXiao-An Cao
Xiao-An Cao
XLXue-Rui Li
Xue-Rui Li
YLYong-Sheng Liu
Yong-Sheng Liu
XCXue-Peng Cai
Xue-Peng Cai

20 June 2019 in Research in Veterinary Science
Verified
Journal Article
Open access
PDF file
LLLingxia Li
Lingxia Li
JWJinyan Wu
Jinyan Wu
XCXiaoan Cao
Xiaoan Cao
JZJian-hua Zhou
Jian-hua Zhou
Shuanghui YinShuanghui Yin
Shuanghui Yin
XLXiangtao Liu
Xiangtao Liu
Peste des petits ruminants virus (PPRV) poses a great threat to livestock husbandry, especially goat farming due to its high mortality and morbidity. Dendritic cells (DCs), as the principal stimulators of naive Th cells were widely used in antigen processing and presenting. In the previous study, we tested the effects of PPRV on murine bone marrow derived dendritic cells (BMDCs) including surface markers and cytokines. While the aim of this study is to detect the proteomic profile of BMDCs stimulated with PPRV towards key proteins involved in. Following PPRV stimulation, 110 differentially expressed proteins (DEPs) were identified through iTRAQ labelling with LC–MS/MS approach, of which 94 DEPs were up-regulated and 16 DEPs were down-regulated, respectively. Among them 15 out of 110 DGPs were related to innate immune system, three were involved in cell apoptosis, RPS15a and Smox were related to translation of viral mRNA. Additionally, western blot analysis showed identical results to iTRAQ analysis. There will be profound significance for understanding antigen-presenting of BMDCs after stimulation with PPRV.

1 January 2018 in Acta Virologica
Verified
Journal Article
Closed access
PMP. Ma
P. Ma
XMX.-X. Ma
X.-X. Ma
QCQ.-Y. Chang
Q.-Y. Chang
LLL.-J. Li
L.-J. Li
YWY.-N. Wang
Y.-N. Wang
JZJian-hua Zhou
Jian-hua Zhou
The effects of nucleotide usage in key nucleotide positions +4 and -3 flanking start codon on translation levels mediated by IRES of hepatitis C virus