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Ning-shao Xia

As seen in: Nature, JAMA Oncology
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Articles

Diagnostic Performance of Anti–Epstein-Barr Virus BNLF2b in Suspected Nasopharyngeal Carcinoma

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By Su-Chen Li, Shi-Ji Wu, Min-Zhong Tang, Ting-Dong Li, Ning-shao Xia, Hai-Qiang Mai, Ming-Fang Ji, Lin-Quan Tang, Li Yuan Verified, Xia Yu, Hui-jun Li, Ying-Ying Lin, Wan-Li Liu, Shan Xing, Yan-Song Chen, Ya-xian Wu, Li-Ting Liu, Shan-Shan Guo, Xin Li, Min-Yi Fu, Hao Tang, Jin Ma, Tian-Sheng Gao, Xiao-Fei Lv, Jing Zhong, Zhi-ming Li, Ming Song, Shu-Wei Chen, Xing Lv, Wei-Xiong Xia, Yi-Jun Hua, Lin Wang, Qi YANG, Xiong Zou, Hu Liang, Jing-Jing Miao, Sai-Lan Liu, Xiao-Yun Li, Xue-Song Sun, Jun Zhang, Fu-Gui Li, Zhen-Zhou Xiao, Biao-Hua Wu, Xiu-Fang He, Guo-Xian Long, Jin-Bin Ye, Lu-Jun Li, Qiao-Juan Guo, Xue-Hong Xiao, Shao-Lu Lu, Rui-Ling Xie, Sheng-Xiang Ge
| JAMA Oncology Verified
Diagnostic Performance of Anti–Epstein-Barr Virus BNLF2b in Suspected Nasopharyngeal Carcinoma Key Points Question Which Epstein-Barr virus (EBV)–related biomarkers provide the most reliable diagnostic performance for suspected nasopharyngeal carcinoma (NPC) in outpatient settings?
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The crucial but insufficient role of E2s domain’s residues 490 and 492 in determining the host tropism of hepatitis E virus - Nature Communications

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By Gui-Ping Wen, Zi-Hao Chen, Jun Zhang, Ying Gu, Hai Yu, Shao-wei Li, Ning-shao Xia, Qing-Bing Zheng
| Nature Verified
Abstract Hepatitis E virus (HEV) is a significant pathogen causing acute viral hepatitis globally, posing a particular threat to pregnant women. HEV infects a range of host species, with distinct genotypes exhibiting genotype-specific tropism for different host hepatocytes. The P domain of viral capsid protein plays a central role in host cell attachment, but the molecular determinants that govern its host specificity remain unclear.
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Filament assembly induced by the recognition of target DNA activates the prokaryotic Argonaute SPARDA system - Nature Communications

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By Yu Li, Xiangkai Zhen, Ning-shao Xia, Shaowei Li, Qingbing Zheng
| Nature Verified
Abstract The short prokaryotic Argonaute (pAgo) proteins, in conjunction with their associated effector molecules, constitute a defence mechanism in prokaryotes that protects against phage infections. The SPARDA is characterized by its collateral nuclease activity, which, upon activation through target DNA recognition, non-specifically cleaves a wide range of nucleic acid substrates. Nevertheless, the structural underpinnings of its collateral activity have remained elusive.
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