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Viral Contamination Source in Clinical Microbiology Laboratory 被引量:1
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作者 wang xin ling SONG Juan +4 位作者 SONG Qin Qin YU Jie LUO Xiao Nuan WU Gui Zhen HAN Jun 《Biomedical and Environmental Sciences》 SCIE CAS CSCD 2016年第8期609-611,共3页
To understand the potential causes of laboratory-acquired infections and to provide possible solutions that would protect laboratory personnel, samples from a viral laboratory were screened to determine the main sourc... To understand the potential causes of laboratory-acquired infections and to provide possible solutions that would protect laboratory personnel, samples from a viral laboratory were screened to determine the main sources of contamination with six subtypes of Rhinovirus. Rhinovirus contamination was found in the gloves, cuffs of protective wear, inner surface of biological safety cabinet (BSC) windows, and trash handles. Remarkably, high contamination was found on the inner walls of the centrifuge and the inner surface of centrifuge tube casing in the rotor. Spilling infectious medium on the surface of centrifuge tubes was found to contribute to contamination of centrifuge surfaces. Exposure to sodium hypochlorite containing no less than 0.2 g/L available chlorine decontaminated the surface of the centrifuRe tubes from Rhinovirus after 2 min. 展开更多
关键词 Viral Contamination Source in Clinical Microbiology Laboratory BSC HRV
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Construction of MicroRNA-Target Interaction Networks Based on MicroRNA Expression Profiles of HRV16-infected H1-HeLa Cells
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作者 SONG Qin Qin wang Yan Hai +8 位作者 wang xin ling SHI Bing Tian wang Rui Fang SONG Juan wang Wen Jun XIA Dong XIA Zhi Qiang WEI Qiang HAN Jun 《Biomedical and Environmental Sciences》 SCIE CAS CSCD 2022年第9期854-860,共7页
In the present study we investigated the changes in miRNA levels inhuman rhinovirus 16(HRV16)-infected cells.A small RNA deep sequencing experiment was performed through next-generation sequencing.In total,53 differen... In the present study we investigated the changes in miRNA levels inhuman rhinovirus 16(HRV16)-infected cells.A small RNA deep sequencing experiment was performed through next-generation sequencing.In total,53 differentially expressed miRNAs were confirmed by RT-q PCR,including 37 known mi RNAs and 16 novel miRNAs.Interaction networks between differentially expressed miRNAs and their targets were established by mir DIP and Navigator.The prediction results showed that QKI. 展开更多
关键词 INFECTED Profiles PREDICTION
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