F
Fei Guo
Researcher at Peking Union Medical College
Publications - 94
Citations - 4022
Fei Guo is an academic researcher from Peking Union Medical College. The author has contributed to research in topics: Viral replication & Virus. The author has an hindex of 23, co-authored 79 publications receiving 3034 citations. Previous affiliations of Fei Guo include McGill University & Jewish General Hospital.
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Journal ArticleDOI
Activation and evasion of type I interferon responses by SARS-CoV-2.
Xiaobo Lei,Xiaojing Dong,Ruiyi Ma,Wenjing Wang,Xia Xiao,Zhongqin Tian,Conghui Wang,Ying Wang,Li Li,Lili Ren,Fei Guo,Zhendong Zhao,Zhuo Zhou,Zichun Xiang,Jianwei Wang +14 more
TL;DR: This study shows that Sars-CoV-2 perturbs host innate immune response via both its structural and nonstructural proteins, and thus provides insights into the pathogenesis of SARS-Cov-2.
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The Interferon-Inducible MxB Protein Inhibits HIV-1 Infection
Zhenlong Liu,Qinghua Pan,Shilei Ding,Shilei Ding,Jin Qian,Jin Qian,Fengwen Xu,Jinming Zhou,Shan Cen,Fei Guo,Chen Liang,Chen Liang +11 more
TL;DR: The interferon-inducible myxovirus resistance (Mx) proteins play important roles in combating a wide range of virus infections, but the antiviral activity of MxB is less well established.
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The interaction between HIV-1 Gag and APOBEC3G.
TL;DR: Evidence against an RNA bridge facilitating the Gag/APOBEC3G interaction includes data indicating that 1) the incorporation of APOB EC3G occurs independently of viral genomic RNA, 2) a Gag-APOBec3G complex is immunoprecipitated from cell lysate after RNase treatment, and 3) the zinc coordination motif, rather than the regions flanking this motif, have been implicated in RNA binding in another family member, APOBEC1.
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CRISPR/Cas9-Derived Mutations Both Inhibit HIV-1 Replication and Accelerate Viral Escape.
Zhen Wang,Zhen Wang,Qinghua Pan,Patrick Gendron,Weijun Zhu,Fei Guo,Shan Cen,Mark A. Wainberg,Mark A. Wainberg,Chen Liang,Chen Liang +10 more
TL;DR: Using HIV-1, it is demonstrated that many of these indels are indeed lethal for the virus, but that others lead to the emergence of replication competent viruses that are resistant to Cas9/sgRNA.
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Inhibition of -Primed Reverse Transcription by Human APOBEC3G during Human Immunodeficiency Virus Type 1 Replication
TL;DR: Evidence is provided here that a decrease in the synthesis of the DNA by reverse transcriptase may account for a significant part of the reduction in DNA production in cells with Vif-negative HIV-1, and this reduction can occur independently of DNA deamination.