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Yinghong Xiao on Muck Rack

Yinghong Xiao

As seen in: Nature, MDPI, BioRxiv, Cell Metabolism, Cell Press
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Articles

SARS-CoV-2 Nsp1 regulates translation start site fidelity to promote infection

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By Yinghong Xiao, Lichao Zhang, Ranen Aviner, Michel Tasseto
| BioRxiv
Thank you for your interest in spreading the word about bioRxiv. NOTE: Your email address is requested solely to identify you as the sender of this article. Your Email * Your Name * Send To * Enter multiple addresses on separate lines or separate them with commas. Message Subject (Your Name) has forwarded a page to you from bioRxiv Message Body (Your Name) thought you would like to see this page from the bioRxiv website.
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Reversible Lane Optimization of the Urban Road Network Considering Adjustment Time Constraints

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By Jianrong Cai, Zhixue Li, Yinghong Xiao, Zhaoming Zhou
| MDPI
Abstract : Reversible lanes constitute an important solutions for sustainable transportation, with the aim to solve the practical problem of reversible lane optimization of urban road networks constrained by adjustment time. Considering the relationship between the number of lanes and the capacity of sections, a mixed-integer bilevel programming model of reversible lane optimization constrained by adjustment time is constructed in order to minimize the total travel time of the system.
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Fluorogenic reporter enables identification of compounds that inhibit SARS-CoV-2 - Nature Microbiology

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By Junjiao Yang, Yinghong Xiao, Shiming Peng, Michel Tassetto, Tsuguhisa Nakayama, Jayakar V. Nayak, David J. Erle, Peter Jackson, Raul Andino, Luke R. Bonser
| Nature Verified
Abstract The coronavirus SARS-CoV-2 causes the severe disease COVID-19. SARS-CoV-2 infection is initiated by interaction of the viral spike protein and host receptor angiotensin-converting enzyme 2 (ACE2). We report an improved bright and reversible fluorogenic reporter, named SURF (split UnaG-based reversible and fluorogenic protein–protein interaction reporter), that we apply to monitor real-time interactions between spike and ACE2 in living cells.
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