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Yinuo Wang on Muck Rack

Yinuo Wang

As seen in: Nature, Wiley Online Library, arXiv, Frontiers, Frontiers in Immunology, Frontiers in Public Health, MDPI, ACS Publications, BMC Genomics, Royal Society of Chemistry and
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Articles

One-Pot Sequential Catalysis as a General Method for Pore-Wall Functionalization of Vinylene-Linked Covalent Organic Frameworks

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By Weiliang Jin, Yinuo Wang, Yixian Zhou
| Wiley Online Library Verified
Conflicts of Interest The authors declare no conflicts of interest. Data Availability Statement The data that support the findings of this study are available from the corresponding author upon reasonable request. Supporting Information Filename Description anie75108-sup-0001-SuppMat.docx106.8 MB Experimental details and analysis are given in the Supporting Information of this article.
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SETDB1 cooperates with the CRL4B complex to promote colorectal cancer tumorigenesis by disrupting circadian rhythm

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By Min Zhang, Dong Yan, Jingyao Zhang, Tianyang Gao, Jingwen Cai, Ting Hu, Tianyu Ma, Yinuo Wang, Miaomiao Huo, Die Zhang, Yu Li, Jingjing Zhang, Chang Guo, Tian Zhu, Jiayi Gao, Zengwei Tang, Yan Wang, Xinhui Hao, Baowen Yuan
| Nature Verified
Abstract The circadian rhythm is an intrinsic, self-regulatory physiological system in organisms that is hierarchically governed by core clock genes. Dysregulation of this rhythm is closely associated with tumor progression. However, the specific molecular mechanisms underlying circadian rhythm disruption–mediated colorectal cancer (CRC) remain largely elusive.
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Alternative tandem transcription initiation links noncoding variants to human disease through translational control

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By Xudong Zou, Wei Wang, Yinuo Wang, Hui Chen, Xing Li, Shuxin Chen, Yangcan Li, Qin Li, Chen Hong Yu, Lei Li, Feihong Weng
| Nature Verified
Abstract Alternative tandem transcription initiation is a pervasive mechanism of gene regulation, yet its genetic impact on human disease remains largely unknown. Here, we systematically quantify the genetic regulation of alternative tandem transcription initiation across 25,859 samples from 49 normal human tissues and 33 tumor tissues.
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