Author

W. Xin

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Bioengineering· 1 Biophysics· 1 Pharmacology & Toxicology· 1 Physiology· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 4 Research Focus:cell type annotation· 2 Assay:bulk RNA-seq· 1 Research Focus:cell signaling & trafficking· 1 Assay:ChIP-seq· 1 Assay:cryo-EM· 1 Research Focus:development & morphogenesis· 1 Research Focus:differential expression· 1

Frequent Co-Authors

X. Li· 2 shared A. Chopra· 1 shared B. Pan· 1 shared C. Duerrschmid· 1 shared C. Wu· 1 shared C. Yang· 1 shared C. Yin· 1 shared D. Ma· 1 shared

Activity by Year

2020-2023 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 10 mutual co-author links

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2 shared papersBiophysics

X. Li

Mutual co-authors in cluster

Author profile →

4 papers

Recent·Most cited

SntB triggers the antioxidant pathways to regulate development and aflatoxin biosynthesis in Aspergillus flavus

D. Wu, C. Yang, Y. Yao, D. Ma, H. Lin, L. Hao, W. Xin, K. Ye, M. Sun, Y. Hu, Y. Yang, Z. Zhuang

This study identifies SntB as a regulator of growth, development, and aflatoxin biosynthesis in Aspergillus flavus by modulating antioxidant pathways and gene expression.

bioRxiv · Dec 19, 2023Pharmacology & Toxicology

Structure basis for recognition of 26RFa by the pyroglutamylated RFamide peptide receptor

S. Jin, X. Li, Y. Xu, S. Guo, C. Wu, B. Pan, W. Xin, H. Zhang, W. Hu, Y. Yin, T. Zhang, K. Wu, Q. Yuan, H. E. Xu, X. Xie, Y. Jiang

This study determines the cryo-EM structure of QRFPR bound to 26RFa, revealing the recognition mechanism and aiding drug design for obesity and diabetes.

bioRxiv · Dec 9, 2023 · PreprintBiophysics

Asprosin Neutralizing Antibodies as a Treatment for Metabolic Syndrome

I. Mishra, C. Duerrschmid, Z. Ku, W. Xie, E. S. Silva, J. Hoffman, W. Xin, N. Zhang, Z. An, A. Chopra

This paper shows anti-asprosin monoclonal antibodies reduce appetite, body weight, and blood glucose in metabolic syndrome mouse models.

bioRxiv · Sep 15, 2020 · PreprintPhysiology

Inducing highly physiologically relevant phenotypes of human vascular smooth muscle cells via 3D printing

P. Zhu, X. Li, W. Xin, M. Wang, C. Yin, J. Li, H. Chen, H. Zhu, Y. Sun, J. Jia, N. Zhou

This study uses 3D printing to create vessel architectures that induce more physiologically relevant phenotypes in vascular smooth muscle cells compared to 2D cultures.

bioRxiv · Jul 24, 2020 · PreprintBioengineering