Author

Tianzi Wei

Southern University of Science and TechnologyORCID 0000-0002-5045-8293Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

Click to filter author papers

Molecular Biology· 2 Biochemistry· 1

Signature Assays, Organisms & Methods

Click to filter · or open tag

Approach:experimental assay· 2 Research Focus:gene regulatory network inference· 2 Organism:human· 2 Approach:statistical model· 2 Assay:bulk RNA-seq· 1 Assay:CRISPR screen· 1 Research Focus:differential expression· 1 Research Focus:drug response / drug discovery· 1

Frequent Co-Authors

Risheng Lin· 2 shared Ruilin TianiD· 2 shared Aifang ChengiD· 1 shared Aima Huang· 1 shared Ann‐Kathrin EmmerichsiD· 1 shared Bin ZhangiD· 1 shared Chengli LiuiD· 1 shared Deyi LiuiD· 1 shared

Activity by Year

2024-2025 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 21 mutual co-author links

Click any collaborator node to inspect or filter shared papers

Focal author (center)Selected co-authorORCID co-authorUnlinked name

Curved chords = mutual co-authorship

2 shared papersMolecular Biology

Risheng Lin

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

Molecular BiologyNature CommunicationsPeer-reviewedSep 18, 2025

Stabilizing mammalian RNA thermometer confers neuroprotection in subarachnoid hemorrhage

Min Zhang, Bin Zhang, Chengli Liu…·Florian Heyd

This paper identifies RNA G-quadruplexes as temperature and potassium sensors that regulate alternative splicing and neuroprotection in subarachnoid hemorrhage.

8 citations

mousebulk RNA-seq

𝕏 PostBluesky

Molecular BiologyCell ReportsPeer-reviewedJul 1, 2025

Multimodal CRISPR screens uncover DDX39B as a global repressor of A-to-I RNA editing

Tianzi Wei, Jiaxuan Li, Xiang Lei…·Ruilin Tian

This study identifies DDX39B as a global repressor of A-to-I RNA editing using CRISPR screens and shows its potential as a therapeutic target for anti-HDV therapy.

6 citations

humanCRISPR screen

𝕏 PostBluesky

BiochemistryPLoS BiologyPeer-reviewedMay 20, 2024

Discovery of Alkenyl Oxindole as a Novel PROTAC Moiety for Targeted Protein Degradation via CRL4DCAF11 Recruitment

Ying Wang, Tianzi Wei, Man Zhao…·Guofeng Li

The paper develops JQ1-alkenyl oxindole conjugates that degrade BRD4 via the ubiquitin-proteasome system and recruits CRL4DCAF11, identifying HL435 as a potent antitumor lead.

24 citations

humanproteomics

𝕏 PostBluesky