Author
Yuli Lu
Chinese Academy of SciencesORCID 0000-0001-8156-8682Unclaimed ORCID profile · follow to get notified of new preprints
Biology Disciplines
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2024-2024 · peak 2/yrCo-Author Collaboration Network
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- Molecular BiologyNature CommunicationsPeer-reviewed
CTCF mutation at R567 causes developmental disorders via 3D genome rearrangement and abnormal neurodevelopment
Jie Zhang, Gongcheng Hu, Yuli Lu…·Hongjie Yao
This study shows that a CTCF R567W mutation causes developmental disorders by altering 3D genome structure and neurodevelopmental pathways in mouse and human models.