Wei Zhang

Publication Activity (10 Years)

Years Active: 2024-2024
Publications (10 Years): 6

Top Topics

Pluripotent Stem Cells

Top Venues

Nature communications

This page only lists publications with an associated author ORCID identifier.

Publications

Lihua Chen, Nannan Wang, Tongran Zhang, Feng Zhang, Wei Zhang, Hao Meng, Jingyi Chen, Zhiying Liao, Xiaopeng Xu, Zhuo Ma, Tao Xu, Huisheng Liu
Directed differentiation of pancreatic δ cells from human pluripotent stem cells. Nature communications 15 (1) (2024)
Lihua Chen, Nannan Wang, Tongran Zhang, Feng Zhang, Wei Zhang, Hao Meng, Jingyi Chen, Zhiying Liao, Xiaopeng Xu, Zhuo Ma, Tao Xu, Huisheng Liu
Directed differentiation of pancreatic δ cells from human pluripotent stem cells. Nature communications 15 (1) (2024)
Jie Zhang, Gongcheng Hu, Yuli Lu, Huawei Ren, Yin Huang, Yulin Wen, Binrui Ji, Diyang Wang, Haidong Wang, Huisheng Liu, Ning Ma, Ling-Ling Zhang, Guangjin Pan, Yibo Qu, Hua Wang, Wei Zhang, Zhichiao Miao, Hongjie Yao
CTCF mutation at R567 causes developmental disorders via 3D genome rearrangement and abnormal neurodevelopment. Nature communications 15 (1) (2024)
Jie Zhang, Gongcheng Hu, Yuli Lu, Huawei Ren, Yin Huang, Yulin Wen, Binrui Ji, Diyang Wang, Haidong Wang, Huisheng Liu, Ning Ma, Ling-Ling Zhang, Guangjin Pan, Yibo Qu, Hua Wang, Wei Zhang, Zhichiao Miao, Hongjie Yao
CTCF mutation at R567 causes developmental disorders via 3D genome rearrangement and abnormal neurodevelopment. Nature communications 15 (1) (2024)
Jie Zhang, Gongcheng Hu, Yuli Lu, Huawei Ren, Yin Huang, Yulin Wen, Binrui Ji, Diyang Wang, Haidong Wang, Huisheng Liu, Ning Ma, Ling-Ling Zhang, Guangjin Pan, Yibo Qu, Hua Wang, Wei Zhang, Zhichiao Miao, Hongjie Yao
CTCF mutation at R567 causes developmental disorders via 3D genome rearrangement and abnormal neurodevelopment. Nature communications 15 (1) (2024)
Jie Zhang, Gongcheng Hu, Yuli Lu, Huawei Ren, Yin Huang, Yulin Wen, Binrui Ji, Diyang Wang, Haidong Wang, Huisheng Liu, Ning Ma, Ling-Ling Zhang, Guangjin Pan, Yibo Qu, Hua Wang, Wei Zhang, Zhichiao Miao, Hongjie Yao
CTCF mutation at R567 causes developmental disorders via 3D genome rearrangement and abnormal neurodevelopment. Nature communications 15 (1) (2024)