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Author/Creator Xi, Yanping

1. A novel frameshift variant of LMX1A that leads to autosomal dominant non-syndromic sensorineural hearing loss: functional characterization of the C-terminal domain in LMX1A. Issue 8 (15th December 2022)

Authors:
Xiao, Min; Zheng, Yan; Huang, Kuo-Hsiang; Yu, Shanhe; Zhang, Wenbi; Xi, Yanping; Dou, Yan; Sun, Xiaoxi; Lei, Caixia; Yu, Huiqian
Journal:
Human molecular genetics
Issue:
Volume 32:Issue 8(2023)
Page Start:
1348
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

3. MicroRNAs activate gene transcription epigenetically as an enhancer trigger. Issue 10 (3rd October 2017)

Authors:
Xiao, Min; Li, Jin; Li, Wei; Wang, Yu; Wu, Feizhen; Xi, Yanping; Zhang, Lan; Ding, Chao; Luo, Huaibing; Li, Yan; Peng, Lina; Zhao, Liping; Peng, Shaoliang; Xiao, Yao; Dong, Shihua; Cao, Jie; Yu, Wenqiang
Journal:
RNA biology
Issue:
Volume 14:Issue 10(2017)
Page Start:
1326
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

4. UHRF1 regulates alternative splicing by interacting with splicing factors and U snRNAs in a H3R2me involved manner. Issue 22 (1st July 2021)

Authors:
Xu, Peng; Zhang, Lan; Xiao, Yao; Li, Wei; Hu, Zhiqiang; Zhang, Rukui; Li, Jin; Wu, Feizhen; Xi, Yanping; Zou, Qingping; Wang, Zhentian; Guo, Rui; Ma, Honghui; Dong, Shihua; Xiao, Min; Yang, Zhicong; Ren, Xiaoguang; Wei, Chaochun; Yu, Wenqiang
Journal:
Human molecular genetics
Issue:
Volume 30:Issue 22(2021)
Page Start:
2110
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗