Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Jamas Reilly"'
Autor:
Hualei Hu, Fei Liu, Pan Gao, Yuwen Huang, Danna Jia, Jamas Reilly, Xiang Chen, Yunqiao Han, Kui Sun, Jiong Luo, Pei Li, Zuxiao Zhang, Qing Wang, Qunwei Lu, Daji Luo, Xinhua Shu, Zhaohui Tang, Mugen Liu, Xiang Ren
Publikováno v:
Frontiers in Genetics, Vol 15 (2024)
IntroductionInherited retinal diseases (IRDs) affect ∼4.5 million people worldwide. Elusive pathogenic variants in over 280 genes are associated with one or more clinical forms of IRDs. It is necessary to understand the complex interaction among re
Externí odkaz:
https://doaj.org/article/f5ed54188b194288bb2e9b4c7b5afde4
Autor:
Kui Sun, Yunqiao Han, Jingzhen Li, Shanshan Yu, Yuwen Huang, Yangjun Zhang, Jamas Reilly, Jiayi Tu, Pan Gao, Danna Jia, Xiang Chen, Hualei Hu, Mengmeng Ren, Pei Li, Jiong Luo, Xiang Ren, Xianqin Zhang, Xinhua Shu, Fei Liu, Mugen Liu, Zhaohui Tang
Publikováno v:
iScience, Vol 26, Iss 11, Pp 108103- (2023)
Summary: DEAH-Box Helicase 38 (DHX38) is a pre-mRNA splicing factor and also a disease-causing gene of autosomal recessive retinitis pigmentosa (arRP). The role of DHX38 in the development and maintenance of the retina remains largely unknown. In thi
Externí odkaz:
https://doaj.org/article/40b0dbf83a734a25a3991847a39c4778
Autor:
Yangjun Zhang, Danna Jia, Jamas Reilly, Xiang Chen, Yunqiao Han, Mugen Liu, Xiliang Liu, Pan Gao, Yuwen Huang, Jiayi Tu, Xinhua Shu, Kui Sun, Daji Luo, Yuntong Zhao, Yuexia Lv, Yayun Qin, Jingzhen Li, Fei Liu, Zhaohui Tang, Shanshan Yu
Publikováno v:
Nucleic Acids Research
Dysfunction of splicing factors often result in abnormal cell differentiation and apoptosis, especially in neural tissues. Mutations in pre-mRNAs processing factor 31 (PRPF31) cause autosomal dominant retinitis pigmentosa, a progressive retinal degen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4a12b45f21aedba8b35ed5325ddde0a8
https://doi.org/10.1093/nar/gkab003
https://doi.org/10.1093/nar/gkab003