Zobrazeno 1 - 10
of 23
pro vyhledávání: '"Danna, Jia"'
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
Publikováno v:
Journal of Education, Health and Sport, Vol 63 (2024)
Introduction: Atopic dermatitis (AD) is a chronic and refractory inflammatory skin disease characterized by relapsing eczematous and pruritic skin lesions. Understanding the specific gene expression patterns associated with AD is crucial for advan
Externí odkaz:
https://doaj.org/article/20fd17f1d7ec4d34a7ba8f5099fa4209
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:
Danna Jia, Pan Gao, Yuexia Lv, Yuwen Huang, James Reilly, Kui Sun, Yunqiao Han, Hualei Hu, Xiang Chen, Zuxiao Zhang, Pei Li, Jiong Luo, Xinhua Shu, Zhaohui Tang, Fei Liu, Mugen Liu, Xiang Ren
Publikováno v:
Cell Death and Disease, Vol 13, Iss 11, Pp 1-11 (2022)
Abstract Mutations in TUB-like protein 1 (TULP1) are associated with severe early-onset retinal degeneration in humans. However, the pathogenesis remains largely unknown. There are two homologous genes of TULP1 in zebrafish, namely tulp1a and tulp1b.
Externí odkaz:
https://doaj.org/article/a4488838773d40f3b42c175e4b6f0088
Autor:
Xiliang Liu, Shanshan Han, Fei Liu, Shanshan Yu, Yayun Qin, Jingzhen Li, Danna Jia, Pan Gao, Xiang Chen, Zhaohui Tang, Mugen Liu, Yuwen Huang
Publikováno v:
Frontiers in Cell and Developmental Biology, Vol 11 (2023)
Introduction: Pathogenic mutations in RPGRORF15, one of two major human RPGR isoforms, were responsible for most X-linked retinitis pigmentosa cases. Previous studies have shown that RPGR plays a critical role in ciliary protein transport. However, t
Externí odkaz:
https://doaj.org/article/69d6994a47384e4d83e6baa71b388944
Autor:
Fei Liu, Yayun Qin, Yuwen Huang, Pan Gao, Jingzhen Li, Shanshan Yu, Danna Jia, Xiang Chen, Yuexia Lv, Jiayi Tu, Kui Sun, Yunqiao Han, James Reilly, Xinhua Shu, Qunwei Lu, Zhaohui Tang, Chengqi Xu, Daji Luo, Mugen Liu
Publikováno v:
PLoS Genetics, Vol 18, Iss 3, p e1009841 (2022)
Neural retina leucine zipper (NRL) is an essential gene for the fate determination and differentiation of the precursor cells into rod photoreceptors in mammals. Mutations in NRL are associated with the autosomal recessive enhanced S-cone syndrome an
Externí odkaz:
https://doaj.org/article/5ec87f08a1f5433195e0b9eaee7ac910
Autor:
Xiang Chen, Yuwen Huang, Pan Gao, Yuexia Lv, Danna Jia, Kui Sun, Yunqiao Han, Hualei Hu, Zhaohui Tang, Xiang Ren, Mugen Liu
Publikováno v:
Biomedicines, Vol 9, Iss 11, p 1699 (2021)
Zebrafish is an excellent model for exploring the development of the inner ear. Its inner ear has similar functions to that of humans, specifically in the maintenance of hearing and balance. Mafba is a component of the Maf transcription factor family
Externí odkaz:
https://doaj.org/article/6c0a53ae4aa84d7fad47c93bfed74606
Publikováno v:
ICCREM 2022.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e74430e402e6cd60ee6ff16178c1fc99
https://doi.org/10.1061/9780784484562.002
https://doi.org/10.1061/9780784484562.002
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
Autor:
Xiongchao Chen, Yuwen Huang, Dizhou Luo, Miao Liu, Pan Gao, Reilly J, Chanjuan Xu, Fuyong Liu, Lv Y, Kui Sun, Jiayi Tu, Shaojun Yu, Xinhua Shu, Jingwen Li, Yayun Qin, Danna Jia, Yunqiao Han, Zhouping Tang, Qunwei Lu
The neural retina leucine zipper (NRL) is an essential gene for the fate determination and differentiation of rod photoreceptors in mammals. Mutations in NRL have been associated with autosomal recessive enhanced S-cone syndrome and autosomal dominan
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2dbf02d4f7105c8da7d16394dd34c4b7
https://doi.org/10.1101/2021.09.29.462301
https://doi.org/10.1101/2021.09.29.462301
