Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Zhijiao Xu"'
Autor:
Pengchao Feng, Zhijiao Xu, Jialin Chen, Meizhen Liu, Yu Zhao, Daqi Wang, Lei Han, Li Wang, Bo Wan, Xingshun Xu, Dali Li, Yilai Shu, Yimin Hua
Publikováno v:
Molecular Therapy: Nucleic Acids, Vol 28, Iss , Pp 280-292 (2022)
A wide spectrum of SLC26A4 mutations causes Pendred syndrome and enlarged vestibular aqueduct, both associated with sensorineural hearing loss (SNHL). A splice-site mutation, c.919-2A>G (A-2G), which is common in Asian populations, impairs the 3′ s
Externí odkaz:
https://doaj.org/article/3bb612608a534a3f9a9cb1f10d711e3e
Autor:
Ziwen Zheng, Guo Li, Chong Cui, Fang Wang, Xiaohan Wang, Zhijiao Xu, Huiping Guo, Yuxin Chen, Honghai Tang, Daqi Wang, Mingqian Huang, Zheng-Yi Chen, Xingxu Huang, Huawei Li, Geng-Lin Li, Xiaoxiang Hu, Yilai Shu
Publikováno v:
Signal Transduction and Targeted Therapy, Vol 7, Iss 1, Pp 1-13 (2022)
Abstract CRISPR/RfxCas13d (CasRx) editing system can specifically and precisely cleave single-strand RNAs, which is a promising treatment for various disorders by downregulation of related gene expression. Here, we tested this RNA-editing approach on
Externí odkaz:
https://doaj.org/article/eee9aef78fce4fff90a9e45b4bc297b6
Autor:
Xi Gu, Daqi Wang, Zhijiao Xu, Jinghan Wang, Luo Guo, Renjie Chai, Genglin Li, Yilai Shu, Huawei Li
Publikováno v:
Genome Biology, Vol 22, Iss 1, Pp 1-23 (2021)
Abstract Background Aging, noise, infection, and ototoxic drugs are the major causes of human acquired sensorineural hearing loss, but treatment options are limited. CRISPR/Cas9 technology has tremendous potential to become a new therapeutic modality
Externí odkaz:
https://doaj.org/article/028e049833014bf5a04fbda2914558cc
Autor:
Xi Gu, Xinde Hu, Daqi Wang, Zhijiao Xu, Fang Wang, Di Li, Geng-lin Li, Hui Yang, Huawei Li, Erwei Zuo, Yilai Shu
Publikováno v:
Cell Res
Autor:
Mingqian Huang, Fang Wang, Zheng-Yi Chen, Yilai Shu, Yuanyuan Xue, Geng Lin Li, Zhijiao Xu, Di Li, Daqi Wang, Renjie Chai, Jun Shen, Jinan Zhou, Xi Gu, Erwei Zuo, Jinghan Wang, Hui Yang, Yige Li, Xinde Hu, Huawei Li
Publikováno v:
Mol Ther
Myosin VI(MYO6) is an unconventional myosin that is vital for auditory and vestibular function. Pathogenic variants in the human MYO6 gene cause autosomal-dominant or -recessive forms of hearing loss. Effective treatments for Myo6 mutation causin
Autor:
Qingquan Xiao, Zhijiao Xu, Yuanyuan Xue, Chunlong Xu, Lei Han, Yuanhua Liu, Fang Wang, Runze Zhang, Shuang Han, Xing Wang, Geng-Lin Li, Huawei Li, Hui Yang, Yilai Shu
Publikováno v:
Science Translational Medicine. 14
Programmable RNA editing tools enable the reversible correction of mutant transcripts, reducing the potential risk associated with permanent genetic changes associated with the use of DNA editing tools. However, the potential of these RNA tools to tr
Autor:
Pengchao, Feng, Zhijiao, Xu, Jialin, Chen, Meizhen, Liu, Yu, Zhao, Daqi, Wang, Lei, Han, Li, Wang, Bo, Wan, Xingshun, Xu, Dali, Li, Yilai, Shu, Yimin, Hua
Publikováno v:
Molecular therapy. Nucleic acids. 28
A wide spectrum of
Autor:
Ziwen Zheng, Guo Li, Chong Cui, Fang Wang, Xiaohan Wang, Zhijiao Xu, Huiping Guo, Yuxin Chen, Honghai Tang, Daqi Wang, Mingqian Huang, Zheng-Yi Chen, Xingxu Huang, Huawei Li, Geng-Lin Li, Xiaoxiang Hu, Yilai Shu
Publikováno v:
Signal transduction and targeted therapy. 7(1)
CRISPR/RfxCas13d (CasRx) editing system can specifically and precisely cleave single-strand RNAs, which is a promising treatment for various disorders by downregulation of related gene expression. Here, we tested this RNA-editing approach on Beethove
Autor:
Gu, Xi, Daqi Wang, Zhijiao Xu, Jinghan Wang, Guo, Luo, Renjie Chai, Genglin Li, Shu, Yilai, Huawei Li
Additional file 4. Source data of blots and gels.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6c7f4db96eac6842c253ff2605943e26
Autor:
Gu, Xi, Daqi Wang, Zhijiao Xu, Jinghan Wang, Guo, Luo, Renjie Chai, Genglin Li, Shu, Yilai, Huawei Li
Additional file 8. Review history.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::088a27c4c6d4c1b612e586d1d937a322