Zobrazeno 1 - 10
of 51
pro vyhledávání: '"Lianqun Wu"'
Autor:
Mingsu Shi, Yanxi Fang, Yu Liang, Yuxiang Hu, Jiaqiu Huang, Weiyi Xia, Hewei Bian, Qiao Zhuo, Lianqun Wu, Chen Zhao
Publikováno v:
BMC Genomics, Vol 24, Iss 1, Pp 1-13 (2023)
Abstract Background Oculomotor nerve palsy (ONP) is a neuroparalytic disorder resulting in dysfunction of innervating extraocular muscles (EOMs), of which the pathological characteristics remain underexplored. Methods In this study, medial rectus mus
Externí odkaz:
https://doaj.org/article/6059c68f703245f39c8dda9b4709711e
Publikováno v:
Frontiers in Molecular Neuroscience, Vol 16 (2023)
IntroductionOculomotor nerve palsy (ONP) arises from primary abnormalities in the central neural pathways that control the extraocular muscles (EOMs). Long non-coding RNAs (lncRNAs) have been found to be involved in the pathogenesis of various neurop
Externí odkaz:
https://doaj.org/article/41b40a5629cf4c85a5de19645538a575
Autor:
Jiancheng Huang, Meng Chen, Yu Liang, Yuxiang Hu, Weiyi Xia, Yihan Zhang, Chen Zhao, Lianqun Wu
Publikováno v:
Frontiers in Endocrinology, Vol 14 (2023)
Externí odkaz:
https://doaj.org/article/a1c7730aca864c818951f67dfacceafe
Autor:
Meng Chen, Zhaozhao Zhao, Lianqun Wu, Jiancheng Huang, Peng Yu, Jiang Qian, Ting Ni, Chen Zhao
Publikováno v:
Cell Death and Disease, Vol 13, Iss 9, Pp 1-10 (2022)
Abstract Retinoblastoma (RB) is the most common pediatric intraocular malignancy and is a serious vision- and life-threatening disease. The biallelic mutation of the retinoblastoma gene RB1 is the initial event in the malignant transformation of RB,
Externí odkaz:
https://doaj.org/article/6e698b08375b47a8b880c047c5a5783f
Autor:
Jiancheng Huang, Meng Chen, Yu Liang, Yuxiang Hu, Weiyi Xia, Yihan Zhang, Chen Zhao, Lianqun Wu
Publikováno v:
Frontiers in Endocrinology, Vol 13 (2022)
ObjectiveThyroid-associated ophthalmopathy (TAO) is a disfiguring autoimmune disease, which destroys the structure of orbital tissues and even threatens vision. Metabolic reprograming is critical in autoimmune diseases; however, the metabolic basis o
Externí odkaz:
https://doaj.org/article/a6bbd11f476d44d49a94af260ab31d47
Autor:
Yu Liang, Lingjie Kong, Yuelu Zhang, Yihan Zhang, Mingsu Shi, Jiaqiu Huang, Hongyu Kong, Siyi Qi, Yunlong Yang, Jiaxu Hong, Meidong Zhu, Xiangjia Zhu, Xinghuai Sun, Shujie Zhang, Lianqun Wu, Chen Zhao
Publikováno v:
Theranostics; 2024, Vol. 14 Issue 4, p1500-1516, 17p
Autor:
Jiancheng Huang, Meng Chen, Yu Liang, Yuxiang Hu, Weiyi Xia, Yihan Zhang, Chen Zhao, Lianqun Wu
Publikováno v:
Frontiers in Endocrinology; 2023, p1-10, 10p
Autor:
Yu Liang, Sijia Ding, Xiying Wang, Chunchun Hu, Yihan Zhang, Yan Hu, Yuye Zhang, Hongyu Kong, Weiyi Xia, Qinghe Jing, Yuxiang Hu, Chen Zhao, Lianqun Wu
Publikováno v:
Frontiers in Cell and Developmental Biology, Vol 9 (2021)
In response to pathological stimulation, methylation status conversion of the genome drives changes of cell feature and is able to promote disease development. Yet the role of methylation in the development of thyroid-associated ophthalmopathy (TAO)
Externí odkaz:
https://doaj.org/article/86007a945e7648989a466985339acbb4
Publikováno v:
Children, Vol 9, Iss 11, p 1605 (2022)
Congenital fibrosis of the extraocular muscles (CFEOM) is a genetic disorder belonging to the congenital cranial dysinnervation disorders and is characterized by nonprogressive restrictive ophthalmoplegia. It is phenotypically and genotypically heter
Externí odkaz:
https://doaj.org/article/dfc0a6e018a543f78ef6c6a867388804
Publikováno v:
British Journal of Ophthalmology; Sep2023, Vol. 107 Issue 9, p1377-1382, 6p