Zobrazeno 1 - 10
of 48
pro vyhledávání: '"Hongyan Ge"'
Publikováno v:
Advances in Ophthalmology Practice and Research, Vol 4, Iss 4, Pp 194-201 (2024)
Background: Cataracts are a common eye disease and a major cause of blindness in China and worldwide. In China, the incidence of cataracts among people over 60 years old is as high as 80%. Surgery is the primary treatment for various types of catarac
Externí odkaz:
https://doaj.org/article/7177a467eac54bfcbd8b8d53acc4d46c
Autor:
Yu Mi, Chaoqun Wei, Liyao Sun, Huirui Liu, Jiayue Zhang, Jialin Luo, Xiaohan Yu, Jie He, Hongyan Ge, Ping Liu
Publikováno v:
Biomedicine & Pharmacotherapy, Vol 157, Iss , Pp 114048- (2023)
Summary: Background: Cataracts are the main cause of reversible blindness worldwide. The ageing of the lens caused by ultraviolet B (UVB) radiation is mostly related to oxidative stress (OS). Little is known about whether OS induced by UVB enhances t
Externí odkaz:
https://doaj.org/article/8d38a04d45fa4d3e894718a1b5e1af02
Publikováno v:
Buildings, Vol 12, Iss 11, p 1922 (2022)
Deep foundation pit (DFP) projects have been a high incidence area of safety accidents because of their own high danger and complexity. Therefore, it is necessary to study the resilience of their construction safety system. This paper systematically
Externí odkaz:
https://doaj.org/article/5db09d53c87f4aa4bb9eae55de1adea7
Autor:
Haiyang Yu, Liyao Sun, Jing Cui, Yan Li, Yu Yan, Xi Wei, Chao Wang, Fanqian Song, Wentong Jiang, Yifan Liu, Hongyan Ge, Hua Qian, Xiaoguang Li, Xianling Tang, Ping Liu
Publikováno v:
EBioMedicine, Vol 44, Iss , Pp 542-553 (2019)
Background: Corneal neovascularization (angiogenesis and lymphangiogenesis) compromises corneal transparency and transplant survival, however, the molecular mechanisms of corneal host epithelial and stromal cells in neovascularization have not yet be
Externí odkaz:
https://doaj.org/article/56dfba73c7844e3fb72f05a4baf8f6c2
Publikováno v:
Frontiers in Genetics, Vol 11 (2020)
Retinoblastoma (RB) is the most common intraocular tumor in childhood. Long non-coding RNA (lncRNA) nuclear paraspeckle assembly transcript 1 (NTAT1) has been reported to be related to RB progression. This study aims to study the molecular mechanism
Externí odkaz:
https://doaj.org/article/d03227a3edb54ae9882e0a1f3efc5028
Publikováno v:
Journal of Ophthalmology, Vol 2019 (2019)
Background. Notch/Dll4 involvement in cornea neovascularization (CRNV) and lymphangiogenesis is unclear. This study aimed to explore the role of notch signaling in basic fibroblast growth factor- (bFGF-) induced corneal lymphangiogenesis and hemangio
Externí odkaz:
https://doaj.org/article/cd3b0afc6b7d4008b804fe1729c5428a
Publikováno v:
Clinical Laboratory; 2024, Vol. 70 Issue 7, p1288-1293, 6p
Publikováno v:
Biochemical Genetics. 60:24-38
Glucocorticoid-induced cataract (GIC)-associated biomarkers were screened by ceRNA network construction. The GIC samples' GSE3040 were obtained from the NCBI-GEO database. R's Limma package was used to identify differentially expressed RNAs (DERs) be
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::552e4ffde51516bfe51048e0f5ff0a2d
https://doi.org/10.1007/s10528-021-10078-3
https://doi.org/10.1007/s10528-021-10078-3
Autor:
Shudan Wang, Lingjia Liu, Tomas Blanco, Hongyan Ge, Yutong Xia, Kunpeng Pang, Yihe Chen, Reza Dana
Publikováno v:
The ocular surface. 26
Allergic conjunctivitis is the most common cause leading to ocular redness (OR). Herein, using an animal model of allergic OR, we evaluated the therapeutic efficacy of topical blockade of substance P (SP) in treating red eye.Allergic OR was induced i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::26fd23470ec3512a4bedb827f77f6151
https://pubmed.ncbi.nlm.nih.gov/36067981
https://pubmed.ncbi.nlm.nih.gov/36067981
Autor:
Liyao Sun, Chao Wang, Zhijian Li, Fanqian Song, Hongyan Ge, Ping Liu, Xianling Tang, Hanruo Liu
Publikováno v:
Graefe's Archive for Clinical and Experimental Ophthalmology. 258:2737-2751
The present study investigated a pathogenic mutation and its mechanism on membranous cataract in a congenital membranous cataract family. An autosomal dominant four-generation Chinese congenital membranous cataract family was recruited and whole-exom
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d48c85f581bfb54bc9229c02a506024e
https://doi.org/10.1007/s00417-020-04846-x
https://doi.org/10.1007/s00417-020-04846-x