Zobrazeno 1 - 10
of 26
pro vyhledávání: '"Shuqiong Hu"'
Publikováno v:
Health Science Reports, Vol 7, Iss 2, Pp n/a-n/a (2024)
Abstract Background Several observational studies have suggested an association between low serum bilirubin levels and Behçet's disease uveitis. However, the causal inference between bilirubin level and juvenile idiopathic arthritis‐associated uve
Externí odkaz:
https://doaj.org/article/d57e1b49fe7046b1b18e442836058e2e
Publikováno v:
BMC Ophthalmology, Vol 18, Iss 1, Pp 1-14 (2018)
Abstract Background The purpose of this study is to discuss whether genetic variants (rs2230199, rs1047286, rs2230205, and rs2250656) in the C3 gene account for a significant risk of advanced AMD. Methods We performed a meta-analysis using electronic
Externí odkaz:
https://doaj.org/article/ca81fea80e444f94ad05db0bb26acdbc
Publikováno v:
Petroleum Exploration and Development, Vol 40, Iss 4, Pp 507-513 (2013)
By using Bush viscometer, dynamic and static laser scatter instrument, scanning electron microscope and core flow experimental apparatus, experiments were conducted to study the viscosity, molecular coil dimensions, molecular configuration and static
Externí odkaz:
https://doaj.org/article/5f26c56ada03496b9248d60bae623ebe
Publikováno v:
European Journal of Clinical Nutrition. 77:75-81
To investigate the causal effects of plasma Polyunsaturated fatty acids (PUFAs) on the risk of juvenile idiopathic arthritis (JIA) and ocular comorbidity through Mendelian randomization (MR) analysis.Genetic variants (formerly single nucleotide polym
Publikováno v:
International Ophthalmology. 43:589-596
The objective of this article was to examine the potential effect of juvenile idiopathic arthritis-associated uveitis (JIAU) on the risk of major depressive and anxiety disorders through Mendelian randomization (MR) study.Genetic instrumental variabl
Publikováno v:
Ophthalmic Research. 65:264-275
Background: Though the risk of protein tyrosine phosphatase nonreceptor 22 (PTPN22) and cytotoxic T-lymphocyte antigen-4 (CTLA-4) genetic variants with uveitis have been developed, the combined results still remain uncertain and controversial. Object
Publikováno v:
Ophthalmic Research. 64:192-204
Age-related macular degeneration (AMD) causes irreversible vision loss, and targeted anti-vascular endothelial growth factor (VEGF) therapy is now the most common and effective treatment. The aim of this meta-analysis is to discuss whether genetic po
Publikováno v:
Ophthalmic research. 65(3)
Though the risk of protein tyrosine phosphatase nonreceptor 22 (PTPN22) and cytotoxic T-lymphocyte antigen-4 (CTLA-4) genetic variants with uveitis have been developed, the combined results still remain uncertain and controversial.The aim of this stu
Publikováno v:
BMC Ophthalmology, Vol 18, Iss 1, Pp 1-14 (2018)
BMC Ophthalmology
BMC Ophthalmology
Background The purpose of this study is to discuss whether genetic variants (rs2230199, rs1047286, rs2230205, and rs2250656) in the C3 gene account for a significant risk of advanced AMD. Methods We performed a meta-analysis using electronic database