Additional evidence to support the role of a common variant near the complement factor I gene in susceptibility to age-related macular degeneration.
作者信息
Kondo Naoshi, Bessho Hiroaki, Honda Shigeru, Negi Akira
出版信息
Eur J Hum Genet. 2010 Jun;18(6):634-5. doi: 10.1038/ejhg.2009.243. Epub 2010 Jan 20.
Abstract
摘要
相似文献
1
Additional evidence to support the role of a common variant near the complement factor I gene in susceptibility to age-related macular degeneration.支持补体因子I基因附近常见变异在年龄相关性黄斑变性易感性中作用的更多证据。
Eur J Hum Genet. 2010 Jun;18(6):634-5. doi: 10.1038/ejhg.2009.243. Epub 2010 Jan 20.
2
Variation near complement factor I is associated with risk of advanced AMD.补体因子I附近的变异与晚期年龄相关性黄斑变性的风险相关。
Eur J Hum Genet. 2009 Jan;17(1):100-4. doi: 10.1038/ejhg.2008.140. Epub 2008 Aug 6.
3
No evidence of association between complement factor I genetic variant rs10033900 and age-related macular degeneration.补体因子I基因变异rs10033900与年龄相关性黄斑变性之间无关联证据。
Eur J Hum Genet. 2012 Jan;20(1):1-2; author reply 3. doi: 10.1038/ejhg.2011.118. Epub 2011 Oct 12.
4
Common variant rs10033900 near the complement factor I gene is associated with age-related macular degeneration risk in Han Chinese population.补体因子I基因附近的常见变异体rs10033900与汉族人群年龄相关性黄斑变性风险相关。
Eur J Hum Genet. 2014 Dec;22(12):1417-9. doi: 10.1038/ejhg.2014.37. Epub 2014 Mar 19.
5
Interactions among different genetic loci in age-related macular degeneration.年龄相关性黄斑变性中不同基因座之间的相互作用。
Ophthalmic Genet. 2018 Apr;39(2):189-193. doi: 10.1080/13816810.2017.1393829. Epub 2017 Oct 31.
6
Genetic variants within chromosome 4q28.3 are not reproducibly associated with age-related macular degeneration (AMD).
Acta Ophthalmol. 2011 Nov;89(7):e603-4. doi: 10.1111/j.1755-3768.2010.01986.x. Epub 2010 Aug 25.
7
Geographic distribution of rare variants associated with age-related macular degeneration.与年龄相关性黄斑变性相关的罕见变异的地理分布。
Mol Vis. 2018 Jan 27;24:75-82. eCollection 2018.
8
Rare Genetic Variants in Complement Factor I Lead to Low FI Plasma Levels Resulting in Increased Risk of Age-Related Macular Degeneration.补体因子 I 中的罕见遗传变异导致 FI 血浆水平降低，从而增加与年龄相关的黄斑变性的风险。
Invest Ophthalmol Vis Sci. 2020 Jun 3;61(6):18. doi: 10.1167/iovs.61.6.18.
9
Support for the involvement of complement factor I in age-related macular degeneration.支持补体因子I参与年龄相关性黄斑变性。
Eur J Hum Genet. 2010 Jan;18(1):15-6. doi: 10.1038/ejhg.2009.113.
10
Age-related macular degeneration: Complement in action.年龄相关性黄斑变性：补体的作用
Immunobiology. 2016 Jun;221(6):733-9. doi: 10.1016/j.imbio.2015.11.007. Epub 2015 Dec 19.
引用本文的文献
1
CRISPR Manipulation of Age-Related Macular Degeneration Haplotypes in the Complement System: Potential Future Therapeutic Applications/Avenues.CRISPR 技术对补体系统中与年龄相关性黄斑变性相关单倍型的操作：潜在的未来治疗应用/途径。
Int J Mol Sci. 2024 Jan 30;25(3):1697. doi: 10.3390/ijms25031697.
2
Characterization of polymorphisms in and genes and their association with exudative age-related macular degeneration in Algerian patients.阿尔及利亚患者中 基因和 基因多态性的特征及其与渗出性年龄相关性黄斑变性的关联。
Mol Biol Res Commun. 2022 Jun;11(2):105-111. doi: 10.22099/mbrc.2022.43634.1743.
3
Complement family member CFI polymorphisms and AMD susceptibility from a comprehensive analysis.从综合分析看补体家族成员 CFI 多态性与 AMD 的易感性。
Biosci Rep. 2020 Apr 30;40(4). doi: 10.1042/BSR20200406.
4
Haplotypes of rs1120638, rs9621532, rs833068, rs10033900, rs3793784, and rs56209061 Gene Polymorphisms in Age-Related Macular Degeneration.rs1120638、rs9621532、rs833068、rs10033900、rs3793784 和 rs56209061 基因多态性与年龄相关性黄斑变性。
Dis Markers. 2019 Sep 8;2019:9602949. doi: 10.1155/2019/9602949. eCollection 2019.
5
Complement System and Age-Related Macular Degeneration: Implications of Gene-Environment Interaction for Preventive and Personalized Medicine.补体系统与年龄相关性黄斑变性：基因-环境相互作用对预防医学和个体化医学的影响。
Biomed Res Int. 2018 Aug 26;2018:7532507. doi: 10.1155/2018/7532507. eCollection 2018.
6
Association of polymorphisms of complement factor I rs141853578 (G119R) with age-related macular degeneration in Iranian population.补体因子I rs141853578（G119R）多态性与伊朗人群年龄相关性黄斑变性的关联
Int Ophthalmol. 2019 Mar;39(3):551-556. doi: 10.1007/s10792-018-0835-0. Epub 2018 Feb 1.
7
Association between complement factor I gene polymorphisms and the risk of age-related macular degeneration: a Meta-analysis of literature.补体因子I基因多态性与年龄相关性黄斑变性风险的关联：文献的Meta分析
Int J Ophthalmol. 2016 Feb 18;9(2):298-305. doi: 10.18240/ijo.2016.02.23. eCollection 2016.
8
9
Lysosomes: Regulators of autophagy in the retinal pigmented epithelium.溶酶体：视网膜色素上皮细胞中自噬的调节因子。
Exp Eye Res. 2016 Mar;144:46-53. doi: 10.1016/j.exer.2015.08.018. Epub 2015 Aug 28.
10
Tag SNPs of CFI contributed to the susceptibility for non-small cell lung cancer in Chinese population.补体因子I的标签单核苷酸多态性与中国人群非小细胞肺癌的易感性相关。
Tumour Biol. 2015 Mar;36(3):1955-62. doi: 10.1007/s13277-014-2801-4. Epub 2014 Nov 15.
本文引用的文献
1
2
Support for the involvement of complement factor I in age-related macular degeneration.支持补体因子I参与年龄相关性黄斑变性。
Eur J Hum Genet. 2010 Jan;18(1):15-6. doi: 10.1038/ejhg.2009.113.
3
4
Variation near complement factor I is associated with risk of advanced AMD.补体因子I附近的变异与晚期年龄相关性黄斑变性的风险相关。
Eur J Hum Genet. 2009 Jan;17(1):100-4. doi: 10.1038/ejhg.2008.140. Epub 2008 Aug 6.
5
Elastin gene polymorphisms in neovascular age-related macular degeneration and polypoidal choroidal vasculopathy.新生血管性年龄相关性黄斑变性和息肉状脉络膜血管病变中的弹性蛋白基因多态性
Invest Ophthalmol Vis Sci. 2008 Mar;49(3):1101-5. doi: 10.1167/iovs.07-1145.
6
A note on exact tests of Hardy-Weinberg equilibrium.关于哈迪-温伯格平衡精确检验的一则注释。
Am J Hum Genet. 2005 May;76(5):887-93. doi: 10.1086/429864. Epub 2005 Mar 23.
Zotero 插件