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Polymorphisms in ARMS2 (LOC387715) and LOXL1 genes in the Japanese with age-related macular degeneration.

作者信息

Lepre Tiziana, Cascella Raffaella, Missiroli Filippo, De Felici Cecilia, Taglia Fabiana, Zampatti Stefania, Cusumano Andrea, Ricci Federico, Giardina Emiliano, Eandi Chiara Maria, Novelli Giuseppe

出版信息

Am J Ophthalmol. 2011 Aug;152(2):325-6; author reply 326. doi: 10.1016/j.ajo.2011.04.021.

DOI:10.1016/j.ajo.2011.04.021
PMID:21784201
Abstract
摘要

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1
Polymorphisms in ARMS2 (LOC387715) and LOXL1 genes in the Japanese with age-related macular degeneration.日本年龄相关性黄斑变性患者中ARMS2（LOC387715）和LOXL1基因的多态性
Am J Ophthalmol. 2011 Aug;152(2):325-6; author reply 326. doi: 10.1016/j.ajo.2011.04.021.
2
Polymorphisms in ARMS2 (LOC387715) and LOXL1 genes in the Japanese with age-related macular degeneration.
Am J Ophthalmol. 2011 Sep;152(3):499. doi: 10.1016/j.ajo.2011.04.022.
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Polymorphisms in ARMS2 (LOC387715) and LOXL1 genes in the Japanese with age-related macular degeneration.日本年龄相关性黄斑变性患者 ARMS2（LOC387715）和 LOXL1 基因的多态性。
Am J Ophthalmol. 2011 Mar;151(3):550-6.e1. doi: 10.1016/j.ajo.2010.08.048. Epub 2011 Jan 13.
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Association of LOC387715/ARMS2 (rs10490924) Gene Polymorphism with Age-Related Macular Degeneration in the Brazilian Population.巴西人群中LOC387715/ARMS2（rs10490924）基因多态性与年龄相关性黄斑变性的关联
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Analysis of LOXL1 single nucleotide polymorphisms in Polish population with pseudoexfoliation syndrome.波兰人群中假性剥脱综合征与 LOXL1 单核苷酸多态性的分析。
Acta Ophthalmol. 2011 Feb;89(1):e64-6. doi: 10.1111/j.1755-3768.2010.02083.x.
6
Age-related macular degeneration is associated with an unstable ARMS2 (LOC387715) mRNA.年龄相关性黄斑变性与不稳定的ARMS2（LOC387715）信使核糖核酸相关。
Nat Genet. 2008 Jul;40(7):892-6. doi: 10.1038/ng.170. Epub 2008 May 30.
7
A variant of mitochondrial protein LOC387715/ARMS2, not HTRA1, is strongly associated with age-related macular degeneration.与年龄相关性黄斑变性密切相关的是线粒体蛋白LOC387715/ARMS2的一种变体，而非HTRA1。
Proc Natl Acad Sci U S A. 2007 Oct 9;104(41):16227-32. doi: 10.1073/pnas.0703933104. Epub 2007 Sep 20.
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LOXL1 gene sequence variants and vascular disease in exfoliation syndrome and exfoliative glaucoma.LOXL1 基因序列变异与晶状体蛋白相关的葡萄膜炎和青光眼患者的血管疾病的关系。
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Polymorphisms in C2, CFB and C3 are associated with progression to advanced age related macular degeneration associated with visual loss.补体2（C2）、补体因子B（CFB）和补体3（C3）基因多态性与进展为伴有视力丧失的晚期年龄相关性黄斑变性有关。
J Med Genet. 2009 May;46(5):300-7. doi: 10.1136/jmg.2008.062737. Epub 2008 Nov 17.
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Polymorphisms in the LOC387715/ARMS2 putative gene and the risk for Alzheimer's disease.LOC387715/ARMS2假定基因多态性与阿尔茨海默病风险
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