Commentary: The genetics of pseudoexfoliation syndrome/glaucoma.
作者信息
Behera Geeta, Kaliaperumal Subashini
机构信息
Department of Ophthalmology, Jawaharlal Institute of Post-Graduate Medical Education and Research (JIPMER), Puducherry, India.
出版信息
Indian J Ophthalmol. 2022 Jun;70(6):2028-2029. doi: 10.4103/ijo.IJO_30_22.
Abstract
摘要
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本文引用的文献
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Prevalence of risk alleles in the lysyl oxidase-like 1 gene in pseudoexfoliation glaucoma patients in India.印度假性剥脱性青光眼患者赖氨酰氧化酶样 1 基因风险等位基因的流行情况。
Indian J Ophthalmol. 2022 Jun;70(6):2024-2028. doi: 10.4103/ijo.IJO_2664_21.
2
Pseudoexfoliation syndrome and glaucoma: from genes to disease mechanisms.假性剥脱综合征与青光眼：从基因到发病机制。
Curr Opin Ophthalmol. 2021 Mar 1;32(2):118-128. doi: 10.1097/ICU.0000000000000736.
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The road ahead in genetics and genomics.遗传学和基因组学的未来之路。
Nat Rev Genet. 2020 Oct;21(10):581-596. doi: 10.1038/s41576-020-0272-6. Epub 2020 Aug 24.
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Integral role for lysyl oxidase-like-1 in conventional outflow tissue function and behavior.赖氨酰氧化酶样蛋白 1 在传统流出组织功能和行为中的整体作用。
FASEB J. 2020 Aug;34(8):10762-10777. doi: 10.1096/fj.202000702RR. Epub 2020 Jul 5.
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The protective variant rs7173049 at LOXL1 locus impacts on retinoic acid signaling pathway in pseudoexfoliation syndrome.LOXL1基因座上的保护性变体rs7173049影响剥脱性青光眼综合征中的视黄酸信号通路。
Hum Mol Genet. 2019 Aug 1;28(15):2531-2548. doi: 10.1093/hmg/ddz075.
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Genetic association study of exfoliation syndrome identifies a protective rare variant at LOXL1 and five new susceptibility loci.剥脱综合征的遗传关联研究确定了LOXL1基因上一个具有保护作用的罕见变异以及五个新的易感基因座。
Nat Genet. 2017 Jul;49(7):993-1004. doi: 10.1038/ng.3875. Epub 2017 May 29.
7
A common variant mapping to CACNA1A is associated with susceptibility to exfoliation syndrome.一个定位到CACNA1A基因的常见变异与剥脱综合征易感性相关。
Nat Genet. 2015 Apr;47(4):387-92. doi: 10.1038/ng.3226. Epub 2015 Feb 23.
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The composition of exfoliation material and the cells involved in its production.脱落物质的组成及其产生过程中涉及的细胞。
J Glaucoma. 2014 Oct-Nov;23(8 Suppl 1):S12-4. doi: 10.1097/IJG.0000000000000123.
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