[1] SORKOU KN, MANTHOU ME, ZIAKAS N, et al.Severe abnormalities of lens epithelial cells in exfoliation syndrome:a transmission electron microscopy study of patients with age-related cataract[J].Medicina(Kaunas), 2019, 55(6):235.
[2] PHILIP S, NAJAFI A, TANTRAWORASIN A, et al.Macula vessel density and foveal avascular zone parameters in exfoliation glaucoma compared to primary open-angle glaucoma[J].Invest Ophthalmol Vis Sci, 2019, 60(4):1244. doi: 10.1167/iovs.18-25986
[3] GAYATHRI R, CORAL K, SHARMILA F, et al.Correlation of aqueous humor lysyl oxidase activity with TGF-β levels and LOXL1 genotype in pseudoexfoliation[J].Curr Eye Res, 2016, 41(10):1331. doi: 10.3109/02713683.2015.1125505
[4] SHARMA S, MARTIN S, SYKES MJ, et al.Biological effect of LOXL1 coding variants associated with pseudoexfoliation syndrome[J].Exp Eye Res, 2016, 146:212. doi: 10.1016/j.exer.2016.03.013
[5] ALAY C, TEKELI O, YANIK ODABAS O, et al.Evaluation of the retinal nerve fiber layer and ganglion cell complex thicknesses in patients with exfoliation syndrome[J].Turk J Med Sci, 2019, 49(1):272. doi: 10.3906/sag-1803-27
[6] THORLEIFSSON G, MAGNUSSON KP, SULEM P, et al.Common sequence variants in the LOXL1 gene confer susceptibility to exfoliation glaucoma[J].Science, 2007, 317(5843):1397. doi: 10.1126/science.1146554
[7] DE JUAN-MARCOS L, ESCUDERO-DOMINGUEZ FA, HERNANDEZ-GALILEA E, et al.Association of lysyl oxidase-like 1 gene polymorphisms in pseudoexfoliation syndrome and pseudoexfoliation glaucoma in a spanish population[J].Ophthalmic Genet, 2016, 37(1):25.
[8] MAYINU, CHEN X.Evaluation of LOXL1 polymorphisms in exfoliation syndrome in the Uygur population[J].Mol Vis, 2011, 17(3):1734.
[9] LITTLE J, HIGGINS JP, IOANNIDIS JP, et al.STrengthening the REporting of Genetic Association studies(STREGA)——an extension of the STROBE statement[J].Eur J Clin Invest, 2009, 39(4):247. doi: 10.1111/j.1365-2362.2009.02125.x
[10] ASFUROGLU M, CAVDARLI B, KOZ OG, et al.Association of lysyl oxidase-like 1 gene polymorphism in turkish patients with pseudoexfoliation syndrome and pseudoexfoliation glaucoma[J].J Glaucoma, 2017, 26(2):e54.
[11] ALVAREZ L, GARCIA M, GONZALEZ-IGLESIAS H, et al.LOXL1 gene variants and their association with pseudoexfoliation glaucoma(XFG)in Spanish patients[J].BMC Med Genet, 2015, 16:72.
[12] DUBEY SK, HEJTMANCIK JF, KRISHNADAS SR, et al.Lysyl oxidase-like 1 gene in the reversal of promoter risk allele in pseudoexfoliation syndrome[J].JAMA Ophthalmol, 2014, 132(8):949. doi: 10.1001/jamaophthalmol.2014.845
[13] PARK DY, WON HH, CHO HK, et al.Evaluation of lysyl oxidase-like 1 gene polymorphisms in pseudoexfoliation syndrome in a Korean population[J].Mol Vis, 2013, 19(1):448.
[14] JAIMES M, RIVERA-PARRA D, MIRANDA-DUARTE A, et al.Prevalence of high-risk alleles in the LOXL1 gene and its association with pseudoexfoliation syndrome and exfoliation glaucoma in a Latin American population[J].Ophthalmic Genet, 2012, 33(1):12. doi: 10.3109/13816810.2011.615078
[15] WOLF C, GRAMER E, MULLER-MYHSOK B, et al.Lysyl oxidase-like 1 gene polymorphisms in German patients with normal tension glaucoma, pigmentary glaucoma and exfoliation glaucoma[J].J Glaucoma, 2010, 19(2):136. doi: 10.1097/IJG.0b013e31819f9330
[16] SAGONG M, GU BY, CHA SC.Association of lysyl oxidase-like 1 gene polymorphisms with exfoliation syndrome in Koreans[J].Mol Vis, 2011, 17(5):2808.
[17] LEMMELA S, FORSMAN E, ONKAMO P, et al.Association of LOXL1 gene with Finnish exfoliation syndrome patients[J].J Hum Genet, 2009, 54(5):289. doi: 10.1038/jhg.2009.28
[18] CHEN L, JIA L, WANG N, et al.Evaluation of LOXL1 polymorphisms in exfoliation syndrome in a Chinese population[J].Mol Vis, 2009, 15(3):2349.
[19] OZAKI M, LEE KY, VITHANA EN, et al.Association of LOXL1 gene polymorphisms with pseudoexfoliation in the Japanese[J].Invest Ophthalmol Vis Sci, 2008, 49(9):3976. doi: 10.1167/iovs.08-1805
[20] CHALLA P.Genetics of pseudoexfoliation syndrome[J].Curr Opin Ophthalmol, 2009, 20(2):88. doi: 10.1097/ICU.0b013e328320d86a
[21] YANG X, ZABRISKIE NA, HAU VS, et al.Genetic association of LOXL1 gene variants and exfoliation glaucoma in a Utah cohort[J].Cell Cycle, 2008, 7(4):521. doi: 10.4161/cc.7.4.5388
[22] TANITO M, MINAMI M, AKAHORI M, et al.LOXL1 variants in elderly Japanese patients with exfoliation syndrome/glaucoma, primary open-angle glaucoma, normal tension glaucoma, and cataract[J].Mol Vis, 2008, 14(2):1898.
[23] FUSE N, MIYAZAWA A, NAKAZAWA T, et al.Evaluation of LOXL1 polymorphisms in eyes with exfoliation glaucoma in Japanese[J].Mol Vis, 2008, 14(1):1338.
[24] ARAGON-MARTIN JA, RITCH R, LIEBMANN J, et al.Evaluation of LOXL1 gene polymorphisms in exfoliation syndrome and exfoliation glaucoma[J].Mol Vis, 2008, 14(2):533.
[25] PASUTTO F, KRUMBIEGEL M, MARDIN CY, et al.Association of LOXL1 common sequence variants in German and Italian patients with pseudoexfoliation syndrome and pseudoexfoliation glaucoma[J].Invest Ophthalmol Vis Sci, 2008, 49(4):1459. doi: 10.1167/iovs.07-1449
[26] FAN BJ, PASQUALE L, GROSSKREUTZ CL, et al.DNA sequence variants in the LOXL1 gene are associated with pseudoexfoliation glaucoma in a U.S.clinic-based population with broad ethnic diversity[J].BMC Med Genet, 2008, 9:5.
[27] ZENKEL M, SCHLÖTZER-SCHREHARDT U.Expression and regulation of LOXL1 and elastin-related genes in eyes with exfoliation syndrome[J].J Glaucoma, 2014, 23(8):48.
[28] METAXAKI I, CONSTANTOULAKIS P, PAPADIMITROPOULOS M, et al.Association of lysyl oxidase-like 1 gene common sequence variants in Greek patients with pseudoexfoliation syndrome and pseudoexfoliation glaucoma[J].Mol Vis, 2013, 19(4):1446.
[29] SKAAT A, JASIEN JV, RITCH R.Efficacy of topically administered rho-kinase inhibitor AR-12286 in patients with exfoliation syndrome and ocular hypertension or glaucoma[J].J Glaucoma, 2016, 25(9):e807. doi: 10.1097/IJG.0000000000000508
[30] HAYASHI H, GOTOH N, UEDA Y, et al.Lysyl oxidase-like 1 polymorphisms and exfoliation syndrome in the Japanese population[J].Am J Ophthalmol, 2008, 145(3):582. doi: 10.1016/j.ajo.2007.10.023
[31] SCHLÖTZER-SCHREHARDT U, PASUTTO F, SOMMER P, et al.Genotype-correlated expression of lysyl oxidase-like 1 in ocular tissues of patients with pseudoexfoliation syndrome/glaucoma and normal patients[J].Am J Pathol, 2008, 173(6):1724. doi: 10.2353/ajpath.2008.080535
[32] COUSINS CC, KANG JH, BOVEE C, et al.Nailfold capillary morphology in exfoliation syndrome[J].Eye(Lond), 2017, 31(5):698.
[33] LEE KY, HO SL, THALAMUTHU A, et al.Association of LOXL1 polymorphisms with pseudoexfoliation in the Chinese[J].Mol Vis, 2009, 15(6):1120.
[34] TANG JZ, WANG XQ, MA HF, et al.Association between polymorphisms in lysyl oxidase-like 1 and susceptibility to pseudoexfoliation syndrome and pseudoexfoliation glaucoma[J].PLoS One, 2014, 9(3):903.
[35] 唐聪, 季青山, 钟敬祥, 等.剥脱综合征与LOXL1基因多态性相关性的meta分析[J].中国病理生理杂志, 2014(5):914. doi: 10.3969/j.issn.1000-4718.2014.05.026
[36] CHAKRABARTI S, RAO KN, KAUR I, et al.The LOXL1 gene variations are not associated with primary open-angle and primary angle-closure glaucomas[J].Invest Ophthalmol Vis Sci, 2008, 49(6):2343. doi: 10.1167/iovs.07-1557
[37] GONG WF, CHIANG SW, CHEN LJ, et al:Evaluation of LOXL1 polymorphisms in primary open-angle glaucoma in southern and northern Chinese[J].Mol Vis, 2008, 14(1):2381.