Common sequence variants in the LOXL1 gene confer susceptibility to exfoliation glaucoma
Thorleifsson G, Magnusson KP, Sulem P, et al. Common sequence variants in the LOXL1 gene confer susceptibility to exfoliation glaucoma. Science. 2007;317:1397-1400.
Lysyl oxidase-like 1 polymorphisms and exfoliation syndrome in the Japanese population
Hayashi H, Gotoh N, Ueda Y, et al. Lysyl oxidase-like 1 polymorphisms and exfoliation syndrome in the Japanese population. Am J Ophthalmol. 2008;145:582-585.
Major LOXL1 risk allele is reversed in exfoliation glaucoma in a black South African population
Williams SE, Whigham BT, Liu Y, et al. Major LOXL1 risk allele is reversed in exfoliation glaucoma in a black South African population. Mol Vis. 2010;16:705-712.
Genotype-correlated expression of lysyl oxidase-like 1 in ocular tissues of patients with pseudoexfoliation syndrome/glaucoma and normal patients
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. Am J Pathol. 2008;173:1724-1735.
Fan BJ, Pasquale LR, Rhee D, et al. LOXL1 promoter haplotypes are associated with exfoliation syndrome in a U.S. Caucasian population. Invest Ophthalmol Vis Sci. 2011; 52:2372-2378.
A single nucleotide polymorphism in the promoter of the LOXL1 gene and its relationship to pelvic organ prolapse and preterm premature rupture of membranes
Ferrell G, Lu M, Stoddard P, et al. A single nucleotide polymorphism in the promoter of the LOXL1 gene and its relationship to pelvic organ prolapse and preterm premature rupture of membranes. Reprod Sci. 2009;16:438-446.
Regulation of lysyl oxidase-like 1 (LOXL1) and elastin-related genes by pathogenic factors associated with pseudoexfoliation syndrome
Zenkel M, Krysta A, Pasutto F, et al. Regulation of lysyl oxidase-like 1 (LOXL1) and elastin-related genes by pathogenic factors associated with pseudoexfoliation syndrome. Invest Ophthalmol Vis Sci. 2011;52:8488-8495.
Disruption of the blood-aqueous barrier and lens abnormalities in mice lacking Lysl Oxidase-like 1 (LOXL1)
Wiggs JL, Dawlyk B, Connolly E, et al. Disruption of the blood-aqueous barrier and lens abnormalities in mice lacking Lysl Oxidase-like 1 (LOXL1). Invest Ophthalmol Vis Sci. 2014; 55:856-864.