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Paper Details

Genetic variants and cellular stressors associated with exfoliation syndrome modulate promoter activity of a lncRNA within the LOXL1 locus.
Hum Mol Genet
60
2015
3'-end of exon 1, 40 kb, 7-kb region, AS1, Exfoliation syndrome, LOXL1, LOXL1 genomic locus, LOXL1 locus, LOXL1-AS1, LOXL1-AS1 lncRNA, XFG, XFS, canal endothelial cells, exfoliation glaucoma, exfoliation syndrome, fibrillinopathy, functional variants, genetic risk variants, human, human lens epithelial cells, intron 1, irreversible blindness, lncRNA, long non-coding RNA, lysyl, lysyl oxidase-like 1, lysyl oxidase-like 1 (LOXL1) gene, promoter, systemic
Author NameAffiliation
Yutao LiuGeorgia Regents University
Lingyun SongCenter for Genomic and Computational Biology and Department of Pediatrics, Duke University
Alexias SafiCenter for Genomic and Computational Biology and Department of Pediatrics, Duke University
Eranga N VithanaSingapore Eye Research Institute
Gregory E CrawfordCenter for Genomic and Computational Biology and Department of Pediatrics, Duke University
Gregory E CrawfordCenter for Genomic and Computational Biology and Department of Pediatrics, Duke University
Tin AungSingapore Eye Research Institute
Chiea Chuen KhorSingapore Eye Research Institute
Allison E Ashley-Koch
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