Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
8591135 | The Ocular Surface | 2018 | 37 Pages |
Abstract
Dry eye disease (DED) is a complex condition with a multifactorial etiology that can be difficult to manage successfully. While external factors are modifiable, treatment success is limited if genetic factors contribute to the disease. The purpose of this review is to compile research describing normal and abnormal ocular surface function on a molecular level, appraise genetic studies involving DED or DED-associated diseases, and introduce the basic methods used for conducting genetic epidemiology studies.
Keywords
MGDFASMMP-9PPARHuman β-defensinsMUCTRAF6CCR5DEDEGFRBLIMP-1PLTPPRDM1FATP4B lymphocyte-induced maturation protein-1HBDsGvHDSNPsTGF-β1RNA-seqqPCRLPREDADHTNF-κBEsr1MAPKRheumatoid arthritismeibomian gland dysfunctionGenetic epidemiologyinterleukin-Dry eye diseaseTransforming growth factor-beta 1RNA sequencingtumor necrosis factor-alphaDihydrotestosteronereal time quantitative polymerase chain reactionTNF-αLymphoproliferationSystemic lupus erythematosusSLEMatrix metalloproteinase-9TranscriptomicsBMPgenome wide association studiesGWASBiomarkersAIREPhospholipid transfer proteinfatty acid transport protein 4bone morphogenic proteinmitogen-activated protein kinaseSingle nucleotide polymorphismsGraft versus host diseaseEstrogen receptor alphaEpidermal growth factor receptorperoxisome proliferator-activated receptorglucocorticoid receptors
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Authors
Ling Lee, Qian Garrett, Judith Flanagan, Subhabrata Chakrabarti, Eric Papas,