Molecular bases of corneal endothelial dystrophies

The phrase “corneal endothelial dystrophies” embraces a group of bilateral corneal conditions that are characterized by a non-inflammatory and progressive degradation of corneal endothelium. Corneal endothelial cells exhibit a high pump site density and, along with barrier function, are responsible...

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Veröffentlicht in:	Experimental eye research 2012-02, Vol.95 (1), p.24-34
Hauptverfasser:	Schmedt, Thore, Silva, Mariana Mazzini, Ziaei, Alireza, Jurkunas, Ula
Format:	Artikel
Sprache:	eng
Schlagworte:	Amino Acid Sequence Animals apoptosis congenital hereditary endothelial dystrophy (CHED) Cornea - blood supply Corneal Dystrophies, Hereditary - genetics Corneal Dystrophies, Hereditary - metabolism Corneal Dystrophies, Hereditary - pathology Endothelial Cells - metabolism Endothelial Cells - pathology Eye Proteins - genetics Eye Proteins - metabolism fuchs endothelial corneal dystrophy (FECD) Fuchs' Endothelial Dystrophy - genetics Fuchs' Endothelial Dystrophy - metabolism Fuchs' Endothelial Dystrophy - pathology Genetic Predisposition to Disease genetics guttae Heredity Humans Molecular Sequence Data Mutation oxidative stress Pedigree Phenotype posterior polymorphous corneal dystrophy (PPCP) Risk Factors sodium biocarbonate transporter-like protein 11 (SLC4A11)
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