The genetics of Fuchs' corneal dystrophy - Wikidata - wikimedia - TriplyDB

The genetics of Fuchs' corneal dystrophy

The genetics of Fuchs' corneal dystrophy

http://www.wikidata.org/entity/Q36754678

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Variation in DNA Base Excision Repair Genes in Fuchs Endothelial Corneal Dystrophy Mitochondrial polymorphism A10398G and Haplogroup I are associated with Fuchs' endothelial corneal dystrophy.Polymorphism of the flap endonuclease 1 gene in keratoconus and Fuchs endothelial corneal dystrophy.The effects of Rho-associated kinase inhibitor Y-27632 on primary human corneal endothelial cells propagated using a dual media approach RNA toxicity and missplicing in the common eye disease fuchs endothelial corneal dystrophy.Association of common variants in TCF4 and PTPRG with Fuchs' corneal dystrophy: a systematic review and meta-analysis.Fuchs Endothelial Corneal Dystrophy: Strong Association with rs613872 Not Paralleled by Changes in Corneal Endothelial TCF4 mRNA Level.Fuchs endothelial corneal dystrophy in patients with myotonic dystrophy: a case series Oxidative stress in the pathogenesis of keratoconus and Fuchs endothelial corneal dystrophy.Corneal Backscatters as an Objective Index for Assessing Fuchs' Endothelial Corneal Dystrophy: A Pilot Study.CTG18.1 repeat expansion may reduce TCF4 gene expression in corneal endothelial cells of German patients with Fuchs' dystrophy.Polymorphism of the APEX nuclease 1 gene in keratoconus and Fuchs endothelial corneal dystrophy.

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The genetics of Fuchs' corneal dystrophy

http://www.wikidata.org/entity/Q36754678

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2012 nî lūn-bûn

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The genetics of Fuchs' corneal dystrophy

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The genetics of Fuchs' corneal dystrophy

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The genetics of Fuchs' corneal dystrophy

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The genetics of Fuchs' corneal dystrophy

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Expert Review of Ophthalmology

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The genetics of Fuchs' corneal dystrophy

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Benjamin W Iliff

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John D Gottsch

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S Amer Riazuddin

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Stem cell markers in the human posterior limbus and corneal endothelium of unwounded and wounded corneas

NaBC1 is a ubiquitous electrogenic Na+ -coupled borate transporter essential for cellular boron homeostasis and cell growth and proliferation

Mutations in LOXHD1, an evolutionarily conserved stereociliary protein, disrupt hair cell function in mice and cause progressive hearing loss in humans

Age-severity relationships in families linked to FCD2 with retroillumination photography

The miR-200 family inhibits epithelial-mesenchymal transition and cancer cell migration by direct targeting of E-cadherin transcriptional repressors ZEB1 and ZEB2

Fuchs’ corneal dystrophy

Borate transporter SLC4A11 mutations cause both Harboyan syndrome and non-syndromic corneal endothelial dystrophy

Immunohistochemistry and electron microscopy of early-onset fuchs corneal dystrophy in three cases with the same L450W COL8A2 mutation

The miR-200 family and miR-205 regulate epithelial to mesenchymal transition by targeting ZEB1 and SIP1

Evidence of oxidative stress in human corneal diseases

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363-375

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scholarly article

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10.1586/EOP.12.39

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