Cargando…

Polymorphisms of the Homologous Recombination Gene RAD51 in Keratoconus and Fuchs Endothelial Corneal Dystrophy

Purpose. We investigated the association between genotypes and haplotypes of the c.-61G>T (rs 1801320) and c.-98G>C (rs 1801321) polymorphisms of the RAD51 gene and the occurrence of keratoconus (KC) and Fuchs endothelial corneal dystrophy (FECD) in dependence on some environmental factors. Me...

Descripción completa

Detalles Bibliográficos
Autores principales:	Synowiec, Ewelina, Wojcik, Katarzyna A., Izdebska, Justyna, Binczyk, Ewelina, Blasiak, Janusz, Szaflik, Jerzy, Szaflik, Jacek P.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Hindawi Publishing Corporation 2013
Materias:	Research Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3809973/ https://www.ncbi.nlm.nih.gov/pubmed/24223453 http://dx.doi.org/10.1155/2013/851817

Ejemplares similares

Polymorphism of the Flap Endonuclease 1 Gene in Keratoconus and Fuchs Endothelial Corneal Dystrophy
por: Wojcik, Katarzyna A., et al.
Publicado: (2014)

Polymorphism of the Transferrin Gene in Eye Diseases: Keratoconus and Fuchs Endothelial Corneal Dystrophy
por: Wójcik, Katarzyna A., et al.
Publicado: (2013)

Oxidative Stress in the Pathogenesis of Keratoconus and Fuchs Endothelial Corneal Dystrophy
por: Wojcik, Katarzyna A., et al.
Publicado: (2013)

Variation in DNA Base Excision Repair Genes in Fuchs Endothelial Corneal Dystrophy
por: Wójcik, Katarzyna A., et al.
Publicado: (2015)

Polymorphism of the DNA Base Excision Repair Genes in Keratoconus
por: Wojcik, Katarzyna A., et al.
Publicado: (2014)

DNA damage and repair in Fuchs endothelial corneal dystrophy
por: Czarny, Piotr, et al.
Publicado: (2012)

Lack of association between polymorphisms of the DNA base excision repair genes MUTYH and hOGG1 and keratoconus in a Polish subpopulation
por: Synowiec, Ewelina, et al.
Publicado: (2015)

Fuchs Endothelial Corneal Dystrophy: Strong Association with rs613872 Not Paralleled by Changes in Corneal Endothelial TCF4 mRNA Level
por: Ołdak, Monika, et al.
Publicado: (2015)

Genetic polymorphism of the iron-regulatory protein-1 and -2 genes in age-related macular degeneration
por: Synowiec, Ewelina, et al.
Publicado: (2012)

Systemic immunosuppression with mycophenolate mofetil to prevent corneal graft rejection after high-risk penetrating keratoplasty: a 2-year follow-up study
por: Szaflik, Jacek P., et al.
Publicado: (2015)

An association between polymorphism of the heme oxygenase-1 and -2 genes and age-related macular degeneration
por: Synowiec, Ewelina, et al.
Publicado: (2011)

Lack of association between the c.544G>A polymorphism of the heme oxygenase-2 gene and age-related macular degeneration
por: Wysokinski, Daniel, et al.
Publicado: (2011)

Protective effect of chitosan oligosaccharide lactate against DNA double-strand breaks induced by a model methacrylate dental adhesive
por: Szczepanska, Joanna, et al.
Publicado: (2011)

Oxidative Stress and Cellular Protein Accumulation Are Present in Keratoconus, Macular Corneal Dystrophy, and Fuchs Endothelial Corneal Dystrophy
por: Vottonen, Linda, et al.
Publicado: (2023)

First Identification of a Triple Corneal Dystrophy Association: Keratoconus, Epithelial Basement Membrane Corneal Dystrophy and Fuchs’ Endothelial Corneal Dystrophy
por: Mazzotta, Cosimo, et al.
Publicado: (2014)

Successive Acanthamoeba Corneal Isolates Identified in Poland Monitored in Terms of In Vitro Dynamics
por: Chomicz, Lidia, et al.
Publicado: (2023)

Genetics of Meesmann corneal dystrophy: a novel mutation in the keratin 3 gene in an asymptomatic family suggests genotype-phenotype correlation
por: Szaflik, Jacek P., et al.
Publicado: (2008)

Coincident keratoconus and Fuchs' endothelial dystrophy: Dual dystrophies mask progression
por: Wang, Nancy, et al.
Publicado: (2020)

An association between environmental factors and the IVS4+44C>A polymorphism of the DMT1 gene in age-related macular degeneration
por: Wysokinski, Daniel, et al.
Publicado: (2012)

BLM and RAD51 Genes Polymorphism and Susceptibility to Breast Cancer
por: Sassi, Agnieszka, et al.
Publicado: (2013)

Variability of the Transferrin Receptor 2 Gene in AMD
por: Wysokinski, Daniel, et al.
Publicado: (2014)

Corneal Hydration Control in Fuchs' Endothelial Corneal Dystrophy
por: Wacker, Katrin, et al.
Publicado: (2016)

Immersion Biometry for Intraocular Lens Power Calculation with Fourth-Generation Formulas
por: Skrzypecki, Janusz, et al.
Publicado: (2020)

The Genetic Basis of Fuchs Endothelial Corneal Dystrophy
por: Feizi, Sepehr
Publicado: (2010)

Fuchs endothelial corneal dystrophy: current perspectives
por: Vedana, Gustavo, et al.
Publicado: (2016)

Regenerative medicine in Fuchs' endothelial corneal dystrophy
por: Yuan, Amy E, et al.
Publicado: (2020)

Polymorphisms of Homologous Recombination RAD51, RAD51B, XRCC2, and XRCC3 Genes and the Risk of Prostate Cancer
por: Nowacka-Zawisza, Maria, et al.
Publicado: (2015)

DNA Damage/Repair and Polymorphism of the hOGG1 Gene in Lymphocytes of AMD Patients
por: Wozniak, Katarzyna, et al.
Publicado: (2009)

Fuchs' Endothelial Corneal Dystrophy in Patients With Myotonic Dystrophy, Type 1
por: Winkler, Nelson S., et al.
Publicado: (2018)

Fuchs' Endothelial Corneal Dystrophy and RNA Foci in Patients With Myotonic Dystrophy
por: Mootha, V. Vinod, et al.
Publicado: (2017)

Cataract surgery in patients with Fuchs' endothelial corneal dystrophy
por: Kaup, Soujanya, et al.
Publicado: (2019)

Update on the Surgical Management of Fuchs Endothelial Corneal Dystrophy
por: Blitzer, Andrea L., et al.
Publicado: (2020)

Mitochondrial Dysfunction and Mitophagy in Fuchs Endothelial Corneal Dystrophy
por: Kumar, Varun, et al.
Publicado: (2021)

Unmasking of subclinical keratoconus with Descemet membrane endothelial keratoplasty in Fuchs endothelial dystrophy
por: Yung, Madeline, et al.
Publicado: (2022)

Genetic analysis of patients with Fuchs endothelial corneal dystrophy in India
por: Hemadevi, Boomiraj, et al.
Publicado: (2010)

Genetic screen of African Americans with Fuchs endothelial corneal dystrophy
por: Minear, Mollie A., et al.
Publicado: (2013)

Perspective of Future Potent Therapies for Fuchs Endothelial Corneal Dystrophy
por: Okumura, Naoki, et al.
Publicado: (2018)

REVIEW: Current understanding of the pathogenesis of Fuchs’ endothelial corneal dystrophy
por: Nanda, Gargi Gouranga, et al.
Publicado: (2019)

Genetic mutations and molecular mechanisms of Fuchs endothelial corneal dystrophy
por: Liu, Xuerui, et al.
Publicado: (2021)

Automated Image Segmentation of the Corneal Endothelium in Patients With Fuchs Dystrophy
por: Shilpashree, Palanahalli S., et al.
Publicado: (2021)

Cannot write session to /tmp/vufind_sessions/sess_98taea1ut7n6c9476f2t6or23b