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Articles: Basic Science/Genetics |
Prior Articles
A single-base substitution within an intronic repetitive element causes dominant retinitis pigmentosa with reduced penetrance
Human Mutation, 07/21/09
Increased Prevalence of Autoimmunity in Patients With White Spot Syndromes and Their Family Members
Archives of Ophthalmology, 07/20/09 The retinoic acid receptor alpha (RARA) gene is not associated with myopia, hypermetropia, and ocular biometric measures
Molecular Vision, 07/20/09
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Fine-mapping of candidate region in Amish and Ashkenazi families confirms linkage of refractive error to a QTL on 1p34-p36
Molecular Vision, 07/20/09
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Mitochondrial DNA mutation m.3635G>A may be associated with Leber hereditary optic neuropathy in Chinese
Biochemical and Biophysical Research Communications, 07/20/09 Phenotypic Variability Due to a Novel Glu292Lys Variation in Exon 8 of the BEST1 Gene Causing Best Macular Dystrophy
Archives of Ophthalmology, 07/16/09 The genetics of central corneal thickness
British Journal of Ophthalmology, 07/15/09 No association of CTLA-4 polymorphisms with susceptibility to Behcet's disease
British Journal of Ophthalmology, 07/15/09 Molecular analysis of FOXC1 in subjects presenting with severe developmental eye anomalies
Molecular Vision, 07/15/09
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Genetic Etiology and Clinical Consequences of Complete and Incomplete Achromatopsia
Ophthalmology, 07/14/09 A preliminary investigation into the relationship between ocular surface temperature and lipid layer thickness
Contact Lens and Anterior Eye, 07/13/09 Expression of hypoxia-inducible factor-1 alpha and -2 alpha in human choroidal neovascular membranes
Graefe's Archive for Clinical and Experimental Ophthalmology, 07/13/09 A novel mutation in CRYAB associated with autosomal dominant congenital nuclear cataract in a Chinese family
Molecular Vision, 07/10/09
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Primary T-cell Lymphoma of the Retina and Cerebellum: Immunophenotypic and Gene Rearrangement Confirmation
American Journal of Ophthalmology, 07/09/09 Genotyping microarray for CSNB-associated genes
Investigative Ophthalmology and Visual Science, 07/08/09 The Natural History of Stargardt Disease with Specific Sequence Mutation in the ABCA4 Gene
Investigative Ophthalmology and Visual Science, 07/08/09 Comparison of the histology, gene expression profile, and phenotype of cultured human limbal epithelial cells from different limbal regions
Investigative Ophthalmology and Visual Science, 07/08/09 Suppression of ICAM-1 in Retinal and Choroidal Endothelial Cells by Plasmid Small-interfering RNA in Vivo
Investigative Ophthalmology and Visual Science, 07/07/09 Complement factor H and LOC387715 gene polymorphisms in a Greek population with age-related macular degeneration
Graefe's Archive for Clinical and Experimental Ophthalmology, 07/06/09 Mitochondrial proteomics in experimental autoimmune uveitis oxidative stress
Investigative Ophthalmology and Visual Science, 07/06/09
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Indexed Journals: American Journal of Ophthalmology, Retina, Eye, Cornea
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