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Articles: Basic Science/Genetics |
Prior Articles
The contribution of lipid layer movement to tear film thinning and breakup
Investigative Ophthalmology and Visual Science, 04/16/09
Detailed ophthalmological evaluation of 43 individuals with PAX6 mutations
Investigative Ophthalmology and Visual Science, 04/16/09 Impact of Cell Source on Human Cornea Reconstructed by Tissue Engineering
Investigative Ophthalmology and Visual Science, 04/16/09 Regulatory sequences in the 3' Untranslated region of the human cGMP-Phosphodiesterase beta-Subunit gene
Investigative Ophthalmology and Visual Science, 04/16/09 Preferential Fluid Flow in the Human Trabecular Meshwork Near Collector Channels
Investigative Ophthalmology and Visual Science, 04/15/09 Disease Boundaries in the Retina of Patients with Usher Syndrome Caused by MYO7A Gene Mutations
Investigative Ophthalmology and Visual Science, 04/15/09 Genetic analysis of complement factor H related 5, CFHR5, in patients with age-related macular degeneration
Molecular Vision, 04/14/09
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TGFB1 as a Susceptibility Gene for High Myopia
Archives of Ophthalmology, 04/14/09 Fine mapping linkage analysis identifies a novel susceptibility locus for myopia on chromosome 2q37 adjacent to but not overlapping MYP12
Molecular Vision, 04/14/09
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Rationale, Design, Methodology, and Baseline Data of a Population-Based Study in Rural China
Ophthalmic Epidemiology, 04/10/09 A Comparative Analysis of Monocular Excursion Measures
Strabismus, 04/09/09 Which Leber congenital amaurosis patients are eligible for gene therapy trials
Journal of American Association for Pediatric Ophthalmology and Strabismus, 04/08/09 High Myopia Is Not Associated with the SNPs in the TGIF, Lumican, TGFB1, and HGF Genes
Investigative Ophthalmology and Visual Science, 04/07/09 Different WDR36 mutation pattern in Chinese patients with primary open-angle glaucoma
Molecular Vision, 04/06/09
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Novel ABCA4 compound heterozygous mutations cause severe progressive autosomal recessive cone-rod dystrophy presenting as Stargardt disease
Molecular Vision, 04/06/09
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Age-Related Macular Degeneration Associated ARMS2 is not a Mitochondrial but Cytosolic Protein
Investigative Ophthalmology and Visual Science, 04/03/09 The cytoplasmic accumulations of the cataract-associated mutant, Connexin50P88S, are long-lived and form in the endoplasmic reticulum
Experimental Eye Research, 04/02/09 Adaptive Optics Scanning Laser Ophthalmoscopy Images in a Family with the Mitochondrial DNA T8993C Mutation
Investigative Ophthalmology and Visual Science, 04/01/09 GSTM1 and GSTT1 Deletion Genotypes in Various Spontaneous Optic Neuropathies in Arabs
British Journal of Ophthalmology, 03/31/09 Reproducibility of the mfERG between instruments
Documenta Ophthalmologica, 03/30/09
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Indexed Journals: American Journal of Ophthalmology, Retina, Eye, Cornea
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