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Articles: Basic Science/Genetics |
Prior Articles
Mutation analysis of congenital cataract in a Basotho family identified a new missense allele in CRYBB2
Molecular Vision, 07/31/09
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Association of the Lumican gene functional 3' UTR polymorphism with high myopia
Investigative Ophthalmology and Visual Science, 07/31/09 Morphogenic and genetic differences between Candida albicans strains are associated with keratomycosis virulence
Molecular Vision, 07/31/09
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A novel UBIAD1 mutation identified in a Chinese family with Schnyder crystalline corneal dystrophy
Molecular Vision, 07/30/09 ERK- and Akt-dependent neuroprotection by Erythropoietin (Epo) against glyoxal-AGEs via modulation of Bcl-xL, Bax and BAD
Investigative Ophthalmology and Visual Science, 07/29/09 MLGA: a cost-effective approach to the diagnosis of gene deletions in eye development anomalies
Molecular Vision, 07/29/09
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T-helper 17 lymphocytes in ocular cicatricial pemphigoid
Molecular Vision, 07/29/09
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Analysis of p53 mutations and the expression of p53 and p21WAF1/CIP1 protein in 15 cases of sebaceous carcinoma of the eyelid
Investigative Ophthalmology and Visual Science, 07/28/09 Constitutive and oxidative-stress-induced expression of VEGF in the RPE are differently regulated by different Mitogen-activated protein kinases
Graefe's Archive for Clinical and Experimental Ophthalmology, 07/27/09 Novel hydrophobic cavity represents retinol-binding site in interphotoreceptor retinoid-binding protein (IRBP)
Investigative Ophthalmology and Visual Science, 07/27/09 Bves Overexpression in Trabecular Meshwork Cells Inhibits RhoA Signaling
Investigative Ophthalmology and Visual Science, 07/27/09 Identification of Vimentin as a Novel Target of HSF4 in Lens Development and Cataract by Proteomic Analysis
Investigative Ophthalmology and Visual Science, 07/27/09 Familial Exudative Vitreoretinopathy and DiGeorge Syndrome: A New Locus for Familial Exudative Vitreoretinopathy on Chromosome 22q11.2
Ophthalmology, 07/27/09 Association of the single nucleotide polymorphisms in the extracellular matrix metalloprotease-9 gene with PACG in southern China
Molecular Vision, 07/24/09
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Analyses of Single Nucleotide Polymorphisms and Haplotype Linkage of Loc387715 and the Htra1 Gene in Exudative Age-Related Macular Degeneration in A Chinese Cohort
Retina, 07/23/09 OPA1 increases the risk of normal but not high tension glaucoma
Journal of Medical Genetics, 07/23/09 The Association of Haplotype at the Lumican Gene with High Myopia Susceptibility in Taiwanese Patients
Ophthalmology, 07/22/09 Iris hyperpigmentation in a Chinese family with ocular albinism and the GPR143 mutation
American Journal of Medical Genetics, 07/22/09 The Levator Aponeurosis Contains Smooth Muscle Fibers: New Findings in Caucasians
Ophthalmic Plastic and Reconstructive Surgery, 07/21/09 A single-base substitution within an intronic repetitive element causes dominant retinitis pigmentosa with reduced penetrance
Human Mutation, 07/21/09
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Indexed Journals: American Journal of Ophthalmology, Retina, Eye, Cornea
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