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Articles: Basic Science/Genetics |
Prior Articles
Approximating Lens Power
Optometry and Vision Science, 05/11/09
Cellular and Molecular Origin of Circumpapillary Dysgenesis of the Pigment Epithelium
Ophthalmology, 05/07/09 Characterization of Severe Rod-Cone Dystrophy in a Consanguineous Family with a Splice Site Mutation in the MERTK Gene
British Journal of Ophthalmology, 05/06/09 Prevalence of myocilin gene mutations in a novel UK cohort of POAG patients
Eye, 05/05/09 Nerve Growth Factor promotes in vitro human conjunctival epithelial cells differentiation and mucin gene expression
Investigative Ophthalmology and Visual Science, 05/04/09 Light responses in rods of vitamin A-deprived Xenopus
Investigative Ophthalmology and Visual Science, 05/04/09 Blue cone monochromacy: Causative mutations and associated phenotypes
Molecular Vision, 05/04/09
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Numerical analysis of interferograms for evaluation of tear film build-up time
Ophthalmic and Physiological Optics, 05/04/09 Clinical phenotype of posterior polymorphous corneal dystrophy in a family with a novel ZEB1 mutation
Acta Ophthalmologica, 05/01/09 Aicardi syndrome: The importance of an ophthalmologist in its diagnosis
Indian Journal of Ophthalmology, 05/01/09
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COL1A1, COL2A1 Genes and Myopia Susceptibility: Evidence of Association and Suggestive Linkage to the COL2A1 Locus
Investigative Ophthalmology and Visual Science, 04/30/09 Mutational Spectrum of SLC4A11 in Autosomal Recessive CHED in Saudi Arabia
Investigative Ophthalmology and Visual Science, 04/30/09 Activation of beta-Catenin Signalling Pathway and Its Impact on RPE Cell Cycle
Investigative Ophthalmology and Visual Science, 04/30/09 Lentivirus-Mediated sFlt-1 Gene Fragment Transfer Suppresses Retinal Neovascularization
Current Eye Research, 04/29/09 Analysis of single nucleotide polymorphisms of CRYGA and CRYGB genes in control population of western Indian origin
Indian Journal of Ophthalmology, 04/28/09
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Clinical Utility of the ABCR400 Microarray
Archives of Ophthalmology, 04/27/09 Analysis of mutations of the PITX2 transcription factor found in Axenfeld-Rieger Syndrome patients
Investigative Ophthalmology and Visual Science, 04/24/09 Myopia and polymorphisms in genes for matrix metalloproteinases
Investigative Ophthalmology and Visual Science, 04/24/09 Two novel FBN1 mutations associated with ectopia lentis and marfanoid habitus in two Chinese families
Molecular Vision, 04/24/09
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Familial Presentation of Idiopathic Intracranial Hypertension
Neuro-Ophthalmology, 04/24/09
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Indexed Journals: American Journal of Ophthalmology, Retina, Eye, Cornea
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