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Articles: Basic Science/Genetics |
Prior Articles
Compound heterozygosity for a novel and a recurrent MFRP gene mutation in a family with the nanophthalmos-retinitis pigmentosa complex
Molecular Vision, 09/09/09
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Muscarinic acetylcholine receptor 1 gene polymorphisms associated with high myopia
Molecular Vision, 09/09/09
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Cis-urocanic acid suppresses UV-B-induced interleukin-6 and -8 secretion and cytotoxicity in human corneal and conjunctival epithelial cells in vitro
Molecular Vision, 09/09/09
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A novel mutation in GRK1 causes Oguchi disease in a consanguineous Pakistani family
Molecular Vision, 09/09/09
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Disease-causing mutations in the CLRN1 gene alter normal CLRN1 protein trafficking to the plasma membrane
Molecular Vision, 09/09/09
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Mutations that are a common cause of Leber congenital amaurosis in northern America are rare in Southern India
Molecular Vision, 09/09/09
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Calcium-independent phospholipase A2 regulates retinal pigment epithelium proliferation and may be important in the pathogenesis of retinal diseases
Experimental Eye Research, 09/08/09 Cell differentiation in the retina of an epibenthonic teleost, the Tench (Tinca tinca, Linneo 1758)
Experimental Eye Research, 09/08/09 Nr2e3-directed transcriptional regulation of genes involved in photoreceptor development and cell-type specific phototransduction
Experimental Eye Research, 09/08/09 Human iris pigment epithelial cells suppress T-cell activation via direct cell contact
Experimental Eye Research, 09/08/09 Clusterin Protects Human Retinal Pigment Epithelial Cells from Oxidative Stress-induced Apoptosis
Investigative Ophthalmology and Visual Science, 09/08/09 The -174GG Interleukin-6 Genotype Is Protective From Retinopathy and Nephropathy in Juvenile Onset Type 1 Diabetes Mellitus
Pediatric Research, 09/04/09 Mutations in ASCC3L1 on chromosome 2q11.2 are associated with autosomal dominant retinitis pigmentosa in a Chinese Family
Investigative Ophthalmology and Visual Science, 09/04/09 Microarray-based mutation analysis of 183 spanish families suffering from usher syndrome
Investigative Ophthalmology and Visual Science, 09/03/09 Impact of the Transfer of sFlt-1 Gene Fragments on the ERK1/2 Pathway of VEGF In Vitro
Current Eye Research, 09/02/09 NR2E3 mutations in enhanced S-cone sensitivity syndrome (ESCS), Goldmann-Favre syndrome (GFS), clumped pigmentary retinal degeneration (CPRD), and retinitis pigmentosa (RP)
Human Mutation, 09/02/09 Comparison of cryopreserved and air-dried human amniotic membrane for ophthalmologic applications
Graefe's Archive for Clinical and Experimental Ophthalmology, 09/01/09 Cone-rod dystrophy and a frameshift mutation in the PROM1 gene
Molecular Vision, 08/31/09
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Customized pachymetric guided epithelial debridement for corneal collagen cross linking
BMC Ophthalmology, 08/31/09
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Beta-Defensin 1 haplotype associated with postoperative endophthalmitis
Acta Ophthalmologica, 08/28/09
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Indexed Journals: American Journal of Ophthalmology, Retina, Eye, Cornea
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250 Available Pages
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