Search Results - "YASUMA, R"
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Whole genome sequencing in patients with retinitis pigmentosa reveals pathogenic DNA structural changes and NEK2 as a new disease gene
Published in Proceedings of the National Academy of Sciences - PNAS (01-10-2013)“…We performed whole genome sequencing in 16 unrelated patients with autosomal recessive retinitis pigmentosa (ARRP), a disease characterized by progressive…”
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Degeneration of retinal on bipolar cells induced by serum including autoantibody against TRPM1 in mouse model of paraneoplastic retinopathy
Published in PloS one (25-11-2013)“…The paraneoplastic retinopathies (PRs) are a group of eye diseases characterized by a sudden and progressive dysfunction of the retina caused by an antibody…”
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TRPM1 mutations are associated with the complete form of congenital stationary night blindness
Published in Molecular vision (12-03-2010)“…To identify human transient receptor potential cation channel, subfamily M, member 1 (TRPM1) gene mutations in patients with congenital stationary night…”
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Elevated C-reactive protein levels and ARMS2/HTRA1 gene variants in subjects without age-related macular degeneration
Published in Molecular vision (31-12-2010)“…To investigate the association between the serum high sensitivity C-reactive protein (hs-CRP) levels and variants in age-related maculopathy susceptibility 2…”
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Axial length increases and related changes in highly myopic normal eyes with myopic complications in fellow eyes
Published in Retina (Philadelphia, Pa.) (01-01-2012)“…To determine whether the axial length (AL) in highly myopic normal adult eyes with myopic complications in the fellow eyes increases significantly during a…”
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Intravitreal injection of bevacizumab for macular edema secondary to branch retinal vein occlusion:results after 12 months and multiple regression analysis
Published in Retina (Philadelphia, Pa.) (01-10-2009)“…To evaluate the 12-month follow-up results of intravitreal bevacizumab therapy for macular edema secondary to branch retinal vein occlusion and to identify the…”
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C9-R95X polymorphism in patients with neovascular age-related macular degeneration
Published in Investigative ophthalmology & visual science (31-01-2012)“…A non-sense mutation at codon 95 in the gene encoding complement factor C9 (C9-R95X) is found most frequently among Japanese. The authors investigated the…”
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Suppression of choroidal neovascularization and quantitative and qualitative inhibition of VEGF and CCL2 by heparin
Published in Investigative ophthalmology & visual science (16-05-2011)“…To study the effect of heparin on the development of laser-induced choroidal neovascularization (CNV) and to assess the underlying molecular mechanisms. Bone…”
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IL18 does not reduce choroidal neovascularization and causes retinal dysfunction in mice
Published in Acta ophthalmologica (Oxford, England) (01-08-2013)“…Purpose It was reported that intravitreous administration anti‐mouse IL18 antibody increases the size of laser‐induced choroidal neovascularization (CNV)…”
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Angiogenic role of glycerol in laser‐induced choroidal neovascularization
Published in Acta ophthalmologica (Oxford, England) (01-08-2013)“…Purpose It has been reported that intravitreous administration of anti‐mouse IL18 antibody increases laser‐induced choroidal neovascularization (CNV) in mice…”
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Intravenous immune globulin suppresses angiogenesis in mice and humans
Published in Signal transduction and targeted therapy (01-01-2016)“…Human intravenous immune globulin (IVIg), a purified IgG fraction composed of ~60% IgG1 and obtained from the pooled plasma of thousands of donors, is…”
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Degeneration of Retinal ON Bipolar Cells Induced by Serum Including Autoantibody against TRPM1 in Mouse Model of Paraneoplastic Retinopathy: e81507
Published in PloS one (01-11-2013)“…The paraneoplastic retinopathies (PRs) are a group of eye diseases characterized by a sudden and progressive dysfunction of the retina caused by an antibody…”
Get full text
Journal Article