Search Results - "Yasuma, Tetsuhiro R."

Whole genome sequencing in patients with retinitis pigmentosa reveals pathogenic DNA structural changes and NEK2 as a new disease gene by Nishiguchi, Koji M., Tearle, Richard G., Liu, Yangfan P., Oh, Edwin C., Miyake, Noriko, Benaglio, Paola, Harper, Shyana, Koskiniemi-Kuendig, Hanna, Venturini, Giulia, Sharon, Dror, Koenekoop, Robert K., Nakamura, Makoto, Kondo, Mineo, Ueno, Shinji, Yasuma, Tetsuhiro R., Beckmann, Jacques S., Ikegawa, Shiro, Matsumoto, Naomichi, Terasaki, Hiroko, Berson, Eliot L., Katsanis, Nicholas, Rivolta, Carlo

“…We performed whole genome sequencing in 16 unrelated patients with autosomal recessive retinitis pigmentosa (ARRP), a disease characterized by progressive…”
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TRPM1 mutations are associated with the complete form of congenital stationary night blindness by Nakamura, Makoto, Sanuki, Rikako, Yasuma, Tetsuhiro R, Onishi, Akishi, Nishiguchi, Koji M, Koike, Chieko, Kadowaki, Mikiko, Kondo, Mineo, Miyake, Yozo, Furukawa, Takahisa

“…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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Axial length increases and related changes in highly myopic normal eyes with myopic complications in fellow eyes by Takahashi, Akiko, Ito, Yasuki, Iguchi, Yuko, Yasuma, Tetsuhiro R, Ishikawa, Kohei, Terasaki, Hiroko

“…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 by Kondo, Mineo, Kondo, Nagako, Ito, Yasuki, Kachi, Shu, Kikuchi, Masato, Yasuma, Tetsuhiro R, Ota, Ichiro, Kensaku, Miyake, Terasaki, Hiroko

“…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 by Nishiguchi, Koji M, Yasuma, Tetsuhiro R, Tomida, Daisuke, Nakamura, Makoto, Ishikawa, Kohei, Kikuchi, Masato, Ohmi, Yuhsuke, Niwa, Toshimitsu, Hamajima, Nobuyuki, Furukawa, Koichi, Terasaki, Hiroko

“…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 by Tomida, Daisuke, Nishiguchi, Koji M, Kataoka, Keiko, Yasuma, Tetsuhiro R, Iwata, Eiji, Uetani, Ruka, Kachi, Shu, Terasaki, Hiroko

“…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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Elevated C-reactive protein levels and ARMS2/HTRA1 gene variants in subjects without age-related macular degeneration by Yasuma, Tetsuhiro R, Nakamura, Makoto, Nishiguchi, Koji M, Kikuchi, Masato, Kaneko, Hiroki, Niwa, Toshimitsu, Hamajima, Nobuyuki, Terasaki, Hiroko

“…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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Reply by Kondo, Mineo, Ito, Yasuki, Kachi, Shu, Kikuchi, Masato, Yasuma, Tetsuhiro R., Terasaki, Hiroko, Kondo, Nagako, Ota, Ichiro, Miyake, Kensaku

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