HuGE Literature Finder
Records 1-4
Low-frequency coding variants in CETP and CFB are associated with susceptibility of exudative age-related macular degeneration in the Japanese population.
Human molecular genetics 2016 Nov 25 (22): 5027-5034. Momozawa Yukihide, Akiyama Masato, Kamatani Yoichiro, Arakawa Satoshi, Yasuda Miho, Yoshida Shigeo, Oshima Yuji, Mori Ryusaburo, Tanaka Koji, Mori Keisuke, Inoue Satoshi, Terasaki Hiroko, Yasuma Tetsuhiro, Honda Shigeru, Miki Akiko, Inoue Maiko, Fujisawa Kimihiko, Takahashi Kanji, Yasukawa Tsutomu, Yanagi Yasuo, Kadonosono Kazuaki, Sonoda Koh-Hei, Ishibashi Tatsuro, Takahashi Atsushi, Kubo Michia |
Low-frequency coding variants in CETP and CFB are associated with susceptibility of exudative age-related macular degeneration in the Japanese population.
Human molecular genetics 2016 Oct . Momozawa Yukihide, Akiyama Masato, Kamatani Yoichiro, Arakawa Satoshi, Yasuda Miho, Yoshida Shigeo, Oshima Yuji, Mori Ryusaburo, Tanaka Koji, Mori Keisuke, Inoue Satoshi, Terasaki Hiroko, Yasuma Tetsuhiro, Honda Shigeru, Miki Akiko, Inoue Maiko, Fujisawa Kimihiko, Takahashi Kanji, Yasukawa Tsutomu, Yanagi Yasuo, Kadonosono Kazuaki, Sonoda Koh-Hei, Ishibashi Tatsuro, Takahashi Atsushi, Kubo Michia |
Associations of 6p21.3 Region with Age-related Macular Degeneration and Polypoidal Choroidal Vasculopathy.
Scientific reports 2016 6 20914. Ye Zimeng, Shuai Ping, Zhai Yaru, Li Fang, Jiang Lingxi, Lu Fang, Wen Feng, Huang Lulin, Zhang Dingding, Liu Xiaoqi, Lin Ying, Luo Huaichao, Zhang Houbin, Zhu Xianjun, Wu Zhengzheng, Yang Zhenglin, Gong Bo, Shi |
Genetic variation in complement regulators and susceptibility to age-related macular degeneration.
Immunobiology 2012 Feb 217 (2): 158-61. Cipriani Valentina, Matharu Baljinder K, Khan Jane C, Shahid Humma, Stanton Chloe M, Hayward Caroline, Wright Alan F, Bunce Catey, Clayton David G, Moore Anthony T, Yates John R |
Polymorphisms in C2, CFB and C3 are associated with progression to advanced age related macular degeneration associated with visual loss.
Journal of medical genetics 2009 May 46 (5): 300-7. Francis P J, Hamon S C, Ott J, Weleber R G, Klein M |
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- Page last updated:Jan 19, 2021
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