Atypical intravitreal growth of retinoblastoma with a multi-branching configuration

Por Nishina, Sachiko, Katagiri, Satoshi, Nakazawa, Atsuko, Kiyotani, Chikako, Yokoi, Tadashi, Azuma, Noriyuki
Publicado no Am J Ophthalmol Case Rep (2017)

Generation of retinal ganglion cells with functional axons from human induced pluripotent stem cells

Por Tanaka, Taku, Yokoi, Tadashi, Tamalu, Fuminobu, Watanabe, Shu-Ichi, Nishina, Sachiko, Azuma, Noriyuki
Publicado no Sci Rep (2015)

Genotype–phenotype correlation of PAX6 gene mutations in aniridia

Por Yokoi, Tadashi, Nishina, Sachiko, Fukami, Maki, Ogata, Tsutomu, Hosono, Katsuhiro, Hotta, Yoshihiro, Azuma, Noriyuki
Publicado no Hum Genome Var (2016)

Electroretinographic effects of retinal dragging and retinal folds in eyes with familial exudative vitreoretinopathy

Por Yaguchi, Yukari, Katagiri, Satoshi, Fukushima, Yoko, Yokoi, Tadashi, Nishina, Sachiko, Kondo, Mineo, Azuma, Noriyuki
Publicado no Sci Rep (2016)

Retinal Structure and Function in Eyes with Optic Nerve Hypoplasia

Por Katagiri, Satoshi, Nishina, Sachiko, Yokoi, Tadashi, Mikami, Masashi, Nakayama, Yuri, Tanaka, Michiko, Azuma, Noriyuki
Publicado no Sci Rep (2017)

Effects of neuroactive agents on axonal growth and pathfinding of retinal ganglion cells generated from human stem cells

Por Yokoi, Tadashi, Tanaka, Taku, Matsuzaka, Emiko, Tamalu, Fuminobu, Watanabe, Shu-Ichi, Nishina, Sachiko, Azuma, Noriyuki
Publicado no Sci Rep (2017)

Establishment of Functioning Human Corneal Endothelial Cell Line with High Growth Potential

Por Yokoi, Tadashi, Seko, Yuko, Yokoi, Tae, Makino, Hatsune, Hatou, Shin, Yamada, Masakazu, Kiyono, Tohru, Umezawa, Akihiro, Nishina, Hiroshi, Azuma, Noriyuki
Publicado em 2012

Clinical features of a toddler with bilateral bullous retinoschisis with a novel RS1 mutation

Por Katagiri, Satoshi, Tanaka, Shin, Yokoi, Tadashi, Hayashi, Takaaki, Matsuzaka, Emiko, Ueda, Kazuko, Yoshida-Uemura, Tomoyo, Arakawa, Akira, Nishina, Sachiko, Kadonosono, Kazuaki, Azuma, Noriyuki
Publicado no Am J Ophthalmol Case Rep (2016)

Molecular Diagnosis of 34 Japanese Families with Leber Congenital Amaurosis Using Targeted Next Generation Sequencing

Por Hosono, Katsuhiro, Nishina, Sachiko, Yokoi, Tadashi, Katagiri, Satoshi, Saitsu, Hirotomo, Kurata, Kentaro, Miyamichi, Daisuke, Hikoya, Akiko, Mizobuchi, Kei, Nakano, Tadashi, Minoshima, Shinsei, Fukami, Maki, Kondo, Hiroyuki, Sato, Miho, Hayashi, Takaaki, Azuma, Noriyuki, Hotta, Yoshihiro
Publicado no Sci Rep (2018)

Two Novel Mutations in the EYS Gene Are Possible Major Causes of Autosomal Recessive Retinitis Pigmentosa in the Japanese Population

Por Hosono, Katsuhiro, Ishigami, Chie, Takahashi, Masayo, Park, Dong Ho, Hirami, Yasuhiko, Nakanishi, Hiroshi, Ueno, Shinji, Yokoi, Tadashi, Hikoya, Akiko, Fujita, Taichi, Zhao, Yang, Nishina, Sachiko, Shin, Jae Pil, Kim, In Taek, Yamamoto, Shuichi, Azuma, Noriyuki, Terasaki, Hiroko, Sato, Miho, Kondo, Mineo, Minoshima, Shinsei, Hotta, Yoshihiro
Publicado em 2012