Takeshi Iwata (Akiko Suga)

ORCID

Publication Activity (10 Years)

Years Active: 2022-2024
Publications (10 Years): 4

Top Venues

Communications biology

Human mutation

This page only lists publications with an associated author ORCID identifier.

Publications

Takeshi Iwata, Yuriko Minegishi, Megumi Yamamoto, Koji Ueda, Takeshi Iwata
Compound heterozygous mutations in a mouse model of Leber congenital amaurosis reveal the role of CCT2 in photoreceptor maintenance. Communications biology 7 (1) (2024)
Takeshi Iwata, Yuriko Minegishi, Megumi Yamamoto, Koji Ueda, Takeshi Iwata
Compound heterozygous mutations in a mouse model of Leber congenital amaurosis reveal the role of CCT2 in photoreceptor maintenance. Communications biology 7 (1) (2024)
Takeshi Iwata, Yuriko Minegishi, Megumi Yamamoto, Koji Ueda, Takeshi Iwata
Compound heterozygous mutations in a mouse model of Leber congenital amaurosis reveal the role of CCT2 in photoreceptor maintenance. Communications biology 7 (1) (2024)
Akiko Suga, Kazutoshi Yoshitake, Naoko Minematsu, Kazushige Tsunoda, Kaoru Fujinami, Yozo Miyake, Kazuki Kuniyoshi, Takaaki Hayashi, Kei Mizobuchi, Shinji Ueno, Hiroko Terasaki, Taro Kominami, Nobuhisa Nao-I, Go Mawatari, Atsushi Mizota, Kei Shinoda, Mineo Kondo, Kumiko Kato, Tetsuju Sekiryu, Makoto Nakamura, Sentaro Kusuhara, Hiroyuki Yamamoto, Shuji Yamamoto, Kiyofumi Mochizuki, Hiroyuki Kondo, Itsuka Matsushita, Shuhei Kameya, Takeo Fukuchi, Tetsuhisa Hatase, Masayuki Horiguchi, Yoshiaki Shimada, Atsuhiro Tanikawa, Shuichi Yamamoto, Gen Miura, Nana Ito, Akira Murakami, Takuro Fujimaki, Yoshihiro Hotta, Koji Tanaka, Takeshi Iwata
Genetic characterization of 1210 Japanese pedigrees with inherited retinal diseases by whole-exome sequencing. Human mutation (2022)

Takeshi Iwata.css-eqlu8i{font-size:small;padding-left:4px;} (Akiko Suga)

Publication Activity (10 Years)

Top Topics

Top Venues

Takeshi Iwata (Akiko Suga)