The Molecular Biology Society of Japan

4066 results (3571 - 3580)

[3P-0794] EIF2B5toy: A spontaneous novel mutation in mouse leading to motor dysfunction.

〇Mika Terumitsu(Tsujita)1, Hiroki Kitaura1, Ikuo Miura2, Kanako Oda3, Naohiko Seike4, Yasuko Toyoshima4, Shigeharu Wakana2, Hironaka Igarashi1, Tsutomu Nakada1 (1.CIHBS, BRI, Niigata Univ., 2.Japan mouse clinic, RIKEN BRC, 3.DCEM, BRI, Niigata Univ., 4.Dept. of Pathol., BRI, Niigata)

The 39th Annual Meeting of the Molecular Biology Society of Japan

[3P-0795] Enamel defect of murine hypophosphatasia.

〇Seiko Nemoto(Yamamoto)1, Eri Yokoi2, Kei Ogawa1, Kunihiko Shimizu1, Takehiko Shimizu1 (1.Dept. of Ped, Sch. Dent. at Matsudo, Nihon Univ., 2.Dept. of Ped, Sch. Dent. at Matsudo, Nihon Univ. Grad.)

The 39th Annual Meeting of the Molecular Biology Society of Japan

[3P-0799] Identification of ATM heterozygous mutation as a genetic determinat for the individual differences of radiation-induced cancer risk using genome editing technology

〇Tatsuo Miyamoto1, Ekaterina Royba1, Silvia Natsuko Akutsu1, Satoshi Tashiro2, Takashi Yamamoto3, Shinya Matsuura1 (1.Dept. of Genet and Cell Biol., RIRBM., Hiroshima Univ., 2.Dept. of Cellular Biol., RIRBM., Hiroshima Univ., 3.Dept. of Math and Life Sci., Grad. Sch. of Sci., Hiroshima Univ.)

The 39th Annual Meeting of the Molecular Biology Society of Japan

[3P-0800] The genetic background of patients suspected of mitochondrial disorders

〇Masakazu Kohda1, Yoshihito Kishita2, Yosuke Mizuno2, Atsuko Imai3, Akihiro Nakaya3, Tomoko Hirata1, Yukiko Yatsuka2, Nurun N. Borna2, Hiroko Harashima4, Kei Murayama5, Akira Ohtake4, Yasushi Okazaki1,2 (1.Div. of Trans. Res., Genomic Med., Saitama Univ., 2.Div. of Func. Genomics, Genomic Med., Saitama Univ., 3.Dept. of Genome Info., Osaka Univ. Grad. School of Med., 4.Dept. of Pediatrics, Saitama Med. Univ., 5.Dept. of Metabolism, Chiba Children's Hospital, Chiba)

The 39th Annual Meeting of the Molecular Biology Society of Japan

4066 results (3571 - 3580)