[3P-0791] Disruption of synaptic structure induced by ALS causing gene TDP-43 in Drosophila visual system

〇Kento Ohmae¹, Fumio Takahashi¹, Emiko Suzuki², Satoko Hakeda(Suzuki)¹, Takashi Suzuki¹ (1.Grad. Sch. of Life Sci. and Tec., Tokyo Tech, 2.Natl. Inst. of Genetics and Dept. of Genetics)

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

[3P-0792] Selected mRNA translation and ribosomopathies: Studying the molecular pathogenesis of congenital anemia using zebrafish

〇Tamayo Uechi¹, Yukari Nakajima¹, Maki Yoshihama¹, Yutaka Suzuki², Sumio Sugano², Naoya Kenmochi¹ (1.Frontier Sci. Res. Ctr, Univ. of Miyazaki, 2.Grad. Sch. of Frontier Sci., Univ. of Tokyo)

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

[3P-0793] Telomere shortening and progeria-related pathologies in WRN/TERT double-knockout mice

〇Shuichi Shibuya^1,2, Kinue Iizuka¹, Koutaro Yokote¹, Takahiko Shimizu¹ (1.Chiba Univ. Grad. Sch. of Med., 2.JSPS Research Fellow DC1)

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

[3P-0794] EIF2B5^toy: 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-0796] PTEN knockout medaka: analysis of the mutated phenotype detected in embryos and its application as a disease model

〇Yuriko Matsuzaki¹, Tetsushi Sakuma², Takashi Yamamoto², Hideyuki Saya¹ (1.Div. of Gene Reg., IAMR, Keio Univ., Sch. Med., 2.Dept.of Math. and Life Sci., Grad. Sch. of Sci.,Hiroshima Univ.)

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

[3P-0797] An establishment of humanized GH model mice for dominantly inherited growth hormone deficiency using gene exchangeable system

〇Emika Kubo¹, Daisuke Ariyasu¹, Kimi Araki¹ (1.Dept. of Dev. Genet., Res. Dev. and Analy., Univ. of Kumamoto)

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

[3P-0798] in vivo analysis using humanized GH model mice for dominanly inherited growth hormone deficiency

〇Daisuke Ariyasu¹, Emika Kubo¹, Shinsuke Shibata², Kimi Araki¹ (1.Dept. of Dev. Genet., Res. Dev. and Analy., Univ. of Kumamoto, 2.Elect. Microsc. Lab, Univ. of Keio)

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 Okazaki^1,2 (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