[2AW-03-7] Depletion of ribosomal proteins and mRNA-specific translation control: studying the molecular pathogenesis of congenital anemia using zebrafish

^○Tamayo Uechi¹, Yukari Nakajima², Mariko Nagatomo², Maki Yoshihama², Yutaka Suzuki³, Naoya Kenmochi² (1.Facul. of Med., Univ. of Miyazaki, 2.Frontier Sci. Res. Ctr., Univ. of Miyazaki, 3.Grad. Sch. of Fron. Sci., Univ. of Tokyo)

The 45th Annual Meeting of the Molecular Biology Society of Japan |Thu. Dec 1, 2022 10:50 AM - 11:05 AM

[2AW-03-8] The decoding of ubiquitin-code for clearance of ribosome collision by RQT complex

^○Yoshitaka Matsuo, Toshifumi Inada (IMSUT)

The 45th Annual Meeting of the Molecular Biology Society of Japan |Thu. Dec 1, 2022 11:05 AM - 11:20 AM

[2AW-03-Discussion] Discussion

The 45th Annual Meeting of the Molecular Biology Society of Japan |Thu. Dec 1, 2022 11:20 AM - 11:29 AM

[2AW-03-Conclusion] Conclusion

^○Akio Yamashita (The University of Ryukyus)

The 45th Annual Meeting of the Molecular Biology Society of Japan |Thu. Dec 1, 2022 11:29 AM - 11:30 AM

[2PW-03-1] Japanese rare diseases models and mechanisms network (J-RDMM)

^○Ituro Inoue (National Institute of Genetics, Human Genetics Laboratory)

The 45th Annual Meeting of the Molecular Biology Society of Japan |Thu. Dec 1, 2022 4:15 PM - 4:20 PM

[2PW-03-2] Unrevealing the pathomechanism of human monogenic diseases

^○Noriko Miyake (Dept. of Hum. Genet., NCGMRI)

The 45th Annual Meeting of the Molecular Biology Society of Japan |Thu. Dec 1, 2022 4:20 PM - 4:40 PM

[2PW-03-8] From comprehensive genomic to functional analysis in human rare diseases: Genes to models

^○Tadashi Kaname (Dept Gen Med, Cntr Child Health Dev (NCCHD))

The 45th Annual Meeting of the Molecular Biology Society of Japan |Thu. Dec 1, 2022 4:40 PM - 5:00 PM

[2PW-03-3] Research on pathophysiological analysis of rare diseases using disease iPS cells

^○Megumu Saito (CiRA, Kyoto Univ.)

The 45th Annual Meeting of the Molecular Biology Society of Japan |Thu. Dec 1, 2022 5:00 PM - 5:20 PM

[2PW-03-4] Endothelin A receptor mutations cause rare human diseases by enhancing ligand binding capacity through allosteric effects

^○Yukiko Kurihara¹, Toru Ekimoto², Gordon Christopher³, Akiyasu Iwase¹, Yasunobu Uchijima¹, Ryo Sugiyama¹, Mitsunori Ikeguchi², Jeanne Amiel³, Hiroki Kurihara¹ (1.Dept. of Physiol. Chem. Metab., Grad. Sch. of Med., Univ. of Tokyo, 2.Dept. of Med. Life Sci., Grad. Sch. of Med. Life Sci., Yokohama City Univ., 3.INSERUM, Necker Hosp.)

The 45th Annual Meeting of the Molecular Biology Society of Japan |Thu. Dec 1, 2022 5:20 PM - 5:35 PM

[2PW-03-5] Mouse Pcdhgc4, of which loss-of-function causes neurodevelopmental disorder with microcephaly in human, regulates neuronal survival and positioning

^○Ryosuke Kaneko^1,2, Martijn Schonewille³, Takayuki Yoshida⁴, Ryuon Higuchi¹, Haruka Umezawa¹, Kouichi Hashimoto⁴, Nobuaki Tamamaki⁵, Yuchio Yanagaw², Takeshi Yagi¹ (1.Osaka Univ, FBS, 2.Gunma Univ, Grad Sch Med, 3.Erasmus MC, 4.Hiroshima Univ, Grad Sch Biomed Health Sci, 5.Kumamoto Univ, Grad Sch Life Sci)

The 45th Annual Meeting of the Molecular Biology Society of Japan |Thu. Dec 1, 2022 5:35 PM - 5:50 PM