The Molecular Biology Society of Japan

4066 results (4001 - 4010)

[3LBA-072] Deficiency of Ski3 gene impairs mitochondrial function and lipid metabolism

〇Kohei Ohnuma1, Yoshihito Kishita2, Hiromi Nyuzuki2, Yukiko Sato-Miyata1, Masakazu Kohda2, Kei Murayama3, Satomi Takeo1, Yasushi Okazaki2, Toshiro Aigaki1 (1.Dept. of Biol. Sci., Grad. Sch. of Sci., Tokyo Metropolitan University, 2.Res. Center for Gen. Med., Saitama Medical University, 3.Dept. of Met., Chiba Children's Hospital)

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

[3LBA-074] Reverse Cholesterol Transport regulated by micro RNA-33

〇Ritsuko Hanada1, Tomohiro Nishino2, Takahiro Horie2, Yasuhide Kuwabara2, Hitoo Nishi2, Tetsushi Nakao2, Masataka Nishiga2, Fumiko Nakazeki2, Yuuya Ide2, Satoshi Koyama2, Masahiro Kimura2, Randolph Ruiz Rodriguez2, Naoya Sowa2, Takeshi Kimura2 (1.Dept. of Med. Sci., Grad. Sch. of Med. Univ. of Kyoto, 2.Dept. of Med. Sci., Grad. Sch. of Med. Univ. of Kyoto)

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

[3LBA-078] Genetic effetcs of FUS/TLS heterozygous deletion on polyglutamine disease model mice

〇Yoshihiro Kino1,2,3,4, Chila Washizu3, Masaru Kurosawa2,3,4, Mizuki Yamada3, Hiroshi Doi6, Toru Yakumi5, Hiroaki Adachi7, Masahisa Katsuno7, Gen Sobue7, Geoffrey G. Hichs8, Nobutaka Hattori2, Tomomi Shimogori4, Nobuyuki Nukina2,3,9 (1.Dept. of Bioinfo and Mol. Neuropathol., Meiji Pharm. Univ., 2.Dept. of NeuroSci. for Neurodegen. Dis., Juntendo Univ Grad. Sch. of Med., 3.Lab. for Struct. Neuropathol., BSI, RIKEN, 4.Lab. for Mol. Mech. of Thalamus Dev.,BSI, RIKEN, 5.Lab. for Mental Biol., BSI, RIKEN, 6.Dept. of Clin. Neurol. and Stroke Med., Grad. Sch. of Med., Yokohama City Univ., 7.Dept. of Neurol., Nagoya Univ. Grad. sch. of Med., 8.Manitoba Ins. of Cell Biol., Univ. of Manitoba, 9.Lab. for Structural Neuropathol., Doshisha Univ. Grad. Sch. of Brain Sci.)

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

[3LBA-079] Male-dominant long haired phenotype of Syrian hamster is caused by 1-bp deletion of Fgf5, and its verification of species specific gender difference

〇Gou Takahashi1, Yasuhiro Yoshizawa2,3, Kiko Takahashi4, Gaku Simoi1,4, Yuichi Kameyama1,4, Ryoichi Hashizume1,4, Kenta Wada1,4 (1.Grad. Sch. of Bioindustry., Tokyo Univ. of Agri., 2.Grad. Sch. of Med., Chiba Univ., 3.Chiba Cancer Center Research Institute., 4.Fac. of Bioindustry., Tokyo Univ. of Agri.)

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

4066 results (4001 - 4010)