American journal of physiology. Cell physiology 321(3) C596-C606 2021年9月 [査読有り]
Ceiling culture-derived preadipocytes (ccdPAs) and adipose-derived stem cells (ASCs) can be harvested from human subcutaneous fat tissue using the specific gravity method. Both cell types possess a similar spindle shape without lipid droplets. We ...
Hayato Tada Akihiro Nomura Masatsune Ogura Katsunori Ikewaki Yasushi Ishigaki Kyoko Inagaki Kazuhisa Tsukamoto Kazushige Dobashi Kimitoshi Nakamura Mika Hori Kota Matsuki Shizuya Yamashita Shinji Yokoyama Masa Aki Kawashiri Mariko Harada-Shiba Mariko Harada-Shiba Shun Ishibashi Shinji Yokoyama Hitoshi Shimano Koutaro Yokote Hideaki Bujo Shizuya Yamashita Kazuhisa Tsukamoto Toshio Hayashi Katsunori Ikewaki Takanari Gotoda Kazushige Dobashi Yoshihiro Miyamoto Misa Takegami Yoshiki Sekijima Yasushi Ishigaki Hiroaki Okazaki Atsushi Nohara Shingo Koyama Kyoko Inagaki Koh Ono Masahiro Koseki Hiroyuki Daida Manabu Takahashi Kimitoshi Nakamura Takashi Miida Masa Aki Kawashiri Tetsuo Minamino Sachiko Okazaki Jun Wada Masatsune Ogura Hirotoshi Ohmura Mika Hori Kota Matsuki Masashi Yamamoto Yasuo Takeuchi Atsuko Nakatsuka Daisaku Masuda Satoshi Hirayama Masayuki Kuroda Takashi Yamaguchi Takeyoshi Murano Hayato Tada
Journal of Atherosclerosis and Thrombosis 28(8) 791-801 2021年 [査読有り]
Sitosterolemia is an inherited metabolic disorder characterized by increased levels of plant sterols, such as sitosterol. This disease is caused by loss-of-function genetic mutations in ATP-binding cassette (ABC) subfamily G member 5 or member 8 (...
Journal of Atherosclerosis and Thrombosis 28(9) 883-904 2021年 [査読有り]
Primary chylomicronemia (PCM) is a rare and intractable disease characterized by marked accumulation of chylomicrons in plasma. The levels of plasma triglycerides (TGs) typically range from 1,000 - 15,000 mg/dL or higher. PCM is caused by defects ...
Journal of Atherosclerosis and Thrombosis 28(9) 905-925 2021年 [査読有り]
Cerebrotendinous xanthomatosis (CTX) is an autosomal recessive lipid storage disorder caused by mutations in the CYP27A1 gene, which encodes the mitochondrial enzyme sterol 27-hydroxylase. Decreased sterol 27-hydroxylase activity results in impair...
Kuroda M Aso M Yamamoto TT Wada J Ishikawa K Maezawa Y Teramoto N Kubota Y Tawada A Aoyagi Y Asada S Kirinashizawa M Onitake A Matsuura Y Yasunaga K Konno S Nishino K Yamamoto M Miyoshi J Kobayashi N Tanio M Ikeuchi T Igari H Mitsukawa N Hanaoka H Saito Y Yokote K
Aso M Yamamoto TT Kuroda M Wada J Kubota Y Ishikawa K Maezawa Y Teramoto N Tawada A Asada S Aoyagi Y Kirinashizawa M Onitake A Matsuura Y Yasunaga K Konno S Nishino K Yamamoto M Miyoshi J Kobayashi N Tanio M Ikeuchi T Igari H Mitsukawa N Hanaoka H Yokote K Saito Y
The American Society of Gene & Cell Therapy (ASGCT), 26th Annual Meeting 2023年5月
大学院国際学術研究院