Zobrazeno 1 - 10
of 62
pro vyhledávání: '"Tatsuya, Furuichi"'
Autor:
Soichiro Saito, Shuji Mizumoto, Tsukasa Yonekura, Rina Yamashita, Kenta Nakano, Tadashi Okubo, Shuhei Yamada, Tadashi Okamura, Tatsuya Furuichi
Publikováno v:
PLoS ONE, Vol 18, Iss 4, p e0284292 (2023)
SLC35A3 is considered an uridine diphosphate N-acetylglucosamine (UDP-GlcNAc) transporter in mammals and regulates the branching of N-glycans. A missense mutation in SLC35A3 causes complex vertebral malformation (CVM) in cattle. However, the biologic
Externí odkaz:
https://doaj.org/article/37f802978ebc4c5f9b1d7095a09c706e
Autor:
Kazuki Kodama, Hiroaki Takahashi, Nobuyasu Oiji, Kenta Nakano, Tadashi Okamura, Kimie Niimi, Eiki Takahashi, Long Guo, Shiro Ikegawa, Tatsuya Furuichi
Publikováno v:
FEBS Open Bio, Vol 10, Iss 6, Pp 1096-1103 (2020)
Desbuquois dysplasia (DD) type 1 is a rare skeletal dysplasia characterized by a short stature, round face, progressive scoliosis, and joint laxity. The causative gene has been identified as calcium‐activated nucleotidase 1 (CANT1), which encodes a
Externí odkaz:
https://doaj.org/article/fc5c8ae823b246b7aa3e657464d34bda
Publikováno v:
Japanese Journal of Veterinary Research; 2024, Vol. 72 Issue 1, p28-35, 8p
Autor:
Long Guo, Nobuyasu Oiji, Hiroaki Takahashi, Tadashi Okamura, Shiro Ikegawa, Tatsuya Furuichi, Kazuki Kodama, Kimie Niimi, Kenta Nakano, Eiki Takahashi
Publikováno v:
FEBS Open Bio, Vol 10, Iss 6, Pp 1096-1103 (2020)
FEBS Open Bio
FEBS Open Bio
Desbuquois dysplasia (DD) type 1 is a rare skeletal dysplasia characterized by a short stature, round face, progressive scoliosis, and joint laxity. The causative gene has been identified as calcium‐activated nucleotidase 1 (CANT1), which encodes a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::65638ae656713e15f4b1fe4a8937dd41
https://doaj.org/article/fc5c8ae823b246b7aa3e657464d34bda
https://doaj.org/article/fc5c8ae823b246b7aa3e657464d34bda
Autor:
Nobuyasu Oiji, Long Guo, Yuriko Sato, Manami Tsukamoto, Shiro Ikegawa, Tatsuya Furuichi, Kentaro Tomii, Masaki Saito, Ryutaro Fukumura, Yoichi Gondo, Yu Yamamori, Kazuhiro Yagami
Publikováno v:
Mammalian Genome. 30:329-338
Cysteine-rich transmembrane bone morphogenetic protein regulator 1 (CRIM1) is a type I transmembrane protein involved in the organogenesis of many tissues via its interactions with growth factors including BMP, TGF-β, and VEGF. In this study, we use
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c0da86d11bf11ffaa485a74fbbd39d99
https://doi.org/10.1007/s00335-019-09822-3
https://doi.org/10.1007/s00335-019-09822-3
Autor:
Carolina A Yoshida, Hisato Komori, Zenjiro Maruyama, Toshihiro Miyazaki, Keishi Kawasaki, Tatsuya Furuichi, Ryo Fukuyama, Masako Mori, Kei Yamana, Kouhei Nakamura, Wenguang Liu, Satoru Toyosawa, Takeshi Moriishi, Hiroshi Kawaguchi, Kenji Takada, Toshihisa Komori
Publikováno v:
PLoS ONE, Vol 7, Iss 3, p e32364 (2012)
RUNX2 and SP7 are essential transcription factors for osteoblast differentiation at an early stage. Although RUNX2 inhibits osteoblast differentiation at a late stage, the function of SP7 at the late stage of osteoblast differentiation is not fully e
Externí odkaz:
https://doaj.org/article/e639d011c37e43edae07c19f4d69c22e
Autor:
Takeshi Moriishi, Zenjiro Maruyama, Ryo Fukuyama, Masako Ito, Toshihiro Miyazaki, Hideki Kitaura, Hidetake Ohnishi, Tatsuya Furuichi, Yosuke Kawai, Ritsuko Masuyama, Hisato Komori, Kenji Takada, Hiroshi Kawaguchi, Toshihisa Komori
Publikováno v:
PLoS ONE, Vol 6, Iss 11, p e27487 (2011)
Bcl2 subfamily proteins, including Bcl2 and Bcl-X(L), inhibit apoptosis. As osteoblast apoptosis is in part responsible for osteoporosis in sex steroid deficiency, glucocorticoid excess, and aging, bone loss might be inhibited by the upregulation of
Externí odkaz:
https://doaj.org/article/2a5a87095d354acfbb744dbee1880200
Autor:
Masahiro Nakajima, Atsushi Takahashi, Ikuyo Kou, Cristina Rodriguez-Fontenla, Juan J Gomez-Reino, Tatsuya Furuichi, Jin Dai, Akihiro Sudo, Atsumasa Uchida, Naoshi Fukui, Michiaki Kubo, Naoyuki Kamatani, Tatsuhiko Tsunoda, Konstantinos N Malizos, Aspasia Tsezou, Antonio Gonzalez, Yusuke Nakamura, Shiro Ikegawa
Publikováno v:
PLoS ONE, Vol 5, Iss 3, p e9723 (2010)
Osteoarthritis (OA) is a common disease that has a definite genetic component. Only a few OA susceptibility genes that have definite functional evidence and replication of association have been reported, however. Through a genome-wide association stu
Externí odkaz:
https://doaj.org/article/5809b0301a1448538a3bc0858415925e
Autor:
Toshiyuki Fukada, Natacha Civic, Tatsuya Furuichi, Shinji Shimoda, Kenji Mishima, Hiroyuki Higashiyama, Yayoi Idaira, Yoshinobu Asada, Hiroshi Kitamura, Satoru Yamasaki, Shintaro Hojyo, Manabu Nakayama, Osamu Ohara, Haruhiko Koseki, Heloisa G Dos Santos, Luisa Bonafe, Russia Ha-Vinh, Andreas Zankl, Sheila Unger, Marius E Kraenzlin, Jacques S Beckmann, Ichiro Saito, Carlo Rivolta, Shiro Ikegawa, Andrea Superti-Furga, Toshio Hirano
Publikováno v:
PLoS ONE, Vol 3, Iss 11, p e3642 (2008)
BackgroundZinc (Zn) is an essential trace element and it is abundant in connective tissues, however biological roles of Zn and its transporters in those tissues and cells remain unknown.Methodology/principal findingsHere we report that mice deficient
Externí odkaz:
https://doaj.org/article/11b68611f81346d0b0d970e52409dbcd
Autor:
Toshiyuki Fukada, Natacha Civic, Tatsuya Furuichi, Shinji Shimoda, Kenji Mishima, Hiroyuki Higashiyama, Yayoi Idaira, Yoshinobu Asada, Hiroshi Kitamura, Satoru Yamasaki, Shintaro Hojyo, Manabu Nakayama, Osamu Ohara, Haruhiko Koseki, Heloisa G. dos Santos, Luisa Bonafe, Russia Ha-Vinh, Andreas Zankl, Sheila Unger, Marius E. Kraenzlin, Jacques S. Beckmann, Ichiro Saito, Carlo Rivolta, Shiro Ikegawa, Andrea Superti-Furga, Toshio Hirano
Publikováno v:
PLoS ONE, Vol 3, Iss 11 (2008)
Externí odkaz:
https://doaj.org/article/0ff28593c41b4b8bac48ae81f46cd1c3