Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Nobuyasu Oiji"'
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
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
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
Autor:
Tatsuya, Furuichi, Manami, Tsukamoto, Masaki, Saito, Yuriko, Sato, Nobuyasu, Oiji, Kazuhiro, Yagami, Ryutaro, Fukumura, Yoichi, Gondo, Long, Guo, Shiro, Ikegawa, Yu, Yamamori, Kentaro, Tomii
Publikováno v:
Mammalian genome : official journal of the International Mammalian Genome Society. 30(11-12)
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