Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Toshiki Tanase"'
Autor:
Yuko Nitahara-Kasahara, Shuji Mizumoto, Yukiko U. Inoue, Shota Saka, Guillermo Posadas-Herrera, Aki Nakamura-Takahashi, Yuki Takahashi, Ayana Hashimoto, Kohei Konishi, Shinji Miyata, Chiaki Masuda, Emi Matsumoto, Yasunobu Maruoka, Takahiro Yoshizawa, Toshiki Tanase, Takayoshi Inoue, Shuhei Yamada, Yoshihiro Nomura, Shin'ichi Takeda, Atsushi Watanabe, Tomoki Kosho, Takashi Okada
Publikováno v:
Disease Models & Mechanisms, Vol 14, Iss 12 (2021)
Musculocontractural Ehlers-Danlos syndrome (mcEDS) is caused by generalized depletion of dermatan sulfate (DS) due to biallelic pathogenic variants in CHST14 encoding dermatan 4-O-sulfotransferase 1 (D4ST1) (mcEDS-CHST14). Here, we generated mouse mo
Externí odkaz:
https://doaj.org/article/18ac308ec99e4737bca148fc2a47dc8c
Autor:
Chiaki Masuda, Yuki Takahashi, Atsushi Watanabe, Shota Saka, Yukiko U. Inoue, Shuji Mizumoto, Takashi Okada, Kohei Konishi, Toshiki Tanase, Shinji Miyata, Aki Nakamura-Takahashi, Yuko Nitahara-Kasahara, Takahiro Yoshizawa, Shuhei Yamada, Takayoshi Inoue, Yasunobu Maruoka, Guillermo Posadas-Herrera, Emi Matsumoto, Tomoki Kosho, Yoshihiro Nomura, Takeda Shin'ichi, Ayana Hashimoto
Publikováno v:
Disease Models & Mechanisms
article-version (VoR) Version of Record
Disease Models & Mechanisms, Vol 14, Iss 12 (2021)
article-version (VoR) Version of Record
Disease Models & Mechanisms, Vol 14, Iss 12 (2021)
Musculocontractural Ehlers-Danlos syndrome (mcEDS) is caused by generalized depletion of dermatan sulfate (DS) due to biallelic pathogenic variants in CHST14 encoding dermatan 4-O-sulfotransferase 1 (D4ST1) (mcEDS-CHST14). Here, we generated mouse mo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cfdc92750701ccb78a4d66397db77c83
https://doi.org/10.1242/dmm.048963
https://doi.org/10.1242/dmm.048963
Autor:
Takashi Okada, Satoru Matsunaga, Aki Nakamura-Takahashi, Yuko Nitahara-Kasahara, Akira Yamaguchi, Seikou Shintani, Watanabe Atsushi, Masataka Kasahara, Toshiki Tanase, Shinichi Abe, Yukihiko Hirai
Publikováno v:
Calcified tissue international.
Hypophosphatasia (HPP) is a systemic skeletal disease caused by mutations in the gene encoding tissue-nonspecific alkaline phosphatase (TNALP). We recently reported that survival of HPP model mice can be prolonged using an adeno-associated virus (AAV
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2db7f758c7b88c3bd69b7ff1636cd283
http://hdl.handle.net/10130/5101
http://hdl.handle.net/10130/5101