Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Yuriko Teranishi"'
Autor:
Ryoko Sasaki, Mary Ann Suico, Keisuke Chosa, Yuriko Teranishi, Takashi Sato, Asuka Kagami, Shunsuke Kotani, Hikaru Kato, Yuki Hitora, Sachiko Tsukamoto, Tomohiro Yamashita, Takeshi Yokoyama, Mineyuki Mizuguchi, Hirofumi Kai, Tsuyoshi Shuto
Publikováno v:
Journal of Pharmacological Sciences, Vol 151, Iss 1, Pp 54-62 (2023)
Hereditary ATTR amyloidosis is caused by the point mutation in serum protein transthyretin (TTR) that destabilizes its tetrameric structure to dissociate into monomer. The monomers form amyloid fibrils, which are deposited in peripheral nerves and or
Externí odkaz:
https://doaj.org/article/73aa628980de4100b6bdb344612c5194
Autor:
Takeshi Yokoyama, Shun Takaki, Keisuke Chosa, Takashi Sato, Mary Ann Suico, Yuriko Teranishi, Tsuyoshi Shuto, Mineyuki Mizuguchi, Hirofumi Kai
Publikováno v:
Journal of Pharmacological Sciences, Vol 129, Iss 4, Pp 240-243 (2015)
Familial amyloid polyneuropathy (FAP) is a genetic, adult-onset, neurodegenerative disorder caused by amyloid formation of transthyretin (TTR), a thyroxine-binding protein. Mutation in TTR causes a propensity of TTR tetramer to dissociate to monomer,
Externí odkaz:
https://doaj.org/article/4cbd743c7ee9416aab2b4f630f72e43b
Autor:
Ryoko Sasaki, Mary Ann Suico, Keisuke Chosa, Yuriko Teranishi, Takashi Sato, Asuka Kagami, Shunsuke Kotani, Hikaru Kato, Yuki Hitora, Sachiko Tsukamoto, Tomohiro Yamashita, Takeshi Yokoyama, Mineyuki Mizuguchi, Hirofumi Kai, Tsuyoshi Shuto
Publikováno v:
Journal of pharmacological sciences. 151(1)
Hereditary ATTR amyloidosis is caused by the point mutation in serum protein transthyretin (TTR) that destabilizes its tetrameric structure to dissociate into monomer. The monomers form amyloid fibrils, which are deposited in peripheral nerves and or
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2a22ebf61bf53e9c8f9f7fc0b14a2296
https://pubmed.ncbi.nlm.nih.gov/36522123
https://pubmed.ncbi.nlm.nih.gov/36522123
Autor:
Mary Ann Suico, Keisuke Chosa, Tsuyoshi Shuto, Yuriko Wakita, Nami Hashimoto, Shingo Kawano, Hiroshi Morioka, Ryoko Sasaki, Yoshiki Imai, Yuriko Teranishi, Hirofumi Kai, Takashi Sato
Publikováno v:
Biological and Pharmaceutical Bulletin. 41:628-636
Transthyretin (TTR) is a tetrameric beta-sheet-rich protein that is important in the plasma transport of thyroxine and retinol. Mutations in the TTR gene cause TTR tetramer protein to dissociate to monomer, which is the rate-limiting step in familial
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fb70d5e2a98cff7b0c3e9f5c65c6aadc
https://doi.org/10.1248/bpb.b17-01021
https://doi.org/10.1248/bpb.b17-01021
Autor:
Takashi Sato, Takeshi Yokoyama, Keisuke Chosa, Tsuyoshi Shuto, Hirofumi Kai, Mineyuki Mizuguchi, Yuriko Teranishi, Mary Ann Suico, Shun Takaki
Publikováno v:
Journal of Pharmacological Sciences, Vol 129, Iss 4, Pp 240-243 (2015)
Familial amyloid polyneuropathy (FAP) is a genetic, adult-onset, neurodegenerative disorder caused by amyloid formation of transthyretin (TTR), a thyroxine-binding protein. Mutation in TTR causes a propensity of TTR tetramer to dissociate to monomer,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d930ab10d6c74c39d09eeef55566f0f6
https://doi.org/10.1016/j.jphs.2015.09.006
https://doi.org/10.1016/j.jphs.2015.09.006