Zobrazeno 1 - 10
of 21
pro vyhledávání: '"Sachiho Kida"'
Autor:
Sachiho Kida, Yuri Koshimura, Eiji Yoden, Aya Yoshioka, Hideto Morimoto, Atsushi Imakiire, Noboru Tanaka, Satowa Tanaka, Ayaka Mori, Jun Ito, Asuka Inoue, Ryuji Yamamoto, Kohtaro Minami, Tohru Hirato, Kenichi Takahashi, Hiroyuki Sonoda
Publikováno v:
Molecular Therapy: Methods & Clinical Development, Vol 29, Iss , Pp 439-449 (2023)
Mucopolysaccharidosis I (MPS I), a lysosomal storage disease caused by dysfunction of α-L-iduronidase (IDUA), is characterized by the deposition of dermatan sulfate (DS) and heparan sulfate (HS) throughout the body, which causes several somatic and
Externí odkaz:
https://doaj.org/article/c4fd5548bc6941a2962304a79b9b0f89
Autor:
Asuka Inoue, Jun Ito, Sachiho Kida, Atsushi Imakiire, Kazuki Miyauchi, Yuri Koshimura, Shinji Kakimoto, Hideto Morimoto, Ryuji Yamamoto, Kohtaro Minami, Tohru Hirato, Hiroyuki Sonoda
Publikováno v:
Molecular Genetics and Metabolism. 138:107163
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e226238ef6f404379a1cece897a8a399
https://doi.org/10.1016/j.ymgme.2022.107163
https://doi.org/10.1016/j.ymgme.2022.107163
Autor:
Eiji Yoden, Takashi Onouchi, Saki Fujiyama, Sachiho Kida, Hidehiko Hashimoto, Wataru Machida, Noboru Tanaka, Hideto Morimoto, Tadao Shibasaki, Kohtaro Minami, Tohru Hirato, Hiroyuki Sonoda, Kenichi Takahashi
Publikováno v:
Molecular Genetics and Metabolism. 138:107364
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1188c3d2d80e5f41b234379c3ec59eb2
https://doi.org/10.1016/j.ymgme.2022.107364
https://doi.org/10.1016/j.ymgme.2022.107364
Autor:
Masafumi Kinoshita, Kohtaro Minami, Kenichi Takahashi, Tohru Hirato, Haruna Takagi, Sachiho Kida, Ryuji Yamamoto, Yuri Koshimura, Eiji Yoden, Hiroyuki Sonoda, Hideto Morimoto, Noboru Tanaka
Publikováno v:
Molecular therapy : the journal of the American Society of Gene Therapy. 29(5)
Mucopolysaccharidosis II (MPS II), a lysosomal storage disease caused by mutations in iduronate-2-sulfatase (IDS), is characterized by a wide variety of somatic and neurologic symptoms. The currently approved intravenous enzyme replacement therapy wi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::50c859c7c0c81ce55d1348dfde95254d
https://pubmed.ncbi.nlm.nih.gov/33508431
https://pubmed.ncbi.nlm.nih.gov/33508431
Autor:
Asuka Inoue, Satowa Tanaka, Sachiho Kida, Yuri Koshimura, Shinji Kakimoto, Atsushi Imakiire, Jun Ito, Kazuki Miyauchi, Hideto Morimoto, Kohtaro Minami, Tohru Hirato, Hiroyuki Sonoda
Publikováno v:
Molecular Genetics and Metabolism. 135:S60
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8dc77fe302402a4cc72535c97276915d
https://doi.org/10.1016/j.ymgme.2021.11.150
https://doi.org/10.1016/j.ymgme.2021.11.150
Publikováno v:
Molecular Genetics and Metabolism. 135:S85
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::62b6353575953e10a97aac6c202c2d45
https://doi.org/10.1016/j.ymgme.2021.11.220
https://doi.org/10.1016/j.ymgme.2021.11.220
Autor:
Hideto Morimoto, Kazuki Miyauchi, Atsushi Imakiire, Satowa Tanaka, Jun Ito, Kohtaro Minami, Shinji Kakimoto, Hiroyuki Sonoda, Sachiho Kida, Tohru Hirato, Yuri Koshimura
Publikováno v:
Molecular Genetics and Metabolism. 132:S105-S106
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::12111ad8b3ec69a33bd12e2d47d426eb
https://doi.org/10.1016/j.ymgme.2020.12.258
https://doi.org/10.1016/j.ymgme.2020.12.258
Autor:
Kenichi Takahashi, Kohtaro Minami, Ryuji Yamamoto, Hiroyuki Sonoda, Hideto Morimoto, Sachiho Kida, Masafumi Kinoshita, Haruna Takagi, Noboru Tanaka, Tohru Hirato, Yuri Koshimura, Eiji Yoden
Publikováno v:
Molecular Genetics and Metabolism. 132:S73
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bf109b6f1068358da6be3347b2458946
https://doi.org/10.1016/j.ymgme.2020.12.169
https://doi.org/10.1016/j.ymgme.2020.12.169
Autor:
Chikako Hashimoto, Shinji Takamatsu, Motoya Sato, Tomoaki Sobajima, Makoto Yamada, Yoshihiro Kamada, Akira Suzuki, Satoshi Yamaguchi, Akiko Yamamoto, Ken-ichi Hirano, Hironori Nagasaka, Hironobu Fujii, Yuichi Yoshida, Yusuke Ebisutani, Sachiho Kida, Eiji Miyoshi, Akihiro Kimura, Tetsuo Takehara, Shinichiro Shinzaki
Publikováno v:
American Journal of Physiology-Gastrointestinal and Liver Physiology. 311:G859-G868
Glycosylation is involved in various pathophysiological conditions. N-Acetylglucosaminyltransferase V (GnT-V), catalyzing β1–6 branching in asparagine-linked oligosaccharides, is one of the most important glycosyltransferases involved in cancer an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9d134ad0b0bef66fcd5fcdb05adbc7b2
https://doi.org/10.1152/ajpgi.00231.2016
https://doi.org/10.1152/ajpgi.00231.2016
Autor:
Tadao Shibasaki, Ryuji Yamamoto, Sachiho Kida, Masafumi Kinoshita, Hideto Morimoto, Noboru Tanaka, Katsuhiko Tachibana
Publikováno v:
Molecular genetics and metabolism. 125(1-2)
Mucopolysaccharidosis type II (MPS II or Hunter syndrome) is a lysosomal storage disorder caused by a deficiency of iduronate-2-sulfatase (IDS), an enzyme that catabolizes glycosaminoglycans (GAGs) including heparan sulfate (HS) and dermatan sulfate
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bc6df7c1bf73931b3f51cd0bcd14900b
https://pubmed.ncbi.nlm.nih.gov/30064964
https://pubmed.ncbi.nlm.nih.gov/30064964