Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Eiji Yoden"'
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:
Ryuji Yamamoto, Eiji Yoden, Noboru Tanaka, Masafumi Kinoshita, Atsushi Imakiire, Tohru Hirato, Kohtaro Minami
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 27, Iss , Pp 100758- (2021)
Pabinafusp alfa is a fusion protein comprising a humanized anti-human transferrin receptor (TfR) antibody and human iduronate-2-sulfatase. It was developed as a novel modality to target central nervous system-related symptoms observed in patients wit
Externí odkaz:
https://doaj.org/article/5e52b45ea09645e9b710b6de626d81d7
Autor:
Atsushi Imakiire, Yasunori Sugano, Tadao Shibasaki, Eiji Yoden, Kazuki Miyauchi, Ryuji Yamamoto, Hideto Morimoto, Kohtaro Minami, Tohru Hirato, Hiroyuki Sonoda, Kenichi Takahashi
Publikováno v:
Molecular Genetics and Metabolism. 138:107162
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9dc7856692f3a871412c02ae5dc731de
https://doi.org/10.1016/j.ymgme.2022.107162
https://doi.org/10.1016/j.ymgme.2022.107162
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:
Tohru Hirato, Kohtaro Minami, Masafumi Kinoshita, Eiji Yoden, Atsushi Imakiire, Ryuji Yamamoto, Noboru Tanaka
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 27, Iss, Pp 100758-(2021)
Molecular Genetics and Metabolism Reports
Molecular Genetics and Metabolism Reports
Pabinafusp alfa is a fusion protein comprising a humanized anti-human transferrin receptor (TfR) antibody and human iduronate-2-sulfatase. It was developed as a novel modality to target central nervous system-related symptoms observed in patients wit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f0bad9d33274408b77250340e21baeff
http://www.sciencedirect.com/science/article/pii/S2214426921000525
http://www.sciencedirect.com/science/article/pii/S2214426921000525
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:
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:
Tohru Hirato, Eiji Yoden, Noboru Tanaka, Yae Ito, Yoshikazu Komurasaki, Hideto Morimoto, Masato Horie, Kazutoshi Mihara, Kohtaro Minami, Ryuji Yamamoto
Publikováno v:
Molecular genetics and metabolism. 125(1-2)
Fabry disease (FD) is an X-linked lysosomal storage disease. It is caused by deficiency of the enzyme α-galactosidase A (α-Gal A), which leads to excessive deposition of neutral glycosphingolipids, especially globotriaosylceramide (GL-3), in cells
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0947baf2939568811cca60189ed08776
https://pubmed.ncbi.nlm.nih.gov/30054149
https://pubmed.ncbi.nlm.nih.gov/30054149
Autor:
Kenichi Takahashi, Hideto Morimoto, Tohru Hirato, Masafumi Kinoshita, Ryuji Yamamoto, Haruna Takagi, Kohtaro Minami, Hiroyuki Sonoda, Katsuhiko Tachibana, Galina Golovina, Yuri Koshimura, Eiji Yoden
Publikováno v:
Molecular Genetics and Metabolism. 123:S134
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7db7be2bc0f353f2b6cc33c089eae753
https://doi.org/10.1016/j.ymgme.2017.12.368
https://doi.org/10.1016/j.ymgme.2017.12.368
Publikováno v:
Molecular Genetics and Metabolism. 114:S64
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b0342a25e085354796eab19a15412089
https://doi.org/10.1016/j.ymgme.2014.12.135
https://doi.org/10.1016/j.ymgme.2014.12.135