Zobrazeno 1 - 10
of 34
pro vyhledávání: '"Hideto Morimoto"'
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:
Hideto Morimoto, Hiroki Morioka, Atsushi Imakiire, Ryuji Yamamoto, Tohru Hirato, Hiroyuki Sonoda, Kohtaro Minami
Publikováno v:
Molecular Therapy: Methods & Clinical Development, Vol 25, Iss , Pp 534-544 (2022)
Deposition of heparan sulfate (HS) in the brain of patients with mucopolysaccharidosis II (MPS II) is believed to be the leading cause of neurodegeneration, resulting in several neurological signs and symptoms, including neurocognitive impairment. We
Externí odkaz:
https://doaj.org/article/4eedbba9a32d4c1babcaa2d7cd77f6c7
Autor:
Kohtaro Minami, Hideto Morimoto, Hiroki Morioka, Atsushi Imakiire, Masafumi Kinoshita, Ryuji Yamamoto, Tohru Hirato, Hiroyuki Sonoda
Publikováno v:
International journal of molecular sciences. 23(19)
Heparan sulfate (HS) is an essential glycosaminoglycan (GAG) as a component of proteoglycans, which are present on the cell surface and in the extracellular matrix. HS-containing proteoglycans not only function as structural constituents of the basal
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
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
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
Autor:
Hideto Morimoto, Hiroki Morioka, Atsushi Imakiire, Ryuji Yamamoto, Tohru Hirato, Hiroyuki Sonoda, Kohtaro Minami
Publikováno v:
Molecular Genetics and Metabolism. 138:107230
Autor:
Norio Sakai, Yuji Sato, Hiroyuki Sonoda, Mathias Schmidt, Kazunori Tanizawa, Mariko Yamaoka, Sairei So, Ana Maria Martins, Hideto Morimoto, Toshiaki Ikeda, Yoshikatsu Eto, Tatsuyoshi Yamamoto, Torayuki Okuyama, Kohtaro Minami, Roberto Giugliani, Kimitoshi Nakamura
Publikováno v:
International Journal of Molecular Sciences, Vol 22, Iss 10938, p 10938 (2021)
International Journal of Molecular Sciences
Volume 22
Issue 20
International Journal of Molecular Sciences
Volume 22
Issue 20
Enzyme replacement therapy (ERT) improves somatic manifestations in mucopolysaccharidoses (MPS). However, because intravenously administered enzymes cannot cross the blood–brain barrier (BBB), ERT is ineffective against the progressive neurodegener
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
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