Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Asuka Hamamoto"'
Autor:
Asuka Hamamoto, Natsuki Kita, Siddabasave Gowda B. Gowda, Hiroyuki Takatsu, Kazuhisa Nakayama, Makoto Arita, Shu-Ping Hui, Hye-Won Shin
Publikováno v:
Cell Structure and Function, Vol 49, Iss 1, Pp 1-10 (2023)
Gaucher disease (GD) is a recessively inherited lysosomal storage disorder characterized by a deficiency of lysosomal glucocerebrosidase (GBA1). This deficiency results in the accumulation of its substrate, glucosylceramide (GlcCer), within lysosomes
Externí odkaz:
https://doaj.org/article/dac1dd9dc36f40f89f54c83bb79bee6d
Autor:
Natsuki Kita, Asuka Hamamoto, Siddabasave Gowda B. Gowda, Hiroyuki Takatsu, Kazuhisa Nakayama, Makoto Arita, Shu-Ping Hui, Hye-Won Shin
Publikováno v:
Journal of Lipid Research, Vol 65, Iss 3, Pp 100508- (2024)
Lipid transport is an essential cellular process with importance to human health, disease development, and therapeutic strategies. Type IV P-type ATPases (P4-ATPases) have been identified as membrane lipid flippases by utilizing nitrobenzoxadiazole (
Externí odkaz:
https://doaj.org/article/b37a55b4e42d4457a8be6c49887a8ab6
Autor:
Shinji TAMURA, Asuka HAMAMOTO
Publikováno v:
Nihon Kikai Gakkai ronbunshu, Vol 81, Iss 824, Pp 14-00568-14-00568 (2015)
Frahm damper is the dynamic absorber without damping. This damper suppresses vibration in some range of excitation frequency using anti-resonance point of frequency response function. In this study, two DOF Frahm damper attached to two DOF system is
Externí odkaz:
https://doaj.org/article/385c4116cda9407e8ab0390b787b1ec0
Autor:
Yumeka Muranaka, Ryo Shigetomi, Yugo Iwasaki, Asuka Hamamoto, Kazuhisa Nakayama, Hiroyuki Takatsu, Hye-Won Shin
Publikováno v:
Biochemical Journal; 9/15/2024, Vol. 481 Issue 18, p1187-1202, 16p
Autor:
Asuka Hamamoto, Natsuki Kita, Gowda, Siddabasave Gowda B., Hiroyuki Takatsu, Kazuhisa Nakayama, Makoto Arita, Shu-Ping Hui, Hye-Won Shin
Publikováno v:
Cell Structure & Function; 2024, Vol. 49 Issue 1, p1-10, 10p
Autor:
Hiroki Inoue, Hye-Won Shin, Yumeka Muranaka, Masahiro Takayama, Tsukasa Yagi, Riki Nakabuchi, Hiroyuki Takatsu, Asuka Hamamoto, Kazuhisa Nakayama
Publikováno v:
Journal of Cell Science. 134(20)
ATP11C, a member of the P4-ATPase family, translocates phosphatidylserine and phosphatidylethanolamine at the plasma membrane. We previously revealed that its C-terminal splice variant ATP11C-b exhibits polarized localization in motile cell lines, su
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8d0f69da1ac710eff85f7d9fcc541e77
http://hdl.handle.net/2433/266563
http://hdl.handle.net/2433/266563
Autor:
Masahiro, Takayama, Hiroyuki, Takatsu, Asuka, Hamamoto, Hiroki, Inoue, Tomoki, Naito, Kazuhisa, Nakayama, Hye-Won, Shin
Publikováno v:
Journal of cell science. 132(17)
ATP11C, a member of the P4-ATPase family, is a major phosphatidylserine (PS)-flippase located at the plasma membrane. ATP11C deficiency causes a defect in B-cell maturation, anemia and hyperbilirubinemia. Although there are several alternatively spli
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e24f957459bf37bd5e1a0c2de7eff64c
https://pubmed.ncbi.nlm.nih.gov/31371488
https://pubmed.ncbi.nlm.nih.gov/31371488
Autor:
Masahiro Takayama, Hiroki Inoue, Hye-Won Shin, Asuka Hamamoto, Hiroyuki Takatsu, Tomoki Naito, Kazuhisa Nakayama
Publikováno v:
Journal of Cell Science.
ATP11C, a member of the P4-ATPase family, is a major phosphatidylserine (PS)-flippase located at the plasma membrane. ATP11C deficiency causes a defect in B-cell maturation, anemia, and hyperbilirubinemia. Although there are several alternatively spl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6c7af119bc4f2377d18f9fe7c4fad249
https://doi.org/10.1242/jcs.231720
https://doi.org/10.1242/jcs.231720
Autor:
Asuka Hamamoto, Shinji Tamura
Publikováno v:
Transactions of the JSME (in Japanese). 81:14-00568
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a25e1a548d6657dd8fc5e21b7690684b
https://doi.org/10.1299/transjsme.14-00568
https://doi.org/10.1299/transjsme.14-00568