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pro vyhledávání: '"Chikako Tasaki"'
Autor:
Hitoshi Sakuraba, Youichi Tajima, Chikako Tasaki, Keisuke Kitakaze, Daisuke Tsuji, Takatsugu Hirokawa, Kohji Itoh
Publikováno v:
Biochemistry and Biophysics Reports
GM2 gangliosidoses are autosomal recessive lysosomal storage diseases (LSDs) caused by mutations in the HEXA, HEXB and GM2A genes, which encode the human lysosomal β-hexosaminidase (Hex) α- and β-subunits, and GM2 activator protein (GM2A), respect
Autor:
Daisuke Asanuma, Eiji Sugiyama, Hitoshi Sakuraba, Kohei Sato, Daisuke Tsuji, Kohji Itoh, Keisuke Kitakaze, Nobuo Maita, Mako Kamiya, Mitsutoshi Setou, Tadayasu Togawa, Akira Otaka, Takatsugu Hirokawa, Yasuteru Urano, Chikako Tasaki, Yasumichi Mizutani
Publikováno v:
Journal of Clinical Investigation. 126:1691-1703
GM2 gangliosidoses, including Tay-Sachs and Sandhoff diseases, are neurodegenerative lysosomal storage diseases that are caused by deficiency of β-hexosaminidase A, which comprises an αβ heterodimer. There are no effective treatments for these dis
Autor:
Chikako Tasaki, Yasumichi Mizutani, Yasuteru Urano, Eiji Sugiyama, Mako Kamiya, Mitsutoshi Setou, Kohji Itoh, Mariko Ikuo, Keisuke Kitakaze
Publikováno v:
Molecular Genetics and Metabolism. 114:S65
Publikováno v:
Bulletin of the Chemical Society of Japan. 56:1305-1307
The effect of α-cyclodextrin (α-CD) on the electroreduction of benzaldehyde was investigated. The reduction in aqueous system produces benzyl alcohol and 1,2-diphenyl-1,2-ethanediol (hydrobenzoin, dimerization product). The addition of α-CD caused
Akademický článek
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Autor:
Keisuke Kitakaze1, Yasumichi Mizutani1, Eiji Sugiyama2, Chikako Tasaki1, Daisuke Tsuji1, Nobuo Maita3, Takatsugu Hirokawa4, Daisuke Asanuma5, Mako Kamiya6, Kohei Sato7, Mitsutoshi Setou2,8,9,10, Yasuteru Urano5,6, Tadayasu Togawa11, Akira Otaka7, Hitoshi Sakuraba12, Kohji Itoh1 kitoh@tokushima-u.ac.jp
Publikováno v:
Journal of Clinical Investigation. May2016, Vol. 126 Issue 5, p1691-1703. 13p. 1 Diagram, 1 Chart, 4 Graphs.