Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Hiroya Imai"'
Autor:
Yoichi HARADA, Keiichi YAMASHITA, Taro YANAGAWA, Hiroya IMAI, Takuro EHARA, Masataka TORII, Masaki IKEGAMI, Mototaka HAYASHI, Eishi SATO, Toru HATAYAMA, Takuji KONO
Publikováno v:
Surgery for Cerebral Stroke. 50:266-273
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d17e87187ca83d7790998ac6668d512f
https://doi.org/10.2335/scs.50.266
https://doi.org/10.2335/scs.50.266
Autor:
Masaru Kiyomoto, Taro Yanagawa, Hiroya Imai, Eishi Sato, Masataka Torii, Masaki Tanaka, Takuro Ehara, Takuji Kono, Keiichi Yamashita, Toru Hatayama, Yoichi Harada
Publikováno v:
Clinical neurology and neurosurgery. 189
Objective Opening of mastoid air cells (MACs), a complication of lateral suboccipital craniotomy for microvascular decompression (MVD), might cause cerebrospinal fluid (CSF) leakage and meningitis. Only a few studies have investigated the association
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::29f0b56448695705cc9e2393727713c1
https://pubmed.ncbi.nlm.nih.gov/31809889
https://pubmed.ncbi.nlm.nih.gov/31809889
Autor:
Noriyoshi Masuoka, Hiroya Imai, Kohji Ishihara, Megumi Kitagawa, Nobuyoshi Nakajima, Hiroki Hamada, Kei Shimoda
Publikováno v:
Bioscience, Biotechnology, and Biochemistry. 76:1552-1554
Plant-cultured cells of Catharanthus roseus converted trans-resveratrol into its 3-O-β-D-glucopyranoside, 4'-O-β-D-glucopyranoside, 3-O-(6-O-β-D-xylopyranosyl)-β-D-glucopyranoside, and 3-O-(6-O-α-L-arabinopyranosyl)-β-D-glucopyranoside. The 3-O
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5f573b5ccc6609cd43299233acba30e1
https://doi.org/10.1271/bbb.120126
https://doi.org/10.1271/bbb.120126
Publikováno v:
Natural product communications. 8(1)
Two glucosyltransferase isozymes from Phytolacca americana, PaGT3 and PaGT2, catalyzed stereo- and regio-selective monoglucosylation of 3,5,3',4'-tetrahydroxy-trans-stilbene to yield 3,5,3',4'-tetrahydroxy-trans-stilbene-4'-O-beta-D-glucopyranoside.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c77a4a5757a4ccfed617b0c378fba10c
https://pubmed.ncbi.nlm.nih.gov/23472474
https://pubmed.ncbi.nlm.nih.gov/23472474
Publikováno v:
Natural product communications. 7(4)
Time course experiment revealed that cultured plant cells of Eucalyptus perriniana regioselectively glucosylated silybin to silybin-23-beta-D-glucoside in up to 70% yield.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d72f65009131692c81368bd88bfcfc17
https://pubmed.ncbi.nlm.nih.gov/22574460
https://pubmed.ncbi.nlm.nih.gov/22574460
Autor:
Takehiro Sato, Tomoya Iwakiri, Hiroya Imai, Hiroki Hamada, Shin-ichi Ozaki, Kei Shimoda, Toru Nakayama
Publikováno v:
Biotechnology Letters
A glucosyltransferase (GT) of Phytolacca americana (PaGT3) was expressed in Escherichia coli and purified for the synthesis of two O-β-glucoside products of trans-resveratrol. The reaction was moderately regioselective with a ratio of 4′-O-β-gluc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a99e28b2432466555496cbca3c7f660e
https://pubmed.ncbi.nlm.nih.gov/22048846
https://pubmed.ncbi.nlm.nih.gov/22048846
Autor:
Kei Shimoda, Yushi Uchimura, Hiroya Imai, Megumi Kitagawa, Hirotaka Hirano, Hatsuyuki Hamada, Hiroki Hamada
Publikováno v:
Biochemistry Insights, Vol 4 (2011)
Reduction and glycosylation of benzophenone, which is an endocrine disrupting chemical, were investigated using immobilized marine microalga and plant cells from the viewpoint of bioremediation of benzophenone. Immobilized marine microalga of Chrysoc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doajarticles::741d672b680667b50ec50d0644f84203
https://doaj.org/article/db8be6fb29624c22bb7b08b380500ff4
https://doaj.org/article/db8be6fb29624c22bb7b08b380500ff4
Publikováno v:
Natural Product Communications. 8:1934578X1300800
Two glucosyltransferase isozymes from Phytolacca americana, PaGT3 and PaGT2, catalyzed stereo- and regio-selective monoglucosylation of 3,5,3′,4′- tetrahydroxy-trans-stilbene to yield 3,5,3′,4′-tetrahydroxy-trans-stilbene-4′-O-β-D-glucopyr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3839b59cf8436d312a972552b5b0995a
https://doi.org/10.1177/1934578x1300800128
https://doi.org/10.1177/1934578x1300800128
Publikováno v:
Natural Product Communications. 7:1934578X1200700
Time course experiment revealed that cultured plant cells of Eucalyptus perriniana regioselectively glucosylated silybin to silybin-23-β-D-glucoside in up to 70% yield.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::972369899e4bfa73aa16ee05df04d24c
https://doi.org/10.1177/1934578x1200700429
https://doi.org/10.1177/1934578x1200700429
Autor:
Hiroya Imai, Yushi Uchimura, Hatsuyuki Hamada, Hiroki Hamada, Megumi Kitagawa, Kei Shimoda, Hirotaka Hirano
Publikováno v:
Biochemistry Insights, Vol 2011, Iss 4, Pp 35-40 (2011)
Reduction and glycosylation of benzophenone, which is an endocrine disrupting chemical, were investigated using immobilized marine microalga and plant cells from the viewpoint of bioremediation of benzophenone. Immobilized marine microalga of Chrysoc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::86891bcb06c565ef3633f884401448f5
https://doi.org/10.4137/bci.s8212
https://doi.org/10.4137/bci.s8212