Zobrazeno 1 - 10
of 77
pro vyhledávání: '"Mariko Aso"'
Publikováno v:
Indian Journal of Dermatology, Vol 69, Iss 2, Pp 204-204 (2024)
Externí odkaz:
https://doaj.org/article/84c2be6deccd4eaba99392d0472ed360
Autor:
Takeru Araki, Yasufumi Fuchi, Shuhei Murayama, Ryoma Shiraishi, Tokimi Oyama, Mariko Aso, Ichio Aoki, Shigeki Kobayashi, Ken-ichi Yamada, Satoru Karasawa
Publikováno v:
Nanomaterials, Vol 8, Iss 10, p 782 (2018)
We synthesized (2,4-trifluoromethyl-7-N-bis(2,5,8,11-tetraoxatridecane-13-yl)-aminoquinoline) TFMAQ-diEg4, an emissive aminoquinoline derivative that incorporated two tetraethyleneglycol chains into an amino group. TFMAQ-diEg4 showed fluorescence and
Externí odkaz:
https://doaj.org/article/95b46e29817c4d0d8b2de4fde5152a24
Publikováno v:
Nishi Nihon Hifuka. 82:348-351
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f1a93251aee3ca71650bb446c1bcd340
https://doi.org/10.2336/nishinihonhifu.82.348
https://doi.org/10.2336/nishinihonhifu.82.348
Publikováno v:
Nishi Nihon Hifuka. 82:10-13
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::982e1489f83b2fe735c60b2272addecc
https://doi.org/10.2336/nishinihonhifu.82.10
https://doi.org/10.2336/nishinihonhifu.82.10
Publikováno v:
Tetrahedron Letters. 59:4528-4531
A dendritic bisphosphonate carrying three bisphosphonate (BP) units in close proximity was designed as a ligand to conjugate large therapeutic molecules for their bone selective delivery. The Bu3P-catalyzed conjugate addition of nitromethane to vinyl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dda1c1a6a1305cd8d2a6c8e52d74fb3c
https://doi.org/10.1016/j.tetlet.2018.11.028
https://doi.org/10.1016/j.tetlet.2018.11.028
Autor:
Mariko Aso, Monji Koga, Yukihiro Tasaki, Kaori Takayanagi, Toshiyuki Nakayama, Shinichi Imafuku
Publikováno v:
Nishi Nihon Hifuka. 82:335-336
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6a4dc56e7a414cdad302b8cb139e16f9
https://doi.org/10.2336/nishinihonhifu.82.335
https://doi.org/10.2336/nishinihonhifu.82.335
Autor:
John Walter Mirc, Kazuteru Usui, Mariko Aso, Manami Kurita, Hiroshi Suemune, Shintaro Matsumoto, Yoshitaka Higuchi
Publikováno v:
ChemBioChem. 17:2346-2352
Oligodeoxynucleotides (ODNs) containing 2-N-tert-butylaminoxyl-2'-deoxyadenosine (A*) residues were synthesized to allow accurate monitoring of adenine motion by EPR spectroscopy through the agency of direct linkage of the acyclic aminoxyl group to t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b25d1eb286abccc72f9719214375d544
https://doi.org/10.1002/cbic.201600465
https://doi.org/10.1002/cbic.201600465
Autor:
Mariko Aso, Bo Yang, Kazuteru Usui, Hiroshi Suemune, Noboru Koga, Midori Sasagaki, Daiki Okado, Yasuhiro Matsui
Publikováno v:
Tetrahedron. 71:5414-5419
5-N-tert-Butylaminoxylcytidine was synthesized as a new spin-labelled cytidine to detect guanosine by EPR spectroscopy. Metal-halogen exchange reaction of TBS-protected N-benzoyl-5-iodocytidine followed by a reaction with 2-methyl-2-nitrosopropane af
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dcf6aa662bd072581d0febc431413382
https://doi.org/10.1016/j.tet.2015.05.080
https://doi.org/10.1016/j.tet.2015.05.080
Autor:
Yurino Matsuura, Yumi Tsuneura, Satoshi Morimoto, Yayoi Yonenaga, Hiroyuki Tanaka, Mariko Aso, Hitoshi Kurose, Seiichi Sakamoto
Publikováno v:
Monoclonal Antibodies in Immunodiagnosis and Immunotherapy. 33:414-419
Most of the functions of D-amino acids (D-AA) remain unclear because of little analytic methods for specific detection/determination. In this study, a highly specific monoclonal antibody to D-glutamic acid (D-Glu-MAb) was produced using a hybridoma m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::41e37b4805d19f03ba7653ef5d86c7da
https://doi.org/10.1089/mab.2014.0048
https://doi.org/10.1089/mab.2014.0048
Autor:
Kazuteru Usui, Mariko Aso, Bo Yang, Chiyoe Ota, Chiemi Gatanaga, Tsutomu Katayama, Yuka Inadomi, Hiroshi Suemune
Publikováno v:
ACS chemical biology. 11(8)
We have developed oligodeoxynucleotides (ODNs) that modify primary amines to produce 5,6-dimethoxy 3-methyleneisoindolin-1-one. Compared to the oxygen isosteric fluorophore, 4,5-dimethoxyphthalimide, this methyleneisoindolinone was more stable and ex
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a8ab1b341892ce565ea1c75cdca99678
https://pubmed.ncbi.nlm.nih.gov/27253874
https://pubmed.ncbi.nlm.nih.gov/27253874