Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Hide-Nori Tanaka"'
Autor:
Shogo Hamajima, Naoko Komura, Hide-Nori Tanaka, Akihiro Imamura, Hideharu Ishida, Tsuyoshi Ichiyanagi, Hiromune Ando
Publikováno v:
Molecules, Vol 28, Iss 1, p 102 (2022)
Chemical synthesis of 3-deoxy-d-manno-2-octulosonic acid (Kdo)-containing glycans, such as bacterial lipopolysaccharides (LPSs) and capsular polysaccharides (CPSs), is in high demand for the development of vaccines against pathogenic bacteria. We hav
Externí odkaz:
https://doaj.org/article/7dda1693ce254c84a610edfd9a38b88b
Autor:
Hide-Nori Tanaka
Publikováno v:
Trends in Glycoscience and Glycotechnology. 35:E34-E37
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8b096c70cfbd17b6b43129c11d7a18dc
https://doi.org/10.4052/tigg.2312.2e
https://doi.org/10.4052/tigg.2312.2e
Autor:
Shogo Hamajima, Naoko Komura, Hide-Nori Tanaka, Akihiro Imamura, Hideharu Ishida, Haruka Noguchi, Tsuyoshi Ichiyanagi, Hiromune Ando
Publikováno v:
Organic Letters. 24:8672-8676
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::11cf8a3311744e5d4baf6202af107bce
https://doi.org/10.1021/acs.orglett.2c03542
https://doi.org/10.1021/acs.orglett.2c03542
Autor:
Rui Hagino, Keita Mozaki, Naoko Komura, Akihiro Imamura, Hideharu Ishida, Hiromune Ando, Hide-Nori Tanaka
Publikováno v:
ACS Omega. 7:32795-32804
Poly(ADP-ribosyl)ation is a post-translational modification that produces poly(ADP-ribose) with a branched structure every 20-50 units; such branching structure has been previously suggested to be involved in regulating chromatin remodeling. To eluci
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::13f8b602d00c158e23e7b70a7d3fffb3
https://doi.org/10.1021/acsomega.2c04732
https://doi.org/10.1021/acsomega.2c04732
Publikováno v:
Advances in carbohydrate chemistry and biochemistry. 81
The synthesis of sialic acid-containing molecules has posed a formidable challenge to carbohydrate chemists for over 50 years. Our research group has intensively searched for robust chemistry to enable the construction of a broad spectrum of sialic a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::fc76a8f4afde85597b80b02d5dd3b33f
https://pubmed.ncbi.nlm.nih.gov/36435533
https://pubmed.ncbi.nlm.nih.gov/36435533
Autor:
Shogo, Hamajima, Naoko, Komura, Hide-Nori, Tanaka, Akihiro, Imamura, Hideharu, Ishida, Haruka, Noguchi, Tsuyoshi, Ichiyanagi, Hiromune, Ando
Publikováno v:
Organic letters. 24(47)
We describe a method for the α-selective glycosidation of 3-deoxy-d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e9834bd35294117060e3fd0d0c3e9fca
https://pubmed.ncbi.nlm.nih.gov/36399121
https://pubmed.ncbi.nlm.nih.gov/36399121
Autor:
Tsuyoshi Asano, Taro Udagawa, Naoko Komura, Akihiro Imamura, Hideharu Ishida, Hiromune Ando, Hide-Nori Tanaka
Publikováno v:
Carbohydrate Research. 527:108808
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::797ed2a7ea70091ea89bc9451bb5ea55
https://doi.org/10.1016/j.carres.2023.108808
https://doi.org/10.1016/j.carres.2023.108808
Autor:
Maina Takahashi, Naoko Komura, Yukako Yoshida, Eriko Yamaguchi, Ami Hasegawa, Hide-Nori Tanaka, Akihiro Imamura, Hideharu Ishida, Kenichi G. N. Suzuki, Hiromune Ando
Publikováno v:
RSC chemical biology. 3(7)
Gangliosides are a family of sialic-acid-containing glycosphingolipids that form dynamic domains (lipid rafts) with proteins in cell plasma membranes (PMs), and are involved in various biological processes. The dynamic behavior of gangliosides can be
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::09e0ee11315992f417e69ca189550304
https://pubmed.ncbi.nlm.nih.gov/35866169
https://pubmed.ncbi.nlm.nih.gov/35866169
Publikováno v:
Special Volume in Memory of Hidetoshi Yamada Part 1 ISBN: 9780323985888
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a3e8a4462b5857e9ab268c4831b258ef
https://doi.org/10.1016/bs.accb.2022.09.003
https://doi.org/10.1016/bs.accb.2022.09.003
Autor:
Hayato Ozaki, Takuya Asano, Hide-Nori Tanaka, Naoko Komura, Hiromune Ando, Hideharu Ishida, Akihiro Imamura
Publikováno v:
Carbohydrate research. 512
In this paper, the chemical synthesis of polylactosamine fragments up to docosasaccharide (22-mer) via the blockwise synthetic approach is reported. We used suitably protected tetrasaccharide and octasaccharide sequences as key building blocks. The u
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ffb023c3900d3b2712d3bef1297f1a26
https://pubmed.ncbi.nlm.nih.gov/35092907
https://pubmed.ncbi.nlm.nih.gov/35092907