Masashi Ueki
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Previous Organizations / Institutes
The organizations / institutes from the scholar's other articles in the past ten years
Research Subjects
Masashi Ueki has a total of 24 co-authors. Here are the top co-authors by number of shared publications:
- Akinobu Honda
Glycometabolic Biochemistry Laboratory, RIKEN Cluster for Pioneering Research Institute, RIKEN
1 shared publication Haruhiko Fujihira
Glycometabolic Biochemistry Laboratory, RIKEN Pioneering Research Institute, RIKEN, 2-1 Hirosawa, Wako, Saitama, 351-0198, Japan; Division of glycobiologics, Juntendo University Graduate School of Medicine, 2-1-1 Hongo, Bunkyo-ku, Tokyo, 113-8421, Japan
1 shared publicationHiroto Hirayama
Glycometabolic Biochemistry Laboratory, RIKEN Pioneering Research Institute, RIKEN, 2-1 Hirosawa, Wako, Saitama, 351-0198, Japan; Institute for Glyco-Core Research (iGCORE), Gifu University, Gifu, Japan
1 shared publicationHisayuki Kanamori
Animal Cell Incubator Laboratory, RIKEN Innovation Center, 2-1 Hirosawa, Wako, Saitama 351-0198, Japan; Mixing Technology Laboratory, Satake Chemical Equipment Mfg., Ltd., 60 Niizo, Toda, Saitama 335-0021, Japan
1 shared publication- Ichiro Matsuo
Gunma University
1 shared publication - Ilaria Casolaro
ASST Ovest Milanese, Milano, Italy
1 shared publication
Latest Publications
- Open Access
- 6 November 2025
- Published by Elsevier in Journal of Biological Chemistry
- Vol. 301 (12) , 110906
Structural characterization of zebrafish Ngly2, an ovary-enriched acid PNGase required for egg-free glycan production
- 6 November 2025
- Published by Elsevier in Journal of Biological Chemistry
- Vol. 301 (12) , 110906
Open AccessStructural characterization of zebrafish Ngly2, an ovary-enriched acid PNGase required for egg-free glycan production
- 6 January 2024
- Published by Elsevier in Journal of Bioscience and Bioengineering
- Vol. 137 (2) , 149-155
Large-scale cultivation of human iPS cells in bioreactor with reciprocal mixing
- 6 January 2024
- Published by Elsevier in Journal of Bioscience and Bioengineering
- Vol. 137 (2) , 149-155
Large-scale cultivation of human iPS cells in bioreactor with reciprocal mixing
- 1 November 2021
- Published by Elsevier in Journal of Bioscience and Bioengineering
- Vol. 132 (5) , 531-536
Improved cultivation of Chinese hamster ovary cells in bioreactor with reciprocal mixing
- 1 November 2021
- Published by Elsevier in Journal of Bioscience and Bioengineering
- Vol. 132 (5) , 531-536
Improved cultivation of Chinese hamster ovary cells in bioreactor with reciprocal mixing
- Open Access
Antibacterial Properties of Silver Nanoparticles Embedded on Polyelectrolyte Hydrogels Based on α-Amino Acid Residues
Polyelectrolyte hydrogels bearing l-phenylalanine (PHE), l-valine (AVA), and l-histidine (Hist) residues were used as scaffolds for the formation of silver nanoparticles by reduction of Ag+ ions with NaBH4. The interaction with the metal ion allowed a prompt collapse of the swollen hydrogel, due to the neutralization reaction of basic groups present on the polymer. The imidazole nitrogen of the hydrogel with Hist demonstrated greater complexing capacity with the Ag+ ion compared to the hydrogels with carboxyl groups. The subsequent reduction to metallic silver allowed for the restoration of the hydrogel’s degree of swelling to the starting value. Transmission electron microscopy (TEM) and spectroscopic analyses showed, respectively, a uniform distribution of the 15 nm spherical silver nanoparticles embedded on the hydrogel and peak optical properties around a wavelength of 400 nm due to the surface plasmonic effect. Unlike native hydrogels, the composite hydrogels containing silver nanoparticles showed good antibacterial activity as gram+/gram− bactericides, and higher antifungal activity against S. cerevisiae.
Open AccessAntibacterial Properties of Silver Nanoparticles Embedded on Polyelectrolyte Hydrogels Based on α-Amino Acid Residues
Polyelectrolyte hydrogels bearing l-phenylalanine (PHE), l-valine (AVA), and l-histidine (Hist) residues were used as scaffolds for the formation of silver nanoparticles by reduction of Ag+ ions with NaBH4. The interaction with the metal ion allowed a prompt collapse of the swollen hydrogel, due to the neutralization reaction of basic groups present on the polymer. The imidazole nitrogen of the hydrogel with Hist demonstrated greater complexing capacity with the Ag+ ion compared to the hydrogels with carboxyl groups. The subsequent reduction to metallic silver allowed for the restoration of the hydrogel’s degree of swelling to the starting value. Transmission electron microscopy (TEM) and spectroscopic analyses showed, respectively, a uniform distribution of the 15 nm spherical silver nanoparticles embedded on the hydrogel and peak optical properties around a wavelength of 400 nm due to the surface plasmonic effect. Unlike native hydrogels, the composite hydrogels containing silver nanoparticles showed good antibacterial activity as gram+/gram− bactericides, and higher antifungal activity against S. cerevisiae.
- Open Access
- 1 January 1998
- Published by Japan Antibiotics Research Association in The Journal of Antibiotics
- Vol. 51 (9) , 883-885
UK-1, a Novel Cytotoxic Metabolite from Streptomyces sp. 517-02. IV. Antifungal Action of Methyl UK-1.
Japan's largest platform for academic e-journals: J-STAGE is a full text database for reviewed academic papers published by Japanese societies
- 1 January 1998
- Published by Japan Antibiotics Research Association in The Journal of Antibiotics
- Vol. 51 (9) , 883-885
Open AccessUK-1, a Novel Cytotoxic Metabolite from Streptomyces sp. 517-02. IV. Antifungal Action of Methyl UK-1.
Japan's largest platform for academic e-journals: J-STAGE is a full text database for reviewed academic papers published by Japanese societies