Zobrazeno 1 - 10
of 105
pro vyhledávání: '"Jun-ichi Saito"'
Publikováno v:
Surfaces, Vol 7, Iss 3, Pp 550-559 (2024)
The iron (Fe) specimens selected as the substrate metal for this study were surface-treated using fluorine gas, and their wettability with liquid sodium (Na) was evaluated using the sliding angle. Additionally, the surface morphology and binding stat
Externí odkaz:
https://doaj.org/article/a19b31331f1d420eb1fe6f0afd348ddc
Autor:
Toshimasa Harumoto, Atsuko Sato, Yuki Takayama, Hikaru Miyagi, Jun-Ichi Saito, Fumikazu Shinohara
Publikováno v:
PLoS ONE, Vol 15, Iss 7, p e0236710 (2020)
Argonaute (AGO) proteins are the key component of the RNA interference machinery that suppresses gene expression by forming an RNA-induced silencing complex (RISC) with microRNAs (miRNAs). Each miRNA is involved in various cellular processes, such as
Externí odkaz:
https://doaj.org/article/01a1ca5097524f528647920742a29080
Autor:
Naohisa Takesue, Jun-ichi Saito
Publikováno v:
Crystals, Vol 10, Iss 11, p 956 (2020)
The effective ionic charges of lead-free perovskite dielectric complex compounds were investigated with molecular orbital calculation. The base model was a double perovskite cluster that consisted of octahedral oxygen cages with a transition metal io
Externí odkaz:
https://doaj.org/article/378ca6d00921422c80ef73dbf5fe90e8
Publikováno v:
Metals, Vol 5, Iss 3, Pp 1212-1240 (2015)
A new kind of suspension liquid was developed by dispersing Ti nanoparticles (10 nm) in liquid Na, which was then determined by TEM (transmission electron microscopy) analysis. The volume fraction was estimated to be 0.0088 from the analyzed Ti conce
Externí odkaz:
https://doaj.org/article/05b1f1b289aa4477920dc0d29bf7311f
Publikováno v:
Acta Crystallographica Section D Structural Biology. 79:435-441
Structure determination of G-protein-coupled receptors (GPCRs) is key for the successful development of efficient drugs targeting GPCRs. BRIL is a thermostabilized apocytochrome b 562 (with M7W/H102I/R106L mutations) from Escherichia coli and is ofte
Publikováno v:
Journal of The Japan Institute of Electronics Packaging. 25:481-487
Autor:
Akira Asai, Ryuichiro Nakai, Jun-ichi Saito, Hiroshi Ishida, Yasuo Watanabe, Yuichi Takahashi, Ryoko Okada-Iwasaki
Figure legends of supplementary figure S1-S5
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2d677685c87f248c6b813bf2b1a5450d
https://doi.org/10.1158/1535-7163.22508332
https://doi.org/10.1158/1535-7163.22508332
Autor:
Akira Asai, Ryuichiro Nakai, Jun-ichi Saito, Hiroshi Ishida, Yasuo Watanabe, Yuichi Takahashi, Ryoko Okada-Iwasaki
Supplementary Fig. S1: A, CTNNB1 siRNAs suppress the target gene and B, the target protein. C, CTNNB1 siRNAs inhibit reporter activity and D, change the expression of Wnt/β-catenin downstream genes.; Supplementary Fig. S2: A, K-756 does not inhibit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0d23dd1d518ae26fd58f9735f46db6d9
https://doi.org/10.1158/1535-7163.22508335.v1
https://doi.org/10.1158/1535-7163.22508335.v1
Autor:
Akira Asai, Ryuichiro Nakai, Jun-ichi Saito, Hiroshi Ishida, Yasuo Watanabe, Yuichi Takahashi, Ryoko Okada-Iwasaki
Supplementary Table S1: The correlation coefficients of the gene expression profiles between CTNNB1 siRNAs and XAV939- or K-756-treated cells. Supplementary Table S2: The reporter inhibitory activity and cell growth inhibitory activity of K-756, XAV9
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3bdc88303c81b5dd5fcc749aaf597d3f
https://doi.org/10.1158/1535-7163.22508329.v1
https://doi.org/10.1158/1535-7163.22508329.v1