Zobrazeno 1 - 10
of 25
pro vyhledávání: '"Tsuneji SUZUKI"'
Publikováno v:
ACS Applied Materials & Interfaces. 7:17131-17137
Organic nanolayers attract much attention for the isolation and adhesion promotion of the Cu line and insulator in Cu interconnection of microelectronic devices. This paper proposes a strategy for selective formation of adhesion nanolayer on the insu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5b1f2d98c9ae31e5fd790f36307cf42e
https://doi.org/10.1021/acsami.5b03835
https://doi.org/10.1021/acsami.5b03835
Publikováno v:
The Bulletin of the Japanese Bird Banding Association. 17:9-15
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a4b2ad5e1809f26f5cea07f7190116e2
https://doi.org/10.14491/jbba.ar125
https://doi.org/10.14491/jbba.ar125
Publikováno v:
IEEE International Interconnect Technology Conference.
A strategy for the selective formation of a pore sealing layer on mesoporous low-k applicable for a Cu dual damascene interconnection process is herein proposed. An ultra-thin, adhesive, and conformal pore sealing layer was formed on mesoporous low-k
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1c1492caa04d3e506febd4cb0e948f93
https://doi.org/10.1109/iitc.2014.6831890
https://doi.org/10.1109/iitc.2014.6831890
Autor:
Yukiyasu Mariko, Tomoyuki Ando, Takashi Tsuruo, Yasuhito Nosaka, Osamu Nakanishi, Katsutoshi Tsuchiya, Tsuneji Suzuki, Takashi Yamashita, Akiko Saito
Publikováno v:
Proceedings of the National Academy of Sciences. 96:4592-4597
Synthetic benzamide derivatives were investigated for their ability to inhibit histone deacetylase (HDA). In this study, one of the most active benzamide derivatives, MS-27-275, was examined with regard to its biological properties and antitumor effi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6c8ec8a7528ee0326896a3beffccd602
https://doi.org/10.1073/pnas.96.8.4592
https://doi.org/10.1073/pnas.96.8.4592
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 9:659-662
We synthesized the glucuronides of MS-209 to identify the two main unknown metabolites in human urine. Reaction of MS-209 and glucuronyl trichloroacetimidate gave two β-isomers, which were each glucuronate of ( R )- and ( S )-MS-209. These spectrum
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fc135a1fe23685adcf35e0454da66469
https://doi.org/10.1016/s0960-894x(99)00056-6
https://doi.org/10.1016/s0960-894x(99)00056-6
Publikováno v:
MRS Proceedings. 1559
Pore sealing has become a critical issue for the implementation of porous low-k dielectrics and for realizing acceptable reliability performance of the interconnect. This study focuses on fabrication of ultra-thin, conformal and plasma resistant pore
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c7e5d9d7df39920d787b25ddad53f159
https://doi.org/10.1557/opl.2013.690
https://doi.org/10.1557/opl.2013.690
Publikováno v:
MRS Proceedings. 1428
It was found for the first time that the control of the size of pore sealant is important to prevent diffusions of pore sealant into pores of porous low-k films and to achieve a good toluene seal property. Two pore sealants (PS-A, B) were prepared an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::86737b488702643652c4e7162e196b7f
https://doi.org/10.1557/opl.2012.1354
https://doi.org/10.1557/opl.2012.1354
Autor:
Akiko Saito, Osamu Nakanishi, Tomoyuki Ando, Nobuyuki Fukazawa, Katsutoshi Tsuchiya, Yukiyasu Mariko, Tsuneji Suzuki, Takashi Yamashita
Publikováno v:
Journal of Medicinal Chemistry. 42:3001-3003
Newly synthesized benzamide derivatives were evaluated for their inhibitory activity against histone deacetylase. The structure of these derivatives was unrelated to the known inhibitors, and IC(50) values of the active compounds were in the range of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::16620ef07b417dba1a91d9d55e4c91ed
https://doi.org/10.1021/jm980565u
https://doi.org/10.1021/jm980565u
Autor:
Hiroyuki, Seimiya, Tomoko, Oh-hara, Tsuneji, Suzuki, Imad, Naasani, Toshiyuki, Shimazaki, Katsutoshi, Tsuchiya, Takashi, Tsuruo
Publikováno v:
Molecular cancer therapeutics. 1(9)
Epidemiological studies suggest potent anticancer effects of tea catechins. Previously, we have reported (I. Naasani et aL, Biochem. Biophys. Res. Commun., 249: 391-396, 1998) that epigallocatechin gallate (EGCG), a major tea catechin, strongly and d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::fcfe5bfdab11b80a4339a4ff4387d09a
https://pubmed.ncbi.nlm.nih.gov/12479362
https://pubmed.ncbi.nlm.nih.gov/12479362
Publikováno v:
Journal of medicinal chemistry. 40(13)
The effect of 24 newly synthesized quinoline derivatives on tumor cell multidrug resistance (MDR) was examined in vitro. At low concentrations, these compounds enhanced the accumulation of [3H]vincristine in K562/ADM cells and reversed tumor cell MDR
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e3055dfce423b95f6635f34c6bc79b4e
https://pubmed.ncbi.nlm.nih.gov/9207946
https://pubmed.ncbi.nlm.nih.gov/9207946