H
Hiroshi Yamaguchi
Researcher at Nippon Telegraph and Telephone
Publications - 571
Citations - 14406
Hiroshi Yamaguchi is an academic researcher from Nippon Telegraph and Telephone. The author has contributed to research in topics: Resonator & Molecular beam epitaxy. The author has an hindex of 47, co-authored 519 publications receiving 13016 citations. Previous affiliations of Hiroshi Yamaguchi include Osaka University & Imperial College London.
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Improved resonance characteristics of GaAs beam resonators by epitaxially induced strain
Hiroshi Yamaguchi,Kazutoshi Kato,Kazutoshi Kato,Y. Nakai,Y. Nakai,Koji Onomitsu,Shin'ichi Warisawa,Sunao Ishihara +7 more
TL;DR: In this article, the authors used a strained GaAs film grown on relaxed In0.1Ga0.9As buffer layers to increase the frequency of the fundamental mode by applying tensile strain.
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Single-Turn GaAs/InAs Nanotubes Fabricated Using the Supercritical CO2 Drying Technique
TL;DR: In this paper, a supercritical CO2 drying technique was applied to fabricate free-standing semiconductor nanotubes, in order to solve the problem of tube collapsing caused by the capillary forces in the final drying process.
Journal Article
IS012 MEF2B is a component of a smooth muscle-specific complex that binds an A/T-rich element important for smooth muscle myosin heavy chain gene expression
TL;DR: It is demonstrated that the SMHC promoter region (−1594 to −1462 base pairs) containing the A/T-rich element can activate the heterologous thymidine kinase promoter in smooth muscle cells, but not in fibroblasts.
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Graphene-Based Nano-Electro-Mechanical Switch with High On/Off Ratio
TL;DR: In this article, local buckling of the nanomembrane structures was shown to reduce the contact conductance between graphene and a metal-coated nanoprobe in scanning probe microscopy, which could represent a new path to electrical switching at the nanoscale.
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An enantioselective total synthesis of aspergillides A and B
TL;DR: An enantioselective total synthesis of aspergillides A and B has been accomplished on the basis of a unified synthetic strategy that exploits stereodivergent intramolecular oxa-conjugate cyclization and Yamaguchi macrolactonization.