Year |
Citation |
Score |
2017 |
Yang J, Wen X, Xia H, Sheng R, Ma Q, Kim J, Tapping P, Harada T, Kee TW, Huang F, Cheng YB, Green M, Ho-Baillie A, Huang S, Shrestha S, et al. Acoustic-optical phonon up-conversion and hot-phonon bottleneck in lead-halide perovskites. Nature Communications. 8: 14120. PMID 28106061 DOI: 10.1038/Ncomms14120 |
0.642 |
|
2016 |
Harada T, Lincoln SF, Kee TW. Excited-state dynamics of the medicinal pigment curcumin in a hydrogel. Physical Chemistry Chemical Physics : Pccp. PMID 27711741 DOI: 10.1039/C6Cp05648B |
0.616 |
|
2015 |
Leung MH, Harada T, Dai S, Kee TW. Nanoprecipitation and Spectroscopic Characterization of Curcumin-Encapsulated Polyester Nanoparticles. Langmuir : the Acs Journal of Surfaces and Colloids. PMID 26439894 DOI: 10.1021/Acs.Langmuir.5B02773 |
0.628 |
|
2015 |
Harada T, McTernan HL, Pham DT, Lincoln SF, Kee TW. Femtosecond transient absorption spectroscopy of the medicinal agent curcumin in diamide linked γ-cyclodextrin dimers. The Journal of Physical Chemistry. B. 119: 2425-33. PMID 25198794 DOI: 10.1021/Jp507272F |
0.623 |
|
2014 |
Harada T, Pham DT, Lincoln SF, Kee TW. The capture and stabilization of curcumin using hydrophobically modified polyacrylate aggregates and hydrogels. The Journal of Physical Chemistry. B. 118: 9515-23. PMID 25029529 DOI: 10.1021/Jp5060205 |
0.623 |
|
2013 |
Harada T, Giorgio L, Harris TJ, Pham DT, Ngo HT, Need EF, Coventry BJ, Lincoln SF, Easton CJ, Buchanan G, Kee TW. Diamide linked γ-cyclodextrin dimers as molecular-scale delivery systems for the medicinal pigment curcumin to prostate cancer cells. Molecular Pharmaceutics. 10: 4481-90. PMID 24160991 DOI: 10.1021/Mp400309S |
0.625 |
|
2013 |
Leung MH, Harada T, Kee TW. Delivery of curcumin and medicinal effects of the copper(II)-curcumin complexes. Current Pharmaceutical Design. 19: 2070-83. PMID 23116313 DOI: 10.2174/138161213805289237 |
0.624 |
|
2011 |
Harada T, Pham DT, Leung MH, Ngo HT, Lincoln SF, Easton CJ, Kee TW. Cooperative binding and stabilization of the medicinal pigment curcumin by diamide linked γ-cyclodextrin dimers: a spectroscopic characterization. The Journal of Physical Chemistry. B. 115: 1268-74. PMID 21194191 DOI: 10.1021/Jp1096025 |
0.623 |
|
Low-probability matches (unlikely to be authored by this person) |
2015 |
Ghosh S, Winchester A, Muchharla B, Wasala M, Feng S, Elias AL, Krishna MB, Harada T, Chin C, Dani K, Kar S, Terrones M, Talapatra S. Ultrafast Intrinsic Photoresponse and Direct Evidence of Sub-gap States in Liquid Phase Exfoliated MoS2Thin Films. Scientific Reports. 5: 11272. PMID 26175112 DOI: 10.1038/Srep11272 |
0.143 |
|
2016 |
Man MK, Margiolakis A, Deckoff-Jones S, Harada T, Wong EL, Krishna MB, Madéo J, Winchester A, Lei S, Vajtai R, Ajayan PM, Dani KM. Imaging the motion of electrons across semiconductor heterojunctions. Nature Nanotechnology. PMID 27723731 DOI: 10.1038/Nnano.2016.183 |
0.126 |
|
2016 |
Kobashi K, Harada T, Adachi Y, Mori M, Ihara M, Hayasaka D. Comparative ecotoxicity of imidacloprid and dinotefuran to aquatic insects in rice mesocosms. Ecotoxicology and Environmental Safety. 138: 122-129. PMID 28040617 DOI: 10.1016/j.ecoenv.2016.12.025 |
0.117 |
|
2011 |
Shimokawa J, Harada T, Yokoshima S, Fukuyama T. Total synthesis of gelsemoxonine. Journal of the American Chemical Society. 133: 17634-7. PMID 21980918 DOI: 10.1351/Pac-Con-11-10-25 |
0.069 |
|
2016 |
Harada T, Shimokawa J, Fukuyama T. Unified Total Synthesis of Five Gelsedine-Type Alkaloids: (-)-Gelsenicine, (-)-Gelsedine, (-)-Gelsedilam, (-)-14-Hydroxygelsenicine, and (-)-14,15-Dihydroxygelsenicine. Organic Letters. PMID 27580209 DOI: 10.1021/Acs.Orglett.6B02263 |
0.062 |
|
2017 |
Harada T, Spence S, Margiolakis A, Deckoff-Jones S, Ploeger R, Shugar AN, Hamm JF, Dani KM, Dani AR. Obtaining Cross-Sections of Paint Layers in Cultural Artifacts Using Femtosecond Pulsed Lasers. Materials (Basel, Switzerland). 10. PMID 28772468 DOI: 10.3390/Ma10020107 |
0.046 |
|
2010 |
Li R, Harada T, Honjoh K, Miyamoto T. Phylogenetic analysis and Shiga toxin production profiling of Shiga toxin-producing/enterohemorrhagic Escherichia coli clinical isolates. Microbial Pathogenesis. 49: 246-51. PMID 20558273 DOI: 10.1016/j.micpath.2010.06.005 |
0.018 |
|
Hide low-probability matches. |