Year |
Citation |
Score |
2021 |
Ogasawara H, Tanaka Y, Taki M, Yamaguchi S. Late-stage functionalisation of alkyne-modified phospha-xanthene dyes: lysosomal imaging using an off-on-off type of pH probe. Chemical Science. 12: 7902-7907. PMID 34168843 DOI: 10.1039/d1sc01705e |
0.302 |
|
2020 |
Iwatate R, Yoshinari A, Yagi N, Grzybowski M, Ogasawara H, Kamiya M, Komatsu T, Taki M, Yamaguschi S, Frommer WB, Nakamura M. Covalent Self-labeling of Tagged Proteins with Chemical Fluorescent Dyes in BY-2 Cells and Arabidopsis Seedlings. The Plant Cell. PMID 32763980 DOI: 10.1105/Tpc.20.00439 |
0.351 |
|
2020 |
Grzybowski M, Taki M, Kajiwara K, Yamaguchi S. Effects of Amino Group Substitution on the Photophysical Properties and Stability of Near-Infrared Fluorescent P-Rhodamines. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 32274865 DOI: 10.1002/Chem.202000957 |
0.404 |
|
2019 |
Wang C, Taki M, Sato Y, Tamura Y, Yaginuma H, Okada Y, Yamaguchi S. A photostable fluorescent marker for the superresolution live imaging of the dynamic structure of the mitochondrial cristae. Proceedings of the National Academy of Sciences of the United States of America. PMID 31337683 DOI: 10.1073/Pnas.1905924116 |
0.37 |
|
2019 |
Griesbeck S, Michail E, Rauch F, Ogasawara H, Wang C, Sato Y, Edkins R, Zhang Z, Taki M, Lambert C, Yamaguchi S, Marder TB. The Effect of Branching on One- and Two-Photon Absorption, Cell Viability and Localization of Cationic Triarylborane Chromophores with Dipolar vs. Octupolar Charge Distributions for Cellular Imaging†. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 31322301 DOI: 10.1002/Chem.201902461 |
0.37 |
|
2019 |
Griesbeck S, Michail E, Wang C, Ogasawara H, Lorenzen S, Gerstner L, Zang T, Nitsch J, Sato Y, Bertermann R, Taki M, Lambert C, Yamaguchi S, Marder TB. Tuning the π-bridge of quadrupolar triarylborane chromophores for one- and two-photon excited fluorescence imaging of lysosomes in live cells. Chemical Science. 10: 5405-5422. PMID 31217943 DOI: 10.1039/C9Sc00793H |
0.447 |
|
2019 |
Griesbeck S, Ferger M, Czernetzki C, Wang C, Bertermann R, Friedrich A, Haehnel M, Sieh D, Taki M, Yamaguchi S, Marder TB. Optimization of Aqueous Stability vs. π-Conjugation in Tetracationic Bis(triarylborane) Chromophores: Applications in Live-Cell Fluorescence Imaging. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 30900778 DOI: 10.1002/Chem.201900723 |
0.317 |
|
2019 |
Griesbeck S, Ferger M, Czernetzi C, Wang C, Bertermann R, Friedrich A, Haehnel M, Sieh D, Taki M, Yamaguchi S, Marder TB. Cover Feature: Optimization of Aqueous Stability versus π‐Conjugation in Tetracationic Bis(triarylborane) Chromophores: Applications in Live‐Cell Fluorescence Imaging (Chem. Eur. J. 32/2019) Chemistry: a European Journal. 25: 7579-7579. DOI: 10.1002/Chem.201901430 |
0.35 |
|
2018 |
Grzybowski M, Taki M, Senda K, Sato Y, Ariyoshi T, Okada Y, Kawakami R, Imamura T, Yamaguchi S. A Highly Photostable Near-infrared Labeling Agent Based on a Phospha-rhodamine for Long-term and Deep Imaging. Angewandte Chemie (International Ed. in English). PMID 29984448 DOI: 10.1002/Anie.201804731 |
0.379 |
|
2017 |
Ogasawara H, Grzybowski M, Hosokawa R, Sato Y, Taki M, Yamaguchi S. A far-red fluorescent probe based on a phospha-fluorescein scaffold for cytosolic calcium imaging. Chemical Communications (Cambridge, England). PMID 29239411 DOI: 10.1039/C7Cc07344E |
0.415 |
|
2017 |
Wang C, Taki M, Sato Y, Fukazawa A, Higashiyama T, Yamaguchi S. Super-Photostable Phosphole-Based Dye for Multiple-Acquisition Stimulated Emission Depletion Imaging. Journal of the American Chemical Society. PMID 28741935 DOI: 10.1021/Jacs.7B04418 |
0.44 |
|
2017 |
Yamaguchi S, Fukazawa A, Taki M. Phosphole P-Oxide-Containing π-Electron Materials: Synthesis and Applications in Fluorescence Imaging Journal of Synthetic Organic Chemistry, Japan. 75: 1179-1187. DOI: 10.5059/Yukigoseikyokaishi.75.1179 |
0.341 |
|
2017 |
Taki M, Azeyanagi S, Hayashi K, Yamaguchi S. Color-tunable fluorescent nanoparticles encapsulating trialkylsilyl-substituted pyrene liquids Journal of Materials Chemistry C. 5: 2142-2148. DOI: 10.1039/C6Tc05208H |
0.369 |
|
2016 |
Osaki H, Chou CM, Taki M, Welke K, Yokogawa D, Irle S, Sato Y, Higashiyama T, Saito S, Fukazawa A, Yamaguchi S. A Macrocyclic Fluorophore Dimer with Flexible Linkers: Bright Excimer Emission with a Long Fluorescence Lifetime. Angewandte Chemie (International Ed. in English). PMID 27121201 DOI: 10.1002/Anie.201602239 |
0.437 |
|
2016 |
Sato Y, Wang C, Fukazawa A, Taki M, Higashiyama T, Yamaguchi S. A super photostable fluorescent dye that survives in repeated STED laser irradiation Plant Morphology. 28: 9-13. DOI: 10.5685/Plmorphol.28.9 |
0.316 |
|
2015 |
Fukazawa A, Suda S, Taki M, Yamaguchi E, Grzybowski M, Sato Y, Higashiyama T, Yamaguchi S. Phospha-fluorescein: a red-emissive fluorescein analogue with high photobleaching resistance. Chemical Communications (Cambridge, England). PMID 26617335 DOI: 10.1039/C5Cc09345G |
0.371 |
|
2015 |
Wang C, Fukazawa A, Taki M, Sato Y, Higashiyama T, Yamaguchi S. A Phosphole Oxide Based Fluorescent Dye with Exceptional Resistance to Photobleaching: A Practical Tool for Continuous Imaging in STED Microscopy. Angewandte Chemie (International Ed. in English). PMID 26493944 DOI: 10.1002/Anie.201507939 |
0.411 |
|
2015 |
Taki M, Ogasawara H, Osaki H, Fukazawa A, Sato Y, Ogasawara K, Higashiyama T, Yamaguchi S. A red-emitting ratiometric fluorescent probe based on a benzophosphole P-oxide scaffold for the detection of intracellular sodium ions. Chemical Communications (Cambridge, England). 51: 11880-3. PMID 26110470 DOI: 10.1039/C5Cc03547C |
0.42 |
|
2015 |
Yamaguchi E, Wang C, Fukazawa A, Taki M, Sato Y, Sasaki T, Ueda M, Sasaki N, Higashiyama T, Yamaguchi S. Inside Cover: Environment-Sensitive Fluorescent Probe: A Benzophosphole Oxide with an Electron-Donating Substituent (Angew. Chem. Int. Ed. 15/2015) Angewandte Chemie International Edition. 54: 4404-4404. DOI: 10.1002/Anie.201502276 |
0.355 |
|
2015 |
Yamaguchi E, Wang C, Fukazawa A, Taki M, Sato Y, Sasaki T, Ueda M, Sasaki N, Higashiyama T, Yamaguchi S. Innentitelbild: Environment-Sensitive Fluorescent Probe: A Benzophosphole Oxide with an Electron-Donating Substituent (Angew. Chem. 15/2015) Angewandte Chemie. 127: 4480-4480. DOI: 10.1002/Ange.201502276 |
0.359 |
|
2014 |
Taki M, Akaoka K, Mitsui K, Yamamoto Y. A mitochondria-targeted turn-on fluorescent probe based on a rhodol platform for the detection of copper(i) Organic and Biomolecular Chemistry. 12: 4999-5005. PMID 24887562 DOI: 10.1039/C4Ob00527A |
0.386 |
|
2012 |
Taki M, Akaoka K, Iyoshi S, Yamamoto Y. Rosamine-based fluorescent sensor with femtomolar affinity for the reversible detection of a mercury ion. Inorganic Chemistry. 51: 13075-7. PMID 23186173 DOI: 10.1021/Ic301822R |
0.399 |
|
2012 |
Hirayama T, Taki M, Akaoka K, Yamamoto Y. Development of a dual functional luminescent sensor for zinc ion based on a peptidic architecture. Bioorganic & Medicinal Chemistry Letters. 22: 7410-3. PMID 23140887 DOI: 10.1016/J.Bmcl.2012.10.061 |
0.391 |
|
2011 |
Iyoshi S, Taki M, Yamamoto Y. Development of a cholesterol-conjugated fluorescent sensor for site-specific detection of zinc ion at the plasma membrane. Organic Letters. 13: 4558-61. PMID 21805969 DOI: 10.1021/Ol201746P |
0.327 |
|
2011 |
Taki M, Asahi F, Hirayama T, Yamamoto Y. Design and synthesis of fluorescent probe for polyhistidine tag using macrocyclic nickel(II) complex and fluorescein conjugate Bulletin of the Chemical Society of Japan. 84: 386-394. DOI: 10.1246/Bcsj.20100288 |
0.395 |
|
2010 |
Taki M, Iyoshi S, Ojida A, Hamachi I, Yamamoto Y. Development of highly sensitive fluorescent probes for detection of intracellular copper(I) in living systems. Journal of the American Chemical Society. 132: 5938-9. PMID 20377254 DOI: 10.1021/Ja100714P |
0.432 |
|
2009 |
Taki M, Watanabe Y, Yamamoto Y. Development of ratiometric fluorescent probe for zinc ion based on indole fluorophore Tetrahedron Letters. 50: 1345-1347. DOI: 10.1016/J.Tetlet.2009.01.026 |
0.465 |
|
2008 |
Taki M, Desaki M, Ojida A, Iyoshi S, Hirayama T, Hamachi I, Yamamoto Y. Fluorescence imaging of intracellular cadmium using a dual-excitation ratiometric chemosensor. Journal of the American Chemical Society. 130: 12564-5. PMID 18761452 DOI: 10.1021/Ja803429Z |
0.373 |
|
2008 |
Iyoshi S, Taki M, Yamamoto Y. Rosamine-based fluorescent chemosensor for selective detection of silver(I) in an aqueous solution. Inorganic Chemistry. 47: 3946-8. PMID 18433117 DOI: 10.1021/Ic800442Y |
0.388 |
|
2007 |
Hirayama T, Iyoshi S, Taki M, Maeda Y, Yamamoto Y. Synthesis of a new bifunctionalised fluorescent label and physical properties of the bound form on model peptide of troponin C. Organic & Biomolecular Chemistry. 5: 2040-5. PMID 17581646 DOI: 10.1039/B705704K |
0.331 |
|
2004 |
Taki M, Wolford JL, O'Halloran TV. Emission ratiometric imaging of intracellular zinc: design of a benzoxazole fluorescent sensor and its application in two-photon microscopy. Journal of the American Chemical Society. 126: 712-3. PMID 14733534 DOI: 10.1021/Ja039073J |
0.702 |
|
2004 |
Taki M, Hattori H, Osako T, Nagatomo S, Shiro M, Kitagawa T, Itoh S. Model complexes of the active site of galactose oxidase. Effects of the metal ion binding sites Inorganica Chimica Acta. 357: 3369-3381. DOI: 10.1016/J.Ica.2004.04.008 |
0.326 |
|
2003 |
Taki M, Wolford JL, O'Halloran TV. Emission ratiometric probes for zinc ion Journal of Inorganic Biochemistry. 96: 237. DOI: 10.1016/S0162-0134(03)80782-1 |
0.682 |
|
2002 |
Taki M, Teramae S, Nagatomo S, Tachi Y, Kitagawa T, Itoh S, Fukuzumi S. Fine-tuning of copper(I)-dioxygen reactivity by 2-(2-pyridyl)ethylamine bidentate ligands. Journal of the American Chemical Society. 124: 6367-77. PMID 12033867 DOI: 10.1021/Ja026047X |
0.305 |
|
2000 |
Taki M, Kumei H, Itoh S, Fukuzumi S. Hydrogen atom abstraction by Cu(II)- and Zn(II)-phenoxyl radical complexes, models for the active form of galactose oxidase Journal of Inorganic Biochemistry. 78: 1-5. PMID 10714699 DOI: 10.1016/S0162-0134(99)00198-1 |
0.313 |
|
2000 |
Taki M, Kumei H, Nagatomo S, Kitagawa T, Itoh S, Fukuzumi S. Active site models for galactose oxidase containing two different phenol groups Inorganica Chimica Acta. 300: 622-632. DOI: 10.1016/S0020-1693(99)00579-4 |
0.303 |
|
2000 |
Itoh S, Taki M, Fukuzumi S. Active site models for galactose oxidase and related enzymes Coordination Chemistry Reviews. 198: 3-20. DOI: 10.1016/S0010-8545(99)00209-X |
0.3 |
|
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