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[Studies on scoring norms and score tables of the Benton test in several developmental groups of normal children and the feeble-minded].

Seishin Igaku Kenkyujo gyosekishu = Bulletin of the Seishin-Igaku Institute

Makita H, Umezu K, Miyamoto C, Hitsuda A, Matsuoka H.
PMID: 5734303
Seishin Igaku Kenkyusho Gyosekishu. 1968;15:81-93.

No abstract available.

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Makita H, Umezu K, Miyamoto C, et al. [Studies on scoring norms and score tables of the Benton test in several developmental groups of normal children and the feeble-minded]. Seishin Igaku Kenkyusho Gyosekishu. 1968;15:81-93
Makita, H., Umezu, K., Miyamoto, C., Hitsuda, A., & Matsuoka, H. (1968). [Studies on scoring norms and score tables of the Benton test in several developmental groups of normal children and the feeble-minded]. Seishin Igaku Kenkyujo gyosekishu = Bulletin of the Seishin-Igaku Institute, 1581-93.
Makita, H, et al. "[Studies on scoring norms and score tables of the Benton test in several developmental groups of normal children and the feeble-minded]." Seishin Igaku Kenkyujo gyosekishu = Bulletin of the Seishin-Igaku Institute vol. 15 (1968): 81-93.
Makita H, Umezu K, Miyamoto C, Hitsuda A, Matsuoka H. [Studies on scoring norms and score tables of the Benton test in several developmental groups of normal children and the feeble-minded]. Seishin Igaku Kenkyusho Gyosekishu. 1968;15:81-93. Japanese. PMID: 5734303.
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Psychological Characteristics in Patients during Treatment for Tobacco Dependence.

Yonago acta medica

Matsuda A, Hasegawa J, Wang X, Tsuno S, Miura N.
PMID: 26306058
Yonago Acta Med. 2015 Jun;58(2):81-4. Epub 2015 Aug 18.

BACKGROUND: Few studies compare mood in tobacco cessation patients with mood in continuing smokers and then estimate the effects of a tobacco cessation program according to status of mood. We investigated whether mood in patients (n = 7) dependent...

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Matsuda A, Hasegawa J, Wang X, et al. Psychological Characteristics in Patients during Treatment for Tobacco Dependence. Yonago Acta Med. 2015;58(2):81-4
Matsuda, A., Hasegawa, J., Wang, X., Tsuno, S., & Miura, N. (2015). Psychological Characteristics in Patients during Treatment for Tobacco Dependence. Yonago acta medica, 58(2), 81-4.
Matsuda, Akiko, et al. "Psychological Characteristics in Patients during Treatment for Tobacco Dependence." Yonago acta medica vol. 58,2 (2015): 81-4.
Matsuda A, Hasegawa J, Wang X, Tsuno S, Miura N. Psychological Characteristics in Patients during Treatment for Tobacco Dependence. Yonago Acta Med. 2015 Jun;58(2):81-4. Epub 2015 Aug 18. PMID: 26306058; PMCID: PMC4546960.
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Photochromism in sound-induced alignment of a diarylethene supramolecular nanofibre.

Chemical communications (Cambridge, England)

Hotta Y, Fukushima S, Motoyanagi J, Tsuda A.
PMID: 25582095
Chem Commun (Camb). 2015 Feb 18;51(14):2790-3. doi: 10.1039/c4cc09702e.

A photochromic supramolecular nanofibre, composed of a diarylethene derivative, exhibits hydrodynamic alignment upon exposure to the audible sound. The aligned nanofibre outputs linear dichroism (LD), whose wavelength region can be switched reversibly with UV and visible light.

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Hotta Y, Fukushima S, Motoyanagi J, et al. Photochromism in sound-induced alignment of a diarylethene supramolecular nanofibre. Chem Commun (Camb). 2015;51(14):2790-3doi: 10.1039/c4cc09702e.
Hotta, Y., Fukushima, S., Motoyanagi, J., & Tsuda, A. (2015). Photochromism in sound-induced alignment of a diarylethene supramolecular nanofibre. Chemical communications (Cambridge, England), 51(14), 2790-3. https://doi.org/10.1039/c4cc09702e
Hotta, Yasuhisa, et al. "Photochromism in sound-induced alignment of a diarylethene supramolecular nanofibre." Chemical communications (Cambridge, England) vol. 51,14 (2015): 2790-3. doi: https://doi.org/10.1039/c4cc09702e
Hotta Y, Fukushima S, Motoyanagi J, Tsuda A. Photochromism in sound-induced alignment of a diarylethene supramolecular nanofibre. Chem Commun (Camb). 2015 Feb 18;51(14):2790-3. doi: 10.1039/c4cc09702e. PMID: 25582095.
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Control of reaction pathways in the photochemical reaction of a quinone with tetramethylethylene by metal binding.

Organic & biomolecular chemistry

Yamamoto H, Ohkubo K, Akimoto S, Fukuzumi S, Tsuda A.
PMID: 24947667
Org Biomol Chem. 2014 Sep 28;12(36):7004-17. doi: 10.1039/c4ob00659c.

The present study reports a novel supramolecular photochemical reaction that focuses on the direct electronic interactions between a host reaction substrate and guest metal salts. The reaction pathways in the photochemical reactions of quinone derivatives bearing a methoxy group...

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Yamamoto H, Ohkubo K, Akimoto S, et al. Control of reaction pathways in the photochemical reaction of a quinone with tetramethylethylene by metal binding. Org Biomol Chem. 2014;12(36):7004-17doi: 10.1039/c4ob00659c.
Yamamoto, H., Ohkubo, K., Akimoto, S., Fukuzumi, S., & Tsuda, A. (2014). Control of reaction pathways in the photochemical reaction of a quinone with tetramethylethylene by metal binding. Organic & biomolecular chemistry, 12(36), 7004-17. https://doi.org/10.1039/c4ob00659c
Yamamoto, Hiroaki, et al. "Control of reaction pathways in the photochemical reaction of a quinone with tetramethylethylene by metal binding." Organic & biomolecular chemistry vol. 12,36 (2014): 7004-17. doi: https://doi.org/10.1039/c4ob00659c
Yamamoto H, Ohkubo K, Akimoto S, Fukuzumi S, Tsuda A. Control of reaction pathways in the photochemical reaction of a quinone with tetramethylethylene by metal binding. Org Biomol Chem. 2014 Sep 28;12(36):7004-17. doi: 10.1039/c4ob00659c. PMID: 24947667.
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Carbacaprazamycins: Chemically Stable Analogues of the Caprazamycin Nucleoside Antibiotics.

ACS infectious diseases

Ichikawa S, Yamaguchi M, Hsuan LS, Kato Y, Matsuda A.
PMID: 27622529
ACS Infect Dis. 2015 Apr 10;1(4):151-6. doi: 10.1021/id5000376. Epub 2015 Feb 19.

Carbacaprazamycins, which are chemically stable analogues of caprazamycins, were designed and synthesized. These analogues were active against drug-resistant bacterial pathogens such as methicillin-resistant Staphylococcus aureus and vancomycin-resistant enterococci, and their activities were comparable to those of the parent caprazamycins....

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Ichikawa S, Yamaguchi M, Hsuan LS, et al. Carbacaprazamycins: Chemically Stable Analogues of the Caprazamycin Nucleoside Antibiotics. ACS Infect Dis. 2015;1(4):151-6doi: 10.1021/id5000376.
Ichikawa, S., Yamaguchi, M., Hsuan, L. S., Kato, Y., & Matsuda, A. (2015). Carbacaprazamycins: Chemically Stable Analogues of the Caprazamycin Nucleoside Antibiotics. ACS infectious diseases, 1(4), 151-6. https://doi.org/10.1021/id5000376
Ichikawa, Satoshi, et al. "Carbacaprazamycins: Chemically Stable Analogues of the Caprazamycin Nucleoside Antibiotics." ACS infectious diseases vol. 1,4 (2015): 151-6. doi: https://doi.org/10.1021/id5000376
Ichikawa S, Yamaguchi M, Hsuan LS, Kato Y, Matsuda A. Carbacaprazamycins: Chemically Stable Analogues of the Caprazamycin Nucleoside Antibiotics. ACS Infect Dis. 2015 Apr 10;1(4):151-6. doi: 10.1021/id5000376. Epub 2015 Feb 19. PMID: 27622529.
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Significant association between glycemic status and increased estimated postglomerular resistance in nondiabetic subjects - study of inulin and para-aminohippuric acid clearance in humans.

Physiological reports

Yasumoto M, Tsuda A, Ishimura E, Uedono H, Ohno Y, Ichii M, Ochi A, Nakatani S, Mori K, Uchida J, Emoto M, Nakatani T, Inaba M.
PMID: 25742958
Physiol Rep. 2015 Mar;3(3). doi: 10.14814/phy2.12321.

We investigated whether glomerular hemodynamic parameters in nondiabetic subjects, including healthy subjects, are associated with glycemic status indices, by simultaneous measurement of inulin (Cin) and para-aminohippuric acid (CPHA) clearance. Twenty-six subjects (age 49.5 ± 13.3 years; 13 men and...

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Yasumoto M, Tsuda A, Ishimura E, et al. Significant association between glycemic status and increased estimated postglomerular resistance in nondiabetic subjects - study of inulin and para-aminohippuric acid clearance in humans. Physiol Rep. 2015;3(3)doi: 10.14814/phy2.12321.
Yasumoto, M., Tsuda, A., Ishimura, E., Uedono, H., Ohno, Y., Ichii, M., Ochi, A., Nakatani, S., Mori, K., Uchida, J., Emoto, M., Nakatani, T., & Inaba, M. (2015). Significant association between glycemic status and increased estimated postglomerular resistance in nondiabetic subjects - study of inulin and para-aminohippuric acid clearance in humans. Physiological reports, 3(3), . https://doi.org/10.14814/phy2.12321
Yasumoto, Mari, et al. "Significant association between glycemic status and increased estimated postglomerular resistance in nondiabetic subjects - study of inulin and para-aminohippuric acid clearance in humans." Physiological reports vol. 3,3 (2015). doi: https://doi.org/10.14814/phy2.12321
Yasumoto M, Tsuda A, Ishimura E, Uedono H, Ohno Y, Ichii M, Ochi A, Nakatani S, Mori K, Uchida J, Emoto M, Nakatani T, Inaba M. Significant association between glycemic status and increased estimated postglomerular resistance in nondiabetic subjects - study of inulin and para-aminohippuric acid clearance in humans. Physiol Rep. 2015 Mar;3(3). doi: 10.14814/phy2.12321. PMID: 25742958; PMCID: PMC4393156.
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LecT-Hepa facilitates estimating treatment outcome during interferon therapy in chronic hepatitis C patients.

Clinical proteomics

Zou X, Chi X, Pan Y, Du D, Sun H, Matsuda A, Li W, Kuno A, Zhang X, Narimatsu H, Niu J, Zhang Y.
PMID: 25593566
Clin Proteomics. 2014 Dec 11;11(1):44. doi: 10.1186/1559-0275-11-44. eCollection 2014.

BACKGROUND: A combination treatment of interferon and ribavirin is the standard and the commonly used treatment for chronic hepatitis C (CHC). Developing noninvasive tests like serum indicators that can predict treatment outcome at an early stage of therapy is...

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Zou X, Chi X, Pan Y, et al. LecT-Hepa facilitates estimating treatment outcome during interferon therapy in chronic hepatitis C patients. Clin Proteomics. 2014;11(1):44doi: 10.1186/1559-0275-11-44.
Zou, X., Chi, X., Pan, Y., Du, D., Sun, H., Matsuda, A., Li, W., Kuno, A., Zhang, X., Narimatsu, H., Niu, J., & Zhang, Y. (2014). LecT-Hepa facilitates estimating treatment outcome during interferon therapy in chronic hepatitis C patients. Clinical proteomics, 11(1), 44. https://doi.org/10.1186/1559-0275-11-44
Zou, Xia, et al. "LecT-Hepa facilitates estimating treatment outcome during interferon therapy in chronic hepatitis C patients." Clinical proteomics vol. 11,1 (2014): 44. doi: https://doi.org/10.1186/1559-0275-11-44
Zou X, Chi X, Pan Y, Du D, Sun H, Matsuda A, Li W, Kuno A, Zhang X, Narimatsu H, Niu J, Zhang Y. LecT-Hepa facilitates estimating treatment outcome during interferon therapy in chronic hepatitis C patients. Clin Proteomics. 2014 Dec 11;11(1):44. doi: 10.1186/1559-0275-11-44. eCollection 2014. PMID: 25593566; PMCID: PMC4276098.
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Doubly meso-beta-Linked Diporphyrins from Oxidation of 5,10,15-Triaryl-Substituted Ni(II)- and Pd(II) - Porphyrins.

Angewandte Chemie (International ed. in English)

Tsuda A, Nakano A, Furuta H, Yamochi H, Osuka A.
PMID: 10671257
Angew Chem Int Ed Engl. 2000 Feb;39(3):558-561. doi: 10.1002/(sici)1521-3773(20000204)39:3<558::aid-anie558>3.0.co;2-g.

Lower oxidation potentials than for the monomeric starting materials are displayed by the diporphyrins obtained by one-electron oxidation with tris(4-bromophenyl)ammonium hexachloroantimonate [see, for example, Eq. (1)]. This and the strong red shift observed for the Soret bands of the...

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Tsuda A, Nakano A, Furuta H, et al. Doubly meso-beta-Linked Diporphyrins from Oxidation of 5,10,15-Triaryl-Substituted Ni(II)- and Pd(II) - Porphyrins. Angew Chem Int Ed Engl. 2000;39(3):558-561doi: 10.1002/(sici)1521-3773(20000204)39:3<558::aid-anie558>3.0.co;2-g.
Tsuda, A., Nakano, A., Furuta, H., Yamochi, H., & Osuka, A. (2000). Doubly meso-beta-Linked Diporphyrins from Oxidation of 5,10,15-Triaryl-Substituted Ni(II)- and Pd(II) - Porphyrins. Angewandte Chemie (International ed. in English), 39(3), 558-561. https://doi.org/10.1002/(sici)1521-3773(20000204)39:3<558::aid-anie558>3.0.co;2-g
Tsuda, et al. "Doubly meso-beta-Linked Diporphyrins from Oxidation of 5,10,15-Triaryl-Substituted Ni(II)- and Pd(II) - Porphyrins." Angewandte Chemie (International ed. in English) vol. 39,3 (2000): 558-561. doi: https://doi.org/10.1002/(sici)1521-3773(20000204)39:3<558::aid-anie558>3.0.co;2-g
Tsuda A, Nakano A, Furuta H, Yamochi H, Osuka A. Doubly meso-beta-Linked Diporphyrins from Oxidation of 5,10,15-Triaryl-Substituted Ni(II)- and Pd(II) - Porphyrins. Angew Chem Int Ed Engl. 2000 Feb;39(3):558-561. doi: 10.1002/(sici)1521-3773(20000204)39:3<558::aid-anie558>3.0.co;2-g. PMID: 10671257.
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Nucleosides and Nucleotides. 151. Conversion of (Z)-2'-(Cyanomethylene)-2'-deoxyuridines into Their (E)-Isomers via Addition of Thiophenol to the Cyanomethylene Moiety Followed by Oxidative Syn-elimination Reactions(1).

The Journal of organic chemistry

Hassan AE, Nishizono N, Minakawa N, Shuto S, Matsuda A.
PMID: 11667465
J Org Chem. 1996 Sep 06;61(18):6261-6267. doi: 10.1021/jo960577s.

The Wittig reaction of 1-[3,5-O-(1,1,3,3-tetraisopropyldisiloxane-1,3-diyl)-beta-D-erythro-pentofuranos-2-ulosyl]uracil (6) with Ph(3)P=CHCN afforded (Z)-2'-cyanomethylene derivative 7 exclusively. The (E)-isomer was accessed from its (Z)-isomer through a sequence of addition of thiophenol to the 2'-cyanomethylene moiety of the (Z)-isomer from the alpha-face, selectively, and...

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Hassan AE, Nishizono N, Minakawa N, et al. Nucleosides and Nucleotides. 151. Conversion of (Z)-2'-(Cyanomethylene)-2'-deoxyuridines into Their (E)-Isomers via Addition of Thiophenol to the Cyanomethylene Moiety Followed by Oxidative Syn-elimination Reactions(1). J Org Chem. 1996;61(18):6261-6267doi: 10.1021/jo960577s.
Hassan, A. E., Nishizono, N., Minakawa, N., Shuto, S., & Matsuda, A. (1996). Nucleosides and Nucleotides. 151. Conversion of (Z)-2'-(Cyanomethylene)-2'-deoxyuridines into Their (E)-Isomers via Addition of Thiophenol to the Cyanomethylene Moiety Followed by Oxidative Syn-elimination Reactions(1). The Journal of organic chemistry, 61(18), 6261-6267. https://doi.org/10.1021/jo960577s
Hassan, Abdalla E. A., et al. "Nucleosides and Nucleotides. 151. Conversion of (Z)-2'-(Cyanomethylene)-2'-deoxyuridines into Their (E)-Isomers via Addition of Thiophenol to the Cyanomethylene Moiety Followed by Oxidative Syn-elimination Reactions(1)." The Journal of organic chemistry vol. 61,18 (1996): 6261-6267. doi: https://doi.org/10.1021/jo960577s
Hassan AE, Nishizono N, Minakawa N, Shuto S, Matsuda A. Nucleosides and Nucleotides. 151. Conversion of (Z)-2'-(Cyanomethylene)-2'-deoxyuridines into Their (E)-Isomers via Addition of Thiophenol to the Cyanomethylene Moiety Followed by Oxidative Syn-elimination Reactions(1). J Org Chem. 1996 Sep 06;61(18):6261-6267. doi: 10.1021/jo960577s. PMID: 11667465.
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Completely Fused Diporphyrins and Triporphyrin This work was supported by Grant-in-Aids for Scientific Research (No. 11223205) from the Ministry of Education, Science, Sports, and Culture of Japan and by CREST (Core Research for Evolutional Science and Technology) of Japan Science and Technology Corporation (JST). A.T. thanks the JSPS Research Fellowship for Young Scientists. We also thank Dr. M. Shiro of the Rigaku Corporation for his help in obtaining the single-crystal X-ray data of 5.

Angewandte Chemie (International ed. in English)

Tsuda A, Furuta H, Osuka A.
PMID: 10941132
Angew Chem Int Ed Engl. 2000 Jul 17;39(14):2549-2552. doi: 10.1002/1521-3773(20000717)39:14<2549::aid-anie2549>3.0.co;2-a.

No abstract available.

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Tsuda A, Furuta H, Osuka A. Completely Fused Diporphyrins and Triporphyrin This work was supported by Grant-in-Aids for Scientific Research (No. 11223205) from the Ministry of Education, Science, Sports, and Culture of Japan and by CREST (Core Research for Evolutional Science and Technology) of Japan Science and Technology Corporation (JST). A.T. thanks the JSPS Research Fellowship for Young Scientists. We also thank Dr. M. Shiro of the Rigaku Corporation for his help in obtaining the single-crystal X-ray data of 5. Angew Chem Int Ed Engl. 2000;39(14):2549-2552doi: 10.1002/1521-3773(20000717)39:14<2549::aid-anie2549>3.0.co;2-a.
Tsuda, A., Furuta, H., & Osuka, A. (2000). Completely Fused Diporphyrins and Triporphyrin This work was supported by Grant-in-Aids for Scientific Research (No. 11223205) from the Ministry of Education, Science, Sports, and Culture of Japan and by CREST (Core Research for Evolutional Science and Technology) of Japan Science and Technology Corporation (JST). A.T. thanks the JSPS Research Fellowship for Young Scientists. We also thank Dr. M. Shiro of the Rigaku Corporation for his help in obtaining the single-crystal X-ray data of 5. Angewandte Chemie (International ed. in English), 39(14), 2549-2552. https://doi.org/10.1002/1521-3773(20000717)39:14<2549::aid-anie2549>3.0.co;2-a
Tsuda, et al. "Completely Fused Diporphyrins and Triporphyrin This work was supported by Grant-in-Aids for Scientific Research (No. 11223205) from the Ministry of Education, Science, Sports, and Culture of Japan and by CREST (Core Research for Evolutional Science and Technology) of Japan Science and Technology Corporation (JST). A.T. thanks the JSPS Research Fellowship for Young Scientists. We also thank Dr. M. Shiro of the Rigaku Corporation for his help in obtaining the single-crystal X-ray data of 5." Angewandte Chemie (International ed. in English) vol. 39,14 (2000): 2549-2552. doi: https://doi.org/10.1002/1521-3773(20000717)39:14<2549::aid-anie2549>3.0.co;2-a
Tsuda A, Furuta H, Osuka A. Completely Fused Diporphyrins and Triporphyrin This work was supported by Grant-in-Aids for Scientific Research (No. 11223205) from the Ministry of Education, Science, Sports, and Culture of Japan and by CREST (Core Research for Evolutional Science and Technology) of Japan Science and Technology Corporation (JST). A.T. thanks the JSPS Research Fellowship for Young Scientists. We also thank Dr. M. Shiro of the Rigaku Corporation for his help in obtaining the single-crystal X-ray data of 5. Angew Chem Int Ed Engl. 2000 Jul 17;39(14):2549-2552. doi: 10.1002/1521-3773(20000717)39:14<2549::aid-anie2549>3.0.co;2-a. PMID: 10941132.
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Self-activated supramolecular reactions: effects of host-guest recognition on the kinetics of the Diels-Alder reaction of open-chain oligoether quinones with cyclopentadiene.

Journal of the American Chemical Society

Tsuda A, Fukumoto C, Oshima T.
PMID: 12733922
J Am Chem Soc. 2003 May 14;125(19):5811-22. doi: 10.1021/ja021444t.

Diels-Alder reactions of acyclic oligoether-substituted quinones 1b, 1c, 2b, and 2c with cyclopentadiene were accelerated by the addition of alkali and alkaline earth metal perchlorates, and scandium trifluoromethane sulfonate (k(c)/k(f) = 1.2-23 for univalent cations, 11-1160 for divalent cations,...

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Tsuda A, Fukumoto C, Oshima T. Self-activated supramolecular reactions: effects of host-guest recognition on the kinetics of the Diels-Alder reaction of open-chain oligoether quinones with cyclopentadiene. J Am Chem Soc. 2003;125(19):5811-22doi: 10.1021/ja021444t.
Tsuda, A., Fukumoto, C., & Oshima, T. (2003). Self-activated supramolecular reactions: effects of host-guest recognition on the kinetics of the Diels-Alder reaction of open-chain oligoether quinones with cyclopentadiene. Journal of the American Chemical Society, 125(19), 5811-22. https://doi.org/10.1021/ja021444t
Tsuda, Akihiko, et al. "Self-activated supramolecular reactions: effects of host-guest recognition on the kinetics of the Diels-Alder reaction of open-chain oligoether quinones with cyclopentadiene." Journal of the American Chemical Society vol. 125,19 (2003): 5811-22. doi: https://doi.org/10.1021/ja021444t
Tsuda A, Fukumoto C, Oshima T. Self-activated supramolecular reactions: effects of host-guest recognition on the kinetics of the Diels-Alder reaction of open-chain oligoether quinones with cyclopentadiene. J Am Chem Soc. 2003 May 14;125(19):5811-22. doi: 10.1021/ja021444t. PMID: 12733922.
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Synthesis of meso-beta doubly linked porphyrin tapes.

Chemical communications (Cambridge, England)

Tsuda A, Nakamura Y, Osuka A.
PMID: 12772920
Chem Commun (Camb). 2003 May 07;(9):1096-7. doi: 10.1039/b302032k.

The oxidation of 5,15-bis(3,5-di-tert-butylphenyl) Ni(II)-porphyrin 1b with Sc(OTf)3 and DDQ led to production of meso-beta doubly linked Ni(II)-porphyrin tapes that have large pi-electronic communications over the arrays.

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Tsuda A, Nakamura Y, Osuka A. Synthesis of meso-beta doubly linked porphyrin tapes. Chem Commun (Camb). 2003;(9):1096-7doi: 10.1039/b302032k.
Tsuda, A., Nakamura, Y., & Osuka, A. (2003). Synthesis of meso-beta doubly linked porphyrin tapes. Chemical communications (Cambridge, England), (9), 1096-7. https://doi.org/10.1039/b302032k
Tsuda, Akihiko, et al. "Synthesis of meso-beta doubly linked porphyrin tapes." Chemical communications (Cambridge, England) vol. ,9 (2003): 1096-7. doi: https://doi.org/10.1039/b302032k
Tsuda A, Nakamura Y, Osuka A. Synthesis of meso-beta doubly linked porphyrin tapes. Chem Commun (Camb). 2003 May 07;(9):1096-7. doi: 10.1039/b302032k. PMID: 12772920.
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