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State dependence of climatic instability over the past 720,000 years from Antarctic ice cores and climate modeling.

Science advances

, Kawamura K, Abe-Ouchi A, Motoyama H, Ageta Y, Aoki S, Azuma N, Fujii Y, Fujita K, Fujita S, Fukui K, Furukawa T, Furusaki A, Goto-Azuma K, Greve R, Hirabayashi M, Hondoh T, Hori A, Horikawa S, Horiuchi K, Igarashi M, Iizuka Y, Kameda T, Kanda H, Kohno M, Kuramoto T, Matsushi Y, Miyahara M, Miyake T, Miyamoto A, Nagashima Y, Nakayama Y, Nakazawa T, Nakazawa F, Nishio F, Obinata I, Ohgaito R, Oka A, Okuno J, Okuyama J, Oyabu I, Parrenin F, Pattyn F, Saito F, Saito T, Saito T, Sakurai T, Sasa K, Seddik H, Shibata Y, Shinbori K, Suzuki K, Suzuki T, Takahashi A, Takahashi K, Takahashi S, Takata M, Tanaka Y, Uemura R, Watanabe G, Watanabe O, Yamasaki T, Yokoyama K, Yoshimori M, Yoshimoto T.
PMID: 28246631
Sci Adv. 2017 Feb 08;3(2):e1600446. doi: 10.1126/sciadv.1600446. eCollection 2017 Feb.

Climatic variabilities on millennial and longer time scales with a bipolar seesaw pattern have been documented in paleoclimatic records, but their frequencies, relationships with mean climatic state, and mechanisms remain unclear. Understanding the processes and sensitivities that underlie these...

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, Kawamura K, Abe-Ouchi A, et al. State dependence of climatic instability over the past 720,000 years from Antarctic ice cores and climate modeling. Sci Adv. 2017;3(2):e1600446doi: 10.1126/sciadv.1600446.
, Kawamura, K., Abe-Ouchi, A., Motoyama, H., Ageta, Y., Aoki, S., Azuma, N., Fujii, Y., Fujita, K., Fujita, S., Fukui, K., Furukawa, T., Furusaki, A., Goto-Azuma, K., Greve, R., Hirabayashi, M., Hondoh, T., Hori, A., Horikawa, S., Horiuchi, K., Igarashi, M., Iizuka, Y., Kameda, T., Kanda, H., Kohno, M., Kuramoto, T., Matsushi, Y., Miyahara, M., Miyake, T., Miyamoto, A., Nagashima, Y., Nakayama, Y., Nakazawa, T., Nakazawa, F., Nishio, F., Obinata, I., Ohgaito, R., Oka, A., Okuno, J., Okuyama, J., Oyabu, I., Parrenin, F., Pattyn, F., Saito, F., Saito, T., Saito, T., Sakurai, T., Sasa, K., Seddik, H., Shibata, Y., Shinbori, K., Suzuki, K., Suzuki, T., Takahashi, A., Takahashi, K., Takahashi, S., Takata, M., Tanaka, Y., Uemura, R., Watanabe, G., Watanabe, O., Yamasaki, T., Yokoyama, K., Yoshimori, M., & Yoshimoto, T. (2017). State dependence of climatic instability over the past 720,000 years from Antarctic ice cores and climate modeling. Science advances, 3(2), e1600446. https://doi.org/10.1126/sciadv.1600446
, et al. "State dependence of climatic instability over the past 720,000 years from Antarctic ice cores and climate modeling." Science advances vol. 3,2 (2017): e1600446. doi: https://doi.org/10.1126/sciadv.1600446
, Kawamura K, Abe-Ouchi A, Motoyama H, Ageta Y, Aoki S, Azuma N, Fujii Y, Fujita K, Fujita S, Fukui K, Furukawa T, Furusaki A, Goto-Azuma K, Greve R, Hirabayashi M, Hondoh T, Hori A, Horikawa S, Horiuchi K, Igarashi M, Iizuka Y, Kameda T, Kanda H, Kohno M, Kuramoto T, Matsushi Y, Miyahara M, Miyake T, Miyamoto A, Nagashima Y, Nakayama Y, Nakazawa T, Nakazawa F, Nishio F, Obinata I, Ohgaito R, Oka A, Okuno J, Okuyama J, Oyabu I, Parrenin F, Pattyn F, Saito F, Saito T, Saito T, Sakurai T, Sasa K, Seddik H, Shibata Y, Shinbori K, Suzuki K, Suzuki T, Takahashi A, Takahashi K, Takahashi S, Takata M, Tanaka Y, Uemura R, Watanabe G, Watanabe O, Yamasaki T, Yokoyama K, Yoshimori M, Yoshimoto T. State dependence of climatic instability over the past 720,000 years from Antarctic ice cores and climate modeling. Sci Adv. 2017 Feb 08;3(2):e1600446. doi: 10.1126/sciadv.1600446. eCollection 2017 Feb. PMID: 28246631; PMCID: PMC5298857.
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[Health counseling for housewives at St. Luke's Hospital].

[Hokenfu zasshi] The Japanese journal for public health nurse

Matsushita K, Sugimoto K, Sato H, Ando Y, Shinbo A.
PMID: 5191599
Hokenfu Zasshi. 1969 Feb;25(2):10-21.

No abstract available.

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Matsushita K, Sugimoto K, Sato H, et al. [Health counseling for housewives at St. Luke's Hospital]. Hokenfu Zasshi. 1969;25(2):10-21
Matsushita, K., Sugimoto, K., Sato, H., Ando, Y., & Shinbo, A. (1969). [Health counseling for housewives at St. Luke's Hospital]. [Hokenfu zasshi] The Japanese journal for public health nurse, 25(2), 10-21.
Matsushita, K, et al. "[Health counseling for housewives at St. Luke's Hospital]." [Hokenfu zasshi] The Japanese journal for public health nurse vol. 25,2 (1969): 10-21.
Matsushita K, Sugimoto K, Sato H, Ando Y, Shinbo A. [Health counseling for housewives at St. Luke's Hospital]. Hokenfu Zasshi. 1969 Feb;25(2):10-21. Japanese. PMID: 5191599.
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Dihedral-angle modulation of meso-meso-linked ZnII diporphyrin through diamine coordination and its application to reversible switching of excitation energy transfer.

Angewandte Chemie (International ed. in English)

Shinmori H, Ahn TK, Cho HS, Kim D, Yoshida N, Osuka A.
PMID: 12820259
Angew Chem Int Ed Engl. 2003 Jun 23;42(24):2754-8. doi: 10.1002/anie.200351177.

No abstract available.

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Shinmori H, Ahn TK, Cho HS, et al. Dihedral-angle modulation of meso-meso-linked ZnII diporphyrin through diamine coordination and its application to reversible switching of excitation energy transfer. Angew Chem Int Ed Engl. 2003;42(24):2754-8doi: 10.1002/anie.200351177.
Shinmori, H., Ahn, T. K., Cho, H. S., Kim, D., Yoshida, N., & Osuka, A. (2003). Dihedral-angle modulation of meso-meso-linked ZnII diporphyrin through diamine coordination and its application to reversible switching of excitation energy transfer. Angewandte Chemie (International ed. in English), 42(24), 2754-8. https://doi.org/10.1002/anie.200351177
Shinmori, Hideyuki, et al. "Dihedral-angle modulation of meso-meso-linked ZnII diporphyrin through diamine coordination and its application to reversible switching of excitation energy transfer." Angewandte Chemie (International ed. in English) vol. 42,24 (2003): 2754-8. doi: https://doi.org/10.1002/anie.200351177
Shinmori H, Ahn TK, Cho HS, Kim D, Yoshida N, Osuka A. Dihedral-angle modulation of meso-meso-linked ZnII diporphyrin through diamine coordination and its application to reversible switching of excitation energy transfer. Angew Chem Int Ed Engl. 2003 Jun 23;42(24):2754-8. doi: 10.1002/anie.200351177. PMID: 12820259.
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The Space Physics Environment Data Analysis System (SPEDAS).

Space science reviews

Angelopoulos V, Cruce P, Drozdov A, Grimes EW, Hatzigeorgiu N, King DA, Larson D, Lewis JW, McTiernan JM, Roberts DA, Russell CL, Hori T, Kasahara Y, Kumamoto A, Matsuoka A, Miyashita Y, Miyoshi Y, Shinohara I, Teramoto M, Faden JB, Halford AJ, McCarthy M, Millan RM, Sample JG, Smith DM, Woodger LA, Masson A, Narock AA, Asamura K, Chang TF, Chiang CY, Kazama Y, Keika K, Matsuda S, Segawa T, Seki K, Shoji M, Tam SWY, Umemura N, Wang BJ, Wang SY, Redmon R, Rodriguez JV, Singer HJ, Vandegriff J, Abe S, Nose M, Shinbori A, Tanaka YM, UeNo S, Andersson L, Dunn P, Fowler C, Halekas JS, Hara T, Harada Y, Lee CO, Lillis R, Mitchell DL, Argall MR, Bromund K, Burch JL, Cohen IJ, Galloy M, Giles B, Jaynes AN, Le Contel O, Oka M, Phan TD, Walsh BM, Westlake J, Wilder FD, Bale SD, Livi R, Pulupa M, Whittlesey P, DeWolfe A, Harter B, Lucas E, Auster U, Bonnell JW, Cully CM, Donovan E, Ergun RE, Frey HU, Jackel B, Keiling A, Korth H, McFadden JP, Nishimura Y, Plaschke F, Robert P, Turner DL, Weygand JM, Candey RM, Johnson RC, Kovalick T, Liu MH, McGuire RE, Breneman A, Kersten K, Schroeder P.
PMID: 30880847
Space Sci Rev. 2019;215(1):9. doi: 10.1007/s11214-018-0576-4. Epub 2019 Jan 22.

With the advent of the Heliophysics/Geospace System Observatory (H/GSO), a complement of multi-spacecraft missions and ground-based observatories to study the space environment, data retrieval, analysis, and visualization of space physics data can be daunting. The Space Physics Environment Data...

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Angelopoulos V, Cruce P, Drozdov A, et al. The Space Physics Environment Data Analysis System (SPEDAS). Space Sci Rev. 2019;215(1):9doi: 10.1007/s11214-018-0576-4.
Angelopoulos, V., Cruce, P., Drozdov, A., Grimes, E. W., Hatzigeorgiu, N., King, D. A., Larson, D., Lewis, J. W., McTiernan, J. M., Roberts, D. A., Russell, C. L., Hori, T., Kasahara, Y., Kumamoto, A., Matsuoka, A., Miyashita, Y., Miyoshi, Y., Shinohara, I., Teramoto, M., Faden, J. B., Halford, A. J., McCarthy, M., Millan, R. M., Sample, J. G., Smith, D. M., Woodger, L. A., Masson, A., Narock, A. A., Asamura, K., Chang, T. F., Chiang, C. Y., Kazama, Y., Keika, K., Matsuda, S., Segawa, T., Seki, K., Shoji, M., Tam, S. W. Y., Umemura, N., Wang, B. J., Wang, S. Y., Redmon, R., Rodriguez, J. V., Singer, H. J., Vandegriff, J., Abe, S., Nose, M., Shinbori, A., Tanaka, Y. M., UeNo, S., Andersson, L., Dunn, P., Fowler, C., Halekas, J. S., Hara, T., Harada, Y., Lee, C. O., Lillis, R., Mitchell, D. L., Argall, M. R., Bromund, K., Burch, J. L., Cohen, I. J., Galloy, M., Giles, B., Jaynes, A. N., Le Contel, O., Oka, M., Phan, T. D., Walsh, B. M., Westlake, J., Wilder, F. D., Bale, S. D., Livi, R., Pulupa, M., Whittlesey, P., DeWolfe, A., Harter, B., Lucas, E., Auster, U., Bonnell, J. W., Cully, C. M., Donovan, E., Ergun, R. E., Frey, H. U., Jackel, B., Keiling, A., Korth, H., McFadden, J. P., Nishimura, Y., Plaschke, F., Robert, P., Turner, D. L., Weygand, J. M., Candey, R. M., Johnson, R. C., Kovalick, T., Liu, M. H., McGuire, R. E., Breneman, A., Kersten, K., & Schroeder, P. (2019). The Space Physics Environment Data Analysis System (SPEDAS). Space science reviews, 215(1), 9. https://doi.org/10.1007/s11214-018-0576-4
Angelopoulos, V, et al. "The Space Physics Environment Data Analysis System (SPEDAS)." Space science reviews vol. 215,1 (2019): 9. doi: https://doi.org/10.1007/s11214-018-0576-4
Angelopoulos V, Cruce P, Drozdov A, Grimes EW, Hatzigeorgiu N, King DA, Larson D, Lewis JW, McTiernan JM, Roberts DA, Russell CL, Hori T, Kasahara Y, Kumamoto A, Matsuoka A, Miyashita Y, Miyoshi Y, Shinohara I, Teramoto M, Faden JB, Halford AJ, McCarthy M, Millan RM, Sample JG, Smith DM, Woodger LA, Masson A, Narock AA, Asamura K, Chang TF, Chiang CY, Kazama Y, Keika K, Matsuda S, Segawa T, Seki K, Shoji M, Tam SWY, Umemura N, Wang BJ, Wang SY, Redmon R, Rodriguez JV, Singer HJ, Vandegriff J, Abe S, Nose M, Shinbori A, Tanaka YM, UeNo S, Andersson L, Dunn P, Fowler C, Halekas JS, Hara T, Harada Y, Lee CO, Lillis R, Mitchell DL, Argall MR, Bromund K, Burch JL, Cohen IJ, Galloy M, Giles B, Jaynes AN, Le Contel O, Oka M, Phan TD, Walsh BM, Westlake J, Wilder FD, Bale SD, Livi R, Pulupa M, Whittlesey P, DeWolfe A, Harter B, Lucas E, Auster U, Bonnell JW, Cully CM, Donovan E, Ergun RE, Frey HU, Jackel B, Keiling A, Korth H, McFadden JP, Nishimura Y, Plaschke F, Robert P, Turner DL, Weygand JM, Candey RM, Johnson RC, Kovalick T, Liu MH, McGuire RE, Breneman A, Kersten K, Schroeder P. The Space Physics Environment Data Analysis System (SPEDAS). Space Sci Rev. 2019;215(1):9. doi: 10.1007/s11214-018-0576-4. Epub 2019 Jan 22. PMID: 30880847; PMCID: PMC6380193.
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Hydrogen Sulfide Mediates Tumor Cell Resistance to Thioredoxin Inhibitor.

Frontiers in oncology

Mao Z, Yang X, Mizutani S, Huang Y, Zhang Z, Shinmori H, Gao K, Yao J.
PMID: 32219063
Front Oncol. 2020 Mar 10;10:252. doi: 10.3389/fonc.2020.00252. eCollection 2020.

Thioredoxin (Trx) is a pro-oncogenic molecule that underlies tumor initiation, progression and chemo-resistance. PX-12, a Trx inhibitor, has been used to treat certain tumors. Currently, factors predicting tumor sensitivity to PX-12 are unclear. Given that hydrogen sulfide (H

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Mao Z, Yang X, Mizutani S, et al. Hydrogen Sulfide Mediates Tumor Cell Resistance to Thioredoxin Inhibitor. Front Oncol. 2020;10:252doi: 10.3389/fonc.2020.00252.
Mao, Z., Yang, X., Mizutani, S., Huang, Y., Zhang, Z., Shinmori, H., Gao, K., & Yao, J. (2020). Hydrogen Sulfide Mediates Tumor Cell Resistance to Thioredoxin Inhibitor. Frontiers in oncology, 10252. https://doi.org/10.3389/fonc.2020.00252
Mao, Zhimin, et al. "Hydrogen Sulfide Mediates Tumor Cell Resistance to Thioredoxin Inhibitor." Frontiers in oncology vol. 10 (2020): 252. doi: https://doi.org/10.3389/fonc.2020.00252
Mao Z, Yang X, Mizutani S, Huang Y, Zhang Z, Shinmori H, Gao K, Yao J. Hydrogen Sulfide Mediates Tumor Cell Resistance to Thioredoxin Inhibitor. Front Oncol. 2020 Mar 10;10:252. doi: 10.3389/fonc.2020.00252. eCollection 2020. PMID: 32219063; PMCID: PMC7078679.
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Improved Stability and Photodynamic Activity of Water-Soluble 5,15-Diazaporphyrins Incorporated in β-(1,3-1,6)-d-Glucan with On-Off Switch.

Chemistry, an Asian journal

Hino S, Satake S, Shinmori H, Kawabata S, Koumoto K, Suzuki T, Nagasaki T, Sugikawa K, Kawasaki R, Ikeda A.
PMID: 31828944
Chem Asian J. 2020 Feb 03;15(3):365-370. doi: 10.1002/asia.201901582. Epub 2019 Dec 30.

5,15-Diazaporphyrins, which have a large absorption at wavelengths over 600 nm, were dissolved in water by complex formation with β-(1,3-1,6)-d-glucans. Aqueous solutions of these complexes were relatively stable compared with their trimethyl-β-cyclodextrin-complexed analogues. β-Glucan-complexed diazaporphyrins showed quenched fluorescence and...

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Hino S, Satake S, Shinmori H, et al. Improved Stability and Photodynamic Activity of Water-Soluble 5,15-Diazaporphyrins Incorporated in β-(1,3-1,6)-d-Glucan with On-Off Switch. Chem Asian J. 2019;15(3):365-370doi: 10.1002/asia.201901582.
Hino, S., Satake, S., Shinmori, H., Kawabata, S., Koumoto, K., Suzuki, T., Nagasaki, T., Sugikawa, K., Kawasaki, R., & Ikeda, A. (2020). Improved Stability and Photodynamic Activity of Water-Soluble 5,15-Diazaporphyrins Incorporated in β-(1,3-1,6)-d-Glucan with On-Off Switch. Chemistry, an Asian journal, 15(3), 365-370. https://doi.org/10.1002/asia.201901582
Hino, Shodai, et al. "Improved Stability and Photodynamic Activity of Water-Soluble 5,15-Diazaporphyrins Incorporated in β-(1,3-1,6)-d-Glucan with On-Off Switch." Chemistry, an Asian journal vol. 15,3 (2020): 365-370. doi: https://doi.org/10.1002/asia.201901582
Hino S, Satake S, Shinmori H, Kawabata S, Koumoto K, Suzuki T, Nagasaki T, Sugikawa K, Kawasaki R, Ikeda A. Improved Stability and Photodynamic Activity of Water-Soluble 5,15-Diazaporphyrins Incorporated in β-(1,3-1,6)-d-Glucan with On-Off Switch. Chem Asian J. 2020 Feb 03;15(3):365-370. doi: 10.1002/asia.201901582. Epub 2019 Dec 30. PMID: 31828944.
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Characterization of single nucleotide polymorphisms for a forward genetics approach using genetic crosses in C57BL/6 and BALB/c substrains of mice.

Experimental animals

Miura I, Kikkawa Y, Yasuda SP, Shinogi A, Usuda D, Kumar V, Takahashi JS, Tamura M, Masuya H, Wakana S.
PMID: 34980769
Exp Anim. 2021 Dec 28; doi: 10.1538/expanim.21-0181. Epub 2021 Dec 28.

Forward genetics is a powerful approach based on chromosomal mapping of phenotypes and has successfully led to the discovery of many mouse mutations in genes responsible for various phenotypes. Although crossing between genetically remote strains can produce F

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Miura I, Kikkawa Y, Yasuda SP, et al. Characterization of single nucleotide polymorphisms for a forward genetics approach using genetic crosses in C57BL/6 and BALB/c substrains of mice. Exp Anim. 2021;doi: 10.1538/expanim.21-0181.
Miura, I., Kikkawa, Y., Yasuda, S. P., Shinogi, A., Usuda, D., Kumar, V., Takahashi, J. S., Tamura, M., Masuya, H., & Wakana, S. (2021). Characterization of single nucleotide polymorphisms for a forward genetics approach using genetic crosses in C57BL/6 and BALB/c substrains of mice. Experimental animals, . https://doi.org/10.1538/expanim.21-0181
Miura, Ikuo, et al. "Characterization of single nucleotide polymorphisms for a forward genetics approach using genetic crosses in C57BL/6 and BALB/c substrains of mice." Experimental animals vol. (2021). doi: https://doi.org/10.1538/expanim.21-0181
Miura I, Kikkawa Y, Yasuda SP, Shinogi A, Usuda D, Kumar V, Takahashi JS, Tamura M, Masuya H, Wakana S. Characterization of single nucleotide polymorphisms for a forward genetics approach using genetic crosses in C57BL/6 and BALB/c substrains of mice. Exp Anim. 2021 Dec 28; doi: 10.1538/expanim.21-0181. Epub 2021 Dec 28. PMID: 34980769.
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Atrazine transforming polymer prepared by molecular imprinting with post-imprinting process.

Organic & biomolecular chemistry

Yane T, Shinmori H, Takeuchi T.
PMID: 17268641
Org Biomol Chem. 2006 Dec 21;4(24):4469-73. doi: 10.1039/b612407k. Epub 2006 Nov 08.

Molecularly imprinted polymers bearing atrazine transforming activity were prepared by using newly designed templates that are atrazine analogues attached with an allyl or a styryl group via a disulfide bond at the 6-position, methacrylic acid as a functional monomer...

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Yane T, Shinmori H, Takeuchi T. Atrazine transforming polymer prepared by molecular imprinting with post-imprinting process. Org Biomol Chem. 2006;4(24):4469-73doi: 10.1039/b612407k.
Yane, T., Shinmori, H., & Takeuchi, T. (2006). Atrazine transforming polymer prepared by molecular imprinting with post-imprinting process. Organic & biomolecular chemistry, 4(24), 4469-73. https://doi.org/10.1039/b612407k
Yane, Takehisa, et al. "Atrazine transforming polymer prepared by molecular imprinting with post-imprinting process." Organic & biomolecular chemistry vol. 4,24 (2006): 4469-73. doi: https://doi.org/10.1039/b612407k
Yane T, Shinmori H, Takeuchi T. Atrazine transforming polymer prepared by molecular imprinting with post-imprinting process. Org Biomol Chem. 2006 Dec 21;4(24):4469-73. doi: 10.1039/b612407k. Epub 2006 Nov 08. PMID: 17268641.
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Hydrogen sulfide as a potent scavenger of toxicant acrolein.

Ecotoxicology and environmental safety

Mao Z, Huang Y, Li B, Tomoya K, Shinmori H, Zeng X, Gu Z, Yao J.
PMID: 34952378
Ecotoxicol Environ Saf. 2021 Dec 21;229:113111. doi: 10.1016/j.ecoenv.2021.113111. Epub 2021 Dec 21.

Acrolein (ACR) is a metabolic byproduct in vivo and a ubiquitous environmental toxicant. It is implicated in the initiation and development of many diseases through multiple mechanisms, including the induction of oxidative stress. Currently, our understanding of the body...

Cite
Mao Z, Huang Y, Li B, et al. Hydrogen sulfide as a potent scavenger of toxicant acrolein. Ecotoxicol Environ Saf. 2021;229:113111doi: 10.1016/j.ecoenv.2021.113111.
Mao, Z., Huang, Y., Li, B., Tomoya, K., Shinmori, H., Zeng, X., Gu, Z., & Yao, J. (2021). Hydrogen sulfide as a potent scavenger of toxicant acrolein. Ecotoxicology and environmental safety, 229113111. https://doi.org/10.1016/j.ecoenv.2021.113111
Mao, Zhimin, et al. "Hydrogen sulfide as a potent scavenger of toxicant acrolein." Ecotoxicology and environmental safety vol. 229 (2021): 113111. doi: https://doi.org/10.1016/j.ecoenv.2021.113111
Mao Z, Huang Y, Li B, Tomoya K, Shinmori H, Zeng X, Gu Z, Yao J. Hydrogen sulfide as a potent scavenger of toxicant acrolein. Ecotoxicol Environ Saf. 2021 Dec 21;229:113111. doi: 10.1016/j.ecoenv.2021.113111. Epub 2021 Dec 21. PMID: 34952378.
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Hydrogen sulfide as a potent scavenger of toxicant acrolein.

Ecotoxicology and environmental safety

Mao Z, Huang Y, Li B, Tomoya K, Shinmori H, Zeng X, Gu Z, Yao J.
PMID: 34952378
Ecotoxicol Environ Saf. 2021 Dec 21;229:113111. doi: 10.1016/j.ecoenv.2021.113111. Epub 2021 Dec 21.

Acrolein (ACR) is a metabolic byproduct in vivo and a ubiquitous environmental toxicant. It is implicated in the initiation and development of many diseases through multiple mechanisms, including the induction of oxidative stress. Currently, our understanding of the body...

Cite
Mao Z, Huang Y, Li B, et al. Hydrogen sulfide as a potent scavenger of toxicant acrolein. Ecotoxicol Environ Saf. 2021;229:113111doi: 10.1016/j.ecoenv.2021.113111.
Mao, Z., Huang, Y., Li, B., Tomoya, K., Shinmori, H., Zeng, X., Gu, Z., & Yao, J. (2021). Hydrogen sulfide as a potent scavenger of toxicant acrolein. Ecotoxicology and environmental safety, 229113111. https://doi.org/10.1016/j.ecoenv.2021.113111
Mao, Zhimin, et al. "Hydrogen sulfide as a potent scavenger of toxicant acrolein." Ecotoxicology and environmental safety vol. 229 (2021): 113111. doi: https://doi.org/10.1016/j.ecoenv.2021.113111
Mao Z, Huang Y, Li B, Tomoya K, Shinmori H, Zeng X, Gu Z, Yao J. Hydrogen sulfide as a potent scavenger of toxicant acrolein. Ecotoxicol Environ Saf. 2021 Dec 21;229:113111. doi: 10.1016/j.ecoenv.2021.113111. Epub 2021 Dec 21. PMID: 34952378.
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Hydrogen sulfide as a potent scavenger of toxicant acrolein.

Ecotoxicology and environmental safety

Mao Z, Huang Y, Li B, Tomoya K, Shinmori H, Zeng X, Gu Z, Yao J.
PMID: 34952378
Ecotoxicol Environ Saf. 2021 Dec 21;229:113111. doi: 10.1016/j.ecoenv.2021.113111. Epub 2021 Dec 21.

Acrolein (ACR) is a metabolic byproduct in vivo and a ubiquitous environmental toxicant. It is implicated in the initiation and development of many diseases through multiple mechanisms, including the induction of oxidative stress. Currently, our understanding of the body...

Cite
Mao Z, Huang Y, Li B, et al. Hydrogen sulfide as a potent scavenger of toxicant acrolein. Ecotoxicol Environ Saf. 2021;229:113111doi: 10.1016/j.ecoenv.2021.113111.
Mao, Z., Huang, Y., Li, B., Tomoya, K., Shinmori, H., Zeng, X., Gu, Z., & Yao, J. (2021). Hydrogen sulfide as a potent scavenger of toxicant acrolein. Ecotoxicology and environmental safety, 229113111. https://doi.org/10.1016/j.ecoenv.2021.113111
Mao, Zhimin, et al. "Hydrogen sulfide as a potent scavenger of toxicant acrolein." Ecotoxicology and environmental safety vol. 229 (2021): 113111. doi: https://doi.org/10.1016/j.ecoenv.2021.113111
Mao Z, Huang Y, Li B, Tomoya K, Shinmori H, Zeng X, Gu Z, Yao J. Hydrogen sulfide as a potent scavenger of toxicant acrolein. Ecotoxicol Environ Saf. 2021 Dec 21;229:113111. doi: 10.1016/j.ecoenv.2021.113111. Epub 2021 Dec 21. PMID: 34952378.
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Porphyrin Photoabsorption and Fluorescence Variation with Adsorptive Loading on Gold Nanoparticles.

Frontiers in chemistry

Shinohara A, Shao G, Nakanishi T, Shinmori H.
PMID: 34888295
Front Chem. 2021 Nov 23;9:777041. doi: 10.3389/fchem.2021.777041. eCollection 2021.

Here, we report the photophysical structure-property relationship of porphyrins adsorbed on gold nanoparticles. The number of porphyrin-alkanethiolate adsorbates per particle was adjusted by a post-synthetic thiol/thiolate exchange reaction on 1-dodecanethiolate-protected gold nanoparticles. Even with a low loading level of...

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Shinohara A, Shao G, Nakanishi T, et al. Porphyrin Photoabsorption and Fluorescence Variation with Adsorptive Loading on Gold Nanoparticles. Front Chem. 2021;9:777041doi: 10.3389/fchem.2021.777041.
Shinohara, A., Shao, G., Nakanishi, T., & Shinmori, H. (2021). Porphyrin Photoabsorption and Fluorescence Variation with Adsorptive Loading on Gold Nanoparticles. Frontiers in chemistry, 9777041. https://doi.org/10.3389/fchem.2021.777041
Shinohara, Akira, et al. "Porphyrin Photoabsorption and Fluorescence Variation with Adsorptive Loading on Gold Nanoparticles." Frontiers in chemistry vol. 9 (2021): 777041. doi: https://doi.org/10.3389/fchem.2021.777041
Shinohara A, Shao G, Nakanishi T, Shinmori H. Porphyrin Photoabsorption and Fluorescence Variation with Adsorptive Loading on Gold Nanoparticles. Front Chem. 2021 Nov 23;9:777041. doi: 10.3389/fchem.2021.777041. eCollection 2021. PMID: 34888295; PMCID: PMC8650619.
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