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[Nursing of tomorrow].

Kangogaku zasshi

Watanabe M, Suzuki T, Asakawa E, Iwasak Y, Minoda E, Matsuda M.
PMID: 4960512
Kangogaku Zasshi. 1967 Jan;31(1):26-32.

No abstract available.

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Watanabe M, Suzuki T, Asakawa E, et al. [Nursing of tomorrow]. Kangogaku Zasshi. 1967;31(1):26-32
Watanabe, M., Suzuki, T., Asakawa, E., Iwasak, Y., Minoda, E., & Matsuda, M. (1967). [Nursing of tomorrow]. Kangogaku zasshi, 31(1), 26-32.
Watanabe, M, et al. "[Nursing of tomorrow]." Kangogaku zasshi vol. 31,1 (1967): 26-32.
Watanabe M, Suzuki T, Asakawa E, Iwasak Y, Minoda E, Matsuda M. [Nursing of tomorrow]. Kangogaku Zasshi. 1967 Jan;31(1):26-32. Japanese. PMID: 4960512.
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Negative electronic compressibility and tunable spin splitting in WSe2.

Nature nanotechnology

Riley JM, Meevasana W, Bawden L, Asakawa M, Takayama T, Eknapakul T, Kim TK, Hoesch M, Mo SK, Takagi H, Sasagawa T, Bahramy MS, King PD.
PMID: 26389661
Nat Nanotechnol. 2015 Dec;10(12):1043-7. doi: 10.1038/nnano.2015.217. Epub 2015 Sep 21.

Tunable bandgaps, extraordinarily large exciton-binding energies, strong light-matter coupling and a locking of the electron spin with layer and valley pseudospins have established transition-metal dichalcogenides (TMDs) as a unique class of two-dimensional (2D) semiconductors with wide-ranging practical applications. Using...

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Riley JM, Meevasana W, Bawden L, et al. Negative electronic compressibility and tunable spin splitting in WSe2. Nat Nanotechnol. 2015;10(12):1043-7doi: 10.1038/nnano.2015.217.
Riley, J. M., Meevasana, W., Bawden, L., Asakawa, M., Takayama, T., Eknapakul, T., Kim, T. K., Hoesch, M., Mo, S. K., Takagi, H., Sasagawa, T., Bahramy, M. S., & King, P. D. (2015). Negative electronic compressibility and tunable spin splitting in WSe2. Nature nanotechnology, 10(12), 1043-7. https://doi.org/10.1038/nnano.2015.217
Riley, J M, et al. "Negative electronic compressibility and tunable spin splitting in WSe2." Nature nanotechnology vol. 10,12 (2015): 1043-7. doi: https://doi.org/10.1038/nnano.2015.217
Riley JM, Meevasana W, Bawden L, Asakawa M, Takayama T, Eknapakul T, Kim TK, Hoesch M, Mo SK, Takagi H, Sasagawa T, Bahramy MS, King PD. Negative electronic compressibility and tunable spin splitting in WSe2. Nat Nanotechnol. 2015 Dec;10(12):1043-7. doi: 10.1038/nnano.2015.217. Epub 2015 Sep 21. PMID: 26389661.
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Immunoglobulin G4-related sclerosing cholecystitis presenting as gallbladder cancer: a case report.

Surgical case reports

Takahashi K, Ito H, Katsube T, Tsuboi A, Hashimoto M, Ota E, Mita K, Asakawa H, Hayashi T, Fujino K, Okamoto S.
PMID: 26943444
Surg Case Rep. 2015 Dec;1(1):120. doi: 10.1186/s40792-015-0123-4. Epub 2015 Dec 03.

Immunoglobulin G4 (IgG4)-related sclerosing disease is a systemic inflammatory syndrome, and an understanding of its characteristics is currently evolving. IgG4-related cholecystitis is a manifestation of IgG4-related sclerosing disease in the gallbladder. This case report describes the clinical, radiographic, and...

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Takahashi K, Ito H, Katsube T, et al. Immunoglobulin G4-related sclerosing cholecystitis presenting as gallbladder cancer: a case report. Surg Case Rep. 2015;1(1):120doi: 10.1186/s40792-015-0123-4.
Takahashi, K., Ito, H., Katsube, T., Tsuboi, A., Hashimoto, M., Ota, E., Mita, K., Asakawa, H., Hayashi, T., Fujino, K., & Okamoto, S. (2015). Immunoglobulin G4-related sclerosing cholecystitis presenting as gallbladder cancer: a case report. Surgical case reports, 1(1), 120. https://doi.org/10.1186/s40792-015-0123-4
Takahashi, Kodai, et al. "Immunoglobulin G4-related sclerosing cholecystitis presenting as gallbladder cancer: a case report." Surgical case reports vol. 1,1 (2015): 120. doi: https://doi.org/10.1186/s40792-015-0123-4
Takahashi K, Ito H, Katsube T, Tsuboi A, Hashimoto M, Ota E, Mita K, Asakawa H, Hayashi T, Fujino K, Okamoto S. Immunoglobulin G4-related sclerosing cholecystitis presenting as gallbladder cancer: a case report. Surg Case Rep. 2015 Dec;1(1):120. doi: 10.1186/s40792-015-0123-4. Epub 2015 Dec 03. PMID: 26943444; PMCID: PMC4668245.
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Comparative Transcriptome Analysis Identifies CCDC80 as a Novel Gene Associated with Pulmonary Arterial Hypertension.

Frontiers in pharmacology

Sasagawa S, Nishimura Y, Sawada H, Zhang E, Okabe S, Murakami S, Ashikawa Y, Yuge M, Kawaguchi K, Kawase R, Mitani Y, Maruyama K, Tanaka T.
PMID: 27375481
Front Pharmacol. 2016 Jun 07;7:142. doi: 10.3389/fphar.2016.00142. eCollection 2016.

Pulmonary arterial hypertension (PAH) is a heterogeneous disorder associated with a progressive increase in pulmonary artery resistance and pressure. Although various therapies have been developed, the 5-year survival rate of PAH patients remains low. There is thus an important...

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Sasagawa S, Nishimura Y, Sawada H, et al. Comparative Transcriptome Analysis Identifies CCDC80 as a Novel Gene Associated with Pulmonary Arterial Hypertension. Front Pharmacol. 2016;7:142doi: 10.3389/fphar.2016.00142.
Sasagawa, S., Nishimura, Y., Sawada, H., Zhang, E., Okabe, S., Murakami, S., Ashikawa, Y., Yuge, M., Kawaguchi, K., Kawase, R., Mitani, Y., Maruyama, K., & Tanaka, T. (2016). Comparative Transcriptome Analysis Identifies CCDC80 as a Novel Gene Associated with Pulmonary Arterial Hypertension. Frontiers in pharmacology, 7142. https://doi.org/10.3389/fphar.2016.00142
Sasagawa, Shota, et al. "Comparative Transcriptome Analysis Identifies CCDC80 as a Novel Gene Associated with Pulmonary Arterial Hypertension." Frontiers in pharmacology vol. 7 (2016): 142. doi: https://doi.org/10.3389/fphar.2016.00142
Sasagawa S, Nishimura Y, Sawada H, Zhang E, Okabe S, Murakami S, Ashikawa Y, Yuge M, Kawaguchi K, Kawase R, Mitani Y, Maruyama K, Tanaka T. Comparative Transcriptome Analysis Identifies CCDC80 as a Novel Gene Associated with Pulmonary Arterial Hypertension. Front Pharmacol. 2016 Jun 07;7:142. doi: 10.3389/fphar.2016.00142. eCollection 2016. PMID: 27375481; PMCID: PMC4894905.
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Efficiency improvement in the cantilever photothermal excitation method using a photothermal conversion layer.

Beilstein journal of nanotechnology

Inada N, Asakawa H, Kobayashi T, Fukuma T.
PMID: 27335733
Beilstein J Nanotechnol. 2016 Mar 10;7:409-17. doi: 10.3762/bjnano.7.36. eCollection 2016.

Photothermal excitation is a cantilever excitation method that enables stable and accurate operation for dynamic-mode AFM measurements. However, the low excitation efficiency of the method has often limited its application in practical studies. In this study, we propose a...

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Inada N, Asakawa H, Kobayashi T, et al. Efficiency improvement in the cantilever photothermal excitation method using a photothermal conversion layer. Beilstein J Nanotechnol. 2016;7:409-17doi: 10.3762/bjnano.7.36.
Inada, N., Asakawa, H., Kobayashi, T., & Fukuma, T. (2016). Efficiency improvement in the cantilever photothermal excitation method using a photothermal conversion layer. Beilstein journal of nanotechnology, 7409-17. https://doi.org/10.3762/bjnano.7.36
Inada, Natsumi, et al. "Efficiency improvement in the cantilever photothermal excitation method using a photothermal conversion layer." Beilstein journal of nanotechnology vol. 7 (2016): 409-17. doi: https://doi.org/10.3762/bjnano.7.36
Inada N, Asakawa H, Kobayashi T, Fukuma T. Efficiency improvement in the cantilever photothermal excitation method using a photothermal conversion layer. Beilstein J Nanotechnol. 2016 Mar 10;7:409-17. doi: 10.3762/bjnano.7.36. eCollection 2016. PMID: 27335733; PMCID: PMC4901543.
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Resection for Pancreatic Cancer Lung Metastases.

The Korean journal of thoracic and cardiovascular surgery

Okui M, Yamamichi T, Asakawa A, Harada M, Horio H.
PMID: 29124023
Korean J Thorac Cardiovasc Surg. 2017 Oct;50(5):326-328. doi: 10.5090/kjtcs.2017.50.5.326. Epub 2017 Oct 05.

BACKGROUND: Pancreatic cancer is a highly aggressive solid tumor. Patients with metastases from pancreatic cancer have poor survival rates. Here, we report the outcomes of 6 patients for whom resection of lung metastases was performed after a pancreatectomy to...

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Okui M, Yamamichi T, Asakawa A, et al. Resection for Pancreatic Cancer Lung Metastases. Korean J Thorac Cardiovasc Surg. 2017;50(5):326-328doi: 10.5090/kjtcs.2017.50.5.326.
Okui, M., Yamamichi, T., Asakawa, A., Harada, M., & Horio, H. (2017). Resection for Pancreatic Cancer Lung Metastases. The Korean journal of thoracic and cardiovascular surgery, 50(5), 326-328. https://doi.org/10.5090/kjtcs.2017.50.5.326
Okui, Masayuki, et al. "Resection for Pancreatic Cancer Lung Metastases." The Korean journal of thoracic and cardiovascular surgery vol. 50,5 (2017): 326-328. doi: https://doi.org/10.5090/kjtcs.2017.50.5.326
Okui M, Yamamichi T, Asakawa A, Harada M, Horio H. Resection for Pancreatic Cancer Lung Metastases. Korean J Thorac Cardiovasc Surg. 2017 Oct;50(5):326-328. doi: 10.5090/kjtcs.2017.50.5.326. Epub 2017 Oct 05. PMID: 29124023; PMCID: PMC5628959.
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Comparative structural analysis of 2,7-diethoxy-1,8-bis(4-phenoxybenzoyl)naphthalene and its homologues: orientation of the 4-phenoxybenzoyl groups at the 1- and 8-positions of the naphthalene ring.

Acta crystallographica. Section C, Structural chemistry

Yoshiwaka S, Sasagawa K, Noguchi K, Yonezawa N, Okamoto A.
PMID: 25471405
Acta Crystallogr C Struct Chem. 2014 Dec;70:1096-100. doi: 10.1107/S2053229614022967. Epub 2014 Nov 06.

The title molecule, C40H32O6, possesses crystallographically imposed twofold symmetry, with the central two C atoms of the naphthalene unit sited on the rotation axis. The two 4-phenoxybenzoyl groups in the molecule are twisted away from the attached naphthalene unit,...

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Yoshiwaka S, Sasagawa K, Noguchi K, et al. Comparative structural analysis of 2,7-diethoxy-1,8-bis(4-phenoxybenzoyl)naphthalene and its homologues: orientation of the 4-phenoxybenzoyl groups at the 1- and 8-positions of the naphthalene ring. Acta Crystallogr C Struct Chem. 2014;70:1096-100doi: 10.1107/S2053229614022967.
Yoshiwaka, S., Sasagawa, K., Noguchi, K., Yonezawa, N., & Okamoto, A. (2014). Comparative structural analysis of 2,7-diethoxy-1,8-bis(4-phenoxybenzoyl)naphthalene and its homologues: orientation of the 4-phenoxybenzoyl groups at the 1- and 8-positions of the naphthalene ring. Acta crystallographica. Section C, Structural chemistry, 701096-100. https://doi.org/10.1107/S2053229614022967
Yoshiwaka, Sayaka, et al. "Comparative structural analysis of 2,7-diethoxy-1,8-bis(4-phenoxybenzoyl)naphthalene and its homologues: orientation of the 4-phenoxybenzoyl groups at the 1- and 8-positions of the naphthalene ring." Acta crystallographica. Section C, Structural chemistry vol. 70 (2014): 1096-100. doi: https://doi.org/10.1107/S2053229614022967
Yoshiwaka S, Sasagawa K, Noguchi K, Yonezawa N, Okamoto A. Comparative structural analysis of 2,7-diethoxy-1,8-bis(4-phenoxybenzoyl)naphthalene and its homologues: orientation of the 4-phenoxybenzoyl groups at the 1- and 8-positions of the naphthalene ring. Acta Crystallogr C Struct Chem. 2014 Dec;70:1096-100. doi: 10.1107/S2053229614022967. Epub 2014 Nov 06. PMID: 25471405.
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[No title available]

International journal of systematic and evolutionary microbiology

Sasi Jyothsna TS, Tushar L, Sasikala C, Ramana CV.
PMID: 26738915
Int J Syst Evol Microbiol. 2016 Mar;66(3):1268-1274. doi: 10.1099/ijsem.0.000874. Epub 2016 Jan 05.

Twenty-three rod-shaped, endospore-forming, Gram-stain-positive, obligately anaerobic bacteria were isolated from different marine sediment samples of Gujarat. All 23 strains shared 16S rRNA gene sequence similarity of ∼100 %. Strain JC272

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Sasi Jyothsna TS, Tushar L, Sasikala C, et al. . Int J Syst Evol Microbiol. 2016;66(3):1268-1274doi: 10.1099/ijsem.0.000874.
Sasi Jyothsna, T. S., Tushar, L., Sasikala, C., & Ramana, C. V. (2016). . International journal of systematic and evolutionary microbiology, 66(3), 1268-1274. https://doi.org/10.1099/ijsem.0.000874
Sasi Jyothsna, T S, et al. "." International journal of systematic and evolutionary microbiology vol. 66,3 (2016): 1268-1274. doi: https://doi.org/10.1099/ijsem.0.000874
Sasi Jyothsna TS, Tushar L, Sasikala C, Ramana CV. . Int J Syst Evol Microbiol. 2016 Mar;66(3):1268-1274. doi: 10.1099/ijsem.0.000874. Epub 2016 Jan 05. PMID: 26738915.
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Matrix effect on in-source decay products of peptides in matrix-assisted laser desorption/ionization.

Mass spectrometry (Tokyo, Japan)

Asakawa D, Sakakura M, Takayama M.
PMID: 24349903
Mass Spectrom (Tokyo). 2012;1(1):A0002. doi: 10.5702/massspectrometry.A0002. Epub 2012 Jul 05.

MALDI-ISD of peptides were studied using several salicylic acid derivatives, 2,5-dihydroxybenzoic acid (2,5-DHB), 5-aminosalicylic acid (5-ASA), 5-formylsalicylic acid (5-FSA), and 5-nitrosalicylic acid (5-NSA) as matrices. The difference in the nature of the functional group at the 5-position in the...

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Asakawa D, Sakakura M, Takayama M. Matrix effect on in-source decay products of peptides in matrix-assisted laser desorption/ionization. Mass Spectrom (Tokyo). 2012;1(1):A0002doi: 10.5702/massspectrometry.A0002.
Asakawa, D., Sakakura, M., & Takayama, M. (2012). Matrix effect on in-source decay products of peptides in matrix-assisted laser desorption/ionization. Mass spectrometry (Tokyo, Japan), 1(1), A0002. https://doi.org/10.5702/massspectrometry.A0002
Asakawa, Daiki, et al. "Matrix effect on in-source decay products of peptides in matrix-assisted laser desorption/ionization." Mass spectrometry (Tokyo, Japan) vol. 1,1 (2012): A0002. doi: https://doi.org/10.5702/massspectrometry.A0002
Asakawa D, Sakakura M, Takayama M. Matrix effect on in-source decay products of peptides in matrix-assisted laser desorption/ionization. Mass Spectrom (Tokyo). 2012;1(1):A0002. doi: 10.5702/massspectrometry.A0002. Epub 2012 Jul 05. PMID: 24349903; PMCID: PMC3775833.
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Systems pharmacology of adiposity reveals inhibition of EP300 as a common therapeutic mechanism of caloric restriction and resveratrol for obesity.

Frontiers in pharmacology

Nishimura Y, Sasagawa S, Ariyoshi M, Ichikawa S, Shimada Y, Kawaguchi K, Kawase R, Yamamoto R, Uehara T, Yanai T, Takata R, Tanaka T.
PMID: 26441656
Front Pharmacol. 2015 Sep 15;6:199. doi: 10.3389/fphar.2015.00199. eCollection 2015.

Both caloric restriction (CR) and resveratrol (RSV) have beneficial effects on obesity. However, the biochemical pathways that mediate these beneficial effects might be complex and interconnected and have not been fully elucidated. To reveal the common therapeutic mechanism of...

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Nishimura Y, Sasagawa S, Ariyoshi M, et al. Systems pharmacology of adiposity reveals inhibition of EP300 as a common therapeutic mechanism of caloric restriction and resveratrol for obesity. Front Pharmacol. 2015;6:199doi: 10.3389/fphar.2015.00199.
Nishimura, Y., Sasagawa, S., Ariyoshi, M., Ichikawa, S., Shimada, Y., Kawaguchi, K., Kawase, R., Yamamoto, R., Uehara, T., Yanai, T., Takata, R., & Tanaka, T. (2015). Systems pharmacology of adiposity reveals inhibition of EP300 as a common therapeutic mechanism of caloric restriction and resveratrol for obesity. Frontiers in pharmacology, 6199. https://doi.org/10.3389/fphar.2015.00199
Nishimura, Yuhei, et al. "Systems pharmacology of adiposity reveals inhibition of EP300 as a common therapeutic mechanism of caloric restriction and resveratrol for obesity." Frontiers in pharmacology vol. 6 (2015): 199. doi: https://doi.org/10.3389/fphar.2015.00199
Nishimura Y, Sasagawa S, Ariyoshi M, Ichikawa S, Shimada Y, Kawaguchi K, Kawase R, Yamamoto R, Uehara T, Yanai T, Takata R, Tanaka T. Systems pharmacology of adiposity reveals inhibition of EP300 as a common therapeutic mechanism of caloric restriction and resveratrol for obesity. Front Pharmacol. 2015 Sep 15;6:199. doi: 10.3389/fphar.2015.00199. eCollection 2015. PMID: 26441656; PMCID: PMC4569862.
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Ultrafast electronic state conversion at room temperature utilizing hidden state in cuprate ladder system.

Nature communications

Fukaya R, Okimoto Y, Kunitomo M, Onda K, Ishikawa T, Koshihara S, Hashimoto H, Ishihara S, Isayama A, Yui H, Sasagawa T.
PMID: 26481604
Nat Commun. 2015 Oct 20;6:8519. doi: 10.1038/ncomms9519.

Photo-control of material properties on femto- (10(-15)) and pico- (10(-12)) second timescales at room temperature has been a long-sought goal of materials science. Here we demonstrate a unique ultrafast conversion between the metallic and insulating state and the emergence...

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Fukaya R, Okimoto Y, Kunitomo M, et al. Ultrafast electronic state conversion at room temperature utilizing hidden state in cuprate ladder system. Nat Commun. 2015;6:8519doi: 10.1038/ncomms9519.
Fukaya, R., Okimoto, Y., Kunitomo, M., Onda, K., Ishikawa, T., Koshihara, S., Hashimoto, H., Ishihara, S., Isayama, A., Yui, H., & Sasagawa, T. (2015). Ultrafast electronic state conversion at room temperature utilizing hidden state in cuprate ladder system. Nature communications, 68519. https://doi.org/10.1038/ncomms9519
Fukaya, R, et al. "Ultrafast electronic state conversion at room temperature utilizing hidden state in cuprate ladder system." Nature communications vol. 6 (2015): 8519. doi: https://doi.org/10.1038/ncomms9519
Fukaya R, Okimoto Y, Kunitomo M, Onda K, Ishikawa T, Koshihara S, Hashimoto H, Ishihara S, Isayama A, Yui H, Sasagawa T. Ultrafast electronic state conversion at room temperature utilizing hidden state in cuprate ladder system. Nat Commun. 2015 Oct 20;6:8519. doi: 10.1038/ncomms9519. PMID: 26481604; PMCID: PMC4634131.
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Two types of quasi-liquid layers on ice crystals are formed kinetically.

Proceedings of the National Academy of Sciences of the United States of America

Asakawa H, Sazaki G, Nagashima K, Nakatsubo S, Furukawa Y.
PMID: 26831089
Proc Natl Acad Sci U S A. 2016 Feb 16;113(7):1749-53. doi: 10.1073/pnas.1521607113. Epub 2016 Feb 01.

Surfaces of ice are covered with thin liquid water layers, called quasi-liquid layers (QLLs), even below their melting point (0 °C), which govern a wide variety of phenomena in nature. We recently found that two types of QLL phases...

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Asakawa H, Sazaki G, Nagashima K, et al. Two types of quasi-liquid layers on ice crystals are formed kinetically. Proc Natl Acad Sci U S A. 2016;113(7):1749-53doi: 10.1073/pnas.1521607113.
Asakawa, H., Sazaki, G., Nagashima, K., Nakatsubo, S., & Furukawa, Y. (2016). Two types of quasi-liquid layers on ice crystals are formed kinetically. Proceedings of the National Academy of Sciences of the United States of America, 113(7), 1749-53. https://doi.org/10.1073/pnas.1521607113
Asakawa, Harutoshi, et al. "Two types of quasi-liquid layers on ice crystals are formed kinetically." Proceedings of the National Academy of Sciences of the United States of America vol. 113,7 (2016): 1749-53. doi: https://doi.org/10.1073/pnas.1521607113
Asakawa H, Sazaki G, Nagashima K, Nakatsubo S, Furukawa Y. Two types of quasi-liquid layers on ice crystals are formed kinetically. Proc Natl Acad Sci U S A. 2016 Feb 16;113(7):1749-53. doi: 10.1073/pnas.1521607113. Epub 2016 Feb 01. PMID: 26831089; PMCID: PMC4763737.
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