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The role of ex vivo lung perfusion in lung transplantation.

Journal of the Intensive Care Society

Tatham KC, O'Dea KP, Wakabayashi K, Marczin N, Takata M.
PMID: 28979376
J Intensive Care Soc. 2015 Feb;16(1):58-63. doi: 10.1177/1751143714554062. Epub 2014 Dec 09.

Whilst lung transplantation is a viable solution for end-stage lung disease, donor shortages, donor lung inflammation and perioperative lung injury remain major limitations. Ex vivo lung perfusion has emerged as the next frontier in lung transplantation to address and...

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Tatham KC, O'Dea KP, Wakabayashi K, et al. The role of ex vivo lung perfusion in lung transplantation. J Intensive Care Soc. 2014;16(1):58-63doi: 10.1177/1751143714554062.
Tatham, K. C., O'Dea, K. P., Wakabayashi, K., Marczin, N., & Takata, M. (2015). The role of ex vivo lung perfusion in lung transplantation. Journal of the Intensive Care Society, 16(1), 58-63. https://doi.org/10.1177/1751143714554062
Tatham, Kate Colette, et al. "The role of ex vivo lung perfusion in lung transplantation." Journal of the Intensive Care Society vol. 16,1 (2015): 58-63. doi: https://doi.org/10.1177/1751143714554062
Tatham KC, O'Dea KP, Wakabayashi K, Marczin N, Takata M. The role of ex vivo lung perfusion in lung transplantation. J Intensive Care Soc. 2015 Feb;16(1):58-63. doi: 10.1177/1751143714554062. Epub 2014 Dec 09. PMID: 28979376; PMCID: PMC5593288.
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Efficient Synthesis of Cyclic Block Copolymers by Rotaxane Protocol by Linear/Cyclic Topology Transformation.

Chemistry (Weinheim an der Bergstrasse, Germany)

Valentina S, Ogawa T, Nakazono K, Aoki D, Takata T.
PMID: 27037975
Chemistry. 2016 Jun 20;22(26):8759-62. doi: 10.1002/chem.201601266. Epub 2016 May 12.

High-yielding synthesis of cyclic block copolymer (CBC) using the rotaxane protocol by linear-cyclic polymer topology transformation was first demonstrated. Initial complexation of OH-terminated sec-ammonium salt and a crown ether was followed by the successive living ring-opening polymerizations of two...

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Valentina S, Ogawa T, Nakazono K, et al. Efficient Synthesis of Cyclic Block Copolymers by Rotaxane Protocol by Linear/Cyclic Topology Transformation. Chemistry. 2016;22(26):8759-62doi: 10.1002/chem.201601266.
Valentina, S., Ogawa, T., Nakazono, K., Aoki, D., & Takata, T. (2016). Efficient Synthesis of Cyclic Block Copolymers by Rotaxane Protocol by Linear/Cyclic Topology Transformation. Chemistry (Weinheim an der Bergstrasse, Germany), 22(26), 8759-62. https://doi.org/10.1002/chem.201601266
Valentina, Stephanie, et al. "Efficient Synthesis of Cyclic Block Copolymers by Rotaxane Protocol by Linear/Cyclic Topology Transformation." Chemistry (Weinheim an der Bergstrasse, Germany) vol. 22,26 (2016): 8759-62. doi: https://doi.org/10.1002/chem.201601266
Valentina S, Ogawa T, Nakazono K, Aoki D, Takata T. Efficient Synthesis of Cyclic Block Copolymers by Rotaxane Protocol by Linear/Cyclic Topology Transformation. Chemistry. 2016 Jun 20;22(26):8759-62. doi: 10.1002/chem.201601266. Epub 2016 May 12. PMID: 27037975.
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Correction: Host Factors and Biomarkers Associated with Poor Outcomes in Adults with Invasive Pneumococcal Disease.

PloS one

Hanada S, Iwata S, Kishi K, Morozumi M, Chiba N, Wajima T, Takata M, Ubukata K.
PMID: 27031245
PLoS One. 2016 Mar 31;11(3):e0153109. doi: 10.1371/journal.pone.0153109. eCollection 2016.

No abstract available.

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Hanada S, Iwata S, Kishi K, et al. Correction: Host Factors and Biomarkers Associated with Poor Outcomes in Adults with Invasive Pneumococcal Disease. PLoS One. 2016;11(3):e0153109doi: 10.1371/journal.pone.0153109.
Hanada, S., Iwata, S., Kishi, K., Morozumi, M., Chiba, N., Wajima, T., Takata, M., Ubukata, K. (2016). Correction: Host Factors and Biomarkers Associated with Poor Outcomes in Adults with Invasive Pneumococcal Disease. PloS one, 11(3), e0153109. https://doi.org/10.1371/journal.pone.0153109
Hanada, Shigeo, et al. "Correction: Host Factors and Biomarkers Associated with Poor Outcomes in Adults with Invasive Pneumococcal Disease." PloS one vol. 11,3 (2016): e0153109. doi: https://doi.org/10.1371/journal.pone.0153109
Hanada S, Iwata S, Kishi K, Morozumi M, Chiba N, Wajima T, Takata M, Ubukata K. Correction: Host Factors and Biomarkers Associated with Poor Outcomes in Adults with Invasive Pneumococcal Disease. PLoS One. 2016 Mar 31;11(3):e0153109. doi: 10.1371/journal.pone.0153109. eCollection 2016. PMID: 27031245; PMCID: PMC4816381.
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Acute gastric volvulus in a patient with trisomy 21.

Surgical case reports

Arima K, Hashimoto D, Takata N, Doi Y, Yoshinaka I, Harada K, Baba H.
PMID: 26943373
Surg Case Rep. 2015 Dec;1(1):5. doi: 10.1186/s40792-014-0005-1. Epub 2015 Jan 16.

Acute gastric volvulus is a torsion of the stomach by more than 180° and a life-threatening condition. We present a 50-year-old male patient with acute abdominal pain who has Down syndrome/trisomy 21. Computed tomography showed a significant distended stomach...

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Arima K, Hashimoto D, Takata N, et al. Acute gastric volvulus in a patient with trisomy 21. Surg Case Rep. 2015;1(1):5doi: 10.1186/s40792-014-0005-1.
Arima, K., Hashimoto, D., Takata, N., Doi, Y., Yoshinaka, I., Harada, K., & Baba, H. (2015). Acute gastric volvulus in a patient with trisomy 21. Surgical case reports, 1(1), 5. https://doi.org/10.1186/s40792-014-0005-1
Arima, Kota, et al. "Acute gastric volvulus in a patient with trisomy 21." Surgical case reports vol. 1,1 (2015): 5. doi: https://doi.org/10.1186/s40792-014-0005-1
Arima K, Hashimoto D, Takata N, Doi Y, Yoshinaka I, Harada K, Baba H. Acute gastric volvulus in a patient with trisomy 21. Surg Case Rep. 2015 Dec;1(1):5. doi: 10.1186/s40792-014-0005-1. Epub 2015 Jan 16. PMID: 26943373; PMCID: PMC4747932.
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Fe-catalyzed synthesis of substituted N-aryl oxazolidines.

Organic & biomolecular chemistry

Murru S, Lott CS, McGough B, Bernard DM, Srivastava RS.
PMID: 27001918
Org Biomol Chem. 2016 Apr 12;14(15):3681-5. doi: 10.1039/c6ob00185h.

A novel iron-catalyzed synthesis of substituted N-aryl oxazolidines was developed via C-N bond formation and methylenation. The reaction of aryl hydroxylamines with allyl alcohols, in the presence of formaldehyde or its equivalents, afforded variety of oxazolidine heterocycles in very...

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Murru S, Lott CS, McGough B, et al. Fe-catalyzed synthesis of substituted N-aryl oxazolidines. Org Biomol Chem. 2016;14(15):3681-5doi: 10.1039/c6ob00185h.
Murru, S., Lott, C. S., McGough, B., Bernard, D. M., & Srivastava, R. S. (2016). Fe-catalyzed synthesis of substituted N-aryl oxazolidines. Organic & biomolecular chemistry, 14(15), 3681-5. https://doi.org/10.1039/c6ob00185h
Murru, Siva, et al. "Fe-catalyzed synthesis of substituted N-aryl oxazolidines." Organic & biomolecular chemistry vol. 14,15 (2016): 3681-5. doi: https://doi.org/10.1039/c6ob00185h
Murru S, Lott CS, McGough B, Bernard DM, Srivastava RS. Fe-catalyzed synthesis of substituted N-aryl oxazolidines. Org Biomol Chem. 2016 Apr 12;14(15):3681-5. doi: 10.1039/c6ob00185h. PMID: 27001918.
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Pressure-induced metallization of molybdenum disulfide.

Physical review letters

Chi ZH, Zhao XM, Zhang H, Goncharov AF, Lobanov SS, Kagayama T, Sakata M, Chen XJ.
PMID: 25083660
Phys Rev Lett. 2014 Jul 18;113(3):036802. doi: 10.1103/PhysRevLett.113.036802. Epub 2014 Jul 16.

X-ray diffraction, Raman spectroscopy, and electrical conductivity measurements of molybdenum disulfide MoS(2) are performed at pressures up to 81 GPa in diamond anvil cells. Above 20 GPa, we find discontinuous changes in Raman spectra and x-ray diffraction patterns which...

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Chi ZH, Zhao XM, Zhang H, et al. Pressure-induced metallization of molybdenum disulfide. Phys Rev Lett. 2014;113(3):036802doi: 10.1103/PhysRevLett.113.036802.
Chi, Z. H., Zhao, X. M., Zhang, H., Goncharov, A. F., Lobanov, S. S., Kagayama, T., Sakata, M., & Chen, X. J. (2014). Pressure-induced metallization of molybdenum disulfide. Physical review letters, 113(3), 036802. https://doi.org/10.1103/PhysRevLett.113.036802
Chi, Zhen-Hua, et al. "Pressure-induced metallization of molybdenum disulfide." Physical review letters vol. 113,3 (2014): 036802. doi: https://doi.org/10.1103/PhysRevLett.113.036802
Chi ZH, Zhao XM, Zhang H, Goncharov AF, Lobanov SS, Kagayama T, Sakata M, Chen XJ. Pressure-induced metallization of molybdenum disulfide. Phys Rev Lett. 2014 Jul 18;113(3):036802. doi: 10.1103/PhysRevLett.113.036802. Epub 2014 Jul 16. PMID: 25083660.
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Reactions of allyl alcohols and boronic acids with trifluoromethanesulfonyl hypervalent iodonium ylide under copper-catalysis.

Dalton transactions (Cambridge, England : 2003)

Arimori S, Takada M, Shibata N.
PMID: 26226886
Dalton Trans. 2015 Dec 07;44(45):19456-9. doi: 10.1039/c5dt02214b. Epub 2015 Jul 31.

Trifluoromethylsulfinyl and trifluoromethylthio groups are both important substituents for pharmaceuticals, agrochemicals and functional materials. We herein report the trifluoromethylthiolation of allyl alcohols 2 with trifluoromethanesulfonyl hypervalent iodonium ylide 1 under copper catalysis to provide trifluoromethylsulfinyl compounds 3. Trifluoromethylthiolation of...

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Arimori S, Takada M, Shibata N. Reactions of allyl alcohols and boronic acids with trifluoromethanesulfonyl hypervalent iodonium ylide under copper-catalysis. Dalton Trans. 2015;44(45):19456-9doi: 10.1039/c5dt02214b.
Arimori, S., Takada, M., & Shibata, N. (2015). Reactions of allyl alcohols and boronic acids with trifluoromethanesulfonyl hypervalent iodonium ylide under copper-catalysis. Dalton transactions (Cambridge, England : 2003), 44(45), 19456-9. https://doi.org/10.1039/c5dt02214b
Arimori, Sadayuki, et al. "Reactions of allyl alcohols and boronic acids with trifluoromethanesulfonyl hypervalent iodonium ylide under copper-catalysis." Dalton transactions (Cambridge, England : 2003) vol. 44,45 (2015): 19456-9. doi: https://doi.org/10.1039/c5dt02214b
Arimori S, Takada M, Shibata N. Reactions of allyl alcohols and boronic acids with trifluoromethanesulfonyl hypervalent iodonium ylide under copper-catalysis. Dalton Trans. 2015 Dec 07;44(45):19456-9. doi: 10.1039/c5dt02214b. Epub 2015 Jul 31. PMID: 26226886.
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Development and evaluation of rice giant embryo mutants for high oil content originated from a high-yielding cultivar 'Mizuhochikara'.

Breeding science

Sakata M, Seno M, Matsusaka H, Takahashi K, Nakamura Y, Yamagata Y, Angeles ER, Mochizuki T, Kumamaru T, Sato M, Enomoto A, Tashiro K, Kuhara S, Satoh H, Yoshimura A.
PMID: 27436953
Breed Sci. 2016 Jun;66(3):425-33. doi: 10.1270/jsbbs.15135. Epub 2016 May 20.

Rice bran oil is a byproduct of the milling of rice (Oryza sativa L.). It offers various health benefits and has a beneficial fatty acid composition. To increase the amount of rice bran as a sink for triacylglycerol (TAG),...

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Sakata M, Seno M, Matsusaka H, et al. Development and evaluation of rice giant embryo mutants for high oil content originated from a high-yielding cultivar 'Mizuhochikara'. Breed Sci. 2016;66(3):425-33doi: 10.1270/jsbbs.15135.
Sakata, M., Seno, M., Matsusaka, H., Takahashi, K., Nakamura, Y., Yamagata, Y., Angeles, E. R., Mochizuki, T., Kumamaru, T., Sato, M., Enomoto, A., Tashiro, K., Kuhara, S., Satoh, H., & Yoshimura, A. (2016). Development and evaluation of rice giant embryo mutants for high oil content originated from a high-yielding cultivar 'Mizuhochikara'. Breeding science, 66(3), 425-33. https://doi.org/10.1270/jsbbs.15135
Sakata, Mitsukazu, et al. "Development and evaluation of rice giant embryo mutants for high oil content originated from a high-yielding cultivar 'Mizuhochikara'." Breeding science vol. 66,3 (2016): 425-33. doi: https://doi.org/10.1270/jsbbs.15135
Sakata M, Seno M, Matsusaka H, Takahashi K, Nakamura Y, Yamagata Y, Angeles ER, Mochizuki T, Kumamaru T, Sato M, Enomoto A, Tashiro K, Kuhara S, Satoh H, Yoshimura A. Development and evaluation of rice giant embryo mutants for high oil content originated from a high-yielding cultivar 'Mizuhochikara'. Breed Sci. 2016 Jun;66(3):425-33. doi: 10.1270/jsbbs.15135. Epub 2016 May 20. PMID: 27436953; PMCID: PMC4902460.
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Measurement of Phenolic Compounds and Their Effect on Shikonin Production in Lithospermum Cultured Cells.

Bioscience, biotechnology, and biochemistry

Yazaki K, Fukui H, Nishikawa Y, Tabata M.
PMID: 27393163
Biosci Biotechnol Biochem. 1997 Jan;61(10):1674-8. doi: 10.1271/bbb.61.1674.

Shikonin production by Lithospevmum cell cultures is induced by transferring the cells into production medium. Six phenolic compounds, p-hydroxybenzoic acid, caffeic acid, sinapic acid, ferulic acid, syringaldehyde, and salicyclic acid, were detected in both shikonin-producing and non-producing cells. Their...

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Yazaki K, Fukui H, Nishikawa Y, et al. Measurement of Phenolic Compounds and Their Effect on Shikonin Production in Lithospermum Cultured Cells. Biosci Biotechnol Biochem. 1997;61(10):1674-8doi: 10.1271/bbb.61.1674.
Yazaki, K., Fukui, H., Nishikawa, Y., & Tabata, M. (1997). Measurement of Phenolic Compounds and Their Effect on Shikonin Production in Lithospermum Cultured Cells. Bioscience, biotechnology, and biochemistry, 61(10), 1674-8. https://doi.org/10.1271/bbb.61.1674
Yazaki, K, et al. "Measurement of Phenolic Compounds and Their Effect on Shikonin Production in Lithospermum Cultured Cells." Bioscience, biotechnology, and biochemistry vol. 61,10 (1997): 1674-8. doi: https://doi.org/10.1271/bbb.61.1674
Yazaki K, Fukui H, Nishikawa Y, Tabata M. Measurement of Phenolic Compounds and Their Effect on Shikonin Production in Lithospermum Cultured Cells. Biosci Biotechnol Biochem. 1997 Jan;61(10):1674-8. doi: 10.1271/bbb.61.1674. PMID: 27393163.
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Echocardiographic assessment of anomalous origin of the left coronary artery from the pulmonary artery.

Journal of echocardiography

Hayabuchi Y, Sakata M, Inoue M, Mori K, Kagami S.
PMID: 27279049
J Echocardiogr. 2014 Jun;12(2):60-1. doi: 10.1007/s12574-014-0207-3. Epub 2014 Feb 22.

Transthoracic echocardiography of a 4-month-old boy with heart failure revealed poor left ventricular contractility with severe mitral regurgitation. Deformation analysis revealed significantly decreased circumferential strain in the anterior and anteroseptal segments. Furthermore, post-systolic shortening was evident in the anterior...

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Hayabuchi Y, Sakata M, Inoue M, et al. Echocardiographic assessment of anomalous origin of the left coronary artery from the pulmonary artery. J Echocardiogr. 2014;12(2):60-1doi: 10.1007/s12574-014-0207-3.
Hayabuchi, Y., Sakata, M., Inoue, M., Mori, K., & Kagami, S. (2014). Echocardiographic assessment of anomalous origin of the left coronary artery from the pulmonary artery. Journal of echocardiography, 12(2), 60-1. https://doi.org/10.1007/s12574-014-0207-3
Hayabuchi, Yasunobu, et al. "Echocardiographic assessment of anomalous origin of the left coronary artery from the pulmonary artery." Journal of echocardiography vol. 12,2 (2014): 60-1. doi: https://doi.org/10.1007/s12574-014-0207-3
Hayabuchi Y, Sakata M, Inoue M, Mori K, Kagami S. Echocardiographic assessment of anomalous origin of the left coronary artery from the pulmonary artery. J Echocardiogr. 2014 Jun;12(2):60-1. doi: 10.1007/s12574-014-0207-3. Epub 2014 Feb 22. PMID: 27279049.
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SF.

Chemical communications (Cambridge, England)

Das P, Takada M, Matsuzaki K, Saito N, Shibata N.
PMID: 28317050
Chem Commun (Camb). 2017 Mar 30;53(27):3850-3853. doi: 10.1039/c7cc01043e.

Electrophilic pentafluorosulfanyl (SF

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Das P, Takada M, Matsuzaki K, et al. SF. Chem Commun (Camb). 2017;53(27):3850-3853doi: 10.1039/c7cc01043e.
Das, P., Takada, M., Matsuzaki, K., Saito, N., & Shibata, N. (2017). SF. Chemical communications (Cambridge, England), 53(27), 3850-3853. https://doi.org/10.1039/c7cc01043e
Das, Prajwalita, et al. "SF." Chemical communications (Cambridge, England) vol. 53,27 (2017): 3850-3853. doi: https://doi.org/10.1039/c7cc01043e
Das P, Takada M, Matsuzaki K, Saito N, Shibata N. SF. Chem Commun (Camb). 2017 Mar 30;53(27):3850-3853. doi: 10.1039/c7cc01043e. PMID: 28317050.
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Difluoromethanesulfonyl hypervalent iodonium ylides for electrophilic difluoromethylthiolation reactions under copper catalysis.

Royal Society open science

Arimori S, Matsubara O, Takada M, Shiro M, Shibata N.
PMID: 27293790
R Soc Open Sci. 2016 May 25;3(5):160102. doi: 10.1098/rsos.160102. eCollection 2016 May.

Difluoromethanesulfonyl hypervalent iodonium ylides 2 were developed as electrophilic difluoromethylthiolation reagents for a wide range of nucleophiles. Enamines, indoles, β-keto esters, silyl enol ethers and pyrroles were effectively reacted with 2 affording desired difluoromethylthio (SCF2H)-substituted compounds in good to...

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Arimori S, Matsubara O, Takada M, et al. Difluoromethanesulfonyl hypervalent iodonium ylides for electrophilic difluoromethylthiolation reactions under copper catalysis. R Soc Open Sci. 2016;3(5):160102doi: 10.1098/rsos.160102.
Arimori, S., Matsubara, O., Takada, M., Shiro, M., & Shibata, N. (2016). Difluoromethanesulfonyl hypervalent iodonium ylides for electrophilic difluoromethylthiolation reactions under copper catalysis. Royal Society open science, 3(5), 160102. https://doi.org/10.1098/rsos.160102
Arimori, Sadayuki, et al. "Difluoromethanesulfonyl hypervalent iodonium ylides for electrophilic difluoromethylthiolation reactions under copper catalysis." Royal Society open science vol. 3,5 (2016): 160102. doi: https://doi.org/10.1098/rsos.160102
Arimori S, Matsubara O, Takada M, Shiro M, Shibata N. Difluoromethanesulfonyl hypervalent iodonium ylides for electrophilic difluoromethylthiolation reactions under copper catalysis. R Soc Open Sci. 2016 May 25;3(5):160102. doi: 10.1098/rsos.160102. eCollection 2016 May. PMID: 27293790; PMCID: PMC4892452.
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Showing 1 to 12 of 1746 entries