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A double-decker silver(I) coordination polymer of 1-methylpyrene with columnar aromatic stacks. Effect of substituting groups on structure of silver(I) complexes with polycyclic aromatic hydrocarbons.

Inorganic chemistry

Munakata M, Zhong JC, Kuroda-Sowa T, Maekawa M, Suenaga Y, Kasahara M, Konaka H.
PMID: 11754295
Inorg Chem. 2001 Dec 31;40(27):7087-90. doi: 10.1021/ic010668u.

No abstract available.

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Munakata M, Zhong JC, Kuroda-Sowa T, et al. A double-decker silver(I) coordination polymer of 1-methylpyrene with columnar aromatic stacks. Effect of substituting groups on structure of silver(I) complexes with polycyclic aromatic hydrocarbons. Inorg Chem. 2001;40(27):7087-90doi: 10.1021/ic010668u.
Munakata, M., Zhong, J. C., Kuroda-Sowa, T., Maekawa, M., Suenaga, Y., Kasahara, M., & Konaka, H. (2001). A double-decker silver(I) coordination polymer of 1-methylpyrene with columnar aromatic stacks. Effect of substituting groups on structure of silver(I) complexes with polycyclic aromatic hydrocarbons. Inorganic chemistry, 40(27), 7087-90. https://doi.org/10.1021/ic010668u
Munakata, M, et al. "A double-decker silver(I) coordination polymer of 1-methylpyrene with columnar aromatic stacks. Effect of substituting groups on structure of silver(I) complexes with polycyclic aromatic hydrocarbons." Inorganic chemistry vol. 40,27 (2001): 7087-90. doi: https://doi.org/10.1021/ic010668u
Munakata M, Zhong JC, Kuroda-Sowa T, Maekawa M, Suenaga Y, Kasahara M, Konaka H. A double-decker silver(I) coordination polymer of 1-methylpyrene with columnar aromatic stacks. Effect of substituting groups on structure of silver(I) complexes with polycyclic aromatic hydrocarbons. Inorg Chem. 2001 Dec 31;40(27):7087-90. doi: 10.1021/ic010668u. PMID: 11754295.
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Introduction of functionalized C1, C2, and C3 units to imines through the dimethylzinc-air-initiated radical addition.

The Journal of organic chemistry

Yamada K, Yamamoto Y, Maekawa M, Tomioka K.
PMID: 14987007
J Org Chem. 2004 Mar 05;69(5):1531-4. doi: 10.1021/jo035496s.

Introduction of functionalized C1, C2, and C3 units to imines was achieved by using the dimethylzinc-air-initiated alpha-alkoxyalkyl radical addition as a key reaction. The addition to a C[double bond]N double bond chemoselectively occurred in the presence of a C[double...

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Yamada K, Yamamoto Y, Maekawa M, et al. Introduction of functionalized C1, C2, and C3 units to imines through the dimethylzinc-air-initiated radical addition. J Org Chem. 2004;69(5):1531-4doi: 10.1021/jo035496s.
Yamada, K., Yamamoto, Y., Maekawa, M., & Tomioka, K. (2004). Introduction of functionalized C1, C2, and C3 units to imines through the dimethylzinc-air-initiated radical addition. The Journal of organic chemistry, 69(5), 1531-4. https://doi.org/10.1021/jo035496s
Yamada, Ken-ichi, et al. "Introduction of functionalized C1, C2, and C3 units to imines through the dimethylzinc-air-initiated radical addition." The Journal of organic chemistry vol. 69,5 (2004): 1531-4. doi: https://doi.org/10.1021/jo035496s
Yamada K, Yamamoto Y, Maekawa M, Tomioka K. Introduction of functionalized C1, C2, and C3 units to imines through the dimethylzinc-air-initiated radical addition. J Org Chem. 2004 Mar 05;69(5):1531-4. doi: 10.1021/jo035496s. PMID: 14987007.
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Icosaniobate: a new member of the isoniobate family.

Inorganic chemistry

Maekawa M, Ozawa Y, Yagasaki A.
PMID: 17112246
Inorg Chem. 2006 Nov 27;45(24):9608-9. doi: 10.1021/ic0601788.

Icosaniobate [Nb20O54]8- was synthesized by reacting [H4Nb6O19]4- with NO in tetrahydrofuran or MeNO2. A single-crystal X-ray diffraction study of its n-tetrabutylammonium salt [a = 17.7284(18) A, b = 33.542(3) A, c = 34.316(2) A, Z = 4, and space...

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Maekawa M, Ozawa Y, Yagasaki A. Icosaniobate: a new member of the isoniobate family. Inorg Chem. 2006;45(24):9608-9doi: 10.1021/ic0601788.
Maekawa, M., Ozawa, Y., & Yagasaki, A. (2006). Icosaniobate: a new member of the isoniobate family. Inorganic chemistry, 45(24), 9608-9. https://doi.org/10.1021/ic0601788
Maekawa, Masaki, et al. "Icosaniobate: a new member of the isoniobate family." Inorganic chemistry vol. 45,24 (2006): 9608-9. doi: https://doi.org/10.1021/ic0601788
Maekawa M, Ozawa Y, Yagasaki A. Icosaniobate: a new member of the isoniobate family. Inorg Chem. 2006 Nov 27;45(24):9608-9. doi: 10.1021/ic0601788. PMID: 17112246.
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Quantitative flow visualization of fluidized-bed heat exchanger by neutron radiography.

Applied radiation and isotopes : including data, instrumentation and methods for use in agriculture, industry and medicine

Ozawa M, Umekawa H, Furui S, Hayashi K, Takenaka N.
PMID: 15246422
Appl Radiat Isot. 2004 Oct;61(4):715-24. doi: 10.1016/j.apradiso.2004.03.099.

Quantitative flow visualization of a gas-solid fluidized-bed installed vertical tube-bank has been successfully conducted using neutron radiography and image processing technique. The quantitative data of void fraction distribution as well as the fluctuation data are presented. The time-averaged void...

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Ozawa M, Umekawa H, Furui S, et al. Quantitative flow visualization of fluidized-bed heat exchanger by neutron radiography. Appl Radiat Isot. 2004;61(4):715-24doi: 10.1016/j.apradiso.2004.03.099.
Ozawa, M., Umekawa, H., Furui, S., Hayashi, K., & Takenaka, N. (2004). Quantitative flow visualization of fluidized-bed heat exchanger by neutron radiography. Applied radiation and isotopes : including data, instrumentation and methods for use in agriculture, industry and medicine, 61(4), 715-24. https://doi.org/10.1016/j.apradiso.2004.03.099
Ozawa, M, et al. "Quantitative flow visualization of fluidized-bed heat exchanger by neutron radiography." Applied radiation and isotopes : including data, instrumentation and methods for use in agriculture, industry and medicine vol. 61,4 (2004): 715-24. doi: https://doi.org/10.1016/j.apradiso.2004.03.099
Ozawa M, Umekawa H, Furui S, Hayashi K, Takenaka N. Quantitative flow visualization of fluidized-bed heat exchanger by neutron radiography. Appl Radiat Isot. 2004 Oct;61(4):715-24. doi: 10.1016/j.apradiso.2004.03.099. PMID: 15246422.
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Syntheses, structures, and properties of intercalation compounds of silver(I) complex with [2.2]paracyclophane.

Inorganic chemistry

Munakata M, Liu SQ, Konaka H, Kuroda-Sowa T, Suenaga Y, Maekawa M, Nakagawa H, Yamazaki Y.
PMID: 14731025
Inorg Chem. 2004 Jan 26;43(2):633-41. doi: 10.1021/ic0302433.

Reaction of [2.2]paracyclophane (pcp) with silver(I) trifluoroacetate (AgCF(3)CO(2)) and silver(I) pentafluoroproprionate (AgC(2)F(5)CO(2)) has led to isolation of three novel intercalation polymers: [Ag(4)(pcp)(CF(3)CO(2))(4)](C(6)H(6)) (1), [Ag(4)(pcp)(CF(3)CO(2))(4)](C(6)H(3)Me(3)) (2), and [Ag(4)(pcp)(C(2)F(5)CO(2))(4)](pcp) (3). Structure studies using single crystal X-ray diffraction have shown that all...

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Munakata M, Liu SQ, Konaka H, et al. Syntheses, structures, and properties of intercalation compounds of silver(I) complex with [2.2]paracyclophane. Inorg Chem. 2004;43(2):633-41doi: 10.1021/ic0302433.
Munakata, M., Liu, S. Q., Konaka, H., Kuroda-Sowa, T., Suenaga, Y., Maekawa, M., Nakagawa, H., & Yamazaki, Y. (2004). Syntheses, structures, and properties of intercalation compounds of silver(I) complex with [2.2]paracyclophane. Inorganic chemistry, 43(2), 633-41. https://doi.org/10.1021/ic0302433
Munakata, Megumu, et al. "Syntheses, structures, and properties of intercalation compounds of silver(I) complex with [2.2]paracyclophane." Inorganic chemistry vol. 43,2 (2004): 633-41. doi: https://doi.org/10.1021/ic0302433
Munakata M, Liu SQ, Konaka H, Kuroda-Sowa T, Suenaga Y, Maekawa M, Nakagawa H, Yamazaki Y. Syntheses, structures, and properties of intercalation compounds of silver(I) complex with [2.2]paracyclophane. Inorg Chem. 2004 Jan 26;43(2):633-41. doi: 10.1021/ic0302433. PMID: 14731025.
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Spin Seebeck insulator.

Nature materials

Uchida K, Xiao J, Adachi H, Ohe J, Takahashi S, Ieda J, Ota T, Kajiwara Y, Umezawa H, Kawai H, Bauer GE, Maekawa S, Saitoh E.
PMID: 20871606
Nat Mater. 2010 Nov;9(11):894-7. doi: 10.1038/nmat2856. Epub 2010 Sep 26.

Thermoelectric generation is an essential function in future energy-saving technologies. However, it has so far been an exclusive feature of electric conductors, a situation which limits its application; conduction electrons are often problematic in the thermal design of devices....

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Uchida K, Xiao J, Adachi H, et al. Spin Seebeck insulator. Nat Mater. 2010;9(11):894-7doi: 10.1038/nmat2856.
Uchida, K., Xiao, J., Adachi, H., Ohe, J., Takahashi, S., Ieda, J., Ota, T., Kajiwara, Y., Umezawa, H., Kawai, H., Bauer, G. E., Maekawa, S., & Saitoh, E. (2010). Spin Seebeck insulator. Nature materials, 9(11), 894-7. https://doi.org/10.1038/nmat2856
Uchida, K, et al. "Spin Seebeck insulator." Nature materials vol. 9,11 (2010): 894-7. doi: https://doi.org/10.1038/nmat2856
Uchida K, Xiao J, Adachi H, Ohe J, Takahashi S, Ieda J, Ota T, Kajiwara Y, Umezawa H, Kawai H, Bauer GE, Maekawa S, Saitoh E. Spin Seebeck insulator. Nat Mater. 2010 Nov;9(11):894-7. doi: 10.1038/nmat2856. Epub 2010 Sep 26. PMID: 20871606.
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Organic dye materials for optical recording media.

Applied optics

Oba H, Abe M, Umehara M, Sato T, Ueda Y, Kunikane M.
PMID: 18235738
Appl Opt. 1986 Nov 15;25(22):4023. doi: 10.1364/ao.25.004023.

No abstract available.

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Oba H, Abe M, Umehara M, et al. Organic dye materials for optical recording media. Appl Opt. 1986;25(22):4023doi: 10.1364/ao.25.004023.
Oba, H., Abe, M., Umehara, M., Sato, T., Ueda, Y., & Kunikane, M. (1986). Organic dye materials for optical recording media. Applied optics, 25(22), 4023. https://doi.org/10.1364/ao.25.004023
Oba, H, et al. "Organic dye materials for optical recording media." Applied optics vol. 25,22 (1986): 4023. doi: https://doi.org/10.1364/ao.25.004023
Oba H, Abe M, Umehara M, Sato T, Ueda Y, Kunikane M. Organic dye materials for optical recording media. Appl Opt. 1986 Nov 15;25(22):4023. doi: 10.1364/ao.25.004023. PMID: 18235738.
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Crystal structure and carrier transport properties of a new 3D mixed-valence Cu(I)-Cu(II) coordination polymer including pyrrolidine dithiocarbamate ligand.

Dalton transactions (Cambridge, England : 2003)

Okubo T, Tanaka N, Kim KH, Anma H, Seki S, Saeki A, Maekawa M, Kuroda-Sowa T.
PMID: 21180735
Dalton Trans. 2011 Mar 14;40(10):2218-24. doi: 10.1039/c0dt01065k. Epub 2010 Dec 22.

A novel mixed-valence Cu(i)-Cu(ii) coordination polymer having an infinite three-dimensional (3D) structure, {[Cu(I)(4)Cu(II)(2)Br(4)(Pyr-dtc)(4)]·CHCl(3)}(n) (1) (Pyr-dtc(-) = pyrrolidine dithiocarbamate), has been prepared and structurally characterized via X-ray diffraction. This complex consists of 1D Cu(i)-Br chains and bridging mononuclear copper(ii) units...

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Okubo T, Tanaka N, Kim KH, et al. Crystal structure and carrier transport properties of a new 3D mixed-valence Cu(I)-Cu(II) coordination polymer including pyrrolidine dithiocarbamate ligand. Dalton Trans. 2010;40(10):2218-24doi: 10.1039/c0dt01065k.
Okubo, T., Tanaka, N., Kim, K. H., Anma, H., Seki, S., Saeki, A., Maekawa, M., & Kuroda-Sowa, T. (2011). Crystal structure and carrier transport properties of a new 3D mixed-valence Cu(I)-Cu(II) coordination polymer including pyrrolidine dithiocarbamate ligand. Dalton transactions (Cambridge, England : 2003), 40(10), 2218-24. https://doi.org/10.1039/c0dt01065k
Okubo, Takashi, et al. "Crystal structure and carrier transport properties of a new 3D mixed-valence Cu(I)-Cu(II) coordination polymer including pyrrolidine dithiocarbamate ligand." Dalton transactions (Cambridge, England : 2003) vol. 40,10 (2011): 2218-24. doi: https://doi.org/10.1039/c0dt01065k
Okubo T, Tanaka N, Kim KH, Anma H, Seki S, Saeki A, Maekawa M, Kuroda-Sowa T. Crystal structure and carrier transport properties of a new 3D mixed-valence Cu(I)-Cu(II) coordination polymer including pyrrolidine dithiocarbamate ligand. Dalton Trans. 2011 Mar 14;40(10):2218-24. doi: 10.1039/c0dt01065k. Epub 2010 Dec 22. PMID: 21180735.
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{6,6'-Dimeth-oxy-2,2'-[naphthalene-2,3-diylbis(nitrilo-methyl-idyne)]diphenolato}thio-cyanato-cobalt(III) diethyl ether dichloro-methane solvate.

Acta crystallographica. Section E, Structure reports online

Yu Z, Kuroda-Sowa T, Nabei A, Maekawa M, Okubo T.
PMID: 21582048
Acta Crystallogr Sect E Struct Rep Online. 2009 Feb 06;65:m257-8. doi: 10.1107/S1600536809000841.

In the title complex, [Co(C(26)H(20)N(2)O(4))(NCS)]·C(4)H(10)O·CH(2)Cl(2), the penta-coordinated Co(III) atom exhibits a distorted square-pyramidal geometry with an N,N',O,O' tetra-dentate Schiff base ligand in the basal plane and one thio-cyanate ligand at the apical site. The diethyl ether mol-ecule is located...

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Yu Z, Kuroda-Sowa T, Nabei A, et al. {6,6'-Dimeth-oxy-2,2'-[naphthalene-2,3-diylbis(nitrilo-methyl-idyne)]diphenolato}thio-cyanato-cobalt(III) diethyl ether dichloro-methane solvate. Acta Crystallogr Sect E Struct Rep Online. 2009;65:m257-8doi: 10.1107/S1600536809000841.
Yu, Z., Kuroda-Sowa, T., Nabei, A., Maekawa, M., & Okubo, T. (2009). {6,6'-Dimeth-oxy-2,2'-[naphthalene-2,3-diylbis(nitrilo-methyl-idyne)]diphenolato}thio-cyanato-cobalt(III) diethyl ether dichloro-methane solvate. Acta crystallographica. Section E, Structure reports online, 65m257-8. https://doi.org/10.1107/S1600536809000841
Yu, Zhong, et al. "{6,6'-Dimeth-oxy-2,2'-[naphthalene-2,3-diylbis(nitrilo-methyl-idyne)]diphenolato}thio-cyanato-cobalt(III) diethyl ether dichloro-methane solvate." Acta crystallographica. Section E, Structure reports online vol. 65 (2009): m257-8. doi: https://doi.org/10.1107/S1600536809000841
Yu Z, Kuroda-Sowa T, Nabei A, Maekawa M, Okubo T. {6,6'-Dimeth-oxy-2,2'-[naphthalene-2,3-diylbis(nitrilo-methyl-idyne)]diphenolato}thio-cyanato-cobalt(III) diethyl ether dichloro-methane solvate. Acta Crystallogr Sect E Struct Rep Online. 2009 Feb 06;65:m257-8. doi: 10.1107/S1600536809000841. PMID: 21582048; PMCID: PMC2968487.
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The Cytoplasm-to-Vacuole Targeting Pathway: A Historical Perspective.

International journal of cell biology

Umekawa M, Klionsky DJ.
PMID: 22481942
Int J Cell Biol. 2012;2012:142634. doi: 10.1155/2012/142634. Epub 2012 Feb 20.

From today's perspective, it is obvious that macroautophagy (hereafter autophagy) is an important pathway that is connected to a range of developmental and physiological processes. This viewpoint, however, is relatively recent, coinciding with the molecular identification of autophagy-related (Atg)...

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Umekawa M, Klionsky DJ. The Cytoplasm-to-Vacuole Targeting Pathway: A Historical Perspective. Int J Cell Biol. 2012;2012:142634doi: 10.1155/2012/142634.
Umekawa, M., & Klionsky, D. J. (2012). The Cytoplasm-to-Vacuole Targeting Pathway: A Historical Perspective. International journal of cell biology, 2012142634. https://doi.org/10.1155/2012/142634
Umekawa, Midori, and Klionsky, Daniel J. "The Cytoplasm-to-Vacuole Targeting Pathway: A Historical Perspective." International journal of cell biology vol. 2012 (2012): 142634. doi: https://doi.org/10.1155/2012/142634
Umekawa M, Klionsky DJ. The Cytoplasm-to-Vacuole Targeting Pathway: A Historical Perspective. Int J Cell Biol. 2012;2012:142634. doi: 10.1155/2012/142634. Epub 2012 Feb 20. PMID: 22481942; PMCID: PMC3296166.
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Induced pluripotent stem cells as a next-generation biomedical interface.

Laboratory investigation; a journal of technical methods and pathology

Hankowski KE, Hamazaki T, Umezawa A, Terada N.
PMID: 21555998
Lab Invest. 2011 Jul;91(7):972-7. doi: 10.1038/labinvest.2011.85. Epub 2011 May 09.

Recent advances in DNA sequencing technologies and subsequent progress in genome-wide association study (GWAS) are rapidly changing the landscape of human diseases. Our knowledge on disease-gene linkage has been exponentially growing, and soon we will obtain complete maps of...

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Hankowski KE, Hamazaki T, Umezawa A, et al. Induced pluripotent stem cells as a next-generation biomedical interface. Lab Invest. 2011;91(7):972-7doi: 10.1038/labinvest.2011.85.
Hankowski, K. E., Hamazaki, T., Umezawa, A., & Terada, N. (2011). Induced pluripotent stem cells as a next-generation biomedical interface. Laboratory investigation; a journal of technical methods and pathology, 91(7), 972-7. https://doi.org/10.1038/labinvest.2011.85
Hankowski, Katherine E, et al. "Induced pluripotent stem cells as a next-generation biomedical interface." Laboratory investigation; a journal of technical methods and pathology vol. 91,7 (2011): 972-7. doi: https://doi.org/10.1038/labinvest.2011.85
Hankowski KE, Hamazaki T, Umezawa A, Terada N. Induced pluripotent stem cells as a next-generation biomedical interface. Lab Invest. 2011 Jul;91(7):972-7. doi: 10.1038/labinvest.2011.85. Epub 2011 May 09. PMID: 21555998; PMCID: PMC3727242.
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Allogeneic amniotic membrane-derived mesenchymal stromal cell transplantation in a porcine model of chronic myocardial ischemia.

Journal of stem cells & regenerative medicine

Kimura M, Toyoda M, Gojo S, Itakura Y, Kami D, Miyoshi S, Kyo S, Ono M, Umezawa A.
PMID: 24693195
J Stem Cells Regen Med. 2012 Nov 26;8(3):171-80. eCollection 2012.

Introduction. Amniotic membrane contains a multipotential stem cell population and is expected to possess the machinery to regulate immunological reactions. We investigated the safety and efficacy of allogeneic amniotic membrane-derived mesenchymal stromal cell (AMSC) transplantation in a porcine model...

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Kimura M, Toyoda M, Gojo S, et al. Allogeneic amniotic membrane-derived mesenchymal stromal cell transplantation in a porcine model of chronic myocardial ischemia. J Stem Cells Regen Med. 2012;8(3):171-80
Kimura, M., Toyoda, M., Gojo, S., Itakura, Y., Kami, D., Miyoshi, S., Kyo, S., Ono, M., & Umezawa, A. (2012). Allogeneic amniotic membrane-derived mesenchymal stromal cell transplantation in a porcine model of chronic myocardial ischemia. Journal of stem cells & regenerative medicine, 8(3), 171-80.
Kimura, M, et al. "Allogeneic amniotic membrane-derived mesenchymal stromal cell transplantation in a porcine model of chronic myocardial ischemia." Journal of stem cells & regenerative medicine vol. 8,3 (2012): 171-80.
Kimura M, Toyoda M, Gojo S, Itakura Y, Kami D, Miyoshi S, Kyo S, Ono M, Umezawa A. Allogeneic amniotic membrane-derived mesenchymal stromal cell transplantation in a porcine model of chronic myocardial ischemia. J Stem Cells Regen Med. 2012 Nov 26;8(3):171-80. eCollection 2012. PMID: 24693195; PMCID: PMC3908291.
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Showing 13 to 24 of 499 entries