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2010 Book Chapter Toll-like receptor 2 mediated dendritic cell activation: Key target for lipopeptide vaccines designZaman, Mehfuz, Skwarczynski, Marius and Toth, Istvan (2010). Toll-like receptor 2 mediated dendritic cell activation: Key target for lipopeptide vaccines design. Dendritic Cells: Types, Life Cycles and Biological Functions. (pp. 63-80) edited by Lorraine C. Welles. New York, NY, U.S.A.: Nova Science Publishers. |
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2009 Journal Article Development of conformational mimetics of conserved Streptococcus pyogenes minimal epitope as vaccine candidatesZhong, Wei, Skwarczynski, Mariusz and Toth, Istvan (2009). Development of conformational mimetics of conserved Streptococcus pyogenes minimal epitope as vaccine candidates. Current Drug Delivery, 6 (5), 520-527. doi: 10.2174/156720109789941650 |
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2009 Journal Article Development of highly pure alpha-helical lipoglycopeptides as self-adjuvanting vaccinesZhong, Wei, Skwarczynski, Mariusz, Simerska, Pavla, Good, Michael F. and Toth, Istvan (2009). Development of highly pure alpha-helical lipoglycopeptides as self-adjuvanting vaccines. Tetrahedron, 65 (17), 3459-3464. doi: 10.1016/j.tet.2009.02.060 |
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2009 Journal Article Lipid core peptide system for gene, drug, and vaccine deliveryZhong, Wei, Skwarczynski, Mariusz and Toth, Istvan (2009). Lipid core peptide system for gene, drug, and vaccine delivery. Australian Journal of Chemistry, 62 (9), 956-967. doi: 10.1071/CH09149 |
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2009 Journal Article Click peptide by use of the O-acyl isopeptide method: Production of Amyloid Beta peptide from water-soluble analogueTaniguchi, Atsuhiko, Sohma, Youhei, Skwarczynski, Mariusz, Okada, Takuma, Ikeda, Keisuke, Prakash, Halan, Mukai, Hidehito, Kimura, Tooru, Hayashi, Yoshio, Hirota, Shun, Matsuzaki, Katsumi and Kiso, Yoshiaki (2009). Click peptide by use of the O-acyl isopeptide method: Production of Amyloid Beta peptide from water-soluble analogue. Peptide Science, 397-400. |
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2009 Journal Article Application of intramolecular migration reaction in peptide chemistry to chemical biology, chemical pharmaceutics and medicinal chemistryHayashi, Yoshio, Yamazaki, Yuri, Skwarczynski, Mariusz, Sohma, Youhei, Taniguchi, Atsuhiko, Noguchi, Mayo, Kimura, Tooru, Neuteboom, Saskia, Potts, Barbara, Lloyd, G. Kenneth and Kiso, Yoshiaki (2009). Application of intramolecular migration reaction in peptide chemistry to chemical biology, chemical pharmaceutics and medicinal chemistry. Advances in Experimental Medicine and Biology, 611, 513-514. doi: 10.1007/978-0-387-73657-0_223 |
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2009 Journal Article Design and synthesis of lipopeptide-carbohydrate assembled multivalent vaccine candidates using native chemical ligationZhong, Wei, Skwarczynski, Mariusz, Fujita, Yoshio, Simerska, Pavla, Good, Michael F. and Toth, Istvan (2009). Design and synthesis of lipopeptide-carbohydrate assembled multivalent vaccine candidates using native chemical ligation. Australian Journal of Chemistry, 62 (9), 993-999. doi: 10.1071/CH09065 |
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2008 Journal Article Controlled production of amyloid beta peptide from a photo-triggered, water-soluble precursor "click peptide"Taniguchi, Atsuhiko, Skwarczynski, Mariusz, Sohma, Youhei, Okada, Takuma, Ikeda, Keisuke, Prakash, Halan, Mukai, Hidehito, Hayashi, Yoshio, Kimura, Tooru, Hirota, Shun, Matsuzaki, Katsumi and Kiso, Yoshiaki (2008). Controlled production of amyloid beta peptide from a photo-triggered, water-soluble precursor "click peptide". ChemBioChem, 9 (18), 3055-3065. doi: 10.1002/cbic.200800503 |
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2008 Journal Article Development of novel water-soluble photocleavable protective group and its application for design of photoresponsive paclitaxel prodrugsNoguchi, Mayo, Skwarczynski, Mariusz, Prakash, Halan, Hirota, Shun, Kimura, Tooru, Hayashi, Yoshio and Kiso, Yoshiaki (2008). Development of novel water-soluble photocleavable protective group and its application for design of photoresponsive paclitaxel prodrugs. Bioorganic and Medicinal Chemistry, 16 (10), 5389-5397. doi: 10.1016/j.bmc.2008.04.022 |
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2007 Journal Article Application of the O-N intramolecular acyl migration reaction in medicinal chemistrySkwarczynski, Mariusz and Kiso, Yoshiaki (2007). Application of the O-N intramolecular acyl migration reaction in medicinal chemistry. Current Medicinal Chemistry, 14 (26), 2813-2823. doi: 10.2174/092986707782360123 |
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2007 Conference Publication Development of new photoresponsive paclitaxel prodrugNoguchi, Mayo, Skwarczynski, Mariusz, Prakash, Halan, Hirota, Shun, Kimura, Tooru, Hayashi, Yoshio and Kiso, Yoshiaki (2007). Development of new photoresponsive paclitaxel prodrug. 第４４回 ペプチド討論会 (44th Japanese Peptide Symposium), Toyama, Toyama Prefecture, Japan, 7-9 November 2007. Osaka, Japan: Protein Research Foundation. |
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2007 Conference Publication Synthesis of a Novel Water-Soluble Paclitaxel Prodrug, Arginine-Isotaxel, and its Physicochemical and Caco-2 Transport PropertiesSuehisa, Y., Noguchi, M., Skwarczynski, M., Yamamoto, A., Kiso, Y., Hayashi, Y. and Fujita, T. (2007). Synthesis of a Novel Water-Soluble Paclitaxel Prodrug, Arginine-Isotaxel, and its Physicochemical and Caco-2 Transport Properties. 8th Annual Meeting of the International Society for Study of Xenobiotics, Sendai, Japan, 9-12 October 2007. PHILADELPHIA: Informa Healthcare. |
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2007 Journal Article The synthesis of bioactive peptides based on O-Acyl Isopeptide Method: Application of O-acyl isodipeptide unitsAbe, Naoko, Fukao, Fukue, Hayashi, Yoshio, Ito, Nui, Kimura, Tooru, Kiso, Yoshiaki, Nakamura, Setsuko, Skwarczynski, Mariusz, Sohma, Youhei, Taniguchi, Atsuhiko and Yoshiya, Taku (2007). The synthesis of bioactive peptides based on O-Acyl Isopeptide Method: Application of O-acyl isodipeptide units. Peptide Science: Proceedings of the Japanese Peptide Symposium, 44, 187-190. |
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2007 Journal Article "O-acyl isopeptide method" for peptide synthesis: Synthesis of forty kinds of "O-acyl isodipeptide unit" Boc-Ser/Thr(Fmoc-Xaa)-OHYoshiya, Taku, Taniguchi, Atsuhiko, Sohma, Youhei, Fukao, Fukue, Nakamura, Setsuko, Abe, Naoko, Ito, Nui, Skwarczynski, Mariusz, Kimura, Tooru, Hayashi, Yoshio and Kiso, Yoshiaki (2007). "O-acyl isopeptide method" for peptide synthesis: Synthesis of forty kinds of "O-acyl isodipeptide unit" Boc-Ser/Thr(Fmoc-Xaa)-OH. Organic and Biomolecular Chemistry, 5 (11), 1720-1730. doi: 10.1039/b702284k |
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2006 Journal Article Paclitaxel prodrugs: Toward smarter delivery of anticancer agentsSkwarczynski, Mariusz, Hayashi, Yoshio and Kiso, Yoshiaki (2006). Paclitaxel prodrugs: Toward smarter delivery of anticancer agents. J. Med. Chem., 49 (25), 7253-7269. doi: 10.1021/jm0602155 |
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2006 Journal Article 'Click peptide': A novel 'O-acyl isopeptide method' for peptide synthesis and chemical biology-oriented synthesis of amyloid beta peptide analoguesSohma, Youhei, Taniguchi, Atsuhiko, Yoshiya, Taku, Chiyomori, Yousuke, Fukao, Fukue, Nakamura, Setsuko, Skwarczynski, Mariusz, Okada, Takuma, Ikeda, Keisuke, Hayashi, Yoshio, Kimura, Tooru, Hirota, Shun, Matsuzaki, Katsumi and Kiso, Yoshiaki (2006). 'Click peptide': A novel 'O-acyl isopeptide method' for peptide synthesis and chemical biology-oriented synthesis of amyloid beta peptide analogues. Journal of Peptide Science, 12 (12), 823-828. doi: 10.1002/psc.817 |
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2006 Journal Article Application of intramolecular carbonate-carbamate migrationSkwarczynski, M., Noguchi, M., Sohma, Y., Kimura, T., Hayashi, Y. and Kiso, Y. (2006). Application of intramolecular carbonate-carbamate migration. Chimica Oggi, 24 (6), 30-32. |
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2006 Journal Article Development of first photoresponsive prodrug of paclitaxelSkwarczynski, Mariusz, Noguchi, Mayo, Hirota. Shun, Sohma, Youhei, Kimura, Tooru, Hayashi, Yoshio and Kiso, Yoshiaki (2006). Development of first photoresponsive prodrug of paclitaxel. Bioorganic and Medicinal Chemistry Letters, 16 (17), 4492-4496. doi: 10.1016/j.bmcl.2006.06.030 |
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2006 Journal Article 'O-Acyl isopeptide method' for the efficient synthesis of difficult sequence-containing peptides: Use of 'O-acyl isodipeptide unit'Sohma, Youhei, Taniguchi, Atsuhiko, Skwarczynski, Mariusz, Yoshiya, Taku, Fukao, Fukue, Kimura, Tooru, Hayashi, Yoshio and Kiso, Yoshiaki (2006). 'O-Acyl isopeptide method' for the efficient synthesis of difficult sequence-containing peptides: Use of 'O-acyl isodipeptide unit'. Tetrahedron Letters, 47 (18), 3013-3017. doi: 10.1016/j.tetlet.2006.03.017 |
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2006 Journal Article O-N intramolecular alkoxycarbonyl migration of typical protective groups in hydroxyamino acidsSkwarczynski, Mariusz, Sohma, Youhei, Noguchi, Mayo, Kimura, Tooru, Hayashi, Yoshio and Kiso, Yoshiaki (2006). O-N intramolecular alkoxycarbonyl migration of typical protective groups in hydroxyamino acids. Journal of Organic Chemistry, 71 (6), 2542-2545. doi: 10.1021/jo0525579 |
