œAûPŒõ—¹A’Ë’J—S‰îAŒ´“c“ñ˜NA–¯H@‹ÏAu3ˆÊ‚̃rƒjƒ‹Šî‚Ì…˜a‚ðG”}‚·‚éBchF‚ÆBchV‚É‚æ‚鈟‰”ƒoƒNƒeƒŠƒIƒNƒƒƒtƒBƒŠƒhd‚Æ‚»‚̃zƒ‚ƒƒO‘̂̒E…”½‰ž‚È‚ç‚тɂ»‚̉ž—pvA‘æ64‰ñ“ú–{A•¨¶—Šw‰ï”N‰ïAPA-001 (å‘ä, 2023”N3ŒŽ).
²“¡éD^AœAûPŒõ—¹A“c’†—ºˆêAˆÉ“¡ ŽõA–¯H@‹ÏAu3ˆÊ‚Ü‚½‚Í8ˆÊ’uŠ·ƒNƒƒƒtƒBƒ‹—U“±‘Ì‚ð—p‚¢‚½¶‘ÌŠO‚Å‚ÌSGRy‘f”½‰ž‚Æ‚»‚̊“ÁˆÙ«v‘æ64‰ñ“ú–{A•¨¶—Šw‰ï”N‰ïAPB-002 (å‘ä, 2023”N3ŒŽ).
Œ´“c“ñ˜NA–؉º—Y‰îA‹´V „AaŒû ³AŽR–{ Œ’A–¯H@‹ÏAu—ÎF—°‰©Œõ‡¬×‹Û‚̃Nƒƒƒ\[ƒ€F‘f‚̃Qƒ‹‰»‚Æ‚»‚Ì\‘¢‚ÌŠÏŽ@vA“ú–{‰»Šw‰ï‘æ103t‹G”N‰ïAP1-1pm-11 (–ì“c, 2023”N3ŒŽ).
—Ñ ‰À‹PA‰ªN‹MA–¯H@‹ÏA‹{•’qOAu7ˆÊ‚Ée…Šî‚ð—L‚·‚鈟‰”3-ƒqƒhƒƒLƒVƒƒ`ƒ‹ƒNƒƒŠƒ“‚̇¬‚Æ•¨«vA“ú–{‰»Šw‰ï‘æ103t‹G”N‰ïAP1-1pm-18 (–ì“c, 2023”N3ŒŽ).
M. Hirose, J. Harada, Y. Kashiyama, H. Tamiaki,uProposed BciC enzymatic hydrolysis and decarboxylation mechanismvA“ú–{‰»Šw‰ï‘æ103t‹G”N‰ïAE1661-1vn-01 (–ì“c, 2023”N3ŒŽ).
–¯H@‹ÏA‹vŒ´—I^A’†–쌒‰›AuƒNƒƒƒtƒBƒ‹“ñ—ʑ̂̇¬‚Æ‚»‚̃Nƒƒƒ][ƒ€Œ^Ž©ŒÈ‰ï‡vA“ú–{‰»Šw‰ï‘æ103t‹G”N‰ïAK605-2am-08 (–ì“c, 2023”N3ŒŽ).
¼ì—T‘¾A–¯H@‹ÏAu1,3-ƒWƒtƒFƒjƒ‹ƒeƒgƒ‰ƒ]ƒŠƒEƒ€Œnƒƒ\ƒCƒIƒ“‰»‡•¨‚̇¬‚ÆŒõ•¨«vA“ú–{‰»Šw‰ï‘æ103t‹G”N‰ïAK604-2am-08 (–ì“c, 2023”N3ŒŽ).
–¯H@‹ÏAoˆä‚Ђæ‚èAˆÀˆä‚Ý‚¸‚«Au‚މ—n«ƒoƒNƒeƒŠƒIƒNƒƒƒtƒBƒ‹-d—Þ‰‘̂̇¬‚ÆŽ©ŒÈ‰ï‡vA“ú–{‰»Šw‰ï‘æ103t‹G”N‰ïAK605-2am-11 (–ì“c, 2023”N3ŒŽ).
–¯H@‹ÏA‹´–{‘å˜aAu132ˆÊ“ñ’uŠ·ƒNƒƒƒtƒBƒ‹—ނ̇¬‚Æ‚»‚ÌŽ©ŒÈ‰ï‡vA“ú–{‰»Šw‰ï‘æ103t‹G”N‰ïAK605-2am-12 (–ì“c, 2023”N3ŒŽ).
–¯H@‹ÏA’†ä±Œ«ŒáA²X–Ø^ˆêAu8ˆÊ’EƒAƒ‹ƒLƒ‹‰»ƒoƒNƒeƒŠƒIƒNƒƒƒtƒBƒ‹d—Þ‰‘̂̇¬‚ÆŽ©ŒÈ‰ï‡‹““®vA“ú–{‰»Šw‰ï‘æ103t‹G”N‰ïAK605-2am-13 (–ì“c, 2023”N3ŒŽ).
Œ´ LsA–¯H@‹ÏAu17ˆÊ‚É’·½Ž}•ª‚©‚êƒAƒ‹ƒLƒ‹Šî‚ð—L‚·‚éƒoƒNƒeƒŠƒIƒNƒƒƒtƒBƒ‹-d—ޗΑ̂̎©ŒÈ‰ï‡‹““®vA“ú–{‰»Šw‰ï‘æ103t‹G”N‰ïAK605-2am-14 (–ì“c, 2023”N3ŒŽ).
¼Œ´ãÄŒáAΈä’C–A–¯H@‹ÏAuƒiƒtƒ^ƒŒƒ“˜AŒ‹ƒNƒƒƒtƒBƒ‹ƒ_ƒCƒ}[‚ÌŽ©ŒÈWςɂæ‚é’´•ªŽqƒiƒmƒŠƒ“ƒO‚Ì\’zvA“ú–{‰»Šw‰ï‘æ103t‹G”N‰ïAK605-2am-06 (–ì“c, 2023”N3ŒŽ).
–¯H@‹ÏA–Ñ—˜—DØAˆÀˆä‚Ý‚¸‚«AuƒNƒƒƒtƒBƒ‹-BODIPY˜AŒ‹‘̂̇¬‚Æ•¨«vA“ú–{‰»Šw‰ï‘æ103t‹G”N‰ïAK602-2vn-02 (–ì“c, 2023”N3ŒŽ).
–¯H@‹ÏA´…—I—™A¼ì—T‘¾AuƒtƒFƒƒZƒjƒ‹Šî‚ð‚RˆÊ‚É—L‚·‚éƒNƒƒƒtƒBƒ‹—U“±‘̂̇¬‚Æ‚»‚Ì•¨«vA“ú–{‰»Šw‰ï‘æ103t‹G”N‰ïAK602-2vn-04 (–ì“c, 2023”N3ŒŽ).
–¯H@‹ÏA‹g“‡‘‹IAu3ˆÊ‚ɃLƒmƒ“—Þ‚ð—L‚·‚éƒNƒƒƒtƒBƒ‹—U“±‘̂̇¬‚Æ•¨«vA“ú–{‰»Šw‰ï‘æ103t‹G”N‰ïAK602-2vn-05 (–ì“c, 2023”N3ŒŽ).
‰i’J”ü—TA”óŒû^OA–¯H@‹ÏA¼Œ´ãÄŒáAuŽ_‰ž“š«Œõ‘Š´ÜŠJ”‚ÉŒü‚¯‚½ƒyƒvƒ`ƒh-ƒNƒƒƒtƒBƒ‹•¡‡‘̂̇¬‚Æ\‘¢EŒõ•¨«vA“ú–{‰»Šw‰ï‘æ103t‹G”N‰ïAB444-3am-01 (–ì“c, 2023”N3ŒŽ).
–¯H@‹ÏA¯ —Y‘åA—é–Ø ”£Aˆ¢•” —³AuƒAƒNƒŠƒ‹Ž_Œ^Šî‚ð—L‚·‚éƒNƒƒƒtƒBƒ‹‚ðŒõ‘Š´Ü‚Æ‚µ‚½F‘f/”¼“±‘̃nƒCƒuƒŠƒbƒhŒõG”}‚ð—p‚¢‚½‰ÂŽ‹Œõ…‘f¶¬vA“ú–{‰»Šw‰ï‘æ103t‹G”N‰ïAK306-3am-02 (–ì“c, 2023”N3ŒŽ).
–¯H@‹ÏAŽR‰ºŒª^AœAûPŒõ—¹Auπ‹¤–ðŒ^EŠÂkŠÂƒNƒƒƒtƒBƒ‹—U“±‘̂̇¬‚Æ•¨«vA“ú–{‰»Šw‰ï‘æ103t‹G”N‰ïAK702-3am-03 (–ì“c, 2023”N3ŒŽ).
–¯H@‹ÏA‹g‘ºN‘åA¬Š}Œ´ LAuƒNƒƒƒtƒBƒ‹—Þ‚Ì132ˆÊ‚ł̃}ƒCƒPƒ‹•t‰Á”½‰ž‘̂̇¬‚Æ•¨«vA“ú–{‰»Šw‰ï‘æ103t‹G”N‰ïAK702-3am-04 (–ì“c, 2023”N3ŒŽ).
–¯H@‹ÏA—Ñ ä—DAu20ˆÊ‚ɃAƒŠ[ƒ‹Šî‚ð—L‚·‚éƒNƒƒƒtƒBƒ‹—U“±‘̂̇¬‚Ɖñ“]ˆÙ«vA“ú–{‰»Šw‰ï‘æ103t‹G”N‰ïAK702-3vn-08 (–ì“c, 2023”N3ŒŽ).
–¯H@‹ÏAù‘q—ŽqA–؉º—Y‰îAu‚RˆÊ‚É‚¨‚¢‚Äπ‹¤–ðƒXƒy[ƒT[‚ŘAŒ‹‚µ‚½ƒNƒƒƒtƒBƒ‹“ñ—ʑ̂̇¬‚Æ‚»‚Ì•¨«vA“ú–{‰»Šw‰ï‘æ103t‹G”N‰ïAK702-3vn-09 (–ì“c, 2023”N3ŒŽ).
–¯H@‹ÏA”W‘º éDAœAûPŒõ—¹A”ŽR—Sˆê˜YAuƒvƒƒeƒBƒXƒg‚É‚æ‚éƒNƒƒƒtƒBƒ‹—Þ‚Ì\‘¢E‹@”\‰ü•ÏvA“ú–{‰»Šw‰ï‘æ103t‹G”N‰ïAD1411-3vn-11 (–ì“c, 2023”N3ŒŽ).
Y. Hashimoto, T. Takeda, H. Tamiaki, "Synthesis and self-aggregation of C132,C132-disubstituted chlorophyll derivatives," Ž©ŒÈWςƒ´•ªŽqƒS[ƒhƒ“Œ¤‹†ƒZƒ~ƒi[A#9 (ƒXƒCƒXEƒŒƒfƒBƒAƒuƒ‹ƒŒ, 2023”N5ŒŽ).
Y. Hisahara, T. Nakano, H. Tamiaki, "Self-aggregation of synthetic chlorophyll derivatives as models of green photosynthetic bacterial antenna systems," Ž©ŒÈWςƒ´•ªŽqƒS[ƒhƒ“Œ¤‹†ƒZƒ~ƒi[A#20 (ƒXƒCƒXEƒŒƒfƒBƒAƒuƒ‹ƒŒ, 2023”N5ŒŽ).
Y. Hisahara, T. Nakano, H. Tamiaki, "Synthesis of chlorophyll dimers and their self-aggregation in an aqueous micelle," Ž©ŒÈWςƒ´•ªŽqƒS[ƒhƒ“Œ¤‹†‰ï‹cATuesday-#17 (ƒXƒCƒXEƒŒƒfƒBƒAƒuƒ‹ƒŒ, 2023”N5ŒŽ).
Y. Hashimoto, H. Tamiaki, "Supramolecular self-aggregates of synthetic C132-substituted bacteriochlorophyll-d analogs," Ž©ŒÈWςƒ´•ªŽqƒS[ƒhƒ“Œ¤‹†‰ï‹cATuesday-#25 (ƒXƒCƒXEƒŒƒfƒBƒAƒuƒ‹ƒŒ, 2023”N5ŒŽ).
K. Nakakuki, S. Sasaki, H. Tamiaki, gSynthesis of dealkylated bacteriochlorophyll-d analogs and their self-aggregation,h SNCPP23, S-2/P-33 (‘’Ã, 2023”N6ŒŽ).m‘I”²u‰‰n
H. Sasakura, Y. Kinoshita, H. Tamiaki, gSynthesis and optical properties of π-conjugated hexatriene-linked chlorophyll dyad,h SNCPP23, S-3/P-43 (‘’Ã, 2023”N6ŒŽ).m‘I”²u‰‰n
R. Ataka, H. Tamiaki, gSynthesis of chlorophyll derivatives methylated at the inner ring nitrogen atom and C3-substitution effect on their optical properties,h SNCPP23, P-2 (‘’Ã, 2023”N6ŒŽ).
Y. Hashimoto, H. Tamiaki, gSupramolecular self-aggregates of synthetic 132-substituted chlorophyll derivatives,h SNCPP23, P-6 (‘’Ã, 2023”N6ŒŽ).
M. Hayashi, H. Tamiaki, gSynthesis of atropisomerically pure 20-arylated chlorophyll-a derivatives,h SNCPP23, P-7 (‘’Ã, 2023”N6ŒŽ).
Y. Hayashi, H. Tamiaki, T. Miyatake, gSynthesis and properties of zinc 3-hydroxymethylchlorin possessing an oligooxyethylene group at the 7-position,h SNCPP23, P-8 (‘’Ã, 2023”N6ŒŽ).
Y. Hisahara, T. Nakano, H. Tamiaki, gSelf-aggregation of synthetic zinc chlorophyll dyads in aqueous micelle,h SNCPP23, P-9 (‘’Ã, 2023”N6ŒŽ).
Y. Hoshi, H. Suzuki, R. Abe, H. Tamiaki, gSynthesis of chlorophyll-a derivatives with an acrylic acid-type anchor and their photosensitizing activities for hydrogen evolution on TiO2–Pt,h SNCPP23, P-10 (‘’Ã, 2023”N6ŒŽ).
S. Kichishima, H. Tamiaki, gSynthesis and physical properties of chlorophyll derivatives possessing a quinone moiety at the 3-position,h SNCPP23, P-17 (‘’Ã, 2023”N6ŒŽ).
Y. Kinoshita, N. Deromachi, K. Tanaka, H. Tamiaki, gCatalytic organic-hydride transfer to CO2 mediated with ruthenium complexes,h SNCPP23, P-19 (‘’Ã, 2023”N6ŒŽ).
Y. Matsukawa, H. Tamiaki, gHighly fluorescent mesoionic compounds,h SNCPP23, P-26 (‘’Ã, 2023”N6ŒŽ).
Y. Mori, H. Tamiaki, gChlorosome-type self-aggregation of chlorophyll–BODIPY conjugate efficiently absorbing green light,h SNCPP23, P-29 (‘’Ã, 2023”N6ŒŽ).
H. Nomura, Y. Kashiyama, H. Tamiaki, gAnalysis of chlorophyll metabolism by algivorous protists,h SNCPP23, P-34 (‘’Ã, 2023”N6ŒŽ).
N. Hara, H. Tamiaki, gSelf-aggregation of zinc bacteriochlorophyll-d analogs with linear and branch type of alkyl chains,h SNCPP23, O-3 (‘’Ã, 2023”N6ŒŽ).mµ‘Òu‰‰n
¼Œ´ãÄŒáAΈä’C–AœAûP—D•ãA–¯H@‹ÏAuƒiƒtƒ^ƒŒƒ“˜AŒ‹ƒNƒƒƒtƒBƒ‹“ñ—ʑ̂̒uŠ·ˆÊ’u‚̈Ⴂ‚É‚æ‚é’´•ªŽq\‘¢•ω»v‘æ20‰ñƒzƒXƒgEƒQƒXƒg’´•ªŽq‰»ŠwƒVƒ“ƒ|ƒWƒEƒ€A1BO8 (”ª‰¤Žq, 2023”N6ŒŽ).
œAûPŒõ—¹AŒ´“c“ñ˜NA”ŽR—Sˆê˜YA–¯H@‹ÏAuƒNƒƒƒ][ƒ€‚ð\’z‚·‚éƒNƒƒƒtƒBƒ‹•ªŽq‚̶‡¬y‘fBciC‚Ì—\‘z\‘¢‚©‚甌©‚³‚ꂽ2dG”}‹@”\«‚Æ‚»‚̃ƒJƒjƒYƒ€‚̉ð–¾vA‘æ‚R‚O‰ñŒõ‡¬ƒZƒ~ƒi[2023AO-1 (–¼ŒÃ‰®, 2023”N6ŒŽ). [ŽOŽºÜŽóÜ]
ˆÀ‘î—ŽqAbŒ´@äA¬Š}Œ´@LA–¯H@‹ÏAuƒJƒ`ƒIƒ“Œ^ƒNƒƒƒtƒBƒ‹‚̇¬‚Æ‚»‚Ì“WŠJvA‘æ‚R‚O‰ñŒõ‡¬ƒZƒ~ƒi[2023AO-8 (–¼ŒÃ‰®, 2023”N6ŒŽ).
H. Sasakura, H. Tamiaki, gSynthesis of π-Conjugated Chlorophyll Dimer and Their Specific Optical Properties,h ‘æ23‰ñƒeƒgƒ‰‚Öƒhƒƒ“ƒVƒ“ƒ|ƒWƒEƒ€, P1-116 (ƒXƒEƒF[ƒfƒ“Eƒˆ[ƒeƒ{ƒŠ, 2023”N6ŒŽ).
K. Nakakuki, S. Sasaki, H. Tamiaki, gSelf-aggregation of synthetic dealkylated bacteriochlorophyll-d analogs,h ‘æ23‰ñƒeƒgƒ‰‚Öƒhƒƒ“ƒVƒ“ƒ|ƒWƒEƒ€, P1-117 (ƒXƒEƒF[ƒfƒ“Eƒˆ[ƒeƒ{ƒŠ, 2023”N6ŒŽ).
Y. Hoshi, H. Suzuki, R. Abe, H. Tamiaki, gVisible-light illuminated hydrogen evolution using dye-semiconductor hybrids: Effect of acrylic acid-type anchors of chlorophyll-a derivatives photosensitizer,h 31th International Conference on Photochemistry (ICP 2023), P25-105 (ŽD–y, 2023”N7ŒŽ).
Y. Mori, M. Yasui, H. Tamiaki, gDevelopment of chlorosome-type artificial photosynthetic antenna efficiently absorbing green light,h ‘æ20‰ñƒˆ[ƒƒbƒpŒõ¶•¨Šw‰ï‹ci20th ESP 2023jP87 (ƒtƒ‰ƒ“ƒXEƒŠƒˆƒ“, 2023”N8ŒŽ). [Short oral presentation]
’†žŠ—ÁŽqA”óŒû^OA–¯H@‹ÏA¼Œ´ãÄŒáAuƒyƒvƒ`ƒh-ƒNƒƒƒtƒBƒ‹•¡‡‘̂̎©ŒÈWςɂæ‚éƒ`ƒ…[ƒuóŒõ•ßWƒAƒ“ƒeƒiƒ‚ƒfƒ‹‚Ì\’zv, 2023”NŒõ‰»Šw“¢˜_‰ï, 2P16 (L“‡, 2023”N9ŒŽ).
‰i’J”ü—TA”óŒû^OA–¯H@‹ÏA¼Œ´ãÄŒáAupH‰ž“š«Œõ‘Š´ÜŠJ”‚ÉŒü‚¯‚½ƒyƒvƒ`ƒh-ƒNƒƒƒtƒBƒ‹Ž©ŒÈWϑ̂̕]‰¿v, 2023”NŒõ‰»Šw“¢˜_‰ï, 3P16 (L“‡, 2023”N9ŒŽ).
¼ì—T‘¾A–¯H@‹ÏAu‹ŒuŒõ«—L‹@•ªŽq1,3-ƒWƒAƒŠ[ƒ‹ƒeƒgƒ‰ƒ]ƒŠƒEƒ€Œnƒƒ\ƒCƒIƒ“‚̇¬‚Æ”Œõ“Á«v, 2023”NŒõ‰»Šw“¢˜_‰ï, 3P71 (L“‡, 2023”N9ŒŽ).
—Ñ ‰À‹PA–¯H@‹ÏA‹{•’qOAuˆŸ‰”3-ƒqƒhƒƒLƒVƒƒ`ƒ‹ƒNƒƒŠƒ“‚Ì7ˆÊ‚É—L‚·‚éƒIƒŠƒSƒIƒLƒVƒGƒ`ƒŒƒ“Šî‚ª—^‚¦‚鎩ŒÈ‰ï‡‚ւ̉e‹¿v, ‘æ33‰ñŠî‘b—L‹@‰»Šw“¢˜_‰ï, 2P140 (‰ªŽR, 2023”N9ŒŽ).
‹vŒ´—I^A’†–쌒‰›A–¯H@‹ÏAu‚RˆÊCüƒoƒNƒeƒŠƒIƒNƒƒƒtƒBƒ‹d—Þ‰‘̂̇¬‚ÆŽ©ŒÈ‰ï‡v, ‘æ33‰ñŠî‘b—L‹@‰»Šw“¢˜_‰ï, 2P150 (‰ªŽR, 2023”N9ŒŽ).
H. Tamiaki, K. Nakakuki, S. Nishibori, gChlorophylls and their synthetic analogs,h 15th ICTPPO, PL-2 (Œä“aê, 2023”N9ŒŽ). [Šî’²u‰‰]
Y. Kashiyama, H. Tamiaki, gBiochemical elucidation of CPE-accumulating chlorophyll catabolism conserved among diverse eukaryotes,h 15th ICTPPO, O3-1 (Œä“aê, 2023”N9ŒŽ). [µ‘Òu‰‰]
Y. Tsukatani, H. Mitsuaki, J. Harada, H. Tamiaki, gNovel enzymatic activities of geranylgeranyl reductase from Halorhodospira halochloris, resulting in the production of bacteriochlorophyll with an unusual phytadienyl tail,h 15th ICTPPO, P1-1 (Œä“aê, 2023”N9ŒŽ).
S. Sato, R. Tanaka, M. Hirose, H. Tamiaki, H. Ito, gIn vitro analysis of the chelating and dechelating reactions of Stay Green Related (SGR) Mg dechelatase,h 15th ICTPPO, P1-7 (Œä“aê, 2023”N9ŒŽ).
S. Kichishima, H. Tamiaki, gSynthesis and physical properties of chlorophyll–quinone conjugates,h 15th ICTPPO, P3-1 (Œä“aê, 2023”N9ŒŽ).
‹´–{‘å˜aAˆÀˆä‚Ý‚¸‚«A–¯H@‹ÏAu132ˆÊ’uŠ·ƒ|ƒ‹ƒtƒBƒŠƒ“Œ^ƒoƒNƒeƒŠƒIƒNƒƒƒtƒBƒ‹-dƒGƒiƒ“ƒ`ƒIƒ}[‚̇¬‚ÆŽ©ŒÈ‰ï‡v, ‘æ39‰ñ—L‹@‡¬‰»ŠwƒZƒ~ƒi[, P-85 (’W˜H, 2023”N9ŒŽ).
¼–x—Á‰ÔAŒ´@LsA¬Š}Œ´@LA–¯H@‹ÏAuƒtƒ‹ƒIƒƒAƒ‹ƒLƒ‹‰»ƒNƒƒƒtƒBƒ‹—U“±‘̂̇¬‚Æ•¨«vA‘æ46‰ñƒtƒb‘f‰»Šw“¢˜_‰ïAP40 (–‡•û, 2023”N10ŒŽ).
H“¡—ʼn›A‰ÔŽR”Ž‹IA–¯H@‹ÏA–îŠLŽjŽ÷AuƒNƒƒƒtƒBƒ‹’´•ªŽqƒ|ƒŠƒ}[‚ÌŽžŠÔ”“W“I‚È\‘¢“]ˆÚvA‘æ13‰ñCSJ‰»ŠwƒtƒFƒXƒ^AP4-020 (“Œ‹ž, 2023”N10ŒŽ).
ù‘q—ŽqA–؉º—Y‰îA–¯H@‹ÏAu3ˆÊ˜AŒ‹π‹¤–ðŒ^ƒNƒƒƒtƒBƒ‹“ñ—ʑ̂̇¬‚Æ•¨«vA‘æ13‰ñCSJ‰»ŠwƒtƒFƒXƒ^AP7-056 (“Œ‹ž, 2023”N10ŒŽ).
‚‹{ ËA‰ÔŽR”Ž‹IA–¯H@‹ÏA–îŠLŽjŽ÷AuƒNƒƒƒtƒBƒ‹“ñ—ʑ̂̎©ŒÈW‡‚Æ‹à‘®”zˆÊ‚É‚æ‚éW‡‹““®‚̕ω»vA‘æ13‰ñCSJ‰»ŠwƒtƒFƒXƒ^AP9-056 (“Œ‹ž, 2023”N10ŒŽ).
M. Nagatani, M. Yoshikawa, S. Tsukiji, M. Higuchi, H. Tamiaki, S. Matsubara, gPeptide-chlorophyll conjugates for the pH-responsive photosensitizers,h ‘æ33‰ñ“ú–{MRS”NŽŸ‘å‰ïAH-015-008 (‰¡•l, 2023”N11ŒŽ).
‹e’rC•½AŠâè—YŒáA‹g‰ª”ü“ÞAX“c^–çA‘½“c@—³A“à‘ºNаA¬—Ñ—FÆA–؉º—Y‰îAŒÃ‘‘‹`—YA‹v•Û‰À”ÍA–¯H@‹ÏAÎŽR”ŽÍA‰F“cìAuƒ‰ƒbƒg‚Ìs“®‚ɑ΂·‚郊ƒ“Ž‰Ž¿‚Ì‹@”\-ƒŠƒ“Ž‰Ž¿‚Ì•ªŽq\‘¢‚É’…–Ú‚µ‚Ä-vA‘æ99‰ñ“ú–{‰ð–UŠw‰ï‹ß‹EŽx•”ŠwpW‰ïA8 (‹ž“s, 2023”N11ŒŽ).
Y. Matsukawa, H. Tamiaki, gSynthesis and Optical Properties of Tetrazolium Mesoionic Fluorophores,h IKCOC-15, PB(C)-20 (‹ž“s, 2023”N11ŒŽ).
M. Yasui, H. Tamiaki, gSelf-aggregation of synthetic bacteriochlorophyll-d analogs possessing a porphyrin π-skeleton and a chiral esterifying group,h IKCOC-15, PB(C)-34 (‹ž“s, 2023”N11ŒŽ).
K. Yoshimura, S. Ogasawara, H. Tamiaki, gIntroductions of Michael Acceptors at the C132 of Methyl Pheophorbide-a/af,h IKCOC-15, PB(C)-82 (‹ž“s, 2023”N11ŒŽ).
R. Ataka, H.Tamiaki, gSynthesis of N-methylated chlorophyll derivatives having various substituents and comparison of their optical properties,h ‘æ12‰ñƒAƒWƒAŒõ‰»Šw‰ï‹c(APC2023), PP41 (ƒI[ƒXƒgƒ‰ƒŠƒAEƒƒ‹ƒ{ƒ‹ƒ“, 2023”N11ŒŽ).
–¯H@‹ÏAuƒNƒƒƒtƒBƒ‹‚̉ȊwF\‘¢‚Æ(¶)‡¬‚Æ‹@”\vA2023”N“x“ŒŠCŽx•”æ’[‰»ŠwƒZƒ~ƒi[ (Šò•Œ, 2023”N12ŒŽ). [µ‘Òu‰‰]
S. Takamiaya, H. Hanayama, H. Tamiaki, S. Yagai, gControl of Supramolecular Polymorphism in Self-assembly of Scissors-shaped Chlorophyll Dyads,h CEMSupra2024, P-42 (“Œ‹ž, 2024”N1ŒŽ).
–¯H@‹ÏAu—§–½‚Å31”NFƒNƒƒƒtƒBƒ‹‰¤‚ð–ÚŽw‚µ‚ÄvAƒVƒ“ƒ|ƒWƒEƒ€u¶•¨—L‹@‰»Šw‚ÌŒ»Ý‚Æ–¢—ˆv (‘’Ã, 2024”N3ŒŽ). [Šî’²u‰‰]
–¯H@‹ÏAuƒNƒƒƒtƒBƒ‹‚̉ȊwvA‘æ8‰ñŒ³‘fƒuƒƒbƒNŒ¤‹†‰ï (‹ž“s, 2024”N3ŒŽ). [µ‘Òu‰‰]
–¯H@‹ÏAŠÛŽR 从qA¼ì —T‘¾AuƒtƒFƒƒZƒ“‰»ƒNƒƒƒtƒBƒ‹—U“±‘̂̇¬‚Æ•¨«vA“ú–{‰»Šw‰ï‘æ104t‹G”N‰ïAE1133-1am-04 (‘D‹´, 2024”N3ŒŽ).
–¯H@‹ÏAbŒ´ äA¬Š}Œ´@LAuƒJƒ`ƒIƒ“«ƒAƒUƒAƒŠ[ƒ‹Šî‚ð—L‚·‚éƒNƒƒƒtƒBƒ‹—U“±‘̂̇¬‚Æ•¨«vA“ú–{‰»Šw‰ï‘æ104t‹G”N‰ïAE1133-1am-11 (‘D‹´, 2024”N3ŒŽ).
¬Š}Œ´@LAŠÛ–{—m–¾A–¯H@‹ÏAuƒsƒŠƒWƒ“ŽcŠî‚ð—L‚·‚éƒ|ƒŠƒ}[‚ւ̃Jƒ`ƒIƒ“«ƒNƒƒƒtƒBƒ‹—U“±‘Ì‚ÌCü‚Æ‚»‚Ì•¨«vA“ú–{‰»Šw‰ï‘æ104t‹G”N‰ïAP2-1vn-25 (‘D‹´, 2024”N3ŒŽ).
H“¡—ʼn›A‰ÔŽR”Ž‹IA–¯H@‹ÏA–îŠL ŽjŽ÷Auƒfƒ“ƒhƒƒ“CüƒNƒƒƒtƒBƒ‹’´•ªŽqƒƒ[ƒbƒg‚ÌŽ©ŒÈW‡vA“ú–{‰»Šw‰ï‘æ104t‹G”N‰ïAE1123-2am-04 (‘D‹´, 2024”N3ŒŽ).
¼ì —T‘¾A–¯H@‹ÏAu1,3-ƒWƒAƒŠ[ƒ‹ƒeƒgƒ‰ƒ]ƒŠƒEƒ€ŒnŒuŒõ«ƒƒ\ƒCƒIƒ“‰»‡•¨‚Ì”Œõ“Á«‚Æ‹@\Œ¤‹†vA“ú–{‰»Šw‰ï‘æ104t‹G”N‰ïAP4-2vn-10 (‘D‹´, 2024”N3ŒŽ).
œAûP—D•ãAΈä’C–A”óŒû^OA–¯H@‹ÏA¼Œ´ãÄŒáAu”ñ‘Î̂ȃiƒtƒ^ƒŒƒ“˜AŒ‹ƒNƒƒƒtƒBƒ‹“ñ—ʑ̂̇¬‚ÆŽ©ŒÈWÏvA“ú–{‰»Šw‰ï‘æ104t‹G”N‰ïAE1131-2vn-04 (‘D‹´, 2024”N3ŒŽ).
Œ´@LsA–¯H@‹ÏAu17ˆÊ‚É’¼½‚¨‚æ‚ÑŽ}•ª‚©‚êƒAƒ‹ƒLƒ‹½‚𓱓ü‚µ‚½ƒoƒNƒeƒŠƒIƒNƒƒƒtƒBƒ‹d—Þ‚ÌŽ©ŒÈ‰ï‡vA“ú–{‰»Šw‰ï‘æ104t‹G”N‰ïAE1123-3pm-02 (‘D‹´, 2024”N3ŒŽ).
’†žŠ —ÁŽqA”óŒû^OA–¯H@‹ÏA¼Œ´ãÄŒáAuƒyƒvƒ`ƒh-ƒNƒƒƒtƒBƒ‹•¡‡‘Ì‚ð—p‚¢‚½Œõ•ßWƒAƒ“ƒeƒiƒ‚ƒfƒ‹‚̇¬‚ÆŒõ•¨«vA“ú–{‰»Šw‰ï‘æ104t‹G”N‰ïAE1123-3pm-03 (‘D‹´, 2024”N3ŒŽ).
–¯H@‹ÏAåa–´“c‘ñ–AŒ´@LsA¬Š}Œ´ LAuV‚½‚ɘZˆõŠÂ‚ªkŠÂ‚µ‚½ƒNƒƒƒtƒBƒ‹—U“±‘̂̇¬‚Æ•¨«vA“ú–{‰»Šw‰ï‘æ104t‹G”N‰ïAE1141-3vn-07 (‘D‹´, 2024”N3ŒŽ).
–¯H@‹ÏA¼ì@‘¸Au31ˆÊ‚Ƀ`ƒGƒjƒ‹Šî‚ð—L‚·‚éƒNƒƒƒtƒBƒ‹—U“±‘̂̇¬‚Æ•¨«vA“ú–{‰»Šw‰ï‘æ104t‹G”N‰ïAE1133-4pm-11 (‘D‹´, 2024”N3ŒŽ).
”ŽR—Sˆê˜YAŒ©ŽsÃA¡¼IŠóAŠÛŽR –GA匴ç—ÇA”W‘º éDA–¯H@‹ÏAuŒ´¶¶•¨‚̃NƒƒƒtƒBƒ‹‘ãŽÓ‚É‚¨‚¯‚éŠîŽ¿“ÁˆÙ«‚ðin vivoæÃHƒAƒbƒZƒC‚©‚ç“ǂ݉ð‚vA“ú–{‘”—ÞŠw‰ï‘æ48‰ñ‘å‰ï (_ŒË, 2024”N3ŒŽ).
H“¡—ʼn›A‰ÔŽR”Ž‹IA–¯H@‹ÏA–îŠL ŽjŽ÷Auƒfƒ“ƒhƒƒ“CüƒNƒƒƒtƒBƒ‹’´•ªŽqƒƒ[ƒbƒg‚ÌŽ©ŒÈW‡vA‘æ45‰ñŒõ‰»ŠwŽáŽè‚̉ï (”MŠC, 2024”N6ŒŽ).
S. Kichishima, N. Funayama, H. Tamiaki, gPhotoinduced intramolecular electron transfer in chlorophyll-a derivatives directly bonding with quinone,h ICPP-13, S38-P-001 (•Ä‘Eƒoƒbƒtƒ@ƒ[, 2024”N6ŒŽ).
Y. Hashimoto, K. Yamashita, N. Hara, M. Hirose, H. Tamiaki, gChlorophyll-a derivatives fused by a π-conjugated E-ring with unique near-infrared absorption,h ICPP-13, S38-P-002 (•Ä‘Eƒoƒbƒtƒ@ƒ[, 2024”N6ŒŽ).
H. Tamiaki, S. Kichishima, Y. Hashimoto, gChirality in chlorophylls and their derivatives,h ICPP-13, Symposium 38-2 (•Ä‘Eƒoƒbƒtƒ@ƒ[, 2024”N6ŒŽ). [µ‘Òu‰‰]
Œ´“c“ñ˜NA‘剪G‘¢AŽR–{ Œ’A–¯H@‹ÏAuƒoƒNƒeƒŠƒIƒNƒƒƒtƒBƒ‹ c‚Æd‚̇¬Œn‚Å“‚C-20ˆÊƒƒ`ƒ‹Šî“]ˆÚy‘fBchU‚̉ðÍvA‘æ31‰ñŒõ‡¬ƒZƒ~ƒi[2024AP23 (‹ž“s, 2024”N6ŒŽ).
S. Duan, S. Sasaki, X.-F. Wang, H. Tamiaki, gNatural Bio-additive Chlorophyll Derivative Enables 17.30% Efficiency Organic Solar Cells,h IPS-24/ICAPR2024, 1E-12-OR (L“‡, 2024”N7ŒŽ).
H. Tamiaki, Y. Mori, K. Nakakuki, Y. Hashimoto, gArtificial light-harvesting systems as models of photosynthetic antennas in green bacteria,h IPS-24/ICAPR2024, 3E-01-KL (L“‡, 2024”N7ŒŽ). [µ‘Òu‰‰]
X.-F. Wang, C. Zhang, Y. Li, Y. Liu, T. Zheng, Z. Liu, H. Ren, Y. Sun, S. Sasaki, T. Miyasaka, H. Tamiaki, gChlorophyll derivative-based devices for photoenergy conversion and storage,h IPS-24/ICAPR2024, 4E-08-KL (L“‡, 2024”N7ŒŽ). [µ‘Òu‰‰]
S. Kichishima, H. Tamiaki, gIntramolecular electron transfer in chlorophyll–quinone conjugates prepared by Diels–Alder reaction,h 26th ICPOC, 03 (–k‹ž, 2024”N8ŒŽ).
H. Sasakura, H. Tamiaki, gSynthesis and optical properties of π-conjugated chlorophyll dimers,h 26th ICPOC, 64 (–k‹ž, 2024”N8ŒŽ).
Y. Hirose, T. Ishii, H. Tamiaki, M. Higuchi, S. Matsubara, gSelf-Assembly of Naphthalene-Linked Chlorophyll Dimers at Different Substitution Positions and Its Photophysical Properties,h 2024”NŒõ‰»Šw“¢˜_‰ïA1P087 (•Ÿ‰ª, 2024”N9ŒŽ).
ù‘q—ŽqA–¯H@‹ÏAuπ‹¤–ðŒ^˜AŒ‹ƒNƒƒƒtƒBƒ‹“ñ—ʑ̂̇¬‚ÆŒõ•¨«vA2024”NŒõ‰»Šw“¢˜_‰ïA2P006 (•Ÿ‰ª, 2024”N9ŒŽ).
‹g“‡‘‹IA–¯H@‹ÏAuƒLƒmƒ“‚ð3ˆÊŽü•Ó•”‚ÉŽ‚ƒNƒƒƒtƒBƒ‹—U“±‘̂̇¬‚Æ•ªŽq“àŒõ—ã‹N“dŽqˆÚ“®vA2024”NŒõ‰»Šw“¢˜_‰ïA2P007 (•Ÿ‰ª, 2024”N9ŒŽ).
’†žŠ—ÁŽqA”óŒû^OA–¯H@‹ÏA¼Œ´ãÄŒáAuŠÂóƒyƒvƒ`ƒh-ƒNƒƒƒtƒBƒ‹•¡‡‘Ì‚ð—p‚¢‚½Œõ•ßWƒAƒ“ƒeƒiƒ‚ƒfƒ‹‚Ì\’z‚ÆŒõ•¨«•]‰¿vA2024”NŒõ‰»Šw“¢˜_‰ïA3P063 (•Ÿ‰ª, 2024”N9ŒŽ).
H“¡—ʼn›A‰ÔŽR”Ž‹IA–¯H@‹ÏA–îŠL ŽjŽ÷Auƒfƒ“ƒhƒƒ“CüƒNƒƒƒtƒBƒ‹’´•ªŽqƒƒ[ƒbƒg‚ÌŽ©ŒÈW‡vA‘æ34‰ñŠî‘b—L‹@‰»Šw“¢˜_‰ïA2P094 (ŽD–y, 2024”N9ŒŽ).
–¯H@‹ÏAuƒNƒƒƒtƒBƒ‹‚̉ȊwFlHŒõ‡¬‚ð–ÚŽw‚µ‚ÄvA‘æ134‰ñG”}“¢˜_‰ïA2C10 (–¼ŒÃ‰®, 2024”N9ŒŽ). [“Á•Êu‰‰]
J. Harada, H. Oh-oka, K. Yamamoto, H. Tamiaki, gC20-methyl group of bacteriochlorophylls c and e catalyzed by the methyltransferase BchU, working in their synthetic pathways,h 2nd Asia-Oceania International Congress on Photosynthesis (AOICP), O3-3/P3-4 (_ŒË, 2024”N9ŒŽ).
S. Sato, M. Hirose, R. Tanaka, H. Tamiaki, M. Hirose, H. Ito, gExploring the multifaceted catalytic activity of Mg extracting enzyme: demetallation and chelation in chlorophyll derivatives,h 2nd Asia-Oceania International Congress on Photosynthesis (AOICP), P11-4 (_ŒË, 2024”N9ŒŽ).
S. Kichishima, H. Tamiaki, gSynthesis of Pheophytin–Quinone Conjugates and Their Physical Properties in Solution,h 2nd Asia-Oceania International Congress on Photosynthesis (AOICP), O12-2/P12-3 (_ŒË, 2024”N9ŒŽ). [‘I”²u‰‰]
Y. Tsukatani, H. Tamiaki, S. Masuda, gElucidating and engineering pigment biosynthetic pathways committed by chlorophyllide oxidoreductase and chlorophyll synthase,h 2nd Asia-Oceania International Congress on Photosynthesis (AOICP), P12-5 (_ŒË, 2024”N9ŒŽ).
H“¡—ʼn›A‰ÔŽR”Ž‹IA–¯H@‹ÏA–îŠL ŽjŽ÷AuƒNƒƒƒtƒBƒ‹ŠÂó’´•ªŽq‚̃fƒ“ƒhƒƒ“‘¤½‚É‚æ‚éWϧŒävA‘æ14‰ñCSJ‰»ŠwƒtƒFƒXƒ^2024AP4-024 (“Œ‹ž, 2024”N10ŒŽ).
Y. Mori,. Tamiaki, gSelf-aggregates of a bacteriochlorophyll-d analog with a BODIPY appendant as a chlorosomal photosynthetic antenna model efficiently absorbing green light,h SJBCS2024, P-08 (‰FŽ¡, 2024”N11ŒŽ).
–¯H@‹ÏAuƒNƒƒƒtƒBƒ‹‚̉ȊwvA‘ˆî“c‘åŠwæi—HŠw•”‰»ŠwE¶–½‰ÈŠw‰È–³‹@•¨Ž¿‰»ŠwŒ¤‹†Žºu‰‰‰ï (“Œ‹ž, 2024”N12ŒŽ). [µ‘Òu‰‰]
–¯H@‹ÏAuƒNƒƒƒtƒBƒ‹‰ÈŠw‚©‚çlHŒõ‡¬‚ÖvA‘æ19‰ñ‚³‚«‚ª‚¯uŒõƒGƒlƒ‹ƒM[‚Æ•¨Ž¿•ÏŠ·vŒ¤‹†—̈æ‰ï‹c (ìè, 2024”N12ŒŽ). [µ‘Òu‰‰]
’Ë’J—S‰îA–¯H@‹ÏA‘“c^“ñAugF׋ۂɂ¨‚¯‚éƒNƒƒƒtƒBƒ‹‡¬‚ɂ͌n‚PŒ^”½‰ž’†S‚Æ“œŽ‰Ž¿‡¬ˆâ“`Žq‚ª•K—v‚Å‚ ‚évA‘æ66‰ñ“ú–{A•¨¶—Šw‰ï”N‰ïA2P004 (‹à‘ò, 2025”N3ŒŽ).
Œ´“c“ñ˜NAŽR–{ Œ’A–¯H@‹ÏAuŒõ‡¬×‹Û‚̃oƒNƒeƒŠƒIƒNƒƒƒtƒBƒ‹‡¬Œn‚É‘¶Ý‚·‚é3Ží—Þ‚ÌC8ˆÊƒrƒjƒ‹ŠÒŒ³y‘f‚Ì‘¶ÝˆÓ‹`‚ÉŠÖ‚·‚élŽ@vA‘æ66‰ñ“ú–{A•¨¶—Šw‰ï”N‰ïA2P016 (‹à‘ò, 2025”N3ŒŽ).
R. Kudo, H. Tamiaki, H. Hanayama S. Yagai, gDimerization of Chlorophylls Guiding the Construction of Helically Arranged Nanofibers,h Japan-France Workshop on Photo-Electro-Responsive Molecules & Materials (PERMolMat) (ƒpƒŠ, 2025”N3ŒŽ).
H“¡—ʼn›A–¯H ‹ÏAŒ´–ìKŽ¡A‰ÔŽR”Ž‹IA–îŠLŽjŽ÷Auƒfƒ“ƒhƒƒ“‘¤½‚Ì¢‘ã‚É‚æ‚éƒNƒƒƒtƒBƒ‹ƒƒ[ƒbƒg‚ÌÏ‘w§ŒävA“ú–{‰»Šw‰ï‘æ105t‹G”N‰ïA[F]2202-1am-01 (“c, 2025”N3ŒŽ).
œA£Œõ—¹A¬—Ñ—D‰ÀA–¯H ‹ÏAŒIŒ´‘å‹PAŒË’JŠóˆê˜YAu‚ª‚ñ×–EŽE”\‚ð—L‚·‚éƒJƒ‹ƒŒƒeƒBƒLƒ…ƒŠƒ“•W“IŒ^“œ½ƒŠƒKƒ“ƒh‚ÌŠJ”vA“ú–{‰»Šw‰ï‘æ105t‹G”N‰ïA[A]A304-3am-05 (“c, 2025”N3ŒŽ).
Œ´@LsA–¯H ‹ÏAuƒoƒNƒeƒŠƒIƒNƒƒƒtƒBƒ‹-d—ޗΑ̂ɂæ‚é—lX‚ÈŽ©ŒÈ•ªŽqW‡Œ`‘Ô‚Ì‘n»vA“ú–{‰»Šw‰ï‘æ105t‹G”N‰ïA[PB]-3am-04 (“c, 2025”N3ŒŽ).
—Ñ ”ü•äAΈä’C–A–¯H ‹ÏA¼Œ´ãÄŒáAu”zˆÊ•”ˆÊ‚ðŽ‚Âƒiƒtƒ^ƒŒƒ“˜AŒ‹ƒNƒƒƒtƒBƒ‹ƒ_ƒCƒ}[‚̇¬‚Æ‚»‚ÌŽ©ŒÈWÏvA“ú–{‰»Šw‰ï‘æ105t‹G”N‰ïA[F]2202-4am-06 (“c, 2025”N3ŒŽ).
N. Hara, H. Tamiaki, gVarious self-assembly morphology form bacteriochlorophyll-d analogs possessing a branched alkyl chain,h ISMSC2025, P1A_21 (‹ž“s, 2025”N5ŒŽ).
R. Kudo, R. Tsuchida, B. Vedhanarayanan, H. Hanayama, H. Tamiaki, Y. Hori, Y. Shigeta, S. Kawai, S. Yagai, gHelical Pitch Evolution of Columnar Aggregates Consisting of Chlorophyll Supramolecular Rosettes,h ISMSC2025, P2A_20 (PNA_81) (‹ž“s, 2025”N5ŒŽ).
‘å’ë ‹œA–¯H ‹Ï, gCoordination chemistry of (bacterio)chlorophylls in the photosynthetic pigment-protein complexes: uneven distribution of chirality around the 5th ligand,h ‘æ15‰ñ“ú–{Œõ‡¬Šw‰ï”N‰ïAP64 (‚³‚¢‚½‚Ü, 2025”N6ŒŽ).
Œ´“c“ñ˜NAŽR–{ Œ’A–¯H ‹Ï, uŒõ‡¬×‹Û‚̃NƒƒƒtƒBƒ‹F‘f‡¬Œn‚É“‚3‚‚ÌC8ˆÊƒrƒjƒ‹ŠÒŒ³y‘f‚Ì‘¶ÝˆÓ‹`‚ÉŠÖ‚·‚élŽ@vA‘æ15‰ñ“ú–{Œõ‡¬Šw‰ï”N‰ïAP91 (‚³‚¢‚½‚Ü, 2025”N6ŒŽ).
Œ´“c“ñ˜NAŽR–{ Œ’A–¯H ‹ÏAuŽ_‘f”ñ”¶Œ^Œõ‡¬×‹Û‚݂̂ª‚à‚ÂC8 ˆÊƒrƒjƒ‹ŠÒŒ³y‘f‚Ì‹@”\‚ÉŠÖ‚·‚éi‰»“IlŽ@vA‘æ32‰ñŒõ‡¬ƒZƒ~ƒi[2025AP19i‹ž“s, 2025”N6ŒŽ).
–©ìˆêãÄA‹g“‡‘‹IA–¯H ‹ÏA²‰ê‰À‰›AuƒNƒƒƒtƒBƒ‹a—Þ‰‘̂̃Gƒsƒ}[‰»”½‰ž‚Ì‘¬“x˜_“I‰ðÍvA‘æ32‰ñŒõ‡¬ƒZƒ~ƒi[2025AP27i‹ž“s, 2025”N6ŒŽ).
‘å’ë ‹œA¬Š}Œ´ LA–¯H ‹ÏAuƒNƒƒƒtƒBƒ‹—Þ‚ÌŽ²”zˆÊö‘̂ɂ¨‚¯‚é•sÄ”Œ»vA‘æ32‰ñŒõ‡¬ƒZƒ~ƒi[2025AO10i‹ž“s, 2025”N6ŒŽ).
–©ìˆêãÄA‹g“‡‘‹IA–¯H ‹ÏA²‰ê‰À‰›AuŒõ‰»ŠwŒnI‚Åd—v‚ȃNƒƒƒtƒBƒ‹a—Þ‰‘̃Gƒsƒ}[‚̶¬”½‰ž‚Ì‘¬“x˜_“I‰ðÍvA‘æ25‰ñŒõ¶•¨Šw‹¦‰ï”N‰ïi‘’Ã, 2025”N8ŒŽ).
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‰ºŠ_“à—y‹IA¬—Ñ—D‰ÀA–¯H ‹ÏAŒIŒ´‘å‹PAœAûPŒõ—¹AŒË’JŠóˆê˜YAu‚ª‚ñ×–E‚ÌŽE‹@”\‚ð—L‚·‚éƒJƒ‹ƒŒƒeƒBƒLƒ…ƒŠƒ“•W“IƒŠƒKƒ“ƒh‚ÌŠJ”vA‘æ44‰ñ“ú–{“œŽ¿Šw‰ïAPA-24iO‘O, 2025”N10ŒŽ).
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‰ºŠ_“à—y‹IA¬—Ñ—D‰ÀA•“c—zˆêA–¯H ‹ÏAŒIŒ´‘å‹PAœAûPŒõ—¹AŒË’JŠóˆê˜YAuƒJƒ‹ƒŒƒeƒBƒLƒ…ƒŠƒ“‚ð•W“I‚É‚µ‚½‚ª‚ñ×–EŽEƒŠƒKƒ“ƒh‚ÌŠJ”vAGlycoTOKYO2025ƒVƒ“ƒ|ƒWƒEƒ€AP-04 (‰¡•l, 2025”N10ŒŽ). [ƒ|ƒXƒ^[ÜŽóÜ]
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H“¡—ʼn›A‚‹{ ËA–¯H ‹ÏA‰ÔŽR”Ž‹IA–îŠLŽjŽ÷Au“Y‰Á܂ɂæ‚éƒnƒTƒ~Œ^ƒNƒƒƒtƒBƒ‹“ñ—ʑ̂̒´•ªŽqƒiƒmƒtƒ@ƒCƒo[/ƒŠƒ“ƒOŒ`¬Œo˜H‚̧ŒävA‘æ15‰ñCSJ‰»ŠwƒtƒFƒXƒ^2025AP4-024 (“Œ‹ž, 2025”N10ŒŽ).
—Ñ ”ü•äAΈä’C–A–¯H ‹ÏA¼Œ´ãÄŒáAuŠK‘w\‘¢‚Ì\’z‚ð–ÚŽw‚µ‚½”zˆÊ•”ˆÊ‚ðŽ‚ÂƒNƒƒƒtƒBƒ‹“ñ—ʑ̂̇¬‚ÆŽ©ŒÈWÏvA‘æ15‰ñCSJ‰»ŠwƒtƒFƒXƒ^2025AP6-029 (“Œ‹ž, 2025”N10ŒŽ).
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