{"id":2054,"date":"2017-02-09T15:40:31","date_gmt":"2017-02-09T06:40:31","guid":{"rendered":"http:\/\/www.pharm.kyoto-u.ac.jp\/byotai\/?page_id=2054\/"},"modified":"2024-12-02T16:49:01","modified_gmt":"2024-12-02T07:49:01","slug":"2012-2","status":"publish","type":"page","link":"https:\/\/www.pharm.kyoto-u.ac.jp\/byotai\/2012-2\/","title":{"rendered":"2012"},"content":{"rendered":"

2012 (\u8ad6\u6587)<\/h2>\n
    \n
  1. Cui M, Wang X, Yu P, Zhang J, Li Z, Zhang X, Yang Y, Ono M, Jia H, Saji H, Liu B.<\/span>
    \nSynthesis and evaluation of novel\u00a018<\/sup>F labeled 2-pyridinylbenzoxazole and 2-pyridinylbenzothiazole derivatives as ligands for positron emission tomography (PET) imaging of \u03b2-amyloid plaques<\/span>
    \nJ. Med. Chem.\u00a0<\/em>55(21) 9283-9296 (2012)<\/span><\/li>\n
  2. Cui M, Ono M, Kimura H, Ueda M, Nakamoto Y, Togashi K, Okamoto Y, Ihara M, Takahashi R, Liu B, Saji H.<\/span>
    \nNovel\u00a018<\/sup>F-labeled benzoxazole derivatives as potential positron emission tomography probes for imaging of cerebral \u03b2-amyloid plaques in alzheimers disease<\/span>
    \nJ. Med. Chem.\u00a0<\/em>55(21) 9136-9145 (2012)<\/span><\/li>\n
  3. Yu P, Cui M, Wang X, Zhang X, Li Z, Yang Y, Jia J, Zhang J, Ono M, Saji H, Jia H, Liu B.<\/span>
    \n18<\/sup>F-Labeled 2-phenylquinoxaline derivatives as potential positron emission tomography probes for in vivo imaging of \u03b2-amyloid plaques<\/span>
    \nEur. J. Med. Chem.\u00a0<\/em>57\u00a051-58 (2012)<\/span><\/li>\n
  4. Watanabe H, Ono M, Kimura H, Matsumura K, Yoshimura M, Okamoto Y, Ihara M, Takahashi R, Saji H.<\/span>
    \nSynthesis and biological evaluation of novel oxindole derivatives for imaging neurofibrillary tangles in Alzheimer’s disease<\/span>
    \nBioorg. Med. Chem. Lett.\u00a0<\/em>22(17) 5700-5703 (2012)<\/span><\/li>\n
  5. Fujii H, Yamaguchi M, Inoue K, Mutou Y, Ueda M, Saji H, Kizaka-Kondoh S, Moriyama N, Umeda I.O.<\/span>
    \nIn vivo visualization of heterogeneous intratumoral distribution of hypoxia-inducible factor-1\u03b1 activity by the fusion of high-resolution SPECT and morphological imaging tests<\/span>
    \nJ. Biomed. Biotechnol.\u00a0<\/em>2012\u00a0262741 (2012)<\/span><\/li>\n
  6. Takai N, Tanaka Y, Inazawa K, Saji H.<\/span>
    \nQuantitative analysis of pharmaceutical drug distribution in multiple organs by imaging mass spectrometry<\/span>
    \nRapid Commun. Mass Spectrom.\u00a0<\/em>26(13) 1549-1556 (2012)<\/span><\/li>\n
  7. Kanegawa N, Kiyono Y, Sugita T, Kuge Y, Fujibayasi Y, Saji H.<\/span>
    \nNorepinephrine transporter imaging in the brain of a rat model of depression using radioiodinated (2S,\u03b1S)-2-(\u03b1-(2-iodophenoxy)benzyl) morpholine<\/span>
    \nMol. Imaging\u00a0<\/em>11(4) 280-285 (2012)<\/span><\/li>\n
  8. Temma T, Saji H.<\/span>
    \nRadiolabelled probes for imaging of atherosclerotic plaques<\/span>
    \nAm. J. Nucl. Med. Mol. Imaging\u00a0<\/em>2(4) 432-447 (2012)\u00a0Review<\/em><\/span><\/li>\n
  9. Nakase I, Konishi Y, Ueda M, Saji H, Futaki S.<\/span>
    \nAccumulation of arginine-rich cell-penetrating peptides in tumors and the potential for anticancer drug delivery in vivo<\/span>
    \nJ. Control. Release\u00a0<\/em>159(2) 181-188 (2012)<\/span><\/li>\n
  10. Ono M, Watanabe H, Kimura H, Saji H.<\/span>
    \nBODIPY-based molecular probe for imaging of cerebral \u03b2-amyloid plaques<\/span>
    \nACS Chem. Neurosci.\u00a0<\/em>3(4) 319-324 (2012)<\/span><\/li>\n
  11. Ono M, Saji H.<\/span>
    \nMolecular approaches to the treatment, prophylaxis, and diagnosis of Alzheimer’s disease: Novel PET\/SPECT imaging probes for diagnosis of Alzheimer’s disease<\/span>
    \nJ. Pharmacol. Sci.\u00a0<\/em>118(3) 338-344 (2012)\u00a0Review.<\/em><\/span><\/li>\n
  12. Cheng Y, Ono M, Kimura H, Ueda M, Saji H.<\/span>
    \nTechnetium-99m labeled pyridyl benzofuran derivatives as single photon emission computed tomography imaging probes for \u03b2-amyloid plaques in Alzheimer’s brains<\/span>
    \nJ. Med. Chem.\u00a0<\/em>55(5) 2279-2286 (2012)<\/span><\/li>\n
  13. Shimizu Y, Temma T, Hara I, Yamahara R, Ozeki E.-I, Ono M, Saji H.<\/span>
    \nDevelopment of novel nanocarrier-based near-infrared optical probes for in vivo tumor imaging<\/span>
    \nJ. Fluoresc.\u00a0<\/em>22(2) 719-727 (2012)<\/span><\/li>\n
  14. Ono M, Ohgami M, Haratake M, Saji H, Nakayama M.<\/span>
    \nA novel bifunctional chelating agent based on bis(hydroxamamide) for\u00a099m<\/sup>Tc labeling of polypeptides<\/span>
    \nJ. Labelled Comp. Radiopharm. <\/em>55(2) 71-79 (2012)<\/span><\/li>\n
  15. Matsumura K, Ono M, Kimura H, Ueda M, Nakamoto Y, Togashi K, Okamoto Y, Ihara M, Takahashi R, Saji H.<\/span>
    \n18<\/sup>F-labeled phenyldiazenyl benzothiazole for in vivo imaging of neurofibrillary tangles in Alzheimer’s disease brains<\/span>
    \nACS Med. Chem. Lett.\u00a0<\/em>3(1) 58-62 (2012)<\/span><\/li>\n
  16. Kimura H, Mori D, Harada N, Ono M, Ohmomo Y, Kajimoto T, Kawashima H, Saji H.<\/span>
    \nMicrowave-assisted synthesis of organometallic complexes of\u00a099m<\/sup>Tc(CO)3<\/sub>\u00a0and Re(CO)3<\/sub>: Its application to radiopharmaceuticals<\/span>
    \nChem. Pharm. Bull.\u00a0<\/em>60(1) 79-85 (2012)<\/span><\/li>\n<\/ol>\n","protected":false},"excerpt":{"rendered":"

    2012 (\u8ad6\u6587) Cui M, Wang X, Yu P, Zhang J, Li Z, Zhang X, Yang Y, Ono M, Jia H, Saji H, Liu B. Synthesis and eval […]<\/p>\n","protected":false},"author":14,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"_acf_changed":false,"footnotes":""},"class_list":["post-2054","page","type-page","status-publish","hentry"],"acf":[],"_links":{"self":[{"href":"https:\/\/www.pharm.kyoto-u.ac.jp\/byotai\/wp-json\/wp\/v2\/pages\/2054","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/www.pharm.kyoto-u.ac.jp\/byotai\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/www.pharm.kyoto-u.ac.jp\/byotai\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/www.pharm.kyoto-u.ac.jp\/byotai\/wp-json\/wp\/v2\/users\/14"}],"replies":[{"embeddable":true,"href":"https:\/\/www.pharm.kyoto-u.ac.jp\/byotai\/wp-json\/wp\/v2\/comments?post=2054"}],"version-history":[{"count":3,"href":"https:\/\/www.pharm.kyoto-u.ac.jp\/byotai\/wp-json\/wp\/v2\/pages\/2054\/revisions"}],"predecessor-version":[{"id":3213,"href":"https:\/\/www.pharm.kyoto-u.ac.jp\/byotai\/wp-json\/wp\/v2\/pages\/2054\/revisions\/3213"}],"wp:attachment":[{"href":"https:\/\/www.pharm.kyoto-u.ac.jp\/byotai\/wp-json\/wp\/v2\/media?parent=2054"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}