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12. A 211At-labelled mGluR1 inhibitor induces cancer senescence to elicit long-lasting anti-tumor efficacy

15. Scandium triflate-catalyzed N-[18F]Fluoroalkylation of aryl- or heteroaryl-amines with [18F]epifluorohydrin under mild condi-tions

17. Automated radiosynthesis of [11C]MTP38—a phosphodiesterase 7 imaging tracer—using [11C]hydrogen cyanide for clinical applications

18. サイクロトロンによる放射性標識薬剤の製造・開発への利用状況<R2>

19. ecDHFRイメージング用の遺伝子レポーターPETトレーサー[18F]FHP-TMPの開発

20. Automated radiosynthesis of 18F-fluoromethylated tracers using the simplified one-pot 18F-fluoromethylation via [18F]fluoromethyl tosylate

21. Development of [18F]FHP-TMP as a PET gene reporter tracer for imaging of E.coli dihydrofolate reductase in the mammalian brain

22. Demonstration of intracellular pH-weighting PET imaging using a new-type PET probe responsible for monoacylglycerol lipase activity in the brain

25. Radiosynthesis and quality control testing of the tau imaging positron emission tomography tracer [18F]PM‐PBB3 for clinical applications

26. サイクロトロンによる放射性標識薬剤の製造・開発への利用状況

27. Automated radiosynthesis of [ 11 C]MTP38—a phosphodiesterase 7 imaging tracer—using [ 11 C]hydrogen cyanide for clinical applications

28. 簡易的1ポット[18F]フルオロアルキル化標識法を用いた[18F]フルオロメチルコリンの合成検討

29. Additional file 1 of Automated radiosynthesis of two 18F-labeled tracers containing 3-fluoro-2-hydroxypropyl moiety, [18F]FMISO and [18F]PM-PBB3, via [18F]epifluorohydrin

30. Automated radiosynthesis of two 18F-labeled tracers containing 3-fluoro-2-hydroxypropyl moiety, [18F]FMISO and [18F]PM-PBB3, via [18F]epifluorohydrin

31. [11C]SL25.1188の臨床提供に向けた安定的製造法及び品質検査法の確立

32. モノアシルグリセロールリパーゼを標的としたPETプローブを用いた脳内pHイメージング法の開発

33. 多種多様な診断及び治療用放射性薬剤の安定的製造

34. 様々な標識中間体を用いた標識合成法の開発

35. Development of 2-(2-(3-(4-([18F]Fluoromethoxy- d2)phenyl)-7-methyl-4-oxo-3,4-dihydroquinazolin-2-yl)ethyl)-4-isopropoxyisoindoline-1,3-dione for Positron-Emission-Tomography Imaging of Phosphodiesterase 10A in the Brain

36. Automated Synthesis of (rac)‐, (R)‐, and (S)‐[18F]Epifluorohydrin and Their Application for Developing PET Radiotracers Containing a 3‐[18F]Fluoro‐2‐hydroxypropyl Moiety

38. Automated radiosynthesis of [11C]MTP38—a phosphodiesterase 7 imaging tracer—using [11C]hydrogen cyanide for clinical applications.

40. 1つの反応容器を用いた[18F]フルオロエチル化合成法の確立―[18F]FEDAC及び[18F]FET合成について

41. 承認申請を見据えた[64Cu]Cu-ATSM注射液の品質検査法の設定

42. Additional file 1: of Radiosynthesis and in vivo evaluation of 11C-labeled BMS-193885 and its desmethyl analog as PET tracers for neuropeptide Y1 receptors

44. In vivo characterizations of [11C]BMS193885 and [11C]Desmethyl-BMS193885 as a PET tracer for neuropeptide Y Y1 receptors

45. Radiosynthesis and quality control testing of the tau imaging positron emission tomography tracer [18F]PM‐PBB3 for clinical applications.

46. Synthesis and evaluation of a new 11C-labeled growth hormone secretagogue receptor 1a probe

47. Simple method for introduction of 3-[18F]fluoro-2-hydroxypropyl group and application for synthesis of 18F-labeled ligand

48. Automated Synthesis of (rac )-, (R )-, and (S )-[18 F]Epifluorohydrin and Their Application for Developing PET Radiotracers Containing a 3-[18 F]Fluoro-2-hydroxypropyl Moiety

49. Synthesis of two novel [18F]fluorobenzene-containing radiotracers via spirocyclic iodonium ylides and positron emission tomography imaging of translocator protein (18 kDa) in ischemic brain

50. Comparison between [ 18 F]fluorination and [ 18 F]fluoroethylation reactions for the synthesis of the PDE10A PET radiotracer [ 18 F]MNI-659

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