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本文引用的文献

1
Detailed radiosynthesis of [ F]mG4P027 as a positron emission tomography radiotracer for mGluR4.
J Labelled Comp Radiopharm. 2023 Feb;66(2):34-40. doi: 10.1002/jlcr.4011. Epub 2023 Jan 19.
2
Development and Validation of a PET/SPECT Radiopharmaceutical in Oncology.
Mol Imaging Biol. 2022 Feb;24(1):1-7. doi: 10.1007/s11307-021-01645-6. Epub 2021 Sep 20.
3
Positron emission tomographic imaging in drug discovery.
Drug Discov Today. 2022 Jan;27(1):280-291. doi: 10.1016/j.drudis.2021.07.025. Epub 2021 Jul 28.
4
Chemistry Considerations for the Clinical Translation of Oncology PET Radiopharmaceuticals.
Mol Pharm. 2020 Jul 6;17(7):2245-2259. doi: 10.1021/acs.molpharmaceut.0c00328. Epub 2020 Jun 5.
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HPLC-free in situF-fluoromethylation of bioactive molecules by azidation and MTBD scavenging.
Chem Commun (Camb). 2019 Sep 26;55(78):11798-11801. doi: 10.1039/c9cc04901k.
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Therapeutic strategies for Parkinson disease: beyond dopaminergic drugs.
Nat Rev Drug Discov. 2018 Nov;17(11):804-822. doi: 10.1038/nrd.2018.136. Epub 2018 Sep 28.
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An mGlu4-Positive Allosteric Modulator Alleviates Parkinsonism in Primates.
Mov Disord. 2018 Oct;33(10):1619-1631. doi: 10.1002/mds.27462. Epub 2018 Sep 14.
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Guidance on validation and qualification of processes and operations involving radiopharmaceuticals.
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Synthesis and evaluation of N-(methylthiophenyl)picolinamide derivatives as PET radioligands for metabotropic glutamate receptor subtype 4.
Bioorg Med Chem Lett. 2016 Jan 1;26(1):133-9. doi: 10.1016/j.bmcl.2015.11.015. Epub 2015 Nov 10.

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