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dc.contributor.authorChoi, Y.-
dc.contributor.authorHa, S.-
dc.contributor.authorLee, Y.-S.-
dc.contributor.authorKim, Y.K.-
dc.contributor.authorLee, D.S.-
dc.contributor.authorKim, D.J.-
dc.date.accessioned2024-01-19T23:32:35Z-
dc.date.available2024-01-19T23:32:35Z-
dc.date.created2021-09-02-
dc.date.issued2018-02-
dc.identifier.issn1869-3474-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/121781-
dc.description.abstractThe pathological features of Alzheimer’s disease are senile plaques which are aggregates of β-amyloid peptides and neurofibrillary tangles in the brain. Neurofibrillary tangles are aggregates of hyperphosphorylated tau proteins, and these induce various other neurodegenerative diseases, such as progressive supranuclear palsy, corticobasal degeneration, frontotemporal lobar degeneration, frontotemporal dementia and parkinsonism linked to chromosome 17 (FTDP-17), and chronic traumatic encephalopathy. In the case of Alzheimer’s disease, the measurement of neurofibrillary tangles associated with cognitive decline is suitable for differential diagnosis, disease progression assessment, and to monitor the effects of therapeutic treatment. This review discusses considerations for the development of tau ligands for imaging and summarizes the results of the first-in-human and preclinical studies of the tau tracers that have been developed thus far. The development of tau ligands for imaging studies will be helpful for differential diagnosis and for the development of therapeutic treatments for tauopathies including Alzheimer’s disease. ? 2017, Korean Society of Nuclear Medicine.-
dc.languageEnglish-
dc.publisherSpringer Verlag-
dc.titleDevelopment of tau PET Imaging Ligands and their Utility in Preclinical and Clinical Studies-
dc.typeArticle-
dc.identifier.doi10.1007/s13139-017-0484-7-
dc.description.journalClass1-
dc.identifier.bibliographicCitationNuclear Medicine and Molecular Imaging, v.52, no.1, pp.24 - 30-
dc.citation.titleNuclear Medicine and Molecular Imaging-
dc.citation.volume52-
dc.citation.number1-
dc.citation.startPage24-
dc.citation.endPage30-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscopus-
dc.description.journalRegisteredClasskci-
dc.identifier.kciidART002315569-
dc.identifier.scopusid2-s2.0-85040942047-
dc.type.docTypeReview-
dc.subject.keywordPlusamyloid beta protein-
dc.subject.keywordPlusradioligand-
dc.subject.keywordPlusradiopharmaceutical agent-
dc.subject.keywordPlustau protein-
dc.subject.keywordPlusAlzheimer disease-
dc.subject.keywordPluschromosome 17-
dc.subject.keywordPluschronic traumatic encephalopathy-
dc.subject.keywordPluscognition-
dc.subject.keywordPluscorticobasal degeneration-
dc.subject.keywordPlusdegenerative disease-
dc.subject.keywordPlusdisease exacerbation-
dc.subject.keywordPlusfrontotemporal dementia-
dc.subject.keywordPlushuman-
dc.subject.keywordPlusneurofibrillary tangle-
dc.subject.keywordPlusparkinsonism-
dc.subject.keywordPluspositron emission tomography-
dc.subject.keywordPluspriority journal-
dc.subject.keywordPlusprogressive supranuclear palsy-
dc.subject.keywordPlusReview-
dc.subject.keywordPlussenile plaque-
dc.subject.keywordPlustauopathy-
dc.subject.keywordAuthorAlzheimer’s disease-
dc.subject.keywordAuthorImaging ligands-
dc.subject.keywordAuthorPet-
dc.subject.keywordAuthorRadiopharmaceutical-
dc.subject.keywordAuthorTau-
dc.subject.keywordAuthorTauopathy-
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KIST Article > 2018
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