Abstract
The type-1 glycine transporter (GlyT1) is a target of interest for the development of new medications for schizophrenia. A specific and selective positron emission tomography (PET) GlyT1 ligand would help understand disease heterogeneity and support drug development studies to determine whether a drug is able to engage this target. During the last 3-4 years, a number of potential ligands have been reported both for preclinical and clinical use. Here, we review the most promising candidates reported to date and make recommendations with regard to their use in clinical studies.
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Passchier, J., Gunn, R.N., van Waarde, A. (2014). Imaging Type 1 Glycine Transporters in the CNS Using Positron Emission Tomography. In: Dierckx, R., Otte, A., de Vries, E., van Waarde, A., Luiten, P. (eds) PET and SPECT of Neurobiological Systems. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-42014-6_12
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DOI: https://doi.org/10.1007/978-3-642-42014-6_12
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