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The development and clinical implementation of GlyT1 inhibitors for the treatment of schizophrenia have advanced significantly, supported by robust preclinical and clinical data (Table 1)
Generation of the C1-2 and C3-1 iPSC lines followed institutional IRB and ISCRO guidelines and was approved by the Johns Hopkins University School of Medicine
Scheller H
The identification of distinct ERG synthases in bacteria and fungi has significantly advanced this research field [[47], [48], [49], [50]]
