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5 616 acts through antagonism of the host cell dopamine D4 receptor and subsequent repression of the ER
6 is a novel, highly selective radioligand for dopamine D4 receptors and may be used to investigate the
7 ridones and piperidines, including potential dopamine D4 receptor antagonists 2 and 3, that have been
8 ave reported that polymorphisms of the human dopamine D4 receptor (D4R) gene are associated with pers
11 ric disorders, and a polymorphism within the dopamine D4 receptor (DRD4) gene has been frequently imp
13 of L-750,667 bound specifically to the human dopamine D4 receptor expressed in HEK cells and saturati
16 gnitive endophenotypes, and variation in the dopamine D4 receptor gene (DRD4) explains at least a por
17 th polymorphisms in some dopamine genes (the dopamine D4 receptor gene and the dopamine transporter g
22 and [3H]raclopride has been used to quantify dopamine D4 receptors in postmortem schizophrenic brain
28 of NMDA-type glutamate receptors by the PFC dopamine D4 receptor (one of the principal targets of an
29 icant nor consistent observation of striatal dopamine D4 receptors or D4-like binding sites was obser
30 receptors and may be used to investigate the dopamine D4 receptor population in the central nervous s
31 dicate that the decrease of cAMP elicited by dopamine D4 receptor stimulation may be secondary to dec
34 ell death are, at least in part, mediated by dopamine D4 receptors via the regulation of cGMP-operate
37 zole (36) is a nanomolar antagonist at human dopamine D4 receptors with > 500-fold selectivity over h