↑ Neve KA 、Seamans JK、Trantham - Davidson H (2004年8 月)。「ドーパミン受容体シグナル伝達」。Journal of Receptor and Signal Transduction Research。24 ( 3 ) : 165–205。CiteSeerX 10.1.1.465.5011。doi : 10.1081/RRS-200029981。PMID 15521361。S2CID 12407397。
1 2 Van Tol HH、Wu CM、Guan HC、Ohara K、Bunzow JR、Civelli O、Kennedy J、Seeman P、Niznik HB、Jovanovic V (1992年7月)。「ヒト集団における複数のドーパミンD4受容体変異体」。Nature。358 ( 6382 ) : 149–52。Bibcode : 1992Natur.358..149T。doi : 10.1038 / 358149a0。PMID 1319557。S2CID 4345839。
↑ Ninomiya S, Anjiki A, Nishide Y, Mori M, Deguchi Y, Satoh T (2013年7月). "厩舎飼育馬のドーパミンD4受容体遺伝子の多型は欲求不満に対する行動反応の違いと関連している" . Animals . 3 (3): 663–9 . doi : 10.3390/ani3030663 . PMC 4494454 . PMID 26479526 .
↑Timm, K.; Mägi, M.; Telva, K.; Tilgar, V. (2019). "The behavioural response of Great Tits to novel environment and handling is affected by the DRD4 gene". Ibis. 161 (2): 91–100. doi:10.1111/ibi.12604.
12345Posner MI, Rothbart MK, Sheese BE, Voelker P (May 2012). "Control networks and neuromodulators of early development". Developmental Psychology. 48 (3): 827–35. doi:10.1037/a0025530. PMC3253251. PMID21942663.
↑Bernaerts P, Tirelli E (June 2003). "Facilitatory effect of the dopamine D4 receptor agonist PD168,077 on memory consolidation of an inhibitory avoidance learned response in C57BL/6J mice". Behavioural Brain Research. 142 (1–2): 41–52. doi:10.1016/s0166-4328(02)00371-6. PMID12798264. S2CID21960608.
↑Browman KE, Curzon P, Pan JB, Molesky AL, Komater VA, Decker MW, Brioni JD, Moreland RB, Fox GB (September 2005). "A-412997, a selective dopamine D4 agonist, improves cognitive performance in rats". Pharmacology Biochemistry and Behavior. 82 (1): 148–55. doi:10.1016/j.pbb.2005.08.002. PMID16154186. S2CID31796938.
↑Woolley ML, Waters KA, Reavill C, Bull S, Lacroix LP, Martyn AJ, Hutcheson DM, Valerio E, Bate S, Jones DN, Dawson LA (December 2008). "Selective dopamine D4 receptor agonist (A-412997) improves cognitive performance and stimulates motor activity without influencing reward-related behaviour in rat". Behavioural Pharmacology. 19 (8): 765–76. doi:10.1097/FBP.0b013e32831c3b06. PMID19020411. S2CID36272297.
↑ Nakane M, Cowart MD, Hsieh GC, Miller L, Uchic ME, Chang R, Terranova MA, Donnelly-Roberts DL, Namovic MT, Miller TR, Wetter JM, Marsh K, Stewart AO, Brioni JD, Moreland RB (2005年7月). "2-[4-(3,4-ジメチルフェニル)ピペラジン-1-イルメチル]-1Hベンゾイミダゾール(A-381393)、選択的ドーパミンD4受容体拮抗薬". Neuropharmacology . 49 (1): 112–21 . doi : 10.1016/j.neuropharm.2005.02.004 . PMID 15992586 . S2CID 7529599 .
1 2 Prante O、Tietze R、Hocke C、Löber S、Hübner H、Kuwert T、Gmeiner P (2008 年 3 月)。「ピラゾロ [1,5-a]ピリジンをベースとしたドーパミン D4 受容体リガンドの合成、放射性フッ素化、および in vitro 評価: PET 用逆アゴニスト放射性リガンドの発見」。Journal of Medicinal Chemistry。51 ( 6 ) : 1800–10。doi : 10.1021 /jm701375u。PMID 18307287。
↑Kulagowski JJ, Broughton HB, Curtis NR, Mawer IM, Ridgill MP, Baker R, Emms F, Freedman SB, Marwood R, Patel S, Patel S, Ragan CI, Leeson PD (May 1996). "3-((4-(4-Chlorophenyl)piperazin-1-yl)-methyl)-1H-pyrrolo-2,3-b-pyridine: an antagonist with high affinity and selectivity for the human dopamine D4 receptor". Journal of Medicinal Chemistry. 39 (10): 1941–2. doi:10.1021/jm9600712. PMID8642550.
↑Patel S, Freedman S, Chapman KL, Emms F, Fletcher AE, Knowles M, Marwood R, Mcallister G, Myers J, Curtis N, Kulagowski JJ, Leeson PD, Ridgill M, Graham M, Matheson S, Rathbone D, Watt AP, Bristow LJ, Rupniak NM, Baskin E, Lynch JJ, Ragan CI (November 1997). "Biological profile of L-745,870, a selective antagonist with high affinity for the dopamine D4 receptor". The Journal of Pharmacology and Experimental Therapeutics. 283 (2): 636–47. doi:10.1016/S0022-3565(24)37092-2. PMID9353380.
↑Patel S, Patel S, Marwood R, Emms F, Marston D, Leeson PD, Curtis NR, Kulagowski JJ, Freedman SB (December 1996). "Identification and pharmacological characterization of [125I]L-750,667, a novel radioligand for the dopamine D4 receptor". Molecular Pharmacology. 50 (6): 1658–64. doi:10.1016/S0026-895X(25)09627-0. PMID8967990.
↑Berry CB, Bubser M, Jones CK, Hayes JP, Wepy JA, Locuson CW, Daniels JS, Lindsley CW, Hopkins CR (September 2014). "Discovery and Characterization of ML398, a Potent and Selective Antagonist of the D4 Receptor with in Vivo Activity". ACS Medicinal Chemistry Letters. 5 (9): 1060–4. doi:10.1021/ml500267c. PMC4160761. PMID25221667.