Dopamine receptor (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Dopamine receptor" in English language version.

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  • Rondou P, Haegeman G, Van Craenenbroeck K (June 2010). "The dopamine D4 receptor: biochemical and signalling properties". Cellular and Molecular Life Sciences. 67 (12): 1971–86. doi:10.1007/s00018-010-0293-y. PMC 11115718. PMID 20165900. S2CID 21432517.
  • Cools AR, Van Rossum JM (1976). "Excitation-mediating and inhibition-mediating dopamine-receptors: a new concept towards a better understanding of electrophysiological, biochemical, pharmacological, functional and clinical data". Psychopharmacologia. 45 (3): 243–254. doi:10.1007/bf00421135. PMID 175391. S2CID 40366909.
  • Neve KA, Seamans JK, Trantham-Davidson H (August 2004). "Dopamine receptor signaling". Journal of Receptor and Signal Transduction Research. 24 (3): 165–205. doi:10.1081/RRS-200029981. PMID 15521361. S2CID 12407397.
  • Neves SR, Ram PT, Iyengar R (2002). "G protein pathways". Science. 296 (5573): 1636–9. Bibcode:2002Sci...296.1636N. doi:10.1126/science.1071550. PMID 12040175. S2CID 20136388.
  • Suzuki M, Hurd YL, Sokoloff P, Schwartz JC, Sedvall G (1998). "D3 dopamine receptor mRNA is widely expressed in the human brain". Brain Res. 779 (1–2): 58–74. doi:10.1016/S0006-8993(97)01078-0. PMID 9473588. S2CID 46096849.
  • Langley K, Marshall L, van den Bree M, Thomas H, Owen M, O'Donovan M, et al. (2004). "Association of the dopamine D4 receptor gene 7-repeat allele with neuropsychological test performance of children with ADHD". Am J Psychiatry. 161 (1): 133–8. doi:10.1176/appi.ajp.161.1.133. PMID 14702261. S2CID 25892078.
  • Williams GV, Castner SA (2006). "Under the curve: critical issues for elucidating D1 receptor function in working memory". Neuroscience. 139 (1): 263–76. doi:10.1016/j.neuroscience.2005.09.028. PMID 16310964. S2CID 20906770.
  • Cavallotti C, Massimo M, Paolo B, Maurizio S, Fiorenzo M (2010). "Dopamine receptor subtypes in the native human heart". Heart and Vessels. 25 (5): 432–7. doi:10.1007/s00380-009-1224-4. hdl:11573/230067. PMID 20676967. S2CID 36507640.
  • Hussain T, Lokhandwala MF (2003). "Renal dopamine receptors and hypertension". Exp. Biol. Med. (Maywood). 228 (2): 134–42. doi:10.1177/153537020322800202. PMID 12563019. S2CID 10896819.
  • Mihara K, Kondo T, Suzuki A, Yasui-Furukori N, Ono S, Sano A, et al. (2003). "Relationship between functional dopamine D2 and D3 receptors gene polymorphisms and neuroleptic malignant syndrome". Am. J. Med. Genet. B Neuropsychiatr. Genet. 117B (1): 57–60. doi:10.1002/ajmg.b.10025. PMID 12555236. S2CID 44866985.
  • Hummel M, Unterwald EM (2002). "D1 dopamine receptor: a putative neurochemical and behavioral link to cocaine action". J. Cell. Physiol. 191 (1): 17–27. doi:10.1002/jcp.10078. PMID 11920678. S2CID 40444893.
  • Gornick MC, Addington A, Shaw P, Bobb AJ, Sharp W, Greenstein D, et al. (2007). "Association of the dopamine receptor D4 (DRD4) gene 7-repeat allele with children with attention-deficit/hyperactivity disorder (ADHD): an update". Am. J. Med. Genet. B Neuropsychiatr. Genet. 144B (3): 379–82. doi:10.1002/ajmg.b.30460. PMID 17171657. S2CID 25065281.
  • Berridge KC, Robinson TE (1998). "What is the role of dopamine in reward: hedonic impact, reward learning, or incentive salience?". Brain Research. Brain Research Reviews. 28 (3): 309–369. doi:10.1016/s0165-0173(98)00019-8. PMID 9858756. S2CID 11959878.
  • Di Chiara G, Bassareo V, Fenu S, De Luca MA, Spina L, Cadoni C, et al. (2004). "Dopamine and drug addiction: the nucleus accumbens shell connection". Neuropharmacology. 47 (Suppl 1): 227–41. doi:10.1016/j.neuropharm.2004.06.032. PMID 15464140. S2CID 25983940.
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  • Jose PA, Eisner GM, Felder RA (2003). "Regulation of blood pressure by dopamine receptors". Nephron Physiol. 95 (2): 19–27. doi:10.1159/000073676. PMID 14610323. S2CID 28595227.
  • Lang AE, Obeso JA (May 2004). "Challenges in Parkinson's disease: restoration of the nigrostriatal dopamine system is not enough". The Lancet. Neurology. 3 (5): 309–16. doi:10.1016/S1474-4422(04)00740-9. PMID 15099546. S2CID 6551470.
  • Nestler EJ (1 January 2004). "Molecular mechanisms of drug addiction". Neuropharmacology. 47 (Suppl 1): 24–32. doi:10.1016/j.neuropharm.2004.06.031. PMID 15464123. S2CID 11266116.
  • Scheler G (2004). "Regulation of neuromodulator receptor efficacy--implications for whole-neuron and synaptic plasticity". Prog. Neurobiol. 72 (6): 399–415. arXiv:q-bio/0401039. doi:10.1016/j.pneurobio.2004.03.008. PMID 15177784. S2CID 9353254.
  • Silvestri S, Seeman MV, Negrete JC, Houle S, Shammi CM, Remington GJ, et al. (2000). "Increased dopamine D2 receptor binding after long-term treatment with antipsychotics in humans: a clinical PET study". Psychopharmacology. 152 (2): 174–80. doi:10.1007/s002130000532. PMID 11057521. S2CID 20804595.
  • Ilieva IP, Hook CJ, Farah MJ (January 2015). "Prescription Stimulants' Effects on Healthy Inhibitory Control, Working Memory, and Episodic Memory: A Meta-analysis". J. Cogn. Neurosci. 27 (6): 1069–1089. doi:10.1162/jocn_a_00776. PMID 25591060. S2CID 15788121. The present meta-analysis was conducted to estimate the magnitude of the effects of methylphenidate and amphetamine on cognitive functions central to academic and occupational functioning, including inhibitory control, working memory, short-term episodic memory, and delayed episodic memory. In addition, we examined the evidence for publication bias. Forty-eight studies (total of 1,409 participants) were included in the analyses. We found evidence for small but significant stimulant enhancement effects on inhibitory control and short-term episodic memory. Small effects on working memory reached significance, based on one of our two analytical approaches. Effects on delayed episodic memory were medium in size. However, because the effects on long-term and working memory were qualified by evidence for publication bias, we conclude that the effect of amphetamine and methylphenidate on the examined facets of healthy cognition is probably modest overall. In some situations, a small advantage may be valuable, although it is also possible that healthy users resort to stimulants to enhance their energy and motivation more than their cognition. ... Earlier research has failed to distinguish whether stimulants' effects are small or whether they are nonexistent (Ilieva et al., 2013; Smith & Farah, 2011). The present findings supported generally small effects of amphetamine and methylphenidate on executive function and memory. Specifically, in a set of experiments limited to high-quality designs, we found significant enhancement of several cognitive abilities. ...

    The results of this meta-analysis cannot address the important issues of individual differences in stimulant effects or the role of motivational enhancement in helping perform academic or occupational tasks. However, they do confirm the reality of cognitive enhancing effects for normal healthy adults in general, while also indicating that these effects are modest in size.

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upenn.edu

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  • Ilieva IP, Hook CJ, Farah MJ (January 2015). "Prescription Stimulants' Effects on Healthy Inhibitory Control, Working Memory, and Episodic Memory: A Meta-analysis". J. Cogn. Neurosci. 27 (6): 1069–1089. doi:10.1162/jocn_a_00776. PMID 25591060. S2CID 15788121. The present meta-analysis was conducted to estimate the magnitude of the effects of methylphenidate and amphetamine on cognitive functions central to academic and occupational functioning, including inhibitory control, working memory, short-term episodic memory, and delayed episodic memory. In addition, we examined the evidence for publication bias. Forty-eight studies (total of 1,409 participants) were included in the analyses. We found evidence for small but significant stimulant enhancement effects on inhibitory control and short-term episodic memory. Small effects on working memory reached significance, based on one of our two analytical approaches. Effects on delayed episodic memory were medium in size. However, because the effects on long-term and working memory were qualified by evidence for publication bias, we conclude that the effect of amphetamine and methylphenidate on the examined facets of healthy cognition is probably modest overall. In some situations, a small advantage may be valuable, although it is also possible that healthy users resort to stimulants to enhance their energy and motivation more than their cognition. ... Earlier research has failed to distinguish whether stimulants' effects are small or whether they are nonexistent (Ilieva et al., 2013; Smith & Farah, 2011). The present findings supported generally small effects of amphetamine and methylphenidate on executive function and memory. Specifically, in a set of experiments limited to high-quality designs, we found significant enhancement of several cognitive abilities. ...

    The results of this meta-analysis cannot address the important issues of individual differences in stimulant effects or the role of motivational enhancement in helping perform academic or occupational tasks. However, they do confirm the reality of cognitive enhancing effects for normal healthy adults in general, while also indicating that these effects are modest in size.

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