DRD2, dopamine receptor D2, 1813

N. diseases: 437; N. variants: 42
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.600 Biomarker disease BEFREE <b>Results</b>: Adenosine A2A-dopamine D2 receptor (A2AR/D2R) heteromer formation was monitored in caudate from healthy and Parkinson's disease (PD) subjects. 31340557 2019
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.600 GeneticVariation disease BEFREE Dopamine D2 receptor TaqIA and TaqIB polymorphisms in Parkinson's disease. 12722176 2003
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.600 GeneticVariation disease BEFREE Dopamine D2 receptor-mediated neuroprotection in a G2019S Lrrk2 genetic model of Parkinson's disease. 29434188 2018
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.600 GeneticVariation disease BEFREE Dopamine D2 receptor activation potently inhibits striatal glutamatergic transmission in a G2019S LRRK2 genetic model of Parkinson's disease. 29908325 2018
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.600 Biomarker disease BEFREE Drd2 is also the primary target of both antipsychotics and Parkinson's disease medications. 30604007 2019
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.600 PosttranslationalModification disease BEFREE DRD2 methylation to differentiate dementia with Lewy bodies from Parkinson's disease. 31659741 2020
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.600 Biomarker disease BEFREE Dopamine D2 receptor agonist, Ropinirole, has been found to promote neuroprotection in Parkinson´s disease and restless leg syndrome. 31816341 2020
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.600 Biomarker disease BEFREE A dopamine D2 receptor agonist, pramipexole, has been found to elicit neuroprotection in patients with Parkinson's disease and restless leg syndrome. 31235613 2019
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.600 Biomarker disease MGD Absence of dopaminergic control on melanotrophs leads to Cushing's-like syndrome in mice. 9717839 1998
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.600 Biomarker disease MGD Absence of opiate rewarding effects in mice lacking dopamine D2 receptors. 9252189 1997
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.600 Therapeutic disease CTD_human ABT-431: the diacetyl prodrug of A-86929, a potent and selective dopamine D1 receptor agonist: in vitro characterization and effects in animal models of Parkinson's disease. 8558425 1996
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.600 Biomarker disease MGD Activity, non-selective attention and emotionality in dopamine D2/D3 receptor knock-out mice. 11864730 2002
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.600 GeneticVariation disease BEFREE Among non-Hispanic whites, homozygous carriers of Taq1A DRD2 (rs1800497) polymorphism had an increased risk of PD compared to homozygous wildtype carriers (OR=1.5, 95% CI 1.0-2.3). 21663922 2011
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.600 Biomarker disease MGD Antiproliferative role of dopamine: loss of D2 receptors causes hormonal dysfunction and pituitary hyperplasia. 9247268 1997
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.600 GeneticVariation disease BEFREE Antipsychotics and serotoninergic antidepressants may potentially attenuate PD risk, and lithium and bupropion may augment risk, through MAPT, GBA, CCDC62, HIP1R, BDNF, and DRD2 transcription, with MAPT, GBA, and CCDC62 being strongly associated with PD risk in recent meta-analyses. 22507762 2012
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.600 GeneticVariation disease BEFREE Association of the DRD2 and DRD3 polymorphisms with response to pramipexole in Parkinson's disease patients. 19396436 2009
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.600 GeneticVariation disease BEFREE Further, DRD2 variants have been implicated in Parkinson's disease (PD) and in iatrogenically-induced movement disorders, as well as in certain migraineurs. 11256581 2000
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.600 GeneticVariation disease BEFREE Genetic variation in the DRD2 gene may influence the risk of developing PD, thus confirming that the DRD2 gene is a susceptibility locus for PD. 10634251 2000
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.600 GeneticVariation disease BEFREE Genotype combinations characterized by the presence of two variant genotypes on their corresponding loci revealed that four combinations of GSTT1 null and MnSOD(-9Val) or GST null and MAOB-G or CYP2E1*5B and MAO-B-AG or CYP2E1*5B and DRD2 (Taq1A-het) genotypes in the patients exhibited severalfold higher and significant association with risk to PD. 18327668 2008
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.600 GeneticVariation disease BEFREE Human genetic studies also show a significant association of DRD2 polymorphisms with disorders including schizophrenia and Parkinson's disease. 29107444 2017
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.600 Biomarker disease BEFREE In conclusion, we suggest that L-DOPA may attenuate the neuropathology of PD by regulating signaling related to DRD2 in neuronal cells under α-syn-induced toxicity. 28687316 2017
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.600 GeneticVariation disease BEFREE In the current study, we determined whether a dopamine D2 receptor DNA sequence polymorphism interacts with L-DOPA during motor tasks in patients with Parkinson's disease (PD). 23439215 2013
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.600 GeneticVariation disease BEFREE In the present study, we investigated this effect in Parkinson's disease (PD) patients carrying the DRD2 TaqIA A1 allelic variant. 17147698 2007
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.600 Biomarker disease BEFREE In the present study, we used 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine-induced PD mouse model to investigate whether Drd2 could suppress astrocytic NLRP3 inflammasome activation. 29786071 2018
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.600 GeneticVariation disease BEFREE In this study, we investigated the hypothesis that a TaqI repeat fragment length polymorphism in the dopamine D2 receptor gene may be associated with PD. 11104188 2000