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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
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1995 | 1 |
1996 | 1 |
2013 | 1 |
2015 | 2 |
2024 | 0 |
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Page 1
What can crystal structures of aminergic receptors tell us about designing subtype-selective ligands?
Pharmacol Rev. 2015;67(1):198-213. doi: 10.1124/pr.114.009944.
Pharmacol Rev. 2015.
PMID: 25527701
Free PMC article.
Review.
Differentiating dopamine D2 ligands by their sensitivities to modification of the cysteine exposed in the binding-site crevice.
Javitch JA, Fu D, Chen J.
Javitch JA, et al.
Mol Pharmacol. 1996 Apr;49(4):692-8.
Mol Pharmacol. 1996.
PMID: 8609898
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Using Bioluminescence Resonance Energy Transfer (BRET) to Characterize Agonist-Induced Arrestin Recruitment to Modified and Unmodified G Protein-Coupled Receptors.
Donthamsetti P, Quejada JR, Javitch JA, Gurevich VV, Lambert NA.
Donthamsetti P, et al.
Curr Protoc Pharmacol. 2015 Sep 1;70:2.14.1-2.14.14. doi: 10.1002/0471141755.ph0214s70.
Curr Protoc Pharmacol. 2015.
PMID: 26331887
Free PMC article.
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A single glycine in extracellular loop 1 is the critical determinant for pharmacological specificity of dopamine D2 and D3 receptors.
Michino M, Donthamsetti P, Beuming T, Banala A, Duan L, Roux T, Han Y, Trinquet E, Newman AH, Javitch JA, Shi L.
Michino M, et al.
Mol Pharmacol. 2013 Dec;84(6):854-64. doi: 10.1124/mol.113.087833. Epub 2013 Sep 23.
Mol Pharmacol. 2013.
PMID: 24061855
Free PMC article.
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Residues in the fifth membrane-spanning segment of the dopamine D2 receptor exposed in the binding-site crevice.
Javitch JA, Fu D, Chen J.
Javitch JA, et al.
Biochemistry. 1995 Dec 19;34(50):16433-9. doi: 10.1021/bi00050a026.
Biochemistry. 1995.
PMID: 8845371
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