183 Publications (Page 4 of 8)
2011
Mapping the catechol binding site in dopamine D₁ receptors: synthesis and evaluation of two parallel series of bicyclic dopamine analogues.
Bonner, Lisa A⋅Laban, Uros⋅Chemel, Benjamin R⋅Juncosa, Jose I⋅Lill, Markus A⋅Watts, Val J and Nichols, David E
ChemMedChem, vol. 6, (no. 6), pp. 1024-40, 2011/Jun/6. | Journal Article
 
Molecular and pharmacological characterization of two D(1)-like dopamine receptors in the Lyme disease vector, Ixodes scapularis.
Meyer, Jason M⋅Ejendal, Karin F⋅Watts, Val J and Hill, Catherine
Insect biochemistry and molecular biology, vol. 41, (no. 8), pp. 563-71, 2011/Aug. | Journal Article
 
Molecular and pharmacological characterization of two D1-like dopamine receptors in the Lyme disease vector, Ixodes scapularis
Meyer, Jason M⋅Ejendal, Karin F⋅Watts, Val J and Hill, Catherine
Insect Biochemistry and Molecular Biology, vol. 41, (no. 8), pp. 563-571, 2011. | Journal Article
 
Probing the steric space at the floor of the D1 dopamine receptor orthosteric binding domain: 7α-, 7β-, 8α-, and 8β-methyl substituted dihydrexidine analogues.
Cueva, Juan P⋅Gallardo-Godoy, Alejandra⋅Juncosa, Jose I⋅Vidi, Pierre A⋅Lill, Markus A⋅Watts, Val J and Nichols, David E
Journal of medicinal chemistry, vol. 54, (no. 15), pp. 5508-21, 2011/Aug/11. | Journal Article
2010
AGS3 blocks D2L dopamine receptor‐mediated heterologous sensitization of adenylyl cyclase 2
Conley, Jason Michael and Watts, Val J
The FASEB journal, vol. 24, (no. S1), pp. 587.5, April 2010. | Journal Article
 
Facile synthesis of octahydrobenzo[h]isoquinolines: novel and highly potent D1 dopamine agonists.
Bonner, Lisa A⋅Chemel, Benjamin R⋅Watts, Val J and Nichols, David E
Bioorganic & medicinal chemistry, vol. 18, (no. 18), pp. 6763-70, 2010/Sep/15. | Journal Article
 
Facile synthesis of octahydrobenzo[h]isoquinolines: Novel and highly potent D sub(1) dopamine agonists
Bonner, Lisa A⋅Chemel, Benjamin R⋅Watts, Val J and Nichols, David E
Bioorganic and Medicinal Chemistry, vol. 18, (no. 18), pp. 6763-6770, 2010. | Journal Article
 
Heterologous sensitization of human AC5: dependence on heterotrimeric G proteins
Ejendal, Karin F K⋅Sadana, Rachna⋅Vidi, Pierre‐Alexandre⋅Dessauer, Carmen W and Watts, Val J
The FASEB journal, vol. 24, (no. S1), pp. 962.5, April 2010. | Journal Article
 
Ligand-induced regulation and localization of cannabinoid CB1 and dopamine D2L receptor heterodimers.
Przybyla, Julie A and Watts, Val J
The Journal of pharmacology and experimental therapeutics, vol. 332, (no. 3), pp. 710-9, 2010/Mar. | Journal Article
 
Ligand‐specific roles for transmembrane 5 serine residues in D1 dopamine receptor binding and activation
Chemel, Benjamin Reed⋅Bonner, Lisa A.⋅Watts, Val J. and Nichols, David E.
The FASEB journal, vol. 24, (no. S1), pp. 584.2, April 2010. | Journal Article
 
Structures of G [alpha [superscript i1]] Bound to a GDP-Selective Peptide Provides Insight into Guanine Nucleotide Exchange
Johnston, Christopher⋅Willard, Francis⋅Jezyk, Mark⋅Fredericks, Zoey⋅Bodor, Erik⋅Jones, Miller⋅Blaesius, Rainer⋅Watts, Val⋅Harden, T.⋅Sondek, John⋅Ramer, J.⋅Siderovski, David⋅ and
Structure, vol. 13, (no. (7) ; 07, 2005), 2010-07-19. | Journal Article
 
Visualization of G protein-coupled receptor (GPCR) interactions in living cells using bimolecular fluorescence complementation (BiFC).
Vidi, Pierre-Alexandre⋅Przybyla, Julie A⋅Hu, Cheng Deng and Watts, Val J
Current protocols in neuroscience / editorial board, Jacqueline N. Crawley ... [et al.], vol. Chapter 5, pp. Unit 5.29, 2010/Apr. | Journal Article
2009
Comparison of the enantiomers of (+/-)-doxanthrine, a high efficacy full dopamine D(1) receptor agonist, and a reversal of enantioselectivity at D(1) versus alpha(2C) adrenergic receptors.
Przybyla, Julie A⋅Cueva, Juan P⋅Chemel, Benjamin R⋅Hsu, K J⋅Riese, David J⋅McCorvy, John D⋅Chester, Julia A⋅Nichols, David E and Watts, Val J
European neuropsychopharmacology : the journal of the European College of Neuropsychopharmacology, vol. 19, (no. 2), pp. 138-46, 2009/Feb. | Journal Article
 
Comparison of the enantiomers of (+/-)-doxanthrine, a high efficacy full dopamine D sub(1 receptor agonist, and a reversal of enantioselectivity at D) sub(1) versus alpha sub(2C adrenergic receptors)
Przybyla, Julie⋅Przybyla, Julie A⋅Cueva, Juan⋅Cueva, Juan P⋅Chemel, Benjamin⋅Chemel, Benjamin R⋅Hsu, KJoseph⋅Hsu, K.⋅Riese, David⋅Riese, David J⋅McCorvy, John D⋅McCorvy, John⋅Chester, Julia⋅Chester, Julia A⋅Nichols, David E⋅Nichols, David⋅Watts, Val and Watts, Val J
European Neuropsychopharmacology, vol. 19, (no. 2), pp. 138-146, 2009. | Journal Article
 
Fluorescent and Bioluminescent Protein-Fragment Complementation Assays in the Study of G Protein-Coupled Receptor Oligomerization and Signaling
Vidi, Pierre-Alexandre and Watts, Val
Molecular Pharmacology, vol. 75, (no. 4), pp. 739, 20090401. | Journal Article
 
The intracellular II-III loops of Cav1.2 and Cav1.3 uncouple L-type voltage-gated Ca2+ channels from glucagon-like peptide-1 potentiation of insulin secretion in INS-1 cells via displacement from lipid rafts.
Jacobo, Sarah M⋅Guerra, Marcy L⋅Jarrard, Rachel E⋅Przybyla, Julie A⋅Liu, Guohong⋅Watts, Val J and Hockerman, Gregory H
The Journal of pharmacology and experimental therapeutics, vol. 330, (no. 1), pp. 283-93, 2009/Jul. | Journal Article
2008
Adenosine A(2A) receptors assemble into higher-order oligomers at the plasma membrane.
Vidi, Pierre-Alexandre⋅Chen, Jiji⋅Irudayaraj, Joseph and Watts, Val J
FEBS letters, vol. 582, (no. 29), pp. 3985-90, 2008/Dec/10. | Journal Article
 
Adenosine A sub(2) sub(A) receptors assemble into higher-order oligomers at the plasma membrane
Vidi, PA⋅Chen, J.⋅Irudayaraj, JMK and Watts, Val J
FEBS Letters, vol. 582, (no. 29), pp. 3985-3990, 2008. | Journal Article
 
A point mutation to Galphai selectively blocks GoLoco motif binding: direct evidence for Galpha.GoLoco complexes in mitotic spindle dynamics.
Willard, Francis S⋅Zheng, Zhen⋅Guo, Juan⋅Digby, Gregory J⋅Kimple, Adam J⋅Conley, Jason M⋅Johnston, Christopher A⋅Bosch, Dustin⋅Willard, Melinda D⋅Watts, Val J⋅Lambert, Nevin A⋅Ikeda, Stephen R⋅Du, Quansheng and Siderovski, David P
The Journal of biological chemistry, vol. 283, (no. 52), pp. 36698-710, 2008/Dec/26. | Journal Article
 
A Point Mutation to Gαi Selectively Blocks GoLoco Motif Binding: DIRECT EVIDENCE FOR Gα·GoLoco COMPLEXES IN MITOTIC SPINDLE DYNAMICS.
Willard, Francis S⋅Zheng, Zhen⋅Guo, Juan⋅Digby, Gregory J⋅Kimple, Adam J⋅Conley, Jason M⋅Johnston, Christopher A⋅Bosch, Dustin⋅Willard, Melinda D⋅Watts, Val J⋅Lambert, Nevin A⋅Ikeda, Stephen R⋅Du, Quansheng and Siderovski, David P
Journal of biological chemistry., vol. 283, (no. 52), pp. 36698-36710, 2008. | Journal Article
 
D1 versus D2 dopamine receptor selectivity is determined by intramolecular hydrogen bonding patterns in catechol‐containing novel dopamine analogues
Chemel, Benjamin R⋅Bonner, Lisa A⋅Watts, Val J and Nichols, David E
The FASEB journal, vol. 22, (no. S1), 2008-03-00. | Journal Article
 
Direct visualization of adenosine A 2A and dopamine D 2L receptor oligomers in a neuronal cell model
Vidi, Pierre‐Alexandre⋅Chemel, Benjamin R. and Watts, Val J.
The FASEB journal, vol. 22, (no. S1), 2008-03-00. | Journal Article
 
Ligand-dependent oligomerization of dopamine D(2) and adenosine A(2A) receptors in living neuronal cells.
Vidi, Pierre-Alexandre⋅Chemel, Benjamin R⋅Hu, Chang Deng and Watts, Val J
Molecular pharmacology, vol. 74, (no. 3), pp. 544-51, 2008/Sep. | Journal Article
2007
Adenylyl Cyclase 5: A New Clue in the Search for the "Fountain of Youth"?
Chester, Julia A and Watts, Val J
Signal Transduction Knowledge Environment, vol. 2007, (no. 413), pp. pe64-pe64, 2007. | Journal Article
 
Adenylyl Cyclase Isoforms as Novel Therapeutic Targets: An Exciting Example of Excitotoxicity Neuroprotection
Watts, Val J
Molecular Interventions, vol. 7, (no. 2), pp. 70-73, 2007. | Journal Article