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DA-11263

Funded outputs count: 21
Funder award ID: DA-11263
OpenAlex ID: G4583170779
Localization of the κ Opioid Receptor in Lipid Rafts
2006 · Wei Xu, Su-In Yoon, et al. · Journal of Pharmacology and Experimental Therapeutics · 85
Distribution and ultrastructural localization of GEC1 in the rat CNS
2006 · Y. Wang, S.L. Dun, et al. · Neuroscience · 13
The Seventh Transmembrane Domains of the δ and κ Opioid Receptors Have Different Accessibility Patterns and Interhelical Interactions
2005 · Wei Xu, Mercedes Campillo, et al. · Biochemistry · 24
Comparison of Pharmacological Activities of Three Distinct κ Ligands (Salvinorin A, TRK-820 and 3FLB) on κ Opioid Receptors in Vitro and Their Antipruritic and Antinociceptive Activities in Vivo
2004 · Yulin Wang, Kang Tang, et al. · Journal of Pharmacology and Experimental Therapeutics · 191
κ Opioid Receptor Interacts with Na+/H+-exchanger Regulatory Factor-1/Ezrin-Radixin-Moesin-binding Phosphoprotein-50 (NHERF-1/EBP50) to Stimulate Na+/H+ Exchange Independent of Gi/Go Proteins
2004 · Peng Huang, Deborah Steplock, et al. · Journal of Biological Chemistry · 43
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Heterodimerization and cross-desensitization between the μ-opioid receptor and the chemokine CCR5 receptor
2003 · Chongguang Chen, Jin Li, et al. · European Journal of Pharmacology · 157
Differential Effects of Agonists on Adenylyl Cyclase Superactivation Mediated by the κ Opioid Receptors: Adenylyl Cyclase Superactivation Is Independent of Agonist-Induced Phosphorylation, Desensitization, Internalization, and Down-Regulation
2003 · Yulin Wang, Jian-Guo Li, et al. · Journal of Pharmacology and Experimental Therapeutics · 19
Recombinant Opioid Receptors: Structure-Function Relationship
2003 · Julija Filipovska, Ivone Gomes, et al. · Humana Press eBooks
Selective inactivation of CCR5 and decreased infectivity of R5 HIV-1 strains mediated by opioid-induced heterologous desensitization
2003 · Imre Szabo, Michele A Wetzel, et al. · Journal of Leukocyte Biology · 86
Differential Regulation of the Human κ Opioid Receptor by Agonists: Etorphine and Levorphanol Reduced Dynorphin A- and U50,488H-Induced Internalization and Phosphorylation
2003 · Jian-Guo Li, Fengqin Zhang, et al. · Journal of Pharmacology and Experimental Therapeutics · 49
The Local Environment at the Cytoplasmic End of TM6 of the μ Opioid Receptor Differs from Those of Rhodopsin and Monoamine Receptors: Introduction of an Ionic Lock between the Cytoplasmic Ends of Helices 3 and 6 by a L6.30(275)E Mutation Inactivates the μ Opioid Receptor and Reduces the Constitutive Activity of Its T6.34(279)K Mutant
2002 · Peng Huang, Irache Visiers, et al. · Biochemistry · 34
(−)U50,488H [(trans)-3,4-Dichloro-N-methyl-N-[2-(1-pyrrolidinyl)-cyclohexyl]benzeneacetamide] Induces Internalization and Down-Regulation of the Human, but not the Rat, κ-Opioid Receptor: Structural Basis for the Differential Regulation
2002 · Fengqin Zhang, Jin Li, et al. · Journal of Pharmacology and Experimental Therapeutics · 32
Molecular Basis of Differences in (−)(trans)-3,4-Dichloro-N-methyl-N-[2-(1-pyrrolidiny)-cyclohexyl]benzeneacetamide-Induced Desensitization and Phosphorylation between Human and Rat κ-Opioid Receptors Expressed in Chinese Hamster Ovary Cells
2002 · Jin Li, Jian-Guo Li, et al. · Molecular Pharmacology · 51
Inverse Agonist Up-Regulates the Constitutively Active D3.49(164)Q Mutant of the Rat μ-Opioid Receptor by Stabilizing the Structure and Blocking Constitutive Internalization and Down-Regulation
2001 · Jin Li, Chongguang Chen, et al. · Molecular Pharmacology · 46
Functional Role of a Conserved Motif in TM6 of the Rat μ Opioid Receptor: Constitutively Active and Inactive Receptors Result from Substitutions of Thr6.34(279) with Lys and Asp
2001 · Peng Huang, Jin Li, et al. · Biochemistry · 85
Constitutive Activation of the μ Opioid Receptor by Mutation of D3.49(164), but Not D3.32(147): D3.49(164) Is Critical for Stabilization of the Inactive Form of the Receptor and for Its Expression
2001 · Jin Li, Peng Huang, et al. · Biochemistry · 68
Comparison of the Amino Acid Residues in the Sixth Transmembrane Domains Accessible in the Binding-Site Crevices of μ, δ, and κ Opioid Receptors
2001 · Wei Xu, Jin Li, et al. · Biochemistry · 31
Comparison of Pharmacological Activities of Buprenorphine and Norbuprenorphine: Norbuprenorphine Is a Potent Opioid Agonist
2001 · Peng Huang, George B. Kehner, et al. · Journal of Pharmacology and Experimental Therapeutics · 340
The Conserved Cysteine 7.38 Residue Is Differentially Accessible in the Binding-Site Crevices of the μ, δ, and κ Opioid Receptors
2000 · Wei Xu, Chongguang Chen, et al. · Biochemistry · 26
Mechanisms of Agonist-Induced Down-Regulation of the Human κ-Opioid Receptor: Internalization Is Required for Down-Regulation
2000 · Jian-Guo Li, Jeffrey L. Benovic, et al. · Molecular Pharmacology · 94
U50,488H-induced Internalization of the Human κ Opioid Receptor Involves a β-Arrestin- and Dynamin-dependent Mechanism
1999 · Jian-Guo Li, Lai-Yi Luo, et al. · Journal of Biological Chemistry · 152
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