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Pharmacokinetics and pharmacodynamics of oral oxycodone in healthy human subjects: Role of circulating active metabolites

Clinical pharmacology and therapeutics, 2006-05, Vol.79 (5), p.461-479

2006

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Agonist-induced regulation and trafficking of κ opioid receptors

Life Sciences, 2004-06, Vol.75 (5), p.511-536

LIUCHEN, L

2004

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Molecular cloning and expression of a rat κ opioid receptor

Biochemical journal, 1993-11, Vol.295 (3), p.629-633

1993

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Differential binding domains of peptide and non-peptide ligands in the cloned rat kappa opioid receptor

The Journal of biological chemistry, 1994-12, Vol.269 (48), p.30195-30199

1994

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Determination of the amino acid residue involved in [3H]beta-funaltrexamine covalent binding in the cloned rat mu-opioid receptor

The Journal of biological chemistry, 1996-08, Vol.271 (35), p.21422-21429

1996

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Cloning of a human κ opioid receptor from the brain

Life sciences (1973), 1995, Vol.56 (9), p.PL201-PL207

1995

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Characterization of irreversible binding of beta-funaltrexamine to the cloned rat mu opioid receptor

The Journal of biological chemistry, 1995-07, Vol.270 (30), p.17866-17870

1995

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Sequence of κ-opioid receptor cDNA in the R1.1 thymoma cell line

Journal of neuroimmunology, 1995-10, Vol.62 (1), p.113-117

1995

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Substance P release in the rat periaqueductal gray and preoptic anterior hypothalamus after noxious cold stimulation: effect of selective mu and kappa opioid agonists

The Journal of pharmacology and experimental therapeutics, 1997-08, Vol.282 (2), p.1055

1997

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Intracerebroventricular treatment with an antisense oligodeoxynucleotide to κ-opioid receptors inhibited κ-agonist-induced analgesia in rats

Brain research, 1994-12, Vol.667 (1), p.129-132

1994

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Beta-[3H]funaltrexamine-labeled mu-opioid receptors: species variations in molecular mass and glycosylation by complex-type, N-linked oligosaccharides

Molecular pharmacology, 1993-10, Vol.44 (4), p.749-756

1993

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The region in the μ opioid receptor conferring selectivity for sufentanil over the δ receptor is different from that over the κ receptor

FEBS letters, 1996-04, Vol.384 (2), p.198-202

1996

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An antisense oligodeoxynucleotide to μ-opioid receptors inhibits μ-opioid receptor agonist-induced analgesia in rats

European journal of pharmacology, 1995-02, Vol.275 (1), p.105-108

1995

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Antisense confirmation of μ- and κ-opioid receptor mediation of morphine's effects on body temperature in rats

Drug and alcohol dependence, 1996-12, Vol.43 (3), p.119-124

1996

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Irreversible Binding of cis-(+)-3-Methylfentanyl Isothiocyanate to the δ Opioid Receptor and Determination of Its Binding Domain (∗)

The Journal of biological chemistry, 1996-01, Vol.271 (3), p.1430-1434

1996

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Identification and characterization of [ 125I] arginine vasopressin binding sites on human peripheral blood mononuclear cells

Life sciences (1973), 1993, Vol.52 (1), p.95-105

1993

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Differential release of substance P and somatostatin in the rat spinal cord in response to noxious cold and heat; effect of dynorphin A(1-17)

The Journal of pharmacology and experimental therapeutics, 1990-02, Vol.252 (2), p.539

1990

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Effect of intracerebroventricular beta-funaltrexamine on mu opioid receptors in the rat brain: consideration of binding condition

The Journal of pharmacology and experimental therapeutics, 1995-06, Vol.273 (3), p.1047

1995

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In vivo treatment with antisense oligodeoxynucleotide to κ-opioid receptors inhibited κ-agonist-induced analgesia in rats

Regulatory peptides, 1994-11, Vol.54 (1), p.1-2

1994

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Covalent labeling of mu opioid binding site by [3H]beta-funaltrexamine

Molecular pharmacology, 1987-09, Vol.32 (3), p.321-329

1987

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Immunohistochemical evidence for a substance P-containing trigeminovascular pathway to pial arteries in cats

Brain research, 1983-05, Vol.268 (1), p.162-166

1983

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Irreversible binding of N-methyl- N-[(1S)-1-(4-isothiocyanatophenyl)-2-(1-pyrrolidinyl)ethyl-3,4-dichlorophenylacetamide to the cloned rat κ opioid receptor

Life sciences (1973), 1997, Vol.61 (8), p.787-794

1997

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Properties of a κ-opioid receptor expressed in CHO cells: interaction with multiple G-proteins is not specific for any individual G α subunit and is similar to that of other opioid receptors

Brain research. Molecular brain research., 1995-04, Vol.29 (2), p.336-346

1995

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Involvement of β-endorphin (β-E) in supraspinal substance P (SP) antinociception

Regulatory peptides, 1994-11, Vol.54 (1), p.329-330

1994

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Use of a μ-antisense oligodeoxynucleotide as a μ opioid receptor noncompetitive antagonist in vivo

Neurochemical research, 1996-11, Vol.21 (11), p.1363-1368

1996

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Pharmacokinetics and pharmacodynamics of oral oxycodone in healthy human subjects: Role of circulating active metabolites

Agonist-induced regulation and trafficking of κ opioid receptors

Molecular cloning and expression of a rat κ opioid receptor

Differential binding domains of peptide and non-peptide ligands in the cloned rat kappa opioid receptor

Determination of the amino acid residue involved in [3H]beta-funaltrexamine covalent binding in the cloned rat mu-opioid receptor

Cloning of a human κ opioid receptor from the brain

Characterization of irreversible binding of beta-funaltrexamine to the cloned rat mu opioid receptor

Sequence of κ-opioid receptor cDNA in the R1.1 thymoma cell line

Substance P release in the rat periaqueductal gray and preoptic anterior hypothalamus after noxious cold stimulation: effect of selective mu and kappa opioid agonists

Intracerebroventricular treatment with an antisense oligodeoxynucleotide to κ-opioid receptors inhibited κ-agonist-induced analgesia in rats

Beta-[3H]funaltrexamine-labeled mu-opioid receptors: species variations in molecular mass and glycosylation by complex-type, N-linked oligosaccharides

The region in the μ opioid receptor conferring selectivity for sufentanil over the δ receptor is different from that over the κ receptor

An antisense oligodeoxynucleotide to μ-opioid receptors inhibits μ-opioid receptor agonist-induced analgesia in rats

Antisense confirmation of μ- and κ-opioid receptor mediation of morphine's effects on body temperature in rats

Irreversible Binding of cis-(+)-3-Methylfentanyl Isothiocyanate to the δ Opioid Receptor and Determination of Its Binding Domain (∗)

Identification and characterization of [ 125I] arginine vasopressin binding sites on human peripheral blood mononuclear cells

Differential release of substance P and somatostatin in the rat spinal cord in response to noxious cold and heat; effect of dynorphin A(1-17)

Effect of intracerebroventricular beta-funaltrexamine on mu opioid receptors in the rat brain: consideration of binding condition

In vivo treatment with antisense oligodeoxynucleotide to κ-opioid receptors inhibited κ-agonist-induced analgesia in rats

Covalent labeling of mu opioid binding site by [3H]beta-funaltrexamine

Immunohistochemical evidence for a substance P-containing trigeminovascular pathway to pial arteries in cats

Irreversible binding of N-methyl- N-[(1S)-1-(4-isothiocyanatophenyl)-2-(1-pyrrolidinyl)ethyl-3,4-dichlorophenylacetamide to the cloned rat κ opioid receptor

Properties of a κ-opioid receptor expressed in CHO cells: interaction with multiple G-proteins is not specific for any individual G α subunit and is similar to that of other opioid receptors

Involvement of β-endorphin (β-E) in supraspinal substance P (SP) antinociception

Use of a μ-antisense oligodeoxynucleotide as a μ opioid receptor noncompetitive antagonist in vivo

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