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Molecular Cloning and Functional Expression of a New Human CC-Chemokine Receptor Gene

Biochemistry (Easton), 1996-03, Vol.35 (11), p.3362-3367

1996

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Isolation and structure of the endogenous agonist of opioid receptor-like ORL1 receptor

Nature (London), 1995-10, Vol.377 (6549), p.532-535

1995

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Functional characterization of a human receptor for neuropeptide FF and related peptides

British journal of pharmacology, 2001-05, Vol.133 (1), p.138-144

2001

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Structure–activity relationships of neuropeptide FF and related peptidic and non-peptidic derivatives

Peptides (New York, N.Y. : 1980), 2006-05, Vol.27 (5), p.990-996

2006

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Functional Inactivation of the Nociceptin Receptor by Alanine Substitution of Glutamine 286 at the C Terminus of Transmembrane Segment VI: Evidence from a Site-Directed Mutagenesis Study of the ORL1 Receptor Transmembrane-Binding Domain

Molecular pharmacology, 2000-03, Vol.57 (3), p.495-502

2000

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Comparison of the structure-activity relationships of nociceptin and dynorphin A using chimeric peptides

FEBS letters, 1997-11, Vol.417 (3), p.333-336

1997

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Nonpeptide Small Molecule Agonist and Antagonist Original Leads for Neuropeptide FF1 and FF2 Receptors

Journal of medicinal chemistry, 2014-11, Vol.57 (21), p.8903-8927

2014

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Solubilization and reconstitution of the mu-opioid receptor expressed in human neuronal SH-SY5Y and CHO cells

Peptides (New York, N.Y. : 1980), 2014-05, Vol.55, p.79-84

2014

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Study of the N-terminal part of peptidic selective NPFF2 agonists

Peptides (New York, N.Y. : 1980), 2012-09, Vol.37 (1), p.157-160

2012

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Solubilization and functional reconstitution of human neuropeptide FF2 receptors

Analytical biochemistry, 2010-03, Vol.398 (2), p.225-229

2010

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Anti-analgesia of a selective NPFF2 agonist depends on opioid activity

Biochemical and biophysical research communications, 2005-10, Vol.336 (1), p.197-203

2005

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Pharmacological characterization of the mouse NPFF2 receptor

Peptides (New York, N.Y. : 1980), 2010-02, Vol.31 (2), p.215-220

2010

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N(ω)-Carbamoylation of the Argininamide Moiety: An Avenue to Insurmountable NPY Y1 Receptor Antagonists and a Radiolabeled Selective High-Affinity Molecular Tool ([(3)H]UR-MK299) with Extended Residence Time

Journal of medicinal chemistry, 2015-11, Vol.58 (22), p.8834-8849

2015

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Replacement of Gln280 by His in TM6 of the human ORL1 receptor increases affinity but reduces intrinsic activity of opioids

FEBS letters, 1996-10, Vol.395 (1), p.17-21

1996

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[Phe1ψ(CH2-NH)Gly2]nociceptin-(1-13)-NH2 is an agonist of the nociceptin (ORL1) receptor

European journal of pharmacology, 1998-05, Vol.349 (1), p.R5-R6

1998

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Structure-activity relationships of neuropeptide FF: role of C-terminal regions

Peptides (New York, N.Y. : 1980), 2001-09, Vol.22 (9), p.1471-1478

2001

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Distinct mechanisms for activation of the opioid receptor-like 1 and kappa-opioid receptors by nociceptin and dynorphin A

Molecular pharmacology, 1999-02, Vol.55 (2), p.324-331

1999

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Characterization of two novel tritiated radioligands for labelling Neuropeptide FF (NPFF(1) and NPFF(2)) receptors

Neurochemistry international, 2009-12, Vol.55 (8), p.815-819

2009

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Different domains of the ORL1 and κ-opioid receptors are involved in recognition of nociceptin and dynorphin A

FEBS letters, 1998-05, Vol.427 (2), p.296-300

1998

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Pharmacological characterization of human NPFF(1) and NPFF(2) receptors expressed in CHO cells by using NPY Y(1) receptor antagonists

European journal of pharmacology, 2002-09, Vol.451 (3), p.245-256

2002

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Molecular Cloning and Functional Expression of a New Human CC-Chemokine Receptor Gene

Isolation and structure of the endogenous agonist of opioid receptor-like ORL1 receptor

Functional characterization of a human receptor for neuropeptide FF and related peptides

Structure–activity relationships of neuropeptide FF and related peptidic and non-peptidic derivatives

Functional Inactivation of the Nociceptin Receptor by Alanine Substitution of Glutamine 286 at the C Terminus of Transmembrane Segment VI: Evidence from a Site-Directed Mutagenesis Study of the ORL1 Receptor Transmembrane-Binding Domain

Comparison of the structure-activity relationships of nociceptin and dynorphin A using chimeric peptides

Nonpeptide Small Molecule Agonist and Antagonist Original Leads for Neuropeptide FF1 and FF2 Receptors

Solubilization and reconstitution of the mu-opioid receptor expressed in human neuronal SH-SY5Y and CHO cells

Study of the N-terminal part of peptidic selective NPFF2 agonists

Solubilization and functional reconstitution of human neuropeptide FF2 receptors

Anti-analgesia of a selective NPFF2 agonist depends on opioid activity

Pharmacological characterization of the mouse NPFF2 receptor

N(ω)-Carbamoylation of the Argininamide Moiety: An Avenue to Insurmountable NPY Y1 Receptor Antagonists and a Radiolabeled Selective High-Affinity Molecular Tool ([(3)H]UR-MK299) with Extended Residence Time

Replacement of Gln280 by His in TM6 of the human ORL1 receptor increases affinity but reduces intrinsic activity of opioids

[Phe1ψ(CH2-NH)Gly2]nociceptin-(1-13)-NH2 is an agonist of the nociceptin (ORL1) receptor

Structure-activity relationships of neuropeptide FF: role of C-terminal regions

Distinct mechanisms for activation of the opioid receptor-like 1 and kappa-opioid receptors by nociceptin and dynorphin A

Characterization of two novel tritiated radioligands for labelling Neuropeptide FF (NPFF(1) and NPFF(2)) receptors

Different domains of the ORL1 and κ-opioid receptors are involved in recognition of nociceptin and dynorphin A

Pharmacological characterization of human NPFF(1) and NPFF(2) receptors expressed in CHO cells by using NPY Y(1) receptor antagonists

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