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The absence of a direct correlation between the loss of [D-Ala2, MePhe4,Gly5-ol]Enkephalin inhibition of adenylyl cyclase activity and agonist-induced mu-opioid receptor phosphorylation

The Journal of biological chemistry, 1999-04, Vol.274 (14), p.9207-9215

1999

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Receptor density and recycling affect the rate of agonist-induced desensitization of mu-opioid receptor

Molecular pharmacology, 2000-08, Vol.58 (2), p.388-398

2000

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A-425619 [1-isoquinolin-5-yl-3-(4-trifluoromethyl-benzyl)-urea], a novel transient receptor potential type V1 receptor antagonist, relieves pathophysiological pain associated with inflammation and tissue injury in rats

The Journal of pharmacology and experimental therapeutics, 2005-07, Vol.314 (1), p.410-421

2005

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A-425619 [1-isoquinolin-5-yl-3-(4-trifluoromethyl-benzyl)-urea], a novel and selective transient receptor potential type V1 receptor antagonist, blocks channel activation by vanilloids, heat, and acid

The Journal of pharmacology and experimental therapeutics, 2005-07, Vol.314 (1), p.400-409

2005

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Pharmacology of α7 nicotinic acetylcholine receptor mediated extracellular signal‐regulated kinase signalling in PC12 cells

British journal of pharmacology, 2009-02, Vol.156 (4), p.638-648

2009

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Capsaicin Infused Into the PAG Affects Rat Tail Flick Responses to Noxious Heat and Alters Neuronal Firing in the RVM

Journal of neurophysiology, 2003-10, Vol.90 (4), p.2702-2710

2003

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Covalently Induced Activation of the δ Opioid Receptor by a Fluorogenic Affinity Label, 7‘-(Phthalaldehydecarboxamido)naltrindole (PNTI)

Journal of medicinal chemistry, 2001-03, Vol.44 (7), p.1017-1020

2001

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Dynamic aspects of colicin N translocation through the Escherichia coli outer membrane

Journal of Bacteriology, 1996-09, Vol.178 (17), p.5316-5319

1996

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[3H]A-778317 [1-((R)-5-tert-butyl-indan-1-yl)-3-isoquinolin-5-yl-urea]: a novel, stereoselective, high-affinity antagonist is a useful radioligand for the human transient receptor potential vanilloid-1 (TRPV1) receptor

The Journal of pharmacology and experimental therapeutics, 2007-10, Vol.323 (1), p.285-293

2007

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High content screen microscopy analysis of A beta sub(1) sub(-) sub(4) sub(2)-induced neurite outgrowth reduction in rat primary cortical neurons: Neuroprotective effects of alpha 7 neuronal nicotinic acetylcholine receptor ligands

Brain research, 2007-06, Vol.1151, p.227-235

2007

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Colicin N interaction with sensitive Escherichia coli cells: in situ and kinetic approaches

Research in microbiology, 1998-10, Vol.149 (9), p.645-651

1998

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Identification of serine 356 and serine 363 as the amino acids involved in etorphine-induced down-regulation of the mu-opioid receptor

The Journal of biological chemistry, 1998-12, Vol.273 (51), p.34488-34495

1998

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Naphthalene Dicarboxaldehyde as an Electrophilic Fluorogenic Moiety for Affinity Labeling: Application to Opioid Receptor Affinity Labels with Greatly Improved Fluorogenic Properties

Journal of medicinal chemistry, 2002-07, Vol.45 (14), p.2887-2890

2002

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Pharmacology of alpha7 nicotinic acetylcholine receptor mediated extracellular signal-regulated kinase signalling in PC12 cells

British journal of pharmacology, 2009-02, Vol.156 (4), p.638

2009

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Reporter Affinity Labels: An o-Phthalaldehyde Derivative of β-Naltrexamine as a Fluorogenic Ligand for Opioid Receptors

Journal of medicinal chemistry, 2000-06, Vol.43 (13), p.2489-2492

2000

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Pharmacology of a7 nicotinic acetylcholine receptor mediated extracellular signal-regulated kinase signalling in PC12 cells

British journal of pharmacology, 2009, Vol.156 (4), p.638-648

2009

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Phosphorylation of Ser363, Thr370, and Ser375 residues within the carboxyl tail differentially regulates mu-opioid receptor internalization

The Journal of biological chemistry, 2001-04, Vol.276 (16), p.12774-12780

2001

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Affinity labels as tools for the identification of opioid receptor recognition sites

Farmaco (Società chimica italiana : 1989), 2001-03, Vol.56 (3), p.191-196

2001

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Characterization of the receptor and translocator domains of colicin N

European journal of biochemistry, 1993-06, Vol.214 (3), p.635-639

1993

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In vitro Approaches to Investigation of the Early Steps of Colicin‐Ompf Interaction

European journal of biochemistry, 1994-09, Vol.224 (2), p.723-728

1994

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Indol-3-ylcycloalkyl Ketones: Effects of N1 Substituted Indole Side Chain Variations on CB2 Cannabinoid Receptor Activity

Journal of medicinal chemistry, 2010-01, Vol.53 (1), p.295-315

2010

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On the Semantic Transparency of Visual Notations: Experiments with UML

SDL 2015: Model-Driven Engineering for Smart Cities, 2015, p.122-137

2015

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Discovery of (R)-(3-fluoropyrrolidin-1-yl)(6-((5-(trifluoromethyl)pyridin-2-yl)oxy)quinolin-2-yl)methanone (ABBV-318) and analogs as small molecule Nav1.7/ Nav1.8 blockers for the treatment of pain

Bioorganic & medicinal chemistry, 2022-06, Vol.63, p.116743-116743, Article 116743

2022

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Adolescent alcohol drinking interaction with the gut microbiome: implications for adult alcohol use disorder

Advances in Drug and Alcohol Research, 2024-01, Vol.4

2024

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Blockade of mGluR1 receptor results in analgesia and disruption of motor and cognitive performances: effects of A‐841720, a novel non‐competitive mGluR1 receptor antagonist

British journal of pharmacology, 2006-11, Vol.149 (6), p.761-774

2006

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The absence of a direct correlation between the loss of [D-Ala2, MePhe4,Gly5-ol]Enkephalin inhibition of adenylyl cyclase activity and agonist-induced mu-opioid receptor phosphorylation

Receptor density and recycling affect the rate of agonist-induced desensitization of mu-opioid receptor

A-425619 [1-isoquinolin-5-yl-3-(4-trifluoromethyl-benzyl)-urea], a novel transient receptor potential type V1 receptor antagonist, relieves pathophysiological pain associated with inflammation and tissue injury in rats

A-425619 [1-isoquinolin-5-yl-3-(4-trifluoromethyl-benzyl)-urea], a novel and selective transient receptor potential type V1 receptor antagonist, blocks channel activation by vanilloids, heat, and acid

Pharmacology of α7 nicotinic acetylcholine receptor mediated extracellular signal‐regulated kinase signalling in PC12 cells

Capsaicin Infused Into the PAG Affects Rat Tail Flick Responses to Noxious Heat and Alters Neuronal Firing in the RVM

Covalently Induced Activation of the δ Opioid Receptor by a Fluorogenic Affinity Label, 7‘-(Phthalaldehydecarboxamido)naltrindole (PNTI)

Dynamic aspects of colicin N translocation through the Escherichia coli outer membrane

[3H]A-778317 [1-((R)-5-tert-butyl-indan-1-yl)-3-isoquinolin-5-yl-urea]: a novel, stereoselective, high-affinity antagonist is a useful radioligand for the human transient receptor potential vanilloid-1 (TRPV1) receptor

High content screen microscopy analysis of A beta sub(1) sub(-) sub(4) sub(2)-induced neurite outgrowth reduction in rat primary cortical neurons: Neuroprotective effects of alpha 7 neuronal nicotinic acetylcholine receptor ligands

Colicin N interaction with sensitive Escherichia coli cells: in situ and kinetic approaches

Identification of serine 356 and serine 363 as the amino acids involved in etorphine-induced down-regulation of the mu-opioid receptor

Naphthalene Dicarboxaldehyde as an Electrophilic Fluorogenic Moiety for Affinity Labeling: Application to Opioid Receptor Affinity Labels with Greatly Improved Fluorogenic Properties

Pharmacology of alpha7 nicotinic acetylcholine receptor mediated extracellular signal-regulated kinase signalling in PC12 cells

Reporter Affinity Labels: An o-Phthalaldehyde Derivative of β-Naltrexamine as a Fluorogenic Ligand for Opioid Receptors

Pharmacology of a7 nicotinic acetylcholine receptor mediated extracellular signal-regulated kinase signalling in PC12 cells

Phosphorylation of Ser363, Thr370, and Ser375 residues within the carboxyl tail differentially regulates mu-opioid receptor internalization

Affinity labels as tools for the identification of opioid receptor recognition sites

Characterization of the receptor and translocator domains of colicin N

In vitro Approaches to Investigation of the Early Steps of Colicin‐Ompf Interaction

Indol-3-ylcycloalkyl Ketones: Effects of N1 Substituted Indole Side Chain Variations on CB2 Cannabinoid Receptor Activity

On the Semantic Transparency of Visual Notations: Experiments with UML

Discovery of (R)-(3-fluoropyrrolidin-1-yl)(6-((5-(trifluoromethyl)pyridin-2-yl)oxy)quinolin-2-yl)methanone (ABBV-318) and analogs as small molecule Nav1.7/ Nav1.8 blockers for the treatment of pain

Adolescent alcohol drinking interaction with the gut microbiome: implications for adult alcohol use disorder

Blockade of mGluR1 receptor results in analgesia and disruption of motor and cognitive performances: effects of A‐841720, a novel non‐competitive mGluR1 receptor antagonist

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