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The novel nonapeptide acein targets angiotensin converting enzyme in the brain and induces dopamine release

British journal of pharmacology, 2016-04, Vol.173 (8), p.1314-1328

2016

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New Trisubstituted 1,2,4-Triazole Derivatives as Potent Ghrelin Receptor Antagonists. 3. Synthesis and Pharmacological in Vitro and in Vivo Evaluations

Journal of medicinal chemistry, 2008-02, Vol.51 (3), p.689-693

2008

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Study of a lipophilic captopril analogue binding to angiotensin I converting enzyme

Journal of peptide science, 2010-02, Vol.16 (2), p.91-97

2010

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Toward Potent Ghrelin Receptor Ligands Based on Trisubstituted 1,2,4-Triazole Structure. 2. Synthesis and Pharmacological in Vitro and in Vivo Evaluations

Journal of medicinal chemistry, 2007-11, Vol.50 (23), p.5790-5806

2007

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Homogeneous time-resolved fluorescence-based assay to screen for ligands targeting the growth hormone secretagogue receptor type 1a

Analytical biochemistry, 2011-01, Vol.408 (2), p.253-262

2011

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Cross-interactions of Two p38 Mitogen-activated Protein (MAP) Kinase Inhibitors and Two Cholecystokinin (CCK) Receptor Antagonists with the CCK1 Receptor and P38 MAP Kinase

The Journal of biological chemistry, 2005-06, Vol.280 (22), p.21384-21393

2005

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Synthesis and Pharmacological in Vitro and in Vivo Evaluations of Novel Triazole Derivatives as Ligands of the Ghrelin Receptor. 1

Journal of medicinal chemistry, 2007-04, Vol.50 (8), p.1939-1957

2007

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Activation of the Ghrelin Receptor is Described by a Privileged Collective Motion: A Model for Constitutive and Agonist-induced Activation of a Sub-class A G-Protein Coupled Receptor (GPCR)

Journal of molecular biology, 2010-01, Vol.395 (4), p.769-784

2010

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Regulation of ERK1/2 activity by ghrelin‐activated growth hormone secretagogue receptor 1A involves a PLC/PKCɛ pathway

British journal of pharmacology, 2006-06, Vol.148 (3), p.350-365

2006

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Involvement of tryptophan W276 and of two surrounding amino acid residues in the high constitutive activity of the ghrelin receptor GHS-R1a

European journal of pharmacology, 2010-09, Vol.643 (2), p.153-161

2010

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New Active Series of Growth Hormone Secretagogues

Journal of medicinal chemistry, 2003-03, Vol.46 (7), p.1191-1203

2003

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C-terminal heptapeptide of gastrin inhibits astrocytomas motility by interacting with a new gastrin binding site

The Journal of pharmacology and experimental therapeutics, 2002-07, Vol.302 (1), p.274

2002

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Trisubstituted 1,2,4-triazoles as ligands for the ghrelin receptor: On the significance of the orientation and substitution at position 3

Bioorganic & medicinal chemistry letters, 2008, Vol.18 (1), p.164-168

2008

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The Third Intracellular Loop of the Rat and Mouse Cholecystokinin-A Receptors Is Responsible for Different Patterns of Gene Activation

Molecular pharmacology, 2000-12, Vol.58 (6), p.1381-1388

2000

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L‐365,260 inhibits in vitro acid secretion by interacting with a PKA pathway

British journal of pharmacology, 1999-05, Vol.127 (1), p.259-267

1999

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Cholecystokinin 1 receptor modulates the MEKK1‐induced c‐Jun trans‐activation: structural requirements of the receptor

British journal of pharmacology, 2006-04, Vol.147 (8), p.951-958

2006

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Common or distinct receptors for gastrin and cholecystokinin in gastric mucosa?

Biochimica et biophysica acta, 1989-03, Vol.1010 (3), p.357-362

1989

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A synthetic glycine-extended bombesin analogue interacts with the GRP/bombesin receptor

European journal of pharmacology, 2000-09, Vol.403 (1), p.17-25

2000

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Are C-terminal octapeptide of cholecystokinin and [Leu 11]gastrin-(5–17) different in stimulating acid secretion in isolated rabbit gastric glands?

European journal of pharmacology, 1995-12, Vol.294 (2), p.511-519

1995

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Involvement of tryptophan W276 and of two surrounding amino acid residues in the high constitutive activity of the ghrelin receptor GHS-R1 a

European journal of pharmacology, 2010, Vol.643 (2-3), p.153-161

2010

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Regulation of ERK1/2 activity by ghrelin‐activated growth hormone secretagogue receptor 1A involves a PLC/PKC ɛ pathway

British journal of pharmacology, 2009-01, Vol.148 (3), p.350-365

2009

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Regulation of ERK1/2 activity by ghrelin-activated growth hormone secretagogue receptor 1A involves a PLC/PKCvarepsilon pathway

British journal of pharmacology, 2006-06, Vol.148 (3), p.350-365

2006

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Regulation of ERK1/2 activity by ghrelin-activated growth hormone secretagogue receptor 1A involves a PLC/PKC[varepsilon] pathway

British journal of pharmacology, 2006-06, Vol.148 (3), p.350

2006

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Cholecystokinin 1 receptor modulates the MEKK1-induced c-Jun trans-activation: structural requirements of the receptor

British journal of pharmacology, 2006-04, Vol.147 (8), p.951-8

2006

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Regulation of ERK1/2 activity by ghrelin-activated growth hormone secretagogue receptor 1Α involves a PLC/PKCε pathway

British journal of pharmacology, 2006, Vol.148 (3), p.350-365

2006

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The novel nonapeptide acein targets angiotensin converting enzyme in the brain and induces dopamine release

New Trisubstituted 1,2,4-Triazole Derivatives as Potent Ghrelin Receptor Antagonists. 3. Synthesis and Pharmacological in Vitro and in Vivo Evaluations

Study of a lipophilic captopril analogue binding to angiotensin I converting enzyme

Toward Potent Ghrelin Receptor Ligands Based on Trisubstituted 1,2,4-Triazole Structure. 2. Synthesis and Pharmacological in Vitro and in Vivo Evaluations

Homogeneous time-resolved fluorescence-based assay to screen for ligands targeting the growth hormone secretagogue receptor type 1a

Cross-interactions of Two p38 Mitogen-activated Protein (MAP) Kinase Inhibitors and Two Cholecystokinin (CCK) Receptor Antagonists with the CCK1 Receptor and P38 MAP Kinase

Synthesis and Pharmacological in Vitro and in Vivo Evaluations of Novel Triazole Derivatives as Ligands of the Ghrelin Receptor. 1

Activation of the Ghrelin Receptor is Described by a Privileged Collective Motion: A Model for Constitutive and Agonist-induced Activation of a Sub-class A G-Protein Coupled Receptor (GPCR)

Regulation of ERK1/2 activity by ghrelin‐activated growth hormone secretagogue receptor 1A involves a PLC/PKCɛ pathway

Involvement of tryptophan W276 and of two surrounding amino acid residues in the high constitutive activity of the ghrelin receptor GHS-R1a

New Active Series of Growth Hormone Secretagogues

C-terminal heptapeptide of gastrin inhibits astrocytomas motility by interacting with a new gastrin binding site

Trisubstituted 1,2,4-triazoles as ligands for the ghrelin receptor: On the significance of the orientation and substitution at position 3

The Third Intracellular Loop of the Rat and Mouse Cholecystokinin-A Receptors Is Responsible for Different Patterns of Gene Activation

L‐365,260 inhibits in vitro acid secretion by interacting with a PKA pathway

Cholecystokinin 1 receptor modulates the MEKK1‐induced c‐Jun trans‐activation: structural requirements of the receptor

Common or distinct receptors for gastrin and cholecystokinin in gastric mucosa?

A synthetic glycine-extended bombesin analogue interacts with the GRP/bombesin receptor

Are C-terminal octapeptide of cholecystokinin and [Leu 11]gastrin-(5–17) different in stimulating acid secretion in isolated rabbit gastric glands?

Involvement of tryptophan W276 and of two surrounding amino acid residues in the high constitutive activity of the ghrelin receptor GHS-R1 a

Regulation of ERK1/2 activity by ghrelin‐activated growth hormone secretagogue receptor 1A involves a PLC/PKC ɛ pathway

Regulation of ERK1/2 activity by ghrelin-activated growth hormone secretagogue receptor 1A involves a PLC/PKCvarepsilon pathway

Regulation of ERK1/2 activity by ghrelin-activated growth hormone secretagogue receptor 1A involves a PLC/PKC[varepsilon] pathway

Cholecystokinin 1 receptor modulates the MEKK1-induced c-Jun trans-activation: structural requirements of the receptor

Regulation of ERK1/2 activity by ghrelin-activated growth hormone secretagogue receptor 1Α involves a PLC/PKCε pathway

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