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Past, present and future of vasopressin and oxytocin receptor oligomers, prototypical GPCR models to study dimerization processes

Current opinion in pharmacology, 2010-02, Vol.10 (1), p.59-66

2010

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Activity of Mambaquaretin toxin on kidney disease via its interaction with vasopressin V2 receptor

Toxicon (Oxford), 2016-06, Vol.116, p.76-76

2016

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CL110 - Le syndrome d’antidiurèse inappropriée néphrogénique (NSIAD) : une pathologie récente et encore méconnue

Archives de pédiatrie : organe officiel de la Société française de pédiatrie, 2010-06, Vol.17 (6), p.30-30

2010

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ATP induces intracellular calcium increases and actin cytoskeleton disaggregation via P2x receptors

Cell calcium (Edinburgh), 2001-05, Vol.29 (5), p.299-309

2001

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Red fluorescent turn-on ligands for imaging and quantifying G protein-coupled receptors in live cells

Chembiochem : a European journal of chemical biology, 2014, Vol.15, p.359-363

2014

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Structure-activity relationship studies on cholecystokinin: analogues with partial agonist activity

American journal of physiology: Gastrointestinal and liver physiology, 1988-02, Vol.254 (2 Pt 1), p.G176-G182

1988

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Characterization of a G Protein-activated Phosphoinositide 3-Kinase in Vascular Smooth Muscle Cell Nuclei

The Journal of biological chemistry, 2001-06, Vol.276 (25), p.22170-22176

2001

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Design and synthesis of cyclic and linear peptide-agarose tools for baiting interacting protein partners of GPCRs

Bioorganic & medicinal chemistry letters, 2006-02, Vol.16 (3), p.521-524

2006

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Characterization of the regulatory domain of gizzard calponin. Interactions of the 145-163 region with F-actin, calcium-binding proteins, and tropomyosin

The Journal of biological chemistry, 1995-04, Vol.270 (15), p.8867-8876

1995

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Peptide and pseudopeptide analogues of cholecystokinin, chemical modifications of the Met28-Gly29 region

Tetrahedron, 1988, Vol.44 (14), p.4415-4430

1988

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Use of Glycolamidic Ester Link. (G.E.L.) for the Preparation of Protected Peptides

Protein and peptide letters, 1995-08, Vol.2 (1), p.287-290

1995

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A pseudopeptide that is a potent cholecystokinin agonist in the peripheral system is able to inhibit the dopamine-like effects of cholecystokinin in the striatum

The Journal of biological chemistry, 1988-08, Vol.263 (22), p.10641-10645

1988

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External pancreatic secretion in the rat: Supramaximal inhibition induced by the cholecystokinin octapeptide [CCK(26–33)] and analogs altered on the 28–29 bond

Peptides (New York, N.Y. : 1980), 1989, Vol.10 (5), p.1041-1047

1989

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SYNTHESIS OF PSEUDO-PEPTIDE AND PEPTIDE ANALOGUES OF THE C-TERMINAL HEPTAPEPTIDE OF CHOLECYSTOKININ AND PRELIMINARY RESULTS ON THEIR IN VITRO ACTIVITY ON RAT PANCREATIC ACINI

Porto Carras, Chalkidiki, Greece, Aug. 31–Sept. 5, 1986, 2019, Vol.19., p.455-458

2019

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Synthesis of an endothelin cyclic analogue using an original multidimensional protection scheme

Tetrahedron letters, 1994-07, Vol.35 (30)

1994

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Synthetic Rat V1a Vasopressin Receptor Fragments Interfere with Vasopressin Binding via Specific Interaction with the Receptor

The Journal of biological chemistry, 1997-08, Vol.272 (34), p.21027-21036

1997

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Endothelin receptor synthetic N-terminal fragment interacts with the receptor itself

Peptides (New York, N.Y. : 1980), 1996, Vol.17 (3), p.521-526

1996

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Continuous flow synthesis of a biologically active small protein and a large peptide

Tetrahedron letters, 1992-07, Vol.33 (28), p.4005-4008

1992

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Endothelin 1: conformation and aggregation

Peptide research, 1992-03, Vol.5 (2), p.97

1992

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Synthesis and biological activities of pseudopeptide analogs of the C-terminal heptapeptide of cholecystokinin. On the importance of the peptide bonds

Journal of medicinal chemistry, 1987-08, Vol.30 (8), p.1366-1373

1987

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Pharmacological activity of cholecystokinin analogues modified in the Met 28-Gly 29 region

European journal of pharmacology, 1990-09, Vol.186 (2), p.213-222

1990

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Peptide and pseudopeptide analogues of cholecystokinin, chemical modifications of the met 28-gly 29 region

Tetrahedron, 1988, Vol.44 (14), p.4415-4430

1988

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Continuous flow synthesis of peptides using a polyacrylamide gel resin (Expansin™)

International Journal of Peptide and Protein Research, 1992-03, Vol.39 (3), p.278-284

1992

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Synthesis and biological activity of some partially modified retro-inverso analogs of cholecystokinin

Journal of medicinal chemistry, 1989-10, Vol.32 (10), p.2331-2339

1989

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Pharmacological activity of cholecystokinin analogues modified in the Met28-Gly29 region

European journal of pharmacology, 1990-09, Vol.186 (2-3), p.213-222

1990

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Past, present and future of vasopressin and oxytocin receptor oligomers, prototypical GPCR models to study dimerization processes

Activity of Mambaquaretin toxin on kidney disease via its interaction with vasopressin V2 receptor

CL110 - Le syndrome d’antidiurèse inappropriée néphrogénique (NSIAD) : une pathologie récente et encore méconnue

ATP induces intracellular calcium increases and actin cytoskeleton disaggregation via P2x receptors

Red fluorescent turn-on ligands for imaging and quantifying G protein-coupled receptors in live cells

Structure-activity relationship studies on cholecystokinin: analogues with partial agonist activity

Characterization of a G Protein-activated Phosphoinositide 3-Kinase in Vascular Smooth Muscle Cell Nuclei

Design and synthesis of cyclic and linear peptide-agarose tools for baiting interacting protein partners of GPCRs

Characterization of the regulatory domain of gizzard calponin. Interactions of the 145-163 region with F-actin, calcium-binding proteins, and tropomyosin

Peptide and pseudopeptide analogues of cholecystokinin, chemical modifications of the Met28-Gly29 region

Use of Glycolamidic Ester Link. (G.E.L.) for the Preparation of Protected Peptides

A pseudopeptide that is a potent cholecystokinin agonist in the peripheral system is able to inhibit the dopamine-like effects of cholecystokinin in the striatum

External pancreatic secretion in the rat: Supramaximal inhibition induced by the cholecystokinin octapeptide [CCK(26–33)] and analogs altered on the 28–29 bond

SYNTHESIS OF PSEUDO-PEPTIDE AND PEPTIDE ANALOGUES OF THE C-TERMINAL HEPTAPEPTIDE OF CHOLECYSTOKININ AND PRELIMINARY RESULTS ON THEIR IN VITRO ACTIVITY ON RAT PANCREATIC ACINI

Synthesis of an endothelin cyclic analogue using an original multidimensional protection scheme

Synthetic Rat V1a Vasopressin Receptor Fragments Interfere with Vasopressin Binding via Specific Interaction with the Receptor

Endothelin receptor synthetic N-terminal fragment interacts with the receptor itself

Continuous flow synthesis of a biologically active small protein and a large peptide

Endothelin 1: conformation and aggregation

Synthesis and biological activities of pseudopeptide analogs of the C-terminal heptapeptide of cholecystokinin. On the importance of the peptide bonds

Pharmacological activity of cholecystokinin analogues modified in the Met 28-Gly 29 region

Peptide and pseudopeptide analogues of cholecystokinin, chemical modifications of the met 28-gly 29 region

Continuous flow synthesis of peptides using a polyacrylamide gel resin (Expansin™)

Synthesis and biological activity of some partially modified retro-inverso analogs of cholecystokinin

Pharmacological activity of cholecystokinin analogues modified in the Met28-Gly29 region

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