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Potent and Long-Acting Corticotropin Releasing Factor (CRF) Receptor 2 Selective Peptide Competitive Antagonists

Journal of medicinal chemistry, 2002-10, Vol.45 (21), p.4737-4747

2002

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Phosphorylation of CREB at Ser-133 induces complex formation with CREB-binding protein via a direct mechanism

Molecular and Cellular Biology, 1996-02, Vol.16 (2), p.694-703

1996

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Costs of Incidence-Based Central Retinal Vein Occlusion in France

Value in health, 2013-11, Vol.16 (7), p.A504-A504

2013

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First-principle calculations of dark matter scattering off light nuclei

Physical review. C, 2017-09, Vol.96 (3), Article 035805

2017

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Identification of a Functional Binding Site for Activin on the Type I Receptor ALK4

The Journal of biological chemistry, 2003-06, Vol.278 (23), p.21129-21135

2003

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Potent, Structurally Constrained Agonists and Competitive Antagonists of Corticotropin-Releasing Factor

Proceedings of the National Academy of Sciences - PNAS, 1995-11, Vol.92 (23), p.10575-10579

1995

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Expression, Purification, and Characterization of a Soluble Form of the First Extracellular Domain of the Human Type 1 Corticotropin Releasing Factor Receptor

The Journal of biological chemistry, 2001-08, Vol.276 (34), p.31528-31534

2001

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PUK23 The Care Pathway for an Adult Patient with Type 2 Diabetes Suffering from Chronic Kidney Disease (CKD) in France

Value in health, 2020-12, Vol.23, p.S754-S755

2020

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Sampling general N-body interactions with auxiliary fields

Europhysics letters, 2017-09, Vol.119 (6), p.60006

2017

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Potent Somatostatin Undecapeptide Agonists Selective for Somatostatin Receptor 1 (sst1)

Journal of medicinal chemistry, 2001-06, Vol.44 (13), p.2238-2246

2001

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Surface potentials of magnetron sputtered transparent conducting oxides

Thin solid films, 2009-12, Vol.518 (4), p.1197-1203

2009

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Electronic structure of In2O3 and Sn-doped In2O3 by hard x-ray photoemission spectroscopy

Physical review. B, Condensed matter and materials physics, 2010-04, Vol.81 (16)

2010

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Nature of the band gap of In2O3 revealed by first-principles calculations and x-ray spectroscopy

Physical review letters, 2008-04, Vol.100 (16), p.167402-167402

2008

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Consensus Bioactive Conformation of Cyclic GnRH Antagonists Defined by NMR and Molecular Modeling

Journal of medicinal chemistry, 2000-03, Vol.43 (5), p.819-828

2000

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Somatostatin Receptor 1 Selective Analogues: 4. Three-Dimensional Consensus Structure by NMR

Journal of medicinal chemistry, 2005-01, Vol.48 (2), p.523-533

2005

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PSS5 COMPARING TWO TREAT-AND-EXTEND ANTI-VEGF REGIMENS FOR MANAGING WET AGE-RELATED MACULAR DEGENERATION - IMPLICATIONS FOR THE NATIONAL HEALTH SYSTEM IN FRANCE

Value in health, 2019-11, Vol.22, p.S886-S886

2019

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Constrained Corticotropin-Releasing Factor Antagonists with i-(i + 3) Glu−Lys Bridges

Journal of medicinal chemistry, 1997-10, Vol.40 (22), p.3651-3658

1997

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Novel sst2-Selective Somatostatin Agonists. Three-Dimensional Consensus Structure by NMR

Journal of medicinal chemistry, 2006-07, Vol.49 (15), p.4487-4496

2006

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Surface energy controlled preferential orientation of thin films

Journal of physics. D, Applied physics, 2010-02, Vol.43 (5), p.055301

2010

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Design of Monocyclic (1−3) and Dicyclic (1−3/4−10) Gonadotropin Releasing Hormone (GnRH) Antagonists

Journal of medicinal chemistry, 2000-03, Vol.43 (5), p.797-806

2000

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Design of Potent Dicyclic (4−10/5−8) Gonadotropin Releasing Hormone (GnRH) Antagonists

Journal of medicinal chemistry, 2000-03, Vol.43 (5), p.784-796

2000

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Constrained Corticotropin-Releasing Factor (CRF) Agonists and Antagonists with i−(i+3) Glu-Xaa-dXbb-Lys Bridges

Journal of medicinal chemistry, 1998-12, Vol.41 (25), p.5002-5011

1998

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Conformationally Restricted Competitive Antagonists of Human/Rat Corticotropin-Releasing Factor

Journal of medicinal chemistry, 1994-05, Vol.37 (10), p.1450-1459

1994

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Design of Potent Dicyclic (1−5/4−10) Gonadotropin Releasing Hormone (GnRH) Antagonists

Journal of medicinal chemistry, 2000-03, Vol.43 (5), p.807-818

2000

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Human Growth Hormone-Releasing Hormone hGHRH(1−29)-NH2: Systematic Structure−Activity Relationship Studies

Journal of medicinal chemistry, 1998-02, Vol.41 (5), p.717-727

1998

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