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Campiglia Pietro
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http://hub.abes.fr/oup/periodical/cardiovascres/2009/volume_84/issue_3/101093cvrcvp252/authorship/6
http://hub.abes.fr/acs/periodical/jmcmar/2005/volume_48/issue_9/101021jm040867y/authorship/4
http://hub.abes.fr/acs/periodical/jmcmar/2008/volume_51/issue_10/101021jm7013056/authorship/2
http://hub.abes.fr/acs/periodical/jmcmar/2008/volume_51/issue_8/101021jm701604t/authorship/4
http://hub.abes.fr/acs/periodical/jmcmar/2007/volume_50/issue_8/101021jm0612158/authorship/2
http://hub.abes.fr/acs/periodical/jmcmar/2002/volume_45/issue_20/101021jm025549i/authorship/3
http://hub.abes.fr/acs/periodical/jmcmar/2005/volume_48/issue_4/101021jm0408565/authorship/3
http://hub.abes.fr/acs/periodical/jmcmar/2004/volume_47/issue_7/101021jm0309912/authorship/3
http://hub.abes.fr/acs/periodical/jmcmar/2008/volume_51/issue_9/101021jm701181n/authorship/8
http://hub.abes.fr/acs/periodical/jmcmar/2004/volume_47/issue_16/101021jm040837v/authorship/3
http://hub.abes.fr/acs/periodical/jmcmar/2005/volume_48/issue_23/101021jm058043j/authorship/3
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Urotensin-II Receptor Ligands. From Agonist to Antagonist Activity
The G protein coupled receptor kinase 2 plays an essential role in beta-adrenergic receptor-induced insulin resistance
Design and Microwave-Assisted Synthesis of Novel Macrocyclic Peptides Active at Melanocortin Receptors: Discovery of Potent and Selective hMC5R Receptor Antagonists
Synthesis and Cytotoxic Evaluation of Novel Spirohydantoin Derivatives of theDihydrothieno[2,3-b]naphtho-4,9-dione System
Unraveling the Active Conformation of Urotensin II.
A Different Molecular Mechanism Underlying Antimicrobial and Hemolytic Actions of Temporins A and L
Unraveling the Active Conformation of Urotensin II
Design, Synthesis, and Cytotoxic Evaluation of a New Series of 3-SubstitutedSpiro[(dihydropyrazine-2,5-dione)-6,3‘-(2‘,3‘-dihydrothieno[2,3-b]naphtho-4‘,9‘-dione)]Derivatives
A New, Potent Urotensin II ReceptorPeptide Agonist Containing a PenResidue at the Disulfide Bridge
Morphiceptin Analogues Containing a Dipeptide Mimetic Structure: AnInvestigation on the Bioactive Topology at the μ-Receptor
Spiro[(dihydropyrazin-2,5-dione)-6,3′-(2′,3′-dihydrothieno[2,3-b]naphtho-4′,9′-dione)]-Based Cytotoxic Agents: Structure-Activity Relationship Studies on the Substituent at N4-Position of the Diketopiperazine Domain
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