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http://hub.abes.fr/acs/periodical/jacsat/2008/volume_130/issue_31/101021ja0765520/authorship/6
http://hub.abes.fr/acs/periodical/jmcmar/2007/volume_50/issue_14/101021jm0700971/authorship/1
http://hub.abes.fr/acs/periodical/jmcmar/2007/volume_50/issue_13/101021jm0614782/authorship/6
http://hub.abes.fr/acs/periodical/jmcmar/2005/volume_48/issue_26/101021jm050911p/authorship/1
http://hub.abes.fr/oup/periodical/proeng/2003/volume_16/issue_12/101093proteingzg117/authorship/3
http://hub.abes.fr/oup/periodical/ndt/2009/volume_24/issue_1/101093ndtgfn454/authorship/5
http://hub.abes.fr/acs/periodical/jmcmar/2002/volume_45/issue_15/101021jm0109762/authorship/2
http://hub.abes.fr/acs/periodical/jmcmar/2005/volume_48/issue_8/101021jm0493562/authorship/3
http://hub.abes.fr/acs/periodical/jacsat/2008/volume_130/issue_15/101021ja077620l/authorship/8
http://hub.abes.fr/acs/periodical/jmcmar/1998/volume_41/issue_17/101021jm980147p/authorship/7
http://hub.abes.fr/acs/periodical/jmcmar/2004/volume_47/issue_22/101021jm049914c/authorship/1
http://hub.abes.fr/acs/periodical/jmcmar/2006/volume_49/issue_18/101021jm060485n/authorship/3
http://hub.abes.fr/acs/periodical/jmcmar/2007/volume_50/issue_6/101021jm060903o/authorship/7
http://hub.abes.fr/acs/periodical/jmcmar/2008/volume_51/issue_24/101021jm801142b/authorship/11
http://hub.abes.fr/acs/periodical/jmcmar/2008/volume_51/issue_10/101021jm800044k/authorship/1
http://hub.abes.fr/acs/periodical/jmcmar/2008/volume_51/issue_3/101021jm7012425/authorship/6
http://hub.abes.fr/acs/periodical/jmcmar/2000/volume_43/issue_2/101021jm9911231/authorship/4
http://hub.abes.fr/acs/periodical/jmcmar/2006/volume_49/issue_13/101021jm060247s/authorship/5
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Architecture of P2Y Nucleotide Receptors: Structural Comparison Based onSequence Analysis, Mutagenesis, and Homology Modeling
Structure−Activity Relationships of Uridine 5‘-Diphosphate Analogues at the Human P2Y6Receptor
Evaluation of Small-Molecule Modulators of the Luteinizing Hormone/Choriogonadotropin andThyroid Stimulating Hormone Receptors: Structure−Activity Relationships and SelectiveBinding Patterns
Bidirectional, Iterative Approach to the Structural Delineation of the Functional “Chemoprint”in GPR40 for Agonist Recognition
N-Cycloalkyl Derivatives of Adenosine and 1-Deazaadenosine as Agonists andPartial Agonists of the A1 Adenosine Receptor
Molecular Modeling of the Human P2Y2 Receptor and Design of a Selective Agonist,2‘-Amino-2‘-deoxy-2-thiouridine 5‘-Triphosphate
Functional properties of subunit interactions in human cytidine deaminase
Discovery of Novel Agonists and Antagonists of the Free Fatty Acid Receptor 1 (FFAR1) Using Virtual Screening
Combined treatment with renin-angiotensin system blockers and polyunsaturated fatty acids in proteinuric IgA nephropathy: a randomized controlled trial
P2Y1 Antagonists: Combining Receptor-Based Modeling and QSAR for a QuantitativePrediction of the Biological Activity Based on Consensus Scoring
N6-Alkyl-2-alkynyl Derivatives of Adenosine as Potent and Selective Agonists atthe Human Adenosine A3 Receptor and a Starting Point for Searching A2BLigands
A Virtual Screen for Diverse Ligands: Discovery of Selective G Protein-Coupled Receptor Antagonists
Atomistic Insights into Rhodopsin Activation from a Dynamic Model
Human P2Y6 Receptor: MolecularModeling Leads to the Rational Design ofa Novel Agonist Based on a UniqueConformational Preference
On the Applicability of GPCR Homology Models to Computer-Aided Drug Discovery: A Comparison between In Silico and Crystal Structures of the β2-Adrenergic Receptor
Effects of 5‘-Phosphate Derivatives of2-Hexynyl Adenosine and2-Phenylethynyl Adenosine on Responsesof Human Platelets Mediated by P2YReceptors
Synthesis and Biological Activity of a New Series of N6-Arylcarbamoyl,2-(Ar)alkynyl-N6-arylcarbamoyl, and N6-Carboxamido Derivatives ofAdenosine-5‘-N-ethyluronamide as A1 and A3 Adenosine Receptor Agonists
Examining the Chirality, Conformation and Selective Kinase Inhibition of 3-((3R,4R)-4-methyl-3-(methyl(7H-pyrrolo[2,3-d]pyrimidin-4-yl)amino)piperidin-1-yl)-3-oxopropanenitrile (CP-690,550)
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