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Chessari Gianni
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http://hub.abes.fr/oup/periodical/nar/2003/volume_31/issue_5/101093nargkg237/authorship/2
http://hub.abes.fr/acs/periodical/jmcmar/2003/volume_46/issue_21/101021jm0308693/authorship/3
http://hub.abes.fr/acs/periodical/joceah/2000/volume_65/issue_17/101021jo0002036/authorship/3
http://hub.abes.fr/acs/periodical/jmcmar/2007/volume_50/issue_6/101021jm0611962/authorship/3
http://hub.abes.fr/acs/periodical/jacsat/2001/volume_123/issue_48/101021ja011311s/authorship/1
http://hub.abes.fr/acs/periodical/jmcmar/2007/volume_50/issue_4/101021jm061277y/authorship/3
http://hub.abes.fr/acs/periodical/jmcmar/2007/volume_50/issue_6/101021jm061197u/authorship/7
http://hub.abes.fr/acs/periodical/jmcmar/2008/volume_51/issue_13/101021jm8000373/authorship/2
http://hub.abes.fr/acs/periodical/jmcmar/2006/volume_49/issue_4/101021jm050850v/authorship/4
http://hub.abes.fr/acs/periodical/jmcmar/2007/volume_50/issue_24/101021jm070829p/authorship/9
http://hub.abes.fr/acs/periodical/jmcmar/2008/volume_51/issue_2/101021jm701359z/authorship/3
http://hub.abes.fr/acs/periodical/jmcmar/2005/volume_48/issue_20/101021jm050543p/authorship/2
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Modeling Water Molecules in Protein−Ligand Docking Using GOLD
Singly Bridged Calix[8]crowns
Sequence-specific minor groove binding by bis-benzimidazoles: water molecules in ligand recognition
Application of Fragment Screening and Fragment Linking to the Discovery of Novel ThrombinInhibitors
Application of Fragment-Based Lead Generation to the Discovery of Novel, Cyclic Amidineβ-Secretase Inhibitors with Nanomolar Potency, Cellular Activity, and High Ligand Efficiency
Application of Fragment Screening by X-ray Crystallography to β-Secretase
Trisubstituted Acridine Derivatives as Potent and Selective TelomeraseInhibitors
Application of Fragment Screening by X-ray Crystallography to the Discovery ofAminopyridines as Inhibitors of β-Secretase
Recent Developments in Fragment-Based Drug Discovery
Detection of Localized Water Clusters in a ChargedPeptidyl Resin
Diverse, High-Quality Test Set for the Validation of Protein−Ligand Docking Performance
Fragment-Based Discovery of Mexiletine Derivatives as Orally Bioavailable Inhibitors of Urokinase-Type Plasminogen Activator
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