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Sebti Said M.
Sebti Saïd M.
Sebti Said
Sebti Saïd M.
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Said
Said M.
Saïd M.
Saïd M.
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http://hub.abes.fr/acs/periodical/jmcmar/2004/volume_47/issue_2/101021jm030236o/authorship/12
http://hub.abes.fr/acs/periodical/jmcmar/2008/volume_51/issue_17/101021jm800113p/authorship/8
http://hub.abes.fr/acs/periodical/jacsat/2005/volume_127/issue_29/101021ja050122x/authorship/9
http://hub.abes.fr/acs/periodical/jmcmar/2008/volume_51/issue_16/101021jm8002526/authorship/9
http://hub.abes.fr/acs/periodical/jacsat/2005/volume_127/issue_15/101021ja0446404/authorship/6
http://hub.abes.fr/acs/periodical/jmcmar/2005/volume_48/issue_11/101021jm0491039/authorship/12
http://hub.abes.fr/acs/periodical/jmcmar/2006/volume_49/issue_19/101021jm060081v/authorship/12
http://hub.abes.fr/acs/periodical/jmcmar/2002/volume_45/issue_1/101021jm0103099/authorship/6
http://hub.abes.fr/acs/periodical/bichaw/1995/volume_34/issue_38/101021bi00038a037/authorship/6
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Burkitt Lymphoma Daudi Cells Contain Two Distinct Farnesyltransferases with Different Divalent Cation Requirements
Terphenyl-Based Bak BH3 α-Helical Proteomimetics asLow-Molecular-Weight Antagonists of Bcl-xL
Structurally Simple, Potent, Plasmodium Selective Farnesyltransferase Inhibitors That Arrestthe Growth of Malaria Parasites
Design and Synthesis of Potent Nonpeptidic Farnesyltransferase InhibitorsBased on a Terphenyl Scaffold
Terephthalamide Derivatives as Mimetics of Helical Peptides: Disruption of the Bcl-xL/Bak Interaction
Inhibitors of Src Homology-2 Domain Containing Protein Tyrosine Phosphatase-2 (Shp2) Based on Oxindole Scaffolds
Protein Farnesyltransferase Inhibitors Exhibit Potent Antimalarial Activity
Potent, Plasmodium-Selective Farnesyltransferase Inhibitors That Arrest the Growth of Malaria Parasites: Structure−Activity Relationships of Ethylenediamine-Analogue Scaffolds and Homology Model Validation
Design and Synthesis of Peptidomimetic Protein Farnesyltransferase Inhibitorsas Anti-Trypanosoma brucei Agents
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