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Lubben Thomas H.
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http://hub.abes.fr/acs/periodical/bichaw/1991/volume_30/issue_40/101021bi00104a021/authorship/4
http://hub.abes.fr/acs/periodical/jmcmar/2006/volume_49/issue_21/101021jm060777o/authorship/17
http://hub.abes.fr/acs/periodical/jmcmar/2006/volume_49/issue_22/101021jm060955d/authorship/7
http://hub.abes.fr/acs/periodical/jmcmar/2003/volume_46/issue_20/101021jm034122o/authorship/8
http://hub.abes.fr/acs/periodical/jmcmar/2006/volume_49/issue_12/101021jm051283e/authorship/6
http://hub.abes.fr/acs/periodical/jmcmar/2003/volume_46/issue_16/101021jm034088d/authorship/12
http://hub.abes.fr/acs/periodical/jmcmar/2006/volume_49/issue_12/101021jm060199b/authorship/15
http://hub.abes.fr/acs/periodical/jmcmar/2006/volume_49/issue_17/101021jm060818g/authorship/6
http://hub.abes.fr/acs/periodical/jmcmar/2007/volume_50/issue_8/101021jm061436d/authorship/9
http://hub.abes.fr/acs/periodical/bichaw/2006/volume_45/issue_24/101021bi060184f/authorship/10
http://hub.abes.fr/acs/periodical/jacsat/2003/volume_125/issue_14/101021ja0296733/authorship/7
http://hub.abes.fr/acs/periodical/bichaw/1990/volume_29/issue_24/101021bi00476a003/authorship/2
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Chaperonin-facilitated refolding of ribulose bisphosphate carboxylase and ATP hydrolysis by chaperonin 60 (groEL) are potassium dependent
Discovery of ((4R,5S)-5-Amino-4-(2,4,5-trifluorophenyl)cyclohex-1-enyl)-(3-(trifluoromethyl)-5,6-dihydro-[1,2,4]triazolo[4,3-a]pyrazin-7(8H)-yl)methanone(ABT-341), a Highly Potent, Selective, OrallyEfficacious, and Safe Dipeptidyl Peptidase IVInhibitor for the Treatment of Type 2 Diabetes
Discovery of a Potent, Selective Protein TyrosinePhosphatase 1B Inhibitor Using a Linked-Fragment Strategy
Fragment Screening and Assembly: AHighly Efficient Approach to a Selectiveand Cell Active Protein TyrosinePhosphatase 1B Inhibitor
Discovery, Structure−Activity Relationship, and Pharmacological Evaluation of(5-Substituted-pyrrolidinyl-2-carbonyl)-2-cyanopyrrolidines as Potent Dipeptidyl Peptidase IVInhibitors
Crystal Structures of DPP-IV (CD26) from Rat Kidney Exhibit FlexibleAccommodation of Peptidase-Selective Inhibitors
Aminopyridine-Based c-Jun N-Terminal Kinase Inhibitors with Cellular Activity and MinimalCross-Kinase Activity
Discovery of 2-[4-{{2-(2S,5R)-2-Cyano-5-ethynyl-1-pyrrolidinyl]-2-oxoethyl]amino]-4-methyl-1-piperidinyl]-4-pyridinecarboxylic Acid (ABT-279): A Very Potent, Selective,Effective, and Well-Tolerated Inhibitor of Dipeptidyl Peptidase-IV, Useful for the Treatment ofDiabetes
Discovery, Structure−Activity Relationship, and Pharmacological Evaluation of (5-Substituted-pyrrolidinyl-2-carbonyl)-2-cyanopyrrolidines as Potent Dipeptidyl Peptidase IV Inhibitors.
Discovery and Structure−Activity Relationships of Piperidinone- and Piperidine-ConstrainedPhenethylamines as Novel, Potent, and Selective Dipeptidyl Peptidase IV Inhibitors
Selective Protein Tyrosine Phosphatase1B Inhibitors: Targeting the SecondPhosphotyrosine Binding Site withNon-Carboxylic Acid-Containing Ligands
Complex interactions between the chaperonin 60 molecular chaperone and dihydrofolate reductase
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