18 results on '"Otterbein, Ludovic"'
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2. The Crystal Structure of Uncomplexed Actin in the ADP State
3. In Vitro Validation of Acetyltransferase Activity of GlmU as an Antibacterial Target in Haemophilus influenzae
4. Heterologous production of a laccase from the basidiomycete Pycnoporus cinnabarinus in the dimorphic yeast Yarrowia lipolytica
5. Isolation of a new laccase isoform from the white-rot fungi Pycnoporus cinnabarinus strain ss3
6. Crystal Structures of S100A6 in the Ca 2+-Free and Ca 2+-Bound States : The Calcium Sensor Mechanism of S100 Proteins Revealed at Atomic Resolution
7. From fragments to leads: novel bacterial NAD+-dependent DNA ligase inhibitors
8. Inhibitors of the acetyltransferase domain of N-acetylglucosamine-1-phosphate-uridylyltransferase/glucosamine-1-phosphate-acetyltransferase (GlmU). Part 2: Optimization of physical properties leading to antibacterial aryl sulfonamides
9. Inhibitors of acetyltransferase domain of N-acetylglucosamine-1-phosphate-uridyltransferase/glucosamine-1-phosphate-acetyltransferase (GlmU). Part 1: Hit to lead evaluation of a novel arylsulfonamide series
10. From fragments to leads: novel bacterial NAD + -dependent DNA ligase inhibitors
11. Development of potent, orally active 1-substituted-3,4-dihydro-2-quinolone glycogen phosphorylase inhibitors
12. Novel thienopyrrole glycogen phosphorylase inhibitors: Synthesis, in vitro SAR and crystallographic studies
13. N-(5-Chloro-1,3-benzodioxol-4-yl)-7-[2-(4-methylpiperazin-1-yl)ethoxy]-5- (tetrahydro-2H-pyran-4-yloxy)quinazolin-4-amine, a Novel, Highly Selective, Orally Available, Dual-Specific c-Src/Abl Kinase Inhibitor
14. Crystallization, X-ray characterization and selenomethionine phasing of Mlc1p bound to IQ motifs from myosin V
15. Crystal Structures of S100A6 in the Ca2+-Free and Ca2+-Bound States
16. Isolation of a new laccase isoform from the white-rot fungiPycnoporus cinnabarinusstrain ss3
17. Molecular cloning of the cDNA encoding laccase from Pycnoporus cinnabarinus I-937 and expression in Pichia pastoris
18. N-(5-Chloro-1,3-benzodioxol-4-yl)-7-2-(4-methylpiperazin-1-yl)ethoxy-5- (tetrahydro-2H-pyran-4-yloxy)quinazolin-4-amine, a Novel, Highly Selective, Orally Available, Dual-Specific c-Src/Abl Kinase Inhibitor
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