18 results on '"Bowers Albert"'
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2. Inter-Modular Linkers play a crucial role in governing the biosynthesis of non-ribosomal peptides.
3. Dehydroamino acids: chemical multi-tools for late-stage diversification.
4. Large-Scale Bioinformatics Analysis of Bacillus Genomes Uncovers Conserved Roles of Natural Products in Bacterial Physiology.
5. VprBP/DCAF1 Regulates the Degradation and Nonproteolytic Activation of the Cell Cycle Transcription Factor FoxM1.
6. Enzymatic Basis of 'Hybridity' in Thiomarinol Biosynthesis.
7. Enzymatic Basis of 'Hybridity' in Thiomarinol Biosynthesis.
8. Thiopeptide antibiotics stimulate biofilm formation in Bacillus subtilis.
9. Dithiolopyrrolones: biosynthesis, synthesis, and activity of a unique class of disulfide-containing antibiotics.
10. The genome-wide distribution of non-B DNA motifs is shaped by operon structure and suggests the transcriptional importance of non-B DNA structures in Escherichia coli.
11. A Backup Plan for Self-Protection: S-Methylation of Holomycin Biosynthetic Intermediates in Streptomyces clavuligerus.
12. LETTERS.
13. Correction: Dithiolopyrrolones: biosynthesis, synthesis, and activity of a unique class of disulfide-containing antibiotics.
14. ChemInform Abstract: Biochemical and Biosynthetic Preparation of Natural Product Like Cyclic Peptide Libraries.
15. ChemInform Abstract: Discovery, Biological Activity, Synthesis and Potential Therapeutic Utility of Naturally Occurring Histone Deacetylase Inhibitors.
16. ChemInform Abstract: One-Pot Syntheses of Dissymmetric Diamides Based on the Chemistry of Cyclic Monothioanhydrides. Scope and Limitations and Application to the Synthesis of Glycodipeptides.
17. ChemInform Abstract: Cyclic Thioanhydrides: Linchpins for Multicomponent Coupling Reactions Based on the Reaction of Thioacids with Electron-Deficient Sulfonamides and Azides.
18. 4,6-O-[1-Cyano-2-(2-iodophenyl)ethylidene] Acetals. Improved Second-Generation Acetals for the Stereoselective Formation of β-D-Mannopyranosides and Regioselective Reductive Radical Fragmentation to β-D-Rhamnopyranosides. Scope and Limitations.
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