17 results on '"Gijsen H"'
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2. BACE inhibitor treatment of mice induces hyperactivity in a Seizure-related gene 6 family dependent manner without altering learning and memory.
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3. The interrelationship between bone and fat: from cellular see-saw to endocrine reciprocity.
4. A Canine Model to Evaluate Efficacy and Safety of [gamma]-Secretase Inhibitors and Modulators.
5. Activation of the cannabinoid 2 (CB2) receptor inhibits murine mesenteric afferent nerve activity.
6. ChemInform Abstract: Evaluation of Furan Photooxygenation as a Device for Construction of the Zaragozic Acid (Squalestatin) Core.
7. ChemInform Abstract: Recent Advances in the Chemoenzymatic Synthesis of Carbohydrates and Carbohydrate Mimetics.
8. ChemInform Abstract: Synthesis of a Cyclitol via a Tandem Enzymatic Aldol - Intramolecular Horner-Wadsworth-Emmons Reaction.
9. ChemInform Abstract: Sequential Three- and Four-Substrate Aldol Reactions Catalyzed by Aldolases.
10. ChemInform Abstract: Structure, Occurrence, Biosynthesis, Biological Activity, Synthesis, and Chemistry of Aromadendrane Sesquiterpenoids.
11. ChemInform Abstract: Sequential One-Pot Aldol Reactions Catalyzed by 2-Deoxyribose-5- phosphate Aldolase and Fructose-1,6-diphosphate Aldolase.
12. ChemInform Abstract: Unprecedented Asymmetric Aldol Reactions with Three Aldehyde Substrates Catalyzed by 2-Deoxyribose-5-phosphate Aldolase.
13. ChemInform Abstract: Thermal Rearrangement of Bicyclogermacrane-1,8-dione (III). Synthesis of Humulenedione (V) and (-)-Cubenol (XI), Starting from Natural (+)- Aromadendrene (I). Part 5.
14. ChemInform Abstract: Rearrangement Reactions of Aromadendrane Derivatives. Synthesis of (+)- Maaliol (X), Starting from Natural (+)-Aromadendrene (I). Part 4.
15. ChemInform Abstract: Synthesis of Mono- and Dihydroxy Aromadendrane Sesquiterpenes, Starting from Natural (+)-Aromadendrene. Part 3.
16. ChemInform Abstract: The Synthesis of (-)-Kessane, Starting from Natural (+)-Aromadendrene. Part 2.
17. ChemInform Abstract: The Conversion of Natural (+)-Aromadendrene into Chiral Synthons.
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