Found: 15
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Presenilin is the molecular target of both acidic and non-acidic gamma-secretase modulators
- Published in:
- 2012
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- Publication type:
- Abstract
Wirkstoffe nach Zahlen: reaktionsbasierter De-novo-Entwurf von potenten und selektiven Leitstrukturen für die Krebsforschung.
- Published in:
- Angewandte Chemie, 2013, v. 125, n. 17, p. 4774, doi. 10.1002/ange.201206897
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- Publication type:
- Article
From Virtual Screening to Bioactive Compounds by Visualizing and Clustering of Chemical Space.
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- Molecular Informatics, 2012, v. 31, n. 1, p. 21, doi. 10.1002/minf.201100147
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- Publication type:
- Article
Flexible, Heat-Resistant, and Flame-Retardant Glass Fiber Nonwoven/Glass Platelet Composite Separator for Lithium-Ion Batteries.
- Published in:
- Energies (19961073), 2018, v. 11, n. 4, p. 999, doi. 10.3390/en11040999
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- Publication type:
- Article
Functionalization of Fatty Acid Mimetics for Solid-Phase Coupling and Subsequent Target Identification.
- Published in:
- Archiv der Pharmazie, 2010, v. 343, n. 11/12, p. 625, doi. 10.1002/ardp.201000091
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- Publication type:
- Article
DOGS: Reaction-Driven de novo Design of Bioactive Compounds.
- Published in:
- PLoS Computational Biology, 2012, v. 8, n. 2, p. 1, doi. 10.1371/journal.pcbi.1002380
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- Publication type:
- Article
Titelbild: Self-Assembly and Cross-Linking of Bionanoparticles at Liquid–Liquid Interfaces (Angew. Chem. 16/2005).
- Published in:
- Angewandte Chemie, 2005, v. 117, n. 16, p. 2357, doi. 10.1002/ange.200590052
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- Publication type:
- Article
Self-Assembly and Cross-Linking of Bionanoparticles at Liquid–Liquid InterfacesThis work was supported by the DOE (DE-FG-02-96ER45 and DE-FG02-04ER46126), the NSF for MRSEC at UMass Amherst (DMR 9400488), the Army Research Laboratory through the MURI program, the Max Planck Society, the DFG within the French–German Network on Complex Fluids, and the MAX KADE Foundation. This work benefited from Argonne's Advanced Photon Source (15-ID) and Intense Pulsed Neutron Source supported by the US Department of Energy, Basic Energy Sciences, Office of Science, under contract no. W-31-109-Eng-38. ChemMatCARS Sector 15 is principally supported by the National Science Foundation/Department of Energy under grant no. CHE0087817 and by the Illinois Board of Higher Education. Q.W. thanks the University of South Carolina and USC Nanocenter for financial support. A.F. and P.C. thank Helmuth Möhwald for stimulating discussions.
- Published in:
- Angewandte Chemie, 2005, v. 117, n. 16, p. 2472, doi. 10.1002/ange.200462653
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- Publication type:
- Article
Reversible tuning of a block-copolymer nanostructure via electric fields.
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- Nature Materials, 2008, v. 7, n. 2, p. 142, doi. 10.1038/nmat2068
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- Publication type:
- Article
Cover Picture: Self-Assembly and Cross-Linking of Bionanoparticles at Liquid–Liquid Interfaces (Angew. Chem. Int. Ed. 16/2005).
- Published in:
- Angewandte Chemie International Edition, 2005, v. 44, n. 16, p. 2305, doi. 10.1002/anie.200590052
- By:
- Publication type:
- Article
Self-Assembly and Cross-Linking of Bionanoparticles at Liquid–Liquid InterfacesThis work was supported by the DOE (DE-FG-02-96ER45 and DE-FG02-04ER46126), the NSF for MRSEC at UMass Amherst (DMR 9400488), the Army Research Laboratory through the MURI program, the Max Planck Society, the DFG within the French–German Network on Complex Fluids, and the MAX KADE Foundation. This work benefited from Argonne's Advanced Photon Source (15-ID) and Intense Pulsed Neutron Source supported by the US Department of Energy, Basic Energy Sciences, Office of Science, under contract no. W-31-109-Eng-38. ChemMatCARS Sector 15 is principally supported by the National Science Foundation/Department of Energy under grant no. CHE0087817 and by the Illinois Board of Higher Education. Q.W. thanks the University of South Carolina and USC Nanocenter for financial support. A.F. and P.C. thank Helmuth Möhwald for stimulating discussions.
- Published in:
- Angewandte Chemie International Edition, 2005, v. 44, n. 16, p. 2420, doi. 10.1002/anie.200462653
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- Publication type:
- Article
From Molecular Shape to Potent Bioactive Agents II: Fragment-Based de novo Design.
- Published in:
- ChemMedChem, 2009, v. 4, n. 1, p. 45, doi. 10.1002/cmdc.200800314
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- Publication type:
- Article
From Molecular Shape to Potent Bioactive Agents I: Bioisosteric Replacement of Molecular Fragments.
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- ChemMedChem, 2009, v. 4, n. 1, p. 41, doi. 10.1002/cmdc.200800313
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- Publication type:
- Article
The Treatment of Dyslipidemia-What's Left in the Pipeline?
- Published in:
- ChemMedChem, 2008, v. 3, n. 2, p. 206, doi. 10.1002/cmdc.200700165
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- Publication type:
- Article
Drugs by Numbers: Reaction-Driven De Novo Design of Potent and Selective Anticancer Leads.
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- Angewandte Chemie International Edition, 2013, v. 52, n. 17, p. 4676, doi. 10.1002/anie.201206897
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- Publication type:
- Article