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Impact of Apolipoprotein E (ApoE) Polymorphism on Brain ApoE Levels

The Journal of neuroscience, 2008-11, Vol.28 (45), p.11445-11453

2008

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Bilayer Kitaev models: Phase diagrams and novel phases

Physical review. B, 2018-10, Vol.98 (15), Article 155101

2018

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P55 - Characterization of in vivo disposition of CTI-1601: A mitochondria targeted therapy for friedreich’s ataxia

Drug metabolism and pharmacokinetics, 2020, Vol.35 (1), p.S38-S38

2020

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Enhanced clearance of Aβ in brain by sustaining the plasmin proteolysis cascade

Proceedings of the National Academy of Sciences - PNAS, 2008-06, Vol.105 (25), p.8754-8759

2008

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Series expansion studies of the J 1 − J 2 Heisenberg bilayer

Physical review. B, 2023-09, Vol.108 (11), Article 115131

2023

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Two-triplon excitations of the Kitaev-Heisenberg bilayer

Physical review. B, 2021-09, Vol.104 (11), p.1, Article 115123

2021

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Tool support for implementing a methodology in magnet development projects at CERN

Proceedings of the Design Society, 2024, Vol.4, p.2615-2624

2024

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Successfully Navigating Food and Drug Administration Orphan Drug and Rare Pediatric Disease Designations for AAV9-hPCCA Gene Therapy: The National Institutes of Health Platform Vector Gene Therapy Experience

Human gene therapy, 2023-03, Vol.34 (5-6), p.217

2023

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Design and Synthesis of 5,5′-Disubstituted Aminohydantoins as Potent and Selective Human β-Secretase (BACE1) Inhibitors

Journal of medicinal chemistry, 2010-02, Vol.53 (3), p.1146-1158

2010

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Die kompetenzorientierte Klassenarbeit. Neue Aufgabenformate zur Messung von kommunikativen Fertigkeiten

Der fremdsprachliche Unterricht. Französisch, 2010, Vol.44 (104), p.14-21

2010

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Kompetenzorientierte Leistungsmessung im Französischunterricht. Neue Aufgabenformate bei der Messung von Schülerkompetenzen in Klassenarbeiten

Französisch heute, 2010, Vol.41 (2), p.62-72

2010

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Aminoimidazoles as Potent and Selective Human β-Secretase (BACE1) Inhibitors

Journal of medicinal chemistry, 2009-10, Vol.52 (20), p.6314-6323

2009

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Begacestat (GSI-953): a novel, selective thiophene sulfonamide inhibitor of amyloid precursor protein gamma-secretase for the treatment of Alzheimer's disease

The Journal of pharmacology and experimental therapeutics, 2009-11, Vol.331 (2), p.598

2009

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Bilayer Kitaev models: Phase diagrams and novel phases

Physical review. B, 2018-10, Vol.98 (15), p.155101

2018

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Design and synthesis of aminohydantoins as potent and selective human β-secretase (BACE1) inhibitors with enhanced brain permeability

Bioorganic & medicinal chemistry letters, 2010-11, Vol.20 (22), p.6597-6605

2010

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Regional oral absorption, hepatic first-pass effect, and non-linear disposition of salmon calcitonin in beagle dogs

European journal of pharmaceutics and biopharmaceutics, 2000-09, Vol.50 (2), p.205-211

2000

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Discovery of Begacestat, a Notch-1-Sparing γ-Secretase Inhibitor for the Treatment of Alzheimer’s Disease

Journal of medicinal chemistry, 2008-12, Vol.51 (23), p.7348-7351

2008

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Di-substituted pyridinyl aminohydantoins as potent and highly selective human β-secretase (BACE1) inhibitors

Bioorganic & medicinal chemistry, 2010-01, Vol.18 (2), p.630-639

2010

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Acylguanidines as Small-Molecule β-Secretase Inhibitors

Journal of medicinal chemistry, 2006-10, Vol.49 (21), p.6158-6161

2006

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Utility of Pharmacodynamic Measures for Assessing the Oral Bioavailability of Peptides. 1. Administration of Recombinant Salmon Calcitonin in Rats

Journal of pharmaceutical sciences, 1995-11, Vol.84 (11), p.1374-1378

1995

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Thiophene substituted acylguanidines as BACE1 inhibitors

Bioorganic & medicinal chemistry letters, 2007-10, Vol.17 (19), p.5353-5356

2007

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"The Lonely Romantic": Nature, Education, and Cultural Pessimism in the Early Works of Hermann Hesse

Wagner, Erik Paul

2015

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Discovery and initial optimization of 5,5′-disubstituted aminohydantoins as potent β-secretase (BACE1) inhibitors

Bioorganic & medicinal chemistry letters, 2010-01, Vol.20 (2), p.632-635

2010

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Acylguanidine inhibitors of β-secretase: Optimization of the pyrrole ring substituents extending into the S 1 ′ substrate binding pocket

Bioorganic & medicinal chemistry letters, 2008-01, Vol.18 (2), p.767-771

2008

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Acylguanidine inhibitors of β-secretase : Optimization of the pyrrole ring substituents extending into the S'1 substrate binding pocket

Bioorganic & medicinal chemistry letters, 2008-01, Vol.18 (2), p.767-771

2008

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Impact of Apolipoprotein E (ApoE) Polymorphism on Brain ApoE Levels

Bilayer Kitaev models: Phase diagrams and novel phases

P55 - Characterization of in vivo disposition of CTI-1601: A mitochondria targeted therapy for friedreich’s ataxia

Enhanced clearance of Aβ in brain by sustaining the plasmin proteolysis cascade

Series expansion studies of the J 1 − J 2 Heisenberg bilayer

Two-triplon excitations of the Kitaev-Heisenberg bilayer

Tool support for implementing a methodology in magnet development projects at CERN

Successfully Navigating Food and Drug Administration Orphan Drug and Rare Pediatric Disease Designations for AAV9-hPCCA Gene Therapy: The National Institutes of Health Platform Vector Gene Therapy Experience

Design and Synthesis of 5,5′-Disubstituted Aminohydantoins as Potent and Selective Human β-Secretase (BACE1) Inhibitors

Die kompetenzorientierte Klassenarbeit. Neue Aufgabenformate zur Messung von kommunikativen Fertigkeiten

Kompetenzorientierte Leistungsmessung im Französischunterricht. Neue Aufgabenformate bei der Messung von Schülerkompetenzen in Klassenarbeiten

Aminoimidazoles as Potent and Selective Human β-Secretase (BACE1) Inhibitors

Begacestat (GSI-953): a novel, selective thiophene sulfonamide inhibitor of amyloid precursor protein gamma-secretase for the treatment of Alzheimer's disease

Bilayer Kitaev models: Phase diagrams and novel phases

Design and synthesis of aminohydantoins as potent and selective human β-secretase (BACE1) inhibitors with enhanced brain permeability

Regional oral absorption, hepatic first-pass effect, and non-linear disposition of salmon calcitonin in beagle dogs

Discovery of Begacestat, a Notch-1-Sparing γ-Secretase Inhibitor for the Treatment of Alzheimer’s Disease

Di-substituted pyridinyl aminohydantoins as potent and highly selective human β-secretase (BACE1) inhibitors

Acylguanidines as Small-Molecule β-Secretase Inhibitors

Utility of Pharmacodynamic Measures for Assessing the Oral Bioavailability of Peptides. 1. Administration of Recombinant Salmon Calcitonin in Rats

Thiophene substituted acylguanidines as BACE1 inhibitors

"The Lonely Romantic": Nature, Education, and Cultural Pessimism in the Early Works of Hermann Hesse

Discovery and initial optimization of 5,5′-disubstituted aminohydantoins as potent β-secretase (BACE1) inhibitors

Acylguanidine inhibitors of β-secretase: Optimization of the pyrrole ring substituents extending into the S 1 ′ substrate binding pocket

Acylguanidine inhibitors of β-secretase : Optimization of the pyrrole ring substituents extending into the S'1 substrate binding pocket

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