Last Updated: 09/26/2026
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Found 14 publications
Answering the Rehabilitation 2030 Call.
Journal: PM & R : the journal of injury, function, and rehabilitation
Published: December 05, 2023
Novel Small Molecules Targeting the Intrinsically Disordered Structural Ensemble of α-Synuclein Protect Against Diverse α-Synuclein Mediated Dysfunctions.
Journal: Scientific reports
Published: May 01, 2019
Targeting the intrinsically disordered structural ensemble of α-synuclein by small molecules as a potential therapeutic strategy for Parkinson's disease.
Journal: PloS one
Published: September 24, 2013
Thermodynamic and kinetic characterization of hydroxyethylamine β-secretase-1 inhibitors.
Journal: Biochemical and biophysical research communications
Published: September 03, 2013
Development of a novel β-secretase binding assay using the AlphaScreen platform.
Journal: Journal of biomolecular screening
Published: April 02, 2013
Structure and function of Parkin E3 ubiquitin ligase reveals aspects of RING and HECT ligases.
Journal: Nature communications
Published: December 13, 2012
Design and synthesis of hydroxyethylamine (HEA) BACE-1 inhibitors: prime side chromane-containing inhibitors.
Journal: Bioorganic & medicinal chemistry letters
Published: December 03, 2012
Design and synthesis of thiophene dihydroisoquinolines as novel BACE1 inhibitors.
Journal: Bioorganic & medicinal chemistry letters
Published: December 03, 2012
Label free fragment screening using surface plasmon resonance as a tool for fragment finding - analyzing parkin, a difficult CNS target.
Journal: PloS one
Published: November 21, 2012
Design and synthesis of highly selective, orally active Polo-like kinase-2 (Plk-2) inhibitors.
Journal: Bioorganic & medicinal chemistry letters
Published: November 19, 2012
Structure-based design of novel dihydroisoquinoline BACE-1 inhibitors that do not engage the catalytic aspartates.
Journal: Bioorganic & medicinal chemistry letters
Published: November 16, 2012
Discovery of a novel [3.2.1] benzo fused bicyclic sulfonamide-pyrazoles as potent, selective and efficacious γ-secretase inhibitors.
Journal: Bioorganic & medicinal chemistry letters
Published: October 03, 2012
Last Updated: 09/26/2026