A novel DYRK1A (Dual specificity tyrosine phosphorylation-regulated kinase 1A) inhibitor for the treatment of Alzheimer's disease: effect on Tau and amyloid pathologies in vitro

Author:

Coutadeur Séverine1,Benyamine Hélène1,Delalonde Laurence1,de Oliveira Catherine1,Leblond Bertrand1,Foucourt Alicia2,Besson Thierry2,Casagrande Anne-Sophie1,Taverne Thierry1,Girard Angélique1,Pando Matthew P.1,Désiré Laurent1

Affiliation:

1. Diaxonhit; Paris France

2. Normandie Univ; COBRA; UMR 6014 & FR 3038; Univ Rouen; INSA Rouen; CNRS; IRCOF; 1 rue Tesnière; Mont St Aignan Cedex; Paris France

Funder

MESR

LABEX SynOrg

Publisher

Wiley

Subject

Cellular and Molecular Neuroscience,Biochemistry

Reference46 articles.

1. Specific tau phosphorylation sites correlate with severity of neuronal cytopathology in Alzheimer's disease;Augustinack;Acta Neuropathol.,2002

2. High-content siRNA screening of the kinome identifies kinases involved in Alzheimer's disease-related tau hyperphosphorylation;Azorsa;BMC Genom,2010

3. Tau-mediated neurodegeneration in Alzheimer's disease and related disorders;Ballatore;Nat. Rev. Neurosci.,2007

4. Sequence characteristics, subcellular localization, and substrate specificity of DYRK-related kinases, a novel family of dual specificity protein kinases;Becker;J. Biol. Chem.,1998

5. DYRK1A: a potential drug target for multiple down syndrome neuropathologies;Becker;CNS Neurol. Disord. Drug Targets.,2014

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