Structural analysis of pathogenic mutations in theDYRK1Agene in patients with developmental disorders-Reference-Cited by-同舟云学术

Structural analysis of pathogenic mutations in theDYRK1Agene in patients with developmental disorders

Published:2017-01-04 Issue: Volume: Page:ddw409
ISSN:0964-6906
Container-title:Human Molecular Genetics
language:en
Short-container-title:Hum. Mol. Genet.

Author:

Evers Jochem M.G.,Laskowski Roman A.,Bertolli Marta,Clayton-Smith Jill,Deshpande Charu,Eason Jacqueline,Elmslie Frances,Flinter Frances,Gardiner Carol,Hurst Jane A.,Kingston Helen,Kini Usha,Lampe Anne K.,Lim Derek,Male Alison,Naik Swati,Parker Michael J.,Price Sue,Robert Leema,Sarkar Ajoy,Straub Volker,Woods Geoff,Thornton Janet M.,Wright Caroline F.,

Publisher

Oxford University Press (OUP)

Subject

Genetics (clinical),Genetics,Molecular Biology,General Medicine

Reference42 articles.

1. The MNB/DYRK1A protein kinase: Genetic and biochemical properties

2. DYRK1A accumulates in splicing speckles through a novel targeting signal and induces speckle disassembly

3. Dual-Specificity Tyrosine Phosphorylation-Regulated Kinase 1A Does Not Require Tyrosine Phosphorylation for Activity in Vitro

4. Identification of the autophosphorylation sites and characterization of their effects in the protein kinase DYRK1A

5. Activation-Loop Autophosphorylation Is Mediated by a Novel Transitional Intermediate Form of DYRKs

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