β‐Arrestin and casein kinase 1/2 define distinct branches of non‐canonical WNT signalling pathways-Reference-Cited by-同舟云学术

β‐Arrestin and casein kinase 1/2 define distinct branches of non‐canonical WNT signalling pathways

Published:2008-10-24 Issue:12 Volume:9 Page:1244-1250
ISSN:1469-221X
Container-title:EMBO reports
language:en
Short-container-title:EMBO Rep

Author:

Bryja Vítězslav¹²,Schambony Alexandra³,Čajánek Lukáš¹,Dominguez Isabel⁴,Arenas Ernest¹,Schulte Gunnar⁵

Affiliation:

1. Laboratory of Molecular Neurobiology, Department of Medical Biochemistry & Biophysics, Karolinska Institutet Scheeles vag 1 S‐171 77 Stockholm Sweden

2. Institute of Biophysics of Academy of Sciences of the Czech Republic & Institute of Experimental Biology, Faculty of Science, Masaryk University Kotlarska 2 611 37 Brno Czech Republic

3. Zoologisches Institut II, Universität Karlsruhe (TH) Kaiserstrasse 12 D‐76131 Karlsruhe Germany

4. Boston University, Boston 650 Albany Street Massachusetts 02118 USA

5. Section of Receptor Biology & Signaling, Department of Physiology & Pharmacology, Karolinska Institutet Nanna Svartz väg 2 S‐171 77 Stockholm Sweden

Publisher

EMBO

Subject

Genetics,Molecular Biology,Biochemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1038/embor.2008.193

Reference25 articles.

1. Inhibition of endocytosis blocks Wnt signalling to ?-catenin by promoting dishevelled degradation

2. beta-Arrestin is a necessary component of Wnt/beta-catenin signaling in vitro and in vivo

3. Wnt-3a utilizes a novel low dose and rapid pathway that does not require casein kinase 1-mediated phosphorylation of Dvl to activate β-catenin

4. Wnt-5a induces Dishevelled phosphorylation and dopaminergic differentiation via a CK1-dependent mechanism

5. Casein Kinase 2 Is Activated and Essential for Wnt/β-Catenin Signaling

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