The Usher syndrome 1C protein harmonin regulates canonical Wnt signaling

The Usher syndrome 1C protein harmonin regulates canonical Wnt signaling

Human Usher syndrome (USH) is the most common form of hereditary combined deaf-blindness. USH is a complex genetic disorder, and the pathomechanisms underlying the disease are far from being understood, especially in the eye and retina. The USH1C gene encodes the scaffold protein harmonin which orga...

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Bibliographic Details
Main Authors: Jessica Schäfer, Nicole Wenck, Katharina Janik, Joshua Linnert, Katarina Stingl, Susanne Kohl, Kerstin Nagel-Wolfrum, Uwe Wolfrum
Format: Article
Language:English
Published: Frontiers Media S.A. 2023-02-01
Series:Frontiers in Cell and Developmental Biology
Subjects:
Usher syndrome
USH1C
β-catenin
translational read-through inducing drugs
ataluren/PTC124
colorectal cancer
Online Access:https://www.frontiersin.org/articles/10.3389/fcell.2023.1130058/full

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https://www.frontiersin.org/articles/10.3389/fcell.2023.1130058/full

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