Usherin defects lead to early-onset retinal dysfunction in zebrafish-Reference-Cited by-同舟云学术

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Usherin defects lead to early-onset retinal dysfunction in zebrafish

Published:2018-08 Issue: Volume:173 Page:148-159
ISSN:0014-4835
Container-title:Experimental Eye Research
language:en
Short-container-title:Experimental Eye Research

Author:

Dona Margo,Slijkerman Ralph,Lerner Kimberly,Broekman Sanne,Wegner Jeremy,Howat Taylor,Peters Theo,Hetterschijt Lisette,Boon Nanda,de Vrieze Erik,Sorusch Nasrin,Wolfrum Uwe^ORCID,Kremer Hannie,Neuhauss Stephan^ORCID,Zang Jingjing,Kamermans Maarten^ORCID,Westerfield Monte,Phillips Jennifer,van Wijk Erwin

Funder

Stichting Nederlands Oogheelkundig Onderzoek

Stichting Blindenhulp

Stichting Researchfonds Nijmegen

Landelijke Stichting voor Blinden en Slechtzienden

Foundation Fighting Blindness USA

Stichting Wetenschappelijk Onderzoek Doof-Blindheid

Stichting Ushersyndroom

FAUN Stiftung Nuernberg

Forschung contra Blindheit - Initiative Usher syndrome e.V

JGU Mainz S1

German Research Council (DFG)

National Institute of Health

Vision for A Cure

The Megan Project

University of Oregon Usher Syndrome Research Fund

Publisher

Elsevier BV

Subject

Cellular and Molecular Neuroscience,Sensory Systems,Ophthalmology

Reference60 articles.

1. Usherin, the defective protein in Usher syndrome type IIA, is likely to be a component of interstereocilia ankle links in the inner ear sensory cells;Adato;Hum. Mol. Genet.,2005

2. The USH2A c.2299delG mutation: dating its common origin in a Southern European population;Aller;EJHG (Eur. J. Hum. Genet.),2010

3. Enrichment of LOVD-USHbases with 152 USH2A genotypes defines an extensive mutational spectrum and highlights missense hotspots;Baux;Hum. Mutat.,2014

4. Rod contributions to the electroretinogram of the dark-adapted developing zebrafish;Bilotta;Dev. Dynam.,2001

5. Complexes of Usher proteins preassemble at the endoplasmic reticulum and are required for trafficking and ER homeostasis;Blanco-Sanchez;Dis. Model. Mech.,2014

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